Department of Psychology, Rutgers University, Piscataway, NJ 08854, USA.
J Pharmacol Exp Ther. 2010 Feb;332(2):667-83. doi: 10.1124/jpet.109.158253. Epub 2009 Nov 11.
To investigate striatal mechanisms underlying the acute effects of stimulants on motor behavior, firing rates (FRs) of striatal neurons related specifically to vertical head movement were studied exclusively during vertical head movements. Precocaine FRs were recorded after intraperitoneal saline injection (time 1; T1), and rats performed conditioned vertical head movements (>10,000) similar to those induced by stimulants. After cocaine injection (0, 5, 10, or 20 mg/kg; T2), animals continued in the task. The proportion of long head movements was increased by low doses but decreased by the high dose, which induced stereotypic head movements. Comparing each neuron's FR during movements that were matched between T1 and T2 (e.g., regarding direction, distance), cocaine's effects depended on predrug FR and dose. Plots regressing T2FR on T1FR showed dose-dependent, "clockwise" rotations of regression lines in plots of all the neurons' average FRs and of individual neurons' FRs during different movements. All three doses elevated normally low FRs; the high dose also suppressed many higher FRs. Enhancement of a neuron's FR associated with weak and suppression of FR associated with strong corticostriatal inputs contradict several current theories of dopamine (DA) function. Induction of stereotypy by a single, high-dose injection suggests that this cocaine level exceeded that in other studies using cocaine self-administration, in which stereotypy develops only after several sessions. Suppressive effects observed only at the high dose and in numerous electrophysiological studies of DA agonist effects may be unrepresentative of uniform elevations in lateral striatal firing related to movement observed at lower cocaine levels.
为了研究纹状体在兴奋剂对运动行为的急性影响中的机制,专门在进行垂直头部运动期间研究了与垂直头部运动特别相关的纹状体神经元的放电率 (FRs)。可卡因注射前 (T1) 记录了预可卡因 FRs,并在 T2 后注射了可卡因 (0、5、10 或 20 mg/kg),动物继续进行任务。低剂量增加了长头运动的比例,但高剂量减少了诱导刻板运动的比例。比较 T1 和 T2 之间匹配的运动中每个神经元的 FR(例如,关于方向、距离),可卡因的作用取决于预药物 FR 和剂量。将 T2FR 回归到 T1FR 的图显示了所有神经元平均 FR 和个体神经元在不同运动期间 FR 的图中回归线的剂量依赖性“顺时针”旋转。所有三种剂量都升高了正常的低 FRs;高剂量还抑制了许多更高的 FRs。与弱皮质纹状体输入相关的神经元 FR 的增强和与强皮质纹状体输入相关的 FR 的抑制与多巴胺 (DA) 功能的几种当前理论相矛盾。单次高剂量注射诱导刻板行为表明,这种可卡因水平超过了使用可卡因自我给药的其他研究中的水平,在这些研究中,只有在几个疗程后才会出现刻板行为。仅在高剂量和大量 DA 激动剂作用的电生理研究中观察到的抑制作用可能不能代表与较低可卡因水平相关的与运动相关的外侧纹状体放电的均匀升高。