Eriksson E, Svensson K, Clark D
Life Sci. 1985 May 13;36(19):1819-27. doi: 10.1016/0024-3205(85)90154-7.
Recent behavioural and biochemical investigations have suggested that the alpha-2 receptor agonist B-HT 920 is also a centrally acting dopamine (DA) agonist with a selectivity for autoreceptors. It is presently demonstrated that B-HT 920, in contrast to the structurally related alpha-2 agonist B-HT 933, effectively reduces the firing rate of nigral DA neurons both after intravenous and microiontophoretic administration. Furthermore, B-HT 920, but not B-HT 933, decreases plasma levels of prolactin in reserpine pretreated rats. The electrophysiological as well as the neuroendocrine effects of the drug were antagonised by DA antagonists but not by alpha-2 receptor antagonists. The data support the contention that B-HT 920 acts as an agonist at central DA autoreceptors. Furthermore, they reinforce the hypothesis that lactotroph DA receptors are more similar to DA autoreceptors than to postsynaptic DA receptors in the brain.
最近的行为学和生物化学研究表明,α-2受体激动剂B-HT 920也是一种对自身受体具有选择性的中枢作用多巴胺(DA)激动剂。目前已证明,与结构相关的α-2激动剂B-HT 933不同,B-HT 920在静脉注射和微量离子导入给药后均能有效降低黑质DA神经元的放电频率。此外,B-HT 920而非B-HT 933可降低利血平预处理大鼠的催乳素血浆水平。该药物的电生理和神经内分泌作用被DA拮抗剂拮抗,但未被α-2受体拮抗剂拮抗。这些数据支持了B-HT 920作为中枢DA自身受体激动剂的观点。此外,它们强化了这样一种假说,即促乳素细胞DA受体在大脑中与DA自身受体比与突触后DA受体更相似。