Potegal M
Psychopharmacology (Berl). 1986;89(4):444-8. doi: 10.1007/BF02412119.
The GABA uptake inhibitor ethyl (R,S)-nipecotate produces a dose-dependent suppression of aggression in highly aggressive hamsters but not in minimally aggressive ones. This suppression occurs at doses below those producing peripheral cholinergic effects; at the highest dose used it persists after these effects have dissipated. Doses sufficient to suppress aggression have no significant effect on grooming, locomotor activity and other behaviors but do affect sunflower seed acceptance. The differential effects of the drug on highly and minimally aggressive animals may indicate that their differences in aggression are due to differences in endogenous GABAergic activity. These results, together with previous evidence for parallel circadian variation in GABA uptake and aggressive behavior, suggest that GABA uptake may be an important endogenous regulator of aggression.
γ-氨基丁酸(GABA)摄取抑制剂乙基(R,S)-哌啶甲酸盐可剂量依赖性地抑制高度好斗仓鼠的攻击性,但对攻击性极低的仓鼠却无此作用。这种抑制作用发生的剂量低于产生外周胆碱能效应的剂量;在使用的最高剂量下,外周胆碱能效应消失后,该抑制作用仍持续存在。足以抑制攻击性的剂量对梳理行为、运动活动及其他行为无显著影响,但会影响向日葵籽的接受情况。该药物对高度好斗和攻击性极低动物的不同作用可能表明,它们在攻击性上的差异源于内源性GABA能活性的差异。这些结果,连同先前关于GABA摄取与攻击行为存在平行昼夜节律变化的证据,提示GABA摄取可能是攻击性的一个重要内源性调节因子。