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年龄相关的非诺贝特对肝组织中 SIRT1、SIRT3 及脂质代谢相关基因表达的影响。

Age-related effects of fenofibrate on the hepatic expression of sirtuin 1, sirtuin 3, and lipid metabolism-related genes.

作者信息

Zubrzycki Adrian, Wrońska Agata, Wierzbicki Piotr M, Kmieć Zbigniew

机构信息

Department of Histology, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.

出版信息

Acta Biochim Pol. 2023 Apr 6;70(2):285-293. doi: 10.18388/abp.2020_6538.

Abstract

BACKGROUND

Sirtuin 1 (Sirt1) and sirtuin 3 (Sirt3) participate in the regulation of lipid metabolism. Our aim was to investigate the effects of the hypolipemic drug fenofibrate (FN) on hepatic Sirt1 and Sirt3 expression, in relation to the expression of lipid metabolism-related genes and in the context of aging.

METHODS AND RESULTS

Young and old male Wistar rats were fed standard chow or supplemented with 0.1% or 0.5% FN for 30 days (n=7-10 in each group). In young rats, 0.1% FN did not affect Sirt1 expression, however, 0.5% FN decreased Sirt1 and both doses reduced Sirt3 protein levels. In old rats, 0.5% FN decreased hepatic Sirt1 mRNA and both doses reduced Sirt1 protein levels, but not Sirt3 expression. Although hepatic Pparα protein levels did not change, FN treatment of young rats induced Cpt1b expression, whereas Lcad, Acox1, Pmp70, and Hmgcs2 expression increased only after 0.1% FN, and Fas2 expression decreased after 0.5% FN. In the liver of old rats, both doses increased Cpt1b and Lcad expression. Only 0.1% FN increased Pmp70 and Hmgcs2 expression, and only 0.5% FN increased Acox1 and Fas2 mRNA levels.

CONCLUSIONS

Treatment with fenofibrate at low or high doses may downregulate the expression of Sirt1 and Sirt3 proteins in the rat liver. The dosage of FN affects molecular changes, and aging alters the response to 0.5% FN.

摘要

背景

Sirtuin 1(Sirt1)和 Sirtuin 3(Sirt3)参与脂质代谢的调节。我们的目的是研究降脂药非诺贝特(FN)对肝脏 Sirt1 和 Sirt3 表达的影响,以及与脂质代谢相关基因表达的关系,并探讨其在衰老过程中的作用。

方法和结果

年轻和年老雄性 Wistar 大鼠分别给予标准饲料或补充 0.1%或 0.5% FN 喂养 30 天(每组 7-10 只)。在年轻大鼠中,0.1% FN 不影响 Sirt1 表达,但 0.5% FN 降低了 Sirt1 和 Sirt3 蛋白水平。在老年大鼠中,0.5% FN 降低了肝 Sirt1 mRNA 表达,两种剂量均降低了 Sirt1 蛋白水平,但 Sirt3 表达没有变化。虽然肝 Pparα 蛋白水平没有变化,但 FN 处理年轻大鼠诱导了 Cpt1b 表达,而 Lcad、Acox1、Pmp70 和 Hmgcs2 表达仅在 0.1% FN 后增加,Fas2 表达在 0.5% FN 后下降。在老年大鼠肝脏中,两种剂量均增加了 Cpt1b 和 Lcad 表达。仅 0.1% FN 增加了 Pmp70 和 Hmgcs2 表达,仅 0.5% FN 增加了 Acox1 和 Fas2 mRNA 水平。

结论

低剂量或高剂量的非诺贝特治疗可能下调大鼠肝脏中 Sirt1 和 Sirt3 蛋白的表达。FN 的剂量影响分子变化,而衰老改变了对 0.5% FN 的反应。

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