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      Genipin alleviates high‐fat diet‐induced hyperlipidemia and hepatic lipid accumulation in mice via miR‐142a‐5p/ SREBP ‐1c axis

      1 , 1 , 1 , 1 , 2 , 3 , 1 , 1 , 4
      The FEBS Journal
      Wiley

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          Abstract

          <p class="first" id="d5618562e134">Hyperlipidemia is a chronic disorder which plays an important role in the development of cardiovascular diseases, type 2 diabetes, atherosclerosis, hypertension, and nonalcoholic fatty liver disease. Genipin (GNP) is a metabolite from genipioside, which is an active component of the traditional Chinese medicine Gardenia jasminoides Ellis, and has been recognized as a beneficial compound against metabolic disorders. However, whether it can correct overnutrition-induced dyslipidemia is still unknown. In this study, the effects of GNP on attenuating hyperlipidemia and hepatic lipid accumulation were investigated using normal and obese mice induced with a high-fat diet (HFD) and primary hepatocytes treated with free fatty acids. We also sought to identify potential targets of GNP to mediate its effects in the liver. We found that obese mice treated with GNP showed a decrease in the body weight, serum lipid levels, as well as hepatic lipid accumulation. Besides, GNP regulated hepatic expression levels of lipid metabolic genes, which are important in maintaining systemic lipid homeostasis. At the molecular level, GNP increased the expression levels of miR-142a-5p, which bound to 3' untranslated region of Srebp-1c, an important regulator of lipogenesis, which thus led to the inhibition of lipogenesis. Collectively, our data demonstrated that GNP effectively antagonized HFD-induced hyperlipidemia and hepatic lipid accumulation in mice. Such effects were achieved by regulating miR-142a-5p/SREBP-1c axis. </p>

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          Author and article information

          Contributors
          Journal
          The FEBS Journal
          FEBS J
          Wiley
          1742-464X
          1742-4658
          December 30 2017
          February 2018
          December 26 2017
          February 2018
          : 285
          : 3
          : 501-517
          Affiliations
          [1 ]Jiangsu Key Laboratory for Molecular and Medical Biotechnology School of Life Sciences Nanjing Normal University China
          [2 ]Department of Geriatric Cardiology the First Affiliated Hospital of Nanjing Medical University China
          [3 ]The Joint Research Center of Guangzhou University and Keele University for Gene Interference and Application School of Life Sciences Guangzhou University China
          [4 ]School of Life Science and Technology China Pharmaceutical University Nanjing China
          Article
          10.1111/febs.14349
          29197188
          93f4d2d2-67db-4d4a-925c-c26e9e88a664
          © 2018

          http://onlinelibrary.wiley.com/termsAndConditions#vor

          http://doi.wiley.com/10.1002/tdm_license_1.1

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