Identification of Spinal Circuits Transmitting and Gating Mechanical Pain
Author(s) -
Bo Duan,
Longzhen Cheng,
Steeve Bourane,
Olivier Britz,
Christopher Padilla,
Lidia GarcíaCampmany,
Michael J. Krashes,
Wendy Knowlton,
Tomoko Velasquez,
Xiangyu Ren,
Sarah E. Ross,
Bradford B. Lowell,
Yun Wang,
Martyn Goulding,
Qiufu Ma
Publication year - 2014
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.11.003
Subject(s) - inhibitory postsynaptic potential , excitatory postsynaptic potential , nociceptor , neuroscience , nociception , spinal cord , biology , dynorphin , electrophysiology , opioid peptide , opioid , receptor , biochemistry
Pain information processing in the spinal cord has been postulated to rely on nociceptive transmission (T) neurons receiving inputs from nociceptors and Aβ mechanoreceptors, with Aβ inputs gated through feed-forward activation of spinal inhibitory neurons (INs). Here, we used intersectional genetic manipulations to identify these critical components of pain transduction. Marking and ablating six populations of spinal excitatory and inhibitory neurons, coupled with behavioral and electrophysiological analysis, showed that excitatory neurons expressing somatostatin (SOM) include T-type cells, whose ablation causes loss of mechanical pain. Inhibitory neurons marked by the expression of dynorphin (Dyn) represent INs, which are necessary to gate Aβ fibers from activating SOM(+) neurons to evoke pain. Therefore, peripheral mechanical nociceptors and Aβ mechanoreceptors, together with spinal SOM(+) excitatory and Dyn(+) inhibitory neurons, form a microcircuit that transmits and gates mechanical pain. PAPERCLIP:
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