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饮食干预可挽救母体肥胖诱导的子代行为缺陷和神经炎症。

Dietary intervention rescues maternal obesity induced behavior deficits and neuroinflammation in offspring.

作者信息

Kang Silvia S, Kurti Aishe, Fair Damien A, Fryer John D

出版信息

J Neuroinflammation. 2014 Sep 12;11:156. doi: 10.1186/s12974-014-0156-9.

Abstract

Obesity induces a low-grade inflammatory state and has been associated with behavioral and cognitive alterations. Importantly, maternal environmental insults can adversely impact subsequent offspring behavior and have been linked with neurodevelopmental disorders such as autism spectrum disorder (ASD) and attention deficit hyperactivity disorder (AHDH). It is unknown if maternal obesity significantly alters offspring sociability, a key ASD feature, and if altering maternal diet will provide an efficacious intervention paradigm for behavioral deficits. Here we investigated the impact of maternal high fat diet (HFD) and maternal dietary intervention during lactation on offspring behavior and brain inflammation in mice. We found that maternal HFD increased anxiety and decreased sociability in female offspring. Additionally, female offspring from HFD-fed dams also exhibited increased brain IL-1β and TNFα and microglial activation. Importantly, maternal dietary intervention during lactation was sufficient to alleviate social deficits and brain inflammation. Maternal obesity during gestation alone was sufficient to increase hyperactivity in male offspring, a phenotype that was not ameliorated by dietary intervention. These data suggest that maternal HFD acts as a prenatal/perinatal insult that significantly impacts offspring behavior and inflammation and that dietary intervention during lactation may be an easily translatable, efficacious intervention to offset some of these manifestations.

摘要

肥胖会引发一种低度炎症状态,并与行为和认知改变有关。重要的是,母体环境损伤会对后代随后的行为产生不利影响,并与自闭症谱系障碍(ASD)和注意力缺陷多动障碍(AHDH)等神经发育障碍有关。尚不清楚母体肥胖是否会显著改变后代的社交能力(这是ASD的一个关键特征),以及改变母体饮食是否会为行为缺陷提供一种有效的干预模式。在此,我们研究了母体高脂饮食(HFD)以及哺乳期母体饮食干预对小鼠后代行为和脑部炎症的影响。我们发现母体HFD会增加雌性后代的焦虑并降低其社交能力。此外,来自喂食HFD的母鼠的雌性后代还表现出脑部白细胞介素-1β(IL-1β)和肿瘤坏死因子α(TNFα)增加以及小胶质细胞活化。重要的是,哺乳期的母体饮食干预足以缓解社交缺陷和脑部炎症。仅孕期的母体肥胖就足以增加雄性后代的多动,这种表型不会因饮食干预而改善。这些数据表明,母体HFD作为一种产前/围产期损伤,会显著影响后代行为和炎症,并且哺乳期的饮食干预可能是一种易于转化的有效干预措施,以抵消其中一些表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0717/4172780/ed446665b5e7/12974_2014_156_Fig1_HTML.jpg

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