bims-mistre Biomed News
on Mito stress
Issue of 2026–06–07
thirteen papers selected by
Ellen Siobhan Mitchell, MitoQ



  1. Curr Alzheimer Res. 2026 May 22.
       BACKGROUND: Mitochondrial dysfunction has gained recognition as a central and early event in the pathophysiology of Alzheimer's disease (AD), extending beyond classical energy failure to encompass complex and dynamic perturbations in organelle homeostasis. Despite extensive focus on amyloid-beta (Aβ) and tau, accumulating evidence implicates mitochondria as both targets and amplifiers of neurodegenerative cascades. This review provides a comprehensive synthesis of the mechanistic roles and therapeutic implications of mitochondrial dysfunction in AD, highlighting recent advances and emerging paradigms that underscore mitochondria as integrative nodes in disease onset, progression, and biomarker discovery.
    MATERIALS AND METHODS: We critically evaluate literature from molecular, cellular, and systemslevel studies-including postmortem brain tissue, transgenic models, and patient-derived cellsfocusing on key domains such as bioenergetic collapse, redox imbalance, mitochondrial dynamics and quality control, Aβ and tau interactions, calcium dysregulation, and apoptosis. Novel mitochondrial mechanisms such as mitochondria-associated membranes (MAMs), mitochondrial unfolded protein response (UPRmt), and mitonuclear communication are discussed alongside recent translational efforts.
    RESULTS: Alzheimer's disease is characterized by widespread mitochondrial abnormalities, including impaired oxidative phosphorylation, increased reactive oxygen species (ROS), disrupted mitochondrial fission/fusion equilibrium, defective mitophagy, and abnormal calcium buffering. Moreover, direct mitochondrial accumulation of Aβ and tau disrupts protein import, respiratory chain integrity, and transport dynamics.
    DISCUSSION: These dysfunctions synergistically activate caspase-mediated apoptotic pathways, exacerbating synaptic loss and neuronal death. Promising therapeutic avenues involve antioxidants, NAD+ precursors, mitophagy modulators, and MAM-targeted strategies. Concurrently, mitochondrial biomarkers such as circulating mtDNA, cytochrome c, and neuroimaging via 31P-MRS or PET are emerging as tools for early diagnosis and disease monitoring.
    CONCLUSION: Mitochondria constitute a mechanistic nexus in AD, bridging upstream pathological triggers with downstream neurodegeneration. Advancing the field will require patient-specific models (e.g., iPSC-derived neurons, brain organoids), a deeper understanding of mitochondrial heterogeneity, and integration of mitochondrial targets into multi-modal therapeutic strategies. Precision mitochondrial medicine holds promise to transform AD management through mechanismbased diagnosis, stratification, and intervention.
    Keywords:  Alzheimer’s disease; amyloid-beta; mitochondrial dysfunction; neurodegenerative cascades; oxidative phosphorylation; reactive oxygen species; transgenic mode.
