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中风中的蛋白激酶C同工酶

Protein kinase C isozymes in stroke.

作者信息

Chou Wen-Hai, Messing Robert O

机构信息

Ernest Gallo Clinic and Research Center, University of California San Francisco, Emeryville, California 94608, USA.

出版信息

Trends Cardiovasc Med. 2005 Feb;15(2):47-51. doi: 10.1016/j.tcm.2005.01.003.

Abstract

Stroke is a devastating neurologic disease and a leading cause of death and disability worldwide. Thrombolytic agents have been used to re-establish circulation in thromboembolic stroke, but their utility is limited by hemorrhage and reperfusion injury. Studies with experimental stroke models, mouse genetics, and selective peptide inhibitors and activators have implicated protein kinase C (PKC) epsilon in ischemic preconditioning and PKCdelta and gamma in tissue injury. PKCdelta, resident both in neutrophils and in the brain, appears particularly essential for reperfusion injury, and recent work using PKCdelta-specific peptide inhibitors suggests that PKCdelta inhibitors could prove useful in attenuating reperfusion injury and improving outcome following thrombolysis.

摘要

中风是一种毁灭性的神经系统疾病,是全球范围内导致死亡和残疾的主要原因。溶栓药物已被用于恢复血栓栓塞性中风的血液循环,但其效用受到出血和再灌注损伤的限制。对实验性中风模型、小鼠遗传学以及选择性肽抑制剂和激活剂的研究表明,蛋白激酶C(PKC)ε参与缺血预处理,而PKCδ和γ参与组织损伤。PKCδ存在于中性粒细胞和大脑中,似乎对再灌注损伤尤为重要,最近使用PKCδ特异性肽抑制剂的研究表明,PKCδ抑制剂可能有助于减轻再灌注损伤并改善溶栓后的预后。

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