Acute aerobic exercise is associated with a biphasic, temporally ordered shift in serum extracellular vesicle microRNA expression in major depressive disorder.

IF 4.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2026-09-15 eCollection Date: 2026-01-01 DOI:10.3389/fmolb.2026.1910088
Beatriz B Elliott, Viraaj Vishnu Prasad, Alicia Taylor, Ian J Shofner, Karl Kerns, Jacob Meyer, Elizabeth M McNeill
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引用次数: 0

Abstract

Introduction: Acute aerobic exercise (AAE) is known to reduce symptoms of Major Depressive Disorder (MDD), yet the underlying biological mechanisms remain poorly understood. Here, we profiled microRNA (miRNA) expression within the serum extracellular vesicle (EV) enriched fraction (hereafter 'EV-enriched miRNA') of individuals diagnosed with MDD at multiple timepoints: before, during (mid), immediately after, and 75 min following a single 30-min session of moderate aerobic exercise. By characterizing the temporal dynamics of EV-enriched miRNA responses to AAE, our objective was to uncover molecular changes that may mediate exercise-induced molecular adaptations relevant to short- or long-term antidepressant effects of exercise and to identify candidate EV-enriched miRNAs for future mechanistic investigation of MDD.

Methods: An EV-enriched serum fraction was isolated from a minimum of 28 individuals diagnosed with MDD. MicroRNA profiles were then assessed via RNA deep sequencing and analyzed with using DESeq2.

Results: We identified time-dependent, significant (false discovery rate [FDR] ≤ 0.05) changes in EV-enriched microRNAs across AAE, with 15 differentially expressed at mid-AAE, 33 immediately post-AAE, and four at 75 min post-AAE. The response was biphasic and directional: miRNAs were predominantly downregulated during and immediately after exercise (13 of 15 down at mid-AAE; all 33 down post-AAE) and exclusively upregulated during recovery (all four up at 75 min post-AAE). hsa-miR-12523p was the only microRNA differentially expressed across all three postexercise timepoints, showing consistent downregulation. Functional enrichment of predicted targets of significantly differentially expressed miRNAs revealed a temporally ordered shift from RNA processing and stability at mid-AAE, to dendrite, synapse, and axon organization immediately post-AAE, to synaptic transmission and neuronal development at 75 min post-AAE.

Discussion: AAE is associated with time-dependent, directional changes in EV-enriched microRNAs in MDD, whose predicted targets converge on synaptic plasticity pathways implicated in the disorder. Together, this suggests microRNAs may contribute to the beneficial short- and potentially long-term effects of aerobic exercise in individuals with MDD and provides specific targets for future mechanistic investigation.

急性有氧运动与重度抑郁症患者血清细胞外囊泡microRNA表达的双相、时间有序变化有关。
简介:急性有氧运动(AAE)已知可以减轻重度抑郁症(MDD)的症状,但其潜在的生物学机制尚不清楚。在这里,我们分析了诊断为MDD的个体在多个时间点的血清细胞外囊泡(EV)富集部分(以下简称“EV富集miRNA”)中的microRNA (miRNA)表达:在单次30分钟适度有氧运动之前,期间(中期),之后立即和75分钟后。通过表征ev富集miRNA对AAE反应的时间动态,我们的目标是揭示可能介导运动诱导的分子适应的分子变化,这些分子适应与运动的短期或长期抗抑郁作用有关,并为未来MDD的机制研究确定候选ev富集miRNA。方法:从至少28名诊断为重度抑郁症的个体中分离出ev富集的血清部分。然后通过RNA深度测序评估MicroRNA谱,并使用DESeq2进行分析。结果:我们发现ev富集的microrna在AAE期间发生了时间依赖性的显著(错误发现率[FDR]≤0.05)变化,其中15个在AAE中期表达差异,33个在AAE后立即表达差异,4个在AAE后75分钟表达差异。反应是双相和定向的:mirna在运动期间和运动后主要下调(15个中有13个在aae中期下调,33个在aae后下调),在恢复期间完全上调(所有4个在aae后75分钟上调)。hsa-miR-12523p是唯一在所有三个运动后时间点差异表达的microRNA,表现出一致的下调。显著差异表达的miRNAs的预测靶标的功能富集揭示了从aae中期的RNA加工和稳定性,到aae后立即的树突、突触和轴突组织,再到aae后75分钟的突触传递和神经元发育的暂时有序转变。讨论:AAE与MDD中ev富集的microrna的时间依赖性、方向性变化有关,其预测目标集中在与该疾病有关的突触可塑性途径上。总之,这表明microrna可能有助于有氧运动对重度抑郁症患者的短期和潜在的长期有益影响,并为未来的机制研究提供了具体的目标。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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