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Maternal obese-type gut microbiota differentially impact cognition anxiety and compulsive behavior in male and female offspring in mice

机译:母体肥胖型肠道菌群差异影响小鼠雌雄后代的认知焦虑和强迫行为

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摘要

Maternal obesity is known to predispose offspring to metabolic and neurodevelopmental abnormalities. While the mechanisms underlying these phenomena are unclear, high fat diets dramatically alter intestinal microbiota, and gut microbiota can impact physiological function. To determine if maternal diet-induced gut dysbiosis can disrupt offspring neurobehavioral function, we transplanted high fat diet- (HFD) or control low fat diet-associated (CD) gut microbiota to conventionally-housed female mice. Recipient mice were then bred and the behavioral phenotype of male and female offspring was tracked. While maternal behavior was unaffected, neonatal offspring from HFD dams vocalized less upon maternal separation than pups from CD dams. Furthermore, weaned male offspring from HFD dams had significant and selective disruptions in exploratory, cognitive, and stereotypical/compulsive behavior compared to male offspring from CD dams; while female offspring from HFD dams had increases in body weight and adiposity. 16S metagenomic analyses confirmed establishment of divergent microbiota in CD and HFD dams, with alterations in diversity and taxonomic distribution throughout pregnancy and lactation. Likewise, significant alterations in gut microbial diversity and distribution were noted in offspring from HFD dams compared to CD dams, and in males compared to females. Regression analyses of behavioral performance against differentially represented taxa suggest that decreased representation of specific members of the Firmicutes phylum predict behavioral decline in male offspring. Collectively, these data establish that high fat diet-induced maternal dysbiosis is sufficient to disrupt behavioral function in murine offspring in a sex-specific manner. Thus these data reinforce the essential link between maternal diet and neurologic programming in offspring and suggest that intestinal dysbiosis could link unhealthy modern diets to the increased prevalence of neurodevelopmental and childhood disorders.
机译:众所周知,母体肥胖会使后代容易发生代谢异常和神经发育异常。尽管尚不清楚这些现象的机制,但高脂饮食会极大地改变肠道菌群,而肠道菌群会影响生理功能。为了确定母体饮食引起的肠道营养不良是否可以破坏后代的神经行为功能,我们将高脂饮食(HFD)或对照低脂饮食相关(CD)的肠道菌群移植到了常规饲养的雌性小鼠中。然后饲养收件人小鼠,并追踪雄性和雌性后代的行为表型。虽然产妇的行为没有受到影响,但来自HFD大坝的新生儿后代在母体分离时的发声要比CD大坝中的幼崽低。此外,与CD坝的雄性后代相比,HFD大坝的断奶雄性后代在探索,认知和定型/强迫行为方面有显着和选择性的破坏。而来自HFD大坝的雌性后代的体重和肥胖增加。 16S宏基因组学分析证实了CD和HFD大坝中存在不同的菌群,并且在整个怀孕和哺乳期的多样性和分类学分布都有变化。同样,与CD大坝相比,HFD大坝的后代中肠道微生物多样性和分布发生了显着变化,与雌性相比,雄性肠道中的肠道微生物多样性和分布发生了显着变化。针对差异表示的分类单元的行为表现的回归分析表明,沙门氏菌特定成员的减少表示了雄性后代的行为下降。这些数据共同证明,高脂饮食引起的母体营养不良足以以性别特定的方式破坏鼠后代的行为功能。因此,这些数据加强了母亲饮食与后代神经系统程序之间的本质联系,并表明肠道营养不良可能将不健康的现代饮食与神经发育和儿童疾病的患病率增加联系起来。

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