Arnt J, Scheel-Krüger J, Magelund G, Krogsgaard-Larsen P
J Pharm Pharmacol. 1979 May;31(5):306-13. doi: 10.1111/j.2042-7158.1979.tb13506.x.
Contralateral turning behaviour following unilateral intranigral injection of a large series of GABA analogues was investigated. The results indicated that the turning behaviour was induced stereospecifically and was selectively antagonized by the GABA antagonist bicuculline methochloride. The comparative potencies of a series of GABA agonists related to muscimol in general corresponded well to the affinity for 3H-GABA receptor sites and to the depressant action on single neurons using microelectrophoretic administration. However, the GABA agonists trans-aminocrotonic acid and 3-aminopropanesulphonic acid were much weaker than expected from in vitro studies. The GABA-uptake inhibitors nipecotic acid and guvacine showed only weak and short-lasting effects. The GABA-transaminase inhibitor gamma-acetylenic GABA showed delayed effects compared with the agonists which acted immediately. It is proposed that this behavioural effect may be a sensitive and quantitative method for evaluation of GABA agonists in vivo.
研究了在单侧黑质内注射一系列GABA类似物后的对侧转向行为。结果表明,转向行为是立体特异性诱导的,并被GABA拮抗剂甲基荷包牡丹碱选择性拮抗。一系列与蝇蕈醇相关的GABA激动剂的相对效力总体上与对3H-GABA受体位点的亲和力以及使用微电泳给药对单个神经元的抑制作用相当。然而,GABA激动剂反式氨基巴豆酸和3-氨基丙烷磺酸比体外研究预期的要弱得多。GABA摄取抑制剂尼克酸和胍可宁仅表现出微弱且持续时间短的作用。与立即起作用的激动剂相比,GABA转氨酶抑制剂γ-乙炔基GABA表现出延迟作用。有人提出,这种行为效应可能是一种在体内评估GABA激动剂的灵敏且定量的方法。