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Rasagiline is neuroprotective in an experimental model of brain ischemia in the rat

机译:雷沙吉兰在大鼠脑缺血的实验模型中具有神经保护作用

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The neuroprotective effects of intravenous rasagiline were investigated in a rat model of stroke. Middle cerebral artery (MCA) occlusion was performed in male rats and the short- (neurological severity score [NSS], infarct size), intermediate- (cognition) and long-term (necrotic area) effects were assessed. A bolus (3 mg/kg) of rasagiline followed by a 3-h infusion (3 mg/kg/h), initiated immediately after MCA occlusion, reduced infarct size by 48.6% and NSS by 32.7% relative to saline treatment. Cognitive function, tested in a water maze 2–3 weeks after occlusion, also significantly improved compared with saline-treated controls. Necrotic brain area was 35–50% smaller with rasagiline than with saline following a single bolus dose. The single bolus rasagiline dose was as effective as a rasagiline bolus followed by rasagiline infusion in short-term outcomes. The neuroprotective effect of rasagiline was fully reproducible when administered at 2 h following occlusion but not after 4 h.
机译:在中风的大鼠模型中研究了静脉注射雷沙吉兰的神经保护作用。在雄性大鼠中进行大脑中动脉(MCA)阻塞,并评估了短期(神经病学严重程度评分[NSS],梗塞面积),中度(认知)和长期(坏死面积)的影响。与盐水治疗相比,在MCA闭塞后立即开始大剂量雷沙吉兰(3 mg / kg),然后进行3小时输注(3 mg / kg / h),可使梗塞面积减少48.6%,NSS减少32.7%。闭塞后2-3周在水迷宫中测试的认知功能也比生理盐水对照组明显改善。雷沙吉兰单次推注后的坏死脑面积比盐水少35–50%。雷沙吉兰单次推注剂量与雷沙吉兰大推注随后输注雷沙吉兰在短期结局上一样有效。雷沙吉兰的神经保护作用在闭塞后2 h给药时可完全再现,但在4 h后不能再现。

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