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The Anti-Inflammatory Effect of Gabyeobda Tea in High Fat Diet-Induced Obese Mice

가볍다차(茶)가 고지방식이로 유도된 비만 마우스에서 항염증에 미치는 효과

  • Wu, Liangliang (Department of Rehabilitation Medicine of Korean Medicine, College of Korean Medicine, Dongguk University) ;
  • Lim, Soo Kyoung (Department of Rehabilitation Medicine of Korean Medicine, College of Korean Medicine, Dongguk University) ;
  • Shin, Seung-Uoo (Shinkang Korean Medicine Clinic) ;
  • Kim, Hojun (Department of Rehabilitation Medicine of Korean Medicine, College of Korean Medicine, Dongguk University)
  • 오량량 (동국대학교 한의과대학 한방재활의학교실) ;
  • 임수경 (동국대학교 한의과대학 한방재활의학교실) ;
  • 신승우 (신강한의원) ;
  • 김호준 (동국대학교 한의과대학 한방재활의학교실)
  • Received : 2022.05.05
  • Accepted : 2022.06.07
  • Published : 2022.06.30

Abstract

Objectives: The purpose of this study was to investigate the effects of Gabyeobda tea (GT) on anti-inflammation in ice induced high fat diet (HFD). Methods: The C57BL/6 mice fed HFD were administrated with GT once daily for 8 weeks. The changes of body weight, calorie intake levels were measured in mice. The level of serum total cholesterol, triglyceride, high density lipoprotein cholesterol, glutamic oxaloacetic transaminase (GOT), and glutamic pyruvic transaminase (GPT) were measured in mice by enzyme-based assay. It was also observed the histological changes of liver, and fat tissues with hematoxylin and eosin staining. Further real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay were employed to detect inflammatory cytokine levels such as tumor necrosis factor (TNF)-𝛼, interleukin (IL)-6, and IL-1𝛽. Results: HFD+GT group, which was administered with GT with HFD, showed no body weight gain compared with HFD group. However, levels of GOT, GPT, and inflammatory cytokines such as TNF-𝛼, IL-6, and IL-1𝛽 in the blood of HFD+GT group were significantly reduced compared with HFD group. In addition, the messenger RNA (mRNA) expression level of the IL-12 gene was significantly reduced and the mRNA expression level of the IL-10 was increased in the liver. Conclusions: It suggests that Gabyeobda tea can alleviate inflammatory responses induced by high fat diet by inhibiting inflammatory cytokines production.

Keywords

Acknowledgement

본 연구는 2021년도 (주)한방비만학외의 연구비 지원에 의해 이루어졌음.

