Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.

Ghrelin is an endogenous regulator of energy homeostasis synthesized by the stomach to stimulate appetite and positive energy balance. Similarly, the endocannabinoid system is part of our internal machinery controlling food intake and energy expenditure. Both peripheral and central mechanisms regula...

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Autores: Alen, Francisco, Crespo, Inmaculada, Ramírez-López, María Teresa, Jagerovic, Nadine, Goya, Pilar, Rodríguez de Fonseca, Fernando, Gómez de Heras, Raquel, Orio, Laura
Tipo de recurso: artículo
Fecha de publicación:2013
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/17048
Acceso en línea:http://hdl.handle.net/20.500.12105/17048
Access Level:acceso abierto
Palabra clave:Animales
Ghrelina
Masculino
Piperidinas
Ratas
Ratas Wistar
Ingestión de Alimentos
Receptor cannabinoide CB1
Eating
Ghrelin
Male
Piperidines
Pyrazoles
Rats
Rats, Wistar
Receptor, Cannabinoid, CB1
Triazoles
Animals
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oai_identifier_str oai:repisalud.isciii.es:20.500.12105/17048
network_acronym_str ES
network_name_str España
spelling Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism. Alen, Francisco Crespo, Inmaculada Ramírez-López, María Teresa Jagerovic, Nadine Goya, Pilar Rodríguez de Fonseca, Fernando Gómez de Heras, Raquel Orio, Laura Animales Ghrelina Masculino Piperidinas Ratas Ratas Wistar Ingestión de Alimentos Receptor cannabinoide CB1 Eating Ghrelin Male Piperidines Pyrazoles Rats Rats, Wistar Receptor, Cannabinoid, CB1 Triazoles Animals Ghrelin is an endogenous regulator of energy homeostasis synthesized by the stomach to stimulate appetite and positive energy balance. Similarly, the endocannabinoid system is part of our internal machinery controlling food intake and energy expenditure. Both peripheral and central mechanisms regulate CB1-mediated control of food intake and a functional relationship between hypothalamic ghrelin and cannabinoid CB1 receptor has been proposed. First of all, we investigated brain ghrelin actions on food intake in rats with different metabolic status (negative or equilibrate energy balance). Secondly, we tested a sub-anxiogenic ultra-low dose of the CB1 antagonist SR141716A (Rimonabant) and the peripheral-acting CB1 antagonist LH-21 on ghrelin orexigenic actions. We found that: 1) central administration of ghrelin promotes food intake in free feeding animals but not in 24 h food-deprived or chronically food-restricted animals; 2) an ultra-low dose of SR141716A (a subthreshold dose 75 folds lower than the EC50 for induction of anxiety) completely counteracts the orexigenic actions of central ghrelin in free feeding animals; 3) the peripheral-restricted CB1 antagonist LH-21 blocks ghrelin-induced hyperphagia in free feeding animals. Our study highlights the importance of the animaĺs metabolic status for the effectiveness of ghrelin in promoting feeding, and suggests that the peripheral endocannabinoid system may interact with ghrelińs signal in the control of food intake under equilibrate energy balance conditions. Public Library of Science (PLOS) http://hdl.handle.net/20.500.12105/17048
title Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
spellingShingle Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
Alen, Francisco
Animales
Ghrelina
Masculino
Piperidinas
Ratas
Ratas Wistar
Ingestión de Alimentos
Receptor cannabinoide CB1
Eating
Ghrelin
Male
Piperidines
Pyrazoles
Rats
Rats, Wistar
Receptor, Cannabinoid, CB1
Triazoles
Animals
title_short Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
title_full Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
title_fullStr Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
title_full_unstemmed Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
title_sort Ghrelin-induced orexigenic effect in rats depends on the metabolic status and is counteracted by peripheral CB1 receptor antagonism.
author Alen, Francisco
author_facet Alen, Francisco
Crespo, Inmaculada
Ramírez-López, María Teresa
Jagerovic, Nadine
Goya, Pilar
Rodríguez de Fonseca, Fernando
Gómez de Heras, Raquel
Orio, Laura
author_role author
author2 Crespo, Inmaculada
Ramírez-López, María Teresa
Jagerovic, Nadine
Goya, Pilar
Rodríguez de Fonseca, Fernando
Gómez de Heras, Raquel
Orio, Laura
author2_role author
author
author
author
author
author
author
topic Animales
Ghrelina
Masculino
Piperidinas
Ratas
Ratas Wistar
Ingestión de Alimentos
Receptor cannabinoide CB1
Eating
Ghrelin
Male
Piperidines
Pyrazoles
Rats
Rats, Wistar
Receptor, Cannabinoid, CB1
Triazoles
Animals
topic_facet Animales
Ghrelina
Masculino
Piperidinas
Ratas
Ratas Wistar
Ingestión de Alimentos
Receptor cannabinoide CB1
Eating
Ghrelin
Male
Piperidines
Pyrazoles
Rats
Rats, Wistar
Receptor, Cannabinoid, CB1
Triazoles
Animals
description Ghrelin is an endogenous regulator of energy homeostasis synthesized by the stomach to stimulate appetite and positive energy balance. Similarly, the endocannabinoid system is part of our internal machinery controlling food intake and energy expenditure. Both peripheral and central mechanisms regulate CB1-mediated control of food intake and a functional relationship between hypothalamic ghrelin and cannabinoid CB1 receptor has been proposed. First of all, we investigated brain ghrelin actions on food intake in rats with different metabolic status (negative or equilibrate energy balance). Secondly, we tested a sub-anxiogenic ultra-low dose of the CB1 antagonist SR141716A (Rimonabant) and the peripheral-acting CB1 antagonist LH-21 on ghrelin orexigenic actions. We found that: 1) central administration of ghrelin promotes food intake in free feeding animals but not in 24 h food-deprived or chronically food-restricted animals; 2) an ultra-low dose of SR141716A (a subthreshold dose 75 folds lower than the EC50 for induction of anxiety) completely counteracts the orexigenic actions of central ghrelin in free feeding animals; 3) the peripheral-restricted CB1 antagonist LH-21 blocks ghrelin-induced hyperphagia in free feeding animals. Our study highlights the importance of the animaĺs metabolic status for the effectiveness of ghrelin in promoting feeding, and suggests that the peripheral endocannabinoid system may interact with ghrelińs signal in the control of food intake under equilibrate energy balance conditions.
publishDate 2013
format article
url http://hdl.handle.net/20.500.12105/17048
language eng
eu_rights_str_mv openAccess
publisher Public Library of Science (PLOS)
institution Instituto de Salud Carlos III (ISCIII)
collection Repisalud
reponame_str Repisalud
instname_str Instituto de Salud Carlos III (ISCIII)
_version_ 1878438209214480384
publishDateSort 2013
author_browse Alen, Francisco
Crespo, Inmaculada
Goya, Pilar
Gómez de Heras, Raquel
Jagerovic, Nadine
Orio, Laura
Ramírez-López, María Teresa
Rodríguez de Fonseca, Fernando
publisherStr Public Library of Science (PLOS)
score 6,9303427