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  2. Curcumin analog CUR5-8 ameliorates nonalcoholic fatty liver disease in mice with high-fat diet-induced obesity

Curcumin analog CUR5-8 ameliorates nonalcoholic fatty liver disease in mice with high-fat diet-induced obesity

  • Metabolism. 2020 Feb;103:154015. doi: 10.1016/j.metabol.2019.154015.
Eun Soo Lee 1 Mi-Hye Kwon 2 Hong Min Kim 1 Ho Bum Woo 3 Chan Mug Ahn 3 Choon Hee Chung 4
Affiliations

Affiliations

  • 1 Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju 220-701, Republic of Korea.
  • 2 The East Coast Research Institute of Life Science, Gangneung-Wonju National University, Gangneung, Republic of Korea.
  • 3 Department of Basic Science, Yonsei University Wonju College of Medicine, Wonju 220-701, Republic of Korea.
  • 4 Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju 220-701, Republic of Korea. Electronic address: cchung@yonsei.ac.kr.
Abstract

Objective: Nonalcoholic fatty liver disease (NAFLD) occurs when excess fat storage in the liver and it is strongly linked with metabolic syndrome including obesity, Insulin resistance, dyslipidemia and hypertension. Curcumin5-8 (CUR5-8) is a synthetic derivative of naturally active curcumin (CUR) that has anti-oxidative and anti-inflammatory properties. In the present study, we investigated the effects of CUR5-8, a novel CUR analog, on hepatic steatosis in mice with high-fat diet (HFD)-induced obesity.

Methods: Based on their diets for 13 weeks, the mice were categorized into the following six groups: regular diet (RD, n = 10), RD with CUR (RD + CUR, 100 mg/kg/day, n = 10), RD with CUR5-8 (RD + CUR5-8, 100 mg/kg/day, n = 10), high-fat diet-induced obese mice (HFD, n = 10), HFD with CUR (HFD + CUR, 100 mg/kg/day, n = 10), and HFD with CUR5-8 (HFD + CUR5-8, 100 mg/kg/day, n = 10) for 13 weeks. Hematoxylin and eosin (H&E) staining of the sections revealed hepatic steatosis.

Results: CUR5-8 administration prevented increase in body and liver weights in mice with HFD-induced obesity. Compared to the HFD group, Insulin resistance was significantly improved in the HFD + CUR5-8 group. Serum alanine aminotransferase level, which is an indicator of liver damage, was also decreased after CUR5-8 administration. H&E staining revealed that CUR5-8 treatment decreased hepatic steatosis in mice with HFD-induced obesity. Interestingly, CUR5-8, and not CUR, decreased the elevated liver triglyceride level induced by the HFD.

Conclusions: These findings suggest that CUR5-8 ameliorates Insulin resistance and hepatic steatosis in mice with HFD-induced obesity.

Keywords

Autophagy; Curcumin; Diabetes; Lipid metabolism; Nonalcoholic fatty liver disease.

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