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用鲁贝唑治疗大鼠实验性局灶性缺血

Treatment of experimental focal ischemia in rats with lubeluzole.

作者信息

Aronowski J, Strong R, Grotta J C

机构信息

Department of Neurology, University of Texas-Houston Medical School, 77030, USA.

出版信息

Neuropharmacology. 1996 Jun;35(6):689-93. doi: 10.1016/0028-3908(96)84640-5.

Abstract

Lubeluzole is a neuroprotective compound in the final stages of clinical evaluation. We evaluated the effects of intravenous followed by intraperitoneal doses of lubeluzole on histological outcome after reversible tandem middle cerebral/common carotid artery occlusion in Long-Evans rats, with particular emphasis on the time window of efficacy. Lubeluzole, started 15 min after the onset of ischemia, had no adverse physiological or behavioral effects and reduce maximal infarct volume produced by 120 min or more of arterial occlusion by approximately 50%, from 143.2 +/- 11.8 mm3 (p < 0.05). Lubeluzole did not prolong the duration of middle cerebral artery occlusion which could be tolerated before histological damage occurred. Lubeluzole was still effective if started 30 min after the onset of ischemia (34% reduction of maximal infarct volume; p < 0.05), but not after delays of 60 or 120 min. we conclude that lubeluzole has promise as a neuroprotective drug, particularly for more severe strokes, but must be started very rapidly after the onset of ischemia to be effective.

摘要

鲁比前列酮是一种处于临床评估最后阶段的神经保护化合物。我们评估了静脉注射后腹腔注射鲁比前列酮对Long-Evans大鼠可逆性大脑中动脉/颈总动脉串联闭塞后组织学结果的影响,特别强调了疗效的时间窗。在缺血开始15分钟后开始使用鲁比前列酮,没有产生不良的生理或行为影响,并且将120分钟或更长时间动脉闭塞所产生的最大梗死体积减少了约50%,从143.2±11.8立方毫米降至(p<0.05)。鲁比前列酮并未延长在组织学损伤发生前能够耐受的大脑中动脉闭塞持续时间。如果在缺血开始30分钟后开始使用鲁比前列酮仍然有效(最大梗死体积减少34%;p<0.05),但在延迟60或120分钟后则无效。我们得出结论,鲁比前列酮有望成为一种神经保护药物,特别是对于更严重的中风,但必须在缺血开始后非常迅速地开始使用才能有效。

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