Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain

Autores
Perello, Mario; Scott, Michael M.; Sakata, Ichiro; Lee, Charlotte E.; Chuang, Jen Chieh; Osborne Lawrence, Sherri; Rovinsky, Sherry A.; Elmquist, Joel K.; Zigman, Jeffrey M.
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The hormones leptin and ghrelin act in apposition to one another in the regulation of body weight homeostasis. Interestingly, both leptin receptor expression and ghrelin receptor expression have been observed within many of the same nuclei of the central nervous system (CNS), suggesting that these hormones may act on a common population of neurons to produce changes in food intake and energy expenditure. In the present study we explored the extent of this putative direct leptin and ghrelin interaction in the CNS and addressed the question of whether a loss of ghrelin signaling would affect sensitivity to leptin. Using histological mapping of leptin receptor and ghrelin receptor expression, we found that cells containing both leptin receptors and ghrelin receptors are mainly located in the medial part of the hypothalamic arcuate nucleus. In contrast, coexpression was much less extensive elsewhere in the brain. To assess the functional consequences of this observed receptor distribution, we explored the effect of ghrelin receptor deletion on leptin sensitivity. In particular, the responses of ad libitum-fed, diet-induced obese and fasted mice to the anorectic actions of leptin were examined. Surprisingly, we found that deletion of the ghrelin receptor did not affect the sensitivity to exogenously administrated leptin. Thus, we conclude that ghrelin and leptin act largely on distinct neuronal populations and that ghrelin receptor deficiency does not affect sensitivity to the anorexigenic and body weight-lowering actions of leptin. © 2011 Wiley Periodicals, Inc.
Fil: Perello, Mario. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Scott, Michael M.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Sakata, Ichiro. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Lee, Charlotte E.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Chuang, Jen Chieh. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Osborne Lawrence, Sherri. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Rovinsky, Sherry A.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Elmquist, Joel K.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Zigman, Jeffrey M.. University of Texas Southwestern Medical Center; Estados Unidos
Materia
Arcuate Nucleus
Food Intake
Ghsr
Leprb
Obesity
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/67848

id CONICETDig_d0a90423178e72a66f1f44f129b4d6ef
oai_identifier_str oai:ri.conicet.gov.ar:11336/67848
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brainPerello, MarioScott, Michael M.Sakata, IchiroLee, Charlotte E.Chuang, Jen ChiehOsborne Lawrence, SherriRovinsky, Sherry A.Elmquist, Joel K.Zigman, Jeffrey M.Arcuate NucleusFood IntakeGhsrLeprbObesityhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3The hormones leptin and ghrelin act in apposition to one another in the regulation of body weight homeostasis. Interestingly, both leptin receptor expression and ghrelin receptor expression have been observed within many of the same nuclei of the central nervous system (CNS), suggesting that these hormones may act on a common population of neurons to produce changes in food intake and energy expenditure. In the present study we explored the extent of this putative direct leptin and ghrelin interaction in the CNS and addressed the question of whether a loss of ghrelin signaling would affect sensitivity to leptin. Using histological mapping of leptin receptor and ghrelin receptor expression, we found that cells containing both leptin receptors and ghrelin receptors are mainly located in the medial part of the hypothalamic arcuate nucleus. In contrast, coexpression was much less extensive elsewhere in the brain. To assess the functional consequences of this observed receptor distribution, we explored the effect of ghrelin receptor deletion on leptin sensitivity. In particular, the responses of ad libitum-fed, diet-induced obese and fasted mice to the anorectic actions of leptin were examined. Surprisingly, we found that deletion of the ghrelin receptor did not affect the sensitivity to exogenously administrated leptin. Thus, we conclude that ghrelin and leptin act largely on distinct neuronal populations and that ghrelin receptor deficiency does not affect sensitivity to the anorexigenic and body weight-lowering actions of leptin. © 2011 Wiley Periodicals, Inc.Fil: Perello, Mario. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Texas Southwestern Medical Center; Estados UnidosFil: Scott, Michael M.. University of Texas Southwestern Medical Center; Estados UnidosFil: Sakata, Ichiro. University of Texas Southwestern Medical Center; Estados UnidosFil: Lee, Charlotte E.. University of Texas Southwestern Medical Center; Estados UnidosFil: Chuang, Jen Chieh. University of Texas Southwestern Medical Center; Estados UnidosFil: Osborne Lawrence, Sherri. University of Texas Southwestern Medical Center; Estados UnidosFil: Rovinsky, Sherry A.. University of Texas Southwestern Medical Center; Estados UnidosFil: Elmquist, Joel K.. University of Texas Southwestern Medical Center; Estados UnidosFil: Zigman, Jeffrey M.. University of Texas Southwestern Medical Center; Estados UnidosWiley-liss, Div John Wiley & Sons Inc2012-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/67848Perello, Mario; Scott, Michael M.; Sakata, Ichiro; Lee, Charlotte E.; Chuang, Jen Chieh; et al.; Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain; Wiley-liss, Div John Wiley & Sons Inc; Journal Of Comparative Neurology; 520; 2; 2-2012; 281-2940021-9967CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/cne.22690info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.22690info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:33Zoai:ri.conicet.gov.ar:11336/67848instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:47:33.428CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
title Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
spellingShingle Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
Perello, Mario
Arcuate Nucleus
Food Intake
Ghsr
Leprb
Obesity
title_short Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
title_full Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
title_fullStr Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
title_full_unstemmed Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
title_sort Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain
dc.creator.none.fl_str_mv Perello, Mario
Scott, Michael M.