    DOI:  https://doi.org/10.2174/0115672050433653251208201102
  2. J Physiol. 2026 Jun 02.
      Skeletal muscle oxidative capacity is a useful in vivo marker of mitochondrial health and is generally lower in the knee-extensor muscles of older compared with younger adults. The causes of this lower oxidative capacity in older muscle are unclear. We used magnetic resonance spectroscopy to investigate the influence of intramyocellular oxygen availability and the coupling (P/O ratio) between mitochondrial respiration and ATP production on oxidative capacity in the knee-extensor muscles of 14 young and 10 older adults. Participants completed a 24-s contraction protocol followed by 10 min of recovery and 8 min of cuff occlusion while interleaved 31P and 1H spectroscopy data were acquired. Oxidative capacity was calculated as the rate constant of phosphocreatine recovery, and intramyocellular oxygen tension ( PO2${{P}_{{{{\mathrm{O}}}_2}}}$ ) was determined from the deoxymyoglobin signal. Critical PO2${{P}_{{{{\mathrm{O}}}_2}}}$ , the point at which respiration is limited owing to insufficient oxygen availability, and the P/O ratio were determined for each individual. Oxidative capacity was lower in older than younger muscles, whereas neither critical PO2${{P}_{{{{\mathrm{O}}}_2}}}$ nor the P/O ratio differed between groups. On average, PO2${{P}_{{{{\mathrm{O}}}_2}}}$ remained above the critical PO2${{P}_{{{{\mathrm{O}}}_2}}}$ throughout the protocol in both young and older muscle. Oxidative capacity was modestly related to PO2${{P}_{{{{\mathrm{O}}}_2}}}$ during recovery in young but not older muscle, and mitochondrial coupling was unrelated to oxidative capacity. These novel results do not support a primary role for limited oxygen availability or impaired mitochondrial coupling in the lower oxidative capacity of older knee-extensor muscles and suggest instead that other mechanisms, such as lower mitochondrial content, might be responsible. KEY POINTS: Knee-extensor muscle oxidative capacity is generally lower in older age, but the questions of whether this decline is attributable, in part, to insufficient oxygen availability or altered coupling between mitochondrial energy production and oxygen consumption remain open. Interleaved 31P and 1H magnetic resonance spectroscopy was used to measure intramyocellular phosphocreatine and deoxygenated myoglobin in vivo, respectively, in the knee-extensor muscles of young and older adults in response to a 24-s contraction protocol and 8 min of circulatory occlusion. Oxidative capacity was indeed lower in the older muscles, but intracellular oxygen availability during and after contractions was sufficient to support oxidative metabolism and did not differ in young and older muscles. Mitochondrial coupling did not differ by age and was unrelated to oxidative capacity. Thus, the lower knee-extensor muscle oxidative capacity in older age is not a result of inadequate intramyocellular oxygen availability or differences in mitochondrial coupling.
    Keywords:  ATP; P/O ratio; ageing; cellular respiration; deoxymyoglobin; intracellular oxygen tension; knee extensors; phosphocreatine recovery
    DOI:  https://doi.org/10.1113/JP291176
  3. Mol Neurobiol. 2026 Jun 06. pii: 679. [Epub ahead of print]63(1):
      MicroRNA (miRNA) dysregulation contributes to the pathogenesis of neurodegenerative diseases, including Alzheimer's disease (AD), but the role of specific miRNAs in tau-mediated toxicity remains unclear. Here, we investigated the contribution of hsa-miR-125b to tau-induced cellular dysfunction using a stable neuronal cell line overexpressing mutant tau (P301L). We found that hsa-miR-125b levels were significantly elevated in tau-expressing cells compared to controls. Using bioinformatic tools, we identified a strong enrichment of predicted hsa-miR-125b targets involved in mitochondrial function. We validated several of these targets by RT-qPCR and confirmed the downregulation of mitochondrial-related transcripts, including genes encoding components of complexes I, IV, and V of the electron transport chain. To assess functional consequences, we performed Seahorse metabolic flux analysis and observed impaired mitochondrial respiration in tau-overexpressing cells, including reduced basal respiration, ATP production, and spare respiratory capacity. Our findings demonstrate that hsa-miR-125b contributes to tau-induced mitochondrial dysfunction by repressing transcripts essential for mitochondrial homeostasis. We propose that hsa-miR-125b acts as a mechanistic link between tau pathology and metabolic impairment in AD and may represent a promising target for therapeutic intervention.
    Keywords:  APP; Aβ; MiRNAs; Mitochondria; Plaques; Tangles
    DOI:  https://doi.org/10.1007/s12035-026-05982-x
  4. Front Aging. 2026 ;7 1791853
       Background: Aging is a multifaceted biological process driven by interconnected cellular and molecular hallmarks. As geroscience increasingly prioritizes healthspan over lifespan, nutritional interventions targeting multiple aging mechanisms have gained attention as accessible strategies to mitigate age-related functional decline.
