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首页> 外文期刊>Japanese Journal of Pharmacology >Adenosine, oxidative stress and cytoprotection.
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Adenosine, oxidative stress and cytoprotection.

机译:腺苷,氧化应激和细胞保护作用。

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摘要

Adenosine, a metabolite of ATP, serves a number of important physiological roles in the body. These actions contribute to sedation, bradycardia, vasorelaxation, inhibition of lipolysis and regulation of the immune system and are mediated, in part, through activation of three distinct adenosine receptor (AR) subtypes. To date, four receptor types have been cloned: A1, A2A, A2B and A3. It is becoming increasing clear that adenosine contributes significantly to cytoprotection, a function mediated principally by the A1AR and A3AR. In this review, we survey the literature on the role of adenosine and the mechanisms underlying cytoprotection and ischemic preconditioning, a process characterized by cytoprotection derived from repeated brief ischemic challenges. An important recent observation is that the expression of several AR subtypes could be regulated by oxidative stress to provide a greater cytoprotective role. Thus, like other proteins known to be regulated during ischemia, the A1AR and A3AR can be considered as being inducible receptors.
机译:腺苷是ATP的代谢产物,在体内起着许多重要的生理作用。这些作用有助于镇静,心动过缓,血管舒张,抑制脂解和调节免疫系统,并部分地通过激活三种不同的腺苷受体(AR)亚型介导。迄今为止,已经克隆了四种受体类型:A1,A2A,A2B和A3。越来越明显的是,腺苷对细胞保护具有重要作用,这种保护作用主要由A1AR和A3AR介导。在这篇综述中,我们调查了关于腺苷的作用以及细胞保护和缺血预处理的机制的文献,该过程的特征是反复短暂的缺血性挑战引起的细胞保护。最近的一项重要重要观察是,氧化应激可以调节几种AR亚型的表达,从而发挥更大的细胞保护作用。因此,如同已知在缺血期间被调节的其他蛋白质一样,A1AR和A3AR可以被认为是诱导型受体。

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