Effects of Garcinia Cambogia Compounded Supplements on the Formation of Body Fat Induced by a High Energy Diet in Obese Rats
DOI:
https://doi.org/10.17140/OROJ-8-147Keywords:
Obesity; Garcinia cambogia extract; Green coffee bean extract; Mulberry leaf extract; Chromium yeast; Wakame extract.Abstract
Background
Obesity is a public health concern in many countries. Obesity is often accompanied by other diseases and, in addition to its effects
on personal health, also increases national health expenditure and medical costs. Currently, weight loss can be achieved through
several medical means, such as gastric bypass surgery, liposuction, or the use of weight loss drugs. However, these options may
lead to side effects or increased mortality. As such, the development of anti-obesity supplements that are natural and safe merits
greater research attention. Garcinia cambogia extract, green coffee bean extract, mulberry leaf extract, chromium yeast, and wakame
extract are known to have the potential to combat obesity and adjust physical constitutions; however, the effect on fat loss of these
agents in a compound supplement has not been researched or discussed.
Objective
This study investigated the effects of a compound supplement (hereafter referred to as Garcinia cambogia compounded supplements (GC)) containing Garcinia cambogia extract, green coffee bean extract, mulberry leaf extract, chromium yeast, and wakame
extract on fat accumulation induced by a high energy (HE) diet in rats.
Design
Six-week-old, male Sprague–Dawley rats were assigned to a control group or an experimental (HE) group. The control group
comprised 12 rats who were given regular feed. The HE group comprised 36 rats who were given HE diet and were further divided according to whether they received carboxymethyl cellulose (CMC) or GC (305 and 1220 mg/kg, denoted as GC-L and GC-H,
respectively) for 5-weeks. Starting from the sixth-week, the rats were tube-fed various dosages of GC. After the ninth-week, the
rats’ body weight, food intake, body fat mass, serum biochemical properties, and liver fat were analyzed.
Results
The results demonstrated that the HE+GC-L rats had significantly lower weight and body fat mass (569.5±51.3 g; 36.6±9.6 g)
than the HE+CMC rats (618.5±57.1 g; 46.3±12.2 g). Food efficiency and calorie utilization were also significantly lower in the
HE+GC-L rats than in the HE+CMC group (p<0.01). Compared with the HE+CMC group, food efficiency, calorie utilization,
total cholesterol, low-density lipoprotein cholesterol (LDL-C), and concentration of free fatty acids were also significantly lower
in the HE+GC-H rats (p<0.05).
Conclusion
The GC supplementation significantly reduced body weight, body fat mass, body fat percentage, food efficiency, and calorie utilization in rats, and it thus has potential as a natural and safe plant extract dietary supplement. Its long-term effects on the human
body should be investigated in the future.
References
World Health Organization (WHO). Web site. https://www. who.int/news-room/fact-sheets/detail/obesity-and-overweight. Accessed March 8, 2018.
Must A, Spadano J, Coakley EH, Field AE, Colditz G, Dietz WH. The disease burden associated with overweight and obesity. JAMA. 1999; 282(16): 1523-1529. doi: 10.1001/jama.282.16.1523
Madan AK, Orth WS, Tichansky DS, Ternovits CA. Vitamin and trace mineral levels after laparoscopic gastric bypass. Obes Surg. 2006; 16(5): 603-606. doi: 10.1381/096089206776945057
Benotti P, Wood GC, Winegar DA, Petrick AT, Still CD, Argyro-poulos G, et al. Risk factors associated with mortality after Roux-en-Y gastric bypass surgery. Ann Surg. 2014; 259(1): 123-130. doi: 10.1097/SLA.0b013e31828a0ee4
Curry SA. Obesity epidemic: Pharmaceutical weight loss. R I Med J (2013). 2017; 100(2): 18-20.
Filippatos TD, Derdemezis CS, Gazi IF, Nakou ES, Mikhaili-dis DP, Elisaf MS. Orlistat-associated adverse effects and drug interactions: A critical review. Drug Saf. 2008; 31(1): 53-65. doi: 10.2165/00002018-200831010-00005
Sherman MM, Ungureanu S, Rey JA. Naltrexone/bupropion ER (contrave): Newly approved treatment option for chronic weight management in obese adults. P T. 2016; 41(3): 164-172.
Chen TH, Tsai MJ, Fu YS, Weng CF. The exploration of natu-ral compounds for anti-diabetes from distinctive species Garcinia linii with comprehensive review of the Garcinia family. Biomolecules. 2019; 9(11): 641. doi: 10.3390/biom9110641
Ministry of Health and Welfare (Republic of China). Web site. 2017. Web site. https://consumer.fda.gov.tw/Food/MaterialDe-tail.aspx?nodeID=160&id=690. Accessed Jul 22, 2021.
