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Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats
Serotonin (5-hydroxytryptamine; 5-HT) plays an important role in control of locomotion, partly through direct effects on motoneurons. Spinal cord complete transection (SCI) results in changes in 5-HT receptors on motoneurons that influence functional recovery. Activation of 5-HT(2A) and 5-HT(7) rece...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083740/ https://www.ncbi.nlm.nih.gov/pubmed/30147717 http://dx.doi.org/10.1155/2018/4232706 |
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author | Miazga, Krzysztof Fabczak, Hanna Joachimiak, Ewa Zawadzka, Małgorzata Krzemień-Ojak, Łucja Bekisz, Marek Bejrowska, Anna Jordan, Larry M. Sławińska, Urszula |
author_facet | Miazga, Krzysztof Fabczak, Hanna Joachimiak, Ewa Zawadzka, Małgorzata Krzemień-Ojak, Łucja Bekisz, Marek Bejrowska, Anna Jordan, Larry M. Sławińska, Urszula |
author_sort | Miazga, Krzysztof |
collection | PubMed |
description | Serotonin (5-hydroxytryptamine; 5-HT) plays an important role in control of locomotion, partly through direct effects on motoneurons. Spinal cord complete transection (SCI) results in changes in 5-HT receptors on motoneurons that influence functional recovery. Activation of 5-HT(2A) and 5-HT(7) receptors improves locomotor hindlimb movements in paraplegic rats. Here, we analyzed the mRNA of 5-HT(2A) and 5-HT(7) receptors (encoded by Htr2a and Htr7 genes, resp.) in motoneurons innervating tibialis anterior (TA) and gastrocnemius lateralis (GM) hindlimb muscles and the tail extensor caudae medialis (ECM) muscle in intact as well as spinal rats. Moreover, the effect of intraspinal grafting of serotonergic neurons on Htr2a and Htr7 gene expression was examined to test the possibility that the graft origin 5-HT innervation in the spinal cord of paraplegic rats could reverse changes in gene expression induced by SCI. Our results indicate that SCI at the thoracic level leads to changes in Htr2a and Htr7 gene expression, whereas transplantation of embryonic serotonergic neurons modifies these changes in motoneurons innervating hindlimb muscles but not those innervating tail muscles. This suggests that the upregulation of genes critical for locomotor recovery, resulting in limb motoneuron plasticity, might account for the improved locomotion in grafted animals. |
format | Online Article Text |
id | pubmed-6083740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60837402018-08-26 Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats Miazga, Krzysztof Fabczak, Hanna Joachimiak, Ewa Zawadzka, Małgorzata Krzemień-Ojak, Łucja Bekisz, Marek Bejrowska, Anna Jordan, Larry M. Sławińska, Urszula Neural Plast Research Article Serotonin (5-hydroxytryptamine; 5-HT) plays an important role in control of locomotion, partly through direct effects on motoneurons. Spinal cord complete transection (SCI) results in changes in 5-HT receptors on motoneurons that influence functional recovery. Activation of 5-HT(2A) and 5-HT(7) receptors improves locomotor hindlimb movements in paraplegic rats. Here, we analyzed the mRNA of 5-HT(2A) and 5-HT(7) receptors (encoded by Htr2a and Htr7 genes, resp.) in motoneurons innervating tibialis anterior (TA) and gastrocnemius lateralis (GM) hindlimb muscles and the tail extensor caudae medialis (ECM) muscle in intact as well as spinal rats. Moreover, the effect of intraspinal grafting of serotonergic neurons on Htr2a and Htr7 gene expression was examined to test the possibility that the graft origin 5-HT innervation in the spinal cord of paraplegic rats could reverse changes in gene expression induced by SCI. Our results indicate that SCI at the thoracic level leads to changes in Htr2a and Htr7 gene expression, whereas transplantation of embryonic serotonergic neurons modifies these changes in motoneurons innervating hindlimb muscles but not those innervating tail muscles. This suggests that the upregulation of genes critical for locomotor recovery, resulting in limb motoneuron plasticity, might account for the improved locomotion in grafted animals. Hindawi 2018-07-25 /pmc/articles/PMC6083740/ /pubmed/30147717 http://dx.doi.org/10.1155/2018/4232706 Text en Copyright © 2018 Krzysztof Miazga et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Miazga, Krzysztof Fabczak, Hanna Joachimiak, Ewa Zawadzka, Małgorzata Krzemień-Ojak, Łucja Bekisz, Marek Bejrowska, Anna Jordan, Larry M. Sławińska, Urszula Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats |
title | Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats |
title_full | Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats |
title_fullStr | Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats |
title_full_unstemmed | Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats |
title_short | Intraspinal Grafting of Serotonergic Neurons Modifies Expression of Genes Important for Functional Recovery in Paraplegic Rats |
title_sort | intraspinal grafting of serotonergic neurons modifies expression of genes important for functional recovery in paraplegic rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083740/ https://www.ncbi.nlm.nih.gov/pubmed/30147717 http://dx.doi.org/10.1155/2018/4232706 |
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