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Protective effect of chalcone derivative L2H24 on cardiomyocytes injured by H2O2 |
HU Linya1, HONG Chenglyu2, CHEN Qian1, HE Wenfei1, WU Jianzhang1 |
1.School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China; 2.Department of Cardiovascular, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China |
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Cite this article: |
HU Linya,HONG Chenglyu,CHEN Qian, et al. Protective effect of chalcone derivative L2H24 on cardiomyocytes injured by H2O2[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2021, 51(7): 534-541.
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Abstract Objective: To investigate the anti-oxidative protective effect of chalcone derivative L2H24 on H2O2-induced H9c2 cardiomyocytes injury and its related molecular mechanism. Methods: The survival rate of cardiomyocytes was detected by MTT experiment; cell proliferation ability was detected by colony cloning experiment; cell pyroptosis was observed under the inverted microscope; MDA level of lipid peroxidation in cells was detected by thiobarbituric acid color reaction; the expression level of HO-1, Nrf2, Caspase-1 p48, Caspase-1 p20 and IL-1β in the cells was measured by Western blotting analysis. Results: L2H24 not only increased the survival rate of H9c2 cells damaged by H2O2 (P<0.05), promote the formation of cell colonies and reduce the level of cell lipid peroxidation (P<0.05), but also reduced the expression level of Caspase-1 p48, Caspase-1 p20 and IL-1β in cells (P<0.05) and improved the pyrolysis. Furthermore, L2H24 promoted the translocation of Nrf2 into the nucleus and up-regulated the expression level of its downstream antioxidant protein HO-1, which protected cardiomyocytes from H2O2-induced oxidative damage. Conclusion: Chalcone derivative L2H24 plays a protective role against oxidative damage, and its mechanism may be related to the activation of Nrf2/HO-1 signaling pathway.
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Received: 20 January 2021
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