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兔主动脉血管平滑肌对维拉帕米和硝普钠敏感性的年龄相关性变化。

Age-related changes in the sensitivity to verapamil and sodium nitroprusside of vascular smooth muscle of rabbit aorta.

作者信息

Karaki H, Nakagawa H, Urakawa N

出版信息

Br J Pharmacol. 1985 May;85(1):223-8. doi: 10.1111/j.1476-5381.1985.tb08850.x.

Abstract

Age-related changes in the sensitivity to verapamil and sodium nitroprusside were examined in isolated aortic strips of the rabbit. In the aortae of newborn rabbits within 10 days of birth, the resting tone of the muscle was strongly reduced by sodium nitroprusside but not by either Ca-deficient solution or by verapamil. High K-induced contraction and noradrenaline-induced contraction were both inhibited by verapamil or sodium nitroprusside. In the aortae of 24 day-old rabbits, resting tension was slightly reduced by sodium nitroprusside but not by verapamil. High K-induced contraction was less sensitive to sodium nitroprusside than to verapamil whereas noradrenaline-induced contraction was less sensitive to verapamil than to sodium nitroprusside. In the aortae isolated from 60 day-old or older rabbits, resting tension was not affected by either sodium nitroprusside or verapamil. High K-induced contraction was inhibited by verapamil whereas sodium nitroprusside showed only a weak inhibitory effect. Noradrenaline-induced contraction was inhibited by sodium nitroprusside although verapamil had only a slight inhibitory effect. In the aortae of 1 day-old and also in adult rabbits, noradrenaline induced an additional increase in muscle tension when applied during the sustained contraction induced by high K. It is suggested that, in the newborn rabbit aorta, the voltage-dependent Ca channel is sensitive to both verapamil and sodium nitroprusside and the sensitivity to sodium nitroprusside gradually decreases during maturation whereas the receptor-linked Ca channel is also sensitive to both of the inhibitors at birth but the sensitivity to verapamil gradually decreases with age.

摘要

在兔离体主动脉条中研究了对维拉帕米和硝普钠敏感性的年龄相关变化。在出生10天内的新生兔主动脉中,硝普钠可强烈降低肌肉的静息张力,但缺钙溶液或维拉帕米均无此作用。高钾诱导的收缩和去甲肾上腺素诱导的收缩均被维拉帕米或硝普钠抑制。在24日龄兔的主动脉中,硝普钠可使静息张力略有降低,但维拉帕米无此作用。高钾诱导的收缩对硝普钠的敏感性低于对维拉帕米的敏感性,而去甲肾上腺素诱导的收缩对维拉帕米的敏感性低于对硝普钠的敏感性。在60日龄及以上兔分离的主动脉中,硝普钠和维拉帕米均不影响静息张力。高钾诱导的收缩被维拉帕米抑制,而硝普钠仅显示微弱的抑制作用。去甲肾上腺素诱导的收缩被硝普钠抑制,尽管维拉帕米只有轻微的抑制作用。在1日龄兔和成年兔的主动脉中,当在高钾诱导的持续收缩期间应用去甲肾上腺素时,可使肌肉张力进一步增加。提示在新生兔主动脉中,电压依赖性钙通道对维拉帕米和硝普钠均敏感,且在成熟过程中对硝普钠的敏感性逐渐降低,而受体偶联钙通道在出生时对两种抑制剂也敏感,但对维拉帕米的敏感性随年龄逐渐降低。

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