TY - JOUR
T1 - Neuronal SIRT1 regulates macronutrient-based diet selection through FGF21 and oxytocin signalling in mice
AU - Matsui, Sho
AU - Sasaki, Tsutomu
AU - Kohno, Daisuke
AU - Yaku, Keisuke
AU - Inutsuka, Ayumu
AU - Yokota-Hashimoto, Hiromi
AU - Kikuchi, Osamu
AU - Suga, Takayoshi
AU - Kobayashi, Masaki
AU - Yamanaka, Akihiro
AU - Harada, Akihiro
AU - Nakagawa, Takashi
AU - Onaka, Tatsushi
AU - Kitamura, Tadahiro
N1 - Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85055966862&partnerID=8YFLogxK
U2 - 10.1038/s41467-018-07033-z
DO - 10.1038/s41467-018-07033-z
M3 - 学術論文
C2 - 30389922
AN - SCOPUS:85055966862
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 4604
ER -