CHEN Rui-Juan, RUI Qing-Lin, WANG Qiong, TIAN Fang, WU Jian, KONG Xiang-Qing. Shenfu injection attenuates lipopolysaccharide-induced myocardial inflammation and apoptosis in rats [J]. Chin J Nat Med, 2020, 18(3): 226-233. DOI: 10.1016/S1875-5364(20)30025-X
Citation: CHEN Rui-Juan, RUI Qing-Lin, WANG Qiong, TIAN Fang, WU Jian, KONG Xiang-Qing. Shenfu injection attenuates lipopolysaccharide-induced myocardial inflammation and apoptosis in rats [J]. Chin J Nat Med, 2020, 18(3): 226-233. DOI: 10.1016/S1875-5364(20)30025-X

Shenfu injection attenuates lipopolysaccharide-induced myocardial inflammation and apoptosis in rats

  • Shenfu injection (SFI), a Chinese medicinal product, shows potent efficacy in treating sepsis. The aim of the present study was to clarify the protective effects of SFI against lipopolysaccharide (LPS)-induced myocardial inflammation and apoptosis. Experiments were carried out in Sprague-Dawley (SD) rats treated with LPS or LPS + SFI, and in H9C2 cardiomyocytes. The sepsis-associated myocardial inflammation and apoptosis was induced by the intraperitoneal injection of LPS (20 mg·kg1). SFI attenuated the increased expression of tumor necrosis factor (TNF)-α and interleukin (IL)-1β induced by LPS both in serum and heart. In LPS group, cell viability was reduced, and reversed after SFI administration. LPS treatment increased the expression levels of cleaved-caspase 3 and Bax, and those of Bcl2 and Bcl2/Bax. These two trends were reversed by SFI administration. The expression levels of phosphorylated mitogen-activated protein kinase kinase (p-MEK) and phosphorylated extracellular regulated protein kinases (p-ERK) were increased by LPS, and reversed by SFI. MEK inhibitor U0126 attenuated the apoptosis induced by LPS. These results indicate that SFI could treat LPS-induced cardiac dysfunction. In conclusion, SFI attenuates the inflammation and apoptosis induced by LPS via downregulating the MEK and ERK signaling pathways.
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