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V2受体活性对大鼠血管加压素升压反应的影响。

Effects of V2 receptor activity on the pressor response to vasopressin in the rat.

作者信息

Shimizu K, Schwartz J, McGrath B P

机构信息

Monash University Department of Medicine, Melbourne, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1991 May;18(5):349-52. doi: 10.1111/j.1440-1681.1991.tb01461.x.

Abstract
  1. To determine the contribution of V1 and V2 receptor activity on the enhancement of reflex buffering of the pressor response to arginine-vasopressin (AVP), mean arterial pressure (MAP) and heart rate (HR) changes were examined in response to graded injections of phenylephrine, AVP, or Phe2Orn8OT, a potent, selective V1-receptor agonist in the absence and presence of Val4DArg8VP, a potent, selective V2-receptor agonist. 2. There were no significant differences in MAP responses to the V1 agonist in the absence and presence of the V2 agonist in either conscious intact or autonomic-blocked rats. 3. Autonomic blockade with methscopolamine and hexamethonium increased the pressor sensitivity to phenylephrine threefold. In contrast, the pressor sensitivities to AVP and Phe2Orn8OT were increased 14-fold and 11-fold, respectively, by autonomic blockade. 4. V2-receptor activity does not have any inherent vasocative action or synergistic vasoactive action with V1-receptor activity. 5. V2 receptors do not play a role in enhancing reflex buffering of the pressor response to AVP; V1 receptors are suggested to play the role.
摘要
  1. 为了确定V1和V2受体活性对精氨酸加压素(AVP)升压反应反射缓冲增强的作用,在有无强效选择性V2受体激动剂Val4DArg8VP的情况下,通过分级注射去氧肾上腺素、AVP或强效选择性V1受体激动剂Phe2Orn8OT,检测平均动脉压(MAP)和心率(HR)的变化。2. 在清醒完整或自主神经阻断的大鼠中,有无V2激动剂时,对V1激动剂的MAP反应均无显著差异。3. 用甲基东莨菪碱和六甲铵进行自主神经阻断,使对去氧肾上腺素的升压敏感性增加了两倍。相比之下,自主神经阻断使对AVP和Phe2Orn8OT的升压敏感性分别增加了14倍和11倍。4. V2受体活性不具有任何内在的血管活性作用,也不与V1受体活性产生协同血管活性作用。5. V2受体在增强对AVP升压反应的反射缓冲中不起作用;提示V1受体起此作用。

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