References

  1. Ferrero-Miliani L, Nielsen OH, Andersen PS, Girardin SE. Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation. Clin Exp Immunol. 2007 ; 147(2) : 227-35. https://doi.org/10.1111/j.1365-2249.2006.03261.x
  2. Hotamisligil GS. Inflammation and metabolic disorders. Nature. 2006 ; 444(7121) : 860-7. https://doi.org/10.1038/nature05485
  3. Makki K, Froguel P, Wolowczuk I. Adipose tissue in obesity-related inflammation and insulin resistance: cells, cytokines, and chemokines. J ISRN Inflamm. 2013 ; 2013 : 139239.
  4. Cook DG, Mendall MA, Whincup PH, Carey IM, Ballam L, Morris JE, et al. C-reactive protein concentration in children: relationship to adiposity and other cardiovascular risk factors. Atherosclerosis. 2000 ; 149(1) : 139-50. https://doi.org/10.1016/S0021-9150(99)00312-3
  5. Barzilay JI, Abraham L, Heckbert SR, Cushman M, Kuller LH, Resnick HE, et al. The relation of markers of inflammation to the development of glucose disorders in the elderly: the cardiovascular health study. Diabetes. 2001 ; 50(10) : 2384-9. https://doi.org/10.2337/diabetes.50.10.2384
  6. Kim MS. Inflammation in obesity-induced metabolic disease. Bulletin of Food Technology. 2010 ; 23(1) : 28-39.
  7. Deka A, Vita JA. Tea and cardiovascular disease. Pharmacological Research. 2011 ; 64(2) : 136-45. https://doi.org/10.1016/j.phrs.2011.03.009
  8. Park JH, Lee E, Park E. Effect of pumpkin, corn silk, adzuki bean, and their mixture on weight control and antioxidant activities in high fat diet-induced obesity rats. Journal of the Korean Society of Food Science and Nutrition. 2016 ; 45(9) : 1239-48. https://doi.org/10.3746/JKFN.2016.45.9.1239
  9. Hosny H, Omran N, Handoussa H. Edible seeds with potential anti-obesity impact: a review. International Journal of Plant Based Pharmaceuticals. 2022 ; 2(1) : 64-81.
  10. Ma XT, Zhang FY, Bai TF, Hao B. The law of the prescription for non-alcoholic steatohepatitis: a data mining analysis. Med Data Min. 2020 ; 3(1) : 28-32.
  11. Chang S, Wang JH, Choi HS, Chin YW, Kim HJ. The effect of Scutellariae Radix combined with metformin on obesity-relating biomarker in high fat fed C57BL/6 mice [J]. Journal of Korean Medicine for Obesity Research. 2017 ; 17(1) : 20-8. https://doi.org/10.15429/jkomor.2017.17.1.20
  12. Brouns F, Bjorck I, Frayn KN, Gibbs AL, Lang V, Slama G, et al. Glycaemic index methodology [J]. Nutrition Research Reviews. 2005 ; 518(1) : 145-71.
  13. Fabbrini E, Sullivan S, Klein S. Obesity and nonalcoholic fatty liver disease: biochemical, metabolic, and clinical implications. Hepatology. 2010 ; 51(2) : 679-89. https://doi.org/10.1002/hep.23280
  14. Abdelmalek MF, Diehl AM. Nonalcoholic fatty liver disease as a complication of insulin resistance. Med Clin North Am. 2007 ; 91(6) : 1125-49. https://doi.org/10.1016/j.mcna.2007.06.001
  15. Wu KT, Kuo PL, Su SB, Chen YY, Yeh ML, Huang CI, et al. Nonalcoholic fatty liver disease severity is associated with the ratios of total cholesterol and triglycerides to high-density lipoprotein cholesterol. Clin Lipidol. 2016 ; 10(2) : 420-5. https://doi.org/10.1016/j.jacl.2015.12.026
  16. Grundy SM. Hypertriglyceridemia, atherogenic dyslipidemia, and the metabolic syndrome. The American Journal of Cardiology. 1998 ; 81(4) : 18B-25B. https://doi.org/10.1016/S0002-9149(98)00033-2
  17. Wu Y, Tan F, Zhang T, Xie B, Ran L, Zhao X. The anti-obesity effect of lotus leaves on high-fat-diet-induced obesity by modulating lipid metabolism in C57BL/6J mice. Applied Biological Chemistry. 2020 ; 63(1) : 1-11. https://doi.org/10.1186/s13765-019-0484-7
  18. Wu J, Ye X, Yang S, Yu H, Zhong L, Gong Q. Systems pharmacology study of the anti-liver injury mechanism of Citri Reticulatae Pericarpium. J Front Pharmacol. 2021 ; 12 : 618846. https://doi.org/10.3389/fphar.2021.618846
  19. Shoelson SE, Herrero L, Naaz A. Obesity, inflammation, and insulin resistance. Gastroenterology. 2007 ; 132(6) : 2169-80. https://doi.org/10.1053/j.gastro.2007.03.059
  20. Nesto R. C-reactive protein, its role in inflammation, type 2 diabetes and cardiovascular disease, and the effects of insulin-sensitizing treatment with thiazolidinediones. Diabetic Medicine. 2004 ; 21(8) : 810-7. https://doi.org/10.1111/j.1464-5491.2004.01296.x
  21. Fulop T, Tessier D, Carpentier A. The metabolic syndrome. Pathologie-biologie. 2006 ; 54(7) ; 375-86.
  22. Men X, Choi SI, Han X, Kwon HY, Jang GW, Choi YE, et al. Physicochemical, nutritional and functional properties of Cucurbita moschata. Food Science and Biotechnology. 2021 ; 30(2) : 171-83. https://doi.org/10.1007/s10068-020-00835-2
  23. Kim C, Kim MB, Hwang JK. Red bean extract inhibits immobilization-induced muscle atrophy in C57BL/6N mice. Journal of Medicinal Food. 2020 ; 23(1) : 29-36. https://doi.org/10.1089/jmf.2019.4426
  24. Sherwood ER, Toliver-Kinsky T. Mechanisms of the inflammatory response. Best Practice & Research Clinical Anaesthesiology. 2004 ; 18(3) : 385-405. https://doi.org/10.1016/j.bpa.2003.12.002
  25. Jung SH, Park HS, Kim KS, Choi WH, Ahn CW, Kim BT, et al. Effect of weight loss on some serum cytokines in human obesity: increase in IL-10 after weight loss. The Journal of Nutritional Biochemistry. 2008 ; 19(6) : 371-5. https://doi.org/10.1016/j.jnutbio.2007.05.007
  26. Wang P, Wu P, Siegel MI, Egan RW, Billah MM. Interleukin (IL)-10 inhibits nuclear factor κB (NFκB) activation in human monocytes: IL-10 and IL-4 suppress cytokine synthesis by different mechanisms (*). Journal of Biological Chemistry. 1995 ; 270(16) : 9558-63. https://doi.org/10.1074/jbc.270.16.9558
  27. Lindmark E, Tenno T, Chen J, Siegbahn A. IL-10 inhibits LPS-induced human monocyte tissue factor expression in whole blood. British Journal of Haematology. 1998 ; 102(2) : 597-604. https://doi.org/10.1046/j.1365-2141.1998.00808.x