Document Detail


Leptin regulates the reward value of nutrient.
MedLine Citation:
PMID:  22081158     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We developed an assay for quantifying the reward value of nutrient and used it to analyze the effects of metabolic state and leptin. In this assay, mice chose between two sippers, one of which dispensed water and was coupled to optogenetic activation of dopaminergic (DA) neurons and the other of which dispensed natural or artificial sweeteners. This assay measured the reward value of sweeteners relative to lick-induced optogenetic activation of DA neurons. Mice preferred optogenetic stimulation of DA neurons to sucralose, but not to sucrose. However, the mice preferred sucralose plus optogenetic stimulation versus sucrose. We found that food restriction increased the value of sucrose relative to sucralose plus optogenetic stimulation, and that leptin decreased it. Our data suggest that leptin suppresses the ability of sucrose to drive taste-independent DA neuronal activation and provide new insights into the mechanism of leptin's effects on food intake.
Authors:
Ana I Domingos; Jake Vaynshteyn; Henning U Voss; Xueying Ren; Viviana Gradinaru; Feng Zang; Karl Deisseroth; Ivan E de Araujo; Jeffrey Friedman
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2011-11-13
Journal Detail:
Title:  Nature neuroscience     Volume:  14     ISSN:  1546-1726     ISO Abbreviation:  Nat. Neurosci.     Publication Date:  2011 Dec 
Date Detail:
Created Date:  2011-11-28     Completed Date:  2012-01-20     Revised Date:  2014-11-09    
Medline Journal Info:
Nlm Unique ID:  9809671     Medline TA:  Nat Neurosci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1562-8     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Analysis of Variance
Animals
Choice Behavior / drug effects,  physiology
Dopamine Plasma Membrane Transport Proteins / genetics
Dose-Response Relationship, Drug
Drinking Behavior / drug effects
Fasting / metabolism
Food*
Food Preferences / drug effects*
Gene Expression Regulation / drug effects
Image Processing, Computer-Assisted
Lasers
Leptin / metabolism,  pharmacology*
Luminescent Proteins / genetics
Magnetic Resonance Imaging
Mice
Mice, Inbred C57BL
Mice, Transgenic
Neurons / drug effects,  physiology,  radiation effects
Oxygen / blood
Proteins / genetics
Proto-Oncogene Proteins c-fos / metabolism
RNA, Untranslated
Reward*
Rhodopsin / genetics
Sucrose / administration & dosage,  analogs & derivatives
Sweetening Agents / administration & dosage
Tyrosine 3-Monooxygenase / metabolism
Ventral Tegmental Area / blood supply,  cytology,  metabolism,  radiation effects
Grant Support
ID/Acronym/Agency:
DC009997/DC/NIDCD NIH HHS; MH075957/MH/NIMH NIH HHS; R01 MH075957/MH/NIMH NIH HHS
Chemical
Reg. No./Substance:
0/Dopamine Plasma Membrane Transport Proteins; 0/Gt(ROSA)26Sor non-coding RNA, mouse; 0/Leptin; 0/Luminescent Proteins; 0/Proteins; 0/Proto-Oncogene Proteins c-fos; 0/RNA, Untranslated; 0/Sweetening Agents; 0/channelrhodopsin 2, mouse; 56038-13-2/trichlorosucrose; 57-50-1/Sucrose; 9009-81-8/Rhodopsin; EC 1.14.16.2/Tyrosine 3-Monooxygenase; S88TT14065/Oxygen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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