Cargando…

Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice

Obesity is one of the major public health issues, and its prevalence is steadily increasing all the world over. The endocannabinoid system (ECS) has been shown to be involved in the intake of palatable food via activation of cannabinoid 1 receptor (CB(1)R). However, the involvement of lingual CB(1)R...

Descripción completa

Detalles Bibliográficos
Autores principales: Brissard, Léa, Leemput, Julia, Hichami, Aziz, Passilly-Degrace, Patricia, Maquart, Guillaume, Demizieux, Laurent, Degrace, Pascal, Khan, Naim Akhtar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213063/
https://www.ncbi.nlm.nih.gov/pubmed/30241419
http://dx.doi.org/10.3390/nu10101347
_version_ 1783367685682233344
author Brissard, Léa
Leemput, Julia
Hichami, Aziz
Passilly-Degrace, Patricia
Maquart, Guillaume
Demizieux, Laurent
Degrace, Pascal
Khan, Naim Akhtar
author_facet Brissard, Léa
Leemput, Julia
Hichami, Aziz
Passilly-Degrace, Patricia
Maquart, Guillaume
Demizieux, Laurent
Degrace, Pascal
Khan, Naim Akhtar
author_sort Brissard, Léa
collection PubMed
description Obesity is one of the major public health issues, and its prevalence is steadily increasing all the world over. The endocannabinoid system (ECS) has been shown to be involved in the intake of palatable food via activation of cannabinoid 1 receptor (CB(1)R). However, the involvement of lingual CB(1)R in the orosensory perception of dietary fatty acids has never been investigated. In the present study, behavioral tests on CB(1)R(−/−) and wild type (WT) mice showed that the invalidation of Cb(1)r gene was associated with low preference for solutions containing rapeseed oil or a long-chain fatty acid (LCFA), such as linoleic acid (LA). Administration of rimonabant, a CB(1)R inverse agonist, in mice also brought about a low preference for dietary fat. No difference in CD36 and GPR120 protein expressions were observed in taste bud cells (TBC) from WT and CB(1)R(−/−) mice. However, LCFA induced a higher increase in [Ca(2+)](i) in TBC from WT mice than that in TBC from CB(1)R(−/−) mice. TBC from CB(1)R(−/−) mice also exhibited decreased Proglucagon and Glp-1r mRNA and a low GLP-1 basal level. We report that CB(1)R is involved in fat taste perception via calcium signaling and GLP-1 secretion.
format Online
Article
Text
id pubmed-6213063
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62130632018-11-06 Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice Brissard, Léa Leemput, Julia Hichami, Aziz Passilly-Degrace, Patricia Maquart, Guillaume Demizieux, Laurent Degrace, Pascal Khan, Naim Akhtar Nutrients Article Obesity is one of the major public health issues, and its prevalence is steadily increasing all the world over. The endocannabinoid system (ECS) has been shown to be involved in the intake of palatable food via activation of cannabinoid 1 receptor (CB(1)R). However, the involvement of lingual CB(1)R in the orosensory perception of dietary fatty acids has never been investigated. In the present study, behavioral tests on CB(1)R(−/−) and wild type (WT) mice showed that the invalidation of Cb(1)r gene was associated with low preference for solutions containing rapeseed oil or a long-chain fatty acid (LCFA), such as linoleic acid (LA). Administration of rimonabant, a CB(1)R inverse agonist, in mice also brought about a low preference for dietary fat. No difference in CD36 and GPR120 protein expressions were observed in taste bud cells (TBC) from WT and CB(1)R(−/−) mice. However, LCFA induced a higher increase in [Ca(2+)](i) in TBC from WT mice than that in TBC from CB(1)R(−/−) mice. TBC from CB(1)R(−/−) mice also exhibited decreased Proglucagon and Glp-1r mRNA and a low GLP-1 basal level. We report that CB(1)R is involved in fat taste perception via calcium signaling and GLP-1 secretion. MDPI 2018-09-21 /pmc/articles/PMC6213063/ /pubmed/30241419 http://dx.doi.org/10.3390/nu10101347 Text en © 2018 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
Brissard, Léa
Leemput, Julia
Hichami, Aziz
Passilly-Degrace, Patricia
Maquart, Guillaume
Demizieux, Laurent
Degrace, Pascal
Khan, Naim Akhtar
Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice
title Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice
title_full Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice
title_fullStr Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice
title_full_unstemmed Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice
title_short Orosensory Detection of Dietary Fatty Acids Is Altered in CB(1)R(−/−) Mice
title_sort orosensory detection of dietary fatty acids is altered in cb(1)r(−/−) mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213063/
https://www.ncbi.nlm.nih.gov/pubmed/30241419
http://dx.doi.org/10.3390/nu10101347
work_keys_str_mv AT brissardlea orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT leemputjulia orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT hichamiaziz orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT passillydegracepatricia orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT maquartguillaume orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT demizieuxlaurent orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT degracepascal orosensorydetectionofdietaryfattyacidsisalteredincb1rmice
AT khannaimakhtar orosensorydetectionofdietaryfattyacidsisalteredincb1rmice