Increased Glyceride-Glycerol Synthesis in Liver and Brown Adipose Tissue of Rat: In-Vivo Contribution of Glycolysis and Glyceroneogenesis


Autoria(s): Chaves, Valeria E.; Frasson, Danubia; Garofalo, Maria A. R.; Navegantes, Luiz C. C.; Migliorini, Renato H.; Kettelhut, Isis C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

30/10/2013

30/10/2013

2012

Resumo

We have previously shown that a high-protein, carbohydrate-free diet can decrease the production of glycerol-3-phosphate (G3P) from glucose and increase glyceroneogenesis in both brown (BAT) and epididymal (EAT) adipose tissue. Here, we utilized an in-vivo approach to examine the hypothesis that there is reciprocal regulation in the G3P synthesis from glucose (via glycolysis) and glyceroneogenesis in BAT, EAT and liver of fasted rats and cafeteria diet-fed rats. Glyceroneogenesis played a prominent role in the generation of G3P in the liver (similar to 70 %) as well as in BAT and EAT (similar to 80 %) in controls rats. The cafeteria diet induced an increase in the total glyceride-glycerol synthesis and G3P synthesis from glucose and a decrease in glyceroneogenesis in BAT; this diet did not affect either the total glyceride-glycerol synthesis or G3P generation from glyceroneogenesis or glycolysis in the liver or EAT. Fasting induced an increase in total glyceride-glycerol synthesis and glyceroneogenesis and a decrease in G3P synthesis from glucose in the liver but did not affect either the total glyceride-glycerol synthesis or G3P synthesis from glyceroneogenesis in BAT and EAT, despite a reduction in glycolysis in these tissues. These data demonstrate that reciprocal changes in the G3P generation from glucose and from glyceroneogenesis in the rat liver and BAT occur only when the synthesis of glycerides-glycerol is increased. Further, our data suggest that this increase may be essential for the systemic recycling of fatty acids by the liver from fasted rats and for the maintenance of the thermogenic capacity of BAT from cafeteria diet-fed rats.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Pesquisa (CNPq)

Conselho Nacional de Pesquisa (CNPq)

Identificador

LIPIDS, HEIDELBERG, v. 47, n. 8, supl. 1, Part 3, pp. 773-780, AUG, 2012

0024-4201

http://www.producao.usp.br/handle/BDPI/36940

10.1007/s11745-012-3683-0

http://dx.doi.org/10.1007/s11745-012-3683-0

Idioma(s)

eng

Publicador

SPRINGER HEIDELBERG

HEIDELBERG

Relação

LIPIDS

Direitos

closedAccess

Copyright SPRINGER HEIDELBERG

Palavras-Chave #GLYCERONEOGENESIS #GLYCEROL-3-PHOSPHATE #GLYCOLYSIS #PHOSPHOENOLPYRUVATE CARBOXYKINASE #EPIDIDYMAL ADIPOSE TISSUE #BROWN ADIPOSE TISSUE #LIVER #CARBOHYDRATE-FREE DIET #CARBOXYKINASE GENE-EXPRESSION #FATTY-ACID SYNTHESIS #HIGH-PROTEIN #PHOSPHOENOLPYRUVATE CARBOXYKINASE #CAFETERIA DIET #GLUCOSE-UPTAKE #LIPOGENESIS #FLUX #GLYCEROL-3-PHOSPHATE #BIOCHEMISTRY & MOLECULAR BIOLOGY #NUTRITION & DIETETICS
Tipo

article

original article

publishedVersion