Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats

Detalhes bibliográficos
Autor(a) principal: Cristina-Silva, Caroline [UNESP]
Data de Publicação: 2017
Outros Autores: Martins, Victor [UNESP], Gargaglioni, Luciane H. [UNESP], Bicego, Kenia C. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00424-017-1966-2
http://hdl.handle.net/11449/163136
Resumo: The periaqueductal gray matter (PAG) is rich in mu and kappa opioid receptors, and this system is involved in thermoregulation, analgesia, and defensive behaviors. No study approached the involvement of the PAG opioids in body temperature (Tb) regulation during psychological stress such as restraint. Because activation of mu and kappa receptors increases and reduces Tb, respectively, we tested the hypothesis that they exert excitatory and inhibitory modulation, respectively, of the restraint-induced fever in rats. To this end, Tb, heat loss index (HLI, inference for peripheral vasoconstriction/vasodilation), and oxygen consumption (inference for thermogenesis) were monitored in unanesthetized rats, restrained or unrestrained, before and after intra-PAG microinjection of the selective mu opioid receptor antagonist (D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 cyclic, CTAP; 1 and 10 mu g/100 nL) or the selective kappa opioid receptor antagonist (nor-binaltorphimine dihydrochloride, nor-BNI; 1 and 4 mu g/100 nL) or saline (100 nL). CTAP and nor-BNI did not change the Tb or HLI of euthermic animals. During restraint, Tb increased (1.0 +/- 0.1 A degrees C) in all groups; however, this effect was lower in those animals treated with CTAP and higher in animals treated with nor-BNI. The HLI decreased during restraint and increased after animals were released, but this response was not affected by any treatment. Restraint stress increased oxygen consumption (35.9 +/- 3.9% elevation), but this response was diminished by CTAP and overstimulated by nor-BNI. Confirming our hypothesis, the results indicate that the mu and kappa opioid receptors in the PAG of rats play a pyrogenic and antipyretic role, respectively, during fever induced by restraint by affecting the thermogenic but not the heat conservation effector.
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spelling Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in ratsBody temperatureHeat loss indexOxygen consumptionOpioid receptorsNor-BNICTAPThe periaqueductal gray matter (PAG) is rich in mu and kappa opioid receptors, and this system is involved in thermoregulation, analgesia, and defensive behaviors. No study approached the involvement of the PAG opioids in body temperature (Tb) regulation during psychological stress such as restraint. Because activation of mu and kappa receptors increases and reduces Tb, respectively, we tested the hypothesis that they exert excitatory and inhibitory modulation, respectively, of the restraint-induced fever in rats. To this end, Tb, heat loss index (HLI, inference for peripheral vasoconstriction/vasodilation), and oxygen consumption (inference for thermogenesis) were monitored in unanesthetized rats, restrained or unrestrained, before and after intra-PAG microinjection of the selective mu opioid receptor antagonist (D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 cyclic, CTAP; 1 and 10 mu g/100 nL) or the selective kappa opioid receptor antagonist (nor-binaltorphimine dihydrochloride, nor-BNI; 1 and 4 mu g/100 nL) or saline (100 nL). CTAP and nor-BNI did not change the Tb or HLI of euthermic animals. During restraint, Tb increased (1.0 +/- 0.1 A degrees C) in all groups; however, this effect was lower in those animals treated with CTAP and higher in animals treated with nor-BNI. The HLI decreased during restraint and increased after animals were released, but this response was not affected by any treatment. Restraint stress increased oxygen consumption (35.9 +/- 3.9% elevation), but this response was diminished by CTAP and overstimulated by nor-BNI. Confirming our hypothesis, the results indicate that the mu and kappa opioid receptors in the PAG of rats play a pyrogenic and antipyretic role, respectively, during fever induced by restraint by affecting the thermogenic but not the heat conservation effector.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Sao Paulo State Univ, Dept Anim Morphol & Physiol, Coll Agr & Vet Sci, BR-14884900 Jaboticabal, SP, BrazilNatl Inst Sci & Technol Comparat Physiol INCT Fis, Jaboticabal, SP, BrazilUniv Estadual Paulista, Dept Morfol & Fisiol Anim, Fac Ciencias Agr & Vet, Via Acesso Paulo Donato Castellane S-N, BR-14884900 Jaboticabal, SP, BrazilSao Paulo State Univ, Dept Anim Morphol & Physiol, Coll Agr & Vet Sci, BR-14884900 Jaboticabal, SP, BrazilUniv Estadual Paulista, Dept Morfol & Fisiol Anim, Fac Ciencias Agr & Vet, Via Acesso Paulo Donato Castellane S-N, BR-14884900 Jaboticabal, SP, BrazilFAPESP: 2013/02813-9FAPESP: 2015/04849-6SpringerUniversidade Estadual Paulista (Unesp)Natl Inst Sci & Technol Comparat Physiol INCT FisCristina-Silva, Caroline [UNESP]Martins, Victor [UNESP]Gargaglioni, Luciane H. [UNESP]Bicego, Kenia C. [UNESP]2018-11-26T17:40:15Z2018-11-26T17:40:15Z2017-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1151-1161application/pdfhttp://dx.doi.org/10.1007/s00424-017-1966-2Pflugers Archiv-european Journal Of Physiology. New York: Springer, v. 469, n. 9, p. 1151-1161, 2017.0031-6768http://hdl.handle.net/11449/16313610.1007/s00424-017-1966-2WOS:000407627800010WOS000407627800010.