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纤溶酶原激活物抑制剂-1与代谢紊乱中的生物钟

Plasminogen activator inhibitor-1 and the circadian clock in metabolic disorders.

作者信息

Oishi Katsutaka

机构信息

Clock Cell Biology Research Group, Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology, Central 6, 1-1-1 Higashi, Tsukuba, Ibaraki, Japan.

出版信息

Clin Exp Hypertens. 2009 May;31(3):208-19. doi: 10.1080/10641960902822468.

Abstract

Plasma PAI-1 levels robustly fluctuate in a circadian manner and consequently contribute to hypofibrinolysis during the early morning. The circadian expression of PAI-1 gene is thought to be directly regulated by the circadian clock proteins such as CLOCK and BMAL1/BMAL2 which drive the endogenous biological clock. Plasma PAI-1 levels are increased in the beginning of the active phase in both diurnal humans and in nocturnal rodents, suggesting that the rhythmic PAI-1 expression is commonly indispensable for organisms. A series of our recent studies revealed that circadian clock proteins are important for hypofibrinolysis induced by metabolic disorders such as obesity and diabetes.

摘要

血浆纤溶酶原激活物抑制因子-1(PAI-1)水平以昼夜节律的方式剧烈波动,因此在清晨会导致纤溶功能低下。PAI-1基因的昼夜节律表达被认为直接受昼夜节律钟蛋白如CLOCK和BMAL1/BMAL2的调控,这些蛋白驱动着内源性生物钟。在昼行性人类和夜行性啮齿动物的活跃期开始时,血浆PAI-1水平都会升高,这表明PAI-1的节律性表达对生物体普遍不可或缺。我们最近的一系列研究表明,昼夜节律钟蛋白对于肥胖和糖尿病等代谢紊乱诱导的纤溶功能低下很重要。

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