water extract alleviates insulin resistance and hepatic lipid accumulation in mice fed a high-fat diet.

Jinya Dong, Wen Li, Xiaocui Du, Xiaofang He, Bin Deng, Hongmei Zheng, Yang Tian, Jun Sheng, Chongye Fang
Author Information
  1. Jinya Dong: Yunnan Research Center for Advanced Tea Processing, Yunnan Agricultural University, Kunming, China.
  2. Wen Li: Yunnan Rural Science and Technology Service Center, Kunming, Yunnan, China.
  3. Xiaocui Du: Yunnan Research Center for Advanced Tea Processing, Yunnan Agricultural University, Kunming, China.
  4. Xiaofang He: Yunnan Research Center for Advanced Tea Processing, Yunnan Agricultural University, Kunming, China.
  5. Bin Deng: Yunnan Rural Science and Technology Service Center, Kunming, Yunnan, China.
  6. Hongmei Zheng: Yunnan Rural Science and Technology Service Center, Kunming, Yunnan, China.
  7. Yang Tian: College of Food Science and Technology, Yunnan Agricultural University, Kunming, China.
  8. Jun Sheng: Yunnan Research Center for Advanced Tea Processing, Yunnan Agricultural University, Kunming, China.
  9. Chongye Fang: Yunnan Research Center for Advanced Tea Processing, Yunnan Agricultural University, Kunming, China.

Abstract

Background: Garcinia cambogia is widely used as a weight-loss supplement, and it is reported to be negatively associated with metabolic diseases including insulin resistance (IR), type 2 diabetes mellitus (T2DM), non-alcoholic fatty liver disease (NAFLD), and dyslipidemia.
Objective: This study aimed to investigate the effect of G. cambogia water extract (GE) on high-fat diet (HFD)-induced obesity, IR, and hepatic lipid accumulation.
Design: C57BL/6 male mice were fed HFD with or without GE, GED and GEP for 16 weeks, and the mice were subjected to insulin tolerance tests and liver histological analysis. The hydroxycitric acid (HCA) levels of GE, GED, and GEP were measured by high-performance liquid chromatography.
Results: The results showed that GE significantly reduced HFD-induced body weight gain ( < 0.001), alleviated IR ( < 0.01), reduced serum total cholesterol (TC) ( < 0.001), and attenuated HFD-induced hepatic lipid accumulation. To investigate the constituent that was responsible for these effects, we separated GE into the component that dissolved in ethanol (GED) and the component that was precipitated by ethanol (GEP). Further mouse experiments showed that both GED and GEP were effective, but GED (which was used at a dose of 4 g/L) was more effective than GEP (which was used at a lower dose of 1 g/L). The HCA levels in GED and GEP were similar, although less than in GE. HCA may be the effective component in GE.
Conclusion: This study provides evidence that G. cambogia can be used as a natural supplement to alleviate IR and hepatic lipid accumulation.

