• J Pain · Apr 2019

    Review

    CONTRIBUTIONS OF NOCIRESPONSIVE AREA 3A TO NORMAL AND ABNORMAL SOMATOSENSORY PERCEPTION.

    • Barry L Whitsel, Charles J Vierck, Robert S Waters, Mark Tommerdahl, and Oleg V Favorov.
    • Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina.
    • J Pain. 2019 Apr 1; 20 (4): 405419405-419.

    AbstractTraditionally, cytoarchitectonic area 3a of primary somatosensory cortex (SI) has been regarded as a proprioceptive relay to motor cortex. However, neuronal spike-train recordings and optical intrinsic signal imaging, obtained from nonhuman sensorimotor cortex, show that neuronal activity in some of the cortical columns in area 3a can be readily triggered by a C-nociceptor afferent drive. These findings indicate that area 3a is a critical link in cerebral cortical encoding of secondary/slow pain. Also, area 3a contributes to abnormal pain processing in the presence of activity-dependent reversal of gamma-aminobutyric acid A receptor-mediated inhibition. Accordingly, abnormal processing within area 3a may contribute mechanistically to generation of clinical pain conditions. PERSPECTIVE: Optical imaging and neurophysiological mapping of area 3a of SI has revealed substantial driving from unmyelinated cutaneous nociceptors, complementing input to areas 3b and 1 of SI from myelinated nociceptors and non-nociceptors. These and related findings force a reconsideration of mechanisms for SI processing of pain.Copyright © 2019. Published by Elsevier Inc.

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