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内皮素受体拮抗剂在实验性中风中的治疗潜力

Therapeutic potential of endothelin receptor antagonists in experimental stroke.

作者信息

Patel T R, Galbraith S L, McAuley M A, Doherty A M, Graham D I, McCulloch J

机构信息

Wellcome Surgical Institute, University of Glasgow, Scotland.

出版信息

J Cardiovasc Pharmacol. 1995;26 Suppl 3:S412-5.

PMID:8587430
Abstract

This investigation demonstrates an increase in endothelin (ET)-mediated vascular tone in peri-ischemic areas after experimental focal cerebral ischemia (middle cerebral artery occlusion) in the cat. Adventitial application of the butenolide antagonist PD155080 (30 microM), after MCA occlusions resulted in marked increases in caliber of dilated (10.6 +/- 1.6% change from preinjection baseline) and constricted vessels (68.7 +/- 17.5% change from pre-injection baseline). Cerebral blood flow (measured by laser Doppler flowmetry) was reduced after MCA occlusion to 50% of preocclusion levels. Intravenous administration of PD156707 30 min after MCA occlusion restored cerebral blood flow to preocclusion baseline levels at 6 h. The volume of ischemic damage in the cerebral hemisphere after MCA occlusion was significantly reduced (by 45%) after intravenous administration of PD156707.

摘要

本研究表明,在猫实验性局灶性脑缺血(大脑中动脉闭塞)后,缺血周边区域内皮素(ET)介导的血管张力增加。大脑中动脉闭塞后,在血管外膜应用丁烯内酯拮抗剂PD155080(30微摩尔),导致扩张血管(与注射前基线相比变化10.6±1.6%)和收缩血管(与注射前基线相比变化68.7±17.5%)的管径显著增加。大脑中动脉闭塞后,脑血流量(通过激光多普勒血流仪测量)降至闭塞前水平的50%。大脑中动脉闭塞30分钟后静脉注射PD156707,6小时时脑血流量恢复到闭塞前基线水平。静脉注射PD156707后,大脑中动脉闭塞后大脑半球的缺血损伤体积显著减少(减少45%)。

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