Electroacupuncture pretreatment protects septic rats from acute lung injury by relieving inflammation and regulating macrophage polarization

被引:3
作者
Zhou, Jun [1 ,2 ]
Li, Lan [3 ]
Qu, Mengjian [3 ]
Tan, Jinqu [3 ]
Sun, Guanghua [3 ]
Luo, Fu [3 ]
Zhong, Peirui [3 ]
He, Chengqi [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Rehabil Med, 37 Guoxue Xiang, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Key Lab Rehabil Med, Chengdu, Peoples R China
[3] Univ South China, Dept Rehabil, Affiliated Hosp 1, Hengyang, Peoples R China
基金
中国国家自然科学基金;
关键词
acute lung injury; electroacupuncture pretreatment; inflammation; macrophage; polarization; ENDOTOXEMIA; ZUSANLI; MODEL;
D O I
10.1177/09645284221118588
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Macrophage polarization toward the M2 phenotype may attenuate inflammation and have a therapeutic effect in acute lung injury (ALI). Objective: To investigate the role of electroacupuncture (EA) pretreatment on the inflammatory response and macrophage polarization in a septic rat model of lipopolysaccharide (LPS)-induced ALI. Methods: Male Sprague Dawley rats (n = 24) were randomly divided into three groups (n = 8 each): control (Ctrl), ALI (LPS) and pre-EA (LPS + EA pretreatment). ALI and pre-EA rats were injected with LPS via the caudal vein. Pulmonary edema was assessed by left upper pulmonary lobe wet-to-dry (W/D) ratios. Lung injury scores were obtained from paraffin-embedded and hematoxylin and eosin-stained sections of the left lower pulmonary lobe. Inflammatory activation was quantified using serum tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, transforming growth factor (TGF)-beta and IL-10 levels measured by enzyme linked immunosorbent assay (ELISA). Macrophage phenotype was determined by real-time quantitative polymerase chain reaction (RT-qPCR) and Western blotting. Results: Mean lung W/D ratio was significantly lower and serum IL-1 beta levels were decreased in pre-EA rats compared to ALI rats (P < 0.05). TNF-alpha mRNA expression was decreased and mannose receptor (MR) and Arg1 mRNA expression was increased in the lung tissues of pre-EA rats compared to ALI rats (P < 0.01). Arg1 protein expression was similarly increased in the lung tissues of pre-EA rats compared to ALI rats (P < 0.05). Conclusion: EA pretreatment may play a protective role by promoting macrophage polarization to the M2 phenotype in a septic rat model of LPS-induced ALI.
引用
收藏
页码:175 / 182
页数:8
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