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Cortical Representation of Pain and Touch:Evidence from Combined Functional Neuroimaging and Electrophysiology in Non-human Primates

Cortical Representation of Pain and Touch:Evidence from Combined Functional Neuroimaging and Electrophysiology in Non-human Primates

作     者:Li Min Chen 

作者机构:Departments of Radiology and Radiological Sciences and Psychology Institute of Imaging Science Vanderbilt University Medical Center 

出 版 物:《Neuroscience Bulletin》 (神经科学通报(英文版))

年 卷 期:2018年第34卷第1期

页      面:165-177页

核心收录:

学科分类:0710[理学-生物学] 1006[医学-中西医结合] 1002[医学-临床医学] 1001[医学-基础医学(可授医学、理学学位)] 10[医学] 100602[医学-中西医结合临床] 

基  金:supported by NIH Grant R01 NS069909 an imaging track Grant from the Dana Foundation 

主  题:Nociception Non-human primate Cortex Functional MRI Functional connectivity 

摘      要:Human functional MRI studies in acute and various chronic pain conditions have revolutionized how we view pain, and have led to a new theory that complex multi-dimensional pain experience (sensory-discriminative, affective/motivational, and cognitive) is represented by concurrent activity in widely-distributed brain regions (termed a network or pain matrix). Despite these break- through discoveries, the specific functions proposed for these regions remain elusive, because detailed electrophys- iological characterizations of these regions in the primate brain are lacking. To fill in this knowledge gap, we have studied the cortical areas around the central and lateral sulci of the non-human primate brain with combined submillimeter resolution functional imaging (optical imaging and fMRI) and intracranial electrophysiological recording. In this mini-review, I summarize and present data showing that the cortical circuitry engaged in nociceptive processing is much more complex than previously recognized. Electrophysiological evidence supports the engage- ment of a distinct nociceptive-processing network within SI (i.e., areas 3a, 3b, 1 and 2), SII, and other areas along the lateral sulcus. Deafferentation caused by spinal cord injury profoundly alters the relationships between fMRI and electrophysiological signals. This finding has significant implications for using fMRI to study chronic pain conditions involving deafferentation in humans.

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