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维拉帕米、地尔硫䓬和硝苯地平对麻醉猫动脉压力反射影响的异同

Similarities and differences in the effects of verapamil, diltiazem and nifedipine on arterial baroreflexes of anesthetized cats.

作者信息

Abdel-Rahman A R, Ingenito A J

出版信息

Arch Int Pharmacodyn Ther. 1985 May;275(1):33-46.

PMID:2992401
Abstract

The effects of verapamil, diltiazem and nifedipine on baroreflex sensitivity (BS) were investigated in anesthetized cats at equihypotensive doses of 100, 100 and 10 micrograms/kg, respectively. The gain in BS (ms/mmHg) was calculated from the ratio delta heart period/delta systolic pressure following evoked rises and falls in arterial pressure. Verapamil and diltiazem significantly augmented BS while nifedipine depressed BS during evoked rises in arterial pressure. By contrast, BS was significantly depressed by diltiazem and nifedipine in response to depressor challenges with nitroprusside, while it was unaffected by verapamil. The augmentatory action of verapamil on BS after pressor challenges, was abolished by bilateral vagotomy while the inhibitory action of nifedipine was still evident after vagotomy, suggesting a vagal augmentatory action for verapamil and an involvement of the cardiac sympathetic nerves in the inhibitory action of nifedipine on BS. The differences between the actions of the 3 drugs on BS are not readily explainable by our data but they cannot be attributed to alterations of cardiac autonomic function since at the doses employed none of the drugs affected the cardiac responses to carotid occlusion, i.v. isoproterenol or electrical stimulation of the right vagus. It is concluded that BS is affected differently by the 3 chemically unrelated calcium channel blockers in a way which could either be contributory or deleterious to the antihypertensive effectiveness of these drugs.

摘要

分别以100、100和10微克/千克的等降压剂量,在麻醉猫中研究了维拉帕米、地尔硫卓和硝苯地平对压力反射敏感性(BS)的影响。压力反射敏感性增益(毫秒/毫米汞柱)是根据动脉压诱发升高和降低后的心搏周期变化率与收缩压变化率之比计算得出的。在动脉压诱发升高期间,维拉帕米和地尔硫卓显著增强压力反射敏感性,而硝苯地平则降低压力反射敏感性。相比之下,在使用硝普钠进行降压挑战时,地尔硫卓和硝苯地平显著降低压力反射敏感性,而维拉帕米对此无影响。双侧迷走神经切断术后,维拉帕米对升压挑战后压力反射敏感性的增强作用消失,而迷走神经切断术后硝苯地平的抑制作用仍然明显,这表明维拉帕米具有迷走神经增强作用,而硝苯地平对压力反射敏感性的抑制作用涉及心脏交感神经。这三种药物对压力反射敏感性的作用差异难以用我们的数据解释,但它们不能归因于心脏自主神经功能的改变,因为在所使用的剂量下,没有一种药物影响心脏对颈动脉闭塞、静脉注射异丙肾上腺素或右迷走神经电刺激的反应。结论是,这三种化学结构不相关的钙通道阻滞剂对压力反射敏感性的影响不同,这种影响可能对这些药物的降压效果有促进作用或有害作用。

相似文献

1
Similarities and differences in the effects of verapamil, diltiazem and nifedipine on arterial baroreflexes of anesthetized cats.维拉帕米、地尔硫䓬和硝苯地平对麻醉猫动脉压力反射影响的异同
Arch Int Pharmacodyn Ther. 1985 May;275(1):33-46.
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