Lactobacillus johnsonii HL79 mitigate plateau environment-induced hippocampal dysfunction in mice.

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Baoxing Gan, Xufei Zhang, Jinge Xin, Lixiao Duan, Ning Sun, Yu Chen, Junqi Zeng, Yueying Lian, Hao Li, Hesong Wang, Xueqin Ni, Hailin Ma
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引用次数: 0

Abstract

Plateau environment represents a common terrestrial characterized by multistress conditions including hypobaric hypoxia, low temperature, and intense radiation, yet sustain over 100 million permanent or transient inhabitants. While this extreme environment exerts profound impacts on cerebral architecture and gut microbiota homeostasis, precipitating cognitive deficits and microbiome-derived intestinal pathologies, the mechanistic interplay between plateau environment adaptation and microbial dynamics remains contentious. Here, we employ a microbiota-gut-brain axis framework to investigate whether probiotic intervention can ameliorate hippocampal impairments induced by simulated plateau environment exposure (3500-4000 m) in mice. Through simulated plateau environment exposure experiments, we revealed that extreme high-altitude conditions induced hippocampal memory dysfunction in mice, exacerbated oxidative stress damage in hippocampal tissues, and altered synaptic plasticity-related biomarkers including CREB transcription factor, BDNF protein levels, and electrophysiological power spectra. Administration of HL79 alleviated these burdens, including memory dysfunction and tissue damage, though complete reversal was not achieved. Combined hippocampal transcriptomic analyses suggested that HL79's beneficial effects primarily involved modulation of lipid-related gene expression in the hippocampus, consistent with prior reports of plateau environmental impacts on gene expression. Serum metabolomic results further reinforced this inference that differential metabolites regulated by HL79 are mainly enriched in bile secretion, taurine and hypotaurine metabolism, linoleic acid metabolism, and PPAR signaling pathways, though the precise regulatory mechanisms require further elucidation. This research provides a novel microbiota-gut-brain axis-based regulatory strategy for adaptation to extreme plateau environments and offers new evidence for understanding the relationship between gut microbiota and plateau environment adaptation at high elevations.

约氏乳杆菌HL79减轻高原环境诱导的小鼠海马功能障碍。
高原环境是一种以低气压、低氧、低温和强辐射等多重应激条件为特征的常见陆地环境,但却维持着超过1亿的永久或短暂居民。尽管这种极端环境对大脑结构和肠道微生物群稳态产生了深远的影响,加速了认知缺陷和微生物群衍生的肠道病理,但高原环境适应与微生物动力学之间的机制相互作用仍存在争议。在这里,我们采用微生物-肠-脑轴框架来研究益生菌干预是否可以改善模拟高原环境暴露(3500-4000 m)引起的小鼠海马损伤。通过模拟高原环境暴露实验,我们发现极端高海拔条件会导致小鼠海马记忆功能障碍,加剧海马组织氧化应激损伤,并改变突触可塑性相关的生物标志物,包括CREB转录因子、BDNF蛋白水平和电生理功率谱。给药HL79减轻了这些负担,包括记忆功能障碍和组织损伤,尽管没有完全逆转。综合海马转录组学分析表明,HL79的有益作用主要涉及海马中脂质相关基因表达的调节,这与先前关于高原环境对基因表达影响的报道一致。血清代谢组学结果进一步强化了这一推断,即HL79调控的差异代谢物主要富集于胆汁分泌、牛磺酸和次牛磺酸代谢、亚油酸代谢和PPAR信号通路,但其具体调控机制有待进一步阐明。本研究提供了一种新的基于微生物-肠-脑轴的高原极端环境适应调控策略,为理解高海拔地区肠道微生物群与高原环境适应之间的关系提供了新的证据。
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来源期刊
AMB Express
AMB Express BIOTECHNOLOGY & APPLIED MICROBIOLOGY-
CiteScore
7.20
自引率
2.70%
发文量
141
审稿时长
13 weeks
期刊介绍: AMB Express is a high quality journal that brings together research in the area of Applied and Industrial Microbiology with a particular interest in ''White Biotechnology'' and ''Red Biotechnology''. The emphasis is on processes employing microorganisms, eukaryotic cell cultures or enzymes for the biosynthesis, transformation and degradation of compounds. This includes fine and bulk chemicals, polymeric compounds and enzymes or other proteins. Downstream processes are also considered. Integrated processes combining biochemical and chemical processes are also published.
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