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新型凋亡蛋白酶激活因子-1(Apaf-1)抑制剂用于缺血性心脏病的发现:合成、活性和靶标鉴定。

The discovery of a novel inhibitor of apoptotic protease activating factor-1 (Apaf-1) for ischemic heart: synthesis, activity and target identification.

机构信息

Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China.

Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 201203, China.

出版信息

Sci Rep. 2016 Jul 22;6:29820. doi: 10.1038/srep29820.

Abstract

Apaf-1 is a central component in the apoptosis regulatory network for the treatment of apoptosis related diseases. Excessive Apaf-1 activity induced by myocardial ischemia causes cell injury. No drug targeted to Apaf-1 for treating myocardial ischemia has been reported to the best of our knowledge. In the present work, we synthesized a novel compound, ZYZ-488, which exhibited significant cardioprotective property in significantly increasing the viability of hypoxia-induced H9c2 cardiomyocytes and reducing CK and LDH leakage. Further study suggested the protective activity of ZYZ-488 dependent on its anti-apoptosis effect. This anti-apoptotic effect is most probably related to its disturbing the interaction between Apaf-1 and procaspase-9 as the target fishing and molecular docking indicated. The suppression on the activation of procaspase-9 and procaspase-3 with ZYZ-488 strongly suggested that compound ZYZ-488 could be a novel inhibitor of Apaf-1. In conclusion, ZYZ-488 as a novel small molecule competitive inhibitor of Apaf-1, with the great potential for treating cardiac ischemia.

摘要

凋亡酶激活因子-1(Apaf-1)是细胞凋亡调控网络的核心组成部分,可用于治疗与细胞凋亡相关的疾病。心肌缺血时,Apaf-1 活性过度增加会导致细胞损伤。据我们所知,目前尚无针对 Apaf-1 的药物用于治疗心肌缺血。在本研究中,我们合成了一种新型化合物 ZYZ-488,该化合物在显著增加缺氧诱导的 H9c2 心肌细胞活力和降低肌酸激酶(CK)和乳酸脱氢酶(LDH)漏出方面表现出显著的心脏保护作用。进一步的研究表明,ZYZ-488 的保护活性依赖于其抗凋亡作用。这种抗凋亡作用可能与其干扰 Apaf-1 和前胱冬酶-9 之间的相互作用有关,因为靶标钓取和分子对接实验表明了这一点。ZYZ-488 抑制前胱冬酶-9 和前胱冬酶-3 的激活,强烈表明化合物 ZYZ-488 可能是 Apaf-1 的新型抑制剂。总之,ZYZ-488 作为 Apaf-1 的新型小分子竞争性抑制剂,具有治疗心肌缺血的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55d/4957240/f16909dafac0/srep29820-f1.jpg

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