Publication | Open Access
Matrine attenuating cardiomyocyte apoptosis in doxorubicin-induced cardiotoxicity through improved mitochondrial membrane potential and activation of mitochondrial respiratory chain Complex I pathway
19
Citations
44
References
2024
Year
Heart FailureH9c2 CellsApoptosisCell DeathCardiovascular ToxicityMatrine PretreatmentOxidative StressInflammationDoxorubicin-induced CardiotoxicityAnti-cancer AgentCardiologyCancer ResearchMitochondrial Membrane PotentialCardiomyopathyMedicineCardiomyocyte ApoptosisPharmacologyCell BiologyTumor MicroenvironmentMitochondrial FunctionPhysiologyOncology
The study aimed to demonstrate that matrine can reduce apoptosis in H9c2 cells induced by the cardiotoxic anticancer drug doxorubicin (DOX).The researchers pretreated H9c2 cells with different concentrations of matrine before exposing them to DOX and cultured them for 24 h. They assessed cell survival rates using cell counting kit-8 and MTT assay. Hoechst 33258 dye kits were used to determine apoptosis, while laser confocal JC-1 method was applied to test the mitochondrial membrane potential (MMP). Complex I activities were detected following the manufacturer's protocol. The results indicated that matrine pretreatment significantly increased the survival rate of H9c2 cells injured by DOX. Additionally, matrine reduced apoptosis in H9c2 cells through the improvement of MMP and activity of Complex I, which were damaged by DOX.
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