Trivalent Chromium Supplementation Ameliorates Oleic Acid-Induced Hepatic Steatosis in Mice

被引:0
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作者
Song Wang
Jian Wang
Yajing Liu
Hui Li
Qiao Wang
Zhiwei Huang
Wenbin Liu
Ping Shi
机构
[1] East China University of Science and Technology,State Key Laboratory of Bioreactor Engineering
[2] Shanghai Research Institute of Criminal Science and Technology,Shanghai Key Laboratory of Crime Scene Evidence
[3] Donghua University,College of Chemistry, Chemical Engineering and Biotechnology
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关键词
Steatosis; Trivalent chromium; CD36; DGAT2; Inflammatory cytokines;
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摘要
Trivalent chromium [Cr(III)] is recognized as an essential trace element for human health, whereas its effect on hepatic lipid metabolism has not yet been fully understood. This study aimed to investigate the beneficial effects and potential mechanisms of Cr(III) on hepatic steatosis in an oleic acid (OA) induced mice model. Mice were fed with high OA for 12 weeks to induce lipid accumulation, and co-administrated with Cr(III) supplementation. Indexes of liver lipid accumulation, associated lipid genes expression, fatty acids (FAs) profile and inflammatory cytokines were analyzed. The data showed that Cr(III) supplementation could attenuate disease progress of hepatic steatosis and protect liver from high OA. After Cr(III) supplementation, elevated body weight and liver injury in steatosis mice were reversed, excessive lipid accumulation and FAs were also reduced. The up-regulation of cluster of differentiation 36 (CD36) and diacylglycerol acyltransferase 2 (DGAT2) following steatosis induction were inhibited by Cr(III). Cr(III) reduced the content of pro-inflammatory cytokines (IL-1β and TNF-α, IL-12) and restored the level of anti-inflammatory cytokine (IL-10) to the control values. Our results suggest that Cr(III) supplementation is a novel strategy for alleviating OA-induced hepatic steatosis.
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页码:192 / 201
页数:9
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