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Microcurrent stimulation promotes reverse remodelling in cardiomyocytes

机译:微电流刺激促进心肌细胞的反向重塑

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Abstract Aims It has been shown that electrical stimulation can improve tissue repair in patients. Imbalances in the extracellular matrix composition induce manifestation of heart failure. Here we investigated the application of microcurrent (MC) to modulate the expression of matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinases (TIMPs) in cardiomyocytes in vitro and in vivo to reverse remodelling in the heart in spontaneous hypertensive rats (SHR). Methods Cardiomyocytes from young SHR (7 months) and old SHR (14 months) were stimulated in vitro and in vivo with MC. MMP and TIMP expression were analysed by qPCR and immunofluorescence to evaluate the modulation of MC treatment. Results Modulation of cardiomyocytes with MC enhances proliferation with no morphological changes in vitro . By electrical stimulation dual effects, increase and decrease, on MMP-2, MMP-9, TIMP-3, and TIMP-4 mRNA as well as protein expression were observed, depending on the age of the cardiomyocytes. In our in vivo study, MC down-regulated MMP-2, MMP-9, and TIMP-4 and increased TIMP-3 in young SHR. In old SHR MMP-2, MMP-9, and TIMP-4 were up-regulated, whereas TIMP-3 was unaffected. Conclusions Our data indicate that treatment of MC can modulate the expression of MMPs and TIMPs in vitro and in vivo in SHR. Based on these results new treatments for heart failure could be developed.
机译:摘要目的表明电刺激可以改善患者的组织修复。细胞外基质组成的失衡引起心力衰竭的表现。在这里,我们研究了微电流(MC)在体外和体内调节心肌细胞中基质金属蛋白酶(MMP)和金属蛋白酶组织抑制剂(TIMPs)的表达,以逆转自发性高血压大鼠(SHR)心脏中的重构的应用。方法MC体外和体内刺激年轻SHR(7个月)和老SHR(14个月)的心肌细胞。通过qPCR和免疫荧光分析MMP和TIMP的表达,以评估MC治疗的调节。结果MC对心肌细胞的调节增强了体外增殖,没有形态学改变。通过电刺激的双重作用,根据心肌细胞的年龄,观察到了MMP-2,MMP-9,TIMP-3和TIMP-4 mRNA的增加和减少以及蛋白质表达。在我们的体内研究中,MC下调了年轻SHR中的MMP-2,MMP-9和TIMP-4,并增加了TIMP-3。在旧的SHR中,MMP-2,MMP-9和TIMP-4上调,而TIMP-3不受影响。结论我们的数据表明MC治疗可以调节SHR体内和体外MMP和TIMP的表达。基于这些结果,可以开发出用于心力衰竭的新疗法。

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