靶向sirtuins治疗糖尿病。

Frank K Huynh, Kathleen A Hershberger, Matthew D Hirschey
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引用次数: 47

摘要

Sirtuins是一类依赖NAD+的去乙酰化酶,如去乙酰化酶,具有广泛的生物学功能。最近的研究表明sirtuin作用降低与2型糖尿病有关。营养过剩和衰老是糖尿病的两大危险因素,它们会导致sirtuin功能下降,导致糖脂代谢异常。因此,在2型糖尿病患者中恢复正常水平的sirtuin可能是一种很有前途的治疗糖尿病的方法。本文综述了哺乳动物SIRT1、SIRT3和SIRT6中7种sirtuins的生物学功能,这些sirtuins已显示出突出的代谢作用和早期药物靶向潜力。研究使用sirtuin激活剂治疗糖尿病的临床试验已经在进行中,有望替代目前的糖尿病治疗方法。因此,对sirtuin激活剂的进一步研究是必要的,并可能导致一种新的安全有效的糖尿病治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting sirtuins for the treatment of diabetes.

Sirtuins are a class of NAD+-dependent deacetylases, such as deacetylases, that have a wide array of biological functions. Recent studies have suggested that reduced sirtuin action is correlated with Type 2 diabetes. Both overnutrition and aging, which are two major risk factors for diabetes, lead to decreased sirtuin function and result in abnormal glucose and lipid metabolism. Therefore, restoring normal levels of sirtuin action in Type 2 diabetes may be a promising method of treating diabetes. This article reviews the biological functions of three of the seven mammalian sirtuins - SIRT1, SIRT3 and SIRT6 - that have demonstrated prominent metabolic roles and early potential for drug targeting. Clinical trials investigating the use of sirtuin activators for treating diabetes are already underway and show promise as alternatives to current diabetes therapies. Thus, further research into sirtuin activators is warranted and may lead to a new class of safe, effective diabetes treatments.

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