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生酮饮食可改善自闭症谱系障碍母体免疫激活模型中的行为。

Ketogenic diet improves behaviors in a maternal immune activation model of autism spectrum disorder.

作者信息

Ruskin David N, Murphy Michelle I, Slade Sierra L, Masino Susan A

机构信息

Department of Psychology, Neuroscience Program, Trinity College, Hartford, CT, United States of America.

出版信息

PLoS One. 2017 Feb 6;12(2):e0171643. doi: 10.1371/journal.pone.0171643. eCollection 2017.

Abstract

Prenatal factors influence autism spectrum disorder (ASD) incidence in children and can increase ASD symptoms in offspring of animal models. These may include maternal immune activation (MIA) due to viral or bacterial infection during the first trimesters. Unfortunately, regardless of ASD etiology, existing drugs are poorly effective against core symptoms. For nearly a century a ketogenic diet (KD) has been used to treat seizures, and recent insights into mechanisms of ASD and a growing recognition that immune/inflammatory conditions exacerbate ASD risk has increased interest in KD as a treatment for ASD. Here we studied the effects of KD on core ASD symptoms in offspring exposed to MIA. To produce MIA, pregnant C57Bl/6 mice were injected with the viral mimic polyinosinic-polycytidylic acid; after weaning offspring were fed KD or control diet for three weeks. Consistent with an ASD phenotype of a higher incidence in males, control diet-fed MIA male offspring were not social and exhibited high levels of repetitive self-directed behaviors; female offspring were unaffected. However, KD feeding partially or completely reversed all MIA-induced behavioral abnormalities in males; it had no effect on behavior in females. KD-induced metabolic changes of reduced blood glucose and elevated blood ketones were quantified in offspring of both sexes. Prior work from our laboratory and others demonstrate KDs improve relevant behaviors in several ASD models, and here we demonstrate clear benefits of KD in the MIA model of ASD. Together these studies suggest a broad utility for metabolic therapy in improving core ASD symptoms, and support further research to develop and apply ketogenic and/or metabolic strategies in patients with ASD.

摘要

产前因素会影响儿童自闭症谱系障碍(ASD)的发病率,并会加重动物模型后代的ASD症状。这些因素可能包括孕期头三个月因病毒或细菌感染导致的母体免疫激活(MIA)。遗憾的是,无论ASD的病因如何,现有药物对核心症状的疗效都很差。近一个世纪以来,生酮饮食(KD)一直被用于治疗癫痫,最近对ASD发病机制的深入了解以及越来越多的人认识到免疫/炎症状况会加剧ASD风险,这使得人们对KD作为ASD治疗方法的兴趣增加。在此,我们研究了KD对暴露于MIA的后代的ASD核心症状的影响。为了诱导MIA,给怀孕的C57Bl/6小鼠注射病毒模拟物聚肌苷酸-聚胞苷酸;断奶后,后代被喂食KD或对照饮食三周。与男性发病率较高的ASD表型一致,喂食对照饮食的MIA雄性后代不社交,并表现出高水平的重复性自我导向行为;雌性后代未受影响。然而,喂食KD部分或完全逆转了雄性小鼠所有由MIA诱导的行为异常;对雌性小鼠的行为没有影响。对两性后代进行了KD诱导的血糖降低和血酮升高的代谢变化定量分析。我们实验室和其他机构之前的研究表明,KD可改善几种ASD模型中的相关行为,在此我们证明了KD在ASD的MIA模型中具有明显益处。这些研究共同表明代谢疗法在改善ASD核心症状方面具有广泛的应用前景,并支持进一步开展研究,以开发并将生酮和/或代谢策略应用于ASD患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b9c/5293204/68fec00ee5cb/pone.0171643.g001.jpg

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