Ward A, Takemori A E
J Pharmacol Exp Ther. 1976 Oct;199(1):124-30.
Studies were conducted to determine the role of norepinephrine and 5-hydroxytryptamine in the action of morphine in the coaxially stimulated guinea-pig ileum. 6-hydroxydopamine produced supersensitivity to norepinephrine and decreased the levels of norepinephrine in the ileum. 6-Hydroxydopamine did not interfere with the acute effects of morphine but did interfere with the degree of tolerance developed to morphine, which is in contrast to reported results of the effect of 6-hydroxydopamine on the analgesic response to morphine. No evidence was found that 5,6-dihydroxytryptamine altered the acute or chronic response of the ileum to morphine. Again this is in contrast to results for the analgesic receptor where 5,6-dihydroxytryptamine has been reported to inhibit the development of tolerance to morphine. Thus, the role of the biogenic amines in the action of morphine in the ileum appears to differ from their reported role in the action of morphine in the central nervous system.
开展了多项研究以确定去甲肾上腺素和5-羟色胺在吗啡对同轴刺激的豚鼠回肠作用中的角色。6-羟基多巴胺使回肠对去甲肾上腺素产生超敏反应,并降低了回肠中去甲肾上腺素的水平。6-羟基多巴胺并不干扰吗啡的急性作用,但确实干扰了对吗啡产生耐受的程度,这与报道的6-羟基多巴胺对吗啡镇痛反应的作用结果相反。未发现有证据表明5,6-二羟基色胺改变了回肠对吗啡的急性或慢性反应。这同样与镇痛受体的结果相反,据报道5,6-二羟基色胺可抑制对吗啡耐受性的产生。因此,生物胺在吗啡对回肠作用中的角色似乎与其在吗啡对中枢神经系统作用中所报道的角色不同。