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慢性社会挫败应激破坏脂质合成的调控。

Chronic social defeat stress disrupts regulation of lipid synthesis.

机构信息

Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

J Lipid Res. 2010 Jun;51(6):1344-53. doi: 10.1194/jlr.M002196. Epub 2010 Feb 2.

Abstract

Several psychiatric disorders increase the risk of cardiovascular disease, including posttraumatic stress disorder and major depression. While the precise mechanism for this association has not yet been established, it has been shown that certain disorders promote an unfavorable lipid profile. To study the interaction of stress and lipid dysregulation, we utilized chronic social defeat stress (CSDS), a mouse model of chronic stress with features of posttraumatic stress disorder and major depression. Following exposure to CSDS, mice were given access to either regular chow or a Western-style diet high in fat and cholesterol (HFD). The combination of social stress and HFD resulted in significant perturbations in lipid regulation, including two key features of the metabolic syndrome: increased plasma levels of non-HDL cholesterol and intrahepatic accumulation of triglycerides. These effects were accompanied by a number of changes in the expression of hepatic genes involved in lipid regulation. Transcriptional activity of LXR, SREBP1c, and ChREBP were significantly affected by exposure to HFD and CSDS. We present CSDS as a model of social stress induced lipid dysregulation and propose that social stress alters lipid metabolism by increasing transcriptional activity of genes involved in lipid synthesis.

摘要

几种精神障碍会增加心血管疾病的风险,包括创伤后应激障碍和重度抑郁症。虽然这种关联的确切机制尚未确定,但已经表明某些疾病会导致不利的脂质谱。为了研究应激和脂质失调的相互作用,我们利用慢性社会挫败应激(CSDS),一种具有创伤后应激障碍和重度抑郁症特征的慢性应激小鼠模型。在接触 CSDS 后,小鼠可以接触到普通食物或高脂肪和胆固醇的西式饮食(HFD)。社会压力和 HFD 的结合导致脂质调节的显著紊乱,包括代谢综合征的两个关键特征:非高密度脂蛋白胆固醇的血浆水平升高和肝内甘油三酯的积累。这些影响伴随着与脂质调节相关的许多肝基因表达的变化。LXR、SREBP1c 和 ChREBP 的转录活性受到 HFD 和 CSDS 暴露的显著影响。我们提出 CSDS 作为一种社会应激诱导的脂质失调模型,并提出社会应激通过增加参与脂质合成的基因的转录活性来改变脂质代谢。

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