Monday 18 July 2016

Application of metabonomic analytical techniques in modernization of Chinese medicine.

Abstract

In the recent years, a wide range of metabonomic analytical techniques are widely used in the modern research of traditional Chinese medicine (TCM). At the same time, the international community has attached increasing importance to TCM toxicity problems. Thus, many studies have been implemented to investigate the toxicity mechanisms of TCM. Among these studies, many metabonomic-based methods have been implemented to facilitate TCM toxicity investigation. At present, the most prevailing methods for TCM toxicity research are mainly single analysis techniques using only one analytical means. These techniques include nuclear magnetic resonance (NMR), gas chromatography-mass spectrometry (GC-MS), and liquid chromatography-mass spectrometry (LC-MS), etc.; with these techniques, some favourable outcomes have been gained in the toxic reaction studies of TCM, such as the action target organs assay, the establishment of action pattern, the elucidation of action mechanism and the exploration of action material foundation. However, every analytical technique has its advantages and drawbacks, no existing analytical technique can be versatile. Multi-analysed techniques can partially overcome the shortcomings of single-analysed techniques. Combination of GC-MS and LC-MS metabolic profiling approaches has unravelled the pathological outcomes of aristolochic acid-induced nephrotoxicity, which can not be achieved by single-analysed techniques. It is believed that with the further development of metabonomic analytical techniques, especially multi-analysed techniques, metabonomics will greatly promote TCM toxicity research and be beneficial to the modernization of TCM in terms of extending the application of modern means in the TCM safety assessment, assisting the formulation of TCM safety norms and establishing the international standards indicators.

Introduction

Metabonomics is an emerging subject of the post-genome era, which, together with genomics, transcriptomics and proteomics, jointly constitutes the ‘Systems Biology’. Metabonomics is the branch of science concerned with the quantitative understandings of the metabolite component of integrated living systems and its dynamic responses to the changes of both endogenous factors (such as physiology and development) and exogenous factors (such as environmental factors and xenobiotics). Recently, as a novel systemic approach to study metabolic profile and accelerate the course of drug development, metabonomics has achieved great growth, which is attracting more and more concerns from the academic community. The main subjects of metabonomics are a variety of predominantly low molecular weight metabolites that serve as the substrates and products of metabolic pathways, and its main biological samples are urine, plasma and serum. Integrity of metabonomic processes includes sample collection and pretreatment, data collection and analysis, and metabolic variation interpretation. Generally, the main technologies metabonomics relied are the nuclear magnetic resonance (NMR)-based method, chromatography-based method and mass spectrometry (MS)-based method. Depending on a series analysis of different sample spectra and combination with chemical pattern recognition methods, metabonomics can be used to identify organisms in pathophysiological state, gene function, drug toxicity and efficacy, and associated biomarkers.

Resource: http://www.ncbi.nlm.nih.gov
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Pure Garcinia Cambogia Extract usage as a Weight Loss Supplement

Abstract

The aim of this systematic review is to examine the efficacy of Garcinia extract, hydroxycitric acid (HCA) as a weight reduction agent, using data from randomised clinical trials (RCTs). Electronic and nonelectronic searches were conducted to identify relevant articles, with no restrictions in language or time. Two independent reviewers extracted the data and assessed the methodological quality of included studies. Twenty-three eligible trials were identified and twelve were included. Nine trials provided data suitable for statistical pooling. The meta-analysis revealed a small, statistically significant difference in weight loss favouring HCA over placebo (MD: −0.88 kg; 95% CI: −1.75, −0.00). Gastrointestinal adverse events were twice as common in the HCA group compared with placebo in one included study. It is concluded that the RCTs suggest that Garcinia extracts/HCA can cause short-term weight loss. The magnitude of the effect is small, and the clinical relevance is uncertain. Future trials should be more rigorous and better reported.

Introduction

The prevalence of overweight and obesity has increased over the last decade, and current measures have not been able to stem the tide. A wide variety of weight management strategies are presently available, and some involve the use of dietary supplements marketed as slimming aids. One such slimming aid is Garcinia extract, (-)-hydroxycitric acid (HCA).

HCA is a derivative of citric acid and can be found in plant species native to South Asia such as Garcinia cambogia, Garcinia indica, and Garcinia atroviridis. HCA is usually marketed as a weight loss supplement either alone or in combination with other supplements. Some authors have suggested that HCA causes weight loss by competitively inhibiting the enzyme adenosine triphosphatase-citrate-lyase. HCA has also been reported to increase the release or availability of serotonin in the brain, thereby leading to appetite suppression. Other postulated weight loss mechanisms include inhibition of pancreatic alpha amylase and intestinal alpha glucosidase, thereby leading to a reduction in carbohydrate metabolism.

Animal studies have suggested that HCA causes weight loss, and human trials involving the use of HCA as a weight loss supplement have been carried out.

The primary objective of this systematic review was to examine the efficacy of HCA in reducing body weight in humans, using data from randomised clinical trials.

Methods

Electronic searches of the literature were conducted in the following databases: Medline, Embase, The Cochrane Library, Amed, and Cinahl. The search terms used included dietary supplements, antiobesity agents, body weight, hydroxycitrate, garcinia, and derivatives of these. Each database was searched from inception until March, 2010. We also searched the Internet for relevant conference proceedings and hand searched relevant medical journals, and our own files. The bibliographies of all located articles were also searched.

Only randomised, double-blind, placebo-controlled studies were included in this paper. To be considered for inclusion, studies had to test the efficacy of oral HCA or any of its salts for weight reduction in obese or overweight humans. Included studies also had to report body weight as an outcome. No age, time, or language restrictions were imposed for inclusion of studies. Studies which involved the use of HCA as part of a combination treatment (dietary interventions containing other supplements in addition to HCA), or not involving obese or overweight subjects based on body mass index (BMI) values, were excluded from this paper.

Two independent reviewers assessed the eligibility of studies to be included in the paper. Data were extracted systematically by two independent reviewers according to the patient characteristics, interventions, and results. The methodological quality of all included studies was assessed by the use of a quality assessment checklist adapted from the Consolidated Standard of Reporting Trials (CONSORT) guidelines. In addition, the Jadad score was also used to assess the quality of included studies. Disagreements were resolved through discussion with the other authors.

Data are presented as means with standard deviations. Mean changes in body weight were used as common endpoints to assess the differences between HCA and placebo groups. Using the standard meta-analysis software , we calculated mean differences (MDs) and 95% confidence intervals (CIs). Studies included in the meta-analysis were weighted by SD (a proxy for study size). If a trial had 3 arms, only the HCA and placebo arms were included in the meta-analysis. The I2 statistic was used to assess for statistical heterogeneity amongst studies. A funnel plot was used to test for publication bias.

Resource: http://www.ncbi.nlm.nih.gov
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Sunday 3 July 2016

Explorations of Chemistry and Biology of the Caged Garcinia Xanthones

Abstract

Natural products have been a great source of many small molecule drugs for various diseases. In spite of recent advances in biochemical engineering and fermentation technologies that allow us to explore microorganisms and the marine environment as alternative sources of drugs, more than 70% of the current small molecule therapeutics derive their structures from plants used in traditional medicine. Natural-product-based drug discovery relies heavily on advances made in the sciences of biology and chemistry. Whereas biology aims to investigate the mode of action of a natural product, chemistry aims to overcome challenges related to its supply, bioactivity, and target selectivity. This review summarizes the explorations of the caged Garcinia xanthones, a family of plant metabolites that possess a unique chemical structure, potent bioactivities, and a promising pharmacology for drug design and development.

Introduction

The trees of the genus Garcinia belong to the family of Guttiferae (Clusiaceae) and are found mostly in lowland rainforests of India, Indochina, Indonesia, West and Central Africa, and Brazil. They are slow-growing polygamous trees that produce scented flowers and fruits that often contain a fleshy, edible endocarp. Throughout the years Garcinia trees have retained considerable value as sources for medicines, pigments, gums, waxes, resins, foodstuffs (fruit), fuel (wood, seed oil), and lumber. Arguably, the most widely cultivated and well-known Garcinia tree is Garcinia mangostana. It yields one of the most highly prized tropical fruits, the mangosteen, valued for its delicious endocarp and rind, both of which are thought to have medicinal potential.

