Andreev B V, Ignatov Iu D
Biull Eksp Biol Med. 1986 Oct;102(10):438-40.
The experiments on rats have shown that selective alpha 1 and alpha 2 adrenoceptor blockers (prazosin and yohimbine) and an inhibitor of dopamine-beta-hydrolase FD-008 failed to change the antinociceptive effect of baclofen, a direct GABAB receptor agonist. The antinociceptive effect of THIP and depakin, acting predominantly on GABAA receptors, was significantly reduced by prazosin, FD-008 and yohimbine in vocalization test. In tail-flick test the analgetic effect of THIP and depakin was not altered by prazosin and FD-008, but was increased by yohimbine. The role of adrenergic mechanisms in GABAA and GABAB receptor-mediated analgesia is discussed.
对大鼠的实验表明,选择性α1和α2肾上腺素能受体阻滞剂(哌唑嗪和育亨宾)以及多巴胺-β-羟化酶抑制剂FD-008未能改变直接GABAB受体激动剂巴氯芬的镇痛作用。在发声测试中,主要作用于GABAA受体的四氢异喹啉(THIP)和丙戊酸的镇痛作用被哌唑嗪、FD-008和育亨宾显著降低。在甩尾测试中,THIP和丙戊酸的镇痛作用未被哌唑嗪和FD-008改变,但被育亨宾增强。文中讨论了肾上腺素能机制在GABAA和GABAB受体介导的镇痛中的作用。