West M O
Department of Psychology, Rutgers University, New Brunswick, New Jersey 08903, USA.
J Neurosci. 1998 Nov 1;18(21):9055-68. doi: 10.1523/JNEUROSCI.18-21-09055.1998.
The somatotopic organization of the lateral striatum has been demonstrated by anatomical studies of corticostriatal projections from somatosensory and motor cortices and by single-cell recordings in awake animals. The functional organization in the rat, characterized thus far in the freely moving rat preparation, could be mapped more precisely if a stereotaxic, and possibly an anesthetized, preparation could be used. Because striatal discharges evoked by innocuous somatosensory stimulation are used in mapping, this study tested whether such discharges can be observed during anesthesia, encouraged by responsiveness during anesthesia in somatosensory cortical layers projecting to the striatum. Electrode tracks through lateral striatum of anesthetized rats (pentobarbital or ketamine) revealed spontaneously discharging neurons but no discharges evoked by somatosensory examination (passive manipulation and cutaneous stimulation of 14 body parts). Similar tracks in chronically implanted rats showed evoked firing at numerous sites during wakefulness but not during anesthesia (pentobarbital or urethane). Comparisons of the activity of individual neurons between wakefulness and anesthesia showed that pentobarbital, ketamine, chloral hydrate, urethane, or metofane eliminated evoked firing and suppressed spontaneous firing. Recovery time was greater for neural than for behavioral measures. Thus, mapping as proposed is ruled out, and more importantly, the data show that somatotopically organized lateral striatal neurons stop discharging in response to natural stimulation during anesthesia. Available data indicate they do not reach threshold in response to depolarizations produced by glutamatergic corticostriatal synaptic transmission projected from the somatosensory cortex. These data and demonstrations of anesthetic-induced imbalances in most striatal neurotransmitters emphasize that many results regarding striatal physiology and pharmacology during anesthesia cannot be extrapolated to behavioral conditions, thus indicating the need for more empirical testing in conscious animals.
体感和运动皮层向纹状体的皮质纹状体投射的解剖学研究以及清醒动物的单细胞记录已经证实了外侧纹状体的躯体定位组织。大鼠的功能组织,迄今为止是在自由活动的大鼠制备中进行表征的,如果能使用立体定位且可能是麻醉的制备方法,就可以更精确地绘制图谱。由于无害体感刺激诱发的纹状体放电被用于绘制图谱,本研究受投射到纹状体的体感皮层层在麻醉期间的反应性的鼓舞,测试了在麻醉期间是否能观察到这种放电。穿过麻醉大鼠(戊巴比妥或氯胺酮)外侧纹状体的电极轨迹显示有自发放电的神经元,但没有体感检查(对14个身体部位的被动操作和皮肤刺激)诱发的放电。在慢性植入大鼠中的类似轨迹显示,在清醒时许多部位有诱发放电,但在麻醉(戊巴比妥或乌拉坦)期间没有。清醒和麻醉状态下单个神经元活动的比较表明,戊巴比妥、氯胺酮、水合氯醛、乌拉坦或甲氧氟烷消除了诱发放电并抑制了自发放电。神经恢复时间比行为测量的恢复时间更长。因此,所提议的绘制图谱方法被排除,更重要的是,数据表明,在麻醉期间,按躯体定位组织的外侧纹状体神经元会停止对自然刺激的放电。现有数据表明,它们对体感皮层投射的谷氨酸能皮质纹状体突触传递产生的去极化没有达到阈值。这些数据以及麻醉引起的大多数纹状体神经递质失衡的证明强调,许多关于麻醉期间纹状体生理学和药理学的结果不能外推到行为状态,因此表明需要在清醒动物中进行更多的实证测试。