Literature DB >> 20723946

Functional variability in corticosteroid receptors is a major component of strain differences in fat deposition and metabolic consequences of enriched diets in rat.

Nathalie Marissal-Arvy1, Allan Langlois, Claudine Tridon, Pierre Mormede.   

Abstract

We aimed to distinguish mineralocorticoid (MR) from glucocorticoid receptor (GR) actions in the nutritional differences between the Fischer 344 (F344) and LOU/C (LOU) rat strains. The decrease of urinary Na+/K+ ratio induced via MR activation by aldosterone and decrease of circulating lymphocyte counts exerted via GR activation by dexamethasone revealed a higher efficiency of corticosteroid receptor in LOU than in F344 rats. Afterward, we submitted F344 and LOU male rats to adrenalectomy and to substitution treatments with agonists of MR or GR under 3 successive diets--standard, free choice between chow and pork lard, and an imposed high-fat/high-sugar diet--to explore the involvement of the interactions between activation of corticosteroid receptors and diet on food intake, body composition, and metabolic blood parameters in these rats. Lastly, we measured energy expenditure and substrate oxidization in various experimental conditions in LOU and F344 rats by indirect calorimetry. In LOU rats, we showed greater basal and MR-induced energy expenditure, diet-induced thermogenesis, and lipid oxidization. We showed that the F344 rat strain constitutes a relevant model of the unfavorable effects exerted by glucocorticoids via GR on food preference for high-calorie diets, abdominal fat deposition, diabetes, and other deleterious consequences of visceral obesity. Contrary to F344 rats, the LOU rats did not exhibit the expected visceral fat deposition linked to GR activation. This strain is therefore a relevant model of resistance to diet-induced obesity and to the deleterious effects exerted by glucocorticoids on metabolism.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20723946     DOI: 10.1016/j.metabol.2010.07.005

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  4 in total

1.  Biometric evidence of diet-induced obesity in Lew/Crl rats.

Authors:  Chad W Schmiedt; Robert M Gogal; Stephen B Harvey; Amanda K Torres; Carla L Jarrett; Elizabeth W Uhl; David J Hurley
Journal:  Comp Med       Date:  2011-04       Impact factor: 0.982

2.  Diet-induced impaired glucose tolerance and gestational diabetes in the dog.

Authors:  Mary Courtney Moore; Renuka Menon; Katie C Coate; Maureen Gannon; Marta S Smith; Ben Farmer; Phillip E Williams
Journal:  J Appl Physiol (1985)       Date:  2010-11-18

3.  Transcriptional signatures of regulatory and toxic responses to benzo-[a]-pyrene exposure.

Authors:  Jacob J Michaelson; Saskia Trump; Susanne Rudzok; Carolin Gräbsch; Danielle J Madureira; Franziska Dautel; Juliane Mai; Sabine Attinger; Kristin Schirmer; Martin von Bergen; Irina Lehmann; Andreas Beyer
Journal:  BMC Genomics       Date:  2011-10-13       Impact factor: 3.969

4.  Characterization of clinical and genetic risk factors associated with dyslipidemia after kidney transplantation.

Authors:  Kazuyuki Numakura; Hideaki Kagaya; Ryohei Yamamoto; Naoki Komine; Mitsuru Saito; Tsuruta Hiroshi; Susumu Akihama; Takamitsu Inoue; Shintaro Narita; Norihiko Tsuchiya; Tomonori Habuchi; Takenori Niioka; Masatomo Miura; Shigeru Satoh
Journal:  Dis Markers       Date:  2015-04-06       Impact factor: 3.434

  4 in total

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