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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/67848
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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 |
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1842268866503245824 |
score |
13.13397 |