Metabolic syndrome signs in Wistar rats submitted to different high-fructose ingestion protocols

In search of an adequate model for the human metabolic syndrome, the metabolic characteristics of Wistar rats were analysed after being submitted to different protocols of high fructose ingestion. First, two adult rat groups (aged 90 d) were studied: a control group (C1; n 6) received regular rodent...

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Detalles Bibliográficos
Autores: de Moura, Rodrigo Ferreira [UNESP], Ribeiro, Carla [UNESP], de Oliveira, Juliana Aparecida, Stevanato, Eliane, de Mello, Maria Alice Rostom [UNESP]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2009
País:Brasil
Institución:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/71087
Acceso en línea:http://dx.doi.org/10.1017/S0007114508066774
http://hdl.handle.net/11449/71087
Access Level:acceso abierto
Palabra clave:Body fat
Fructose
Insulin sensitivity
Metabolic syndrome
cholesterol
drinking water
fructose
high density lipoprotein cholesterol
lipid
low density lipoprotein cholesterol
triacylglycerol
age distribution
animal experiment
animal model
body fat
carbohydrate intake
cholesterol blood level
controlled study
experimental rat
food analysis
food composition
fructose metabolism
glucose tolerance
hypertriglyceridemia
insulin sensitivity
lipid blood level
male
metabolic balance
metabolic syndrome X
nonhuman
rat
triacylglycerol blood level
Wistar rat
Animals
Blood Glucose
Cholesterol
Disease Models, Animal
Glucose Tolerance Test
Insulin
Insulin Resistance
Male
Metabolic Syndrome X
Rats
Rats, Wistar
Weight Gain
Animalia
Rattus
Rattus norvegicus
Rodentia
Descripción
Sumario:In search of an adequate model for the human metabolic syndrome, the metabolic characteristics of Wistar rats were analysed after being submitted to different protocols of high fructose ingestion. First, two adult rat groups (aged 90 d) were studied: a control group (C1; n 6) received regular rodent chow (Labina, Purina) and a fructose group (F1; n 6) was fed on regular rodent chow. Fructose was administered as a 10 % solution in drinking water. Second, two adult rat groups (aged 90 d) were evaluated: a control group (C2; n 6) was fed on a balanced diet (AIN-93G) and a fructose group (F2; n 6) was fed on a purified 60 % fructose diet. Finally, two young rat groups (aged 28 d) were analysed: a control group (C3; n 6) was fed on the AIN-93G diet and a fructose group (F3; n 6) was fed on a 60 % fructose diet. After 4-8 weeks, the animals were evaluated. Glucose tolerance, peripheral insulin sensitivity, blood lipid profile and body fat were analysed. In the fructose groups F2 and F3 glucose tolerance and insulin sensitivity were lower, while triacylglycerolaemia was higher than the respective controls C2 and C3 (P < 0.05). Blood total cholesterol, HDL and LDL as well as body fat showed change only in the second protocol. In conclusion, high fructose intake is more effective at producing the signs of the metabolic syndrome in adult than in young Wistar rats. Additionally, diet seems to be a more effective way of fructose administration than drinking water.