[Efficacy and mechanism of Lianhua Qingwen Capsules(LHQW) on chemotaxis of macrophages in acute lung injury (ALI) animal model].

体内 渗透(HVAC) 趋化性 地塞米松 炎症 H&E染色 医学 病理 体外 化学 内科学 免疫学 免疫组织化学 生物 受体 生物化学 物理 生物技术 热力学
作者
Qi Li,Jie Yin,Qingsen Ran,Qing Yang,Li Liu,Zheng Zhao,Yujie Li,Ying Chen,Lidong Sun,Yajie Wang,Xiaogang Weng,Weiyan Cai,Xiaoxin Zhu
出处
期刊:PubMed 卷期号:44 (11): 2317-2323 被引量:12
标识
DOI:10.19540/j.cnki.cjcmm.20190210.001
摘要

This paper was mainly to discuss the potential role and mechanism of Lianhua Qingwen Capsules(LHQW) in inhibiting pathological inflammation in the model of acute lung injury caused by bacterial infection. For in vitro study, the mRNA expression of MCP-1 in RAW264.7 cells and THP-1 cells, the content of MCP-1 in cell supernatant, as well as the effect of LHQW on chemotaxis of macrophages were detected. For in vivo study, mice were randomly divided into 7 groups, including normal group, model group(LPS 5 mg·kg~(-1)), LHQW 300, 600 and 1 200 mg·kg~(-1)(low, middle and high dose) groups, dexamethasone 5 mg·kg~(-1) group and penicillin-streptomycin group. Then, the anal temperature was detected two hours later. Dry weight and wet weight of lung tissues in mice were determined; TNF-α and MCP-1 levels in alveolar lavage fluid and MCP-1 in serum were detected. In addition, the infiltration of alveolar macrophages was also observed and the infiltration count of alveolar macrophages was measured by CCK-8 method. HE staining was also used to observe the inflammatory infiltration of lung tissues in mice. Both of the in vitro and in vivo data consistently have confirmed that: by down-regulating the expression of MCP-1, LHWQ could efficiently decrease the chemotaxis of monocytes toward the pulmonary infection foci, thus blocking the disease development in ALI animal model.
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