The utility of the Garcinia trees in the arts and sciences is well documented. In fact, gamboge, the pulverized gold-colored resin collected primarily from Garcinia hanburyi, and to a lesser extent from Garcinia morella, has a particularly long and rich history in the arts and sciences. For instance, the yellow colorant used on 8th century artifacts from East Asia is presumed to be a gamboge-based water-color. The importation of gamboge in Europe took place in the 15–16th century where it was used mainly as a coloring material by Flemish painters. In fact, this pigment has been noted on a painting by Rembrandt, currently found in the Staatliche Kunstsammlungen Museum in Dresden.The toxicity of gamboge was also noted early on and several accounts warn against licking brushes containing gamboge. In the recent years, gamboge has been utilized primarily for research on identification of biologically active substances. Nonetheless, it is worth noting that Jean Baptiste Perrin used a colloidal suspension of gamboge particles to investigate Brownian motion and derive a value for the Avogadro number in a series of experiments that gave him the Nobel Prize in physics in 1926.

Resource: http://www.ncbi.nlm.nih.gov
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Protective effect of Garcinia against oxidative stress

Abstract
 
Background
Obesity became major health problem in the world, the objective of this work was to examine the effect of high sucrose and high fat diet to induce obesity on antioxidant defense system, biochemical changes in blood and tissue of control, non treated and treated groups by administration of Garcinia cambogia, and explore the mechanisms that link obesity with altered renal function.

Methods

Rats were fed a standard control diet for 12 week (wk) or a diet containing 65% high sucrose (HSD) or 35% fat (HFD) for 8 wk and then HFD group divided into two groups for the following 4 wks. One group was given Garcinia+HFD, the second only high fat, Also the HSD divided into two groups, 1st HSD+Garcinia and 2nd HSD. Blood and renal, mesenteric, Perirenal and epididymal adipose tissues were collected for biochemical assays.

Results

HFD and HSD groups of rats showed a significant increase in feed intake, Body weight (BW) and body mass index (BMI). Also there were significant increases in weights of mesenteric, Perirenal and epididymal adipose tissues in HFD and HSD groups.

HFD and HSD affect the kidney by increasing serum urea and creatinine levels and decreased level of nitric oxide (NO) and increased blood glucose, low density lipoproteins (LDL), triacylglycerol (TG), total cholesterol (TC) and malondialdehyde (MDA). Glucose 6-phosphate dehydrogenase (G6PD) activities were significantly decreased in HFD while there were significant increases in HSD and HSD+G groups p ≤ 0.05 compared with control. Moreover, renal catalase activities and MDA levels were significantly increased while NO level was lowered. These changes improved by Garcinia that decreased the oxidative stress biomarkers and increased NO level.

There were significant positive correlations among BMI, kidney functions (Creatinine and urea), TG and Oxidative markers (renal MDA and catalase).

Conclusions


Rats fed a diet with HFD or HSD showed, hypertriglyceridemia, increased LDL production, increased oxidative stress and renal alteration. Moreover, suggesting association between lipid peroxidation, obesity and nephropathy, while Garcinia ameliorated the damaging effects of the HFD or HSD and decreased feed intake, MDA level and decreased oxidative stress in renal tissues.

Resource: http://www.ncbi.nlm.nih.gov
Resource: http://www.nutritionforest.com/

Monday 27 June 2016

Garcinia Combogia updates on Antiobesity

Abstract

Garcinia is a plant under the family of Clusiaceae that is commonly used as a flavouring agent. Various phytochemicals including flavonoids and organic acid have been identified in this plant. Among all types of organic acids, hydroxycitric acid or more specifically (−)-hydroxycitric acid has been identified as a potential supplement for weight management and as antiobesity agent. Various in vivo studies have contributed to the understanding of the anti-obesity effects of Garcinia/hydroxycitric acid via regulation of serotonin level and glucose uptake. Besides, it also helps to enhance fat oxidation while reducing de novo lipogenesis. However, results from clinical studies showed both negative and positive antiobesity effects of Garcinia/hydroxycitric acid. This review was prepared to summarise the update of chemical constituents, significance of in vivo/clinical anti-obesity effects, and the importance of the current market potential of Garcinia/hydroxycitric acid.
 
Introduction

The world is in health transition. Infection as a major cause of suffering and death is giving way to new epidemics of noncommunicable disorders such as cancer, cardiovascular diseases, and diabetes, which continue to plague the world at an alarming rate. A trend of increasing prevalence of obesity and obesity-related comorbidity and mortality was observed over the last few decades. The International Association of the Study of Obesity (IASO) reported on the country rankings in terms of percentage global prevalence of adult obesity (BMI ≥ 30 kg/m2) in the year of 2012, where Tonga ranks first with 56.0% obese adults (46.6% of obese male and 70.3% of obese female). In the United States, IASO reported that 35.5% of men and 35.8% women were obese (BMI ≥ 30). Overweight and obesity are diagnosed based on the body mass index (BMI), which is defined as quotient of body weight (kg) over the square of stature (m2). 

According to the World Health Organization (WHO) standard, overweight subjects are diagnosed with BMI values in the range of 25–29.99. Obesity itself, defined as BMI ≥ 30, is associated with several chronic and debilitating health problems including hyperlipidemia, hypertension, coronary heart disease, diabetes, cancer, disease of the gall bladder, osteoarthritis, shortage of breath, abnormal dilation of the veins, backache, and even psychological problems.

There are a few drugs in the market to ameliorate or prevent obesity, but there are costs, efficacy, and side effects to be considered. For example, the currently available pharmacological agents, Sibutramine, Rimonabant, Orlistat, and Phentermine which are licensed for weight reduction therapy, appear to possess some adverse effects. Phentermine, for instance, has been reported to cause dry mouth, insomnia, headache, dizziness, fatigue, and palpitation. In year 2010, FDA had announced the market withdrawal of Meridia (Sibutramine) due to its risk of serious cardiovascular events. Natural products and plant-based dietary supplements have been used by people for centuries. Evidence is starting to emerge to shed light on the consumption of herbs as an effective strategy for disease treatment and health maintenance. Several ethnobotanical studies have reported the bioprospecting surveys on the positive application of herbs in the treatments for obesity. Garcinia has been used for centuries in Asian countries for culinary purposes as a condiment and flavoring agent in place of tamarind or lemon and to make meals more filling. Besides its use as a flavouring agent, the dried rind of G. cambogia combined with salt and other organic acids can help to lower the pH and thus provides a bacteriostatic effect in curing fish. G. cambogia contains large amounts of hydroxycitric acid (HCA). Similar to G. cambogia, G. atroviridis and G. indica also contain significant HCA content and are sometimes used interchangeably with G. cambogia in food preparation. The different features among these three different types of Garcinia are summarised.

A myriad of health effects have been attributed to Garcinia (including G. cambogia, G. atroviridis, and G. indica), such as antiobesity effects, antiulcerogenic, antioxidative, antidiabetes, antimicrobial, antifungal, anti-inflammatory, and anticancer effects. In particular, the antiobesity effects of Garcinia or more specifically of its HCA content have been elucidated with unprecedented clarity over the last few decades. Besides its efficacy in the reduction of body weight and food intake, Garcinia/HCA has been proven to be beneficial in ameliorating obesity-related complications such as inflammation, oxidative stress, and insulin resistance. The results obtained from several studies supported the positive effects of HCA administration alone or in combination with other ingredients on body weight loss, reduced food intake, increased fat oxidation, or energy expenditure (EE) whereas some studies did not.

In spite of the vastly reported prominent role of HCA in inducing satiety, reduced energy intake and weight gain, and improved blood parameters and substrate oxidation, controversial results regarding its efficacy and safety as an antiobesity dietary supplement had also been reported. Evidence from the in vitro, in vivo, and clinical trials on the safety of Garcinia/HCA as a dietary supplement for treating obesity had been extensively reviewed. However, the efficacy of Garcinia/HCA remains the subject of debate. Despite the previously stated issues, on conclusive evidence for HCA's efficacy in promoting weight loss and suppressing food intake, the marketing of a plethora of over-the-counter slimming aids containing HCA has taken place. The aim of this review is to critically assess the evidence from a very broad range of reports, rigorous clinical trials, systematic reviews, and meta-analyses on the efficacy and potential of Garcinia/HCA as an antiobesity dietary supplement.
 
Uses in Traditional Medical Systems

Botanical dietary supplements usually contain a complex mixture of phytochemicals which have additive or synergistic interactions. Aside from its use as a preservative and as a condiment in cuisine, Garcinia extract has been used in the traditional Ayurvedic medical system. A decoction of G. cambogia is given as purgative in the treatment of intestinal worms and other parasites, for bilious digestive conditions, for dysentery, rheumatism, and in the treatment of tumours. Less commonly, extracts are employed as cardiotonics to treat angina. In veterinary medicine, it is used as a rinse for diseases of the mouth in cattle. The fruit rind is used in rickets and enlargement of spleen and to heal bone fractures. In Southeast Asian folkloric medicine, a decoction of G. atroviridis (leaves and roots) is sometimes used for the treatment of cough, dandruff, earache, stomach pains associated with pregnancy, and throat irritation. The dried fruit of G. atroviridis is used for improving blood circulation, for the treatment of coughs, as a laxative, and as a expectorant. The fruit is used in a lotion with vinegar to rub over the abdomen of women after confinement. Fruit of G. indica is antiscorbutic, cholagogue, cooling, antibilious, emollient, and demulcent. The anthelmintic properties of the fruit of G. indica contributed to its use in haemorrhoids, dysentery, tumor, pains, and heart complaints. Bilious affected sites are treated with syrup from the fruit juice. Kokum butter is astringent and demulcent and is used in diarrhea and dysentery. It is also applied externally for ulcerations, sinuses, fissures of hand, lip, chapped skin, and skin diseases.
 
