Stoof J C, Mulder A H
Eur J Pharmacol. 1977 Nov 15;46(2):177-80. doi: 10.1016/0014-2999(77)90254-0.
The effects were examined of two inhibitors of GABA-aminotransferase, amino-oxyacetic acid (AOAA) and RMI-71645-16, on depolarization-induced (30 mM K+) dopamine (DA) release from rat striatal slices. When added to the medium, these drugs increased the release of radiolabeled DA, either accumulated by high-affinity uptake or synthesized from 14C-tyrosine. AOAA did not modify the release of 14C-acetylcholine from striatal slices or 3H-noradrenaline from cortical slices. Moreover, 3H-DA release from substantia nigra was not affected. The data suggest the possibility that the effects of GABA-T inhibitors on striatal DA release are mediated by intrinsic GABA-ergic neurons.
研究了两种γ-氨基丁酸转氨酶抑制剂,即氨氧乙酸(AOAA)和RMI-71645-16,对大鼠纹状体切片去极化诱导(30 mM钾离子)的多巴胺(DA)释放的影响。当将这些药物添加到培养基中时,它们增加了放射性标记的多巴胺的释放,这些多巴胺要么通过高亲和力摄取积累,要么由14C-酪氨酸合成。AOAA不会改变纹状体切片中14C-乙酰胆碱的释放或皮质切片中3H-去甲肾上腺素的释放。此外,黑质中3H-多巴胺的释放不受影响。数据表明,γ-氨基丁酸转氨酶抑制剂对纹状体多巴胺释放的影响可能是由内在的γ-氨基丁酸能神经元介导的。