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Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal

The role of food nutrients in mediating the positive effect of dietary restriction (DR) on longevity has been extensively characterized, but how non-nutrient food components regulate lifespan is not well understood. Here, we show that food-associated odors shorten the lifespan of C. elegans under DR...

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Detalles Bibliográficos
Autores principales: Zhang, Bi, Jun, Heejin, Wu, Jun, Liu, Jianfeng, Xu, X.Z. Shawn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009090/
https://www.ncbi.nlm.nih.gov/pubmed/33796867
http://dx.doi.org/10.1038/s43587-021-00039-1
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author Zhang, Bi
Jun, Heejin
Wu, Jun
Liu, Jianfeng
Xu, X.Z. Shawn
author_facet Zhang, Bi
Jun, Heejin
Wu, Jun
Liu, Jianfeng
Xu, X.Z. Shawn
author_sort Zhang, Bi
collection PubMed
description The role of food nutrients in mediating the positive effect of dietary restriction (DR) on longevity has been extensively characterized, but how non-nutrient food components regulate lifespan is not well understood. Here, we show that food-associated odors shorten the lifespan of C. elegans under DR but not those fed ad libitum, revealing a specific effect of food odors on DR-mediated longevity. Food odors act on a neural circuit comprising the sensory neurons ADF and CEP, and the interneuron RIC. This olfactory circuit signals the gut to suppress DR-mediated longevity via octopamine, the invertebrate homolog of norepinephrine, by regulating the energy sensor AMPK through a Gq-PLCβ-CaMKK-dependent mechanism. In mouse primary cells, we find that norepinephrine signaling regulates AMPK through a similar mechanism. Our results identify a brain-gut axis that regulates DR-mediated longevity by relaying olfactory information about food abundance from the brain to the gut.
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spelling pubmed-80090902021-09-15 Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal Zhang, Bi Jun, Heejin Wu, Jun Liu, Jianfeng Xu, X.Z. Shawn Nat Aging Article The role of food nutrients in mediating the positive effect of dietary restriction (DR) on longevity has been extensively characterized, but how non-nutrient food components regulate lifespan is not well understood. Here, we show that food-associated odors shorten the lifespan of C. elegans under DR but not those fed ad libitum, revealing a specific effect of food odors on DR-mediated longevity. Food odors act on a neural circuit comprising the sensory neurons ADF and CEP, and the interneuron RIC. This olfactory circuit signals the gut to suppress DR-mediated longevity via octopamine, the invertebrate homolog of norepinephrine, by regulating the energy sensor AMPK through a Gq-PLCβ-CaMKK-dependent mechanism. In mouse primary cells, we find that norepinephrine signaling regulates AMPK through a similar mechanism. Our results identify a brain-gut axis that regulates DR-mediated longevity by relaying olfactory information about food abundance from the brain to the gut. 2021-03 2021-03-15 /pmc/articles/PMC8009090/ /pubmed/33796867 http://dx.doi.org/10.1038/s43587-021-00039-1 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Zhang, Bi
Jun, Heejin
Wu, Jun
Liu, Jianfeng
Xu, X.Z. Shawn
Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
title Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
title_full Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
title_fullStr Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
title_full_unstemmed Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
title_short Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
title_sort olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009090/
https://www.ncbi.nlm.nih.gov/pubmed/33796867
http://dx.doi.org/10.1038/s43587-021-00039-1
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