补充益生菌对长期睡眠紊乱的雌雄青春期小鼠的睡眠、抑郁样行为以及中枢葡萄糖和乳酸代谢的影响

IF 3.4 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Michael Murack , Anthony K. Kadamani , Alexi Guindon-Riopel , Olivia H. Traynor , Umar Haris Iqbal , Stéphane Bronner , Claude Messier , Nafissa Ismail
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引用次数: 0

摘要

抑郁症的发病率在青春期和青春期明显上升。青春期是性成熟的时期,而青春期则持续到青春期之后,包括生理、社交、情感和认知的成熟。以前的研究表明,长期睡眠中断是诱发抑郁症的一种压力源。益生菌可以预防压力引起的抑郁症。然而,益生菌是否能预防慢性睡眠中断引起的抑郁症以及其中可能涉及的机制尚不清楚。因此,我们研究了青春期益生菌治疗能否预防小鼠在慢性睡眠中断后出现抑郁样行为。我们还研究了益生菌治疗是否能改善睡眠质量,并提高慢性睡眠紊乱小鼠的血清素、色氨酸、葡萄糖和 L-乳酸的浓度。我们假设益生菌治疗可以预防抑郁样行为,改善睡眠质量,提高睡眠中断小鼠的血清素、色氨酸、葡萄糖和 L-乳酸盐浓度。雌雄小鼠(N=120)在出生后第 26 天接受插管和脑电图(EEG)电极植入。小鼠接受 Lacidofil® 或 Cerebiome® 益生菌治疗(PND 33-51),并在光照阶段(睡眠期)的前 4 小时(PND 40-51)睡眠中断。在24小时内(PND 48-49)测量海马L-乳酸盐和葡萄糖浓度以及睡眠情况。抑郁样行为通过尾悬吊试验(PND 49)和强迫游泳试验(PND 50)进行评估。长期睡眠中断会增加抑郁样行为和黑暗阶段的 NREM 持续时间,并减少大脑内测得的所有代谢物和神经调节生物大分子。然而,使用益生菌治疗的小鼠在慢性睡眠中断后并没有表现出抑郁样行为,海马左乳酸也没有减少。脑益生菌能防止前额叶血清素和海马葡萄糖浓度的下降,而拉西多菲能延长光照后半期的非快速眼动持续时间。目前的研究不仅重复了之前将慢性睡眠中断与抑郁联系起来的研究结果,而且还证明了青春期益生菌治疗可以减轻慢性睡眠中断对抑郁样行为的影响,并以菌株依赖的方式减轻对抑郁的神经机制的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of probiotic supplementation on sleep, depression-like behaviour, and central glucose and lactate metabolism in male and female pubertal mice exposed to chronic sleep disruption

The prevalence of depression significantly increases during puberty and adolescence. Puberty is the period during which sexual maturity is attained, while adolescence persists beyond puberty and includes physiological, social, emotional, and cognitive maturation. A stressor that has been shown previously to induce depression is chronic sleep disruption. Probiotics can prevent stress-induced depression. However, it was unclear whether probiotics could prevent depression following chronic sleep disruption and what mechanism may be involved. Therefore, we investigated whether pubertal probiotic treatment could prevent depression-like behavior in mice following chronic sleep disruption. We also examined whether probiotic treatment could improve sleep quality, and increase serotonin, tryptophan, glucose, and L-lactate concentrations in chronically sleep-disrupted mice. We hypothesized that probiotic treatment would prevent depression-like behavior, improve sleep quality, and increase serotonin, tryptophan, glucose, and L-lactate concentrations in sleep-disrupted mice. Male and female mice (N=120) received cannula and electroencephalogram (EEG) electrode implants at postnatal day (PND) 26. Mice received Lacidofil® or Cerebiome® probiotics (PND 33–51) and were sleep-disrupted for the first 4 hours of the light phase (sleep period) (PND 40–51). Hippocampal L-lactate and glucose concentrations and sleep were measured over a 24-h period (PND 48–49). Depression-like behaviour was evaluated using tail suspension (PND 49) and forced swim tests (PND 50). Chronic sleep disruption increased depression-like behaviour and NREM duration in the dark phase, and reduced all metabolites and neuromodulating biomolecules measured within the brain. However, mice treated with probiotics did not display depression-like behaviour or decreased hippocampal L-lactate following chronic sleep disruption. Cerebiome prevented decreases to prefrontal serotonin and hippocampal glucose concentrations, while Lacidofil increased NREM duration in the latter half of the light phase. The current study not only replicates previous findings linking chronic sleep disruption to depression, but also demonstrates that pubertal probiotic treatment can mitigate the effects of chronic sleep disruption on depression-like behaviour and on the neural mechanisms underlying depression in a strain-dependent manner.

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来源期刊
Psychoneuroendocrinology
Psychoneuroendocrinology 医学-精神病学
CiteScore
7.40
自引率
8.10%
发文量
268
审稿时长
66 days
期刊介绍: Psychoneuroendocrinology publishes papers dealing with the interrelated disciplines of psychology, neurobiology, endocrinology, immunology, neurology, and psychiatry, with an emphasis on multidisciplinary studies aiming at integrating these disciplines in terms of either basic research or clinical implications. One of the main goals is to understand how a variety of psychobiological factors interact in the expression of the stress response as it relates to the development and/or maintenance of neuropsychiatric illnesses.
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