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Gomisin A Ameliorates Endoplasmic Reticulum Stress-induced Hepatic Steatosis

Gomisin A의 비알코올성 지방간 보호효과

  • Yun, Ye-Rang (Division of Longevity and Biofunctional Medicine, School of Korean Medicine, Pusan National University) ;
  • Jung, Myeong Ho (Division of Longevity and Biofunctional Medicine, School of Korean Medicine, Pusan National University)
  • Received : 2016.12.29
  • Accepted : 2017.01.12
  • Published : 2017.02.28

Abstract

Previously, we have shown that Schisandra chinensis (Turcz.) Baill. (S. chinensis) has a protective effect against endoplasmic reticulum (ER) stress-induced hepatic steatosis. Gomisin A is a bioactive phytoestrogen derived from S. chinensis. In the present study, the in vitro and in vivo effects of gomisin A on ER stress and hepatic steatosis were investigated. We quantified the expression of markers of ER stress, including glucose regulated protein 78 (GRP78), C/EBP homolog protein (CHOP), and X-box-binding protein-1 (XBP-1), in HepG2 cells treated with tunicamycin or palmitate. Tunicamycin treatment in HepG2 cells induced the expression of markers of ER stress, including GRP78, CHOP, and XBP-1c. However, treatment with gomisin A reduced the expression of markers of ER stress. These inhibitory effects were also observed in palmitate-incubated HepG2 cells. The in vivo inhibitory effects of gomisin A were assessed in mice injected with tunicamycin or fed with a high fat diet (HFD). Gomisin A reduced the expression of markers of ER stress and decreased triglyceride levels in the livers of mice after tunicamycin injection or HFD feeding. Furthermore, gomisin A decreased the expression of inflammatory genes in palmitate-incubated HepG2 cells and the liver of HFD-fed obese mice. These results suggest that gomisin A inhibits ER stress and ameliorates hepatic steatosis induced by ER stress.

본 연구는 소포체스트레스(endoplasmic reticulum stress)에 의해 유발되는 지방간(hepatic steatosis)에 대한 오미자추출물(Schisandra chinensis)의 주요성분인 gomisin A의 지방간 보호 효능에 대하여 연구하였다. 이를 위해 HepG2 세포에 소포체스트레스 유도물질인 tunicamycin 또는 palmitate을 처리하여 세포에서의 지방간 모델을 만들어 실험을 진행 하였으며, 소포체스트레스 표지자(marker)인 GRP78, CHOP, XBP-1의 발현을 측정하였다. Tunicamycin 처리한 세포에서는 GRP78, CHOP, XBP-1의 발현이 증가되었으나, gomisin A를 처리 한 세포에서는 이들의 발현 증가가 억제됨을 확인하였다. 이는 palmitate를 처리한 HepG2 세포에서도 palmitate에 의해 증가하는 소포체스트레스 표지자들이 gomisin A을 처리한 세포에서 발현이 감소함을 확인하였다. 이러한 결과에 의해, gomisin A는 소포체스트레스를 억제함을 알 수 있었다. 다음으로 gomisin A가 in vivo에서 소포체스트레스 및 지방간에 대한 보호효과가 있는지 확인하기 위해, tunicamycin과 고지방(high fat diet)으로 식이 한 쥐에서 소포체스트레스와 지방간의 보호효능에 대해 실험을 진행하였다. Tunicamycin과 고지방식이을 한 쥐의 간에서 중성지방이 증가하였으나, gomisin A를 처리한 쥐의 간에서 중성지방의 수준이 유의적으로 감소함을 확인하였다. 소포체스트레스 표지자들 역시 tunicamycin이나 고지방식이을 한 쥐에서 증가되나 gomisin A를 처리한 쥐에서 감소됨을 확인하였다. Gomisin A의 염증 반응에서의 조절기능을 확인하기 위하여 $TNF-{\alpha}$, IL-6 그리고 MCP1과 같은 염증관련 유전자들의 발현을 분석한 결과, tunicamycin이나 고지방식이을 한 쥐에서 염증유전자들의 발현이 증가하였으나 gomisin A를 처리한 쥐에서는 유의적으로 감소하였다. 종합적으로 본 연구 결과에 의하면, gomsin A는 소포체스트레스를 억제하여 지방간의 생성을 저해함을 알 수 있었다.

