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异麦芽低聚糖增强间歇性禁食对减肥期间和体重反弹时肥胖相关认知障碍的缓解作用。

Isomalto-Oligosaccharide Potentiates Alleviating Effects of Intermittent Fasting on Obesity-Related Cognitive Impairment during Weight Loss and the Rebound Weight Gain.

机构信息

School of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi'an 710062, China.

School of Physical Education, Shaanxi Normal University, Xi'an 710062, China.

出版信息

J Agric Food Chem. 2024 Oct 30;72(43):23875-23892. doi: 10.1021/acs.jafc.4c07351. Epub 2024 Oct 21.

Abstract

Obesity-related cognitive dysfunction poses a significant threat to public health. The present study demonstrated mitigating effects of intermittent fasting (IF) and its combination with isomalto-oligosaccharides and IF (IF + IMO) on cognitive impairments induced by a high-fat-high-fructose (HFHF) diet in mice, with IF + IMO exhibiting superior effects. Transcriptomic analysis of the hippocampus revealed that the protective effects on cognition might be attributed to the suppression of toll-like receptor 4 (TLR4)/NFκB signaling, oxidative phosphorylation, and neuroinflammation. Moreover, both IF and IF + IMO modulated the gut microbiome and promoted the production of short-chain fatty acids, with IF + IMO displaying more pronounced effects. IF + IMO-modulated gut microbiota, metabolites, and molecular targets associated with cognitive impairments were further corroborated using human data from public databases Gmrepo and gutMgene. Furthermore, the fecal microbiome transplantation confirmed the direct impacts of IF + IMO-derived microbiota on improving cognition functions by suppressing TLR4/NFκB signaling and increasing BDNF levels. Notably, prior exposure to IF + IMO prevented weight-regain-induced cognitive decline, suppressed TLR4/NFκB signaling and inflammatory cytokines in the hippocampus, and mitigated weight regain-caused gut dysbacteriosis without altering body weight. Our study underscores that IMO-augmented alleviating effects of IF on obesity-related cognitive impairment particularly during weight-loss and weight-regain periods, presenting a novel nutritional strategy to tackle obesity-related neurodegenerative disorders.

摘要

肥胖相关认知功能障碍对公众健康构成重大威胁。本研究表明,间歇性禁食(IF)及其与异麦芽低聚糖和 IF(IF+IMO)的组合对高脂肪高果糖(HFHF)饮食诱导的小鼠认知障碍具有缓解作用,IF+IMO 具有更好的效果。海马转录组分析表明,其对认知的保护作用可能归因于抑制 toll 样受体 4(TLR4)/NFκB 信号、氧化磷酸化和神经炎症。此外,IF 和 IF+IMO 均调节肠道微生物组并促进短链脂肪酸的产生,IF+IMO 显示出更显著的效果。IF+IMO 调节的与认知障碍相关的肠道微生物组、代谢物和分子靶点,使用来自公共数据库 Gmrepo 和 gutMgene 的人类数据进一步得到证实。此外,粪便微生物群移植证实了 IF+IMO 衍生微生物群通过抑制 TLR4/NFκB 信号和增加 BDNF 水平直接影响改善认知功能。值得注意的是,IF+IMO 的预先暴露可防止体重恢复引起的认知能力下降,抑制海马中的 TLR4/NFκB 信号和炎症细胞因子,并减轻体重恢复引起的肠道菌群失调,而不改变体重。我们的研究强调,IMO 增强了 IF 对肥胖相关认知障碍的缓解作用,特别是在减肥和体重恢复期间,为解决肥胖相关神经退行性疾病提供了一种新的营养策略。

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