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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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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author Yoshimura Megumu
Ko Shanelle W
Xu Hui
Wu Long-Jun
Zhuo Min
author_facet Yoshimura Megumu
Ko Shanelle W
Xu Hui
Wu Long-Jun
Zhuo Min
author_sort Yoshimura Megumu
collection DOAJ
description <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>
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spelling doaj.art-201f97976ba0464a84b722e3501fce9e2022-12-22T01:39:01ZengSAGE PublishingMolecular Pain1744-80692005-11-01113410.1186/1744-8069-1-34Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance PYoshimura MegumuKo Shanelle WXu HuiWu Long-JunZhuo Min<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>http://www.molecularpain.com/content/1/1/34
spellingShingle Yoshimura Megumu
Ko Shanelle W
Xu Hui
Wu Long-Jun
Zhuo Min
Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P
Molecular Pain
title Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P
title_full Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P
title_fullStr Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P
title_full_unstemmed Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P
title_short Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P
title_sort feed forward inhibition a novel cellular mechanism for the analgesic effect of substance p
url http://www.molecularpain.com/content/1/1/34
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AT xuhui feedforwardinhibitionanovelcellularmechanismfortheanalgesiceffectofsubstancep
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AT zhuomin feedforwardinhibitionanovelcellularmechanismfortheanalgesiceffectofsubstancep