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双黄连减轻虾蛋白诱导的小鼠哮喘模型中的气道高反应性和炎症。

Shuang-Huang-Lian Attenuates Airway Hyperresponsiveness and Inflammation in a Shrimp Protein-Induced Murine Asthma Model.

作者信息

Gao Yuan, Fei Qiaoling, Qi Ruijuan, Hou Rui, Han Yixin, Cai Runlan, Sun Guibo, Qi Yun

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China.

出版信息

Evid Based Complement Alternat Med. 2019 Jan 1;2019:4827342. doi: 10.1155/2019/4827342. eCollection 2019.

Abstract

Shuang-Huang-Lian (SHL), an herbal formula of traditional Chinese medicine, is clinically used for bronchial asthma treatment. Our previous study found that SHL prevented basophil activation to suppress Th2 immunity and stabilized mast cells through activating its mitochondrial calcium uniporter. Sporadic clinical reports that SHL was used for the treatment of bronchial asthma can be found. Thus, in this study, we systematically investigated the effects of SHL on asthmatic responses using a shrimp protein (SP)- induced mouse model. SHL significantly inhibited airway inspiratory and expiratory resistance, and histological studies suggested it reduced thickness of airway smooth muscle and infiltration of inflammation cells. It also could alleviate eosinophilic airway inflammation (EAI), including reducing the number of eosinophils and decreasing eotaxin and eosinophil peroxidase levels in the bronchoalveolar lavage fluid (BALF). Further studies indicated that SHL suppressed SP-elevated mouse mast cell protease-1 and IgE levels, prevented Th2 differentiation in mediastinal lymph nodes, and lowered Th2 cytokine (e.g., IL-4, IL-5, and IL-13) production in BALF. In conclusion, SHL attenuates airway hyperresponsiveness and EAI mainly via the inhibition of mast cell activation and Th2 immunity, which may help to elucidate the underlying mechanism of SHL on asthma treatment and support its clinical use.

摘要

双黄连(SHL)是一种中药复方,临床上用于治疗支气管哮喘。我们之前的研究发现,SHL可通过激活线粒体钙单向转运体来防止嗜碱性粒细胞活化,从而抑制Th2免疫反应,并稳定肥大细胞。有零星的临床报告表明SHL可用于治疗支气管哮喘。因此,在本研究中,我们使用虾蛋白(SP)诱导的小鼠模型系统地研究了SHL对哮喘反应的影响。SHL显著抑制气道吸气和呼气阻力,组织学研究表明它可降低气道平滑肌厚度和炎症细胞浸润。它还可以减轻嗜酸性气道炎症(EAI),包括减少嗜酸性粒细胞数量以及降低支气管肺泡灌洗液(BALF)中嗜酸性粒细胞趋化因子和嗜酸性粒细胞过氧化物酶水平。进一步的研究表明,SHL可抑制SP升高的小鼠肥大细胞蛋白酶-1和IgE水平,防止纵隔淋巴结中的Th2分化,并降低BALF中Th2细胞因子(如IL-4、IL-5和IL-13)的产生。总之,SHL主要通过抑制肥大细胞活化和Th2免疫反应来减轻气道高反应性和EAI,这可能有助于阐明SHL治疗哮喘的潜在机制,并支持其临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/343a/6332955/edc087ec0d10/ECAM2019-4827342.001.jpg

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