青附宣肺汤对博来霉素诱导大鼠肺纤维化的干预作用及机制OA
The therapeutic effect of Qingfu Xuanfei Tang on bleomycin-induced pulmonary fibrosis in rats and its mechanism
目的 在博来霉素雾化诱导的肺纤维化(pulmonary fi-brosis,PF)大鼠模型上,评价青附宣肺汤(qingfu xuanfei tang,QFXFT)的抗PF药效并探讨其作用机制.方法 首先,为确定稳定的药效学研究模型,将SD大鼠分为空白对照组、单次气管内雾化博来霉素组(4.5 mg·kg-1)及3次气管内雾化博来霉素组(1.5 mg·kg-1,每周1次),通过肺组织病理学和羟脯氨酸(HYP)含量评估模型稳定性与纤维化程度.继而,采用更优的造模方法复制模型,将成模大鼠随机分为模型组、强的松组(5 mg·kg-1)及QFXFT低、高剂量组(1、2 g·kg-1),连续干预28 d.通过HE和Masson染色评估肺组织病理改变;采用 Western blot 及免疫组化法检测肺组织中 α-SMA、Col-Ⅰ和Col-Ⅲ蛋白的表达水平.结果 模型比较显示,单次给药组大鼠肺组织肺泡炎评分、纤维化程度及HYP含量均明显高于3次给药组(P<0.01).药效实验表明,与模型组相比,QFXFT高剂量组与强的松组均可明显减轻肺泡炎和PF病理损伤,并明显下调肺组织中α-SMA、Col-Ⅰ和Col-Ⅲ的蛋白表达水平(P<0.01).结论 在优化的博来霉素雾化诱导模型中,QFXFT能够明显抑制PF进展,其机制可能与抑制成纤维细胞活化及细胞外基质沉积有关.
Aim To evaluate the anti-pulmonary fi-brosis effect of Qingfu Xuanfei Tang(QFXFT)and ex-plore its mechanism in a bleomycin-induced rat model.Methods First,to establish a stable model for pharmacodynamic study,SD rats were divided into a control group,a single intratracheal aerosolized bleo-mycin group(4.5 mg·kg-1),and a triple intratracheal aerosolized bleomycin group(1.5 mg·kg-1 per time,once a week).Model stability and fibrosis degree were evaluated by lung histopathology and hydroxyproline(HYP)content.Then,the superior modeling method was adopted.Successfully modeled rats were randomly divided into a model group,a prednisone group(5 mg·kg-1),and QFXFT groups(1,2 g·kg-1),receiving continuous intervention for 28 days.The pathological changes were assessed by HE and Masson staining.The protein expression levels of α-SMA,Col-I,and Col-Ⅲ in lung tissue were detected by Western blot and immunohistochemistry.Results Model compari-son showed that the single administration group had significantly higher alveolar inflammation scores,fi-brosis degree,and HYP content than the triple admin-istration group(all P<0.01).Pharmacodynamic ex-periments showed that,compared with the model group,both 2 g·kg-1 QFXFT group and prednisone sig-nificantly alleviated alveolitis and pulmonary fibrosis pathological damage,and significantly down-regulated the protein expression levels of α-SMA,Col-I,and Col-Ⅲ in lung tissue(P<0.01).Conclusions In an optimized bleomycin aerosol-induced model,QFXFT can significantly inhibit the progression of pulmonary fibrosis,and its mechanism may be related to the inhi-bition of fibroblast activation and extracellular matrix deposition.
范佳欣;郑蕾;尧忠柳;张钧岚;蔡雄;林也;刘良
湖南中医药大学第一中医临床学院 湖南 长沙 410007湖南中医药大学第一中医临床学院 湖南 长沙 410007湖南中医药大学第一中医临床学院 湖南 长沙 410007湖南中医药大学中医学院 湖南 长沙 410208湖南中医药大学第一中医临床学院 湖南 长沙 410007||湖南中医药大学中医学院 湖南 长沙 410208湖南中医药大学第一中医临床学院 湖南 长沙 410007||湖南中医药大学中医学院 湖南 长沙 410208广州中医药大学中医证候全国重点实验室,广东 广州 510000
医药卫生
肺纤维化博来霉素青附宣肺汤动物模型药效学α-平滑肌肌动蛋白
pulmonary fibrosisbleomycinQingfu Xuanfei Tanganimal modelpharmacodynamicsα-smooth muscle actin
《中国药理学通报》 2026 (10)
1970-1976,7
国家自然科学基金项目(No 82405235)
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