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钙拮抗剂尼莫地平对沙鼠实验性脑缺血模型的影响。

The effect of the calcium antagonist nimodipine on the gerbil model of experimental cerebral ischemia.

作者信息

Fujisawa A, Matsumoto M, Matsuyama T, Ueda H, Wanaka A, Yoneda S, Kimura K, Kamada T

出版信息

Stroke. 1986 Jul-Aug;17(4):748-52. doi: 10.1161/01.str.17.4.748.

Abstract

The gerbil model was used to assess the therapeutic effects of the calcium antagonist nimodipine on cerebral ischemia. Transient cerebral ischemia was produced in each gerbil by bilateral common carotid occlusion of 10-, 15- or 20-min duration. Nimodipine (0.01 or 0.1 mg/kg) was administered intraperitoneally just before the carotid occlusion or 10-30 min after the removal of the arterial clips. Morbidity of each animal was evaluated using the stroke index, and the sum of stroke indices was calculated for evaluating the overall morbidity during a particular period of reperfusion. Mortality was observed for 24 hours after clip removal. Although, depending on the timing of the drug administration, the low-dose (0.01 mg/kg) nimodipine worsened the morbidity in the gerbils with 10-min ischemia, the high-dose (0.1 mg/kg) of the drug had a clear beneficial effect on the mortality associated with cerebral ischemia. These results are considered worthwhile for further trials to assess the usefulness of nimodipine as a therapeutic agent in the management of the acute ischemic stroke.

摘要

采用沙鼠模型评估钙拮抗剂尼莫地平对脑缺血的治疗效果。通过双侧颈总动脉闭塞10、15或20分钟,在每只沙鼠身上造成短暂性脑缺血。在颈动脉闭塞前或移除动脉夹后10 - 30分钟,腹腔注射尼莫地平(0.01或0.1毫克/千克)。使用中风指数评估每只动物的发病率,并计算中风指数总和以评估特定再灌注期间的总体发病率。移除夹子后观察24小时的死亡率。尽管根据给药时间不同,低剂量(0.01毫克/千克)的尼莫地平会使缺血10分钟的沙鼠发病率恶化,但高剂量(0.1毫克/千克)的该药物对与脑缺血相关的死亡率有明显的有益作用。这些结果被认为值得进一步试验,以评估尼莫地平作为治疗急性缺血性中风药物的有效性。

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