Martin G E, Papp N L, Bacino C B
Brain Res. 1978 Oct 27;155(2):297-312. doi: 10.1016/0006-8993(78)91024-7.
Contraversive turning was evoked by the microinjection of GABAergic agents into the substantia nigra (SN) of the rat. Muscimol, the most potent GABA agonist, evoked contralateral turning when injected into the SN in doses of 0.005, 0.05, 0.5 and 5 microgram, whereas 0.5 microgram of muscimol applied at extranigral sites produced no turning. A shorter lived contraversive turning response was evoked by the intranigral micro-injection of imidazole acetic acid (10 or 50 microgram), ethanolamine-O-sulphate (25 or 50 microgram), or GABA (50 microgram). No increase in GABA-induced turning was produced by local pretreatment with pipecolic acid (5 microgram). When injected into the SN, neither picrotoxin, in doses of 0.1, 0.5, 1.0 or 2.0 microgram, nor bicuculline methiodide (Bm), in doses of 0.1 or 0.2 microgram, elicited a significant amount of turning. Picrotoxin, however, partially blocked the turning evoked by the intranigral injection of muscimol, both via the i.p. and intranigral routes of administration whereas Bm did not. In addition, haloperidol (1 mg/kg i.p.) antagonized the muscimol-induced turning. Hence, we feel GABA mimetic substances injected within the SN might evoke contralateral turning via activation of a heretofore undescribed neural system arising from the SN or by activating the ipsilateral dopaminergic neurons projecting from the SN.
通过向大鼠黑质(SN)微量注射GABA能药物可诱发对侧转向。蝇蕈醇是最有效的GABA激动剂,当以0.005、0.05、0.5和5微克的剂量注射到SN中时,可诱发对侧转向,而在黑质外部位注射0.5微克蝇蕈醇则不会引起转向。通过向黑质内微量注射咪唑乙酸(10或50微克)、乙醇胺 - O - 硫酸盐(25或50微克)或GABA(50微克)可诱发持续时间较短的对侧转向反应。用哌啶酸(5微克)进行局部预处理不会增加GABA诱导的转向。当注射到SN中时,剂量为0.1、0.5、1.0或2.0微克的印防己毒素以及剂量为0.1或0.2微克的荷包牡丹碱甲碘化物(Bm)均未引起明显的转向。然而,印防己毒素通过腹腔注射和黑质内注射途径,部分阻断了黑质内注射蝇蕈醇诱发的转向,而Bm则没有。此外,氟哌啶醇(1毫克/千克,腹腔注射)拮抗蝇蕈醇诱导的转向。因此,我们认为在SN内注射的GABA模拟物质可能通过激活源自SN的迄今未描述的神经系统,或通过激活从SN投射的同侧多巴胺能神经元来诱发对侧转向。