Sakata, Ichiro
Lee, Charlotte E.
Chuang, Jen Chieh
Osborne Lawrence, Sherri
Rovinsky, Sherry A.
Elmquist, Joel K.
Zigman, Jeffrey M.
author Perello, Mario
author_facet Perello, Mario
Scott, Michael M.
Sakata, Ichiro
Lee, Charlotte E.
Chuang, Jen Chieh
Osborne Lawrence, Sherri
Rovinsky, Sherry A.
Elmquist, Joel K.
Zigman, Jeffrey M.
author_role author
author2 Scott, Michael M.
Sakata, Ichiro
Lee, Charlotte E.
Chuang, Jen Chieh
Osborne Lawrence, Sherri
Rovinsky, Sherry A.
Elmquist, Joel K.
Zigman, Jeffrey M.
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Arcuate Nucleus
Food Intake
Ghsr
Leprb
Obesity
topic Arcuate Nucleus
Food Intake
Ghsr
Leprb
Obesity
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv The hormones leptin and ghrelin act in apposition to one another in the regulation of body weight homeostasis. Interestingly, both leptin receptor expression and ghrelin receptor expression have been observed within many of the same nuclei of the central nervous system (CNS), suggesting that these hormones may act on a common population of neurons to produce changes in food intake and energy expenditure. In the present study we explored the extent of this putative direct leptin and ghrelin interaction in the CNS and addressed the question of whether a loss of ghrelin signaling would affect sensitivity to leptin. Using histological mapping of leptin receptor and ghrelin receptor expression, we found that cells containing both leptin receptors and ghrelin receptors are mainly located in the medial part of the hypothalamic arcuate nucleus. In contrast, coexpression was much less extensive elsewhere in the brain. To assess the functional consequences of this observed receptor distribution, we explored the effect of ghrelin receptor deletion on leptin sensitivity. In particular, the responses of ad libitum-fed, diet-induced obese and fasted mice to the anorectic actions of leptin were examined. Surprisingly, we found that deletion of the ghrelin receptor did not affect the sensitivity to exogenously administrated leptin. Thus, we conclude that ghrelin and leptin act largely on distinct neuronal populations and that ghrelin receptor deficiency does not affect sensitivity to the anorexigenic and body weight-lowering actions of leptin. © 2011 Wiley Periodicals, Inc.
Fil: Perello, Mario. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Scott, Michael M.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Sakata, Ichiro. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Lee, Charlotte E.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Chuang, Jen Chieh. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Osborne Lawrence, Sherri. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Rovinsky, Sherry A.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Elmquist, Joel K.. University of Texas Southwestern Medical Center; Estados Unidos
Fil: Zigman, Jeffrey M.. University of Texas Southwestern Medical Center; Estados Unidos
description The hormones leptin and ghrelin act in apposition to one another in the regulation of body weight homeostasis. Interestingly, both leptin receptor expression and ghrelin receptor expression have been observed within many of the same nuclei of the central nervous system (CNS), suggesting that these hormones may act on a common population of neurons to produce changes in food intake and energy expenditure. In the present study we explored the extent of this putative direct leptin and ghrelin interaction in the CNS and addressed the question of whether a loss of ghrelin signaling would affect sensitivity to leptin. Using histological mapping of leptin receptor and ghrelin receptor expression, we found that cells containing both leptin receptors and ghrelin receptors are mainly located in the medial part of the hypothalamic arcuate nucleus. In contrast, coexpression was much less extensive elsewhere in the brain. To assess the functional consequences of this observed receptor distribution, we explored the effect of ghrelin receptor deletion on leptin sensitivity. In particular, the responses of ad libitum-fed, diet-induced obese and fasted mice to the anorectic actions of leptin were examined. Surprisingly, we found that deletion of the ghrelin receptor did not affect the sensitivity to exogenously administrated leptin. Thus, we conclude that ghrelin and leptin act largely on distinct neuronal populations and that ghrelin receptor deficiency does not affect sensitivity to the anorexigenic and body weight-lowering actions of leptin. © 2011 Wiley Periodicals, Inc.
publishDate 2012
dc.date.none.fl_str_mv 2012-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/67848
Perello, Mario; Scott, Michael M.; Sakata, Ichiro; Lee, Charlotte E.; Chuang, Jen Chieh; et al.; Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain; Wiley-liss, Div John Wiley & Sons Inc; Journal Of Comparative Neurology; 520; 2; 2-2012; 281-294
0021-9967
CONICET Digital
CONICET
url http://hdl.handle.net/11336/67848
identifier_str_mv Perello, Mario; Scott, Michael M.; Sakata, Ichiro; Lee, Charlotte E.; Chuang, Jen Chieh; et al.; Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain; Wiley-liss, Div John Wiley & Sons Inc; Journal Of Comparative Neurology; 520; 2; 2-2012; 281-294
0021-9967
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1002/cne.22690
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.22690
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley-liss, Div John Wiley & Sons Inc
publisher.none.fl_str_mv Wiley-liss, Div John Wiley & Sons Inc
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1842268866503245824
score 13.13397