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外周和中枢神经系统疾病中疼痛通路的神经生理学研究。

Neurophysiological studies of pain pathways in peripheral and central nervous system disorders.

作者信息

Treede Rolf-Detlef

机构信息

Institute of Physiology and Pathophysiology, Johannes Gutenberg-University, Saarstr. 21, 55099 Mainz, Germany.

出版信息

J Neurol. 2003 Oct;250(10):1152-61. doi: 10.1007/s00415-003-0237-7.

Abstract

Standard clinical neurophysiological assessment of somatosensory pathways by sensory evoked potentials (SEPs) is limited to the tactile and proprioceptive systems consisting of large fibers in the peripheral nerve, the dorsal columns of the spinal cord and the medial lemniscus in the brainstem. This limitation means that about half of the lesions in the somatosensory system will not be detectable. In recent years, many clinical studies have confirmed that laser evoked potentials (LEPs) allow the assessment of the other half of the somatosensory system. Rapid heating of the skin by infrared laser pulses specifically activates the nociceptive and thermoreceptive pathways consisting of small fibers in the peripheral nerve and the anterolateral spinothalamic tract in the spinal cord and brainstem. Owing to the large degree of convergence of the somatosensory pathways on to common thalamic nuclei, the differential use of LEP vs. SEP is less evident for thalamocortical lesions. In contrast to standard SEPs, the LEP technique can be applied to non-glabrous skin in any dermatome. This review summarizes the principles of clinical neurophysiological studies of pain pathways and the findings obtained in patients with peripheral and central nervous system disorders. These data provide a rational basis for developing clinical indications for LEP testing.

摘要

通过感觉诱发电位(SEP)对躯体感觉通路进行的标准临床神经生理学评估,仅限于由外周神经中的大纤维、脊髓背柱和脑干内侧丘系组成的触觉和本体感觉系统。这种局限性意味着躯体感觉系统中约一半的病变将无法被检测到。近年来,许多临床研究证实,激光诱发电位(LEP)能够评估躯体感觉系统的另一半。红外激光脉冲对皮肤的快速加热会特异性激活由外周神经中的小纤维以及脊髓和脑干中的脊髓丘脑前束组成的伤害性感受和温度感受通路。由于躯体感觉通路在共同丘脑核上有很大程度的汇聚,对于丘脑皮质病变,LEP与SEP的差异使用不太明显。与标准SEP不同,LEP技术可应用于任何皮节的非光滑皮肤。本综述总结了疼痛通路临床神经生理学研究的原理以及在周围和中枢神经系统疾病患者中获得的研究结果。这些数据为制定LEP检测的临床适应症提供了合理依据。

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