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Ablation of AgRP neurons impairs adaption to restricted feeding

While the SCN controls the circadian clock, further evidence suggests the existence of a food-entrainable oscillator (FEO) that links behavior to changes in food availability such as during restricted feeding (RF). We found that the activity of AgRP/NPY neurons changed rhythmically during RF suggest...

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Autores principales: Tan, Keith, Knight, Zachary A., Friedman, Jeffrey M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209355/
https://www.ncbi.nlm.nih.gov/pubmed/25352998
http://dx.doi.org/10.1016/j.molmet.2014.07.002
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author Tan, Keith
Knight, Zachary A.
Friedman, Jeffrey M.
author_facet Tan, Keith
Knight, Zachary A.
Friedman, Jeffrey M.
author_sort Tan, Keith
collection PubMed
description While the SCN controls the circadian clock, further evidence suggests the existence of a food-entrainable oscillator (FEO) that links behavior to changes in food availability such as during restricted feeding (RF). We found that the activity of AgRP/NPY neurons changed rhythmically during RF suggesting that these neurons are a component of the FEO. We next ablated AgRP/NPY neurons in neonates with diphtheria toxin resulting in the loss of ∼50% of AgRP/NPY neurons. Body weight and food intake were unchanged in adult animals after neonatal ablation, as were the responses to leptin treatment, leptin withdrawal, food deprivation and ghrelin treatment. However, ablated animals showed 30% mortality within 4 days of RF. Moreover, the recovery of body weight and food intake in surviving animals lagged behind controls with an absence of food anticipatory activity even after three days. These findings identify AgRP/NPY neurons as a key cellular component of the food-entrained oscillator.
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spelling pubmed-42093552014-10-28 Ablation of AgRP neurons impairs adaption to restricted feeding Tan, Keith Knight, Zachary A. Friedman, Jeffrey M. Mol Metab Original Article While the SCN controls the circadian clock, further evidence suggests the existence of a food-entrainable oscillator (FEO) that links behavior to changes in food availability such as during restricted feeding (RF). We found that the activity of AgRP/NPY neurons changed rhythmically during RF suggesting that these neurons are a component of the FEO. We next ablated AgRP/NPY neurons in neonates with diphtheria toxin resulting in the loss of ∼50% of AgRP/NPY neurons. Body weight and food intake were unchanged in adult animals after neonatal ablation, as were the responses to leptin treatment, leptin withdrawal, food deprivation and ghrelin treatment. However, ablated animals showed 30% mortality within 4 days of RF. Moreover, the recovery of body weight and food intake in surviving animals lagged behind controls with an absence of food anticipatory activity even after three days. These findings identify AgRP/NPY neurons as a key cellular component of the food-entrained oscillator. Elsevier 2014-07-10 /pmc/articles/PMC4209355/ /pubmed/25352998 http://dx.doi.org/10.1016/j.molmet.2014.07.002 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Original Article
Tan, Keith
Knight, Zachary A.
Friedman, Jeffrey M.
Ablation of AgRP neurons impairs adaption to restricted feeding
title Ablation of AgRP neurons impairs adaption to restricted feeding
title_full Ablation of AgRP neurons impairs adaption to restricted feeding
title_fullStr Ablation of AgRP neurons impairs adaption to restricted feeding
title_full_unstemmed Ablation of AgRP neurons impairs adaption to restricted feeding
title_short Ablation of AgRP neurons impairs adaption to restricted feeding
title_sort ablation of agrp neurons impairs adaption to restricted feeding
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209355/
https://www.ncbi.nlm.nih.gov/pubmed/25352998
http://dx.doi.org/10.1016/j.molmet.2014.07.002
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