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藏药佐太对小鼠肝脏中生物钟基因表达有影响。

The Tibetan medicine Zuotai influences clock gene expression in the liver of mice.

作者信息

Li Huan, Li Wen-Kai, Lu Yuan-Fu, Wei Li-Xin, Liu Jie

机构信息

Key Lab for Basic Pharmacology of Ministry of Education, Zunyi Medical College , Zunyi , China.

Northwest Plateau Institute of Bology, Chinese Academia of Sciences , Xining, Qinghai , China.

出版信息

PeerJ. 2016 Jan 26;4:e1632. doi: 10.7717/peerj.1632. eCollection 2016.

Abstract

Background. The circadian clock is involved in drug metabolism, efficacy and toxicity. Drugs could in turn affect the biological clock as a mechanism of their actions. Zuotai is an essential component of many popular Tibetan medicines for sedation, tranquil and "detoxification," and is mainly composed of metacinnabar (β-HgS). The pharmacological and/or toxicological basis of its action is unknown. This study aimed to examine the effect of Zuotai on biological clock gene expression in the liver of mice. Materials and methods. Mice were orally given Zuotai (10 mg/kg, 1.5-fold of clinical dose) daily for 7 days, and livers were collected every 4 h during the 24 h period. Total RNA was extracted and subjected to real-time RT-PCR analysis of circadian clock gene expression. Results. Zuotai decreased the oscillation amplitude of the clock core gene Clock, neuronal PAS domain protein 2 (Npas2), Brain and muscle Arnt-like protein-1 (Bmal1) at 10:00. For the clock feedback negative control genes, Zuotai had no effect on the oscillation of the clock gene Cryptochrome (Cry1) and Period genes (Per1-3). For the clock-driven target genes, Zuotai increased the oscillation amplitude of the PAR-bZip family member D-box-binding protein (Dbp), decreased nuclear factor interleukin 3 (Nfil3) at 10:00, but had no effect on thyrotroph embryonic factor (Tef); Zuotai increased the expression of nuclear receptor Rev-Erbα (Nr1d1) at 18:00, but had little influence on the nuclear receptor Rev-Erbβ (Nr1d2) and RORα. Conclusion. The Tibetan medicine Zuotai could influence the expression of clock genes, which could contribute to pharmacological and/or toxicological effects of Zuotai.

摘要

背景。昼夜节律时钟参与药物代谢、疗效和毒性。药物反过来可能会影响生物钟,这是其作用机制之一。坐台是许多常用藏药中用于镇静、安神和“解毒”的重要成分,主要由朱砂(β-硫化汞)组成。其作用的药理学和/或毒理学基础尚不清楚。本研究旨在探讨坐台对小鼠肝脏生物钟基因表达的影响。

材料与方法。小鼠每天口服坐台(10 mg/kg,临床剂量的1.5倍),连续7天,并在24小时内每4小时采集一次肝脏。提取总RNA,进行生物钟基因表达的实时逆转录聚合酶链反应分析。

结果。坐台在10:00时降低了生物钟核心基因Clock、神经元PAS结构域蛋白2(Npas2)、脑和肌肉芳香烃受体核转运蛋白样蛋白1(Bmal1)的振荡幅度。对于生物钟反馈负调控基因,坐台对生物钟基因隐花色素(Cry1)和周期基因(Per1-3)的振荡没有影响。对于生物钟驱动的靶基因,坐台在10:00时增加了PAR-bZip家族成员D-盒结合蛋白(Dbp)的振荡幅度,降低了核因子白细胞介素3(Nfil3),但对促甲状腺素胚胎因子(Tef)没有影响;坐台在18:00时增加了核受体Rev-Erbα(Nr1d1)的表达,但对核受体Rev-Erbβ(Nr1d2)和RORα影响较小。

结论。藏药坐台可影响生物钟基因的表达,这可能有助于其药理学和/或毒理学效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/474f/4741069/bb2f96d3c810/peerj-04-1632-g001.jpg

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