3. Phytoconstituents

The several compounds which have been isolated from various species of Garcinia are summarised in Table 2. Several types of organic acids such as HCA, citric, tartaric, malic, and succinic acids are isolated from Garcinia. However, HCA is the principal acid of the fruit rinds of G. cambogia, G. indica, and G. atroviridis, with its content ascending as listed. A substantial amount of (−)-HCA, up to 30% by weight is present in the pericarp of the fruit of G. cambogia. In similar studies conducted by Sullivan et al. and Stallings et al., they observed that of the four isomers of HCA [(–)-HCA, (+)-HCA, (–)-allo-HCA, and (+)-allo-HCA], (−)-HCA, which is also known as (2S, 3S)-HCA, was the only potent inhibitor of ATP citrate lyase. (−)-HCA can be chemically synthesized using citric acid as starting material. Synthetic (−)-HCA offers several advantages including higher purity and lactone stable as compared to natural (−)-HCA [81]. On the other hand, (−)-HCA is a good starting material to synthesize other important chiral synthons and compounds [82].

Phytochemicals of Garcinia.

(−)-HCA is one of the important supplements for antiobesity and weight management. Its effect on weight management is mainly contributed by giving the feeling of full and satisfaction while the antiobesity effect is by reduction of de novo lipogenesis and acceleration of fat oxidation. In this paper, we aimed to review the mechanism for antiobesity and weight management effects by (−)-HCA (hereafter referred to as HCA)/G. cambogia/G. atroviridis/G. indica extracts and the assessment of these effects in the clinical settings.

Possible multiple mechanisms that contribute to antiobesity effect of Garcinia/HCA. ↑ indicated increase or stimulation; ↓ indicated reduce or inhibition while ?? indicated that the effect is yet to be confirmed. (A) summary of Serotonin ...

Salts of HCA

On account to the discovery of (−)-HCA as an effective compound in weight management, market demand for the acid has increased tremendously. The commercially available G. cambogia extracts which contain approximately 50% (−)-HCA are prepared from the fruit rind. HCA can exist as a free acid or in the lactone form. The former form is considered to be biologically active. However, the free acid is unstable and is usually converted to its less active lactone form to attain higher stability. To prevent the cyclization of HCA into its less potent lactone, the acid has been combined with various counter ions to form stable salts.

Commercial HCA is available in free acid form and as single, double, or triple salts. Preparations with different counter ions contribute to different degree of solubility as well as bioavailability. For example, Na+ salt of HCA had been shown to be more effective than its lactone in inhibiting lipogenesis. However, Na+ salt is highly hygroscopic when bound to (−)-HCA, which would deemed unfavorable for the production of pharmaceuticals for dry delivery.

To address the need to achieve higher solubility and stability, recent approaches have been focused more on the preparation of (−)-HCA in the form of a double or triple salt. Similar to its single salts, these double or triple salts also serve as good supply for essential ions. A remarkable example of these would be the Ca2+/K+ salt of (−)-HCA (HCA-SX) or Super CitriMax. In contrast to the single salts, HCA-SX is completely soluble in water and thus confers higher bioavailability. A number of studies on the safety of HCA-SX had been reported. Daily intake of HCA-SX at this dosage was shown to be effective in reducing body weight and BMI of healthy and obese adults after clinical trials of 8 weeks. Gene expression studies also provided additional evidence for the safety of HCA-SX, where genes essential for mitochondrial/nuclear proteins and for fundamental support of adipose tissue were shown to be independent of the regulation by HCA-SX.

A typical reduction of food appetite and an increased serotonin availability were observed in all the weight control studies of HCA-SX on both animal and human subjects. These were associated with reduced levels of total cholesterol, LDL, triglycerides, and serum leptin as well as increased HDL level and urinary excretion of fat metabolites. In rats, the salt also caused downregulation of genes encoding abdominal fat leptin while expressions of the plasma leptin genes remained unaltered. Nevertheless, it was postulated that a set of obesity regulatory genes [84] and inhibition to the uptake of [3H]-5-HT release in the brain are involved in the appetite suppressing activity of HCA-SX.

In relation to this, gene expression profiling carried out by a research group demonstrated the modulation of a specific set of genes (about 1% of 9960 genes and ESTs) in the adipocytes by dietary HCA-SX supplementation. Further study on cultured mature human adipocytes revealed significant upregulation of 366 and downregulation of 348 the fat- and obesity-related genes [88]. Notably also in the microarray analyses, HCA-SX demonstrated a distinct effect on appetite suppression whereby genes encoding serotonin receptors were shown to be selectively upregulated by the salt. Besides, HCA-SX was also found to be capable of activating hypoxia inducible factor (HIF), a transcription factor involved in energy metabolism and restored the increase in oxidative stress, inflammation, and insulin resistance in obese Zucker rats.
Antiobesity Effects of Garcinia/HCA

Obesity, particularly caused by accumulation of visceral fat, is a serious risk factor of various life-style diseases such as coronary heart disease, diabetes, hyperlipidemia, hypertension, and cancer [2, 4]. Human obesity is influenced by genetic and environmental factors and particularly by changes in diet and physical activity, which contributes greatly to the development of insulin resistance, a most common underlying abnormality in human obesity [89]. Studies on food sources exerting antiobesity effects have focused on the development of herbal extracts or functional food which can suppress the accumulation of body fat. Several studies were conducted to provide scientific basis on the extensive usage of G. cambogia and G. atroviridis associated with high-fat diet- (HFD-) induced obesity where dyslipidemia, fatty liver, insulin resistance, and hyperleptinemia were acquired along with the overexpression of leptin, TNF-α, resistin, PPARγ2, C/EBPα, and SREBP1c genes in epididymal adipose tissue. The effect of G. cambogia was largely attributed to its HCA content [90, 91]. Subsequent researches proved that the antiobesity effects of G. cambogia/HCA resulted from the combined actions of several mechanisms including suppressing de novo fatty acid biosynthesis and appetite [16, 60] and increasing energy expenditure [39], subsequently reducing body fat accumulation and weight gain in experimental animals [37, 38, 92]. In this review, we arranged the antiobesity effects of Garcinia/HCA based on their distinct mechanisms: (1) serotonin regulation and food intake suppression, (2) decreased de novo lipogenesis, (3) increased fat oxidation, and (4) downregulation of a spectrum of obesity-associated genes.

Serotonin (5-Hydroxytryptamine, 5-HT) Regulation and Food Intake Suppression

HCA, the primary acid in the fruit rinds of G. cambogia, G. atroviridis, and G. indica, has been reported as the active ingredient in inhibiting ATP citrate lyase (EC 4.1.3.8). ATP citrate lyase, which is an extramitochondrial enzyme catalyzing the cleavage of citrate to oxaloacetate and acetyl-CoA, was inhibited by HCA. Thus, the availability of two-carbon units required for the initial steps of fatty acid and cholesterol biosynthesis during carbohydrate feeding was limited. As a result, the consumed carbon source was diverted to glycogen synthesis in liver. A signal was then sent to the brain due to this metabolic alteration, resulting in rising of serotonin level concomitant with a reduced appetite. HCA might exhibite its anorectic effect by a second possible mechanism, namely, reducing acetyl CoA, subsequently decreasing malonyl CoA levels and thereby reducing negative feedback on carnitine acyltransferase (CPT-1). The substrate of CPT-1, long-chain acyl CoA(s), may act as a mediator(s) of appetite. More recently, neuropeptide Y (NPY) had also been implicated in the appetite suppression of HCA. Basal concentration of the neurotransmitter was claimed to be significantly reduced in the hypothalamic tissues as a result of supplementation with HCA-SX [84]. However, the role of NPY in this is still vague to date. Several reports supported the serotonin regulation of HCA. Ohia et al. demonstrated that HCA-SX enhanced serotonin availability in isolated rat brain cortex by acting as a mild serotonin receptor reuptake inhibitor (SRRI), without stimulating the central nervous system. Kaur and Kulkarni conducted a study to elucidate the effect of OB-200G, a polyherbal preparation containing aqueous extracts of G. cambogia, Gymnema sylvestre, Zingiber officinale, Piper longum, and resin from Commiphora mukul on the modulation of food intake by serotonin modulators in female mice. The results obtained were compared with fluoxetine, a drug that was reported to enhance 5-HT neurotransmission. Both OB-200G and fluoxetine significantly (P < 0.05) antagonized the hyperphagic effect of p-chlorophenylalanine (PCPA), 8-hydroxy-2-(di-N-propylamino)-Tetralin (8-OH-DPAT), cyproheptadine, and 2-deoxy-D-glucose (2-DG) which further instigate possible serotonergic involvement in the effects of OB-200G on food intake in female mice. Preuss et al. reported that HCA caused a significant reduction in appetite, weight loss, and plasma leptin level, concomitant with an increase in the serum serotonin level and a favorable lipid profile in human clinical trials. Similar results were also obtained in a study conducted by Asghar et al. They reported on increased brain serotonin level in obese Zucker rats receiving G. cambogia extract, suggesting that the ability of HCA in body weight gain reduction was most probably due to its combined effects on the metabolic and serotonin pathways. In addition, Roy et al. reported that HCA-SX supplementation upregulated prostaglandin D synthase (PDS), aldolase B (AldB), and lipocalin (LCN2) genes in abdominal fat tissue. Further mapping of the candidate genes of known pathways associated with fat metabolism by using functional categorization and pathway construction software showed that supplementation of HCA-SX targeted on the serotonin receptor.

