Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction

Aim. To test the potential role of PPARγ in the endocrine abdominal tissue dysfunction induced by feeding normal rats with a fructose rich diet (FRD) during three weeks. Methodology. Adult normal male rats received a standard commercial diet (CD) or FRD, (10% in drinking water) without or with piogl...

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Autores principales: Alzamendi, Ana, Giovambattista, Andrés, García, María Elisa, Rebolledo, Oscar Remigio, Gagliardino, Juan José, Spinedi, Eduardo
Formato: Articulo
Lenguaje:Inglés
Publicado: 2012
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/68072
https://www.hindawi.com/journals/ppar/2012/259093/
Aporte de:
id I19-R120-10915-68072
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Medicina
Microbiología
Adiposidad
Fructosa
fructose rich diet, endocrine abdominal tissue dysfunction
spellingShingle Medicina
Microbiología
Adiposidad
Fructosa
fructose rich diet, endocrine abdominal tissue dysfunction
Alzamendi, Ana
Giovambattista, Andrés
García, María Elisa
Rebolledo, Oscar Remigio
Gagliardino, Juan José
Spinedi, Eduardo
Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction
topic_facet Medicina
Microbiología
Adiposidad
Fructosa
fructose rich diet, endocrine abdominal tissue dysfunction
description Aim. To test the potential role of PPARγ in the endocrine abdominal tissue dysfunction induced by feeding normal rats with a fructose rich diet (FRD) during three weeks. Methodology. Adult normal male rats received a standard commercial diet (CD) or FRD, (10% in drinking water) without or with pioglitazone (PIO) (i.p. 0.25mg/Kg BW/day; CD-PIO and FRD-PIO). Thereafter, we measured circulating metabolic, endocrine, and oxidative stress (OS) markers, abdominal adipose tissue (AAT) mass, leptin (LEP) and plasminogen activator inhibitor-1 (PAI-1) tissue content/expression, and leptin release by isolated adipocytes incubated with different concentrations of insulin. Results. Plasma glucose, insulin, triglyceride, TBARS, LEP, and PAI-1 levels were higher in FRD rats; PIO coadministration fully prevented all these increments. AAT adipocytes from FRD rats were larger, secreted a higher amount of LEP, and displayed decreased sensitivity to insulin stimulation; these effects were significantly ameliorated by PIO. Whereas AAT LEP and PAI-1 (mRNA) concentrations increased significantly in FRD rats, those of insulin-receptor-substrate- (IRS-) 1 and IRS-2 were reduced. PIO coadministration prevented FRD effects on LEP, PAI-1, and IRS-2 (fully) and IRS-1 (partially) mRNAs in AAT. Conclusion. PPARγ would play a relevant role in the development of the FRD-induced metabolicendocrine dysfunction.
format Articulo
Articulo
author Alzamendi, Ana
Giovambattista, Andrés
García, María Elisa
Rebolledo, Oscar Remigio
Gagliardino, Juan José
Spinedi, Eduardo
author_facet Alzamendi, Ana
Giovambattista, Andrés
García, María Elisa
Rebolledo, Oscar Remigio
Gagliardino, Juan José
Spinedi, Eduardo
author_sort Alzamendi, Ana
title Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction
title_short Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction
title_full Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction
title_fullStr Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction
title_full_unstemmed Effect of Pioglitazone on the Fructose-Induced Abdominal Adipose Tissue Dysfunction
title_sort effect of pioglitazone on the fructose-induced abdominal adipose tissue dysfunction
publishDate 2012
url http://sedici.unlp.edu.ar/handle/10915/68072
https://www.hindawi.com/journals/ppar/2012/259093/
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