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人白蛋白治疗对永久性局灶性脑缺血的神经保护作用:组织病理学和皮质灌注研究

Neuroprotective effect of treatment with human albumin in permanent focal cerebral ischemia: histopathology and cortical perfusion studies.

作者信息

Liu Y, Belayev L, Zhao W, Busto R, Belayev A, Ginsberg M D

机构信息

Cerebral Vascular Disease Research Center, Department of Neurology (D4-5), University of Miami School of Medicine, P.O. Box 016960, Miami, FL 33101, USA.

出版信息

Eur J Pharmacol. 2001 Oct 5;428(2):193-201. doi: 10.1016/s0014-2999(01)01255-9.

Abstract

In recent experimental studies, we demonstrated a highly beneficial neuroprotective effect of moderate- to high-dose human albumin treatment of transient focal cerebral ischemia, but we did not define the effect of albumin therapy in permanent focal cerebral ischemia. In this study, anesthetized Sprague-Dawley rats were subjected to permanent middle cerebral artery occlusion by retrograde insertion of an intraluminal nylon suture coated with poly-L-lysine. Albumin was administered i.v. at 2 h after onset of middle cerebral artery occlusion, in doses of either 1.25 (n=8) or 2.5 g/kg (n=6). In a separate group of animals, albumin (2.5 g/kg) was given 1 h after middle cerebral artery occlusion (n=6). Vehicle-treated rats (n=6) received 0.9% saline in equivalent volumes. Neurological status was evaluated during and 24 h after middle cerebral artery occlusion. One day after middle cerebral artery occlusion, infarct volumes and brain edema were determined. In a separate group of animals, cortical perfusion was assessed by Laser-Doppler perfusion imaging. Albumin (1.25 g/kg; n=3) or vehicle (sodium chloride 0.9%; n=3) was administered at 2 h after onset of middle cerebral artery occlusion. Higher-dose albumin therapy (2.5 g/kg) significantly improved the neurological score compared to vehicle rats at 24 h, when administered at either 1 or 2 h after middle cerebral artery occlusion. Total infarct volume was reduced by albumin (2.5 g/kg given at 2 h) by 32% compared with vehicle-treated rats. Both albumin doses (1.25 and 2.5 g/kg) significantly reduced cortical and striatal infarct areas at several coronal levels when administered at 2 h after middle cerebral artery occlusion. Brain swelling was not affected by albumin treatment. Cortical perfusion declined during middle cerebral artery occlusion in both groups. Treatment with albumin led to 48% increases in cortical perfusion (P<0.002), but saline caused no change. These results support a beneficial effect of albumin therapy in permanent focal cerebral ischemia.

摘要

在最近的实验研究中,我们证明了中高剂量人白蛋白治疗短暂性局灶性脑缺血具有高度有益的神经保护作用,但我们尚未明确白蛋白疗法对永久性局灶性脑缺血的影响。在本研究中,通过逆行插入涂有聚-L-赖氨酸的腔内尼龙缝线,使麻醉的Sprague-Dawley大鼠发生永久性大脑中动脉闭塞。白蛋白在大脑中动脉闭塞开始后2小时静脉注射,剂量为1.25(n = 8)或2.5 g/kg(n = 6)。在另一组动物中,在大脑中动脉闭塞后1小时给予白蛋白(2.5 g/kg)(n = 6)。接受载体治疗的大鼠(n = 6)接受等量的0.9%生理盐水。在大脑中动脉闭塞期间及闭塞后24小时评估神经功能状态。大脑中动脉闭塞一天后,测定梗死体积和脑水肿。在另一组动物中,通过激光多普勒灌注成像评估皮质灌注。在大脑中动脉闭塞开始后2小时给予白蛋白(1.25 g/kg;n = 3)或载体(0.9%氯化钠;n = 3)。当在大脑中动脉闭塞后1小时或2小时给予较高剂量的白蛋白疗法(2.5 g/kg)时,与接受载体治疗的大鼠相比,在24小时时神经评分显著改善。与接受载体治疗的大鼠相比,白蛋白(2小时给予2.5 g/kg)使总梗死体积减少了32%。当在大脑中动脉闭塞后2小时给予白蛋白时,两种剂量(1.25和2.5 g/kg)均显著减少了几个冠状层面的皮质和纹状体梗死面积。白蛋白治疗对脑肿胀无影响。两组在大脑中动脉闭塞期间皮质灌注均下降。白蛋白治疗使皮质灌注增加了48%(P<0.002),但生理盐水未引起变化。这些结果支持白蛋白疗法对永久性局灶性脑缺血具有有益作用。

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