Leonhardt et al. reported that HCA reduced body weight regain in rats after a period of substantial body weight loss. Besides, HCA temporarily reduced food intake of rats with diets of varying nutrient contents (grounded standard rat chow, high glucose, and high glucose + fat). HCA supplementation caused pronounce suppression of food intake during the entire 10 days of ad libitum feeding period in rats fed with high glucose + fat diet, a diet that had a nutritionally relevant level of dietary fat (24% of energy). These data therefore extended those of the previous studies which reported on the anorectic effects of HCA. Moreover, the results obtained were consistent with studies which reported on particularly strong food intake suppression by HCA with high glucose + fat diet and a smaller but still significant suppression with the high glucose diet in other rat models and in different orders. Hence, the feed conversion efficiency [cumulative body weight regain (g)/cumulative food intake (MJ)] in the high glucose and high glucose + fat groups during the 10 ad libitum days was reduced, which indirectly supported that HCA increased energy expenditure in these groups.

Leonhardt and Langhans [39] then extended their study on the long-term effects of HCA on body weight regain and food intake, as well as the effects of HCA on the circadian distribution of food intake and on meal patterns during the dark and light phases. HCA administration significantly reduced the food intake of rats fed with 12% fat diet, but not 1% fat diet, concomitant with significant reduction in weight regain (overall P < 0.01) in both groups. In the study, the rats underwent restrictive feeding for 10 days prior to ad libitum feeding (Experiment 1: normal 1% fat diet and 1% fat diet + 3% HCA; Experiment 2: normal 12% fat diet and 12% fat diet + 3% HCA). The control groups of both experiments had compensated the body weight loss, whereas the HCA-fed rats groups regained only 68 ± 4% (1% fat diet) and 61 ± 8% (12% fat diet) of the body weight regained by their respective control groups after 22 days of such ad libitum feeding. Despite significant reduction in weight regain in rats fed with 1% and 12% fat diet, long-term suppression of HCA on food intake was only detected in combination with 12% fat diet (Experiment 2). This was in line with the results obtained by Leonhardt et al. who suggested that HCA increased energy expenditure. Studies on the effects of HCA on the circadian distribution of food intake and on meal patterns showed that the suppression of food intake occurred predominantly during the dark phase of the first ad libitum days. However later on, HCA suppression of food intake was more effective during the light phase. Further experiments elucidating the effects of HCA in combination with the 12% fat diet on meal size and meal number during the light phase revealed that HCA markedly reduced the meal number, but not the meal size. HCA did not affect any metabolic variables tested (plasma glucose, lactate, triacylglycerol, HDL, free fatty acids, β-hydroxybutyrate, and insulin, hepatic fact, and glycogen concentrations) in both experiments, except decreasing plasma triacylglycerol levels and increasing the liver fat concentration in Experiment 2 (rats fed with 12% fat diet). The fact that HCA did not affect plasma β-hydroxybutyrate (BHB) levels did not support the hypothesis that HCA suppressed food intake via increased hepatic fatty acid oxidation.

However, contradicting results were obtained by Kovacs et al. who reported that two-week supplementation with HCA and HCA combined with medium-chain triglycerides did not result in increased satiety. The findings were in line with previous reports where no significant treatment effects were observed on appetite indices (inclusive of mean, peak or nadir hunger ratings, mean ratings of desire to eat, prospective consumption, fullness or sensations of thirst, stomach growling, headache, distraction, irritability, or, as a check on malingering, itchiness). The lack of efficacy and transient food intake suppression by HCA raised questions about its clinical significance. While negative findings are always open to methodological questions, several questions need to be answered before drawing a definite conclusion. First, the diet administered to the subjects should not promote extreme sensations in the evaluation of the food intake suppression effects of HCA under conditions of energy restriction. However, Mattes and Bormann imposed mild restrictions and thus ruled out this possibility as evidenced by ratings falling in the middle range of the response scales. Second, an energy-restricted diet would prevent the required enzyme alterations (reduction of acetyl-CoA and suppression of formation of carnitine palmitoyltransferase I inhibitor malonyl CoA) which altered substrate metabolism and satiety. However, it was unlikely that the moderate energy restricted diet prescribed in the study conducted by Mattes and Bormann hindered the satiety effect of HCA as it still contained at least 30% of energy from fat.

Several factors might contribute to the controversial results of the efficacy of HCA in human studies. One of contributing factors is the highly variable doses used in the human trials which ranged from 5 to 250 mg/kg of HCA per day. Besides, the discrepancy might also be due to the differences in the preparation or extraction of HCA. For instance, the extraction method might increase the formation of HCA in a lactone form, which is less potent in the inhibition of ATP citrate lyase. In order to prevent the cyclization of HCA into the less potent lactone form, preparation using different counte rions (such as potassium, sodium, or calcium) had been applied, which contributed to the different degrees of stability, bioavailability, or solubility of HCA. In this respect, Louter-Van De Haar et al. conducted a study on the efficacy of three commercially available HCA products on suppression of food intake in male Wistar rats. Many human studies which reported lack of efficacy used Super CitriMax at considerably lower doses . On the contrary, Preuss et al. reported that high doses of Super CitriMax exerted significant effects in human. Thus, Louter-Van De Haar et al. suggested that the reported lack of efficacy of HCA in suppressing food intake in human subjects might be due to the low doses of a relatively low-effective HCA preparation. Nevertheless, significant suppression of food intake was observed in the studies conducted by Leonhardt and Langhans where Sprague-Dawley rats were supplemented with HCA for 10 days after substantial, fasting-induced weight loss. It seemed that HCA might be more effective in regulating weight gain than promoting weight loss; thus it was more useful for weight maintenance after an initial loss. Hence, differences in the experimental setups such as the difference in rat strains could contribute to such discrepancy.

Decreased De Novo Lipogenesis

The reduction of the acetyl-CoA by HCA and thus limiting the availability of building blocks required for fatty acid and cholesterol biosynthesis has led to suggestions that HCA inhibited lipogenesis. Several studies conducted by Sullivan and colleagues had confirmed the inhibition of in vivo and in vitro rates of lipogenesis in several tissues reported to convert carbohydrate into fatty acids (such as liver, adipose tissue, and small intestine), in which HCA was predominantly given to rodent models. Lowenstein demonstrated that HCA greatly inhibited in vivo fatty acid synthesis in rat liver. The rats were placed on chow diet for 7–10 days, followed by 45 h of fasting prior to a scheduled diet high in fructose or glucose for 10 to 15 days. The sodium salt of HCA at dose levels of 2 to 20 mM was administered by intraperitoneal injections 45 min before injection of 3H2O. Fatty acid biosynthesis in rat liver (μ moles 3H2O incorporated/g liver/h) was measured 3.5–5 h after starting of the final feeding. Profound decrease in fatty acid synthesis by 25 to 30 days was obtained with an intraperitoneal dose of 0.1 mmole per kg of body weight (equivalent to approximately 2.9 mg of HCA per 150 g rat). In addition, 50% of inhibition was detected at a dose level of 0.28 mmole per kg body weight.

