敲除腺苷酸环化酶1可减轻吡柔比星诱导的心脏毒性

IF 2.9 4区 医学 Q2 Medicine
Wenqing Zhang, Zhiyun Shu, Peng Huang, HongYuan Cheng, Jiahua Ji, Dexian Wei, Liqun Ren
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引用次数: 0

摘要

本研究旨在探讨腺苷酸环化酶1(ADCY1)对吡拉比星诱导的心肌细胞损伤的影响和可能机制。用吡柔比星(THP)处理 HL-1 细胞以诱导细胞内毒性,并用 CCK-8、Edu、流式细胞术、ROS、ELISA、RT-qPCR 和 Western 印迹法评估小鼠心肌细胞的损伤程度。THP 处理降低了 HL-1 细胞的活力,抑制了细胞增殖,诱导了细胞凋亡,并引发了氧化应激。此外,RT-qPCR 结果显示 ADCY1 在 HL-1 细胞中的表达明显升高,分子对接显示 ADCY1 与 THP 有直接的相互作用。Western 印迹显示 ADCY1、磷酸蛋白激酶 A 和 GRIN2D 的表达也明显升高。敲除 ADCY1 可减轻 THP 诱导的心脏毒性,这可能是通过调节 ADCY1/PKA/GRIN2D 通路实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adenylate cyclase 1 knockdown attenuates pirarubicin-induced cardiotoxicity

This study aimed to investigate the effects and possible mechanisms of adenylate cyclase 1 (ADCY1) on pirarubicin-induced cardiomyocyte injury. HL-1 cells were treated with pirarubicin (THP) to induce intracellular toxicity, and the extent of damage to mouse cardiomyocytes was assessed using CCK-8, Edu, flow cytometry, ROS, ELISA, RT-qPCR and western blotting. THP treatment reduced the viability of HL-1 cells, inhibited proliferation, induced apoptosis and triggered oxidative stress. In addition, the RT-qPCR results revealed that ADCY1 expression was significantly elevated in HL-1 cells, and molecular docking showed a direct interaction between ADCY1 and THP. Western blotting showed that ADCY1, phospho-protein kinase A and GRIN2D expression were also significantly elevated. Knockdown of ADCY1 attenuated THP-induced cardiotoxicity, possibly by regulating the ADCY1/PKA/GRIN2D pathway.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
128
审稿时长
6 months
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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