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J Nutr Biochem ; 81: 108383, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32388252

RESUMO

Nutritional restriction early in life followed by catch-up growth has been associated with increased risk of metabolic syndrome in adulthood. To elucidate whether altered gut colonization underlies the mechanisms responsible of this predisposition gut microbiome was studied before or afterwards catch-up growth. Offspring of dams fed ad libitum (C) or undernourished during pregnancy and suckling (U), were weaned onto high-fat diet (HFD) for 22 weeks (CHF and UHF, respectively) or continued on their diet. HF-feeding induced glucose intolerance (P<.05), insulin resistance (P<.001), and white adipose tissue inflammation (P<.001) in UHF rats compared to CHF. Analyses of gut microbial composition before catch-up growth revealed reduced F/B ratio and significant expansion of the mucolytic genera Akkermansia (P<.05) and Desulfovibrio (P<.05) in U pups. Although relative abundance of Akkermansia remained elevated to adulthood in U rats, HFD normalized its levels to C and CHF. Food-restriction increased intestinal permeability causing disorganization on the tight-junction proteins of colonic epithelium, Zonula Occludens-1 (ZO-1) and occludin, and reducing the mucus thickness layer in U adult rats. The levels of ZO-1 and occludin were not recovered in U rats after HF-feeding. This event was correlated with increased circulating levels of bacterial lipopolysaccharides in both U and UHF adult rats. Even more, serum lipopolysaccharides were already elevated in U rats compared to C group (P<.001) at weaning. Thus, gut dysbiosis and chronic endotoxemia observed in U rats, even before catch-up growth, might anticipate a pro-inflammatory milieu promoting metabolic diseases when fed hyperlipidic diets.


Assuntos
Disbiose/metabolismo , Microbioma Gastrointestinal , Desnutrição/metabolismo , Síndrome Metabólica/metabolismo , Animais , Colo/metabolismo , Dieta Hiperlipídica/efeitos adversos , Endotoxemia/metabolismo , Fezes/microbiologia , Feminino , Intolerância à Glucose/etiologia , Intolerância à Glucose/metabolismo , Humanos , Inflamação/etiologia , Inflamação/metabolismo , Resistência à Insulina , Mucosa Intestinal/metabolismo , Lipopolissacarídeos/sangue , Masculino , Gravidez , Ratos
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