    Objective: This mini review synthesizes recent evidence on how the bioactivities of two food-derived geroprotective compounds, pyrroloquinoline quinone (PQQ) and spermidine (SPD), intersect with the hallmarks of aging and their distinct and overlapping roles in maintaining cellular homeostasis.
    Findings: PQQ primarily functions as a mitochondrial and redox regulator, enhancing mitochondrial biogenesis and bioenergetic capacity through the AMP-activated protein kinase (AMPK) and sirtuin1 (SIRT1)/peroxisome proliferator-activated receptor gamma coactivator 1-alpha pathways. In contrast, SPD acts as a key regulator of cellular quality control by inducing macroautophagy and preserving proteostasis, largely through modulation of histone and autophagy-related protein acetylation. These complementary mechanisms converge on several key hallmarks of aging, including genomic instability, deregulated nutrient sensing, mitochondrial dysfunction, and chronic inflammation.
    Conclusion: The anti-aging mechanisms of PQQ and SPD originate from distinct upstream biochemical processes but converge on shared signaling hubs, including the AMPK/SIRT1 axis and autophagy-related networks. This convergence suggests a coordinated network-level complementarity that may offer a more robust intervention against age-related decline than targeting independent pathways alone.
    Keywords:  anti-aging; autophagy; longevity; mitochondria; nutritional intervention; pyrroloquinoline quinone; spermidine
    DOI:  https://doi.org/10.3389/fragi.2026.1791853
  5. J Neurochem. 2026 Jun;170(6): e70467
      This Preface introduces the Special Issue entitled, "Brain Bioenergetics in Aging: Neurovascular and Neurometabolic Coupling and Fuels," which is comprised of manuscripts contributed by invited speakers and program/organizing committee members who participated in the 15th International Conference on Brain Energy Metabolism (ICBEM) held on September 17-21, 2024, in Ljubljana, Slovenia. The conference covered the latest developments in research related to (i) coordination of neurometabolic and neurovascular coupling and homeostasis of energy metabolism in healthy aging and Alzheimer's disease, (ii) in vivo imaging modalities for study of neurometabolic and neurovascular coupling, (iii) mitochondrial and metabolic alterations and resilience in injured and aging brain, (iv) astrocyte metabolism in Alzheimer's and other neurodegenerative diseases, (v) microglial support of neuronal metabolism and role in neurodegeneration, (vi) neuronal mitochondria and disease, (vii) lipids and transporters in brain function, metabolism and Alzheimer's disease, and (viii) metabolic regulation of cognition. The special issue contains 19 manuscripts on these topics.
    DOI:  https://doi.org/10.1111/jnc.70467
  6. bioRxiv. 2026 May 23. pii: 2026.05.21.726892. [Epub ahead of print]
      Mitochondria are essential for cellular energy production and are particularly critical for brain development and function. Neurons rely predominantly on oxidative phosphorylation for energy production, rendering the brain highly vulnerable to mitochondrial dysfunction. Consequently, impaired mitochondrial function contributes to a broad spectrum of neurological and systemic disorders, making mitochondria attractive therapeutic targets. Despite this importance, there is currently no non-invasive, spatially resolved method to assess mitochondrial function in the intact living brain. Here, we establish a non-invasive functional MRI approach-4D Oxy-wavelet MRI-to probe in vivo mitochondrial electron transport chain (ETC) function in a spatially specific manner across the lifespan, from fetal to adult brains. This method employs a low-rank k -t sub-Nyquist acquisition strategy to achieve simultaneous structural and functional imaging with high spatial (78 μm) and temporal (∼14 ms) resolution, enabling motion-robust imaging in multi-fetal mouse pregnancies. Mitochondrial ETC function is interrogated by measuring oxygen homeostasis responses to brief hypoxic challenges, analyzed using computational time-frequency wavelet profiling. We validate this approach in mouse models of mitochondrial respiratory chain disease and late-onset Alzheimer's disease, from in utero fetuses to adults, and demonstrate reproducibility and specificity using pharmacological hyperemia and ETC complex I inhibition. We further show parallel wavelet responses in placenta and fetal brain, enabling multi-organ interrogation of the placenta-brain axis. Finally, we present first-in-human feasibility data, supporting translational potential for non-invasive assessment of mitochondrial function in living brains across the lifespan.
