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二甲双胍对 AMP 激活的蛋白激酶的作用:理解一个潜在新治疗靶点的转化研究方法。

Metformin action on AMP-activated protein kinase: a translational research approach to understanding a potential new therapeutic target.

机构信息

University Medical Unit, Glasgow Royal Infirmary, UK.

出版信息

Diabet Med. 2010 Oct;27(10):1097-106. doi: 10.1111/j.1464-5491.2010.03098.x.

Abstract

Clinical studies in Type 2 diabetes mellitus have shown that the effects of metformin go beyond improving HbA(1c) and include reductions in cardiovascular endpoints. Metformin therapy has been widely used in the treatment of Type 2 diabetes for many years, yet the precise mode of action remains uncertain. It has recently been proposed that metformin-mediated stimulation of hepatic AMP-activated protein kinase (AMPK) underlies the hypoglycaemic effects of metformin. AMPK is a heterotrimeric enzyme that is expressed in many tissues and plays a central role in the regulation of energy homoeostasis. Furthermore, there is increasing evidence that AMPK is implicated in the pathophysiology of cardiovascular and metabolic diseases. The generation of more specific and potent activators of AMPK, however, could have additional metabolic and vascular benefits for patients with Type 2 diabetes.

摘要

临床研究表明,二甲双胍在 2 型糖尿病中的作用不仅在于改善糖化血红蛋白(HbA1c),还包括降低心血管终点事件。多年来,二甲双胍已广泛用于 2 型糖尿病的治疗,但确切的作用机制仍不确定。最近有研究提出,二甲双胍通过刺激肝脏 AMP 激活的蛋白激酶(AMPK)发挥降血糖作用。AMPK 是一种异三聚体酶,在许多组织中表达,在调节能量稳态中发挥核心作用。此外,越来越多的证据表明 AMPK 与心血管和代谢疾病的病理生理学有关。然而,生成更特异和更强效的 AMPK 激活剂,可能会为 2 型糖尿病患者带来额外的代谢和血管益处。

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