IMIBIO-SL   20937
INSTITUTO MULTIDISCIPLINARIO DE INVESTIGACIONES BIOLOGICAS DE SAN LUIS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Adjustment of a Western Diet-Induced Obesity Mouse Model for Immunometabolic Studies
Autor/es:
MARIA CECILIA DELLA VEDOVA1,2, MARCOS D MUÑOZ1,3, MARTIN RINALDI TOSI1, SILVINA GARCIA1, SANDRA E GOMEZ MEJIBA1,3, AND DARIO C RAMIRE
Lugar:
Seattle
Reunión:
Congreso; SFRBM`s; 2014
Institución organizadora:
Sociedad de Radicales Libres
Resumen:
Adjustment of a Western Diet-Induced Obesity Mouse
Model for Immunometabolic Studies
Maria Cecilia Della-Vedova1,2, Marcos D Muñoz1,3, Martin Rinaldi
Tosi1, Silvina Garcia1, Sandra E Gomez Mejiba1,3, And Dario C
Ramirez1,2
1Lab. Exp. Med. & Ther., IMIBIO-SL, Nat. Bureau of Sci. & Tech.
Res. (CONICET), Argentina, 2Dept. of Biochemstry, School of
Chemistry, Biochemistry & Pharmacy-UNSL, Argentina, 3Dept. of
Nutrition, School of Health Sciences-UNSL, Argentina
The increase in the consumption of chicken fat and fructose,
which are cheaper ingredients for foods, coincides with an
increase in the prevalence of obesity. Due to the world known
difficulties Argentinean scientists to import commercially available
diets herein we aimed at developing a mouse model of dietinduced
obesity that uses local ingredients and that also
highlights the main features of human obesity, including adiposity
and insulin resistance (IR). To accomplish our aim we fed male 6
week-old B6 mice for 16 weeks with a rodent chow diet containing
either 4 (LFD) or 22% (HFD) p/p chicken fat and water containing
or not 10% p/v fructose (F). This experimental design resulted in 4
experimental groups: high fat diet plus water supplemented with
10% fructose (HFD+F); HFD only, low fat diet only (LFD) and
LFD+F. The consumption of food and drink as well as body
weight gain were measured throughout the experiment. At the
end of the feeding period adiposity index, fasten glucemia and IR
(glucose tolerance test) were measured. The results (mean
valuesSEM) showed that compared to mouse from other groups
those from the HFD+F group: i) gained more weight
(HFD+F:29.41±1.07 vs HFD:27.40.93; LFD+F:25.50.70;
LFD:24.770.60); ii) have heavier epididymal fat-pads thus larger
adiposity index ([epididymal fat(g)/body weight] x100
(HFD+F:4.38±1.36 vs HFD:3.34±0.27; LFD+F:2.12±0.17;
LFD:1.43±0.10); iii) like the LFD+F this group drank more water
(ml/mouse/day, HFD+F:8.7±0.46 and LFD+F:7.43±0.47 vs
HFD:4.94±0.56 and LFD:4.52±0.70); iv) ate less (mg/mouse/day,
HFD+F:2.16±0.07 vs HFD:2.55±0.03; LFD+F:2.35±0.06;
LFD:2.95±0.07); v) have more fasten glucemia (HFD+F:27150
vs HFD:23350; LFD+F:212±44; LFD:18345); and vi) are more
IR (AUC as arbitrary units, HFD+F:14468937 vs
HFD:12000450; LFD+F:940570; LFD:8490930). A mouse
model of diet-induced obesity, which will allow us to compare the
contribution of fructose and fat consumption on
immunometabolism has been developed and will provide a tissue
repository to increase the efficiency of animal usage in projects
aimed at dissecting obesity-associated abnormalities. Supported
by PROICO-2-3214(FQBYF)/PROICO10-0414(FCS)