Morphine modulation of pain processing in medial and lateral pain pathways

<p>Abstract</p> <p>Background</p> <p>Despite the wide-spread use of morphine and related opioid agonists in clinic and their powerful analgesic effects, our understanding of the neural mechanisms underlying opioid analgesia at supraspinal levels is quite limited. The pr...

Full description

Bibliographic Details
Main Authors: Woodward Donald J, Chang Jing-Yu, Huang Jin, Wang Jin-Yan, Luo Fei
Format: Article
Language:English
Published: SAGE Publishing 2009-10-01
Series:Molecular Pain
Online Access:http://www.molecularpain.com/content/5/1/60
id doaj-78f5635cad4a44d792f7ba2a1d7b6e80
record_format Article
spelling doaj-78f5635cad4a44d792f7ba2a1d7b6e802020-11-25T03:34:10ZengSAGE PublishingMolecular Pain1744-80692009-10-01516010.1186/1744-8069-5-60Morphine modulation of pain processing in medial and lateral pain pathwaysWoodward Donald JChang Jing-YuHuang JinWang Jin-YanLuo Fei<p>Abstract</p> <p>Background</p> <p>Despite the wide-spread use of morphine and related opioid agonists in clinic and their powerful analgesic effects, our understanding of the neural mechanisms underlying opioid analgesia at supraspinal levels is quite limited. The present study was designed to investigate the modulative effect of morphine on nociceptive processing in the medial and lateral pain pathways using a multiple single-unit recording technique. Pain evoked neuronal activities were simultaneously recorded from the primary somatosensory cortex (SI), ventral posterolateral thalamus (VPL), anterior cingulate cortex (ACC), and medial dorsal thalamus (MD) with eight-wire microelectrode arrays in awake rats.</p> <p>Results</p> <p>The results showed that the noxious heat evoked responses of single neurons in all of the four areas were depressed after systemic injection of 5 mg/kg morphine. The depressive effects of morphine included (i) decreasing the neuronal response magnitude; (ii) reducing the fraction of responding neurons, and (iii) shortening the response duration. In addition, the capability of cortical and thalamic neural ensembles to discriminate noxious from innocuous stimuli was decreased by morphine within both pain pathways. Meanwhile, morphine suppressed the pain-evoked changes in the information flow from medial to lateral pathway and from cortex to thalamus. These effects were completely blocked by pre-treatment with the opiate receptor antagonist naloxone.</p> <p>Conclusion</p> <p>These results suggest that morphine exerts analgesic effects through suppressing both sensory and affective dimensions of pain.</p> http://www.molecularpain.com/content/5/1/60
collection DOAJ
language English
format Article
sources DOAJ
author Woodward Donald J
Chang Jing-Yu
Huang Jin
Wang Jin-Yan
Luo Fei
spellingShingle Woodward Donald J
Chang Jing-Yu
Huang Jin
Wang Jin-Yan
Luo Fei
Morphine modulation of pain processing in medial and lateral pain pathways
Molecular Pain
author_facet Woodward Donald J
Chang Jing-Yu
Huang Jin
Wang Jin-Yan
Luo Fei
author_sort Woodward Donald J
title Morphine modulation of pain processing in medial and lateral pain pathways
title_short Morphine modulation of pain processing in medial and lateral pain pathways
title_full Morphine modulation of pain processing in medial and lateral pain pathways
title_fullStr Morphine modulation of pain processing in medial and lateral pain pathways
title_full_unstemmed Morphine modulation of pain processing in medial and lateral pain pathways
title_sort morphine modulation of pain processing in medial and lateral pain pathways
publisher SAGE Publishing
series Molecular Pain
issn 1744-8069
publishDate 2009-10-01
description <p>Abstract</p> <p>Background</p> <p>Despite the wide-spread use of morphine and related opioid agonists in clinic and their powerful analgesic effects, our understanding of the neural mechanisms underlying opioid analgesia at supraspinal levels is quite limited. The present study was designed to investigate the modulative effect of morphine on nociceptive processing in the medial and lateral pain pathways using a multiple single-unit recording technique. Pain evoked neuronal activities were simultaneously recorded from the primary somatosensory cortex (SI), ventral posterolateral thalamus (VPL), anterior cingulate cortex (ACC), and medial dorsal thalamus (MD) with eight-wire microelectrode arrays in awake rats.</p> <p>Results</p> <p>The results showed that the noxious heat evoked responses of single neurons in all of the four areas were depressed after systemic injection of 5 mg/kg morphine. The depressive effects of morphine included (i) decreasing the neuronal response magnitude; (ii) reducing the fraction of responding neurons, and (iii) shortening the response duration. In addition, the capability of cortical and thalamic neural ensembles to discriminate noxious from innocuous stimuli was decreased by morphine within both pain pathways. Meanwhile, morphine suppressed the pain-evoked changes in the information flow from medial to lateral pathway and from cortex to thalamus. These effects were completely blocked by pre-treatment with the opiate receptor antagonist naloxone.</p> <p>Conclusion</p> <p>These results suggest that morphine exerts analgesic effects through suppressing both sensory and affective dimensions of pain.</p>
url http://www.molecularpain.com/content/5/1/60
work_keys_str_mv AT woodwarddonaldj morphinemodulationofpainprocessinginmedialandlateralpainpathways
AT changjingyu morphinemodulationofpainprocessinginmedialandlateralpainpathways
AT huangjin morphinemodulationofpainprocessinginmedialandlateralpainpathways
AT wangjinyan morphinemodulationofpainprocessinginmedialandlateralpainpathways
AT luofei morphinemodulationofpainprocessinginmedialandlateralpainpathways
_version_ 1724560237372899328