Literature DB >> 9467418

DHEA treatment reduces fat accumulation and protects against insulin resistance in male rats.

D H Han1, P A Hansen, M M Chen, J O Holloszy.   

Abstract

The purpose of this study was to determine whether administration of dehydroepiandrosterone (DHEA) protects male rats against the accumulation of body fat the development of insulin resistance with advancing age. We found that supplementation of the diet with 0.3% DHEA between the ages of 5 months and approximately 25 months resulted in a significantly lower final body weight (DHEA, 593 +/- 18 g vs control, 668 +/- 12 g, p < 0.02), despite no decrease in food intake. Lean body mass was unaffected by the DHEA, and the lower body weight was due to a approximately 25% reduction in body fat. The rate of glucose disposal during a euglycemic, hyperinsulinemic clamp was 30% higher in the DHEA group than in the sedentary controls due to a greater insulin responsiveness. The DHEA administration was as effective in reducing body fat content and maintaining insulin responsiveness as exercise in the form of voluntary wheel running. The DHEA had no significant effect on muscle GLUT4 content. A preliminary experiment provided evidence suggesting that muscle insulin signaling, as reflected in binding of phosphatidylinositol 3-kinase to the insulin receptor substrate-1, was enhanced in the DHEA-treated and wheel running groups as compared to controls. These results provide evidence that DHEA, like exercise, protects against excess fat accumulation and development of insulin resistance in rats.

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Year:  1998        PMID: 9467418     DOI: 10.1093/gerona/53a.1.b19

Source DB:  PubMed          Journal:  J Gerontol A Biol Sci Med Sci        ISSN: 1079-5006            Impact factor:   6.053


  13 in total

1.  Dehydroepiandrosterone protects against oxidative stress-induced endothelial dysfunction in ovariectomized rats.

Authors:  João Paulo Gabriel Camporez; Eliana Hiromi Akamine; Ana Paula Davel; Celso Rodrigues Franci; Luciana Venturini Rossoni; Carla Roberta de Oliveira Carvalho
Journal:  J Physiol       Date:  2011-03-14       Impact factor: 5.182

2.  Dynamic Glucose Disposal is Driven by Reduced Endogenous Glucose Production in Response to Voluntary Wheel Running: A Stable Isotope Approach.

Authors:  Timothy D Allerton; Greg Kowalski; Hardy Hang; Jacqueline Stephens
Journal:  Am J Physiol Endocrinol Metab       Date:  2020-04-28       Impact factor: 4.310

Review 3.  Exercise Promotes Healthy Aging of Skeletal Muscle.

Authors:  Gregory D Cartee; Russell T Hepple; Marcas M Bamman; Juleen R Zierath
Journal:  Cell Metab       Date:  2016-06-14       Impact factor: 27.287

4.  A family-based association study identified CYP17 as a candidate gene for obesity susceptibility in Caucasians.

Authors:  H Yan; Y Guo; T-L Yang; L-J Zhao; H-W Deng
Journal:  Genet Mol Res       Date:  2012-08-06

Review 5.  Dehydroepiandrosterone on metabolism and the cardiovascular system in the postmenopausal period.

Authors:  Caio Jordão Teixeira; Katherine Veras; Carla Roberta de Oliveira Carvalho
Journal:  J Mol Med (Berl)       Date:  2019-11-12       Impact factor: 4.599

6.  DHEA administration and exercise training improves insulin resistance in obese rats.

Authors:  Koji Sato; Motoyuki Iemitsu; Katsuji Aizawa; Noboru Mesaki; Ryuichi Ajisaka; Satoshi Fujita
Journal:  Nutr Metab (Lond)       Date:  2012-05-30       Impact factor: 4.169

7.  Dehydroepiandrosterone regulates insulin-like growth factor-1 system in adult rat hypothalamus.

Authors:  Maria Flavia Ribeiro; Luis Miguel Garcia-Segura
Journal:  Endocrine       Date:  2002-03       Impact factor: 3.925

8.  Dehydroepiandrosterone (DHEA) replacement decreases insulin resistance and lowers inflammatory cytokines in aging humans.

Authors:  Edward P Weiss; Dennis T Villareal; Luigi Fontana; Dong-Ho Han; John O Holloszy
Journal:  Aging (Albany NY)       Date:  2011-05       Impact factor: 5.682

9.  Dehydroepiandrosterone (DHEA) Feeding Protects Liver Steatosis in Obese Breast Cancer Rat Model.

Authors:  Reza Hakkak; Andrea Bell; Soheila Korourian
Journal:  Sci Pharm       Date:  2017-03-20

10.  17α-Estradiol Modulates IGF1 and Hepatic Gene Expression in a Sex-Specific Manner.

Authors:  Silvana Sidhom; Augusto Schneider; Yimin Fang; Samuel McFadden; Justin Darcy; Roshini Sathiaseelan; Allyson K Palmer; Frederik J Steyn; Johannes Grillari; John J Kopchick; Andrzej Bartke; Shadab Siddiqi; Michal M Masternak; Michael B Stout
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2021-04-30       Impact factor: 6.053

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