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胰岛素治疗时机影响内毒素血症大鼠的炎症反应。

Timing of insulin therapy affects the inflammatory response in endotoxemic rats.

机构信息

Medical School of Nanjing University, Nanjing 210093, Jiangsu Province, China.

出版信息

Inflammation. 2012 Apr;35(2):723-9. doi: 10.1007/s10753-011-9367-8.

Abstract

The aim of the present study was to determine whether timing of insulin administration influences the hepatic and serum proinflammatory and anti-inflammatory cytokines during endotoxemia stimulated by lipopolysaccharide (LPS). Eighty-one male Sprague-Dawley rats were divided into different time groups and insulin was given 30 min pre-LPS administration or hour 0, 1, 3, 6, 12, 24 after the induction of endotoxemia, respectively. Hepatic and serum proinflammatory cytokines IL-1β, IL-6, and TNF-α, and anti-inflammatory cytokine IL-10 were detected 24 and 48 h after the induction of endotoxemia. Compared with sham control rats, serum concentrations of proinflammatory cytokines IL-1β, IL-6, and TNF-α and anti-inflammatory cytokine IL-10 significantly increased on 24 and 48 h after induction of endotoxemia. Similarly, LPS administration also significantly increased the hepatic IL-1β, TNF-α, IL-6, and IL-10 protein concentration 48 h after LPS injection. Compared with levels in positive LPS controls animals receiving saline, on 24 and 48 h after LPS injection, insulin administrated ahead of 6 h after LPS injection significantly decreased the serum IL-1β, IL-6, and TNF-a concentration (P < 0.05), and significantly increased anti-inflammatory cytokine IL-10 concentration (P < 0.05); hepatic IL-1β and IL-6 expression were (P < 0.05) significantly decreased compared with levels in positive LPS controls. But, the significant decrease of hepatic TNF-a expression and significant increase of hepatic IL-10 were only seen in the animals in which insulin was administrated at 30 min pre-LPS or coadministrated with LPS. Insulin administrated 6 h after LPS injection lost the ability to significantly reduce serum or hepatic IL-1β, TNF-α, and IL-6 concentrations. Insulin has a protective role in systemic inflammatory response syndrome related to sepsis, such as downregulation of proinflammatory cytokines and upregulation of anti-inflammatory cytokine production. However, timing of insulin administrated may change its effect of inflammatory response in endotoxemic rats. Insulin administrated 6 h after LPS injection weaken the ability to protect inflammatory response related to sepsis.

摘要

本研究旨在探讨胰岛素给药时机对内毒素血症时肝脏和血清中促炎和抗炎细胞因子的影响。81 只雄性 Sprague-Dawley 大鼠分为不同时间组,分别于内毒素诱导前 30min 或内毒素诱导后 0、1、3、6、12、24h 给予胰岛素。内毒素诱导后 24 和 48h 检测肝脏和血清中促炎细胞因子 IL-1β、IL-6 和 TNF-α,以及抗炎细胞因子 IL-10。与假手术对照组大鼠相比,内毒素诱导后 24 和 48h 血清中促炎细胞因子 IL-1β、IL-6 和 TNF-α以及抗炎细胞因子 IL-10 浓度明显升高。同样,LPS 给药后 48h 肝脏中 IL-1β、TNF-α、IL-6 和 IL-10 蛋白浓度也明显升高。与给予生理盐水的阳性 LPS 对照组相比,LPS 注射后 6h 内给予胰岛素可显著降低血清中 IL-1β、IL-6 和 TNF-α浓度(P<0.05),显著增加抗炎细胞因子 IL-10 浓度(P<0.05);与阳性 LPS 对照组相比,肝脏中 IL-1β 和 IL-6 的表达明显降低(P<0.05)。但只有在胰岛素于 LPS 注射前 30min 给予或与 LPS 同时给予时,才能观察到肝 TNF-α表达显著降低和 IL-10 表达显著增加。LPS 注射后 6h 给予胰岛素则丧失了显著降低血清或肝脏中 IL-1β、TNF-α 和 IL-6 浓度的能力。胰岛素对内毒素血症相关全身炎症反应综合征具有保护作用,可下调促炎细胞因子的产生,上调抗炎细胞因子的产生。然而,胰岛素给药时机可能会改变其对内毒素血症大鼠炎症反应的作用。LPS 注射后 6h 给予胰岛素减弱了其对与脓毒症相关的炎症反应的保护作用。

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