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Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models

The compound S38151 is a nanomolar antagonist that acts at the melanin-concentrating hormone receptor 1 (MCH(1)). S38151 is more stable than its purely peptide counterpart, essentially because of the blockade of its N-terminus. Therefore, its action on various models of obesity was studied. Acute in...

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Autores principales: Della-Zuana, Odile, Audinot, Valérie, Levenez, Viviane, Ktorza, Alain, Presse, Françoise, Nahon, Jean-Louis, Boutin, Jean A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527734/
https://www.ncbi.nlm.nih.gov/pubmed/23267345
http://dx.doi.org/10.3389/fendo.2012.00160
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author Della-Zuana, Odile
Audinot, Valérie
Levenez, Viviane
Ktorza, Alain
Presse, Françoise
Nahon, Jean-Louis
Boutin, Jean A.
author_facet Della-Zuana, Odile
Audinot, Valérie
Levenez, Viviane
Ktorza, Alain
Presse, Françoise
Nahon, Jean-Louis
Boutin, Jean A.
author_sort Della-Zuana, Odile
collection PubMed
description The compound S38151 is a nanomolar antagonist that acts at the melanin-concentrating hormone receptor 1 (MCH(1)). S38151 is more stable than its purely peptide counterpart, essentially because of the blockade of its N-terminus. Therefore, its action on various models of obesity was studied. Acute intra-cerebroventricular (i.c.v.) administration of S38151 in wild-type rats counteracted the effect of the stable precursor of melanin-concentrating hormone (MCH), NEI-MCH, in a dose-dependent manner (from 0.5 to 50 nmol/kg). In genetically obese Zucker fa/fa rats, daily i.c.v. administration of S38151 induced dose-dependent (5, 10, and 20 nmol/kg) inhibition of food intake, water intake, and body weight gain, as well as increased motility (maximal effect observed at 20 nmol/kg). In Zucker fa/fa rats, intraperitoneal injection of S38151 (30 mg/kg) induced complete inhibition of food consumption within 1 h. Daily intraperitoneal injection of S38151 (10 and 30 mg/kg) into genetically obese ob/ob mice or diet-induced obese mice is able to limit body weight gain. Furthermore, S38151 administration (10 and 30 mg/kg) does not affect food intake, water intake, or body weight gain in MCHR1-deleted mice, demonstrating that its effects are linked to its interaction with MCH(1). These results validate MCH(1) as a target of interest in obesity. S38151 cannot progress to the clinical phase because it is still too poorly stable in vivo.
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spelling pubmed-35277342012-12-24 Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models Della-Zuana, Odile Audinot, Valérie Levenez, Viviane Ktorza, Alain Presse, Françoise Nahon, Jean-Louis Boutin, Jean A. Front Endocrinol (Lausanne) Endocrinology The compound S38151 is a nanomolar antagonist that acts at the melanin-concentrating hormone receptor 1 (MCH(1)). S38151 is more stable than its purely peptide counterpart, essentially because of the blockade of its N-terminus. Therefore, its action on various models of obesity was studied. Acute intra-cerebroventricular (i.c.v.) administration of S38151 in wild-type rats counteracted the effect of the stable precursor of melanin-concentrating hormone (MCH), NEI-MCH, in a dose-dependent manner (from 0.5 to 50 nmol/kg). In genetically obese Zucker fa/fa rats, daily i.c.v. administration of S38151 induced dose-dependent (5, 10, and 20 nmol/kg) inhibition of food intake, water intake, and body weight gain, as well as increased motility (maximal effect observed at 20 nmol/kg). In Zucker fa/fa rats, intraperitoneal injection of S38151 (30 mg/kg) induced complete inhibition of food consumption within 1 h. Daily intraperitoneal injection of S38151 (10 and 30 mg/kg) into genetically obese ob/ob mice or diet-induced obese mice is able to limit body weight gain. Furthermore, S38151 administration (10 and 30 mg/kg) does not affect food intake, water intake, or body weight gain in MCHR1-deleted mice, demonstrating that its effects are linked to its interaction with MCH(1). These results validate MCH(1) as a target of interest in obesity. S38151 cannot progress to the clinical phase because it is still too poorly stable in vivo. Frontiers Media S.A. 2012-12-21 /pmc/articles/PMC3527734/ /pubmed/23267345 http://dx.doi.org/10.3389/fendo.2012.00160 Text en Copyright © 2012 Della-Zuana, Audinot, Levenez, Ktorza, Presse, Nahon and Boutin. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Endocrinology
Della-Zuana, Odile
Audinot, Valérie
Levenez, Viviane
Ktorza, Alain
Presse, Françoise
Nahon, Jean-Louis
Boutin, Jean A.
Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models
title Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models
title_full Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models
title_fullStr Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models
title_full_unstemmed Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models
title_short Peripheral injections of melanin-concentrating hormone receptor 1 antagonist S38151 decrease food intake and body weight in rodent obesity models
title_sort peripheral injections of melanin-concentrating hormone receptor 1 antagonist s38151 decrease food intake and body weight in rodent obesity models
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527734/
https://www.ncbi.nlm.nih.gov/pubmed/23267345
http://dx.doi.org/10.3389/fendo.2012.00160
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