{"title":"Glutamine Administration After Sublethal Lower Limb Ischemia Reduces Inflammatory Reaction and Offers Organ Protection in Ischemia/Reperfusion Injury.","authors":"Yao-Ming Shih, Juey-Ming Shih, Man-Hui Pai, Yu-Chen Hou, Chiu-Li Yeh, Sung-Ling Yeh","doi":"10.1177/0148607115587949","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>This study investigated the effects of intravenous glutamine (GLN) administration on the expression of adhesion molecules and inflammatory mediators in a mice model of hind limb ischemia/reperfusion (IR) injury.</p><p><strong>Methods: </strong>There were 3 IR groups and 1 normal control (NC) group. The NC group did not undergo the IR procedure. Mice in the IR groups underwent 90 minutes of limb ischemia followed by a variable period of reperfusion. Ischemia was performed by applying a 4.5-oz orthodontic rubber band to the left thigh. Mice in one IR group were sacrificed immediately after reperfusion. The other 2 IR groups were injected once with either 0.75 g GLN/kg body weight (G group) or an equal volume of saline (S group) via tail vein before reperfusion. Mice in the S and G groups were subdivided and sacrificed at 4 or 24 hours after reperfusion.</p><p><strong>Results: </strong>IR enhanced the inflammatory cytokine gene expressions in muscle. Also, plasma interleukin (IL)-6 levels, blood neutrophil percentage, and the adhesion molecule and chemokine receptors expressed by leukocytes were upregulated after reperfusion. The IR-induced muscle inflammatory mediator gene expressions, blood macrophage percentage, and plasma IL-6 concentration had declined at an early or a late phase of reperfusion when GLN was administered. Histologic findings also found that remote lung injury was attenuated during IR insult.</p><p><strong>Conclusions: </strong>A single dose of GLN administration immediately after sublethal lower limb ischemia reduces the inflammatory reaction locally and systemically; this may offer local and distant organ protection in hind limb IR injury.</p>","PeriodicalId":520701,"journal":{"name":"JPEN. Journal of parenteral and enteral nutrition","volume":" ","pages":"1122-1130"},"PeriodicalIF":0.0000,"publicationDate":"2016-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/0148607115587949","citationCount":"16","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JPEN. Journal of parenteral and enteral nutrition","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/0148607115587949","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/6/9 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16
Abstract
Background: This study investigated the effects of intravenous glutamine (GLN) administration on the expression of adhesion molecules and inflammatory mediators in a mice model of hind limb ischemia/reperfusion (IR) injury.
Methods: There were 3 IR groups and 1 normal control (NC) group. The NC group did not undergo the IR procedure. Mice in the IR groups underwent 90 minutes of limb ischemia followed by a variable period of reperfusion. Ischemia was performed by applying a 4.5-oz orthodontic rubber band to the left thigh. Mice in one IR group were sacrificed immediately after reperfusion. The other 2 IR groups were injected once with either 0.75 g GLN/kg body weight (G group) or an equal volume of saline (S group) via tail vein before reperfusion. Mice in the S and G groups were subdivided and sacrificed at 4 or 24 hours after reperfusion.
Results: IR enhanced the inflammatory cytokine gene expressions in muscle. Also, plasma interleukin (IL)-6 levels, blood neutrophil percentage, and the adhesion molecule and chemokine receptors expressed by leukocytes were upregulated after reperfusion. The IR-induced muscle inflammatory mediator gene expressions, blood macrophage percentage, and plasma IL-6 concentration had declined at an early or a late phase of reperfusion when GLN was administered. Histologic findings also found that remote lung injury was attenuated during IR insult.
Conclusions: A single dose of GLN administration immediately after sublethal lower limb ischemia reduces the inflammatory reaction locally and systemically; this may offer local and distant organ protection in hind limb IR injury.
背景:本研究探讨静脉注射谷氨酰胺(GLN)对小鼠后肢缺血再灌注(IR)损伤模型中粘附分子和炎症介质表达的影响。方法:3个IR组和1个正常对照组。NC组不进行IR手术。IR组小鼠进行90分钟肢体缺血,然后进行可变时间的再灌注。通过在左大腿上应用4.5盎司正畸橡皮筋进行缺血。其中1组小鼠在再灌注后立即处死。其余2个IR组在再灌注前经尾静脉注射0.75 g GLN/kg体重(g组)或等体积生理盐水(S组)1次。S组和G组分别于再灌注后4、24小时处死。结果:IR增强了肌肉中炎性细胞因子基因的表达。再灌注后,血浆白细胞介素(IL)-6水平、血液中性粒细胞百分比、白细胞表达的粘附分子和趋化因子受体均上调。给药GLN后,ir诱导的肌肉炎症介质基因表达、血液巨噬细胞百分比和血浆IL-6浓度在再灌注早期或晚期均下降。组织学结果也发现,在IR损伤期间远端肺损伤减轻。结论:亚致死性下肢缺血后立即给予单剂量GLN可减轻局部和全身炎症反应;这可能在后肢IR损伤中提供局部和远处器官保护。