Suppr超能文献

异亮氨酸限制饮食通过肠道菌群-脑轴对高脂诱导肥胖小鼠认知障碍的潜在影响

The Potential Effects of Isoleucine Restricted Diet on Cognitive Impairment in High-Fat-Induced Obese Mice via Gut Microbiota-Brain Axis.

作者信息

Wang Yuli, Rong Xue, Guan Hui, Ouyang Fangxin, Zhou Xing, Li Feng, Tan Xintong, Li Dapeng

机构信息

College of Food Science and Engineering, Shandong Agricultural University Key Laboratory of Food Nutrition and Human Health in Universities of Shandong, Taian, 271018, China.

出版信息

Mol Nutr Food Res. 2023 Oct;67(20):e2200767. doi: 10.1002/mnfr.202200767. Epub 2023 Sep 1.

Abstract

SCOPE

Obesity induced by high-fat diet (HFD) can cause lipid metabolism disorders and cognitive impairment. Isoleucine restriction can effectively alleviate lipid metabolism disorders caused by HFD but the underlying mechanisms on cognition are unknown.

METHODS AND RESULTS

Thirty 3-month-old C57BL/6J mice are divided equally into the following groups: the control group, HFD group, and HFD Low Ile group (67% reduction in isoleucine in high fat feeds). Feeding for 11 weeks with behavioral testing, which shows that isoleucine restriction attenuates HFD-induced cognitive dysfunction. As observed by staining, isoleucine restriction inhibits HFD-induced neuronal damage and microglia activation. Furthermore, isoleucine restriction significantly increases the relative abundance of gut microbiota, decreases the proportion of Proteobacteria, and reduces the levels of lipopolysaccharide (LPS) in serum and brain. Isoleucine restriction reduces protein expression of TLR4/MyD88/NF-κB signaling pathway and inhibits upregulation of proinflammatory cytokine genes and protein expression in mice brain. In addition, isoleucine restriction significantly improves insulin resistance in the brain as well as synaptic plasticity impairment.

CONCLUSION

Isoleucine restriction may be a potential intervention to reduce HFD-induced cognitive impairment by altering gut microbiota, reducing neuroinflammation, insulin resistance, and improving synaptic plasticity in mice brain.

摘要

范围

高脂饮食(HFD)诱导的肥胖可导致脂质代谢紊乱和认知障碍。异亮氨酸限制可有效缓解HFD引起的脂质代谢紊乱,但其对认知的潜在机制尚不清楚。

方法与结果

将30只3月龄C57BL/6J小鼠平均分为以下几组:对照组、HFD组和HFD低异亮氨酸组(高脂饲料中异亮氨酸减少67%)。喂养11周并进行行为测试,结果表明异亮氨酸限制可减轻HFD诱导的认知功能障碍。通过染色观察,异亮氨酸限制可抑制HFD诱导的神经元损伤和小胶质细胞活化。此外,异亮氨酸限制可显著增加肠道微生物群的相对丰度,降低变形菌门的比例,并降低血清和脑中脂多糖(LPS)的水平。异亮氨酸限制可降低TLR4/MyD88/NF-κB信号通路的蛋白表达,并抑制小鼠脑中促炎细胞因子基因的上调和蛋白表达。此外,异亮氨酸限制可显著改善脑内胰岛素抵抗以及突触可塑性损伤。

结论

异亮氨酸限制可能是一种潜在的干预措施,通过改变肠道微生物群、减轻神经炎症、改善胰岛素抵抗以及增强小鼠脑内突触可塑性来减轻HFD诱导的认知障碍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验