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[多胺类物质腐胺、亚精胺和精胺对麻醉犬去甲肾上腺素升压作用的影响]

[Effects of the polyamines putrescine, spermidine and spermine on the hypertensive action of norepinephrine in anesthetized dogs].

作者信息

Ceballos G, Recamier L M, Pérez J, Trujillo J, Yáñez R, Pastelín G

机构信息

Departamento de Farmacología del Instituto Nacional de Cardiología Ignacio Chávez, México.

出版信息

Arch Inst Cardiol Mex. 1990 Jul-Aug;60(4):369-73.

PMID:2268174
Abstract

In anesthetized and vagotomized dogs, we investigate the associative effects on blood pressure of norepinephrine (NE) with the three polyamines putrescine (Pt), spermidine (Sd) and spermine (Se). Experimental series were performed under beta adrenergic blockade (propranolol 0.5 mg/Kg, iv.), alpha adrenergic blockade (phenoxybenzamine 15 mg/Kg, iv.), and under calcium antagonistic action (verapamil 0.3 mg/Kg, iv.). The three polyamines induced a potentiation on the hypertensive effect of NE, they change the dose/response curve to the left side in a potency rank of Se greater than Sd greater than Pt. Such potentiation was not different when a beta adrenergic blockade or calcium antagonism was present; however phenoxybenzamine neutralized it. On the other side, polyamines had a hypotensive effect when were administered alone to the animals. Such effect is related to a histamine releasing properties of the polyamines, and was abolished by previous administration of anihistaminic agents chlorpheniramine (5 mg/kg, iv.) and cimetidine (20 mg/Kg, iv.). In conclusion our results indicate that the potentiation of the hypertensive effect of NE by polyamines, could be attained through a mechanism which involves the alpha adrenergic receptors of the vascular smooth muscle but is not related to the calcium channels that show voltage dependence.

摘要

在麻醉且切断迷走神经的犬中,我们研究了去甲肾上腺素(NE)与三种多胺即腐胺(Pt)、亚精胺(Sd)和精胺(Se)对血压的联合作用。实验系列在β肾上腺素能阻断(普萘洛尔0.5mg/kg,静脉注射)、α肾上腺素能阻断(酚苄明15mg/kg,静脉注射)以及钙拮抗作用(维拉帕米0.3mg/kg,静脉注射)下进行。这三种多胺对NE的升压作用有增强作用,它们使剂量/反应曲线向左移动,增强效力顺序为Se>Sd>Pt。当存在β肾上腺素能阻断或钙拮抗作用时,这种增强作用没有差异;然而酚苄明可使其作用消失。另一方面,多胺单独给予动物时具有降压作用。这种作用与多胺的组胺释放特性有关,并且在预先给予抗组胺药氯苯那敏(5mg/kg,静脉注射)和西咪替丁(20mg/kg,静脉注射)后被消除。总之,我们的结果表明,多胺对NE升压作用的增强可能是通过一种涉及血管平滑肌α肾上腺素能受体但与显示电压依赖性的钙通道无关的机制实现的。

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Arch Inst Cardiol Mex. 1990 Jul-Aug;60(4):369-73.
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