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Time sequence of the intensification of the liver glucose production induced by high-fat diet in mice.

Authors :
Obici S
Tavoni TM
Barrena HC
Curi R
Bazotte RB
Source :
Cell biochemistry and function [Cell Biochem Funct] 2012 Jun; Vol. 30 (4), pp. 335-9. Date of Electronic Publication: 2012 Feb 07.
Publication Year :
2012

Abstract

It is well established that the development of insulin resistance shows a temporal sequence in different organs and tissues. Moreover, considering that the main aspect of insulin resistance in liver is a process of glucose overproduction from gluconeogenesis, we investigated if this metabolic change also shows temporal sequence. For this purpose, a well-established experimental model of insulin resistance induced by high-fat diet (HFD) was used. The mice received HFD (HFD group) or standard diet (COG group) for 1, 7, 14 or 56 days. The HFD group showed increased (P < 0.05 versus COG) epididymal, retroperitoneal and inguinal fat weight from days 1 to 56. In agreement with these results, the HFD group also showed higher body weight (P < 0.05 versus COG) from days 7 to 56. Moreover, the changes induced by HFD on liver gluconeogenesis were progressive because the increment (P < 0.05 versus COG) in glucose production from l-lactate, glycerol, l-alanine and l-glutamine occurred 7, 14, 56 and 56 days after the introduction of the HFD schedule, respectively. Furthermore, glycaemia and cholesterolemia increased (P < 0.05 versus COG) 14 days after starting the HFD schedule. Taken together, the results suggest that the intensification of liver gluconeogenesis induced by an HFD is not a synchronous 'all-or-nothing process' but is specific for each gluconeogenic substrate and is integrated in a temporal manner with the progressive augmentation of fasting glycaemia.<br /> (Copyright © 2012 John Wiley & Sons, Ltd.)

Details

Language :
English
ISSN :
1099-0844
Volume :
30
Issue :
4
Database :
MEDLINE
Journal :
Cell biochemistry and function
Publication Type :
Academic Journal
Accession number :
22315157
Full Text :
https://doi.org/10.1002/cbf.2809