米糠肽对TNF-α的调节:对衰老中肠道微生物群稳定性和认知健康的影响

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jianfei Mu, Qinlu Lin, Shuang Wang, Mingfeng Chen, Jianqiang Wang, Yajuan Chen, Yusheng Li, Ying Liang
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引用次数: 0

摘要

与衰老相关的神经炎症导致认知能力下降;然而,调节肠道微生物群的生物活性化合物,如米糠肽KF-8,缓解这一过程的机制尚不清楚。在这里,KF-8被证明可以通过重塑肠道微生物群来改善老年小鼠的年龄相关特征,特别是通过稳定嗜粘蛋白突变(AKK)来抑制全身炎症和认知缺陷。具体来说,接受KF-8抗生素治疗的小鼠表现出神经炎症和认知能力下降。KF-8和AKK协同减弱血液和海马中的促炎途径,特别是TNF-α。虽然TNF-α抗体反映了KF-8的益处,但TNF-α重组蛋白否定了KF-8的保护作用。KF-8和AKK联合干预与TNF-α抗体结果一致,强调TNF-α的关键作用。我们的研究结果表明,KF-8通过调节肠道微生物群、维持AKK和抑制TNF-α驱动的神经炎症来促进健康衰老,从而挽救老年小鼠的认知功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TNF-α modulation by rice bran peptides: implications for gut microbiota stability and cognitive health in aging.

Aging-related neuroinflammation drives cognitive decline; however, the mechanisms by which gut microbiota-modulating bioactive compounds, such as rice bran peptide KF-8, mitigate this process remain unclear. Here, KF-8 was shown to ameliorate age-related traits in aged mice by reshaping gut microbiota, notably by stabilizing Akkermansia muciniphila (AKK), to suppress systemic inflammation and cognitive deficits. Specifically, antibiotic-treated mice receiving KF-8 exhibited neuroinflammation and declined cognition. KF-8 and AKK synergistically attenuated pro-inflammatory pathways, particularly TNF-α, in the blood and in the hippocampus. While TNF-α antibodies mirrored KF-8's benefits, TNF-α recombinant protein negated KF-8's protective effects. Combined KF-8 and AKK interventions aligned with TNF-α antibody outcomes, underscoring TNF-α's pivotal role. Our findings reveal that KF-8 enhances healthy aging by modulating gut microbiota, sustaining AKK, and suppressing TNF-α-driven neuroinflammation, thereby rescuing cognitive function in aged mice.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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