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非诺多泮在大鼠后肢血管床产生的神经源性血管舒张。

Neurogenic vasodilatation produced by fenoldopam in the rat hindquarters vascular bed.

作者信息

Van der Niepen P, Lefebvre R A, Dupont A G

机构信息

Department of Pharmacology, Free University of Brussels (VUB), Belgium.

出版信息

J Auton Pharmacol. 1987 Dec;7(4):331-8. doi: 10.1111/j.1474-8673.1987.tb00161.x.

Abstract

1 The effects of local administration of the selective DA1-receptor agonist fenoldopam into the isolated autoperfused rat hindquarters were studied in order to investigate the site of action of fenoldopam in this vascular bed. 2 Bolus injections of fenoldopam produced reductions in perfusion pressure in the preconstricted, constant flow perfused rat hindquarters vascular bed. 3 The vasodilator effect of fenoldopam was abolished by sectioning of the lumbar sympathetic nerves and by pretreatment with the ganglion-blocker hexamethonium or the alpha-adrenoreceptor antagonists phentolamine and prazosin. At the same concentration, local infusion of fenoldopam had no effect on vasoconstrictor responses to locally administered noradrenaline and phenylephrine. 4 The vasodilator effect of fenoldopam was antagonized by the non-selective dopamine receptor antagonist RS-sulpiride and by the selective DA1-receptor antagonist SCH 23390, but not by the selective DA2-receptor antagonist domperidone. 5 These results provide no evidence for the presence of postsynaptic DA1-receptors in the rat hindquarters vascular bed; they show that fenoldopam induces neurogenic vasodilatation in this vascular bed, probably via stimulation of ganglionic DA1-receptors.

摘要
  1. 为了研究非诺多泮在该血管床中的作用位点,对选择性DA1受体激动剂非诺多泮局部给药至离体自灌注大鼠后肢的效应进行了研究。2. 单次注射非诺多泮可使预先收缩、恒流灌注的大鼠后肢血管床的灌注压降低。3. 切断腰交感神经以及用神经节阻滞剂六甲铵或α-肾上腺素能受体拮抗剂酚妥拉明和哌唑嗪预处理后,非诺多泮的血管舒张作用消失。在相同浓度下,局部输注非诺多泮对局部给予去甲肾上腺素和去氧肾上腺素的血管收缩反应无影响。4. 非诺多泮的血管舒张作用被非选择性多巴胺受体拮抗剂RS-舒必利和选择性DA1受体拮抗剂SCH 23390拮抗,但不被选择性DA2受体拮抗剂多潘立酮拮抗。5. 这些结果没有提供大鼠后肢血管床中存在突触后DA1受体的证据;它们表明非诺多泮在该血管床中诱导神经源性血管舒张,可能是通过刺激神经节DA1受体实现的。

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