标题:Propofol Protects Rats and Human Alveolar Epithelial Cells Against Lipopolysaccharide-Induced Acute Lung Injury via Inhibiting HMGB1 Expression
作者:Wang, Xiaoyan; Liu, Chengxiao; Wang, Gongming
作者机构:[Wang, Xiaoyan; Liu, Chengxiao; Wang, Gongming] Shandong Univ, Shandong Prov Hosp, Dept Anesthesiol, 324 Jingwu Rd, Jinan 250100, Shandong, Peoples R 更多
通讯作者:Wang, GM
通讯作者地址:[Wang, GM]Shandong Univ, Shandong Prov Hosp, Dept Anesthesiol, 324 Jingwu Rd, Jinan 250100, Shandong, Peoples R China.
来源:INFLAMMATION
出版年:2016
卷:39
期:3
页码:1004-1016
DOI:10.1007/s10753-016-0330-6
关键词:propofol; HMGB1; LPS; NF-kappa B; TLR4; acute lung injury
摘要:High-mobility group box 1 (HMGB1) plays a key role in the development of acute lung injury (ALI). Propofol, a general anesthetic with anti-inflammatory properties, has been suggested to be able to modulate lipopolysaccharide (LPS)-induced ALI. In this study, we investigated the effects of propofol on the expression of HMGB1 in a rat model of LPS-induced ALI. Rats underwent intraperitoneal injection of LPS to mimic sepsis-induced ALI. Propofol bolus (1, 5, or 10 mg/kg) was infused continuously 30 min after LPS administration, followed by infusion at 5 mg/(kg center dot h) through the left femoral vein cannula. LPS increased wet to dry weight ratio and myeloperoxidase activity in lung tissues and caused the elevation of total protein and cells, neutrophils, macrophages, and neutrophils in bronchoalveolar lavage fluid (BALF). Moreover, HMGB1 and other cytokine levels were increased in BALF and lung tissues and pathological changes of lung tissues were excessively aggravated in rats after LPS administration. Propofol inhibited all the above effects. It also inhibited LPS-induced toll-like receptor (TLR)2/4 protein upexpression and NF-kappa B activation in lung tissues and human alveolar epithelial cells. Propofol protects rats and human alveolar epithelial cells against HMGB1 expression in a rat model of LPS-induced ALI. These effects may partially result from reductions in TLR2/4 and NF-kappa B activation.
收录类别:SCOPUS;SCIE
WOS核心被引频次:4
Scopus被引频次:6
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960098340&doi=10.1007%2fs10753-016-0330-6&partnerID=40&md5=1c0061ddffb5623f0b9cb273058ff2db
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