Fleischmann A, Vincent P A, Etgen A M
Department of Psychiatry, Albert Einstein College of Medicine, Bronx, NY 10461.
Brain Res. 1991 Dec 24;568(1-2):138-46. doi: 10.1016/0006-8993(91)91389-i.
MK-801 and dextrorphan, selective non-competitive antagonists at N-methyl-D-aspartate (NMDA) receptors, were used to evaluate the effect of NMDA receptor blockade on sexual and motor behaviors in female rats. Ovariectomized rats were treated with estradiol benzoate (EB) for 48 or 72 h followed by progesterone (P) 3.5-4 h before testing the animals for sexual receptivity. After testing for estrous responsiveness, the effect of NMDA antagonists on several motor behaviors was also assessed. Lordosis frequency and intensity were inhibited in animals that received 0.5 mg/kg MK-801 30 min before EB; the same dose of MK-801 was relatively ineffective when administered 24 h after EB. In neither case did MK-801-treated females differ from controls when motor behaviors were assessed after mating tests. When 30 mg/kg dextrorphan, a short-acting NMDA antagonist, was administered 15 min before P, sexual behavior was not blocked. However, both 0.05 mg/kg MK-801 and 30 mg/kg dextrorphan suppressed ongoing female sexual behavior within 30 min in animals made receptive with EB and P. These deficits in sexual behavior were associated with changes in motor performance. MK-801 (0.1 mg/kg) and dextrorphan (30 mg/kg) abolished movement in the vertical dimension (e.g. jumping and rearing). By contrast, the drugs increased movement in the longitudinal (locomotion) and lateral (circling) dimensions. At 0.2 mg/kg, MK-801 blocked movement in both the vertical and longitudinal dimensions; however, it failed to block circling. Only at 0.4 mg/kg did MK-801 inhibit lateral movements and righting reflexes.(ABSTRACT TRUNCATED AT 250 WORDS)
MK-801和右啡烷是N-甲基-D-天冬氨酸(NMDA)受体的选择性非竞争性拮抗剂,被用于评估NMDA受体阻断对雌性大鼠性行为和运动行为的影响。对去卵巢大鼠用苯甲酸雌二醇(EB)处理48或72小时,然后在测试动物的性接受能力前3.5 - 4小时给予孕酮(P)。在测试动情反应后,还评估了NMDA拮抗剂对几种运动行为的影响。在EB给药前30分钟接受0.5mg/kg MK-801的动物中,脊柱前凸频率和强度受到抑制;相同剂量的MK-801在EB给药24小时后给药则相对无效。在交配试验后评估运动行为时,MK-801处理的雌性大鼠在这两种情况下与对照组均无差异。当在P给药前15分钟给予30mg/kg右啡烷(一种短效NMDA拮抗剂)时,性行为未被阻断。然而,0.05mg/kg MK-801和30mg/kg右啡烷在使动物用EB和P诱导出性接受能力后30分钟内均抑制了正在进行的雌性性行为。这些性行为缺陷与运动表现的变化有关。MK-801(0.1mg/kg)和右啡烷(30mg/kg)消除了垂直方向的运动(如跳跃和竖毛)。相比之下,这些药物增加了纵向(移动)和横向(转圈)方向的运动。在0.2mg/kg时,MK-801阻断了垂直和纵向方向的运动;然而,它未能阻断转圈。只有在0.4mg/kg时,MK-801才抑制横向运动和翻正反射。(摘要截短于250字)