首页|期刊导航|中国中药杂志|基于"肺主治节"理论对玉屏风散合四君子汤干预反复呼吸道感染大鼠肺心共损研究

基于"肺主治节"理论对玉屏风散合四君子汤干预反复呼吸道感染大鼠肺心共损研究OA

Intervention of Yupingfeng Powder and Sijunzi Decoction in treatment of lung and heart co-injury in rats with recurrent respiratory tract infection based on theory of"lung governing management and regulation"

中文摘要英文摘要

利用宏观表征评价和肺心组织损伤比较,验证玉屏风散合四君子汤(Yupingfeng Powder and Sijunzi Decoction,YPSD)对反复呼吸道感染(RRTI)大鼠"肺失治节"的干预作用;基于网络药理学方法预测其共治RRTI和心肌损伤(MD)的可能机制.研究将 30 只大鼠随机分为对照(Co)组、模型(Mo)组、匹多莫德(Pg)组、中药低剂量(Lg)组和中药高剂量(Hg)组.建立RRTI模型并干预后,针对"肺失治节"表现,对宏观表征指标进行评价;比较肺心组织损伤水平;使用网络药理学实验对YPSD作用于RRTI和MD的潜在治疗靶点和可能机制预测;进行体内实验进一步验证.结果表明,YPSD能有效改善RRTI大鼠的宏观表征评价指标,缓解病理过程中肺、心组织的损伤水平.网络药理学结果得到蛋白激酶B(Akt)为核心作用蛋白.体内实验结果显示YPSD能够有效上调肺、心组织被激活的Akt蛋白水平,显著增高B淋巴细胞瘤-2 基因(Bcl-2)与Bcl-2 相关X蛋白(Bax)比值.YPSD能有效干预RRTI大鼠"肺失治节"结局,实现肺心共治作用,对RRTI和MD的干预效果可能依靠调节Akt蛋白的表达水平发挥作用.

This study aims to validate the intervention effect of Yupingfeng Powder and Sijunzi Decoction(YPSD)on"lung's failure in management and regulation"in rats with recurrent respiratory tract infection(RRTI)by utilizing macroscopic characterization evaluation and comparing lung and heart tissue damage.Additionally,it aims to predict the possible mechanisms underlying co-treatment of RRTI and myocardial damage(MD)based on network pharmacology methods.Thirty rats were randomly divided into a control(Co)group,a model(Mo)group,a pidotimod(Pg)group,a low-dose YPSD(Lg)group,and a high-dose YPSD(Hg)group.After the RRTI modeling and interventions,macroscopic characterization indicators were evaluated based on the manifestations of"lung's failure in management and regulation".The levels of lung and heart tissue damage were compared.Network pharmacology experiments were used to predict potential therapeutic targets and possible mechanisms of YPSD in treating RRTI and MD,which were further validated through in vivo experiments.The experimental results showed that YPSD could effectively improve the macroscopic characterization evaluation indicators in RRTI rats and alleviate the damage levels of lung and heart tissue during the pathological process.Network pharmacology results identified protein kinase B(Akt)as the core functional protein.In vivo experimental results demonstrated that YPSD could effectively upregulate the activated Akt protein levels in lung and heart tissue,with a significantly increased ratio of B lymphoblastoma-2 gene(Bcl-2)to Bcl-2-associated X protein(Bax).YPSD can effectively intervene in the outcome of"lung's failure in management and regulation"in RRTI rats,achieving the effect of concurrent lung and heart treatment.Its intervention effects on RRTI and MD may function by regulating the activation level of the Akt protein.

唐丹;田亚静;刘槐洋;高金生;杨金虎;杨晶晶;王嘉铖;安家盛;高绍芳

河北中医药大学 中医学院,河北 石家庄 050091河北中医药大学 中医学院,河北 石家庄 050091河北中医药大学 中西医结合学院 河北省中西医结合肝肾病证研究重点实验室,河北 石家庄 050091河北中医药大学 中医学院,河北 石家庄 050091河北中医药大学 中医学院,河北 石家庄 050091河北中医药大学 中西医结合学院 河北省中西医结合肝肾病证研究重点实验室,河北 石家庄 050091河北中医药大学 中西医结合学院 河北省中西医结合肝肾病证研究重点实验室,河北 石家庄 050091河北中医药大学 研究生学院,河北 石家庄 050091河北中医药大学 中西医结合学院 河北省中西医结合肝肾病证研究重点实验室,河北 石家庄 050091

反复呼吸道感染肺主治节宏观表征肺心共治网络药理学

recurrent respiratory tract infectionlung governing management and regulationmacroscopic characterizationco-treat-ment of lung and heartnetwork pharmacology

《中国中药杂志》 2026 (6)

1657-1666,10

河北省中医药管理局科研计划项目(2024101)

10.19540/j.cnki.cjcmm.20251117.801

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