Semwal RB, Semwal DK, Vermaak I, Viljoen A. A comprehen-sive scientific overview of Garcinia cambogia. Fitoterapia. 2015; 102: 134-148. doi: 10.1016/j.fitote.2015.02.012
Meinhart AD, Damin FM, Caldeirão L, de Jesus Filho M, da Silva LC, da Silva Constant L, et al. Chlorogenic and caffeic acids in 64 fruits consumed in Brazil. Food Chem. 2019; 286: 51-63. doi: 10.1016/j.foodchem.2019.02.004
Narita Y, Inouye K. Inhibitory effects of chlorogenic acids from green coffee beans and cinnamate derivatives on the activity of porcine pancreas α-amylase isozyme I. Food Chem. 2011; 127 (2011): 1532-1539. doi: 10.1016/j.foodchem.2011.02.013
Meng S, Cao J, Feng Q, Peng J, Hu Y. Roles of chlorogen-ic acid on regulating glucose and lipids metabolism: A review. Evid Based Complement Alternat Med. 2013; 2013: 801457. doi: 10.1155/2013/801457
Maeda H. Nutraceutical effects of fucoxanthin for obesity and diabetes therapy: A review. J Oleo Sci. 2015; 64(2): 125-132. doi: 10.5650/jos.ess14226
Li YG, Ji DF, Zhong S, Lv Z-Q, Lin T-B, Chen S, et al. Hybrid of 1-deoxynojirimycin and polysaccharide from mulberry leaves treat diabetes mellitus by activating PDX-1/insulin-1 signaling pathway and regulating the expression of glucokinase, phospho-enolpyruvate carboxykinase and glucose-6-phosphatase in alloxan-induced diabetic mice. J Ethnopharmacol. 2011; 134(3): 961-970. doi: 10.1016/j.jep.2011.02.009
Havel PJ. A scientific review: The role of chromium in insulin resistance. Diabetes Educ. 2004; Suppl: 2-14.
Ministry of Health and Welfare (Republic of China). Web site. http://www.functionalfood.org.tw/hth/eva/body/fat.doc. Ac-cessed July 25, 2018.
Folch J, Lees M, Sloane Stanley GH. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957; 226(1): 497-509. doi: 10.1016/s0021-9258(18)64849-5
Wu N, Sarna LK, Hwang S-Y, Zhu Q, Wang P, Siow YL, et al. Activation of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase during high fat diet feeding. Biochim Biophys Acta. 2013; 1832(10): 1560-1568. doi: 10.1016/j.bbadis.2013.04.024
Buettner R, Parhofer KG, Woenckhaus M, Wrede CE, Kunz-Schughart LA, Schölmerich J, et al. Defining high-fat-diet rat mod-els: metabolic and molecular effects of different fat types. J Mol Endocrinol. 2006; 36(3): 485-501. doi: 10.1677/jme.1.01909
Bailey SA, Zidell RH, Perry RW. Relationships between or-gan weight and body/brain weight in the rat: What is the best analytical endpoint? Toxicol Pathol. 2004; 32(4): 448-466. doi: 10.1080/01926230490465874
Boden G. Obesity and free fatty acids. Endocrinol Metab Clin North Am. 2008; 37(3): 635-ix. doi: 10.1016/j.ecl.2008.06.007 Submit your article to this journal | https://openventio.org/submit-manuscript/
Golzarand M, Omidian M, Toolabi K. Effect of Garcinia cam-bogia supplement on obesity indices: A systematic review and dose-response meta-analysis. Complement Ther Med. 2020; 52: 102451. doi: 10.1016/j.ctim.2020.102451
Preuss HG, Bagchi D, Bagchi M, Rao CV, Dey DK, Satyanaray-ana S. Effects of a natural extract of (-)- hydroxycitric acid (HCA-SX) and a combination of HCA-SX plus niacin-bound chromium and Gymnema sylvestre extract on weight loss. Diabetes Obes Metab. 2004; 6(3): 171-180. doi: 10.1111/j.1462-8902.2004.00328.x
Cho HK, Han YS, Park JM. Ocular complications of Garcinia cambogia extract diet pills: Case report. Eur J Ophthalmol. 2020; 30(6): NP21-NP26. doi: 10.1177/1120672119872364
Andueza N, Giner RM, Portillo MP. Risks associated with the use of garcinia as a nutritional complement to lose weight. Nutri-ents. 2021; 13(2): 450. doi: 10.3390/nu13020450
Ong KW, Hsu A, Tan BK. Anti-diabetic and anti-lipidemic ef-fects of chlorogenic acid are mediated by ampk activation. Biochem Pharmacol. 2013; 85(9): 1341-1351. doi: 10.1016/j.bcp.2013.02.008
Thom E. The effect of chlorogenic acid enriched coffee on glucose absorption in healthy volunteers and its effect on body mass when used long-term in overweight and obese people. J Int Med Res. 2007; 35(6): 900-908. doi: 10.1177/147323000703500620
Wan C-W, Wong CN-Y, Pin W-K, Wong MH-Y, Kwok C-Y, Chan RY-K, et al. Chlorogenic acid exhibits cholesterol lowering and fatty liver attenuating properties by up-regulating the gene expression of PPAR-α in hypercholesterolemic rats induced with a high-cholesterol diet. Phytother Res. 2013; 27(4): 545-551. doi: 10.1002/ptr.4751
Hitoe S, Shimoda H. Seaweed fucoxanthin supplementation improves obesity parameters in mild obese Japanese subjects. Func-tional Foods in Health and Disease. 2017; 7(4): 246-262. doi: 10.31989/ ffhd.v7i4.333
Gammone MA, D’Orazio N. Anti-obesity activity of the ma-rine carotenoid fucoxanthin. Mar Drugs. 2015; 13(4): 2196-2214. doi: 10.3390/md13042196
Sheng Y, Liu J, Zheng S, Liang F, Luo Y, Huang K, et al. Mul-berry leaves ameliorate obesity through enhancing brown adipose tissue activity and modulating gut microbiota. Food Funct. 2019; 10(8): 4771-4781. doi: 10.1039/c9fo00883g
Hua Y, Clark S, Ren J, Sreejayan N. Molecular mechanisms of chromium in alleviating insulin resistance. J Nutr Biochem. 2012; 23(4): 313-319. doi: 10.1016/j.jnutbio.2011.11.001
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