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Maternal high sugar and fat diet benefits offspring brain function via targeting on the gut–brain axis

机译:母体高糖和脂肪饮食通过瞄准肠轴轴来利用后代脑功能

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摘要

A recent study showed that a gestational high fat diet protects 3xTg-AD offspring from memory impairments, synaptic dysfunction, and brain pathology. However, it is unknown whether this diet exerts the same effects on normal mice or on other functions, and if so, how. In the present study, mother mice were pre-fed a high sugar and high fat (HSHF) diet for 1 month and then fertilized; the HSHF diet was continued until birth and then mother mice were returned to a standard diet. The gut microbiota, and intestinal and brain functions of the offspring were dynamically monitored at 7, 14, 28, and 56 days old until 16 months of age. Results showed that the HSHF diet significantly affected the gut microbiota structure of the offspring, especially during the early life stage. In addition, in the HSHF diet offspring, there were influenced on various types of neurons, including cholinergic and GABAergic neurons, on autophagy levels in the brain, and on inflammation levels in the intestinal tract. When the offspring grew older (16 months), we found that some genes of benefit against nervous system disease were activated, such as Lhx8, GPR88, RGS9, CD4, DRD2, RXRG, and Syt6, and the expression of cholinergic and GABAergic neurons biomarker protein increased. Although the inflammation levels in the nervous and peripheral systems showed no obvious differences, the AFP level of individuals on the HSHF diet was much higher than those on the standard diet, suggesting that more accurate and/or personalized nutrition is needed. Taken together, the results show that a maternal HSHF diet benefits the offspring by reducing the risk of nervous diseases, which might depend on LHX8 activation to modulate cholinergic and GABAergic neurons via the gut–brain axis, but still need much more deep studies.
机译:最近的一项研究表明,一种妊娠高脂饮食可以保护来自记忆障碍,突触功能障碍和脑病理学的3XTG-AD后代。然而,尚不清楚这种饮食是否对正常小鼠或其他功能产生相同的效果,如果是的话,如何。在目前的研究中,将母老鼠预先喂养高糖和高脂肪(HSHF)饮食1个月,然后受精; HSHF饮食仍在继续,直到出生,然后母亲小鼠返回标准饮食。后代的肠道微生物肿瘤和肠道和脑功能在7,14,28和56天内动态监测到16个月。结果表明,HSHF饮食显着影响了后代的肠道微生物群结构,特别是在初期期间。此外,在HSHF饮食后代,对各种类型的神经元有影响,包括胆碱能和胃肠杆菌神经元,对大脑的自噬水平以及肠道中的炎症水平。当后代增长(16个月)时,我们发现一些对神经系统疾病有益的基因被激活,如LHX8,GPR88,RGS9,CD4,DRD2,RXRG和SYT6,以及胆碱能和甘蓝神经元生物标志物的表达蛋白质增加。虽然神经和周边系统的炎症水平没有明显的差异,但HSHF饮食中的个体的AFP水平远高于标准饮食中的个体,这表明需要更准确和/或个性化的营养。结果表明,母体HSHF饮食通过降低神经疾病的风险来利用后代,这可能取决于LHX8激活通过肠脑轴调节胆碱能和加巴霉菌神经元,但仍需要更深入的研究。

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