Oka M, Manku M S, Horrobin D F
Prostaglandins Med. 1981 Oct;7(4):267-80. doi: 10.1016/0161-4630(81)90132-4.
Interactions between dopamine and responses to noradrenaline as modulated by prostaglandins (PGs) were studied in the perfused rat mesenteric vascular bed. When perfused alone dopamine up to a concentration of 10(-7)M neither changed baseline pressure nor modified the pressor response to noradrenaline. Dopamine at 10(-9) to 10(-7)M significantly inhibited responses to noradrenaline which had been enhanced by the presence of 10(-10) to 10(-8) M PGE1. In preparations in which vascular responses to noradrenaline had been abolished by indomethacin and restored by adding PGE1, 10(-9) to 10(-7)M dopamine significantly inhibited the restored responses. Dopamine also attenuated the inhibitory effects of prostacyclin on pressor responses to noradrenaline but it did not change the actions of either PGE2 or PGF2 alpha. Pimozide, a mainly centrally acting dopamine antagonist, did not interfere with these peripheral actions of dopamine. The dopamine effects were blocked by another dopamine antagonist, metoclopramide. Dopamine can inhibit the effects of PGE1 and prostacyclin in the rat mesenteric vascular bed, possibly by interacting with specific dopamine receptors.
在灌注的大鼠肠系膜血管床中研究了多巴胺与去甲肾上腺素反应之间的相互作用,该反应受前列腺素(PGs)调节。单独灌注时,浓度高达10(-7)M的多巴胺既不改变基础血压,也不改变对去甲肾上腺素的升压反应。10(-9)至10(-7)M的多巴胺显著抑制了由10(-10)至10(-8)M PGE1增强的对去甲肾上腺素的反应。在血管对去甲肾上腺素的反应已被吲哚美辛消除并通过添加PGE1恢复的制剂中,10(-9)至10(-7)M的多巴胺显著抑制了恢复的反应。多巴胺还减弱了前列环素对去甲肾上腺素升压反应的抑制作用,但它没有改变PGE2或PGF2α的作用。匹莫齐特是一种主要作用于中枢的多巴胺拮抗剂,不干扰多巴胺的这些外周作用。多巴胺的作用被另一种多巴胺拮抗剂甲氧氯普胺阻断。多巴胺可能通过与特定的多巴胺受体相互作用,抑制大鼠肠系膜血管床中PGE1和前列环素的作用。