Keywords

References

  1. Araki, E., Oyadomari, S. and Mori, M. 2003. Endoplasmic reticulum stress and diabetes mellitus. Intern. Med. 42, 7-14. https://doi.org/10.2169/internalmedicine.42.7
  2. Ashraf, N. U. and Sheikh, T. A. 2015. Endoplasmic reticulum stress and oxidative stress in the pathogenesis of Non-alcoholic fatty liver disease. Free Radic. Res. 49, 1405-1418. https://doi.org/10.3109/10715762.2015.1078461
  3. Cao, S. S. and Kaufman, R. J. 2013. Targeting endoplasmic reticulum stress in metabolic disease. Expert Opin. Ther. Targets 17, 437-448. https://doi.org/10.1517/14728222.2013.756471
  4. Choi, M. S., Kwon, K. J., Jeon, S. J., Go, H. S., Han, S. H., Shin, K. H. and Ko, C. Y. 2009. Schizandra chinensis alkaloids inhibit lipopolysaccharide-induced inflammatory responses in BV2 microglial cells. J. Biomol. Tech. 17, 47-56.
  5. Choi, Y. W., Takamatsu, S. and Khan, S. I. 2006. Schisandrene, a dibenzocyclooctadiene lignan from Schisandra chinensis structure-antioxidant activity relationships of dibenzocyclooctadiene. J. Nat. Prod. 69, 356-359. https://doi.org/10.1021/np0503707
  6. Chun, J. N., Cho, M., So, I. and Jeon, J. H. 2014. The protective effects of Schisandra chinensis fruit extract and its lignans against cardiovascular disease: a review of the molecular mechanisms. Fitoterapia 97, 224-233. https://doi.org/10.1016/j.fitote.2014.06.014
  7. Farrell, G. C. and Larter, C. Z. 2006. Nonalcoholic fatty liver disease: from steatosis to cirrhosis. Hepatology 43, S99-S112. https://doi.org/10.1002/hep.20973
  8. Hikino, H., Kiso, Y., Taguchi, H. and Ikeya, Y. 1984. Antihepatotoxic actions of lignoids from Schizandra chinensis fruits. Planta Med. 50, 213-218. https://doi.org/10.1055/s-2007-969681
  9. Hwang, I. S., Kim, J. E., Lee, Y. J., Kwak, M. H., Choi, Y. H. and Hwang, D. Y. 2013. Protective effects of gomisin A isolated from Schisandra chinensis against CCl(4)-induced hepatic and renal injury. Int. J. Mol. Med. 31, 888-898. https://doi.org/10.3892/ijmm.2013.1263
  10. Ikeya, Y., Taguchi, H., Yosioka, I. and Kobayashi, H. 1979. The constituents of Schizandra chinensis Baill. I. Isolation and structure determination of five new lignans, Gomisin A, B, C, F and G, and the absolute structure of schizandrin. Chem. Pharm. Bull. (Tokyo) 27, 1383-1394. https://doi.org/10.1248/cpb.27.1383
  11. Iwata, H., Tezuka, Y. and Kadot, S. 2004. Identification and characterization of potent CYP3A4 inhibitors in Schisandra fruit extract. Drug Metab. Dispos. 32, 1351-1358. https://doi.org/10.1124/dmd.104.000646
  12. Jang, M. K., Nam, J. S., Kim, J. H., Yun, Y. R. and Jung, M. H. 2016. Schisandra chinensis extract ameliorates nonalcoholic fatty liver via inhibition of endoplasmic reticulum stress. J. Ethnopharmacol. 185, 96-104. https://doi.org/10.1016/j.jep.2016.03.021
  13. Kim, D. H., Hung, T. M. and Bae, K. H. 2006. Gomisin A improves scopolamine-induced memoy impairment in mice. Eur. J. Pharmacol. 542, 129-135. https://doi.org/10.1016/j.ejphar.2006.06.015
  14. Kim, S. H., Kim, Y. S., Kang, S. S., Bae, K., Hung, T. M. and Lee, S. M. 2008. Anti-apoptotic and hepatoprotective effects of gomisin A on fulminant hepatic failure induced by D-galactosamine and lipopolysaccharide in mice. J. Pharmacol. Sci. 106, 225-233. https://doi.org/10.1254/jphs.FP0071738
