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Acta Physiol (Oxf) ; 217(3): 240-53, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-27029505

RESUMO

AIM: The maternal environment during pregnancy and lactation plays a determining role in programming energy metabolism in offspring. Among a myriad of maternal factors, disruptions in the light/dark cycle during pregnancy can program glucose intolerance in offspring. Out-of-phase feeding has recently been reported to influence metabolism in adult humans and rodents; however, it is not known whether this environmental factor impacts offspring metabolism when applied during pregnancy and lactation. This study aims to determine whether maternal day-restricted feeding (DF) influences energy metabolism in offspring. METHODS: Pregnant and lactating Wistar rats were subjected to ad libitum (AL) or DF during pregnancy and lactation. The offspring born to the AL and DF dams were intra- and interfostered, which resulted in 4 group types. RESULTS: The male offspring born to and breastfed by the DF dams (DF/DF off) were glucose intolerant, but without parallel insulin resistance as adults. Experiments with isolated pancreatic islets demonstrated that the male DF/DF off rats had reduced insulin secretion with no parallel disruption in calcium handling. However, this reduction in insulin secretion was accompanied by increased miRNA-29a and miRNA34a expression and decreased syntaxin 1a protein levels. CONCLUSION: We conclude that out-of-phase feeding during pregnancy and lactation can lead to glucose intolerance in male offspring, which is caused by a disruption in insulin secretion capacity. This metabolic programming is possibly caused by mechanisms dependent on miRNA modulation of syntaxin 1a.


Assuntos
Restrição Calórica/efeitos adversos , Insulina/metabolismo , Lactação/fisiologia , Prenhez/metabolismo , Animais , Cálcio/metabolismo , Metabolismo Energético/fisiologia , Feminino , Intolerância à Glucose/metabolismo , Técnicas In Vitro , Secreção de Insulina , Ilhotas Pancreáticas/metabolismo , Masculino , MicroRNAs/biossíntese , MicroRNAs/genética , NADP/metabolismo , Gravidez , Ratos , Ratos Wistar , Sintaxina 1/biossíntese , Sintaxina 1/genética
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