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尼索地平抑制猫后肢血管床的肾上腺素能反应。

Nisoldipine inhibits adrenergic responses in the hindquarters vascular bed of the cat.

作者信息

Minkes R K, Bellan J A, Kerstein M D, McNamara D B, Kadowitz P J

机构信息

Department of Pharmacology, Tulane University School of Medicine, New Orleans, LA 70112.

出版信息

Eur J Pharmacol. 1989 Jun 20;165(2-3):259-67. doi: 10.1016/0014-2999(89)90720-6.

Abstract

The effects of the calcium entry blocking agent nisoldipine on adrenergic vasoconstrictor responses were investigated in the hindquarters vascular bed of the cat under conditions of controlled blood flow. Nisoldipine dilated the hindquarters vascular bed and inhibited vasoconstrictor responses to Bay K 8644, a nifedipine analog which promotes calcium entry. During infusion of nisoldipine, vasoconstrictor responses to sympathetic nerve stimulation, norepinephrine, and tyramine were inhibited in a reversible manner. In addition to blocking responses to nerve-released and exogenous norepinephrine, the calcium entry antagonist decreased responses to methoxamine and BHT 933, alpha 1- and alpha 2-adrenoceptor agonists. Responses to methoxamine were reduced by prazosin, an alpha 1-adrenoceptor antagonist, but not by yohimbine, an alpha 2-adrenoceptor blocking agent, whereas responses to BHT 933 were decreased by yohimbine but not by prazosin. The results of these studies suggest that vasoconstrictor responses to neuronally released and exogenous norepinephrine, as well as to selective alpha 1- and alpha 2-adrenoceptor agonists, are dependent in part on an extracellular source of calcium in resistance vessels of the feline hindquarters vascular bed. The inhibitory effect of nisoldipine on vasoconstrictor responses to neuronally released norepinephrine may be important in the antihypertensive actions of calcium entry blocking agents.

摘要

在控制血流的条件下,研究了钙通道阻滞剂尼索地平对猫后肢血管床肾上腺素能血管收缩反应的影响。尼索地平使后肢血管床扩张,并抑制对Bay K 8644(一种促进钙内流的硝苯地平类似物)的血管收缩反应。在输注尼索地平期间,对交感神经刺激、去甲肾上腺素和酪胺的血管收缩反应以可逆方式受到抑制。除了阻断对神经释放的和外源性去甲肾上腺素的反应外,钙通道拮抗剂还降低了对甲氧明和BHT 933(α1和α2肾上腺素能受体激动剂)的反应。α1肾上腺素能受体拮抗剂哌唑嗪可降低对甲氧明的反应,但α2肾上腺素能受体阻断剂育亨宾则不能;而育亨宾可降低对BHT 933的反应,哌唑嗪则不能。这些研究结果表明,对神经释放的和外源性去甲肾上腺素以及对选择性α1和α2肾上腺素能受体激动剂的血管收缩反应部分依赖于猫后肢血管床阻力血管中细胞外钙源。尼索地平对神经释放的去甲肾上腺素引起的血管收缩反应的抑制作用可能在钙通道阻滞剂的降压作用中起重要作用。

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