Vijayaraghavan S, Schmid H A, Mapp K S
Department of Biology, University of California, San Diego, La Jolla 92093-0322.
J Neurochem. 1993 Jul;61(1):324-31. doi: 10.1111/j.1471-4159.1993.tb03571.x.
5-Hydroxytryptamine (5-HT) specifically and reversibly inhibits nicotine-induced currents and catecholamine release in bovine adrenal chromaffin cells in culture. Pharmacological analysis indicates that the inhibition is not mediated by known 5-HT receptor subtypes. The inhibition is noncompetitive over a range of nicotine concentrations between 1 and 100 microM. Preincubation with either 5-HT or substance P significantly protects the response from nicotine-induced desensitization. It is concluded that 5-HT inhibits nicotinic acetylcholine receptors on bovine adrenal chromaffin cells, probably by binding to a noncompetitive site on the receptor itself. Because both blood and the chromaffin cells contain 5-HT, the inhibition provides an opportunity for negative control of catecholamine secretion from the adrenals.
5-羟色胺(5-HT)可特异性且可逆地抑制培养的牛肾上腺嗜铬细胞中尼古丁诱导的电流及儿茶酚胺释放。药理学分析表明,这种抑制作用并非由已知的5-HT受体亚型介导。在1至100微摩尔的尼古丁浓度范围内,该抑制作用是非竞争性的。用5-HT或P物质预孵育可显著保护细胞免受尼古丁诱导的脱敏反应。得出的结论是,5-HT可能通过与受体自身的非竞争性位点结合来抑制牛肾上腺嗜铬细胞上的烟碱型乙酰胆碱受体。由于血液和嗜铬细胞中都含有5-HT,这种抑制作用为肾上腺儿茶酚胺分泌的负调控提供了一个机会。