Effect of fentanyl on TNF-alpha and IL-1beta levels during global ischemia/reperfusion in rats.

W. Oh
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引用次数: 6

Abstract

To reduce surgical stress, fentanyl is frequently used for neurosurgical procedures in which focal and/or global ischemia may occur. However, the effect of fentanyl on cytokine levels during ischemia/reperfusion is still uncertain. The goal of this study was to evaluate the effect of fentanyl infusion on levels of the proinflammatory cytokines, tumor necrosis factor (TNF)-alpha and interleukin (IL)-1beta, during global cerebral ischemia/reperfusion in rats using the intracerebral microdialysis technique. Forty male Sprague-Dawley rats weighing 280-320 g were randomly assigned to each of four groups: group 1 (no fentanyl infusion and only ischemia/reperfusion); group 2 (1.5 ng/ml of fentanyl infusion during ischemia/reperfusion) and group 3 (3 ng/ml of fentanyl infusion during ischemia/reperfusion) (n=5 in each group). The rats were anesthetized with an intraperitoneal injection of pentobarbital (50 mg/kg). They were then intubated and ventilated with room air using an animal ventilator. A CMA-12 probe was inserted into the left hippocampal CA-1 region according to the guidelines. Artificial cerebrospinal fluid was run from the inserted microdialysis probe and infused with or without fentanyl at 3 microl/min using a microinjection syringe pump during ischemia/reperfusion. Ischemia was induced by clamping the carotid arteries. Hemorrhagic hypotension was induced for 17 min via the femoral artery, and reperfusion was accomplished by unclamping the sling and reinfusing the blood via the femoral artery. After 2 h of stabilization, the microdialysate was collected 10 times every 17 min, just before ischemia (control), after ischemia (I) and after reperfusion (R1-R8), and stored at -80 degrees C until analysis using high-performance liquid chromatography During global ischemia/reperfusion, TNF-alpha and IL-1beta significantly increased at reperfusion (R5) compared with the control value (p < 0.05). However, in both cases of fentanyl infusion, TNF-alpha and IL-1beta showed no increase compared with the control value. Fentanyl inhibited an increase of the proinflammatory cytokines, TNF-alpha and IL-1beta levels, during global cerebral ischemia/reperfusion in rats.
芬太尼对大鼠全身缺血/再灌注时tnf - α和il -1 β水平的影响。
为了减少手术压力,芬太尼经常用于可能发生局灶性和/或全局性缺血的神经外科手术。然而,芬太尼对缺血/再灌注期间细胞因子水平的影响仍不确定。本研究的目的是利用脑内微透析技术评估芬太尼输注对大鼠全脑缺血/再灌注过程中促炎细胞因子、肿瘤坏死因子(TNF)- α和白细胞介素(IL)-1 β水平的影响。体重280 ~ 320 g的雄性Sprague-Dawley大鼠40只,随机分为4组:1组(不输注芬太尼,仅缺血/再灌注);2组(缺血/再灌注时芬太尼输注1.5 ng/ml)和3组(缺血/再灌注时芬太尼输注3 ng/ml)(每组n=5)。大鼠腹腔注射戊巴比妥50 mg/kg麻醉。然后用动物呼吸机插管和室内空气通气。按照指南将CMA-12探针插入左侧海马CA-1区。在缺血/再灌注时,从插入的微透析探针中取出人工脑脊液,用微注射注射泵以3微升/分钟的速度输注芬太尼或不输注芬太尼。夹持颈动脉致缺血。经股动脉诱导出血性低血压17 min,取下吊带,经股动脉再输注血液完成再灌注。稳定2 h后,每17 min收集微透析液10次,分别在缺血前(对照)、缺血后(ⅰ)和再灌注后(R1-R8)采集,保存于-80℃,待高效液相色谱分析。全身缺血/再灌注时,再灌注时tnf - α和il -1 β较对照组显著升高(R5) (p < 0.05)。然而,在两组芬太尼输注中,tnf - α和il -1 β与对照组相比没有增加。芬太尼抑制大鼠全脑缺血/再灌注过程中促炎细胞因子、tnf - α和il -1 β水平的升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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