    DOI:  https://doi.org/10.64898/2026.05.21.726892
  7. Exp Physiol. 2026 May 30.
      Cardiovascular disease (CVD) is a leading cause of mortality in women, and CVD risk is accelerated during the menopause transition. This acceleration has traditionally been attributed to the hallmark decline in oestradiol with menopause. However, the menopause transition is also characterized by changes in other sex hormones that exert effects on the vascular endothelium including declines in progesterone and rising follicle stimulating hormone (FSH) and luteinizing hormone (LH) levels. The purpose of this review is to examine the relationships between sex hormones and vascular endothelial function in menopausal women. We emphasize data from clinical and translational studies investigating the effects of oestradiol, progesterone, FSH, LH, and testosterone on vascular endothelial function, and the putative underlying mechanisms including modulation of endothelin-1 signalling, oxidative stress and inflammatory pathways.
    Keywords:  endothelium; perimenopause; reproductive hormones; women's health
    DOI:  https://doi.org/10.1113/EP092848
  8. Aging Cell. 2026 Jun;25(6): e70573
      Mitochondrial dysfunction, impaired proteostasis, and reduced stress resistance and resilience are aging hallmarks. At the core of these hallmarks, the mitochondrial unfolded protein response (mtUPR) is a transcriptional pathway that restores mitochondrial proteostasis in response to proteotoxicity. Although the mtUPR is well studied in invertebrates and cell culture models, how the mtUPR is engaged in aged mammalian tissue is poorly defined. Here, we defined the extent to which repeated physical stress initiates mtUPR transcription in aged mouse skeletal muscle and assessed candidate regulatory mechanisms in vivo. Aged muscle exhibited reduced mitoprotective chaperone and protease availability and greater carbonylation of intermyofibrillar mitochondria relative to young muscle, suggesting diminished proteostatic reserve and increased oxidative burden. Short-term physical stress induced a greater initiation of mtUPR genes in aged muscle than young muscle, coinciding with reduced physiological reserve. Physical stress shifted ATF5 localization from the mitochondria to the nucleus in the muscle of both ages, whereas CHOP mRNA and nuclear localization were selectively elevated in aged muscle. Mechanistically, we show mitochondrial reactive oxygen species (mtROS) contribute to mtUPR initiation in aged skeletal muscle. Using in vivo ChIP-qPCR and in vitro knockdown/inhibition experiments, we provide support for CHOP as a redox-sensitive factor contributing in part to the enhanced mtUPR initiation in aged mouse muscle, potentially linked to JNK signaling. Collectively, these data suggest reduced mitochondrial proteostatic reserve and mtROS signaling in aged muscle contribute to an amplified mtUPR transcriptional response following repetitive physical stress, providing the foundation to explore the mtUPR in mammalian aging.
    DOI:  https://doi.org/10.1111/acel.70573
  9. Mech Ageing Dev. 2026 Jun 01. pii: S0047-6374(26)00058-8. [Epub ahead of print] 112206
      Ageing is the primary risk factor for neurodegeneration and age-related cognitive decline, which is increasingly recognised as a systemic collapse of metabolic crosstalk between neurons and glial cells in the brain. This narrative review elucidates that mitochondrial dynamics - encompassing biogenesis, fusion, fission, and mitophagy - acts as the core regulatory mechanism governing this multicellular interaction network, and drives the cell-specific energy crisis that underpins pathological progression in the ageing brain. We delineate that senescent astrocytes disrupt the astrocyte-neuron lactate shuttle, oligodendrocytes develop ATP deficits triggering myelin breakdown, and microglia undergo maladaptive immunometabolism and metabolic reprogramming via excessive Drp1-mediated mitochondrial fission, which collectively initiates and amplifies chronic neuroinflammation and neurodegenerative damage. Crucially, we highlight intercellular mitochondrial transfer as a vital endogenous rescue mechanism, wherein glial cells donate functional mitochondria to stressed neurons to mitigate damage. Finally, we synthesise emerging therapeutic strategies targeting the glia-neuron mitochondrial social network, providing a holistic framework for restoring brain bioenergetic homeostasis and delaying age-related neurodegenerative progression.
