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Visceral adiposity influences glucose and glycogen metabolism in control and hyperlipidic-fed animals.

Authors :
de Souza, Danielle Kaiser
de Souza, Fabiana A.
de Fraga, Luciano Stürmer
Konrad, Signorá Peres
Bello-Klein, Adriane
Martins da Silva, Roselis Silveira
Kucharski, Luiz Carlos R.
Source :
Nutrición Hospitalaria. mar/abr2013, Vol. 28 Issue 2, p545-552. 8p.
Publication Year :
2013

Abstract

Introduction: Evidences suggest that fat intake, visceral obesity and intracellular lipids are related to insulin impairment. Objective: The objective of the present paper was correlate visceral obesity and metabolic alterations in control (CTR) and hyperlipidic cafeteria diet (CFT) fed animals. Methods: After 6 months of diet treatment, liver and muscle of the male rats were utilized to determined glucose uptake and glycogen metabolism after administration of 0.4I U/kg insulin in vivo, and correlate the visceral adiposity to these two parameters. Results: Ample range of physiologic answers to body composition in metabolic profile of the both diets was found. No differences were found in glycemia and triacylglycerol after insulin action in both groups, however CFT group accumulated higher adiposity, mostly visceral fat, and showed lower glycogen content in the liver. We also found an inverse correlation between visceral adiposity and glucose uptake and a decrease of the glycogen synthase active form in the liver. CTR animals demonstrated an inverse correlation between glucose uptake and visceral adiposity in the muscle. Discussion and conclusion: It was observed a variability of metabolic alterations in animals which can be related to degree of accumulation of abdominal adiposity and ingestion of diet fats. Further studies will be required to clarify the reasons for the observed liver alterations in CFT and muscle alterations in CTR animals. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02121611
Volume :
28
Issue :
2
Database :
Academic Search Index
Journal :
Nutrición Hospitalaria
Publication Type :
Academic Journal
Accession number :
86722538
Full Text :
https://doi.org/10.3305/nh.2013.28.2.61