Disruption of persistent nociceptive behavior in rats with learning impairment.

Despite the subjective nature of pain experience with cognitive and affective dimensions, preclinical pain research has largely focused on its sensory dimension. Here, we examined the relationship between learning/memory and nociceptive behavior in rats with combined learning impairment and persiste...

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Main Authors: Yuxin Ma, Shuxing Wang, Yinghong Tian, Lucy Chen, Guoying Li, Jianren Mao
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3770575?pdf=render
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spelling doaj-52e3fcc643c24c7fb24ec0b442f87fe02020-11-25T01:55:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7453310.1371/journal.pone.0074533Disruption of persistent nociceptive behavior in rats with learning impairment.Yuxin MaShuxing WangYinghong TianLucy ChenGuoying LiJianren MaoDespite the subjective nature of pain experience with cognitive and affective dimensions, preclinical pain research has largely focused on its sensory dimension. Here, we examined the relationship between learning/memory and nociceptive behavior in rats with combined learning impairment and persistent nociception. Learning impairment was induced by bilateral hippocampal injection of a mixed Aβ solution, whereas persistent nociception produced in these rats by complete Freund's adjuvant-induced ankle inflammation. Those rats with learning impairment showed a diminished development of thermal hyperalgesia and mechanical allodynia and a shorter time course of nociceptive behavior without alteration of their baseline nociceptive threshold. In rats with pre-established hyperalgesia and allodynia due to ankle inflammation, bilateral intra-hippocampal injection of cycloheximide (a protein synthesis inhibitor) promoted the earlier recovery of nociceptive behavior. Moreover, expression of Aβ, NR1 subunit of the N-methyl-D-aspartate receptor, and protein kinase Cγ was upregulated, whereas the choline acetyl transferase expression was downregulated, in the hippocampus, thalamus, amygdala, and/or spinal cord of rats with combined learning impairment and persistent nociception. The data indicate that learning impairment could disrupt the response to a state of persistent nociception, suggesting an important role for cognitive maladaptation in the mechanisms of chronic pain. These results also suggest that a preclinical model of combined learning impairment and persistent nociception may be useful to explore the brain mechanisms underlying the transition from acute to chronic pain.http://europepmc.org/articles/PMC3770575?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yuxin Ma
Shuxing Wang
Yinghong Tian
Lucy Chen
Guoying Li
Jianren Mao
spellingShingle Yuxin Ma
Shuxing Wang
Yinghong Tian
Lucy Chen
Guoying Li
Jianren Mao
Disruption of persistent nociceptive behavior in rats with learning impairment.
PLoS ONE
author_facet Yuxin Ma
Shuxing Wang
Yinghong Tian
Lucy Chen
Guoying Li
Jianren Mao
author_sort Yuxin Ma
title Disruption of persistent nociceptive behavior in rats with learning impairment.
title_short Disruption of persistent nociceptive behavior in rats with learning impairment.
title_full Disruption of persistent nociceptive behavior in rats with learning impairment.
title_fullStr Disruption of persistent nociceptive behavior in rats with learning impairment.
title_full_unstemmed Disruption of persistent nociceptive behavior in rats with learning impairment.
title_sort disruption of persistent nociceptive behavior in rats with learning impairment.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Despite the subjective nature of pain experience with cognitive and affective dimensions, preclinical pain research has largely focused on its sensory dimension. Here, we examined the relationship between learning/memory and nociceptive behavior in rats with combined learning impairment and persistent nociception. Learning impairment was induced by bilateral hippocampal injection of a mixed Aβ solution, whereas persistent nociception produced in these rats by complete Freund's adjuvant-induced ankle inflammation. Those rats with learning impairment showed a diminished development of thermal hyperalgesia and mechanical allodynia and a shorter time course of nociceptive behavior without alteration of their baseline nociceptive threshold. In rats with pre-established hyperalgesia and allodynia due to ankle inflammation, bilateral intra-hippocampal injection of cycloheximide (a protein synthesis inhibitor) promoted the earlier recovery of nociceptive behavior. Moreover, expression of Aβ, NR1 subunit of the N-methyl-D-aspartate receptor, and protein kinase Cγ was upregulated, whereas the choline acetyl transferase expression was downregulated, in the hippocampus, thalamus, amygdala, and/or spinal cord of rats with combined learning impairment and persistent nociception. The data indicate that learning impairment could disrupt the response to a state of persistent nociception, suggesting an important role for cognitive maladaptation in the mechanisms of chronic pain. These results also suggest that a preclinical model of combined learning impairment and persistent nociception may be useful to explore the brain mechanisms underlying the transition from acute to chronic pain.
url http://europepmc.org/articles/PMC3770575?pdf=render
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