Literature DB >> 36107313

Nuclear Receptors in Energy Metabolism.

Alina A Walth-Hummel1,2,3, Stephan Herzig1,2,3,4, Maria Rohm5,6,7.   

Abstract

Nuclear receptors are master regulators of energy metabolism through the conversion of extracellular signals into gene expression signatures. The function of the respective nuclear receptor is tissue specific, signal and co-factor dependent. While normal nuclear receptor function is central to metabolic physiology, aberrant nuclear receptor signaling is linked to various metabolic diseases such as type 2 diabetes mellitus, obesity, or hepatic steatosis. Thus, the tissue specific manipulation of nuclear receptors is a major field in biomedical research and represents a treatment approach for metabolic syndrome. This chapter focuses on key nuclear receptors involved in regulating the metabolic function of liver, adipose tissue, skeletal muscle, and pancreatic β-cells. It also addresses the importance of nuclear co-factors for fine-tuning of nuclear receptor function. The mode of action, role in energy metabolism, and therapeutic potential of prominent nuclear receptors is outlined.
© 2022. The Author(s), under exclusive license to Springer Nature Switzerland AG.

Entities:  

Keywords:  Energy homeostasis; Glucose and lipid metabolism; Metabolic syndrome; Nuclear receptor-based therapies; Transcriptional co-factors

Mesh:

Substances:

Year:  2022        PMID: 36107313     DOI: 10.1007/978-3-031-11836-4_4

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   3.650


  146 in total

1.  Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators.

Authors:  I Issemann; S Green
Journal:  Nature       Date:  1990-10-18       Impact factor: 49.962

2.  Peroxisome proliferator-activated receptor alpha mediates the adaptive response to fasting.

Authors:  S Kersten; J Seydoux; J M Peters; F J Gonzalez; B Desvergne; W Wahli
Journal:  J Clin Invest       Date:  1999-06       Impact factor: 14.808

3.  PPARα gene expression correlates with severity and histological treatment response in patients with non-alcoholic steatohepatitis.

Authors:  Sven Francque; An Verrijken; Sandrine Caron; Janne Prawitt; Réjane Paumelle; Bruno Derudas; Philippe Lefebvre; Marja-Riitta Taskinen; Wim Van Hul; Ilse Mertens; Guy Hubens; Eric Van Marck; Peter Michielsen; Luc Van Gaal; Bart Staels
Journal:  J Hepatol       Date:  2015-02-19       Impact factor: 25.083

4.  Different sensitivity of PPARalpha gene expression to nutritional changes in liver of suckling and adult rats.

Authors:  Maribel Panadero; Emilio Herrera; Carlos Bocos
Journal:  Life Sci       Date:  2005-01-14       Impact factor: 5.037

5.  A critical role for the peroxisome proliferator-activated receptor alpha (PPARalpha) in the cellular fasting response: the PPARalpha-null mouse as a model of fatty acid oxidation disorders.

Authors:  T C Leone; C J Weinheimer; D P Kelly
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

6.  The peroxisome proliferator-activated receptor regulates mitochondrial fatty acid oxidative enzyme gene expression.

Authors:  T Gulick; S Cresci; T Caira; D D Moore; D P Kelly
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-08       Impact factor: 11.205

7.  Differential expression and activation of a family of murine peroxisome proliferator-activated receptors.

Authors:  S A Kliewer; B M Forman; B Blumberg; E S Ong; U Borgmeyer; D J Mangelsdorf; K Umesono; R M Evans
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

8.  Expression of putative fatty acid transporter genes are regulated by peroxisome proliferator-activated receptor alpha and gamma activators in a tissue- and inducer-specific manner.

Authors:  K Motojima; P Passilly; J M Peters; F J Gonzalez; N Latruffe
Journal:  J Biol Chem       Date:  1998-07-03       Impact factor: 5.157

9.  Differential expression of peroxisome proliferator-activated receptors (PPARs): tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat.

Authors:  O Braissant; F Foufelle; C Scotto; M Dauça; W Wahli
Journal:  Endocrinology       Date:  1996-01       Impact factor: 4.736

10.  Liver PPARα is crucial for whole-body fatty acid homeostasis and is protective against NAFLD.

Authors:  Alexandra Montagner; Arnaud Polizzi; Edwin Fouché; Simon Ducheix; Yannick Lippi; Frédéric Lasserre; Valentin Barquissau; Marion Régnier; Céline Lukowicz; Fadila Benhamed; Alison Iroz; Justine Bertrand-Michel; Talal Al Saati; Patricia Cano; Laila Mselli-Lakhal; Gilles Mithieux; Fabienne Rajas; Sandrine Lagarrigue; Thierry Pineau; Nicolas Loiseau; Catherine Postic; Dominique Langin; Walter Wahli; Hervé Guillou
Journal:  Gut       Date:  2016-02-01       Impact factor: 23.059

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