Chang Wen-Yue, Qin Qiao-Zhen, Li Xiao-Tong, Wang Jia-Jing, Chen Yue, Ruan Hua-Qiang, Qu Yan-Nv, Jiang Xiao-Xia, He Hui-Xia
Department of Stomatology, First Medical Center of Chinese PLA General Hospital and Medical School of Chinese PLA, Beijing 100853, China.
Institute of Basic Medical Sciences, Beijing 100850, China.
World J Psychiatry. 2025 Jun 19;15(6):104809. doi: 10.5498/wjp.v15.i6.104809.
Hypobaric hypoxia exposure (HHE) often causes neuropsychiatric disorders. Due to its complex mechanism, efficient strategies for alleviating HHE-induced anxiety- and depression-like behaviors remain limited.
To characterize alterations in the oral and gut microbiota following HHE and to explore a potential microbiota-based intervention to mitigate associated psychiatric symptoms.
C57BL/6J mice were exposed to simulated high-altitude hypoxia (5000 m) for 1, 3, 5, or 7 days. Behavioral assessments, including the open field test, elevated plus maze, and forced swim test, were conducted to evaluate anxiety- and depression-like behaviors. Oral and fecal microbiota were analyzed using 16S rRNA sequencing to assess changes in microbial composition and diversity. Immunofluorescence staining was performed to examine c-Fos expression in brain nuclei. A probiotic formulation containing () DSM17648, DDS-1, and UALR-06 was administered to mice subjected to one day of HHE (HH1) to evaluate its therapeutic efficacy.
Behavioral tests revealed that HHE caused anxiety- and depression-like behaviors, which were most pronounced after 1 day of exposure. The IF data revealed significantly increased expression of c-Fos in various brain nuclei after HHE, including the anterior cingulate cortex, paraventricular thalamic nucleus, lateral habenula nucleus, paraventricular hypothalamic nucleus, lateral hypothalamus, and periaqueductal gray. The 16S rRNA sequencing results demonstrated a sharp decline in the abundance of in the oral microbiota of mice exposed to HH1 and a marked decrease in the abundance of and in the fecal microbiota of mice exposed to three days of HHE. Finally, oral administration and gavage of significantly alleviated anxiety- and depression-like behaviors in HH1 mice.
HHE caused significant variations in the oral and fecal microbiota of mice. supplementation alleviated anxiety- and depression-like behaviors in mice. Improving oral flora may relieve HHE-induced psychiatric disorders.
低压缺氧暴露(HHE)常导致神经精神障碍。由于其机制复杂,缓解HHE诱导的焦虑和抑郁样行为的有效策略仍然有限。
表征HHE后口腔和肠道微生物群的变化,并探索基于微生物群的潜在干预措施以减轻相关的精神症状。
将C57BL/6J小鼠暴露于模拟高海拔缺氧(5000米)环境中1、3、5或7天。进行行为评估,包括旷场试验、高架十字迷宫试验和强迫游泳试验,以评估焦虑和抑郁样行为。使用16S rRNA测序分析口腔和粪便微生物群,以评估微生物组成和多样性的变化。进行免疫荧光染色以检查脑核中c-Fos的表达。将含有()DSM17648、DDS-1和UALR-06的益生菌制剂给予经历一天HHE(HH1)的小鼠,以评估其治疗效果。
行为测试表明,HHE引起焦虑和抑郁样行为,在暴露1天后最为明显。免疫荧光数据显示,HHE后包括前扣带回皮质、室旁丘脑核、外侧缰核、室旁下丘脑核、外侧下丘脑和导水管周围灰质在内的各种脑核中c-Fos的表达显著增加。16S rRNA测序结果表明,暴露于HH1的小鼠口腔微生物群中 的丰度急剧下降,暴露于三天HHE的小鼠粪便微生物群中 和 的丰度显著降低。最后,口服和灌胃 显著减轻了HH1小鼠的焦虑和抑郁样行为。
HHE导致小鼠口腔和粪便微生物群发生显著变化。 补充剂减轻了小鼠的焦虑和抑郁样行为。改善口腔菌群可能缓解HHE诱导的精神障碍。