    Keywords:  Cell-Specific Energy Crisis; Immunometabolism; Intercellular Mitochondrial Transfer; Metabolic Reprogramming; Mitochondrial Dynamics
    DOI:  https://doi.org/10.1016/j.mad.2026.112206
  10. Aging Cell. 2026 Jun;25(6): e70578
      Magnesium is traditionally viewed as a permissive electrolyte required for cellular viability. Emerging evidence, however, reveals a more central role for Mg2+ as an active regulator of mitochondrial bioenergetics and metabolic resilience. In this Review, we synthesize recent advances in renal magnesium handling, mitochondrial Mg2+ transport, and MgATP chemistry to propose a unifying framework in which magnesium functions as a bioenergetic checkpoint. At the cellular level, Mg2+ availability specifies the functional pool of ATP, constrains kinase signaling, and stabilizes mitochondrial performance by limiting calcium overload and oxidative stress. At the tissue and organismal levels, disruption of magnesium homeostasis contributes to metabolic inflexibility, insulin resistance, acute kidney injury, and the progressive decline in stress tolerance that accompanies aging. We further discuss how age-associated drift in mitochondrial magnesium may act as a hidden temporal regulator that lowers the threshold for cellular senescence. Finally, we outline emerging therapeutic strategies, including transport-informed and compartment-specific approaches, that move beyond nonspecific supplementation toward precision modulation of magnesium-dependent bioenergetics. Together, this framework positions magnesium as a mechanistic link between mitochondrial function, metabolic disease, and aging, with broad implications for translational intervention.
    Keywords:  aging and senescence; kidney injury; magnesium; metabolic disease; mitochondria
    DOI:  https://doi.org/10.1111/acel.70578
  11. bioRxiv. 2026 May 27. pii: 2026.05.22.727297. [Epub ahead of print]
      Skeletal muscle function is central to the preservation of functional mobility. Given global shifts to an increasingly aged population, it is paramount that researchers and clinicians better understand the effectors of age-related functional decline. Muscle fatiguability acutely modifies skeletal muscle mechanics in ways that may affect joint stability. We have previously reported sex-specific reductions in cellular passive stress and modulus with fatigue in young males, but not females. Here, we assess whether older adults, who are more susceptible to fatigue during dynamic contractions, exhibit changes to cellular passive mechanics following fatiguing exercise. Muscle tissue biopsies were collected from 11 young and 11 older adults to measure passive stress and Young's Modulus at the single fiber and bundle level. Biopsy samples were acquired from rested muscle and immediately following intermittent maximal contractions to task failure. Fatigue was associated with persistent reduction in elastic modulus that was specific to male participants, regardless of age. In muscle fiber bundles, containing both myofibrillar proteins and the extracellular matrix, fatigue-induced changes in modulus were largely negated, with the only significant change observed in young females, who demonstrated enhanced modulus with fatigue. Taken together our findings suggest a preservation of sex-based differences in the acute response to fatigue across the adult lifespan when measured at the myofilament level. However, further research is needed to understand how and whether these findings translate to the whole tissue level.
    New and noteworthy: Acute modifications to muscle tissue mechanics are poorly understood but may have important impacts on functional outcomes in at-risk populations. Our findings suggest myocellular mechanics respond to acute fatigue stress in a sex specific manner that persists across the lifespan.
