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运动神经元病(MND)中的非NMDA受体:使用[3H]CNQX和[3H]海人酸对脊髓和运动皮层进行的定量放射自显影研究。

Non-NMDA receptors in motor neuron disease (MND): a quantitative autoradiographic study in spinal cord and motor cortex using [3H]CNQX and [3H]kainate.

作者信息

Shaw P J, Chinnery R M, Ince P G

机构信息

Department of Clinical Neurosciences, University of Newcastle upon Tyne, UK.

出版信息

Brain Res. 1994 Aug 29;655(1-2):186-94. doi: 10.1016/0006-8993(94)91613-6.

Abstract

The distribution and density of non-NMDA receptors in spinal cord and motor cortex was compared in 10 cases of motor neuron disease (MND) and 8 neurologically normal controls by quantitative autoradiography using [3H]CNQX and [3H]kainate. In the motor cortex of MND cases, an increased density of [3H]kainate binding sites was observed which was most marked in the deep layers. No significant differences were observed in [3H]CNQX binding in the motor cortex between MND and control cases. In the spinal cord significantly increased densities of both [3H]CNQX and [3]kainate binding sites were found in the substantia gelatinosa and the intermediate grey matter in the MND group. The changes in [3H]kainate binding were observed only in the amyotrophic lateral sclerosis (ALS) subgroup of MND, while the changes in [3H]CNQX binding in the spinal cord were more marked in ALS compared to progressive muscular atrophy (PMA) cases. These findings provide evidence in support of a disturbance of glutamatergic neurotransmission in MND and suggest that there may be an increased excitatory drive to motor neurons via non-NMDA receptors. It is unclear at present whether the changes observed represent a compensatory response to loss of motor neurons in MND or a pathophysiological phenomenon contributing to motor neuron degeneration. Modulation of non-NMDA receptor activity may represent a possible target for therapeutic intervention in this disease.

摘要

通过使用[3H]CNQX和[3H]海人酸的定量放射自显影术,比较了10例运动神经元病(MND)患者和8例神经功能正常对照者脊髓和运动皮层中非NMDA受体的分布和密度。在MND患者的运动皮层中,观察到[3H]海人酸结合位点密度增加,在深层最为明显。MND患者和对照者的运动皮层中[3H]CNQX结合未观察到显著差异。在MND组中,脊髓的胶状质和中间灰质中[3H]CNQX和[3H]海人酸结合位点的密度均显著增加。[3H]海人酸结合的变化仅在MND的肌萎缩侧索硬化(ALS)亚组中观察到,而与进行性肌肉萎缩(PMA)病例相比,脊髓中[3H]CNQX结合的变化在ALS中更为明显。这些发现为MND中谷氨酸能神经传递紊乱提供了证据,并表明可能通过非NMDA受体增加了对运动神经元的兴奋性驱动。目前尚不清楚观察到的变化是代表对MND中运动神经元丧失的代偿反应,还是导致运动神经元变性的病理生理现象。调节非NMDA受体活性可能是该疾病治疗干预的一个可能靶点。

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