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Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain

The N‐methyl‐D‐aspartate receptor (NMDAR) is an important mediator of central sensitization and nociception in the rat spinal dorsal horn. The NMDAR subunits and splice variants determine the properties of the receptor. Understanding the expression of NMDAR subunits in spinal cord during the neonata...

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Autores principales: de Geus, Thomas J., Patijn, Jacob, Joosten, Elbert A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894158/
https://www.ncbi.nlm.nih.gov/pubmed/33131183
http://dx.doi.org/10.1002/dneu.22789
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author de Geus, Thomas J.
Patijn, Jacob
Joosten, Elbert A. J.
author_facet de Geus, Thomas J.
Patijn, Jacob
Joosten, Elbert A. J.
author_sort de Geus, Thomas J.
collection PubMed
description The N‐methyl‐D‐aspartate receptor (NMDAR) is an important mediator of central sensitization and nociception in the rat spinal dorsal horn. The NMDAR subunits and splice variants determine the properties of the receptor. Understanding the expression of NMDAR subunits in spinal cord during the neonatal development is important as it may have consequences for the process of central sensitization and nociception in later life. In this review, a systematic literature search was conducted using three databases: Medline, Embase, and PubMed. A quality assessment was performed on predetermined entities of bias. Thirteen articles were identified to be relevant. The results show that NMDAR subunits and splice variants are dynamically expressed during postnatal development in the spinal dorsal horn. During the first 2 weeks, the expression of less excitable GluN2A subunit and more sensitive GluN2B subunit increases while the expression of high excitable GluN2C subunit decreases. During the 2nd week of postnatal development GluN1 subunits with exon 21 spliced in but exon 22 spliced out are predominantly expressed, increasing phosphorylation, and transport to the membrane. The data suggest that in rats, the nociceptive system is most susceptible to central sensitization processes during the first two postnatal weeks. This may have important consequences for nociception and pain responses in later life. From this, we conclude that targeted therapy directed toward specific NMDAR subunits is a promising candidate for mechanism‐based treatment of pain in neonates.
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spelling pubmed-78941582021-03-02 Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain de Geus, Thomas J. Patijn, Jacob Joosten, Elbert A. J. Dev Neurobiol Review Article The N‐methyl‐D‐aspartate receptor (NMDAR) is an important mediator of central sensitization and nociception in the rat spinal dorsal horn. The NMDAR subunits and splice variants determine the properties of the receptor. Understanding the expression of NMDAR subunits in spinal cord during the neonatal development is important as it may have consequences for the process of central sensitization and nociception in later life. In this review, a systematic literature search was conducted using three databases: Medline, Embase, and PubMed. A quality assessment was performed on predetermined entities of bias. Thirteen articles were identified to be relevant. The results show that NMDAR subunits and splice variants are dynamically expressed during postnatal development in the spinal dorsal horn. During the first 2 weeks, the expression of less excitable GluN2A subunit and more sensitive GluN2B subunit increases while the expression of high excitable GluN2C subunit decreases. During the 2nd week of postnatal development GluN1 subunits with exon 21 spliced in but exon 22 spliced out are predominantly expressed, increasing phosphorylation, and transport to the membrane. The data suggest that in rats, the nociceptive system is most susceptible to central sensitization processes during the first two postnatal weeks. This may have important consequences for nociception and pain responses in later life. From this, we conclude that targeted therapy directed toward specific NMDAR subunits is a promising candidate for mechanism‐based treatment of pain in neonates. John Wiley and Sons Inc. 2020-11-20 2020 /pmc/articles/PMC7894158/ /pubmed/33131183 http://dx.doi.org/10.1002/dneu.22789 Text en © 2020 The Authors. Developmental Neurobiology published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
de Geus, Thomas J.
Patijn, Jacob
Joosten, Elbert A. J.
Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain
title Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain
title_full Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain
title_fullStr Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain
title_full_unstemmed Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain
title_short Qualitative review on N‐methyl‐D‐aspartate receptor expression in rat spinal cord during the postnatal development: Implications for central sensitization and pain
title_sort qualitative review on n‐methyl‐d‐aspartate receptor expression in rat spinal cord during the postnatal development: implications for central sensitization and pain
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894158/
https://www.ncbi.nlm.nih.gov/pubmed/33131183
http://dx.doi.org/10.1002/dneu.22789
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