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Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration
BACKGROUND: Antagonists of N-type voltage-gated calcium channels (VGCC), Ca(v)2.2, can manage severe chronic pain with intrathecal use and may be effective systemically. A series of novel ω-conotoxins that selectively inhibit N-type VGCCs was isolated from Conus catus. In the present study, the pote...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853768/ https://www.ncbi.nlm.nih.gov/pubmed/24139484 http://dx.doi.org/10.1186/1744-8069-9-51 |
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author | Sadeghi, Mahsa Murali, Swetha S Lewis, Richard J Alewood, Paul F Mohammadi, Sarasa Christie, MacDonald J |
author_facet | Sadeghi, Mahsa Murali, Swetha S Lewis, Richard J Alewood, Paul F Mohammadi, Sarasa Christie, MacDonald J |
author_sort | Sadeghi, Mahsa |
collection | PubMed |
description | BACKGROUND: Antagonists of N-type voltage-gated calcium channels (VGCC), Ca(v)2.2, can manage severe chronic pain with intrathecal use and may be effective systemically. A series of novel ω-conotoxins that selectively inhibit N-type VGCCs was isolated from Conus catus. In the present study, the potency and reversibility of ω-conotoxins CVID, CVIE and CVIF to inhibit N-type calcium currents were investigated in mouse isolated dorsal root ganglion (DRG) neurons. The systemic potency of each ω-conotoxin to reverse signs of mouse chronic inflammatory pain was also compared. RESULTS: In DRG neurons, the rank order of potency to inhibit N-type calcium currents was CVIE > CVIF > CVID. After subcutaneous administration, CVID and CVIE, but not CVIF, partially reversed impaired weight bearing in mice injected with Freund’s complete adjuvant (CFA) three days prior to testing. No side-effects associated with systemic administration of ω-conotoxins were observed. CONCLUSIONS: The present study indicates a potential for CVID and CVIE to be developed as systemically active analgesics with no accompanying neurological side-effects. |
format | Online Article Text |
id | pubmed-3853768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38537682013-12-07 Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration Sadeghi, Mahsa Murali, Swetha S Lewis, Richard J Alewood, Paul F Mohammadi, Sarasa Christie, MacDonald J Mol Pain Research BACKGROUND: Antagonists of N-type voltage-gated calcium channels (VGCC), Ca(v)2.2, can manage severe chronic pain with intrathecal use and may be effective systemically. A series of novel ω-conotoxins that selectively inhibit N-type VGCCs was isolated from Conus catus. In the present study, the potency and reversibility of ω-conotoxins CVID, CVIE and CVIF to inhibit N-type calcium currents were investigated in mouse isolated dorsal root ganglion (DRG) neurons. The systemic potency of each ω-conotoxin to reverse signs of mouse chronic inflammatory pain was also compared. RESULTS: In DRG neurons, the rank order of potency to inhibit N-type calcium currents was CVIE > CVIF > CVID. After subcutaneous administration, CVID and CVIE, but not CVIF, partially reversed impaired weight bearing in mice injected with Freund’s complete adjuvant (CFA) three days prior to testing. No side-effects associated with systemic administration of ω-conotoxins were observed. CONCLUSIONS: The present study indicates a potential for CVID and CVIE to be developed as systemically active analgesics with no accompanying neurological side-effects. BioMed Central 2013-10-20 /pmc/articles/PMC3853768/ /pubmed/24139484 http://dx.doi.org/10.1186/1744-8069-9-51 Text en Copyright © 2013 Sadeghi 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 Sadeghi, Mahsa Murali, Swetha S Lewis, Richard J Alewood, Paul F Mohammadi, Sarasa Christie, MacDonald J Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration |
title | Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration |
title_full | Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration |
title_fullStr | Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration |
title_full_unstemmed | Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration |
title_short | Novel ω-conotoxins from C. catus reverse signs of mouse inflammatory pain after systemic administration |
title_sort | novel ω-conotoxins from c. catus reverse signs of mouse inflammatory pain after systemic administration |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853768/ https://www.ncbi.nlm.nih.gov/pubmed/24139484 http://dx.doi.org/10.1186/1744-8069-9-51 |
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