Literature DB >> 30047465

Ilexgenin A enhances the effects of simvastatin on non-alcoholic fatty liver disease without changes in simvastatin pharmacokinetics.

Ya-Wen Lu1, Ying-Chao Zhu1, Li Zhang1, Ping Li1, Jie Yang2, Xiao-Dong Wen3.   

Abstract

Cardiovascular disease (CVD) is the most common cause of death in patients with non-alcoholic fatty liver disease (NAFLD). New therapeutic strategies which have the potential for slowing down the evolution of NAFLD and reducing CVD-related mortality are urgently needed. Statins are well recognized in the treatment of dyslipidemia, but their use in the treatment of NAFLD is limited due to the safety concerns. Ilexgenin A (IA) is one of the main bioactive compounds in 'Shan-lv-cha', an herbal tea commonly used in China. In the present study, we investigated the possible synergistic therapeutic effects of IA and simvastatin (SV) on NAFLD. IA or SV showed beneficial effects on the rats with NAFLD by lowering the liver weight, liver index and plasma levels of alanine aminotransferase and aspartate aminotransferase, regulating abnormal metabolism of lipids and ameliorating steatosis in liver. IA significantly enhanced the hypolipidemic and anti-inflammation effects of SV. Furthermore, a sensitive, accurate, convenient and reproducible LC-MS method was developed to investigate the effects of IA on the pharmacokinetics of SV. No significant changes were observed in pharmacokinetic parameters of SV and simvastatin hydroxy acid in the IA plus SV co-treated group in comparison with those in the group treated with SV alone. The mRNA levels and activity of CYP3A1 were not altered by IA. In conclusion, the results obtained from the present study should be helpful for further clinical application of SV and IA alone or in combination.
Copyright © 2018 China Pharmaceutical University. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Ilexgenin A; Non-alcoholic fatty liver; Pharmacokinetics; Simvastatin; Simvastatin acid

Mesh:

Substances:

Year:  2018        PMID: 30047465     DOI: 10.1016/S1875-5364(18)30077-3

Source DB:  PubMed          Journal:  Chin J Nat Med        ISSN: 1875-5364


  2 in total

1.  Urantide decreases hepatic steatosis in rats with experimental atherosclerosis via the MAPK/Erk/JNK pathway.

Authors:  Haipeng Cui; Yingxue Lin; Lide Xie; Juan Zhao
Journal:  Mol Med Rep       Date:  2021-02-19       Impact factor: 2.952

2.  The Effect of Simvastatin on Gut Microbiota and Lipid Metabolism in Hyperlipidemic Rats Induced by a High-Fat Diet.

Authors:  Qing Zhang; Xiaoyun Fan; Rui Ye; Yuzhong Hu; Tingting Zheng; Rui Shi; Wenjian Cheng; Xucong Lv; Lijiao Chen; Peng Liang
Journal:  Front Pharmacol       Date:  2020-04-29       Impact factor: 5.810

  2 in total

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