Ankeeta Ankeeta, Tripathi Ashutosh, Ma Yizhou, Pillai Bindu, Chiappelli Joshua J, Jernberg Jennifer N, Kunitoki Keiko, Adhikari Bhim M, Gao Si, Du Xiaoming, Kabui Loise, Solano Francisco Pallares, Akindona Oluwabunmi, Ye Zhenyao, Chen Shuo, Milad Mohammad, Kochunov Peter, Pillai Anilkumar R, Hong Elliot L
bioRxiv. 2025 Aug 1:2025.07.30.667787. doi: 10.1101/2025.07.30.667787.
Stress response obligates increased mitochondrial activities to meet stress induced high energy requirement. This stress mitochondrial response process involves glucocorticoid but also multiple alternative pathways that are top down regulated by the medial prefrontal cortex (mPFC). These pathways are important for many neuropsychiatric conditions that are sensitive to stress. However, the field lacks a reliable, clinically accessible stress mitochondrial response paradigm to study the process in humans.
We used an established psychological stress challenge combined with assaying salivary cell-free mitochondrial DNA (cf mtDNA), thought to reflect heightened mitochondrial changes or disruptions, in 35 healthy individuals (21 males). We also explored if these stress induced cf mtDNA marker elevations were associated brain metabolites as measured by magnetic resonance spectroscopy (MRS), as well as high resolution brain imaging based cortical thickness focusing on the mPFC.
We found that salivary cf mtDNA was significant elevated immediately after the stress challenge (p=2.0x10-7) and gradually declined after. Exploratory causal analysis showed that this cf mtDNA response was not primarily driven by cortisol response. Instead, individuals with higher baseline dACC lactate+ levels, thought to in part reflect mitochondrial dysfunctions, was significantly associated with the cf mtDNA response (r=0.80, p<0.001). Higher mtDNA response was also significantly associated with thinner dorsomedial prefrontal cortex (r=-0.52, p=0.01). Age had a U-shape effect such that cf mtDNA response trended lower in earlier adulthood but higher in older people, explaining 33.8% of the ct mtDNA response variance (p=0.003).
This stress challenge-salivary cf mtDNA assay paradigm may offer a new, noninvasive approach to evaluate the stress-mitochondrial pathway functioning in aging, psychopharmacology, and neuropsychiatric conditions where psychological stress plays a role.
应激反应需要增加线粒体活性以满足应激诱导的高能量需求。这种应激线粒体反应过程涉及糖皮质激素,但也涉及多个由内侧前额叶皮质(mPFC)自上而下调节的替代途径。这些途径对许多对应激敏感的神经精神疾病很重要。然而,该领域缺乏一种可靠的、临床上可获取的应激线粒体反应范式来研究人类的这一过程。
我们对35名健康个体(21名男性)采用了既定的心理应激挑战,并结合检测唾液游离线粒体DNA(cf mtDNA),其被认为可反映线粒体变化或破坏加剧。我们还探讨了这些应激诱导的cf mtDNA标志物升高是否与通过磁共振波谱(MRS)测量的脑代谢物相关,以及基于高分辨率脑成像的以mPFC为重点的皮质厚度相关。
我们发现,应激挑战后唾液cf mtDNA立即显著升高(p = 2.0×10-7),随后逐渐下降。探索性因果分析表明,这种cf mtDNA反应并非主要由皮质醇反应驱动。相反,基线背侧前扣带回乳酸盐+水平较高的个体(被认为部分反映线粒体功能障碍)与cf mtDNA反应显著相关(r = 0.80,p < 0.001)。较高的mtDNA反应也与背内侧前额叶皮质较薄显著相关(r = -0.52,p = 0.01)。年龄具有U形效应,即cf mtDNA反应在成年早期呈下降趋势,而在老年人中较高,解释了ct mtDNA反应方差的33.8%(p = 0.003)。
这种应激挑战-唾液cf mtDNA检测范式可能提供一种新的非侵入性方法,用于评估心理应激起作用的衰老、精神药理学和神经精神疾病中的应激-线粒体途径功能。