Objective To observe the effect of Xiaoer Feire Kechuan oral solution on the extrapulmonary injury induced by Mycoplasma pneumoniae in infant Wistar rats. Methods Infant Wistar rats were infected intranasally with M. ...Objective To observe the effect of Xiaoer Feire Kechuan oral solution on the extrapulmonary injury induced by Mycoplasma pneumoniae in infant Wistar rats. Methods Infant Wistar rats were infected intranasally with M. pneumoniae once a day for four days. In the treatment groups, Xiaoer Feire Kechuan oral solution was administered daily for four days beginning from the day of infection. On day 5, blood of the rats was collected, and blood routine and biochemistry indexes were measured. All rats were sacrificed, and the weight of brain, heart, liver, and kidney was measured to calculate the organ indexes. The GM1 and GALC-Ab content in brain tissue was determined by ELISA. Pathological changes in the brain, heart, liver, kidney, and cerebellum were observed by HE staining. Results Blood routine indexes fluctuated within the normal range in the infection control group and in three of the Xiaoer Feire Kechuan oral solution groups. The serum LDH, CK, and CRE in all three Xiaoer Feire Kechuan oral solution groups were distinctly lower than those in the infection control group (P < 0.01, P < 0.05). Rat brain index and GALC-Ab content in the brain tissue showed an increase in infection control group. In the Xiaoer Feire Kechuan oral solution groups, the GALC-Ab content in brain tissue was decreased significantly. The heart, liver, and kidney tissues showed mild pathological changes in the infection group, which were reversed by Xiaoer Feire Kechuan oral solution treatment. Conclusions The extrapulmonary injury induced by M. pneumoniae in infant Wistar rats was significantly inhibited by Xiaoer Feire Kechuan oral solution.展开更多
文摘Objective To observe the effect of Xiaoer Feire Kechuan oral solution on the extrapulmonary injury induced by Mycoplasma pneumoniae in infant Wistar rats. Methods Infant Wistar rats were infected intranasally with M. pneumoniae once a day for four days. In the treatment groups, Xiaoer Feire Kechuan oral solution was administered daily for four days beginning from the day of infection. On day 5, blood of the rats was collected, and blood routine and biochemistry indexes were measured. All rats were sacrificed, and the weight of brain, heart, liver, and kidney was measured to calculate the organ indexes. The GM1 and GALC-Ab content in brain tissue was determined by ELISA. Pathological changes in the brain, heart, liver, kidney, and cerebellum were observed by HE staining. Results Blood routine indexes fluctuated within the normal range in the infection control group and in three of the Xiaoer Feire Kechuan oral solution groups. The serum LDH, CK, and CRE in all three Xiaoer Feire Kechuan oral solution groups were distinctly lower than those in the infection control group (P < 0.01, P < 0.05). Rat brain index and GALC-Ab content in the brain tissue showed an increase in infection control group. In the Xiaoer Feire Kechuan oral solution groups, the GALC-Ab content in brain tissue was decreased significantly. The heart, liver, and kidney tissues showed mild pathological changes in the infection group, which were reversed by Xiaoer Feire Kechuan oral solution treatment. Conclusions The extrapulmonary injury induced by M. pneumoniae in infant Wistar rats was significantly inhibited by Xiaoer Feire Kechuan oral solution.
文摘目的探讨特应质在肺炎支原体肺炎(Mycoplasma pneumoniae pneumonia,MPP)儿童病情严重程度和肺外并发症中的作用,并阐明IL-17在其中的作用机制。方法回顾性纳入了2017年2月至2019年2月期间就诊于本院的221例MPP儿童,所有患者均行过敏原检测。采用相关性分析探索特应质和IL-17与病情及肺外并发症等相关性。结果221例MPP患儿中71例合并特应质,44例出现肺外并发症,其中以皮肤表现(36.4%)最为常见。有特应质MPP患者哮喘发作(P<0.001)和既往哮喘病史(P<0.001)比例、总IgE(P<0.001)显著高于无特应质患者,而IL-17(P<0.001)显著低于无特应质患者。有特应质MPP患者中更易出现重症肺炎(48/71 vs 17/150,P<0.001)。有特应质MPP患者出现胸腔积液(P=0.045)、呼吸急促(P<0.001)的比例、需氧疗(P<0.001)、糖皮质激素治疗的比例(P=0.008)以及糖皮质激素治疗时间(P=0.002)显著高于无特应质患者。合并肺外并发症MPP患者血浆IL-17(P=0.009)显著低于无肺外并发症患者,而总IgE水平(P=0.009)和特应质比例(P<0.001)显著高于无肺外并发症患者。结论特应质是导致MPP患儿病情严重和肺外并发症的危险因素之一,可能与IgE释放和IL-17降低相关。
