The effect of electroacupuncture at ST36 on severe thermal injury-induced remote acute lung injury in rats

被引:22
|
作者
Song, Xue-Min [1 ]
Wu, Xiao-Jing [2 ]
Li, Jian-Guo [1 ]
Le, Lin-Li [1 ]
Liang, Hui [1 ]
Xu, Yang [1 ]
Zhang, Zong-Ze [1 ]
Wang, Yan-Lin [1 ]
机构
[1] Wuhan Univ, Res Ctr Anesthesiol & Crit Care Med, Zhongnan Hosp, Wuchang 430071, Hubei Province, Peoples R China
[2] Wuhan Univ, Renmin Hosp, Dept Anesthesiol, Wuchang 430060, Hubei Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Electroacupuncture; ST36; Acute lung injury; HMGB-1; CHOLINERGIC ANTIINFLAMMATORY PATHWAY; SEVERE BURN INJURY; THERAPEUTIC TARGET; HEMORRHAGIC-SHOCK; VAGUS NERVE; SCALD BURN; INFLAMMATION; PROTEIN; MODEL; SEPSIS;
D O I
10.1016/j.burns.2015.03.004
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: Acupuncture at ST36 can produce anti-inflammatory effects, which might be associated with vagus nerve activity. This study,explored the effects of electroacupuncture (EA) at ST36 on severe thermal injury-induced remote acute lung injury in rats. Interventions: Forty male Sprague-Dawley (SD) rats were randomly divided into five groups: (1) the sham (S) group, (2) the thermal injury (TEM) group subjected to 30% total body surface area (30% TBSA) third-degree scald, (3) the EA at ST36 group subjected to EA stimulation at ST36 (3 V, 2 ms, and 3 Hz) after 30% TBSA scald, (4) the EA at non-acupoint group subjected to EA stimulation at non-acupoint after 30% TBSA scald, and (5) the alpha-bungarotoxin (alpha 7 nicotinic acetylcholine receptor subunit antagonist) group administered 1.0 mu g kg(-1) alpha-bun-garotoxin before EA at ST36. Measurements and main results: Thermal injury of 30% TBSA induced leukocytosis in the alveolar space, interstitial edema, and the pro-inflammatory cytokines interleukin (IL)-1 beta, IL-6, and high-mobility group box 1 (HMGB-1); the expression of both HMGB-1 messenger RNA (mRNA) and protein in lung tissue was significantly enhanced. EA at ST36 significantly downregulated the levels of inflammatory cytokines and improved lung tissue injury. However, pretreatment with alpha-bungarotoxin reversed the effects of electrical stimulation of ST36. Conclusions: EA at ST36 might have a potential protective effect on severe thermal injury-induced remote acute lung injury via limitation of inflammatory responses in rats. (C) 2015 Elsevier Ltd and ISM. All rights reserved.
引用
收藏
页码:1449 / 1458
页数:10
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