  15. Min, H. Y., Park, E. J., Hong, J. Y., Kang, Y. J., Kim, S. J. and Lee, S. K. 2008. Antiproliferative effects of dibenzocyclooctadiene lignans isolated from Schisandra chinensis in human cancer cells. Bioorg. Med. Chem. Lett. 18, 523-526. https://doi.org/10.1016/j.bmcl.2007.11.082
  16. Oh, S. Y., Kim, Y. H., Bae, D. S., Um, B. H., Pan, C. H., Kim, C. Y., Lee, H. J. and Lee, J. K. 2010. Anti-inflammatory effects of gomisin N, gomisin J, and schisandrin C isolated from the fruit of Schisandra chinensis. Biosci. Biotechnol. Biochem. 74, 285-291. https://doi.org/10.1271/bbb.90597
  17. Pagliassotti, M. J. 2012. Endoplasmic reticulum stress in nonalcoholic fatty liver disease. Annu. Rev. Nutr. 21, 17-33.
  18. Park, E., Kim, G. H., Yun, S. H., Lim, H. L., Hong, Y., Kwon, S. O., Kwon, J., Chung, Y. H. and Kim, S. I. 2012. Analysis of the endoplasmic reticulum subproteome in the livers of type 2 diabetic mice. Int. J. Mol. Sci. 13, 17230-17243. https://doi.org/10.3390/ijms131217230
  19. Park, H. J., Cho, J. Y., Kim, M. K., Koh, P. O., Cho, K. W. and Kim, C. H. 2012. Anti-obesity effect of Schisandra chinensis in 3T3-L1 cells and high fat diet-induced obese rats. Food Chem. 134, 227-234. https://doi.org/10.1016/j.foodchem.2012.02.101
  20. Passos, E., Ascensao, A., Martins, M. J. and Magalhaes, J. 2015. Endoplasmic reticulum stress response in non-alcoholic steatohepatitis: The possible role of physical exercise. Metabolism 64, 780-792. https://doi.org/10.1016/j.metabol.2015.02.003
  21. Ren, F., Zhou, L., Zhang, X., Wen, T., Shi, H., Xie, B., Li, Z., Chen, D., Wang, Z. and Duan, Z. 2015. Endoplasmic reticulum stress-activated glycogen synthase kinase $3{\beta}$ aggravates liver inflammation and hepatotoxicity in mice with acute liver failure. Inflammation 38, 1151-1165. https://doi.org/10.1007/s10753-014-0080-2
  22. Schroder, M. and Kaufman, R. J. 2005. The mammalian unfolded protein response. Annu. Rev. Biochem. 4, 739-789.
  23. Tajiri, S., Oyadomari, S., Yano, S., Morioka, M., Gotoh, T., Hamada, J. I., Ushio, Y. and Mori, M. 2004. Ischemia-induced neuronal cell death is mediated by the endoplasmic reticulum stress pathway involving CHOP. Cell Death Differ. 11, 403-415. https://doi.org/10.1038/sj.cdd.4401365
  24. Teraoka, R., Shimada, T. and Aburada, M. 2012. The molecular mechanisms of the hepatoprotective effect of Gomisin A against oxidative stress and inflammatory response in rats with carbon tetrachloride-induced acute liver injury. Biol. Pharm. Bull. 35, 171-177. https://doi.org/10.1248/bpb.35.171
  25. Xue, Y., Li, X., Du, X., Li, X., Wang, W., Yang, J., Chen, J., Pu, J. and Sun, H. 2015. Isolation and anti-hepatitis B virus activity of dibenzocyclooctadiene lignans from the fruits of Schisandra chinensis. Phytochemistry 116, 253-261. https://doi.org/10.1016/j.phytochem.2015.03.009
  26. Yamaguchi, O., Higuchi, Y., Hirotani, S., Kashiwase, K., Nakayama, H., Hikoso, S., Takeda, T., Watanabe, T., Asahi, M., Taniike, M., Matsumura, Y., Tsujimoto, I., Hongo, K., Kusakari, Y., Kurihara, S., Nishida, K., Ichijo, H., Hori, M. and Otsu, K. 2003. Targeted deletion of apoptosis signal-regulating kinase 1 attenuates left ventricular remodeling. Proc. Natl. Acad. Sci. USA 100, 15883-15888. https://doi.org/10.1073/pnas.2136717100