Sinnamon H M
Neuroscience & Behavior Program, Wesleyan University, Middletown, CT 06457.
Neuroscience. 1992 Sep;50(1):197-207. doi: 10.1016/0306-4522(92)90392-f.
Previous studies have indicated that the basal forebrain at the level of the preoptic area contains neurons which participate in the initiation of locomotion. This study attempted to localize those neurons by mapping sites at which 25- and 50-microA stimulation (50 Hz, 0.5 ms cathodal pulses, 10-s trains) initiated hindlimb stepping. Anesthetized rats were held in a stereotaxic apparatus supported by a sling so that stepping movements rotated a wheel. Anesthesia was maintained by periodic injections of Nembutal (7 mg/kg) supplemented by lidocaine injections. Stimulation was applied through 50-70-microns diameter pipettes filled with 2 M NaCl at approximately 1600 sites in the basal forebrain, adjacent thalamus, and striatum. A circumscribed grouping of 25-microA locomotor sites, centered in the lateral preoptic area, defined the preoptic locomotor region. It extended into the ventral bed nucleus of the stria terminalis, the lateral part of the medial preoptic area, the anterior hypothalamic area, the medial and rostral parts of the ventral pallidum, medial substantia innominata, and the horizontal limb of the diagonal band. This general region is known to project to the midbrain locomotor region and the ventral tegmental area; it is proposed to initiate locomotion in service of primary motivational systems. Among the structures generally negative for locomotor sites were the dorsal and ventral striata, septal complex, bed nucleus of stria terminalis, and lateral ventral pallidum and substantia innominata. These findings indicate that low current stimulation applied to a circumscribed area centered in the lateral preoptic area produces locomotor stepping in the anesthetized rat. Whether the activated elements in this preoptic locomotor region are cells or fibers is not yet known. The degree of localization afforded by these findings indicates that the areas that are most likely to contain the mediating elements are quite limited in extent.
先前的研究表明,视前区水平的基底前脑包含参与运动起始的神经元。本研究试图通过绘制25微安和50微安刺激(50赫兹,0.5毫秒阴极脉冲,10秒串刺激)引发后肢踏步的位点来定位这些神经元。将麻醉的大鼠置于由吊带支撑的立体定位仪中,使踏步运动带动轮子转动。通过定期注射戊巴比妥(7毫克/千克)并辅以利多卡因注射来维持麻醉。通过直径为50 - 70微米、充满2 M氯化钠的移液管,在基底前脑、相邻丘脑和纹状体的约1600个位点施加刺激。以外侧视前区为中心的一组界限分明的25微安运动位点,确定了视前运动区。它延伸至终纹床核腹侧、内侧视前区外侧部、下丘脑前区、腹侧苍白球内侧和嘴侧部、无名质内侧以及斜角带水平支。已知这个一般区域投射到中脑运动区和腹侧被盖区;推测它在主要动机系统的作用下启动运动。在通常对运动位点呈阴性的结构中,有背侧和腹侧纹状体、隔复合体、终纹床核、腹侧苍白球外侧部和无名质。这些发现表明,对以外侧视前区为中心的一个限定区域施加低电流刺激,可使麻醉大鼠产生运动性踏步。该视前运动区中被激活的成分是细胞还是纤维尚不清楚。这些发现所提供的定位程度表明,最有可能包含介导成分的区域范围相当有限。