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二甲双胍部分通过载脂蛋白A5途径改善小鼠肥胖相关的高甘油三酯血症。

Metformin ameliorates obesity-associated hypertriglyceridemia in mice partly through the apolipoprotein A5 pathway.

作者信息

Li Rong, Chen Lu-Zhu, Zhao Wang, Zhao Shui-Ping, Huang Xian-Sheng

机构信息

Department of Stomatology, The Second Xiangya Hospital, Central South University, Changsha, China.

Department of Cardiovascular Medicine, The Second Xiangya Hospital, Central South University, Changsha, China.

出版信息

Biochem Biophys Res Commun. 2016 Sep 23;478(3):1173-8. doi: 10.1016/j.bbrc.2016.08.087. Epub 2016 Aug 17.

Abstract

INTRODUCTION

Apolipoprotein A5 (apoA5) is a key regulator of triglyceride (TG) metabolism. This study is to investigate the role of apoA5 in obesity-associated hypertriglyceridemia and metformin-related hypotriglyceridemic actions.

METHODS

Two obese mouse models, including high-fat diet-induced obese mice and ob/ob obese mice, were adopted. The effects of low- and high-dose metformin were determined on plasma and hepatic TG and apoA5 of these obese mice. Besides, the effects of metformin on TG and apoA5 were also detected in mouse and human hepatocytes in vitro.

RESULTS

(1) Plasma apoA5 levels in the obese mice were markedly elevated and positively correlated with TG. Hepatic TG contents and apoA5 expressions were also remarkably increased in the obese mice. (2) Metformin dose-dependently decreased hepatic and plasma TG and apoA5 in the obese mice. Similarly, metformin dose-dependently reduced cellular TG contents and apoA5 expressions in hepatocytes in vitro. Compared to APOA5 knock-down (KD), metformin plus APOA5 KD resulted in more TG reduction of hepatocytes.

CONCLUSION

Increased hepatic and plasma apoA5 could be a result of obesity-associated hypertriglyceridemia, and metformin displays hypotriglyceridemic effects on obese mice partly via the apoA5 pathway.

摘要

引言

载脂蛋白A5(apoA5)是甘油三酯(TG)代谢的关键调节因子。本研究旨在探讨apoA5在肥胖相关高甘油三酯血症及二甲双胍相关降甘油三酯作用中的作用。

方法

采用两种肥胖小鼠模型,包括高脂饮食诱导的肥胖小鼠和ob/ob肥胖小鼠。测定低剂量和高剂量二甲双胍对这些肥胖小鼠血浆和肝脏TG及apoA5的影响。此外,还在体外小鼠和人肝细胞中检测了二甲双胍对TG和apoA5的影响。

结果

(1)肥胖小鼠血浆apoA5水平显著升高,且与TG呈正相关。肥胖小鼠肝脏TG含量和apoA5表达也显著增加。(2)二甲双胍可剂量依赖性降低肥胖小鼠肝脏和血浆TG及apoA5水平。同样,二甲双胍在体外可剂量依赖性降低肝细胞内TG含量和apoA5表达。与载脂蛋白A5基因敲低(KD)相比,二甲双胍联合载脂蛋白A5基因敲低可使肝细胞内TG降低更多。

结论

肝脏和血浆apoA5升高可能是肥胖相关高甘油三酯血症的结果,二甲双胍对肥胖小鼠的降甘油三酯作用部分是通过apoA5途径实现的。

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