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPflugers Archiv-european Journal Of Physiology1,479info:eu-repo/semantics/openAccess2024-06-06T18:42:13Zoai:repositorio.unesp.br:11449/163136Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:16:19.280942Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
title Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
spellingShingle Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
Cristina-Silva, Caroline [UNESP]
Body temperature
Heat loss index
Oxygen consumption
Opioid receptors
Nor-BNI
CTAP
title_short Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
title_full Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
title_fullStr Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
title_full_unstemmed Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
title_sort Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
author Cristina-Silva, Caroline [UNESP]
author_facet Cristina-Silva, Caroline [UNESP]
Martins, Victor [UNESP]
Gargaglioni, Luciane H. [UNESP]
Bicego, Kenia C. [UNESP]
author_role author
author2 Martins, Victor [UNESP]
Gargaglioni, Luciane H. [UNESP]
Bicego, Kenia C. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Natl Inst Sci & Technol Comparat Physiol INCT Fis
dc.contributor.author.fl_str_mv Cristina-Silva, Caroline [UNESP]
Martins, Victor [UNESP]
Gargaglioni, Luciane H. [UNESP]
Bicego, Kenia C. [UNESP]
dc.subject.por.fl_str_mv Body temperature
Heat loss index
Oxygen consumption
Opioid receptors
Nor-BNI
CTAP
topic Body temperature
Heat loss index
Oxygen consumption
Opioid receptors
Nor-BNI
CTAP
description The periaqueductal gray matter (PAG) is rich in mu and kappa opioid receptors, and this system is involved in thermoregulation, analgesia, and defensive behaviors. No study approached the involvement of the PAG opioids in body temperature (Tb) regulation during psychological stress such as restraint. Because activation of mu and kappa receptors increases and reduces Tb, respectively, we tested the hypothesis that they exert excitatory and inhibitory modulation, respectively, of the restraint-induced fever in rats. To this end, Tb, heat loss index (HLI, inference for peripheral vasoconstriction/vasodilation), and oxygen consumption (inference for thermogenesis) were monitored in unanesthetized rats, restrained or unrestrained, before and after intra-PAG microinjection of the selective mu opioid receptor antagonist (D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 cyclic, CTAP; 1 and 10 mu g/100 nL) or the selective kappa opioid receptor antagonist (nor-binaltorphimine dihydrochloride, nor-BNI; 1 and 4 mu g/100 nL) or saline (100 nL). CTAP and nor-BNI did not change the Tb or HLI of euthermic animals. During restraint, Tb increased (1.0 +/- 0.1 A degrees C) in all groups; however, this effect was lower in those animals treated with CTAP and higher in animals treated with nor-BNI. The HLI decreased during restraint and increased after animals were released, but this response was not affected by any treatment. Restraint stress increased oxygen consumption (35.9 +/- 3.9% elevation), but this response was diminished by CTAP and overstimulated by nor-BNI. Confirming our hypothesis, the results indicate that the mu and kappa opioid receptors in the PAG of rats play a pyrogenic and antipyretic role, respectively, during fever induced by restraint by affecting the thermogenic but not the heat conservation effector.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-01
2018-11-26T17:40:15Z
2018-11-26T17:40:15Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s00424-017-1966-2
Pflugers Archiv-european Journal Of Physiology. New York: Springer, v. 469, n. 9, p. 1151-1161, 2017.
0031-6768
http://hdl.handle.net/11449/163136
10.1007/s00424-017-1966-2
WOS:000407627800010
WOS000407627800010.pdf
url http://dx.doi.org/10.1007/s00424-017-1966-2
http://hdl.handle.net/11449/163136
identifier_str_mv Pflugers Archiv-european Journal Of Physiology. New York: Springer, v. 469, n. 9, p. 1151-1161, 2017.
0031-6768
10.1007/s00424-017-1966-2
WOS:000407627800010
WOS000407627800010.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pflugers Archiv-european Journal Of Physiology
1,479
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1151-1161
application/pdf
dc.publisher.none.fl_str_mv Springer
publisher.none.fl_str_mv Springer
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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