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玉屏风散改善力竭运动诱导的肺泡-毛细血管屏障损伤——细胞骨架的调节作用

Yu-Ping-Feng Formula Ameliorates Alveolar-Capillary Barrier Injury Induced by Exhausted-Exercise Regulation of Cytoskeleton.

作者信息

Wang Di, Li Quan, Pan Chun-Shui, Yan Li, Sun Kai, Wang Xiao-Yi, Anwaier Gulinigaer, Liao Qian-Zan, Xie Ting-Ting, Fan Jing-Yu, Huo Xin-Mei, Wang Yuan, Han Jing-Yan

机构信息

Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.

Tasly Microcirculation Research Center, Peking University Health Science Center, Beijing, China.

出版信息

Front Pharmacol. 2022 Jun 24;13:891802. doi: 10.3389/fphar.2022.891802. eCollection 2022.

Abstract

Yu-ping-feng powder (YPF) is a compound traditional Chinese medicine extensively used in China for respiratory diseases. However, the role of YPF in alveolar-capillary barrier dysfunction remains unknown. This study aimed to explore the effect and potential mechanism of YPF on alveolar-capillary barrier injury induced by exhausted exercise. Male Sprague-Dawley rats were used to establish an exhausted-exercise model by using a motorized rodent treadmill. YPF at doses of 2.18 g/kg was administrated by gavage before exercise training for 10 consecutive days. Food intake-weight/body weight, blood gas analysis, lung water percent content, BALF protein concentration, morphological observation, quantitative proteomics, real-time PCR, and Western blot were performed. A rat pulmonary microvascular endothelial cell line (PMVEC) subjected to hypoxia was applied for assessing the related mechanism. YPF attenuated the decrease of food intake weight/body weight, improved lung swelling and hemorrhage, alleviated the increase of lung water percent content and BALF protein concentration, and inhibited the impairment of lung morphology. In addition, YPF increased the expression of claudin 3, claudin 18, occludin, VE-cadherin, and β-catenin, attenuated the epithelial and endothelial hyperpermeability and/or , and the stress fiber formation in PMVECs after hypoxia. Quantitative proteomics discovered that the effect of YPF implicated the Siah2-ubiquitin-proteasomal pathway, Gng12-PAK1-MLCK, and RhoA/ROCK, which was further confirmed by Western blot. Data are available via ProteomeXchange with identifier PXD032737. YPF ameliorated alveolar-capillary barrier injury induced by exhausted exercise, which is accounted for at least partly by the regulation of cytoskeleton.

摘要

玉屏风散(YPF)是一种在中国广泛用于治疗呼吸道疾病的复方中药。然而,YPF在肺泡-毛细血管屏障功能障碍中的作用尚不清楚。本研究旨在探讨YPF对力竭运动诱导的肺泡-毛细血管屏障损伤的影响及潜在机制。采用雄性Sprague-Dawley大鼠,通过电动啮齿动物跑步机建立力竭运动模型。在连续10天的运动训练前,通过灌胃给予剂量为2.18 g/kg的YPF。进行食物摄入量-体重/体重、血气分析、肺水百分比含量、支气管肺泡灌洗液(BALF)蛋白浓度、形态学观察、定量蛋白质组学、实时聚合酶链反应(PCR)和蛋白质免疫印迹法检测。应用缺氧处理的大鼠肺微血管内皮细胞系(PMVEC)评估相关机制。YPF减轻了食物摄入量-体重/体重的下降,改善了肺肿胀和出血,减轻了肺水百分比含量和BALF蛋白浓度的升高,并抑制了肺形态学损伤。此外,YPF增加了闭合蛋白3、闭合蛋白18、闭锁蛋白、血管内皮钙黏蛋白和β-连环蛋白的表达,减轻了缺氧后PMVECs的上皮和内皮高通透性及/或应激纤维形成。定量蛋白质组学发现,YPF的作用涉及Siah2-泛素-蛋白酶体途径、Gng12-PAK1-MLCK和RhoA/ROCK,蛋白质免疫印迹法进一步证实了这一点。数据可通过ProteomeXchange获得,标识符为PXD032737。YPF改善了力竭运动诱导的肺泡-毛细血管屏障损伤,这至少部分是由细胞骨架调节所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/babb/9263595/35b9448677fa/fphar-13-891802-g001.jpg

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