Morales Melissa, Spear Linda P
Department of Physiology & Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA,
Psychopharmacology (Berl). 2014 Apr;231(8):1797-807. doi: 10.1007/s00213-013-3278-3. Epub 2013 Sep 17.
NMDA antagonists consistently produce social inhibition in adult animals, although effects of these manipulations on social behavior of adolescents are relatively unknown.
The aim of this study was to assess potential age differences in the socially inhibitory effects of the non-competitive NMDA antagonist, MK-801, as well as NR2 subunit selective effects, given the regional and developmental differences that exist for the NR2 subunit during ontogeny.
In separate experiments, adolescent and adult male Sprague-Dawley rats were treated acutely with MK-801 (0, 0.05, 0.1, 0.2 mg/kg, i.p.), the NR2A antagonist, PEAQX (2.5, 5, 10, 20 mg/kg, s.c.), or the NR2B antagonist, ifenprodil (1.5, 3, 6, 12 mg/kg, i.p.), 10 min prior to a social interaction test.
Adolescents required higher doses of MK-801 (0.1 and 0.2 mg/kg) to induce social suppression, whereas adults demonstrated reductions in social activity after all doses. Likewise, adolescents required higher doses of ifenprodil (6 and 12 mg/kg) to produce social inhibitory effects relative to adults (all doses). In contrast, adults were less sensitive to PEAQX than adolescents, with adults showing social inhibition after 20 mg/kg whereas adolescents showed this effect following 10 and 20 mg/kg. Although locomotor activity was generally reduced at both ages by all drugs tested, ANCOVAs using locomotor activity as a covariate revealed similar patterns of social inhibitory effects.
Adolescents are less sensitive than adults to the disruption of social behavior by NMDA and NR2B-selective receptor antagonism, but not by an NR2A antagonist-age differences that may be related to different subunit expression patterns during development.
NMDA拮抗剂在成年动物中始终会产生社交抑制作用,尽管这些操作对青少年社交行为的影响相对未知。
鉴于NR2亚基在个体发育过程中存在区域和发育差异,本研究旨在评估非竞争性NMDA拮抗剂MK-801的社交抑制作用以及NR2亚基选择性作用中潜在的年龄差异。
在单独的实验中,青春期和成年雄性Sprague-Dawley大鼠在社交互动测试前10分钟,分别接受MK-801(0、0.05、0.1、0.2mg/kg,腹腔注射)、NR2A拮抗剂PEAQX(2.5、5、10、20mg/kg,皮下注射)或NR2B拮抗剂ifenprodil(1.5、3、6、12mg/kg,腹腔注射)的急性处理。
青少年需要更高剂量的MK-801(0.1和0.2mg/kg)才能诱导社交抑制,而所有剂量的MK-801都会使成年大鼠的社交活动减少。同样,相对于成年大鼠(所有剂量),青少年需要更高剂量的ifenprodil(6和12mg/kg)才能产生社交抑制作用。相比之下,成年大鼠对PEAQX的敏感性低于青少年,成年大鼠在20mg/kg后出现社交抑制,而青少年在10和20mg/kg后出现这种效应。尽管所有测试药物在两个年龄段通常都会降低运动活动,但以运动活动作为协变量的协方差分析显示出相似的社交抑制作用模式。
青少年对NMDA和NR2B选择性受体拮抗作用引起的社交行为破坏不如成年大鼠敏感,但对NR2A拮抗剂不敏感——这些年龄差异可能与发育过程中不同的亚基表达模式有关。