Kilpatrick I C, Starr M S
Eur J Pharmacol. 1981 Feb 19;69(4):407-19. doi: 10.1016/0014-2999(81)90444-1.
The intensity, direction and dopamine dependence of circling behaviour were determined following stereotaxic injections of 40 ng muscimol (in 0.2 microliter over 3 min) into different regions of the rat's substantia nigra (SN). Weak, haloperidol-sensitive ipsilateral postural or locomotor asymmetries were invariably obtained from the rostral SN zona compacta (SNC), whilst robust contraversive rotational behaviour was always initiated from the SN zona reticulata (SNR) and caudal SNC. This was most rapid from the central SNR and was markedly attenuated by i.p. pretreatment with haloperidol (0.1 mg/kg) or pimozide (0.25 mg/kg), or by week-old 6-OHDA lesions of the nigrostriatal dopamine (DA) tract. Turning was significantly weaker from the lateral and ventral areas of the SNR, where it was not susceptible to DAergic blockade. Lower circling rates were also obtained if the SNR injections were made rapidly (in 30 sec), in a large volume (0.5 microliter) or at a supramaximal dose level (400 ng), possibly due to increased spread of the drug to remote neurones having an opposite effect on directional behaviour, or to exaggerated stereotypy. The variable action of muscimol at multiple sites in the SN is suggested to account for the earlier conflicting data in the literature.
在将40纳克蝇蕈醇(于3分钟内注射0.2微升)立体定位注射到大鼠黑质(SN)的不同区域后,确定了转圈行为的强度、方向和多巴胺依赖性。从黑质致密部(SNC)的嘴侧总是能获得微弱的、对氟哌啶醇敏感的同侧姿势或运动不对称,而强烈的向对侧旋转行为总是从黑质网状部(SNR)和尾侧SNC引发。从中部SNR引发的旋转行为最为迅速,并且腹腔注射氟哌啶醇(0.1毫克/千克)或匹莫齐特(0.25毫克/千克)预处理,或黑质纹状体多巴胺(DA)束的一周龄6-羟基多巴胺损伤,均能显著减弱这种旋转行为。从SNR的外侧和腹侧区域引发的旋转明显较弱,且不受多巴胺能阻断的影响。如果快速(30秒内)、大容量(0.5微升)或以超最大剂量水平(400纳克)注射到SNR,转圈速率也会降低,这可能是由于药物扩散到对方向行为有相反作用的远处神经元,或由于刻板行为加剧所致。提示蝇蕈醇在SN多个位点的可变作用可解释文献中早期相互矛盾的数据。