The ghrelin signalling system is involved in the consumption of sweets.

The gastric-derived orexigenic peptide ghrelin affects brain circuits involved in energy balance as well as in reward. Indeed, ghrelin activates an important reward circuit involved in natural- as well as drug-induced reward, the cholinergic-dopaminergic reward link. It has been hypothesized that th...

Full description

Bibliographic Details
Main Authors: Sara Landgren, Jeffrey A Simms, Dag S Thelle, Elisabeth Strandhagen, Selena E Bartlett, Jörgen A Engel, Elisabet Jerlhag
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3063250?pdf=render
_version_ 1811282184446672896
author Sara Landgren
Jeffrey A Simms
Dag S Thelle
Elisabeth Strandhagen
Selena E Bartlett
Jörgen A Engel
Elisabet Jerlhag
author_facet Sara Landgren
Jeffrey A Simms
Dag S Thelle
Elisabeth Strandhagen
Selena E Bartlett
Jörgen A Engel
Elisabet Jerlhag
author_sort Sara Landgren
collection DOAJ
description The gastric-derived orexigenic peptide ghrelin affects brain circuits involved in energy balance as well as in reward. Indeed, ghrelin activates an important reward circuit involved in natural- as well as drug-induced reward, the cholinergic-dopaminergic reward link. It has been hypothesized that there is a common reward mechanism for alcohol and sweet substances in both animals and humans. Alcohol dependent individuals have higher craving for sweets than do healthy controls and the hedonic response to sweet taste may, at least in part, depend on genetic factors. Rat selectively bred for high sucrose intake have higher alcohol consumption than non-sucrose preferring rats and vice versa. In the present study a group of alcohol-consuming individuals selected from a population cohort was investigated for genetic variants of the ghrelin signalling system in relation to both their alcohol and sucrose consumption. Moreover, the effects of GHS-R1A antagonism on voluntary sucrose-intake and operant self-administration, as well as saccharin intake were investigated in preclinical studies using rodents. The effects of peripheral grelin administration on sucrose intake were also examined. Here we found associations with the ghrelin gene haplotypes and increased sucrose consumption, and a trend for the same association was seen in the high alcohol consumers. The preclinical data show that a GHS-R1A antagonist reduces the intake and self-administration of sucrose in rats as well as saccharin intake in mice. Further, ghrelin increases the intake of sucrose in rats. Collectively, our data provide a clear indication that the GHS-R1A antagonists reduces and ghrelin increases the intake of rewarding substances and hence, the central ghrelin signalling system provides a novel target for the development of drug strategies to treat addictive behaviours.
first_indexed 2024-04-13T01:47:08Z
format Article
id doaj.art-28499f51ba3540b8a90398e55b377390
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-13T01:47:08Z
publishDate 2011-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-28499f51ba3540b8a90398e55b3773902022-12-22T03:07:58ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0163e1817010.1371/journal.pone.0018170The ghrelin signalling system is involved in the consumption of sweets.Sara LandgrenJeffrey A SimmsDag S ThelleElisabeth StrandhagenSelena E BartlettJörgen A EngelElisabet JerlhagThe gastric-derived orexigenic peptide ghrelin affects brain circuits involved in energy balance as well as in reward. Indeed, ghrelin activates an important reward circuit involved in natural- as well as drug-induced reward, the cholinergic-dopaminergic reward link. It has been hypothesized that there is a common reward mechanism for alcohol and sweet substances in both animals and humans. Alcohol dependent individuals have higher craving for sweets than do healthy controls and the hedonic response to sweet taste may, at least in part, depend on genetic factors. Rat selectively bred for high sucrose intake have higher alcohol consumption than non-sucrose preferring rats and vice versa. In the present study a group of alcohol-consuming individuals selected from a population cohort was investigated for genetic variants of the ghrelin signalling system in relation to both their alcohol and sucrose consumption. Moreover, the effects of GHS-R1A antagonism on voluntary sucrose-intake and operant self-administration, as well as saccharin intake were investigated in preclinical studies using rodents. The effects of peripheral grelin administration on sucrose intake were also examined. Here we found associations with the ghrelin gene haplotypes and increased sucrose consumption, and a trend for the same association was seen in the high alcohol consumers. The preclinical data show that a GHS-R1A antagonist reduces the intake and self-administration of sucrose in rats as well as saccharin intake in mice. Further, ghrelin increases the intake of sucrose in rats. Collectively, our data provide a clear indication that the GHS-R1A antagonists reduces and ghrelin increases the intake of rewarding substances and hence, the central ghrelin signalling system provides a novel target for the development of drug strategies to treat addictive behaviours.http://europepmc.org/articles/PMC3063250?pdf=render
spellingShingle Sara Landgren
Jeffrey A Simms
Dag S Thelle
Elisabeth Strandhagen
Selena E Bartlett
Jörgen A Engel
Elisabet Jerlhag
The ghrelin signalling system is involved in the consumption of sweets.
PLoS ONE
title The ghrelin signalling system is involved in the consumption of sweets.
title_full The ghrelin signalling system is involved in the consumption of sweets.
title_fullStr The ghrelin signalling system is involved in the consumption of sweets.
title_full_unstemmed The ghrelin signalling system is involved in the consumption of sweets.
title_short The ghrelin signalling system is involved in the consumption of sweets.
title_sort ghrelin signalling system is involved in the consumption of sweets
url http://europepmc.org/articles/PMC3063250?pdf=render
work_keys_str_mv AT saralandgren theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT jeffreyasimms theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT dagsthelle theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT elisabethstrandhagen theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT selenaebartlett theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT jorgenaengel theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT elisabetjerlhag theghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT saralandgren ghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT jeffreyasimms ghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT dagsthelle ghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT elisabethstrandhagen ghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT selenaebartlett ghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT jorgenaengel ghrelinsignallingsystemisinvolvedintheconsumptionofsweets
AT elisabetjerlhag ghrelinsignallingsystemisinvolvedintheconsumptionofsweets