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作 者:Xu-Han Zuo Yu Huang Bo-Cen Chen Ming-Yue Zhu Cai-Cai Zhang Han-Yi Jiao Li-Fang Lu Man Xiao Han Wang
机构地区:[1]Key Laboratory of Tropical Translational Medicine of Ministry of Education,School of Basic Medicine and Life Sciences,Hainan Medical University,Haikou,Hainan,China [2]Experiment and Teaching Center for Clinical Skills,Hainan Medical University,Haikou,Hainan,China
出 处:《Asian Pacific Journal of Tropical Biomedicine》2024年第9期410-416,共7页亚太热带生物医学杂志(英文版)
基 金:supported by the Natural Science Foundation of Hainan Province High-level Talent Project(grant number 820RC644);Innovative Research Projects for Postgraduate Students at Hainan Medical University(grant number HYYS2022B08).
摘 要:Objective:To explore whether thrombopoietin can exert a protective effect against doxorubicin-induced cardiotoxicity by modulating the sirtuin 1(SIRT1)signaling pathway.Methods:H9c2 cell viability was determined by CCK-8 and cardiomyocyte apoptosis was detected by TUNEL assay.The protein expressions of SIRT1 and p38 MAPK were measured by Western blot.RT-qPCR was also used to determine SIRT1 mRNA expression.In addition,intracellular reactive oxygen species levels and antioxidant enzyme activities were evaluated.Results:Thrombopoietin treatment reversed doxorubicin-induced decline in H9c2 cell viability.It also increased SIRT1 and decreased p-p38 MAPK protein expressions.In addition,thrombopoietin significantly attenuated doxorubicin-induced apoptosis and oxidative stress,and enhanced antioxidant enzyme activities.However,silencing SIRT1 abrogated the protective effects of thrombopoietin,as evidenced by reduced cell viability and increased oxidative stress and reactive oxygen species levels.Conclusions:Thrombopoietin alleviates doxorubicin-induced cardiomyocyte injury by reducing oxidative stress and apoptosis via the SIRT1/p38 MAPK pathway.However,its protective effects need to be further verified in animal tests.
关 键 词:DOXORUBICIN THROMBOPOIETIN Oxidative stress Sirtuin 1 CARDIOTOXICITY
分 类 号:R542.2[医药卫生—心血管疾病]
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