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首页> 外文期刊>Frontiers in Neurology >Anatomical Location of the Mesencephalic Locomotor Region and Its Possible Role in Locomotion, Posture, Cataplexy, and Parkinsonism
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Anatomical Location of the Mesencephalic Locomotor Region and Its Possible Role in Locomotion, Posture, Cataplexy, and Parkinsonism

机译:中脑运动区的解剖位置及其在运动,姿势,分解代谢和帕金森病中的可能作用

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The mesencephalic (or midbrain) locomotor region (MLR) was first described in 1966 by Shik and colleagues, who demonstrated that electrical stimulation of this region induced locomotion in decerebrate (intercollicular transection) cats. The pedunculopontine tegmental nucleus (PPT) cholinergic neurons and midbrain extrapyramidal area (MEA) have been suggested to form the neuroanatomical basis for the MLR, but direct evidence for the role of these structures in locomotor behavior has been lacking. Here, we tested the hypothesis that the MLR is composed of non-cholinergic spinally projecting cells in the lateral pontine tegmentum. Our results showed that putative MLR neurons medial to the PPT and MEA in rats were non-cholinergic, glutamatergic, and express the orexin (hypocretin) type 2 receptors. Fos mapping correlated with motor behaviors revealed that the dorsal and ventral MLR are activated, respectively, in association with locomotion and an erect posture. Consistent with these findings, chemical stimulation of the dorsal MLR produced locomotion, whereas stimulation of the ventral MLR caused standing. Lesions of the MLR (dorsal and ventral regions together) resulted in cataplexy and episodic immobility of gait. Finally, trans-neuronal tracing with pseudorabies virus demonstrated disynaptic input to the MLR from the substantia nigra via the MEA. These findings offer a new perspective on the neuroanatomic basis of the MLR, and suggest that MLR dysfunction may contribute to the postural and gait abnormalities in Parkinsonism.
机译:Shik及其同事于1966年首次描述了中脑(或中脑)运动区域(MLR),他们证明了该区域的电刺激可诱发小脑(颈间横切)猫的运动。已建议使用人足桥骨被盖核(PPT)胆碱能神经元和中脑锥体束外区域(MEA)形成MLR的神经解剖学基础,但一直缺乏这些结构在运动行为中的作用的直接证据。在这里,我们测试了以下假设:MLR由桥脑外侧盖中的非胆碱能脊柱投射细胞组成。我们的研究结果表明,在大鼠PPT和MEA内侧的推定MLR神经元是非胆碱能,谷氨酸能的,并表达orexin(hypocretin)2型受体。与运动行为相关的Fos作图揭示了背侧和腹侧MLR分别与运动和直立姿势有关而被激活。与这些发现一致,对背侧MLR的化学刺激产生运动,而对腹侧MLR的刺激引起站立。 MLR(背侧和腹侧区域)病变导致步态瘫痪和发作性固定。最后,伪狂犬病病毒的跨神经元示踪表明,黑膜中的黑质通过MEA向MLR产生了突触输入。这些发现为MLR的神经解剖学基础提供了新的观点,并表明MLR功能障碍可能与帕金森病的姿势和步态异常有关。

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