It was reported that G. cambogia/HCA affected respiratory quotient (RQ) and EE in rats and human. Lim et al. showed that short-term administration of HCA decreased the RQ in athletes and in untrained women. Leonhardt et al. further extended their study to determine the effect of HCA on RQ and EE in rats fed ad libitum after a period of substantial weight loss. They reported that HCA markedly decreased RQ and EE during the first two days of ad libitum, reflecting suppression of de novo lipogenesis in rats, which is consistent with the findings of Westerterp-Plantenga and Kovacs in humans.

In this respect, Kovacs and Westerterp-Plantenga further extended their study where the effects of HCA on net fat synthesis as de novo lipogenesis were investigated. A double-blind, placebo-controlled, randomized, and crossover design experiment was conducted on 10 sedentary male subjects. The subjects performed glycogen depletion exercise, followed by a 3-day high-fat low-carbohydrate (F/CHO/P, 60/25/15% energy; 100% of EE; depletion period) intake in order to create a similar glycogen storage capacity. Subsequently, a 7-day high-carbohydrate diet (F/CHO/P, <5/>85/10% energy; 130–175% of EE; overfeeding period) supplemented with either 500 mg of regulator HCA (HOB Ireland Ltd.) or placebo was administered. Each intervention ended with a 60 h stay in the respiratory chamber (days 9 and 10). De novo lipogenesis occurred as indicated by RQ > 1.00 in all subjects. Significantly, lower 24 h EE (P < 0.05; on day 9), resting metabolic rate (P < 0.01; on day 10), and RQ at night (P < 0.05; on day 10) were detected with HCA as compared to placebo. Fat balance and thus net fat synthesis as de novo lipogenesis tended to be lower (P < 0.1) with HCA as compared to placebo. Taken all together, Kovacs and Westerterp-Plantenga concluded that the administration of HCA during overfeeding of carbohydrates may reduce de novo lipogenesis.

However, opinions differ widely with respect to this issue. The mechanism underlying the anorectic effect of HCA is still unclear. Furthermore, whether the suppression of body weight regained was solely due to reduced food intake or whether there was involvement of increased EE remained unknown. Contradictory results were reported on the effects of HCA on EE. Previous reports by Leonhardt and colleagues and the results obtained in pair-feeding studies showed reduction of body weight regain and energy conversion ratio by HCA supporting the finding that HCA increased EE. However, reduced energy conversion ratio could be due to decreased nutrient absorption. Vasselli et al. demonstrated an increment in 24 h EE in rats fed with mixed high-carbohydrate diet ad libitum by directly measuring the EE in a whole-body respirometer, albeit no effect on the RQ was detected. Another study conducted by Leray et al. reported that 6 months of HCA administration did not affected EE in adult neutered cats. Besides, most human studies reported that HCA had no effect on EE. Kriketos et al. reported that HCA administration exhibited no effect on lipid oxidation in men during either rest or moderately intense exercise on a cycle ergometer. However, in these studies, the subjects received a much smaller dose, namely, a daily dose of 3.0 g per subject [nearly equal to 1.5 mg/day/mouse]. Furthermore, their experimental period of 3 days was quite short when compared with other studies.

Blunden reported that when Garcinia extract and insulin were added simultaneously, the number of larger droplets markedly decreased while the smaller droplets (10–20 μm2 or <10 μm2) increased in 3T3-L1 cell. The activity of cytosolic glycerophosphate dehydrogenase (GPDH) which converts dihydroxyacetne phosphate to glycerol 3-phosphate (predominant substrate for triglyceride synthesis) increased from undetectable levels to between 100 and 187 U/mg of cytosolic protein after adipose conversion. However, no significant decrease in enzymatic activity was detected after administration of the Garcinia extract. Taken together, the authors therefore suggested that Garcinia extract interferes with lipid synthesis in fat cells via fatty acid supply inhibition without affecting adipose conversion.
5.3. Increased Fat Oxidation

Ishihara et al. conducted a study on acute and chronic effects of HCA on energy metabolism. Acute administration of 10 mg/100 μL of a 0.48 mol/L HCA solution per mice significantly increased (P < 0.05) serum free fatty acid levels and concentration of glycogen in the gastrocnemius muscle, even though the respiratory exchange ratio was not different from that in the control group. On the other hand, chronic administration of 10 mg HCA twice a day significantly lowered (P < 0.01) the RQ during resting and exercising conditions in mice. Lipid oxidation, calculated from RQ, and oxygen consumption were significantly enhanced, and carbohydrate oxidation was significantly less in these mice during the early stages of running (P < 0.01). Taken all together, the authors therefore suggested that chronic administration of HCA augmented the endurance exercise performance in mice via the attenuation of glycogen consumption caused by the promotion of lipid oxidation during running exercise. Furthermore, Ishihara et al. suggested that chronic HCA administration might have increased EE during the 3-week experimental period.

In addition, Lim et al. also showed that short-term administration of HCA increased fat oxidation during exercise in athletes and in untrained women. Lim et al. conducted a randomized, placebo-controlled study where subjects (athletes) consumed HCA (250 mg) or placebo for 5 days, after each time performing cycle ergometer exercise at 60% VO2 max for 60 min followed by 80% VO2 max until exhaustion. The results obtained showed that the respiratory exchange ratio (RER) was significantly lower in the HCA trial than in the control trial (P < 0.05). Fat oxidation was significantly increased by short-term administration of HCA, and carbohydrate oxidation was significantly decreased (P < 0.05) during exercise in athletes. In a continuation of their study, Lim et al. conducted a similar study to evaluate the effects of HCA administration on fat oxidation during exercise in untrained women. The results showed that HCA decreased the RER and carbohydrate oxidation during 1 hour of exercise. In addition, exercise time to exhaustion was significantly enhanced (P < 0.05).

A more recent approach for determining fat metabolism by HCA was conducted by measuring urinary concentration of malondialdehyde (MDA), acetaldehyde (ACT), formaldehyde (FA), and acetone (ACON) of the tested subjects. The urinary excretion of these four metabolites was proposed to be a consequence of enhanced β-oxidation of fats in body tissues. The effect of HCA-SX had been studied extensively by Preuss et al. on obese human subjects as well as on male and female Sprague-Dawley rats. In the randomized, double-blind, and placebo-controlled clinical studies on obese human, a group of subjects were given 4,667 mg of HCA-SX daily (provided 2,800 mg HCA/day) while the other given a combination of HCA-SX 4,667 mg, 4 mg of niacin-bound chromium (NBC), and 400 mg of gymnema sylvestre extract (GSE) daily. The control group received placebo in 3 equal doses daily at 30 to 60 min before meals. In the trial involving 30 subjects, urinary excretion of fat metabolites was increased by approximately 125–258% whereas in trial involving 60 and 90 obese subjects, the metabolite excretion increased by about 35.6–106.4% and 32–109%, respectively. As excretion of fat metabolites was enhanced in groups receiving the combination formula, it was also suggested that HCS-SX, either alone or in combination with NBC and GSE, could effectively promote breakdown of fats.

Downregulation of a Spectrum of Obesity-Associated Genes

Lipogenic transcription factors, including SREBP1c, liver X receptors, PPARγ, and C/EBPα, are highly expressed in the adipose tissue and actively participate in the lipid metabolism of adipocytes by coordinating lipogenic and adipocyte-specific gene expression [114]. PPARγ interacts with several other transcription factors. C/EBPα and PPARγ interact via a positive feedback loop in the differentiated adipocytes, to induce each other's expression. Besides, coexpression of PPARγ with SREBP1c increases the transcriptional activity of PPARγ. aP2 (a marker of terminal adipocyte differentiation), together with several adipocyte-specific genes, including adiponectin, insulin receptor, leptin, glucose transporter 4 (GLUT4), and glycerol phosphate dehydrogenase, are induced during the adipogenic differentiation process. Leptin, a 167-amino acid hormone and a biomarker of the obesity regulatory gene, is produced by fat tissue and is known to regulate energy intake and metabolism. Leptin binds to the medial nucleus of the hypothalamus and induces a sensation of satiety and thus controlling the appetite.

Fatty acid synthase, acetyl-CoA carboxylase 1, and SREBP1c mRNA concentrations were decreased in the adipose tissue of the obese animal models. On the contrary, the mRNA and protein expression of TNFα (which is involved in proinflammation, apoptosis, lipid metabolism, and insulin resistance) were increased in the adipose tissues of the obese rodents and humans. A high level of TNFα suppressed transcription factors such as PPARγ and C/EBPα which, in turn, activated the GLUT4 gene.

