Seiler N, Grauffel C, Elands J, van den Buuse M, Knödgen B, Sarhan S, Moran P, Gobaille S
Marion Merrel Dow Research Institute, Strasbourg, France.
Pharmacol Biochem Behav. 1995 Feb;50(2):181-9. doi: 10.1016/0091-3057(94)00282-n.
Acute and chronic administration of vigabatrin, a selective inactivator of GABA-T, suppresses haloperidol-induced dyskinesias at low doses without preventing the enhancement of striatal dopamine D2 receptor density or the development of vacuous chewing movements. The long-term administration of vigabatrin does not attenuate its effect. The observations presented in this work support the GABA hypothesis of haloperidol-induced vacuous chewing behavior in rats, and suggest that vigabatrin is an appropriate means to enhance nigral GABAergic activity.
γ-氨基丁酸转氨酶(GABA-T)的选择性灭活剂vigabatrin的急性和慢性给药,在低剂量时可抑制氟哌啶醇诱导的运动障碍,且不会阻止纹状体多巴胺D2受体密度的增加或无意义咀嚼运动的发展。Vigabatrin的长期给药不会减弱其效果。这项工作中的观察结果支持大鼠中氟哌啶醇诱导的无意义咀嚼行为的GABA假说,并表明vigabatrin是增强黑质GABA能活性的合适手段。