Luccarini P, Gahery Y, Blanchet G, Pompeiano O
Laboratoire de Neurosciences Fonctionnelles, Unité de Neurosciences Integratives, C.N.R.S., Marseille, France.
Arch Ital Biol. 1992 Mar;130(2):127-54.
The early component of the postural responses which accompany the limb flexion during unilateral stimulation of the motor cortex in the cat is not of reflex origin, but results from a central command. These postural adjustments are characterized by a decreased force under the limb diagonally opposite to the moving one and an increased force under the other two. Since the lateral vestibular nucleus (LVN) exerts an excitatory influence on ipsilateral limb extensor motoneurons, experiments were performed in cats to establish whether the cortical-induced postural changes were mediated through the LVN. This structure is tonically inhibited by GABAergic synapses originating from Purkinje cells of the cerebellar vermis, so that local microinjection into the LVN of GABA agonists or antagonists should either decrease or increase the spontaneous discharge of their neurons. Unilateral microinjection of 0.25 microliters of the GABA-A agonist muscimol or the GABA-B agonist baclofen (at 2-4 micrograms/microliters saline) into the LVN produced a short-lasting episode of ipsilateral postural hypotonia and contralateral hypertonia, during which the cats were unable to stand on the measurement platform. When, shortly after, some recovery of the postural activity appeared, no changes in threshold, latency or amplitude of the cortical-induced flexion movement were observed; however, the early component of the postural responses decreased in the other three limbs. Moreover, the slope of the response curve of the moving limb remained unmodified, while that of the early component of the postural responses, which involved the remaining limbs, decreased following stimulation of the motor cortex at different stimulus intensities. These effects started a few min after the injection and lasted for about 2-3 h. The effects described above were dose-dependent. Moreover, histological controls indicated that the structure responsible for these postural changes corresponded to the middle part of the LVN. The specificity of the results was shown by the fact that unilateral microinjection of 0.25 microliters of the GABA-A antagonist bicuculline or the GABA-B antagonist phaclofen (at 5-8 micrograms/microliter saline) into the LVN produced a postural asymmetry opposite in sign to that elicited in the same experiments by the corresponding agonists. These injections did not modify the amplitude of the cortical-induced limb flexion, but rather enhanced the amplitude of the early component of the postural responses in the other three limbs.(ABSTRACT TRUNCATED AT 400 WORDS)
在猫的运动皮层单侧刺激期间,伴随肢体屈曲的姿势反应的早期成分并非反射起源,而是源于中枢指令。这些姿势调整的特征是,与运动肢体对角相对的肢体下的力量减小,而另外两条肢体下的力量增加。由于外侧前庭核(LVN)对同侧肢体伸肌运动神经元施加兴奋性影响,因此在猫身上进行了实验,以确定皮层诱导的姿势变化是否通过LVN介导。该结构受到来自小脑蚓部浦肯野细胞的GABA能突触的紧张性抑制,因此向LVN局部微量注射GABA激动剂或拮抗剂应分别减少或增加其神经元的自发放电。向LVN单侧微量注射0.25微升GABA-A激动剂蝇蕈醇或GABA-B激动剂巴氯芬(以2 - 4微克/微升盐水配制)会产生同侧姿势性肌张力减退和对侧肌张力亢进的短暂发作,在此期间猫无法站在测量平台上。之后不久,当姿势活动出现一些恢复时,未观察到皮层诱导的屈曲运动的阈值、潜伏期或幅度有变化;然而,其他三条肢体的姿势反应的早期成分减小。此外,运动肢体的反应曲线斜率保持不变,而涉及其余肢体的姿势反应早期成分的斜率在以不同刺激强度刺激运动皮层后减小。这些效应在注射后几分钟开始,持续约2 - 3小时。上述效应呈剂量依赖性。此外,组织学对照表明,导致这些姿势变化的结构对应于LVN的中部。结果的特异性体现在以下事实上:向LVN单侧微量注射0.25微升GABA-A拮抗剂荷包牡丹碱或GABA-B拮抗剂法氯芬(以5 - 8微克/微升盐水配制)会产生与相应激动剂在相同实验中引发的姿势不对称相反的体征。这些注射并未改变皮层诱导的肢体屈曲幅度,而是增强了其他三条肢体姿势反应早期成分的幅度。(摘要截取自400字)