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Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)

The present study investigated the cholinergic system in the African naked mole-rat (Heterocephalus glaber) with focus on the muscarinic acetylcholine receptor subtypes M(1) and M(4). The protein sequences for the subtypes m(1–5) of the naked mole-rat were compared to that of the house mouse (Mus mu...

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Autores principales: Jørgensen, Kristine B., Krogh-Jensen, Karen, Pickering, Darryl S., Kanui, Titus I., Abelson, Klas S. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698283/
https://www.ncbi.nlm.nih.gov/pubmed/26520141
http://dx.doi.org/10.1007/s00359-015-1048-x
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author Jørgensen, Kristine B.
Krogh-Jensen, Karen
Pickering, Darryl S.
Kanui, Titus I.
Abelson, Klas S. P.
author_facet Jørgensen, Kristine B.
Krogh-Jensen, Karen
Pickering, Darryl S.
Kanui, Titus I.
Abelson, Klas S. P.
author_sort Jørgensen, Kristine B.
collection PubMed
description The present study investigated the cholinergic system in the African naked mole-rat (Heterocephalus glaber) with focus on the muscarinic acetylcholine receptor subtypes M(1) and M(4). The protein sequences for the subtypes m(1–5) of the naked mole-rat were compared to that of the house mouse (Mus musculus) using basic local alignment search tool (BLAST). The presence and function of M(1) and M(4) was investigated in vivo, using the formalin test with the muscarinic receptor agonists xanomeline and VU0152100. Spinal cord tissue from the naked mole-rat was used for receptor saturation binding studies with [(3)H]-N-methylscopolamine. The BLAST test revealed 95 % protein sequence homology showing the naked mole-rat to have the genetic potential to express all five muscarinic acetylcholine receptor subtypes. A significant reduction in pain behavior was demonstrated after administration of 8.4 mg/kg in the formalin test. Administration of 50 mg/kg VU0152100 resulted in a non-significant tendency towards antinociception. The antinociceptive effects were reversed by the muscarinic acetylcholine receptor antagonist atropine. Binding studies indicated presence of muscarinic acetylcholine receptors with a radioligand affinity comparable to that reported in mice. In conclusion, muscarinic acetylcholine receptor subtypes are present in the naked mole-rat and contribute to antinociception in the naked mole-rat.
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spelling pubmed-46982832016-01-08 Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber) Jørgensen, Kristine B. Krogh-Jensen, Karen Pickering, Darryl S. Kanui, Titus I. Abelson, Klas S. P. J Comp Physiol A Neuroethol Sens Neural Behav Physiol Original Paper The present study investigated the cholinergic system in the African naked mole-rat (Heterocephalus glaber) with focus on the muscarinic acetylcholine receptor subtypes M(1) and M(4). The protein sequences for the subtypes m(1–5) of the naked mole-rat were compared to that of the house mouse (Mus musculus) using basic local alignment search tool (BLAST). The presence and function of M(1) and M(4) was investigated in vivo, using the formalin test with the muscarinic receptor agonists xanomeline and VU0152100. Spinal cord tissue from the naked mole-rat was used for receptor saturation binding studies with [(3)H]-N-methylscopolamine. The BLAST test revealed 95 % protein sequence homology showing the naked mole-rat to have the genetic potential to express all five muscarinic acetylcholine receptor subtypes. A significant reduction in pain behavior was demonstrated after administration of 8.4 mg/kg in the formalin test. Administration of 50 mg/kg VU0152100 resulted in a non-significant tendency towards antinociception. The antinociceptive effects were reversed by the muscarinic acetylcholine receptor antagonist atropine. Binding studies indicated presence of muscarinic acetylcholine receptors with a radioligand affinity comparable to that reported in mice. In conclusion, muscarinic acetylcholine receptor subtypes are present in the naked mole-rat and contribute to antinociception in the naked mole-rat. Springer Berlin Heidelberg 2015-10-31 2016 /pmc/articles/PMC4698283/ /pubmed/26520141 http://dx.doi.org/10.1007/s00359-015-1048-x Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Jørgensen, Kristine B.
Krogh-Jensen, Karen
Pickering, Darryl S.
Kanui, Titus I.
Abelson, Klas S. P.
Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)
title Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)
title_full Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)
title_fullStr Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)
title_full_unstemmed Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)
title_short Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber)
title_sort investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the african naked mole-rat (heterocephalus glaber)
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698283/
https://www.ncbi.nlm.nih.gov/pubmed/26520141
http://dx.doi.org/10.1007/s00359-015-1048-x
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