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瑞芬太尼预处理可预防大鼠因缺血再灌注损伤导致的肠道收缩力降低。

Pretreatment with remifentanil protects against the reduced-intestinal contractility related to the ischemia and reperfusion injury in rat.

作者信息

Sayan-Ozacmak Hale, Ozacmak Veysel Haktan, Turan Inci, Barut Figen, Hanci Volkan

机构信息

Department of Physiology, Bulent Ecevit University Medical School, Kozlu, Zonguldak, Turkey.

Department of Physiology, Bulent Ecevit University Medical School, Kozlu, Zonguldak, Turkey.

出版信息

Braz J Anesthesiol. 2015 Nov-Dec;65(6):483-90. doi: 10.1016/j.bjane.2013.09.007. Epub 2014 Nov 6.

Abstract

BACKGROUND AND OBJECTIVES

Serious functional and structural alterations of gastrointestinal tract are observed in failure of blood supply, leading to gastrointestinal dismotility. Activation of opioid receptors provides cardioprotective effect against ischemia-reperfusion (I/R) injury. The aim of the present study was to determine whether or not remifentanil could reduce I/R injury of small intestine.

METHODS

Male Wistar Albino rats were subjected to mesenteric ischemia (30 min) followed by reperfusion (3h). Four groups were designed: sham control; remifentanil alone; I/R control; and remifentanil+I/R. Animals in remifentanil+I/R group were subjected to infusion of remifentanil (2 ug kg(-1)min(-1)) for 60 min, half of which started before inducing ischemia. Collecting the ileum tissues, evaluation of damage was based on contractile responses to carbachol, levels of lipid peroxidation and neutrophil infiltration, and observation of histopathological features in intestinal tissue.

RESULTS

Following reperfusion, a significant decrease in carbachol-induced contractile response, a remarkable increase in both lipid peroxidation and neutrophil infiltration, and a significant injury in mucosa were observed. An average contractile response of remifentanil+I/R group was significantly different from that of the I/R group. Lipid peroxidation and neutrophil infiltration were also significantly suppressed by the treatment. The tissue samples of the I/R group were grade 4 in histopathological evaluation. In remifentanil+I/R group, on the other hand, the mucosal damage was moderate, staging as grade 1.

CONCLUSIONS

The pretreatment with remifentanil can attenuate the intestinal I/R injury at a remarkable degree possibly by lowering lipid peroxidation and leukocyte infiltration.

摘要

背景与目的

在血液供应不足时可观察到胃肠道出现严重的功能和结构改变,进而导致胃肠动力障碍。阿片受体激活可对缺血再灌注(I/R)损伤发挥心脏保护作用。本研究旨在确定瑞芬太尼是否能减轻小肠的I/R损伤。

方法

雄性Wistar白化大鼠经历肠系膜缺血(30分钟),随后再灌注(3小时)。设计四组:假手术对照组;单独使用瑞芬太尼组;I/R对照组;瑞芬太尼+I/R组。瑞芬太尼+I/R组的动物接受瑞芬太尼输注(2μg·kg⁻¹·min⁻¹)60分钟,其中一半在诱导缺血前开始。收集回肠组织,基于对卡巴胆碱的收缩反应、脂质过氧化水平和中性粒细胞浸润情况以及肠道组织的组织病理学特征评估损伤。

结果

再灌注后,观察到卡巴胆碱诱导的收缩反应显著降低、脂质过氧化和中性粒细胞浸润均显著增加以及黏膜出现明显损伤。瑞芬太尼+I/R组的平均收缩反应与I/R组有显著差异。该治疗还显著抑制了脂质过氧化和中性粒细胞浸润。I/R组的组织样本在组织病理学评估中为4级。另一方面,在瑞芬太尼+I/R组中,黏膜损伤为中度,分期为1级。

结论

瑞芬太尼预处理可能通过降低脂质过氧化和白细胞浸润,在很大程度上减轻肠道I/R损伤。

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