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1.
Lipids ; 47(8): 773-80, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22684889

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 (~70 %) as well as in BAT and EAT (~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.


Assuntos
Tecido Adiposo Marrom/metabolismo , Glicerídeos/biossíntese , Glicerol/metabolismo , Glicólise , Fígado/metabolismo , Tecido Adiposo Branco/metabolismo , Animais , Jejum , Glicerofosfatos/biossíntese , Masculino , Ratos , Ratos Wistar
2.
Metabolism ; 61(10): 1473-85, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22592131

RESUMO

The aim of the present study was to investigate the participation of the sympathetic nervous system (SNS) in the control of glycerol-3-P (G3P) generating pathways in white adipose tissue (WAT) of rats in three situations in which the plasma insulin levels are low. WAT from 48 h fasted animals, 3 day-streptozotocin diabetic animals and high-protein, carbohydrate-free (HP) diet-fed rats was surgical denervated and the G3P generation pathways were evaluated. Food deprivation, diabetes and the HP diet provoke a marked decrease in the rate of glucose uptake and glycerokinase (GyK) activity, but a significant increase in the glyceroneogenesis, estimated by the phosphoenolpyruvate carboxykinase (PEPCK) activity and the incorporation of 1-[(14)C]-pyruvate into glycerol-TAG. The denervation provokes a reduction (~70%) in the NE content of WAT in fasted, diabetic and HP diet-fed rats. The denervation induced an increase in WAT glucose uptake of fed, fasted, diabetic and HP diet-fed rats (40%, 60%, 3.2 fold and 35%, respectively). TAG-glycerol synthesis from pyruvate was reduced by denervation in adipocytes of fed (58%) and fasted (36%), saline-treated (58%) and diabetic (23%), and HP diet-fed rats (11%). In these same groups the denervation reduced the PEPCK mRNA expression (75%-95%) and the PEPCK activity (35%-60%). The denervation caused a ~35% decrease in GyK activity of control rats and a further ~35% reduction in the already low enzyme activity of fasted, diabetic and HP diet-fed rats. These data suggest that the SNS plays an important role in modulating G3P generating pathways in WAT, in situations where insulin levels are low.


Assuntos
Tecido Adiposo Branco/metabolismo , Diabetes Mellitus Experimental/metabolismo , Proteínas Alimentares/administração & dosagem , Jejum/metabolismo , Glicerofosfatos/biossíntese , Sistema Nervoso Simpático/fisiologia , Animais , Glicemia/análise , Gluconeogênese , Glucose/metabolismo , Glicerol Quinase/metabolismo , Insulina/sangue , Masculino , Norepinefrina/metabolismo , Ratos , Ratos Wistar , Estreptozocina
3.
Can J Physiol Pharmacol ; 86(7): 416-23, 2008 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18641690

RESUMO

In vivo fatty acid synthesis and the pathways of glycerol-3-phosphate (G3P) production were investigated in brown adipose tissue (BAT) from rats fed a cafeteria diet for 3 weeks. In spite of BAT activation, the diet promoted an increase in the carcass fatty acid content. Plasma insulin levels were markedly increased in cafeteria diet-fed rats. Two insulin-sensitive processes, in vivo fatty acid synthesis and in vivo glucose uptake (which was used to evaluate G3P generation via glycolysis) were increased in BAT from rats fed the cafeteria diet. Direct glycerol phosphorylation, evaluated by glycerokinase (GyK) activity and incorporation of [U-14C]glycerol into triacylglycerol (TAG)-glycerol, was also markedly increased in BAT from these rats. In contrast, the cafeteria diet induced a marked reduction of BAT glyceroneogenesis, evaluated by phosphoenolpyruvate carboxykinase-C activity and incorporation of [1-14C]pyruvate into TAG-glycerol. BAT denervation resulted in an approximately 50% reduction of GyK activity, but did not significantly affect BAT in vivo fatty acid synthesis, in vivo glucose uptake, or glyceroneogenesis. The data suggest that the supply of G3P for BAT TAG synthesis can be adjusted independently from the sympathetic nervous system and solely by reciprocal changes in the generation of G3P via glycolysis and via glyceroneogenesis, with no participation of direct phosphorylation of glycerol by GyK.


Assuntos
Tecido Adiposo Marrom/metabolismo , Ácidos Graxos/biossíntese , Glicerofosfatos/biossíntese , Animais , Western Blotting , Composição Corporal/fisiologia , Denervação , Dieta , Glucose/metabolismo , Glicerol/metabolismo , Guanosina Difosfato/metabolismo , Insulina/metabolismo , Canais Iônicos/metabolismo , Lipase Lipoproteica/efeitos dos fármacos , Lipase Lipoproteica/metabolismo , Masculino , Mitocôndrias/metabolismo , Proteínas Mitocondriais/metabolismo , Norepinefrina/metabolismo , Ácido Pirúvico/metabolismo , Ratos , Ratos Wistar , Triglicerídeos/metabolismo , Proteína Desacopladora 1
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