Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China.
Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 201203, China.
Sci Rep. 2016 Jul 22;6:29820. doi: 10.1038/srep29820.
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.
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。