Day‐restricted feeding during pregnancy and lactation programs glucose intolerance and impaired insulin secretion in male rat offspring

后代 哺乳期 内分泌学 内科学 怀孕 生物 胰岛素抵抗 碳水化合物代谢 胰岛素 医学 遗传学
作者
Juliana de Almeida Faria,Thiago Matos Ferreira de Araújo,Rubia Isler Mancuso,Jessica Meulman,Danilo da Silva Ferreira,Thiago M. Batista,Jean Franciesco Vettorazzi,P. M. R. da Silva,Sandra Rodrigues,Andrezza Pinheiro Bezerra de Menezes Kinote,Everardo M. Carneiro,Silvana Bordin,Gabriel Forato Anhê
出处
期刊:Acta Physiologica [Wiley]
卷期号:217 (3): 240-253 被引量:17
标识
DOI:10.1111/apha.12684
摘要

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.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.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.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.
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