Ozaki N, Kawakita S, Toda N
J Cardiovasc Pharmacol. 1982 May-Jun;4(3):456-61. doi: 10.1097/00005344-198205000-00017.
The effects of dobutamine on helical strips of isolated canine cerebral, coronary, mesenteric, and renal arteries was investigated. Dobutamine contracted only renal arterial strips under resting condition. When renal and mesenteric arterial strips were partially contracted with prostaglandin F2 alpha (PGF2 alpha), dobutamine caused further concentration-related contraction, while coronary arterial strips were relaxed. Cerebral arterial strips, on the other hand, did not significantly respond to dobutamine. After treatment with 10(-5) M dl-phenoxybenzamine hydrochloride (POB) for 1 h, dobutamine-induced contractions of partially precontracted mesenteric and renal arterial strips were converted to relaxations. Relaxations of coronary arteries were not potentiated by the alpha-antagonist, but were attenuated by treatment with 10(-6) M propranolol and 10(-6) M metoprolol to a similar extent. On the other hand, relaxations of mesenteric and renal arterial strips were not inhibited by metoprolol but by propranolol. Droperidol (3 X 10(-5) M) failed to significantly alter the concentration-response curve for dobutamine. These results suggest that dobutamine causes vasoconstriction mediated by apha-adrenergic receptor and vasodilatation mediated by beta 1- and beta 2-adrenoceptors. Dobutamine does not appear to act on dopamine receptors.
研究了多巴酚丁胺对离体犬脑动脉、冠状动脉、肠系膜动脉和肾动脉螺旋条的作用。在静息状态下,多巴酚丁胺仅使肾动脉条收缩。当肾动脉和肠系膜动脉条用前列腺素F2α(PGF2α)部分收缩时,多巴酚丁胺引起进一步的浓度依赖性收缩,而冠状动脉条则舒张。另一方面,脑动脉条对多巴酚丁胺无明显反应。用10(-5)M盐酸苯氧苄胺(POB)处理1小时后,多巴酚丁胺诱导的部分预收缩肠系膜和肾动脉条的收缩转变为舒张。α受体拮抗剂未增强冠状动脉的舒张作用,但用10(-6)M普萘洛尔和10(-6)M美托洛尔处理后,冠状动脉舒张作用在相似程度上减弱。另一方面,美托洛尔未抑制肠系膜和肾动脉条的舒张作用,但普萘洛尔可抑制。氟哌利多(3×10(-5)M)未能显著改变多巴酚丁胺的浓度-反应曲线。这些结果表明,多巴酚丁胺引起由α肾上腺素能受体介导的血管收缩和由β1和β2肾上腺素能受体介导的血管舒张。多巴酚丁胺似乎不作用于多巴胺受体。