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用于减少中风脑损伤的钙拮抗剂。

Calcium antagonists for reduction of brain damage in stroke.

作者信息

Sauter A, Rudin M

机构信息

Central Nervous System Unit of Preclinical Research, Sandoz Ltd., Basel, Switzerland.

出版信息

J Cardiovasc Pharmacol. 1990;15 Suppl 1:S43-7.

PMID:1695302
Abstract

In a rat model of embolic stroke [permanent occlusion of the left middle cerebral artery (MCAO)], isradipine, a 1,4-dihydropyridine calcium antagonist, reduced the infarct size by more than 50%, as determined by both in vivo magnetic resonance imaging (MRI) and postmortem histology. Among several calcium antagonists tested, including nimodipine, nitrendipine, and nifedipine, isradipine was found to be the most potent and most efficacious. These results suggest that isradipine, when administered shortly after stroke onset, may have beneficial effects in patients suffering from brain ischemia. When high blood pressure in spontaneously hypertensive rats (SHR) was normalized by daily injections of isradipine, brain damage caused by a subsequent stroke (MCAO) was substantially reduced by as much as 75% in the cortex compared to controls. These results suggest that isradipine, when used as an antihypertensive drug in humans, may offer the additional benefit of reducing brain damage caused by an eventual stroke. Because high blood pressure is considered an important risk factor for stroke, this additional benefit of isradipine would be particularly valuable in antihypertensive therapy.

摘要

在栓塞性中风大鼠模型(永久性闭塞左大脑中动脉)中,1,4 - 二氢吡啶类钙拮抗剂伊拉地平通过体内磁共振成像(MRI)和死后组织学检查确定,使梗死面积减少超过50%。在测试的几种钙拮抗剂中,包括尼莫地平、尼群地平和硝苯地平,发现伊拉地平是最有效力且最有效果的。这些结果表明,伊拉地平在中风发作后不久给药,可能对脑缺血患者有益。当通过每日注射伊拉地平使自发性高血压大鼠(SHR)的高血压恢复正常时,与对照组相比,随后中风(大脑中动脉闭塞)引起的大脑皮质损伤在皮质中显著减少多达75%。这些结果表明,伊拉地平在人类用作抗高血压药物时,可能具有减少最终中风引起的脑损伤的额外益处。由于高血压被认为是中风的一个重要危险因素,伊拉地平的这种额外益处在抗高血压治疗中特别有价值。

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