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首页> 外文期刊>Environmental toxicology and pharmacology >The effect of Platycodin D on the expression of cytoadherence proteins P1 and P30 in Mycoplasma pneumoniae models
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The effect of Platycodin D on the expression of cytoadherence proteins P1 and P30 in Mycoplasma pneumoniae models

机译:桔梗D对肺炎支原体模型细胞粘附蛋白P1和P30表达的影响

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摘要

Platycodin D is one of the most important monomers of the Qinbaiqingfei pellet (Qinbai), which has already been approved as the first effective new Traditional Chinese Medicine used to fight against Mycoplasma pneumoniae (M. pneumoniae) in clinic in China. In previous studies, pharmacodynamics experiment has proved that Platycodin D has anti-M. pneumoniae effect and the minimum inhibitory concentration (MIC) is 16m μg/ml. This paper further clarified that the mechanism underlying the anti-M. pneumoniae effect of Platycodin D might be due to M. pneumoniae adhesion proteins P1 and P30. P1 and P30 expression levels in M. pneumoniae strain, M. pneumoniae-infected BALB/c mice, and M. pneumoniae-infected A549 cells were determined by reverse transcription PCR. Platycodin D strongly inhibited P1 and P30 expression in M. pneumonia and high dosage of Platycodin D exhibited a greater effect on reducing P1 and P30 expression than low dose Platycodin D. Platycodin D prevented M. pneumoniae infection through inhibiting the expression of adhesion proteins, which might be one of the mechanisms for the anti-M. pneumoniae properties of Qinbai. These results provide a foundation to further explore the mechanisms of action of Qjnbai in future studies.
机译:Platycodin D是秦白清肺丸(秦白)中最重要的单体之一。秦白清肺丸已被批准为中国临床上首个有效的抗肺炎支原体(M. pneumoniae)的新型中药。在以前的研究中,药效学实验证明Platycodin D具有抗M的作用。肺炎效应和最小抑菌浓度(MIC)为16mμg/ ml。本文进一步阐明了抗M的潜在机制。 Platycodin D的肺炎作用可能是由于肺炎支原体粘附蛋白P1和P30引起的。通过逆转录PCR确定肺炎支原体菌株,肺炎支原体感染的BALB / c小鼠和肺炎支原体感染的A549细胞中P1和P30的表达水平。 Platycodin D强烈抑制肺炎支原体中P1和P30的表达,高剂量的Platycodin D表现出比低剂量Platycodin D降低P1和P30更大的作用。Platycodin D通过抑制粘附蛋白的表达来预防肺炎支原体感染。可能是抗M的机制之一。秦柏的肺炎性质。这些结果为进一步研究Qjnbai的作用机理提供了基础。

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