Keywords

References

  1. Curr Vasc Pharmacol. 2017;15(1):30-39 [PMID: 27748199]
  2. Phytochemistry. 2010 Oct;71(14-15):1625-41 [PMID: 20732701]
  3. J Agric Food Chem. 2019 Mar 20;67(11):3188-3197 [PMID: 30827101]
  4. Fitoterapia. 2003 Apr;74(3):267-73 [PMID: 12727492]
  5. Evid Based Complement Alternat Med. 2013;2013:751658 [PMID: 23990846]
  6. J Clin Diagn Res. 2015 Feb;9(2):BF01-4 [PMID: 25859449]
  7. Nutr Hosp. 2015 Dec 01;32(6):2400-8 [PMID: 26667686]
  8. Front Pharmacol. 2021 Feb 19;11:591293 [PMID: 33679386]
  9. Adv Exp Med Biol. 2017;960:1-17 [PMID: 28585193]
  10. Biosci Biotechnol Biochem. 2008 Jul;72(7):1772-80 [PMID: 18603810]
  11. J Adv Pharm Technol Res. 2022 Jan-Mar;13(1):1-6 [PMID: 35223433]
  12. Exp Ther Med. 2018 Jun;15(6):5070-5076 [PMID: 29844801]
  13. Dtsch Arztebl Int. 2014 Jun 27;111(26):447-52 [PMID: 25019921]
  14. Lipids. 1974 Feb;9(2):121-8 [PMID: 4815799]
  15. Crit Rev Food Sci Nutr. 2012;52(7):585-94 [PMID: 22530711]
  16. World J Gastroenterol. 2013 Nov 28;19(44):8160-2 [PMID: 24307814]
  17. J Obes. 2011;2011:509038 [PMID: 21197150]
  18. Front Pharmacol. 2021 Jan 21;11:606514 [PMID: 33551809]
  19. Lipids Health Dis. 2011 May 14;10:74 [PMID: 21569551]
  20. Nutr Metab Cardiovasc Dis. 2019 Sep;29(9):887-905 [PMID: 31377181]
  21. Int J Mol Sci. 2020 May 29;21(11): [PMID: 32485838]
  22. Clin Gastroenterol Hepatol. 2022 Jun;20(6):e1416-e1425 [PMID: 34400337]
  23. Ukr Biochem J. 2016 May-Jun;88(3):78-82 [PMID: 29235331]
  24. J Hepatol. 2016 Jun;64(6):1388-402 [PMID: 27062661]
  25. Lipids. 1974 Feb;9(2):129-34 [PMID: 4815800]
  26. J Complement Integr Med. 2016 Mar;13(1):9-16 [PMID: 26595408]
  27. Metabolism. 2021 Jun;119:154766 [PMID: 33766485]
  28. Cureus. 2022 Sep 27;14(9):e29657 [PMID: 36320966]
  29. Autophagy. 2022 Mar;18(3):518-539 [PMID: 34101546]
  30. Int J Mol Sci. 2022 Aug 29;23(17): [PMID: 36077214]
  31. Nihon Eiseigaku Zasshi. 2015;70(3):197-204 [PMID: 26411937]
  32. J Cell Physiol. 2021 Mar;236(3):1822-1839 [PMID: 32716094]
  33. Physiol Rev. 2013 Jan;93(1):359-404 [PMID: 23303913]
  34. Mutat Res. 2005 Nov 11;579(1-2):149-62 [PMID: 16055158]
  35. Diabetes Obes Metab. 2005 Jan;7(1):47-55 [PMID: 15642075]
  36. Nutrients. 2021 Aug 19;13(8): [PMID: 34445005]
  37. Front Pharmacol. 2021 Apr 12;12:594437 [PMID: 33912032]
  38. Phytother Res. 2014 Jun;28(6):887-91 [PMID: 24133059]
  39. Curr Ther Res Clin Exp. 2003 Sep;64(8):551-67 [PMID: 24944404]
  40. Drug Des Devel Ther. 2015 Aug 20;9:4835-45 [PMID: 26316717]
  41. World J Gastroenterol. 2013 Aug 7;19(29):4689-701 [PMID: 23922466]
  42. BMC Complement Altern Med. 2018 Jan 24;18(1):26 [PMID: 29361938]
  43. Fitoterapia. 2015 Apr;102:134-48 [PMID: 25732350]
  44. Anal Biochem. 2001 May 1;292(1):148-54 [PMID: 11319829]
  45. Phytother Res. 2016 Aug;30(8):1316-29 [PMID: 27145492]
  46. Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Mar;1864(3):271-280 [PMID: 30553055]
  47. Rev Clin Esp. 2020 Oct 31;: [PMID: 33143860]
  48. Food Funct. 2021 Jul 20;12(14):6432-6441 [PMID: 34075995]
  49. Antioxidants (Basel). 2021 Jul 29;10(8): [PMID: 34439474]
  50. Biomed Pharmacother. 2019 Feb;110:500-509 [PMID: 30530230]

Word Cloud

Created with Highcharts 10.0.0GEGEDGEPhepaticlipidaccumulationcambogiausedinsulinIRresistancelivermiceHCA<0componenteffectiveGarciniasupplementnon-alcoholicfattydiseasestudyinvestigateGwaterextracthigh-fatdietHFDobesityfedhydroxycitricacidlevelsshowedreducedHFD-induced001ethanoldoseg/LBackground:widelyweight-lossreportednegativelyassociatedmetabolicdiseasesincludingtype2diabetesmellitusT2DMNAFLDdyslipidemiaObjective:aimedeffect-inducedDesign:C57BL/6malewithout16weekssubjectedtolerancetestshistologicalanalysismeasuredhigh-performanceliquidchromatographyResults:resultssignificantlybodyweightgainalleviated01serumtotalcholesterolTCattenuatedconstituentresponsibleeffectsseparateddissolvedprecipitatedmouseexperiments4lower1similaralthoughlessmayConclusion:providesevidencecannaturalalleviatealleviates

Similar Articles

Cited By