Schmied A, Amalric M, Dormont J F, Farin D
Laboratoire de Neurobiologie et Neuropharmacologie du Développement, CNRS-UA, Université-Paris-Sud, Orsay, France.
Exp Brain Res. 1991;84(2):285-96. doi: 10.1007/BF00231448.
The activity of 61 rubral neurones was recorded in association with microinjections of GABA, muscimol, bicuculline-methiodide or saline, in cat Red Nucleus area, during the performance of a reaction time task. The depressing action of GABA and muscimol on the firing of most neurones (17/23) suggests that, in a behavioural situation, an inhibitory GABAergic control can be exerted on rubral neurones discharging with different patterns during the reaction time task. The motor slowing down induced by GABA and muscimol is in agreement with a general reduction of the rubral output. Injections of bicuculline, whose antagonistic effects on GABA transmission are well established in the Red Nucleus, had various consequences on the firing of rubral neurones: 1) the decreases of activity related to the reaction time task were never suppressed, suggesting that these task-related inactivations are probably not mediated by GABA A receptors; 2) an enhancement of the tonic and phasic discharges was found for 1/4 of the neurones (7/29), which were either activated or not modulated in relation to the reaction time task, suggesting that a sustained GABA A-mediated inhibition, blocked by bicuculline, could be exerted on these neurones; 3) a reduction of the tonic and phasic discharges was observed for other neurones (15/29), which were either activated, inactivated or not modulated in relation to the reaction time task, suggesting that the activity of these neurones could be controlled by inhibitory processes not mediated by GABA A receptors, possibly enhanced or released by bicuculline. The delay in motor triggering induced by bicuculline could be related to the disruption of the pattern or rubral output during the reaction time task, as a result of the opposite changes affecting the firing of rubral neurones. A well-balanced GABAergic activity appears to be critical in the control of rubral firing during the performance of the reaction time task.
在猫红核区域进行反应时任务期间,记录了61个红核神经元的活动,同时向该区域微量注射γ-氨基丁酸(GABA)、蝇蕈醇、甲基荷包牡丹碱或生理盐水。GABA和蝇蕈醇对大多数神经元(17/23)放电的抑制作用表明,在行为情境中,在反应时任务期间以不同模式放电的红核神经元可受到抑制性GABA能控制。GABA和蝇蕈醇引起的运动减慢与红核输出的总体减少一致。甲基荷包牡丹碱对GABA传递的拮抗作用在红核中已得到充分证实,其注射对红核神经元的放电产生了各种影响:1)与反应时任务相关的活动减少从未被抑制,这表明这些与任务相关的失活可能不是由GABAA受体介导的;2)在1/4的神经元(7/29)中发现紧张性和相位性放电增强,这些神经元在反应时任务中要么被激活,要么未被调制,这表明bicuculline可阻断的持续GABAA介导的抑制作用可能作用于这些神经元;3)在其他神经元(15/29)中观察到紧张性和相位性放电减少,这些神经元在反应时任务中要么被激活、失活,要么未被调制,这表明这些神经元的活动可能受非GABAA受体介导的抑制过程控制,bicuculline可能增强或释放了该过程。bicuculline引起的运动触发延迟可能与反应时任务期间红核输出模式的破坏有关,这是影响红核神经元放电的相反变化的结果。在反应时任务执行期间,平衡良好的GABA能活动似乎对控制红核放电至关重要。