Puglisi-Allegra S, Mandel P
Psychopharmacology (Berl). 1980;70(3):287-90. doi: 10.1007/BF00427887.
An inhibitor of GABA-T (sodium n-dipropylacetate), a GABA agonist (muscimol hydrobromide) and an inhibitor of GABA uptake (R,S) nipecotic acid amide were administered to DBA/2 isolated aggressive mice throughout three successive daily experimental sessions. Aggressive responses, measured by an automated device, were inhibited by the highest doses of the three drugs in each daily session. At the lowest doses, sodium, n-dipropylacetate and nipecotic acid amide failed to inhibit aggression in the first session while they were effective in the subsequent sessions. Muscimol was effective in the first session but did not differ significantly from saline in the second and third session. The highest doses of these three drugs did not affect spontaneous motor activity, indicating that the observed drug effects are rather specific.
在连续三天的每日实验过程中,向DBA/2品系的孤立攻击性小鼠施用了γ-氨基丁酸转氨酶抑制剂(二丙基乙酸钠)、γ-氨基丁酸激动剂(氢溴酸蝇蕈醇)和γ-氨基丁酸摄取抑制剂(R,S)-哌啶酸酰胺。通过自动装置测量的攻击反应在每个每日实验过程中均被三种药物的最高剂量所抑制。在最低剂量下,二丙基乙酸钠和哌啶酸酰胺在第一天实验中未能抑制攻击行为,但在随后的实验中有效。蝇蕈醇在第一天实验中有效,但在第二天和第三天实验中与生理盐水相比无显著差异。这三种药物的最高剂量不影响自发运动活动,表明观察到的药物作用具有相当的特异性。