Hughes A D, Sever P S
Department of Clinical Pharmacology, St. Mary's Hospital Medical School, London, UK.
Blood Vessels. 1989;26(2):119-27. doi: 10.1159/000158760.
The effects of a DA1 dopamine receptor selective agonist, fenoldopam, were examined on human blood vessels. Fenoldopam relaxed precontracted human arteries in vitro from brachial, cerebral, cervical, colic, coronary, lumbar, pulmonary, renal and splenic sites. Fenoldopam failed to relax uterine or external iliac arteries or saphenous vein segments. These effects of fenoldopam were not endothelium dependent, but were antagonised by the selective DA1 receptor antagonists, SCH 23390, (+)-butaclamol, and (R)- more than (S)-sulpiride. The effect of fenoldopam may involve cyclic adenosine monophosphate. These studies indicate the presence of DA1 receptors on a variety of large isolated human arteries.
研究了多巴胺1(DA1)受体选择性激动剂非诺多泮对人体血管的作用。非诺多泮可使体外预先收缩的来自肱动脉、脑动脉、颈动脉、结肠动脉、冠状动脉、腰动脉、肺动脉、肾动脉和脾动脉部位的人体动脉舒张。非诺多泮未能使子宫动脉、髂外动脉或大隐静脉段舒张。非诺多泮的这些作用不依赖于内皮,但可被选择性DA1受体拮抗剂SCH 23390、(+)-布他拉莫尔和(R)-舒必利拮抗,(R)-舒必利的拮抗作用强于(S)-舒必利。非诺多泮的作用可能涉及环磷酸腺苷。这些研究表明在多种分离的人体大动脉上存在DA1受体。