妊娠前果糖诱导的 Wistar 大鼠代谢综合征会导致其后代出现性别双态行为变化。

IF 2.7 4区 医学 Q2 DEVELOPMENTAL BIOLOGY
Marié L. Cuervo Sánchez, Facundo H. Prado Spalm, Natalia E. Furland, Ana S. Vallés
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引用次数: 0

摘要

代谢综合征(MetS)以持久的代谢炎症为特征,对认知能力和大脑结构有不利影响,并影响行为。本研究旨在探讨母体代谢综合征是否会对后代的神经发育和新陈代谢产生负面影响。为了验证这一假设,对2个月大的雌性Wistar大鼠进行了为期10周的单独或添加20%果糖的自来水诱导MetS。母鼠与健康雄鼠交配产仔:OC(来自对照组母鼠的后代)和 OMetS(来自患有 MetS 的母鼠的后代)。为隔离产前影响,所有幼崽均由对照组哺乳母鼠哺乳,并在断奶前保持标准饮食和自由饮水。行为评估在出生后第 22 天到第 95 天之间进行,代谢参数在出生后第 100 天进行分析。高架加迷宫、开阔地和大理石埋藏测试的结果显示,OMetS雌鼠的焦虑表型增强。新物体识别测试表明,只有 OMetS 雄性动物存在长期记忆障碍。在互惠社交互动测试中,OMetS的社交互动次数较少,只有雌性OMetS的 "社交不活跃 "行为明显增加。此外,在三室测试中,发现只有 OMetS 女性的社交偏好和社交新奇指数较低。内脏脂肪的增加与高甘油三酯血症是 OMetS 女性死后代谢的相关发现。总之,母体代谢紊乱会对后代的神经行为和新陈代谢造成持久的损害和不利影响,并具有明显的性别二态性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pregestational fructose-induced metabolic syndrome in Wistar rats causes sexually dimorphic behavioral changes in their offspring

Metabolic syndrome (MetS), marked by enduring metabolic inflammation, has detrimental effects on cognitive performance and brain structure, influencing behavior. This study aimed to investigate whether maternal MetS could negatively impact the neurodevelopment and metabolism of offspring. To test this hypothesis, 2 months old female Wistar rats were subjected to a 10-week regimen of tap water alone or supplemented with 20% fructose to induce MetS. Dams were mated with healthy males to generate litters: OC (offspring from control dams) and OMetS (offspring from dams with MetS). To isolate prenatal effects, all pups were breastfed by control nurse dams, maintaining a standard diet and water ad libitum until weaning. Behavioral assessments were conducted between postnatal days (PN) 22 and 95, and metabolic parameters were analyzed post-sacrifice on PN100. Results from the elevated plus maze, the open field, and the marble burying tests revealed a heightened anxiety-like phenotype in OMetS females. The novel object recognition test showed that exclusively OMetS males had long-term memory impairment. In the reciprocal social interaction test, OMetS displayed a lower number of social interactions, with a notable increase in “socially inactive” behavior observed exclusively in females. Additionally, in the three-chamber test, social preference and social novelty indexes were found to be lower solely among OMetS females. An increase in visceral fat concomitantly with hypertriglyceridemia was the relevant postmortem metabolic finding in OMetS females. In summary, maternal MetS leads to enduring damage and adverse effects on offspring neurobehavior and metabolism, with notable sexual dimorphism.

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来源期刊
Developmental Neurobiology
Developmental Neurobiology 生物-发育生物学
CiteScore
6.50
自引率
0.00%
发文量
45
审稿时长
4-8 weeks
期刊介绍: Developmental Neurobiology (previously the Journal of Neurobiology ) publishes original research articles on development, regeneration, repair and plasticity of the nervous system and on the ontogeny of behavior. High quality contributions in these areas are solicited, with an emphasis on experimental as opposed to purely descriptive work. The Journal also will consider manuscripts reporting novel approaches and techniques for the study of the development of the nervous system as well as occasional special issues on topics of significant current interest. We welcome suggestions on possible topics from our readers.
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