Centre for Human Drug Research, Leiden, the Netherlands.
Clinical Pharmacological Research Center (CPRC), Peking Union Medical College Hospital, Beijing, China.
Clin Pharmacol Drug Dev. 2015 Mar;4(2):149-54. doi: 10.1002/cpdd.134. Epub 2014 Aug 28.
Compounds with selectivity for GABAA receptor subtypes may differ significantly from nonselective benzodiazepines in their dopaminergic effects in vivo. To explore the exact role of the GABAA receptor subtypes in the regulation of prolactin secretion and the differential effects of selective and nonselective GABA receptor modulators, the effects of the nonselective benzodiazepine lorazepam, as well as two novel α2 /α3 subunit-selective GABAA receptor modulators AZD7325 and AZD6280, on prolactin levels were measured in healthy male volunteers. Following administration of lorazepam at 2 mg doses and AZD6280 at 10 mg and 40 mg doses, prolactin levels increased significantly compared with placebo (difference 42.0%, 19.8%, and 32.8%, respectively), suggesting that the α2 and/or α3 receptor subtypes are involved in GABAergic modulation of prolactin secretion, although possible roles of the α1 and α5 receptor subtypes are not excluded. The increases in prolactin levels after administration of AZD7325 at 2 mg and 10 mg doses (difference 7.6% and 10.5%, respectively) did not reach statistical significance, suggesting that doses of AZD7325 or intrinsic efficacy at the α2 and α3 receptor subtypes may have been too low.
具有 GABA A 受体亚型选择性的化合物在体内的多巴胺能效应方面可能与非选择性苯二氮䓬类药物有显著差异。为了探索 GABA A 受体亚型在调节催乳素分泌中的确切作用,以及选择性和非选择性 GABA 受体调节剂的差异作用,我们测量了非选择性苯二氮䓬类药物劳拉西泮,以及两种新型的 α2/α3 亚基选择性 GABA A 受体调节剂 AZD7325 和 AZD6280,对健康男性志愿者催乳素水平的影响。与安慰剂相比,劳拉西泮 2mg 剂量和 AZD6280 10mg 和 40mg 剂量给药后,催乳素水平显著升高(分别差异 42.0%、19.8%和 32.8%),提示 α2 和/或 α3 受体亚型参与了 GABA 对催乳素分泌的调制,尽管不能排除 α1 和 α5 受体亚型的可能作用。AZD7325 2mg 和 10mg 剂量给药后催乳素水平的升高(分别差异 7.6%和 10.5%)未达到统计学意义,提示 AZD7325 剂量或在 α2 和 α3 受体亚型中的内在效能可能过低。