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血管加压素能维持清醒自发性高血压大鼠的血压吗?

Does vasopressin sustain blood pressure in conscious spontaneously hypertensive rats?

作者信息

Filep J, Fejes-Tóth G

出版信息

Hypertension. 1986 Jun;8(6):514-9. doi: 10.1161/01.hyp.8.6.514.

DOI:10.1161/01.hyp.8.6.514
PMID:2872162
Abstract

To investigate the possible role of arginine vasopressin in maintaining high blood pressure of spontaneously hypertensive rats (SHR), the effect of two arginine vasopressin pressor antagonists on mean arterial pressure and the pressor responsiveness to exogenous arginine vasopressin were studied in conscious, freely moving SHR and in Wistar-Kyoto rats (WKY). Intravenous injections of either d(CH2)5Tyr(Me)arginine vasopressin, 10 micrograms/kg, or dPTyr(Me)arginine vasopressin, 20 micrograms/kg, had no effect on mean arterial pressure or heart rate of normohydrated SHR, although both antagonists almost completely abolished the pressor response to exogenous arginine vasopressin. Furthermore, dPTyr(Me)arginine vasopressin was ineffective in eliciting a depressor response, even after 24 or 48 hours of water deprivation. During converting enzyme inhibition with SQ 20881, mean arterial pressure and heart rate remained unchanged following arginine vasopressin blockade in both normohydrated and fluid-restricted animals. alpha-Adrenergic receptor blockade reduced the blood pressure of normohydrated SHR, from 160 +/- 7 to 81 +/- 8 mm Hg. When dPTyr(Me)arginine vasopressin was given during alpha-adrenergic receptor blockade there was a small, transient fall in mean arterial pressure. The pressor responsiveness to exogenous arginine vasopressin was similar in hypertensive and normotensive rats. These results suggest that arginine vasopressin does not function as an important pressor hormone in conscious SHR.

摘要

为研究精氨酸加压素在维持自发性高血压大鼠(SHR)高血压状态中可能的作用,我们在清醒、自由活动的SHR和Wistar-Kyoto大鼠(WKY)中研究了两种精氨酸加压素升压拮抗剂对平均动脉压以及对外源性精氨酸加压素升压反应性的影响。静脉注射10微克/千克的d(CH2)5Tyr(Me)精氨酸加压素或20微克/千克的dPTyr(Me)精氨酸加压素,对正常水合状态的SHR的平均动脉压或心率没有影响,尽管两种拮抗剂几乎完全消除了对外源性精氨酸加压素的升压反应。此外,即使在缺水24或48小时后,dPTyr(Me)精氨酸加压素也未能引发降压反应。在用SQ 20881抑制转换酶期间,正常水合和限液动物在精氨酸加压素被阻断后,平均动脉压和心率均保持不变。α-肾上腺素能受体阻断使正常水合SHR的血压从160±7毫米汞柱降至81±8毫米汞柱。当在α-肾上腺素能受体阻断期间给予dPTyr(Me)精氨酸加压素时,平均动脉压有小幅短暂下降。高血压大鼠和正常血压大鼠对外源性精氨酸加压素的升压反应性相似。这些结果表明,精氨酸加压素在清醒的SHR中并非重要的升压激素。

相似文献

1
Does vasopressin sustain blood pressure in conscious spontaneously hypertensive rats?血管加压素能维持清醒自发性高血压大鼠的血压吗?
Hypertension. 1986 Jun;8(6):514-9. doi: 10.1161/01.hyp.8.6.514.
2
Vascular effects of arginine vasopressin during fluid deprivation in the rat.大鼠禁水期间精氨酸加压素的血管效应
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Evidence against a pressor role for vasopressin in spontaneous hypertension.关于血管加压素在自发性高血压中升压作用的反对证据。
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Contribution of vasopressin in dexamethasone-induced hypertension in rats.血管加压素在大鼠地塞米松诱导性高血压中的作用
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引用本文的文献

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Effects of calcium antagonists on endothelin-1-induced myocardial ischaemia and oedema in the rat.钙拮抗剂对大鼠内皮素-1诱导的心肌缺血和水肿的影响。
Br J Pharmacol. 1996 Jun;118(4):893-900. doi: 10.1111/j.1476-5381.1996.tb15483.x.
2
Effects of the ETA/ETB receptor antagonist, bosentan on endothelin-1-induced myocardial ischaemia and oedema in the rat.内皮素A/内皮素B受体拮抗剂波生坦对大鼠内皮素-1诱导的心肌缺血和水肿的影响。
Br J Pharmacol. 1995 Sep;116(2):1745-50. doi: 10.1111/j.1476-5381.1995.tb16657.x.
3
Characterization of receptors mediating vascular responses to endothelin-1 in the conscious rat.
清醒大鼠中介导血管对内皮素-1反应的受体的特性研究
Br J Pharmacol. 1994 Nov;113(3):845-52. doi: 10.1111/j.1476-5381.1994.tb17070.x.