Sensing and signaling mechanisms linking dietary methionine restriction to the behavioral and physiological components of the response
•The liver is the key anatomical site for sensing of dietary methionine restriction.•The liver responds to dietary methionine restriction by releasing FGF21.•FGF21 mediates many of the metabolic effects of dietary methionine restriction. Dietary methionine restriction (MR) is implemented using a sem...
Gespeichert in:
Veröffentlicht in: | Frontiers in neuroendocrinology 2018-10, Vol.51, p.36-45 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | •The liver is the key anatomical site for sensing of dietary methionine restriction.•The liver responds to dietary methionine restriction by releasing FGF21.•FGF21 mediates many of the metabolic effects of dietary methionine restriction.
Dietary methionine restriction (MR) is implemented using a semi-purified diet that reduces methionine by ∼80% and eliminates dietary cysteine. Within hours of its introduction, dietary MR initiates coordinated series of transcriptional programs and physiological responses that include increased energy intake and expenditure, decreased adiposity, enhanced insulin sensitivity, and reduction in circulating and tissue lipids. Significant progress has been made in cataloguing the physiological responses to MR in males but not females, but identities of the sensing and communication networks that orchestrate these responses remain poorly understood. Recent work has implicated hepatic FGF21 as an important mediator of MR, but it is clear that other mechanisms are also involved. The goal of this review is to explore the temporal and spatial organization of the responses to dietary MR as a model for understanding how nutrient sensing systems function to integrate complex transcriptional, physiological, and behavioral responses to changes in dietary composition. |
---|---|
ISSN: | 0091-3022 1095-6808 |
DOI: | 10.1016/j.yfrne.2017.12.002 |