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Hyperalgesic activity of kisspeptin in mice

BACKGROUND: Kisspeptin is a neuropeptide known for its role in the hypothalamic regulation of the reproductive axis. Following the recent description of kisspeptin and its 7-TM receptor, GPR54, in the dorsal root ganglia and dorsal horns of the spinal cord, we examined the role of kisspeptin in the...

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Autores principales: Spampinato, Simona, Trabucco, Angela, Biasiotta, Antonella, Biagioni, Francesca, Cruccu, Giorgio, Copani, Agata, Colledge, William H, Sortino, Maria Angela, Nicoletti, Ferdinando, Chiechio, Santina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284433/
https://www.ncbi.nlm.nih.gov/pubmed/22112588
http://dx.doi.org/10.1186/1744-8069-7-90
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author Spampinato, Simona
Trabucco, Angela
Biasiotta, Antonella
Biagioni, Francesca
Cruccu, Giorgio
Copani, Agata
Colledge, William H
Sortino, Maria Angela
Nicoletti, Ferdinando
Chiechio, Santina
author_facet Spampinato, Simona
Trabucco, Angela
Biasiotta, Antonella
Biagioni, Francesca
Cruccu, Giorgio
Copani, Agata
Colledge, William H
Sortino, Maria Angela
Nicoletti, Ferdinando
Chiechio, Santina
author_sort Spampinato, Simona
collection PubMed
description BACKGROUND: Kisspeptin is a neuropeptide known for its role in the hypothalamic regulation of the reproductive axis. Following the recent description of kisspeptin and its 7-TM receptor, GPR54, in the dorsal root ganglia and dorsal horns of the spinal cord, we examined the role of kisspeptin in the regulation of pain sensitivity in mice. RESULTS: Immunofluorescent staining in the mouse skin showed the presence of GPR54 receptors in PGP9.5-positive sensory fibers. Intraplantar injection of kisspeptin (1 or 3 nmol/5 μl) induced a small nocifensive response in naive mice, and lowered thermal pain threshold in the hot plate test. Both intraplantar and intrathecal (0.5 or 1 nmol/3 μl) injection of kisspeptin caused hyperalgesia in the first and second phases of the formalin test, whereas the GPR54 antagonist, p234 (0.1 or 1 nmol), caused a robust analgesia. Intraplantar injection of kisspeptin combined with formalin enhanced TRPV1 phosphorylation at Ser800 at the injection site, and increased ERK1/2 phosphorylation in the ipsilateral dorsal horn as compared to naive mice and mice treated with formalin alone. CONCLUSION: These data demonstrate for the first time that kisspeptin regulates pain sensitivity in rodents and suggest that peripheral GPR54 receptors could be targeted by novel drugs in the treatment of inflammatory pain.
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spelling pubmed-32844332012-02-25 Hyperalgesic activity of kisspeptin in mice Spampinato, Simona Trabucco, Angela Biasiotta, Antonella Biagioni, Francesca Cruccu, Giorgio Copani, Agata Colledge, William H Sortino, Maria Angela Nicoletti, Ferdinando Chiechio, Santina Mol Pain Research BACKGROUND: Kisspeptin is a neuropeptide known for its role in the hypothalamic regulation of the reproductive axis. Following the recent description of kisspeptin and its 7-TM receptor, GPR54, in the dorsal root ganglia and dorsal horns of the spinal cord, we examined the role of kisspeptin in the regulation of pain sensitivity in mice. RESULTS: Immunofluorescent staining in the mouse skin showed the presence of GPR54 receptors in PGP9.5-positive sensory fibers. Intraplantar injection of kisspeptin (1 or 3 nmol/5 μl) induced a small nocifensive response in naive mice, and lowered thermal pain threshold in the hot plate test. Both intraplantar and intrathecal (0.5 or 1 nmol/3 μl) injection of kisspeptin caused hyperalgesia in the first and second phases of the formalin test, whereas the GPR54 antagonist, p234 (0.1 or 1 nmol), caused a robust analgesia. Intraplantar injection of kisspeptin combined with formalin enhanced TRPV1 phosphorylation at Ser800 at the injection site, and increased ERK1/2 phosphorylation in the ipsilateral dorsal horn as compared to naive mice and mice treated with formalin alone. CONCLUSION: These data demonstrate for the first time that kisspeptin regulates pain sensitivity in rodents and suggest that peripheral GPR54 receptors could be targeted by novel drugs in the treatment of inflammatory pain. BioMed Central 2011-11-23 /pmc/articles/PMC3284433/ /pubmed/22112588 http://dx.doi.org/10.1186/1744-8069-7-90 Text en Copyright ©2011 Spampinato et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Spampinato, Simona
Trabucco, Angela
Biasiotta, Antonella
Biagioni, Francesca
Cruccu, Giorgio
Copani, Agata
Colledge, William H
Sortino, Maria Angela
Nicoletti, Ferdinando
Chiechio, Santina
Hyperalgesic activity of kisspeptin in mice
title Hyperalgesic activity of kisspeptin in mice
title_full Hyperalgesic activity of kisspeptin in mice
title_fullStr Hyperalgesic activity of kisspeptin in mice
title_full_unstemmed Hyperalgesic activity of kisspeptin in mice
title_short Hyperalgesic activity of kisspeptin in mice
title_sort hyperalgesic activity of kisspeptin in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284433/
https://www.ncbi.nlm.nih.gov/pubmed/22112588
http://dx.doi.org/10.1186/1744-8069-7-90
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