Hayamizu et al.evaluated the effects of G. cambogia fruit rind extract containing 60% (–)-HCA on serum leptin and insulin in mice. G. cambogia extract reduced serum total cholesterol, triacylglycerol, and nonesterified fatty acids in mice. Nevertheless, the body weight gain and fat pad weight were not affected in the treatment. No significant difference in blood glucose level was detected between groups, but a significant reduction of serum insulin (P < 0.05) was detected, suggesting that the G. cambogia extract efficiently improved glucose metabolism in the treated animals. In addition, the treatment decreased serum leptin levels and the leptin/WAT ratio. Besides, the changed ratio of body weight correlated positively with leptin levels in their study. Furthermore, it had been reported that leptin suppressed the signal transduction of insulin via cytokine interactions. Hayamizu et al. suggested that the observed effect of G. cambogia extract on serum insulin in their study occurred through leptin-like activity.

The antiobesity effects of Garcinia on visceral fat mass, lipid profiles in the serum and liver, serum adipocytokine levels, and regulation of the expression of multiple adipose tissue genes were reviewed. Kim et al. reported the antiobesity effects of a mixture composed of aqueous extract of G. cambogia, soy peptide, and L-carnitine (1.2 : 0.3 : 0.02, w/w/w) on rats rendered obese by high-fat diet (HFD). An HFD (40% fat calories) with identical composition of the high-fat control diet (CD) applied in the study was fed to five-week-old male Sprague-Dawley rats for 9 weeks to create an obese conditions in rats that mimic to human obesity. Body weight gain, visceral fat-pad weight, and serum and hepatic biochemistry of rats were measured. The 0.38% mixture-supplemented HFD (D + M) reduced the total body weight and the accumulation of visceral fat mass and lowered the blood and hepatic lipid levels, which led to the improvement of insulin resistance in the HFD-induced obese rats. Moreover, the mixture of G. cambogia, soy peptide, and L-carnitine improved dyslipidemia in rat models with HFD-induced obesity. Downregulation of the expression of leptin, tumor necrosis factor-alpha, and sterol regulatory element binding protein 1c genes in the epididymal fat tissue of rats fed with CD + M diet was obtained. In contrary, upregulation of the uncoupling protein 2 (UCP2) gene in epididymal adipose tissues was induced with CD + M diet. No effect on the food intake of the animals was observed in the study, suggesting that the mixture exerted antiobesity effect via modulation of the metabolic derangement induced by HFD during which interactions between the multiple genes implicated in the process of adipogenesis might be involved, rather than simply suppressing appetite. A similar observation was obtained by Kim et al, where in addition to the reduction of food intake, the food efficiency ratio (FER) was also significantly lower in the G. cambogia diet administrated group than in the HFD mice, implying less efficient transformation of the feed mass into body mass.
 
Human Clinical Trials

The antiobesity effects of G. cambogia in terms of promoting weight loss and lowering cholesterol level were extensively studied. However, evidence for the effectiveness of G. cambogia or its derivative products was largely derived from animal studies. Despite the intriguing evidence of antiobesity effects of G. cambogia from in vitro and animal studies, more equivocal results were obtained from randomized double-blind placebo-controlled experiments dealing with human subjects. Hayamizu et al. conducted a crossover design randomized controlled trials (RCTs) to determine the “no observed adverse effect level (NOAEL)” of G. cambogia extract in 44 healthy volunteers (22 males and 22 females) and concluded that G. cambogia is generally safe to be consumed. Several equivocal findings of RCTs were reported on the effectiveness of supplements containing HCA. Some studies reported that HCA exerted no significant effects as compared to the placebo group. All the above findings were in agreement with the most recent meta-analysis of RCTs which revealed that G. cambogia extract possessed limited or no effects on weight-loss in human subjects. Moreover, this study showed no effect on satiety or calorie intake in overweight individuals consuming their habitual diet, which is in agreement with past studies. However, such comparisons must be made with caution as the variations in the formulations, doses administered, RCTs designs, and study populations might contribute to the discrepancy of the results.

Preclinical studies using rodent models have confirmed the body weight reduction, appetite suppression, and subsequently food intake reduction effects of HCA in rats. Clinically, however, HCA failed to perform well. Several factors that might contribute to this scenario are the ATP citrate lyase which might be important only at very high carbohydrate diets, a type of diet that most studies did not prescribe. Besides, a high-fiber diet can bind to HCA and block it, thus reducing its efficacy. HCA and G. cambogia exerted potential effects in weight management, but clinical studies have yet to prove optimum conditions for HCA to be effective. For instance, Sullivan et al.reported that hepatic lipid synthesis was reduced only if HCA was administered before the beginning of feeding, reaching optimum 30–60 minutes prior to feeding. The reason for this remains unknown.
 
Patents and Commercialization

The claims on enhanced human health associated with Garcinia/HCA had been reviewed in Section 4. In particular, the antiobesity effects of Garcinia/HCA were extensively reported. This has resulted in the availability of numerous commercialized weight-management products derived from Garcinia/HCA. Several products of G. cambogia or its derivatives had been patented and commercialized. As of August 2012, a total of 66 patents that apply to G. cambogia or HCA derived from Garcinia were filed with the US Patent and Trademark Office (USPTO) since 1976 (search of US Patents and Trademark Office in year 2012 using Google patent search). These patents are on various aspects, including HCA enrichment from Garcinia rind, HCA and food products/dietary supplements prepared therefrom, methods of production, and their use. The majority of the patents are related to G. cambogia/atroviridis and/or HCA derived from Garcinia on obesity and weight loss.

Conclusions

The nutraceutical industry is flourishing, and interest in establishing scientific credibility has attained importance for many companies and scientists. In the recent years, more clinical trials had been conducted to elucidate the functional effects of Garcinia/HCA supplementation on promoting human health. A multitude of metabolic functions had been reported for HCA or HCA-containing Garcinia extract, such as reducing blood lipids, inducing weight loss, suppressing appetite, and reducing food intake based on results obtained in both animal trials and human clinical trials. These discoveries make the development of evidence-based adjuvant modalities to curb the trend of the increasing prevalence of obesity and obesity-related comorbidity and mortality possible. We have previously reviewed and concluded that Garcinia extract and HCA were generally safe to be consumed. Collective results from 17 clinical studies which involved 873 subjects demonstrated the safety of HCA and HCA-SX for human consumption. These studies provided scientific evidence that intake of HCA and HCA-SX alone did not produce adverse effects and a dietary dosage of up to 2800 mg/day was regarded as the “no observed adverse effect level (NOAEL)” of HCA-SX in human. Based on these animal and human safety data, HCA-SX also received self-affirmed GRAS status in the USA by the Burdock Group in year 2003. However, definitive conclusions that Garcinia/HCA supplements are efficient tools against various health problems especially obesity remain to be proven in larger-scale and longer-term clinical trials, despite substantial public interest in such supplements. Many diet supplements containing Garcinia/HCA marketed as weight management products are the combination of active ingredients rather than containing a single agent. Thus it is difficult to evaluate the effectiveness of single agents when the combination products are tested. In addition, awareness of the safety and efficacy of the weight management supplements available in the market should be raised among health care providers in order to assist their patients in analyzing the risks and benefits of the dietary supplements. Thus, scientific investigations on the potential health promoting effects of herbal preparations as diet supplement are prerequisites for new discoveries of alternative therapies.

Resource: http://www.ncbi.nlm.nih.gov/

How Gracinia Combogia contributes to Glucose Tolerance in Male Wistar Rat

Abstract

Introduction: Obesity leads to derangements in lipid and glucose homeostasis resulting in various metabolic complications. Plants containing vital phytochemicals are known to posses anti obesity properties and have proved to exert beneficial effects in obesity.

Objectives: The present study was aimed to investigate the effects of Garcinia Cambogia on body weight, glucose tolerance and inflammation in high fat diet fed male Wistar rats.

Materials and Methods: Five month old male wistar rats (n=40) were divided into four groups. Two groups were fed with standard rodent diet and the remaining two with 30% high fat diet. One group in each of the two sets received the crude ethanolic extract of Garcinia Cambogia at a dose of 400mg/kg body weight/day for ten weeks. Body weight, intraperitoneal glucose tolerance test, leptin, tumour necrosis factor-α (TNF-α) and renal function (urea, creatinine, uric acid) were studied.

Results: High fat diet fed rats showed increased body weight gain, glucose intolerance, elevated levels of plasma leptin and TNF-α. Supplementation of Garcinia Cambogia extract (GE) along with high fat diet significantly decreased body weight gain, glucose intolerance, plasma leptin and TNF-α level. No significant changes were observed in the renal function parameters in any of the groups.

Conclusion: Supplementation of the Garcinia Cambogia extract with high fat diet reduced body weight gain, inflammation and glucose intolerance.
 
