Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P

<p>Abstract</p> <p>Substance P (SP) is a neuropeptide well known for its contribution to pain transmission in the spinal cord, however, less is known about the possible modulatory effects of SP. A new study by Gu and colleagues, published in <it>Molecular Pain </it>(200...

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Bibliographic Details
Main Authors: Yoshimura Megumu, Ko Shanelle W, Xu Hui, Wu Long-Jun, Zhuo Min
Format: Article
Language:English
Published: SAGE Publishing 2005-11-01
Series:Molecular Pain
Online Access:http://www.molecularpain.com/content/1/1/34
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Summary:<p>Abstract</p> <p>Substance P (SP) is a neuropeptide well known for its contribution to pain transmission in the spinal cord, however, less is known about the possible modulatory effects of SP. A new study by Gu and colleagues, published in <it>Molecular Pain </it>(2005, 1:20), describes its potential role in feed-forward inhibition in lamina V of the dorsal horn of the spinal cord. This inhibition seems to function through a direct excitation of GABAergic interneurons by substance P released from primary afferent fibers and has a distinct temporal phase of action from the well-described glutamate-dependent feed-forward inhibition. It is believed that through this inhibition, substance P can balance nociceptive output from the spinal cord.</p>
ISSN:1744-8069