    DOI:  https://doi.org/10.64898/2026.05.22.727297
  12. Eur J Appl Physiol. 2026 Jun 06.
      Coenzyme Q10 (CoQ10) is an integral component of the mitochondrial electron transfer system. Most studies have administered the oxidised form of CoQ10 (ubiquinone) and observed no effects on mitochondrial respiratory function or endurance exercise performance. The reduced form of CoQ10, ubiquinol (UQH2), has greater bioavailability than ubiquinone, but the effects of UQH2 supplementation on mitochondrial respiratory function and exercise capacity are unclear. Fifty-four healthy, recreationally active males were randomised to receive either 300 mg·day- 1 UQH2 or placebo (PLA) for 6 weeks in a double-blind independent-group design. Before and after the supplementation period, skeletal muscle mitochondrial respiration variables and protein content of the mitochondrial leak proteins, adenine nucleotide translocase1 + 2 (ANT1 + 2) and uncoupling protein-3 (UCP-3), were assessed. In addition, participants completed a severe-intensity cycle test to exhaustion to assess time to the limit of tolerance (TLim) and oxygen uptake (V̇O2) kinetics. Compared to pre-supplementation and PLA, UQH2 supplementation increased plasma [CoQ10] (P < 0.05), and lowered inverse respiratory control ratio (Pre-PLA: 0.064 ± 0.034 vs. Post-PLA: 0.072 ± 0.026; Pre- UQH2: 0.073 ± 0.039 vs. Post-UQH2: 0.044 ± 0.019; P < 0.05), suggestive of improved oxidative phosphorylation coupling efficiency. There were no differences in ANT1 + 2 or UCP-3 protein content post-supplementation compared to pre-supplementation between groups (P > 0.05). End-exercise V̇O2, change in V̇O2 between 2 min and end-exercise, and TLim were not different between groups post-supplementation (P > 0.05). Six-weeks UQH2 supplementation increased plasma [CoQ10] and oxidative phosphorylation coupling efficiency, but did not alter mitochondrial leak proteins, TLim or V̇O2 kinetics during severe-intensity exercise in healthy, active males.
    Keywords:  Coenzyme Q10; Dietary supplement; Exercise performance; Mitochondrial respiratory efficiency; V̇O2 kinetics
    DOI:  https://doi.org/10.1007/s00421-026-06275-w
  13. Free Radic Biol Med. 2026 May 29. pii: S0891-5849(26)00830-0. [Epub ahead of print]253 351-363
      Maternal immune activation (MIA) increases risk for neurodevelopmental and psychiatric disorders, yet the stress programs linking prenatal immune challenge to persistent neuronal dysfunction remain incompletely defined. Here, we show that MIA engages convergent oxidative and ER stress programs accompanied by mitochondrial dysfunction across brain regions. Transcriptomic profiling of offspring hippocampus (HIP) revealed coordinated downregulation of oxidative phosphorylation (OXPHOS) and upregulation of ER protein-processing pathways, consistent with increased neuronal oxidative damage and ER stress markers. In parallel, hippocampal neurons exhibited mitochondrial fragmentation, reduced membrane potential, and a marked reduction in respiratory capacity. In the prefrontal cortex (PFC), MIA induced broad transcriptional remodeling that again highlighted ER stress-related pathways together with a region-specific OXPHOS signature, and these changes were accompanied by mitochondrial structural abnormalities and elevated inflammatory signaling. Finally, the mitochondria-targeted antioxidant MitoQ restored mitochondrial respiration and ameliorated anxiety-like and social behavioral abnormalities in MIA offspring. Together, these findings identify mitochondrial redox imbalance as a mechanistic node linking prenatal immune challenge to circuit-relevant cellular stress programs and support mitochondrial redox modulation as a potential intervention strategy.
    Keywords:  Behavioral abnormalities; Hippocampus; Maternal immune activation (MIA); MitoQ; Mitochondrial dysfunction; Mitochondrial redox imbalance; Oxidative stress; Prefrontal cortex
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.05.326