Introduction

Obesity occurs due to imbalance between food consumption and energy expenditure. It is a vital risk factor for the global burden of chronic disease and disability. Obesity increases the risk of several complications like diabetes mellitus, cardiovascular disease, hypertension and certain cancers. Chronic consumption of fat rich diet leads to dyslipidemia which is characterized by increased plasma levels of total cholesterol (TC), triglyceride (TG), low density lipoprotein cholesterol (LDL-C) and decreased high density lipoprotein cholesterol (HDL-C). Excess fat intake leads to accumulation of lipid in the adipocytes causing hypertrophy of the adipose tissue which produces inflammatory cytokines like TNF-α, resistin, interleukin -6 (IL-6), plasminogen activator inhibitor-1 (PAI-1) and monocyte chemoattractant protein -1 (MCP-1). These cytokines cause local and systemic insulin resistance leading to impairment in insulin signaling.The elevated cytokines also contribute for the development of renal pathologies in diet induced obese animal models. Though several pharmacological modalities are available in the treatment of obesity and its associated complications, there is considerable interest in the naturally available plant products with antiobesity properties.

Phytochemicals possessing antiobesity effects with minimal side effects would be beneficial in the management of obesity. Garcinia Cambogia (Garcinia gummi-gutta) is a tropical edible fruit of the family Clusiaceae grown in south East Asia, south India and Africa. It has a characteristic sweet and sour taste, used commonly for preparing culinary dishes. The fruit rinds of G. cambogia contain 20-30% of (-) Hydroxycitric acid (HCA) which is a competitive inhibitor of the enzyme ATP-citrate lyase, a key enzyme involved in fatty acid and cholesterol biosynthesis (EC 4.1.3.8). The inhibitory effect of HCA on ATP citrate lyase lowers the production of cholesterol, fatty acids and also promotes gluconeogenesis and glycogenesis. Apart from HCA, the fruits of G. cambogia have also been reported to contain secondary metabolites like xanthones, flavonoids, benzophenones like Garcinol/camboginol and Isoxanthohumol. All the three constituents have been reported to possess antioxidant properties. Several animal and human studies have been carried out with HCA, only a few evidences are available in the literature about the beneficial effects of the crude extract of Garcinia Cambogia. Thus the present study was designed to investigate the effects of Garcinia Cambogia on body weight, glucose tolerance and inflammation in rats fed with high fat diet.

Materials and Methods

Preparation of crude Garcinia Cambogia extracts (GE): The Garcinia Cambogia fruits were obtained from Kerala. The fruits were washed, deseeded and the rinds were sun dried. The fruit rinds were crushed, ground and extracted crudely with 70% v/v ethanol with shaking at room temperature for 24 h. The solution was filtered and the filtrate was evaporated under reduced pressure. The semi solid residual material was collected and stored at 40C till use.

Animals and study design

The present study was approved by the Institute Scientific Advisory Committee and Animal Ethics Committee. Five month old male Wistar rats weighing 200 to 250 gm were housed in polypropylene cages with stainless steel grill. The animals were maintained at standard conditions with a 12:12 h light: dark cycle. After acclimatization the rats were randomly divided into four groups (10 rats / group) based on their body weight.
  • Group 1: Control+ vehicle, the rats received standard rodent diet.
  • Group 2: Control + GE, the rats received standard rodent diet along with GE.
  • Group 3: High fat diet +vehicle, rats received 30% High fat diet (HFD).
  • Group 4: High fat diet +GE, rats received 30% High fat diet (HFD) along with GE
The G. cambogia extract was dissolved in drinking water and administered at a dose of 400mg/Kg body wt/day/rat for an experimental duration of ten weeks. Drinking water was given as vehicle for control and HFD groups.
Composition of High fat diet

Diet Ingredients                  (g/100g)
  • Casein                             26
  • Corn starch                        16
  • Sucrose                            16
  • Cellulose                          6.1
  • Safflower oil                      1
  • Butter                             29
  • Standard Mineral mixture           4.2
  • Standard Vitamin mixture           1.2
  • Choline                            0.2
  • DL-Methionine                      0.3
The non-purified high-fat diet was prepared as described by Hsu et al., [16], with 53.78% of total calories derived from fat, 21.8% from protein, and 30.35 % from carbohydrate. The energy of the high-fat diet was 5.02 kcal/g.

Sample collection

At the end of the experiment fasting blood samples were collected and centrifuged at 3500 rpm. The plasma was separated, aliquoted and stored at -800C for further analysis.
Intra peritoneal glucose tolerance test (IPGTT)

Intraperitoneal glucose tolerance test was performed for all rats at the end of the experiment. After 12-15 h of overnight fasting, basal blood samples were collected. Glucose (2g/Kg BW in saline) was administered intraperitoneally and blood samples were collected at 30, 60 and 120 min interval. The plasma was separated and glucose levels were estimated immediately.
 
Biochemical analyses

Plasma glucose, urea, creatinine and uric acid were estimated using standard reagent kits adapted to a fully automated clinical chemistry analyser (AU-400, OLYMPUS, UK). The plasma leptin levels were estimated using Ray BioR rat leptin ELISA kit (Ray Biotech, Inc. USA) and TNF- α levels using Diaclone rat TNF- α ELISA Kit (Diaclone, France).

Statistical Analysis

Results were expressed as Mean ± SD. One-way analysis of variance (ANOVA) with Tukey as post hoc test was used to evaluate the differences between the groups. Statistical Package of Social Service (SPSS version 19) was used for performing statistical analyses. Area under curve (AUC) was analysed using Graph pad Prism 6 software. P-value <0.05 was considered as statistically significant.
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Results

It show rats fed with high fat diet showed significant increase in body weight gain (p<0.001) when compared to control rats. Supplementation with GE along with HFD showed significant decrease in the body weight gain (p<0.001).

Effect of GE on body weight in control and high fat fed rats. All values were expressed as Mean ± SD. N=10 rats/ group. a,b P< 0.05 was considered as statistically significant. a vs Control group. b vs HFD group

It show high fat diet fed rats showed elevated plasma levels of leptin (p<0.001) and TNF-α (p<0.001) when compared to control rats. GE treatment along with HFD decreased leptin (p=0.031) and TNF-α (p=0.013) levels significantly. No significant changes were observed with the renal function parameters urea, creatinine and uric acid in any of the groups.

Effect of GE on plasma leptin, TNF-α, urea, creatinine and uric acid in control and high fat fed rats. All values were expressed as Mean ± SD. N=10 rats/ group. a,b P< 0.05 was considered as statistically significant. a vs Control ...

It shows that there was significant increase in the IPGTT and incremental area under curve (p<0.001) of IPGTT in rats fed with high fat diet when compared to control rats. GE administration along with HFD showed significant decrease in the IPGTT and incremental area under curve (p<0.001).

Effect of GE on intraperitoneal glucose tolerance test (IPGTT) in control and high fat fed rats

Effect of GE on incremental area under curve (AUC) of IPGTT in control and high fat fed rats

Discussion

The persistent rise in the incidence of obesity and its associated complications continues to present monumental challenges to health. Ingestion of excess calories has become a major risk factor for the occurrence of obesity. Leptin, the adipose derived hormone regulates food intake and energy expenditure through interactions with hypothalamic nuclei. Hence it plays a crucial role in the maintenance of body weight . The circulating leptin level is proportional to body fat but in case of diet induced obesity the increased leptin level fails to prevent weight gain. Such unresponsiveness of endogenous or exogenous leptin is referred as ‘leptin resistance’. In our study we found increased body weight gain and plasma leptin level in rats fed with high fat diet. This finding was consistent with the previous literature. Supplementation of GE along with high fat diet showed decreased gain in body weight and plasma leptin level. GE contains hydroxycitric acid (HCA) which is a competitive inhibitor of the citrate cleavage enzyme, ATP citrate lyase. Due to concentration of the GE, the free form of HCA is converted to its lactone form (HCAL). The HCAL is relatively stable but less effective when compared to the free HCA. Previous reports have shown that HCAL is effective in reducing food intake and body weight. The decrease in body weight and leptin observed in our study might be due to the inhibitory effect of HCAL on calorie intake.

