Protective function of tocilizumab in human cardiac myocytes ischemia reperfusion injury

来源 :Asian Pacific Journal of Tropical Medicine | 被引量 : 0次 | 上传用户:lmh860628
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Objective:To investigate the protective function of tocilizumab in human cardiac myocytes ischemia-reperfusion injury.Methods:The human cardiac myocytes were treated by tocilizumab with different concentrations(1.0 mg/mL,3.0 mg/mL,5.0 mg/mL) for 24 h.then cells were cultured in ischemia environment for 24 h and reperfusion environment for 1 h.The MTT and flow cytometry were used to detect the proliferation and apoptosis of human cardiac myocytes,respectively.The mRNA and protein expressions of Bcl-2 and Bax were measured by qRT-PCR and western blot,respectively.Results:Compared to the negative group,pretreated by tocilizumab could significantly enhance the proliferation viability and suppress apoptosis of human cardiac myocytes after suffering ischemia reperfusion injury(P<0.05).The expression of Bcl-2 in tocilizumab treated group were higher than NC group(P<0.05).while the Bax expression were lower(P<0.05).Conclusions:Tocilizumab could significantly inhibit apoptosis and keep the proliferation viability of human cardiac myocytes after suffering ischemia reperfusion injury.Tocilizumab may obtain a widely application in the protection of ischemia reperfusion injury. Methods: The human cardiac myocytes were treated by tocilizumab with different concentrations (1.0 mg / mL, 3.0 mg / mL, 5.0 mg / mL) for 24 h . then cells were cultured in ischemia environment for 24 h and reperfusion environment for 1 h. The MTT and flow cytometry were used to detect the proliferation and apoptosis of human cardiac myocytes, respectively. The mRNA and protein expressions of Bcl-2 and Bax were measured by qRT-PCR and western blot, respectively. Results: Compared to the negative group, pretreated by tocilizumab could significantly enhance the proliferation viability and suppress apoptosis of human cardiac myocytes after suffering ischemia reperfusion injury (P <0.05). expression of Bcl -2 in tocilizumab treated group were higher than NC group (P <0.05) .while the Bax expression were lower (P <0.05) .Conclusions: Tocilizumab could significantly inhibit apoptosis and keep the prol Iferation viability of human cardiac myocytes after suffering ischemia reperfusion injury. Tocilizumab may obtain a wide application in the protection of ischemia reperfusion injury.
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