Difference between revisions of "Carmona 2009 Int J Obes"
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|authors=Carmona MC, Amigo M, Barcelo-Batllori S, Julia M, Esteban Y, Moreno S, Gomis R | |authors=Carmona MC, Amigo M, Barcelo-Batllori S, Julia M, Esteban Y, Moreno S, Gomis R | ||
|year=2009 | |year=2009 | ||
|journal=Int | |journal=Int J Obes | ||
|abstract=OBJECTIVE: We have recently shown the ''in vivo'' anti-obesity effects of sodium tungstate. In this study, we investigate the in ''vitro'' effects of sodium tungstate on adipocyte differentiation and function. | |abstract=OBJECTIVE: We have recently shown the ''in vivo'' anti-obesity effects of sodium tungstate. In this study, we investigate the in ''vitro'' effects of sodium tungstate on adipocyte differentiation and function. | ||
Revision as of 01:21, 5 April 2012
| Carmona MC, Amigó M, Barceló-Batllori S, Julià M, Esteban Y, Moreno S, Gomis R (2009) Dual effects of sodium tungstate on adipocyte biology: inhibition of adipogenesis and stimulation of cellular oxygen consumption. Int J Obes 33: 534-540. |
Carmona MC, Amigo M, Barcelo-Batllori S, Julia M, Esteban Y, Moreno S, Gomis R (2009) Int J Obes
Abstract: OBJECTIVE: We have recently shown the in vivo anti-obesity effects of sodium tungstate. In this study, we investigate the in vitro effects of sodium tungstate on adipocyte differentiation and function.
METHODS: 3T3-F442A cells were allowed to differentiate in the presence of sodium tungstate, and were analyzed for triglyceride (TG) accumulation, adipocyte differentiation and mitochondrial oxygen consumption.
RESULTS: Sodium tungstate treatment of adipose cells decreased TG accumulation and adipocyte differentiation. Expression of key genes for adipocyte function (aP2, ACC, fatty acid synthase (FAS) and lipoprotein lipase (LPL)) and differentiation (CCAAT enhancer-binding protein (C/EBP)alpha and peroxisome proliferator-activated receptor gamma (PPARgamma)) was reduced by sodium tungstate, whereas C/EBPbeta isoform LIP expression level was increased. TG accumulation and changes in C/EBPbeta expression were partially recovered by inactivating the erk1/2 pathway. Finally, tungstate treatment increased the oxygen consumption of adipose cells without changes in the expression of oxidative genes.
CONCLUSIONS: Sodium tungstate inhibits adipocyte differentiation by promoting the translation of LIP, a master dominant-negative regulator of this process, and regulates the mitochondrial oxygen consumption of adipose cells. These effects contribute to the anti-obesity activity of sodium tungstate and confirm its potential as a powerful alternative for the treatment of obesity. • Keywords: Obesity, Sodium tungstate, 3T3-F442A cells, Oxidative genes
• O2k-Network Lab: ES_Barcelona_Gomis R
Labels:
Preparation: Intact Cell; Cultured; Primary"Intact Cell; Cultured; Primary" is not in the list (Intact organism, Intact organ, Permeabilized cells, Permeabilized tissue, Homogenate, Isolated mitochondria, SMP, Chloroplasts, Enzyme, Oxidase;biochemical oxidation, ...) of allowed values for the "Preparation" property.
Regulation: Respiration; OXPHOS; ETS Capacity"Respiration; OXPHOS; ETS Capacity" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property.
HRR: Oxygraph-2k
