Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , |
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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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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1808129303154524160 |