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Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice
Diet affects health through ingested calories and macronutrients, and macronutrient balance affects health span. The mechanisms regulating macronutrient-based diet choices are poorly understood. Previous studies had shown that NAD-dependent deacetylase sirtuin-1 (SIRT1) in part influences the health...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214990/ https://www.ncbi.nlm.nih.gov/pubmed/30389922 http://dx.doi.org/10.1038/s41467-018-07033-z |
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author | Matsui, Sho Sasaki, Tsutomu Kohno, Daisuke Yaku, Keisuke Inutsuka, Ayumu Yokota-Hashimoto, Hiromi Kikuchi, Osamu Suga, Takayoshi Kobayashi, Masaki Yamanaka, Akihiro Harada, Akihiro Nakagawa, Takashi Onaka, Tatsushi Kitamura, Tadahiro |
author_facet | Matsui, Sho Sasaki, Tsutomu Kohno, Daisuke Yaku, Keisuke Inutsuka, Ayumu Yokota-Hashimoto, Hiromi Kikuchi, Osamu Suga, Takayoshi Kobayashi, Masaki Yamanaka, Akihiro Harada, Akihiro Nakagawa, Takashi Onaka, Tatsushi Kitamura, Tadahiro |
author_sort | Matsui, Sho |
collection | PubMed |
description | Diet affects health through ingested calories and macronutrients, and macronutrient balance affects health span. The mechanisms regulating macronutrient-based diet choices are poorly understood. Previous studies had shown that NAD-dependent deacetylase sirtuin-1 (SIRT1) in part influences the health-promoting effects of caloric restriction by boosting fat use in peripheral tissues. Here, we show that neuronal SIRT1 shifts diet choice from sucrose to fat in mice, matching the peripheral metabolic shift. SIRT1-mediated suppression of simple sugar preference requires oxytocin signalling, and SIRT1 in oxytocin neurons drives this effect. The hepatokine FGF21 acts as an endocrine signal to oxytocin neurons, promoting neuronal activation and Oxt transcription and suppressing the simple sugar preference. SIRT1 promotes FGF21 signalling in oxytocin neurons and stimulates Oxt transcription through NRF2. Thus, neuronal SIRT1 contributes to the homeostatic regulation of macronutrient-based diet selection in mice. |
format | Online Article Text |
id | pubmed-6214990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62149902018-11-05 Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice Matsui, Sho Sasaki, Tsutomu Kohno, Daisuke Yaku, Keisuke Inutsuka, Ayumu Yokota-Hashimoto, Hiromi Kikuchi, Osamu Suga, Takayoshi Kobayashi, Masaki Yamanaka, Akihiro Harada, Akihiro Nakagawa, Takashi Onaka, Tatsushi Kitamura, Tadahiro Nat Commun Article Diet affects health through ingested calories and macronutrients, and macronutrient balance affects health span. The mechanisms regulating macronutrient-based diet choices are poorly understood. Previous studies had shown that NAD-dependent deacetylase sirtuin-1 (SIRT1) in part influences the health-promoting effects of caloric restriction by boosting fat use in peripheral tissues. Here, we show that neuronal SIRT1 shifts diet choice from sucrose to fat in mice, matching the peripheral metabolic shift. SIRT1-mediated suppression of simple sugar preference requires oxytocin signalling, and SIRT1 in oxytocin neurons drives this effect. The hepatokine FGF21 acts as an endocrine signal to oxytocin neurons, promoting neuronal activation and Oxt transcription and suppressing the simple sugar preference. SIRT1 promotes FGF21 signalling in oxytocin neurons and stimulates Oxt transcription through NRF2. Thus, neuronal SIRT1 contributes to the homeostatic regulation of macronutrient-based diet selection in mice. Nature Publishing Group UK 2018-11-02 /pmc/articles/PMC6214990/ /pubmed/30389922 http://dx.doi.org/10.1038/s41467-018-07033-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Matsui, Sho Sasaki, Tsutomu Kohno, Daisuke Yaku, Keisuke Inutsuka, Ayumu Yokota-Hashimoto, Hiromi Kikuchi, Osamu Suga, Takayoshi Kobayashi, Masaki Yamanaka, Akihiro Harada, Akihiro Nakagawa, Takashi Onaka, Tatsushi Kitamura, Tadahiro Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice |
title | Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice |
title_full | Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice |
title_fullStr | Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice |
title_full_unstemmed | Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice |
title_short | Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice |
title_sort | neuronal sirt1 regulates macronutrient-based diet selection through fgf21 and oxytocin signalling in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214990/ https://www.ncbi.nlm.nih.gov/pubmed/30389922 http://dx.doi.org/10.1038/s41467-018-07033-z |
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