Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing

In most species, including humans, food preference is primarily controlled by nutrient value. In particular, glucose-containing sugars exert exquisitely strong effects on food choice via gut-generated signals. However, the identity of the visceral signals underlying glucose’s rewarding effects remai...

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Published in:Frontiers in Integrative Neuroscience
Main Authors: Lingli Zhang, Wenfei Han, Chenguanlu Lin, Fei Li, Ivan E. de Araujo
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-11-01
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnint.2018.00057/full
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author Lingli Zhang
Lingli Zhang
Lingli Zhang
Wenfei Han
Wenfei Han
Wenfei Han
Wenfei Han
Chenguanlu Lin
Chenguanlu Lin
Fei Li
Fei Li
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
author_facet Lingli Zhang
Lingli Zhang
Lingli Zhang
Wenfei Han
Wenfei Han
Wenfei Han
Wenfei Han
Chenguanlu Lin
Chenguanlu Lin
Fei Li
Fei Li
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
author_sort Lingli Zhang
collection DOAJ
container_title Frontiers in Integrative Neuroscience
description In most species, including humans, food preference is primarily controlled by nutrient value. In particular, glucose-containing sugars exert exquisitely strong effects on food choice via gut-generated signals. However, the identity of the visceral signals underlying glucose’s rewarding effects remains uncertain. In particular, it is unknown whether sugar metabolism mediates the formation of preferences for glucose-containing sugars. Using the mouse as a model organism, we made use of a combination of conditioning schedules, gastrointestinal nutrient administration, and chromatographic/electrochemical methods to assess the behavioral and neural effects of activating the gut with either metabolizable glucose or a non-metabolizable glucose analog. We show that mice display much superior preferences for flavors associated with intra-gastric infusions of glucose compared to flavors associated with intra-gastric infusions of the non-metabolizable glucose analog α-methyl-D-glucopyranoside (“MDG,” an activator of intestinal sodium/glucose co-transporters). These effects were unaffected by surgical bypassing of the duodenum, suggesting glucose-specific post-absorptive sensing mechanisms. Consistently, intra-portal infusions of glucose, but not of MDG, induced significant rises in dopamine (DA) levels within brain reward circuits. Our data reveal that the unmatched rewarding effects of glucose-containing sugars cannot be accounted for by metabolism-independent activation of sodium/glucose cotransporters; rather, they point to glucose metabolism as the physiological mechanism underlying the potent reward value of sugar-sweetened flavored beverages. In particular, no circulating “gut factors” need to be invoked to explain the reward value of ingested glucose. Thus, instead of circulating gut hormones, portal-mesenteric sensing of glucose emerges as the preferential physiological pathway for sugar reward.
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spelling doaj-art-e63c04f6c4a04b3eb4a299fde405e2a82025-08-19T19:14:55ZengFrontiers Media S.A.Frontiers in Integrative Neuroscience1662-51452018-11-011210.3389/fnint.2018.00057423087Sugar Metabolism Regulates Flavor Preferences and Portal Glucose SensingLingli Zhang0Lingli Zhang1Lingli Zhang2Wenfei Han3Wenfei Han4Wenfei Han5Wenfei Han6Chenguanlu Lin7Chenguanlu Lin8Fei Li9Fei Li10Ivan E. de Araujo11Ivan E. de Araujo12Ivan E. de Araujo13Ivan E. de Araujo14Ivan E. de Araujo15Shanghai Children’s Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaMinistry of Education-Shanghai Key Laboratory of Children’s Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaThe John B. Pierce Laboratory, Yale University, New Haven, CT, United StatesThe John B. Pierce Laboratory, Yale University, New Haven, CT, United StatesDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, United StatesDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, United StatesShanghai Engineering Research Center of Tooth Restoration and Regeneration, School & Hospital of Stomatology, Tongji University, Shanghai, ChinaThe John B. Pierce Laboratory, Yale University, New Haven, CT, United StatesShanghai Engineering Research Center of Tooth Restoration and Regeneration, School & Hospital of Stomatology, Tongji University, Shanghai, ChinaMinistry of Education-Shanghai Key Laboratory of Children’s Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDevelopmental and Behavioral Pediatric Department & Child Primary Care Department, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaThe John B. Pierce Laboratory, Yale University, New Haven, CT, United StatesDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, United StatesDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, United StatesDiabetes, Obesity and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United StatesDepartment of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT, United StatesIn most species, including humans, food preference is primarily controlled by nutrient value. In particular, glucose-containing sugars exert exquisitely strong effects on food choice via gut-generated signals. However, the identity of the visceral signals underlying glucose’s rewarding effects remains uncertain. In particular, it is unknown whether sugar metabolism mediates the formation of preferences for glucose-containing sugars. Using the mouse as a model organism, we made use of a combination of conditioning schedules, gastrointestinal nutrient administration, and chromatographic/electrochemical methods to assess the behavioral and neural effects of activating the gut with either metabolizable glucose or a non-metabolizable glucose analog. We show that mice display much superior preferences for flavors associated with intra-gastric infusions of glucose compared to flavors associated with intra-gastric infusions of the non-metabolizable glucose analog α-methyl-D-glucopyranoside (“MDG,” an activator of intestinal sodium/glucose co-transporters). These effects were unaffected by surgical bypassing of the duodenum, suggesting glucose-specific post-absorptive sensing mechanisms. Consistently, intra-portal infusions of glucose, but not of MDG, induced significant rises in dopamine (DA) levels within brain reward circuits. Our data reveal that the unmatched rewarding effects of glucose-containing sugars cannot be accounted for by metabolism-independent activation of sodium/glucose cotransporters; rather, they point to glucose metabolism as the physiological mechanism underlying the potent reward value of sugar-sweetened flavored beverages. In particular, no circulating “gut factors” need to be invoked to explain the reward value of ingested glucose. Thus, instead of circulating gut hormones, portal-mesenteric sensing of glucose emerges as the preferential physiological pathway for sugar reward.https://www.frontiersin.org/article/10.3389/fnint.2018.00057/fulldopamineflavor preferencesglucose metabolismportal veinstriatumsugar
spellingShingle Lingli Zhang
Lingli Zhang
Lingli Zhang
Wenfei Han
Wenfei Han
Wenfei Han
Wenfei Han
Chenguanlu Lin
Chenguanlu Lin
Fei Li
Fei Li
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Ivan E. de Araujo
Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing
dopamine
flavor preferences
glucose metabolism
portal vein
striatum
sugar
title Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing
title_full Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing
title_fullStr Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing
title_full_unstemmed Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing
title_short Sugar Metabolism Regulates Flavor Preferences and Portal Glucose Sensing
title_sort sugar metabolism regulates flavor preferences and portal glucose sensing
topic dopamine
flavor preferences
glucose metabolism
portal vein
striatum
sugar
url https://www.frontiersin.org/article/10.3389/fnint.2018.00057/full
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