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新型钙拮抗剂莫那普利对大鼠药物诱导的缺血性心电图变化的预防作用。

Preventive effect of a new calcium antagonist, monatepil, on drug-induced ischaemic electrocardiographic changes in rats.

作者信息

Yamamoto T, Nakatsuji K, Hosoki K, Karasawa T

机构信息

Department of Pharmacology, Dainippon Pharmaceutical Co. Ltd, Osaka, Japan.

出版信息

Clin Exp Pharmacol Physiol. 1993 Nov;20(11):673-8. doi: 10.1111/j.1440-1681.1993.tb01651.x.

Abstract
  1. The preventive effects of monatepil, a new calcium antagonist with alpha 1-adrenoceptor blocking activity, on ischaemic electrocardiographic changes in rat models of vasospastic angina were evaluated and compared with those of the existing calcium antagonists (diltiazem, verapamil, nicardipine and nifedipine). 2. In order to assess the contribution of the alpha 1-adrenoceptor blocking action of monatepil to its anti-vasospastic action, the anti-ST depression effect of prazosin, an alpha 1-adrenoceptor blocker, was also examined. 3. Monatepil given orally (3-30 mg/kg) inhibited vasopressin (0.2 IU/kg, i.v.)-induced ST depression which is considered to indicate ischaemic electrocardiographic changes in a vasospastic angina. This effect of monatepil was more potent and long-lasting than that of diltiazem, and was similar to that of verapamil and nicardipine. At a dose of 30 mg/kg, monatepil produced a significant inhibition, even at 7 h after administration. 4. Monatepil given intravenously (0.3 mg/kg) exerted a significant inhibitory effect on methacholine (16 micrograms/kg, intracoronary arterial administration; i.c.a.)-induced ST elevation which seems to be caused by coronary vasospasm. This effect was more potent or equipotent to those of the existing calcium antagonists. 5. These results indicate that monatepil produces the preventive effect on the drug-induced ischaemic electrocardiographic changes in rats and suggest that monatepil may have potential for the treatment of vasospastic angina.
摘要
  1. 评估了一种具有α1 -肾上腺素能受体阻断活性的新型钙拮抗剂莫那普利对血管痉挛性心绞痛大鼠模型缺血性心电图变化的预防作用,并与现有的钙拮抗剂(地尔硫䓬、维拉帕米、尼卡地平和平硝苯地平)进行了比较。2. 为了评估莫那普利的α1 -肾上腺素能受体阻断作用对其抗血管痉挛作用的贡献,还研究了α1 -肾上腺素能受体阻滞剂哌唑嗪的抗ST段压低作用。3. 口服莫那普利(3 - 30毫克/千克)可抑制血管加压素(0.2国际单位/千克,静脉注射)诱导的ST段压低,这种压低被认为表明血管痉挛性心绞痛存在缺血性心电图变化。莫那普利的这种作用比地尔硫䓬更强且更持久,与维拉帕米和尼卡地平相似。在30毫克/千克的剂量下,即使在给药7小时后,莫那普利仍产生显著抑制作用。4. 静脉注射莫那普利(0.3毫克/千克)对乙酰甲胆碱(16微克/千克,冠状动脉内给药;i.c.a.)诱导的ST段抬高有显著抑制作用,这种抬高似乎是由冠状动脉痉挛引起的。该作用比现有的钙拮抗剂更强或相当。5. 这些结果表明莫那普利对大鼠药物诱导的缺血性心电图变化具有预防作用,并提示莫那普利可能具有治疗血管痉挛性心绞痛的潜力。

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