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芬太尼不会增加大鼠局灶性脑缺血后的脑损伤。

Fentanyl does not increase brain injury after focal cerebral ischemia in rats.

作者信息

Soonthon-Brant V, Patel P M, Drummond J C, Cole D J, Kelly P J, Watson M

机构信息

Department of Anesthesiology, University of California, San Diego and Department of Veterans Affairs, Veterans Affairs Medical Center, 92161, USA.

出版信息

Anesth Analg. 1999 Jan;88(1):49-55. doi: 10.1097/00000539-199901000-00010.

Abstract

UNLABELLED

Recent reports have indicated that large-dose opiate anesthesia can increase neuronal injury in rats subjected to forebrain ischemia. However, most episodes of cerebral ischemia in the operating room setting are focal in nature, and the influence of large-dose opioid administration on the tolerance of the brain to focal cerebral ischemia has not been studied. Accordingly, we undertook the present study to evaluate the effect of fentanyl administration on outcome after focal cerebral ischemia. Three groups of fasted Wistar-Kyoto rats (awake, fentanyl, and isoflurane groups; n = 20 per group) were anesthetized with isoflurane (2.5% end-tidal). Pericranial temperature was servocontrolled at 37.0 degrees C. After surgical preparation fentanyl 50 microg/kg was administered IV over 10 min in the fentanyl group. Thereafter, an infusion was established at a rate of 50 microg x kg(-1) x h(-1). The end-tidal concentration of isoflurane was then reduced to 1.1%, one minimum alveolar anesthetic concentration (1 MAC) in all groups. Occlusion of the middle cerebral artery was achieved by advancing a 0.25-mm filament into the anterior cerebral artery via the common carotid artery. In the fentanyl and awake groups, isoflurane administration was then discontinued. In the isoflurane group, isoflurane anesthesia was maintained at 1.0 MAC. After 90 min of focal ischemia, the filament was removed, and the animals were allowed to recover. Seven days later, the volume of cerebral infarction in the animals was determined by image analysis of hematoxylin and eosin-stained coronal brain sections. There was no difference in the infarct volume between the fentanyl and awake groups. The infarct volume was the least in the isoflurane group. The results confirm the ability of isoflurane to reduce brain injury caused by focal cerebral ischemia. Fentanyl neither increased nor decreased brain injury compared with the awake unanesthetized state.

IMPLICATIONS

Fentanyl is commonly used in surgical procedures in which there is a substantial risk of focal cerebral ischemia. Fentanyl did not affect cerebral injury produced by focal ischemia in the rat. The data suggest that, in doses that produce respiratory depression and muscle rigidity, fentanyl does not reduce the tolerance of the brain to a focal ischemic insult.

摘要

未标注

最近的报告表明,大剂量阿片类麻醉剂可增加前脑缺血大鼠的神经元损伤。然而,手术室环境中大多数脑缺血发作本质上是局灶性的,大剂量阿片类药物给药对大脑对局灶性脑缺血耐受性的影响尚未得到研究。因此,我们进行了本研究以评估芬太尼给药对局灶性脑缺血后结局的影响。三组禁食的Wistar-Kyoto大鼠(清醒组、芬太尼组和异氟烷组;每组n = 20)用异氟烷(呼气末浓度2.5%)麻醉。颅骨周围温度通过伺服控制维持在37.0℃。手术准备后,芬太尼组在10分钟内静脉注射50μg/kg芬太尼。此后,以50μg·kg⁻¹·h⁻¹的速率进行输注。然后将所有组的异氟烷呼气末浓度降至1.1%,即一个最低肺泡有效浓度(1MAC)。通过经颈总动脉将一根0.25mm的细丝推进大脑前动脉来实现大脑中动脉闭塞。在芬太尼组和清醒组中,随后停止给予异氟烷。在异氟烷组中,异氟烷麻醉维持在1.0MAC。局灶性缺血90分钟后,取出细丝,让动物恢复。7天后,通过苏木精和伊红染色的冠状脑切片图像分析确定动物脑梗死体积。芬太尼组和清醒组的梗死体积没有差异。异氟烷组的梗死体积最小。结果证实了异氟烷减轻局灶性脑缺血所致脑损伤的能力。与清醒未麻醉状态相比,芬太尼既未增加也未减少脑损伤。

启示

芬太尼常用于存在局灶性脑缺血重大风险的手术过程中。芬太尼不影响大鼠局灶性缺血所致的脑损伤。数据表明,在产生呼吸抑制和肌肉强直的剂量下,芬太尼不会降低大脑对局灶性缺血性损伤的耐受性。

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