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MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice
Melanin-concentrating hormone (MCH) is a 19 amino acid long peptide found in the brain of animals, including fishes, batrachians, and mammals. MCH is implicated in appetite and/or energy homeostasis. Antagonists at its receptor (MCH-R1) could be major tools (or ultimately drugs) to understand the me...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957705/ https://www.ncbi.nlm.nih.gov/pubmed/33673598 http://dx.doi.org/10.3390/molecules26051291 |
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author | Boutin, Jean A. Jullian, Magali Frankiewicz, Lukasz Galibert, Mathieu Gloanec, Philippe Le Diguarher, Thierry Dupuis, Philippe Ko, Amber Ripoll, Laurent Bertrand, Marc Pecquery, Anne Ferry, Gilles Puget, Karine |
author_facet | Boutin, Jean A. Jullian, Magali Frankiewicz, Lukasz Galibert, Mathieu Gloanec, Philippe Le Diguarher, Thierry Dupuis, Philippe Ko, Amber Ripoll, Laurent Bertrand, Marc Pecquery, Anne Ferry, Gilles Puget, Karine |
author_sort | Boutin, Jean A. |
collection | PubMed |
description | Melanin-concentrating hormone (MCH) is a 19 amino acid long peptide found in the brain of animals, including fishes, batrachians, and mammals. MCH is implicated in appetite and/or energy homeostasis. Antagonists at its receptor (MCH-R1) could be major tools (or ultimately drugs) to understand the mechanism of MCH action and to fight the obesity syndrome that is a worldwide societal health problem. Ever since the deorphanisation of the MCH receptor, we cloned, expressed, and characterized the receptor MCH-R1 and started a vast medicinal chemistry program aiming at the discovery of such usable compounds. In the present final work, we describe GPS18169, a pseudopeptide antagonist at the MCH-R1 receptor with an affinity in the nanomolar range and a Ki for its antagonistic effect in the 20 picomolar range. Its metabolic stability is rather ameliorated compared to its initial parent compound, the antagonist S38151. We tested it in an in vivo experiment using high diet mice. GPS18169 was found to be active in limiting the accumulation of adipose tissues and, correlatively, we observed a normalization of the insulin level in the treated animals, while no change in food or water consumption was observed. |
format | Online Article Text |
id | pubmed-7957705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79577052021-03-16 MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice Boutin, Jean A. Jullian, Magali Frankiewicz, Lukasz Galibert, Mathieu Gloanec, Philippe Le Diguarher, Thierry Dupuis, Philippe Ko, Amber Ripoll, Laurent Bertrand, Marc Pecquery, Anne Ferry, Gilles Puget, Karine Molecules Article Melanin-concentrating hormone (MCH) is a 19 amino acid long peptide found in the brain of animals, including fishes, batrachians, and mammals. MCH is implicated in appetite and/or energy homeostasis. Antagonists at its receptor (MCH-R1) could be major tools (or ultimately drugs) to understand the mechanism of MCH action and to fight the obesity syndrome that is a worldwide societal health problem. Ever since the deorphanisation of the MCH receptor, we cloned, expressed, and characterized the receptor MCH-R1 and started a vast medicinal chemistry program aiming at the discovery of such usable compounds. In the present final work, we describe GPS18169, a pseudopeptide antagonist at the MCH-R1 receptor with an affinity in the nanomolar range and a Ki for its antagonistic effect in the 20 picomolar range. Its metabolic stability is rather ameliorated compared to its initial parent compound, the antagonist S38151. We tested it in an in vivo experiment using high diet mice. GPS18169 was found to be active in limiting the accumulation of adipose tissues and, correlatively, we observed a normalization of the insulin level in the treated animals, while no change in food or water consumption was observed. MDPI 2021-02-27 /pmc/articles/PMC7957705/ /pubmed/33673598 http://dx.doi.org/10.3390/molecules26051291 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Boutin, Jean A. Jullian, Magali Frankiewicz, Lukasz Galibert, Mathieu Gloanec, Philippe Le Diguarher, Thierry Dupuis, Philippe Ko, Amber Ripoll, Laurent Bertrand, Marc Pecquery, Anne Ferry, Gilles Puget, Karine MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice |
title | MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice |
title_full | MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice |
title_fullStr | MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice |
title_full_unstemmed | MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice |
title_short | MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice |
title_sort | mch-r1 antagonist gps18169, a pseudopeptide, is a peripheral anti-obesity agent in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957705/ https://www.ncbi.nlm.nih.gov/pubmed/33673598 http://dx.doi.org/10.3390/molecules26051291 |
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