Lipid laden adipocytes show increase in the production of proinflammatory cytokines TNF-α, IL-6, resistin, MCP-1 and PAI-1. These cytokines up regulate the synthesis of adhesion molecules (intracellular adhesion molecule and vascular cell adhesion molecule). Cross talks between endothelial cells, adipocytes and macrophages enhance the inflammatory state leading to synthesis of excess cytokines. All these consequences culminate in systemic and local insulin resistance causing impairment in insulin sensitivity. Evidences suggest that in cultured human muscle cells TNF-α affects insulin stimulated storage of glucose and impairs insulin signaling. Also, it was reported that TNF-α knocked out obese mice showed protection against insulin resistance.These evidences provide the direct role of TNF-α in insulin resistance. To assess the insulin sensitivity generally glucose tolerance test is performed. Rats fed with fat rich diet showed elevated levels of TNF-α and glucose intolerance. Our results are in agreement with the previous reports. Treatment with GE significantly decreased plasma levels of TNF- α and improved glucose intolerance. In addition to HCAL, the GE also contains xanthones, flavonoids and benzophenones which are known to have antioxidant properties. The polyisoprenylated benzophenone garcinol/ camboginol and isoxanthohumol are reported to be present in the fruit rinds of Garcinia Cambogia. The garcinol has been shown to posses antioxidative, anti-inflammatory and antiproliferative properties. In vitro assays have also reported the antioxidant properties of Garcinia Cambogia. A study in catfish have stated that administration of the crude aqueous extract of Garcinia Cambogia fruit reduced body weight gain, glucose, TC, TG, LDL and increased red blood cells (RBC), white blood cells (WBC), platelets, HDL. The antioxidants present in the Garcinia Cambogia fruit might have contributed for the significant reduction in the TNF-α level and glucose intolerance.

In diet induced obese rats the elevated levels of proinflammatory cytokines cause monocyte infiltration and leads to renal damage. To assess the renal function plasma levels of urea, creatinine, and uric acid were estimated. There was no statistical significance in all parameters in any of the groups. There was mild decrease in the levels of blood urea, creatinine and uric acid in high fat rats when compared to control rats. The low protein content in the high fat diet than the standard rodent diet might be the reason for the observed decrease in the levels of urea, creatinine and uric acid.

Conclusion

Supplementation of Garcinia Cambogia showed decrease in body weight gain, inflammation and glucose intolerance. This supports the popular view that inclusion of Garcinia Cambogia in the diet may help in body weight management. However scientific studies to confirm these effects in humans are warranted.

Acknowledgments

We thank Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) for providing the infrastructure and intramural research grants required for the study. We extend our thanks to Dr. A.G. Ramachandran Nair, formerly Professor of Chemistry in Pondicherry University for his valuable assistance in conceptualizing the research work. We would like to thank Dr. Zachariah Bobby, Professor and Head, Department of Biochemistry, JIPMER for the kind supply of Garcinia Cambogia fruits from Kerala for the research work.

Resource: http://www.ncbi.nlm.nih.gov

Thursday 23 June 2016

Garcinia Cambogia: New Research Shows Weight-Loss Benefits of Natural Extract

The pumpkin like fruit from which Garcinia Cambogia is derived (Malabar Tamarind), has long been used to enhance the culinary experience of certain South-East Asian dishes, and is now being recognized as one of the most effective and safest weight loss ingredients available today. The recent popularity of Garcinia Cambogia has many divided on the supplements true effectiveness, sparking two new studies into the matter.

Randomized, double-blind, placebo-controlled research published on Obesity, demonstrated the significant effect Garcinia Cambogia can have regarding weight loss and hip-and-waist circumference when compared to a placebo group. These results were pooled together with results from a separate study, and published in the American Dieting Journal. The Combined results demonstrated significant reduction of weight, waist-and-hip circumference, blood lipid and glucose levels, as well as an increase in quality of life after two weeks. These results were not accomplished by every brand of the supplement, but rather only quality sourced Garcinia Cambogia. View the Verified Garcinia Cambogia used in the study here.

Paul Fenway of the American Dieting Journal explains how “most companies are looking for two published, well-designed clinical studies to support unique structure/function claims for their weight management products. The pooled data, as well as the publication of the 60-subject study on obesity posted in the A.D.J, provides valid confirmation that Garcinia Cambogia is a useful for weight management, providing the product ingested meets the standard." - Paul Fenway

Study Breakdown

After two weeks of supplementing with 700 mg of quality sourced Garcinia Cambogia twice per day, test subjects significantly reduced body weights by 6.8 pounds, and waist-and-hip circumference by 2.5 - 3 inches, on average, compared to the placebo group. After eight weeks, weight was significantly reduced in subjects by 13.5 pounds, and waist-and-hip circumferences were reduced by 5.7 inches. Study participants walked 30 minutes five days per week, and they followed a standard 2,000 calorie daily diet.

Garcinia group: The people in this group took 700 mg of Garcinia Cambogia, 30 minutes before breakfast and dinner (a total of 1400mg).
Placebo group: The placebo group took 700 mg of placebo (a dummy pill) instead, at the same times.

While these preliminary studies are promising, it is the belief of some researchers that more research is needed to definitively provide important information such as how long is it safe to take the supplement: daily, indefinitely, or is six months? "While people have been consuming the fruit for centuries, the extract form with the higher HCA percentages still should be studied in larger studies with longer durations."
For now, the smaller studies suggest the dosages of 1400-3000 mg a day, are relatively safe and effective for weight loss for three months of use, but as always, everyone to check with their physician first before starting any new supplement.

How Garcinia Cambogia Claims to Work

"Garcinia Cambogia fruit rind modulates multiple pathways involved in fat cell formation and fat breakdown."

Unlike other, more traditional weight-loss supplements such as Ephedrine, Synephrine, and Caffeine, Garcinia Cambogia is NOT a stimulant. It does not work by turning up the bodies metabolism, and as such does not carry the dangers of stimulants such as elevated hear-rate and high blood pressure. Garcinia Cambogia Extract is therefore considered safe for dieters, according to the recent studies.
Since Garcinia Cambogia is not a stimulant, it acts differently by inhibiting a enzyme in the body (citric acid lyase) responsible for synthesizing fatty-acids, a process known as de novo-lipogenesis. This blocks the bodies ability to store fat, leaving it free to be immediately used by the body as a source of energy. In addition to this, it helps free already stored fat, allowing the body to burn it off quickly.

Reportedly the effects of Garcinia Cambogia Extract are biphasic, this means it works via two separate pathways. The studies explain how Garcinia Cambogia works on two different levels:
-First, it appears to have an immediate effect on serotonin levels in the brain, the “feel good” chemical. By increasing levels of serotonin, mood is increased and appetite is suppressed; effectively eliminating cravings.

-Second, a chemical in the extract called Hydroxy-citric Acid (HCA) interrupts the bodies ability to synthesize fatty acids, effectively blocking fat from being stored and leaving it readily available as an immediate source of energy. This not only leads to significant fat loss, but greatly increases energy levels and highly enhances feelings of well being.

What to Look For

"Sourcing the right brand of Garcinia Cambogia extract is the majority of the battle in achieving safe weight loss, with this product."

  • - The Garcinia Cambogia is Made in the U.S.A
  • - Must contain 50%-60% HCA
  • - All Natural Ingredients.
  • - No toxic additives or fillers on product's label.
  • - Is a proven product.
  • - High Potency Extraction Process
  • - The Garcinia Cambogia is Verified by Research


With chemical and physical interactions occurring within a supplement, it is difficult to determine the exact efficiency of the product remaining. Manufactures are not required to list the exact amount of fillers within the supplement; therefore it is difficult to determine the amount of non-medicinal ingredients versus medicinal ingredients used. Always use caution when putting anything in your body, and purchase only verified products.

Reasons for Unhealthy Additives in Supplements

"Supplement manufacturers often add in fillers to their garcinia cambogia Extract for numerous reasons." - Paul Fenway A.D.J
1.Easier and faster production (cutting costs): Supplements like garcinia cambogia Extract, involve an extraction procedure which requires more time and more money to acquire and finish product product. Rather then spend the time or money, additives are used leading to an inferior product.

2. More appealing to the eye (colorants): We eat and buy with our eyes, low quality manufactures of garcinia cambogia Extract know this, so artificial colors are used to make their product more appealing to the eye, again leading to an ineffective product.

3. Easier to swallow (coatings): Magnesium Stearate is used as a lubricant so that the pills don’t stick to one another, or to the equipment being used during production. This is the sole reason why magnesium stearate is used in supplements and vitamins. Magnesium Stearate is a toxic ingredient, and should not be added to supplements as it caries serious health consequences. Access garcinia cambogia products that do not contain dangerous additives here.

When in doubt as to whether you should be taking this supplement, always check with your physician. While I am not in favor of taking this supplement with other weight loss supplements due to lack of data for safety, I hope that with the growing public interest that more studies on safety and usage will be done on a larger scale, for this promising supplement.

About Natural Review

Natural Review, is a top-tier provider of natural health product information through clinical research. Research is conducted to aid and promote healthy lifestyles, weight loss, and high quality products to consumers. Natural Review uses highly efficient research methods to gain accurate results on many dieting products without bias, and will only publish results that include safe natural ingredients, in order to assure optimum health and safety. Natural Review is dedicated to providing its viewers quality information that is geared towards living longer, healthier, and happier lives. The primary purpose of this release is to help consumers avoid poor quality products online, while shedding light on quality brands leading to informed buying decisions, and creating a better buying experience.

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