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The effect of Shenmai injection on the proliferation of Rat airway smooth muscle cells in asthma and underlying mechanism

机译:参麦注射液对哮喘大鼠气道平滑肌细胞增殖的影响及其机制

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Background Over-proliferation of airway smooth muscle cell (ASMC) is one of the important contributors to airway remodeling in asthma. The aim of this study was to investigate the effect of Shenmai injection (SMI) on the proliferation of the rat ASMC in asthma. Methods Rats were randomly divided into three groups: the control group, the asthma group, and the SMI treatment group. Reverse transcription-polymerase chain reaction (RT-PCR) and immunocytochemistry staining were used to detect the mRNA and protein expression of transient receptor potential vanilloid 1 (TRPV1) and proliferating cell nuclear antigen (PCNA) in rat ASMC respectively. Intracellular Ca2+ concentration ( [Ca2+]i ) in rat ASMC were measured with Fluo-3/AM by confocal microscopy. The proliferation was detected by MTT assay. Results Compared with the control group, the asthma group showed an increased expression of TRPV1 and [Ca2+]i in rat ASMC. The expression of PCNA and absorbance of MTT assay in asthma rat ASMC was also significantly increased. SMI could significantly decrease the expression of TRPV1 channel and [Ca2+]i in the asthmatic rat ASMC. Furthermore, the expression of PCNA and absorbance of MTT assay in asthmatic rat ASMC was significantly reduced after SMI treatment. Conclusions SMI may prevent asthma-induced ASMC over-proliferation probably by inhibiting the expression of TRPV1 channel, which regulates the intracellular calcium concentration.
机译:背景技术气道平滑肌细胞(ASMC)的过度增殖是哮喘气道重塑的重要因素之一。这项研究的目的是研究参麦注射液(SMI)对哮喘大鼠ASMC增殖的影响。方法将大鼠随机分为三组:对照组,哮喘组和SMI治疗组。用逆转录聚合酶链反应(RT-PCR)和免疫细胞化学染色分别检测大鼠ASMC中瞬时受体电位类香草素1(TRPV1)和增殖细胞核抗原(PCNA)的mRNA和蛋白表达。通过共聚焦显微镜用Fluo-3 / AM测定大鼠ASMC中细胞内Ca 2 + 的浓度[Ca 2 + ] i。通过MTT测定检测增殖。结果与对照组相比,哮喘组大鼠ASMC中TRPV1和[Ca 2 + ] i的表达增加。哮喘大鼠ASMC中PCNA的表达和MTT法的吸光度也显着增加。 SMI可以显着降低哮喘大鼠ASMC中TRPV1通道和[Ca 2 + ] i的表达。此外,SMI处理后哮喘大鼠ASMC中PCNA的表达和MTT测定的吸光度显着降低。结论SMI可能通过抑制TRPV1通道的表达来预防哮喘引起的ASMC过度增殖,而TRPV1通道可以调节细胞内钙的浓度。

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