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尼卡地平在心肌梗死模型中的应用。

Nicardipine in models of myocardial infarction.

作者信息

Alps B J, Calder C, Wilson A

出版信息

Br J Clin Pharmacol. 1985;20 Suppl 1(Suppl 1):29S-49S. doi: 10.1111/j.1365-2125.1985.tb05142.x.

Abstract

In a dog model of partial myocardial ischaemia, superimposed ST segment elevations in epicardial ECGs were inhibited by nicardipine over a cumulative i.v. dose range of 1-20 micrograms kg-1. Over the cumulative i.v. dose range of 0.5-166.5 micrograms kg-1, nicardipine had little overall effect on gross cardiac conduction, at spontaneous heart rate. Dogs that received oral 1-2 mg kg-1 nicardipine daily for 16 weeks and then survived 1 week occlusion of the left anterior descending coronary artery (LAD) developed a superior coronary collateral circulation compared with untreated animals. Nicardipine given by three different dosing schedules to baboons markedly limited myocardial infarction over a 6 h period of LAD occlusion. Compared with a group of completely untreated dogs, there was protection of the myocardium in the animals given nicardipine that survived 3 months occlusion of the LAD.

摘要

在部分心肌缺血的犬模型中,尼卡地平在1-20微克/千克的累积静脉注射剂量范围内可抑制心外膜心电图上叠加的ST段抬高。在0.5-166.5微克/千克的累积静脉注射剂量范围内,尼卡地平对自发心率下的心脏总体传导几乎没有影响。每天口服1-2毫克/千克尼卡地平,持续16周,然后在左冠状动脉前降支(LAD)闭塞1周后存活下来的犬,与未治疗的动物相比,形成了更好的冠状动脉侧支循环。以三种不同给药方案给狒狒注射尼卡地平,在LAD闭塞6小时期间显著限制了心肌梗死。与一组完全未治疗的犬相比,给予尼卡地平的动物在LAD闭塞3个月后存活下来,心肌得到了保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/1400792/25d5a5942b0d/brjclinpharm00136-0037-a.jpg

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