Literature DB >> 22700428

Transgenic mouse models resistant to diet-induced metabolic disease: is energy balance the key?

Laura A A Gilliam1, P Darrell Neufer.   

Abstract

The prevalence and economic burden of obesity and type 2 diabetes is a driving force for the discovery of molecular targets to improve insulin sensitivity and glycemic control. Here, we review several transgenic mouse models that identify promising targets, ranging from proteins involved in the insulin signaling pathway, alterations of genes affecting energy metabolism, and transcriptional metabolic regulators. Despite the diverse endpoints in each model, a common thread that emerges is the necessity for maintenance of energy balance, suggesting pharmacotherapy must target the development of drugs that decrease energy intake, accelerate energy expenditure in a well controlled manner, or augment natural compensatory responses to positive energy balance.

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Year:  2012        PMID: 22700428      PMCID: PMC3422517          DOI: 10.1124/jpet.112.192146

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  65 in total

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Authors:  Frédéric Picard; Martine Géhin; Jean- Sébastien Annicotte; Stéphane Rocchi; Marie-France Champy; Bert W O'Malley; Pierre Chambon; Johan Auwerx
Journal:  Cell       Date:  2002-12-27       Impact factor: 41.582

2.  Mechanisms by which liver-specific PEPCK knockout mice preserve euglycemia during starvation.

Authors:  Pengxiang She; Shawn C Burgess; Masakazu Shiota; Paul Flakoll; E Patrick Donahue; Craig R Malloy; A Dean Sherry; Mark A Magnuson
Journal:  Diabetes       Date:  2003-07       Impact factor: 9.461

3.  Polymorphisms of the FTO gene are associated with variation in energy intake, but not energy expenditure.

Authors:  John R Speakman; Kellie A Rance; Alexandra M Johnstone
Journal:  Obesity (Silver Spring)       Date:  2008-06-12       Impact factor: 5.002

4.  A 3-year intervention with a Mediterranean diet modified the association between the rs9939609 gene variant in FTO and body weight changes.

Authors:  C Razquin; J A Martinez; M A Martinez-Gonzalez; M Bes-Rastrollo; J Fernández-Crehuet; A Marti
Journal:  Int J Obes (Lond)       Date:  2009-11-17       Impact factor: 5.095

5.  Phosphoenolpyruvate carboxykinase and the synthesis of glyceride-glycerol from pyruvate in adipose tissue.

Authors:  F J Ballard; R W Hanson; G A Leveille
Journal:  J Biol Chem       Date:  1967-06-10       Impact factor: 5.157

Review 6.  Diabetes area participation analysis: a review of companies and targets described in the 2008 - 2010 patent literature.

Authors:  Philip A Carpino; Bryan Goodwin
Journal:  Expert Opin Ther Pat       Date:  2010-12       Impact factor: 6.674

7.  c-Cbl-deficient mice have reduced adiposity, higher energy expenditure, and improved peripheral insulin action.

Authors:  Juan C Molero; Thomas E Jensen; Phil C Withers; Michelle Couzens; Herbert Herzog; Christine B F Thien; Wallace Y Langdon; Ken Walder; Maria A Murphy; David D L Bowtell; David E James; Gregory J Cooney
Journal:  J Clin Invest       Date:  2004-11       Impact factor: 14.808

8.  Adipose overexpression of phosphoenolpyruvate carboxykinase leads to high susceptibility to diet-induced insulin resistance and obesity.

Authors:  Sylvie Franckhauser; Sergio Muñoz; Ivet Elias; Tura Ferre; Fatima Bosch
Journal:  Diabetes       Date:  2006-02       Impact factor: 9.461

Review 9.  The effect of obesity on health outcomes.

Authors:  John B Dixon
Journal:  Mol Cell Endocrinol       Date:  2009-07-21       Impact factor: 4.102

10.  Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.

Authors:  Angelo Scuteri; Serena Sanna; Wei-Min Chen; Manuela Uda; Giuseppe Albai; James Strait; Samer Najjar; Ramaiah Nagaraja; Marco Orrú; Gianluca Usala; Mariano Dei; Sandra Lai; Andrea Maschio; Fabio Busonero; Antonella Mulas; Georg B Ehret; Ashley A Fink; Alan B Weder; Richard S Cooper; Pilar Galan; Aravinda Chakravarti; David Schlessinger; Antonio Cao; Edward Lakatta; Gonçalo R Abecasis
Journal:  PLoS Genet       Date:  2007-07       Impact factor: 5.917

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  4 in total

1.  Induced Cre-mediated knockdown of Brca1 in skeletal muscle reduces mitochondrial respiration and prevents glucose intolerance in adult mice on a high-fat diet.

Authors:  Kathryn C Jackson; Michael D Tarpey; Ana P Valencia; Melissa R Iñigo; Stephen J Pratt; Daniel J Patteson; Joseph M McClung; Richard M Lovering; David M Thomson; Espen E Spangenburg
Journal:  FASEB J       Date:  2018-01-26       Impact factor: 5.191

2.  Genetically increasing flux through β-oxidation in skeletal muscle increases mitochondrial reductive stress and glucose intolerance.

Authors:  Cody D Smith; Chien-Te Lin; Shawna L McMillin; Luke A Weyrauch; Cameron A Schmidt; Cheryl A Smith; Irwin J Kurland; Carol A Witczak; P Darrell Neufer
Journal:  Am J Physiol Endocrinol Metab       Date:  2021-04-05       Impact factor: 4.310

3.  MED13-dependent signaling from the heart confers leanness by enhancing metabolism in adipose tissue and liver.

Authors:  Kedryn K Baskin; Chad E Grueter; Christine M Kusminski; William L Holland; Angie L Bookout; Santosh Satapati; Y Megan Kong; Shawn C Burgess; Craig R Malloy; Philipp E Scherer; Christopher B Newgard; Rhonda Bassel-Duby; Eric N Olson
Journal:  EMBO Mol Med       Date:  2014-12       Impact factor: 12.137

Review 4.  AMPK, insulin resistance, and the metabolic syndrome.

Authors:  Neil B Ruderman; David Carling; Marc Prentki; José M Cacicedo
Journal:  J Clin Invest       Date:  2013-07-01       Impact factor: 14.808

  4 in total

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