Evidence map›Paper›PMID 42838474›Full record

ArticleMitochondrion2026

Mitochondrial calcium and ROS: present understanding and future directions.

Chloe I Roth, Alyssa C Vadovsky, Keeler J Steele, Annamaria Raftu, Skyler Shaman, Jada G Roberts, Jason N Bazil

Abstract read
In one paragraph

Article in Mitochondrion, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Chloe I RothDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America.
Alyssa C VadovskyDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America.
Keeler J SteeleDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America.
Annamaria RaftuDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America.
Skyler ShamanDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America.
Jada G RobertsDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America.
Jason N BazilDepartment of Physiology, Michigan State University, East Lansing, MI 48824, United States of America; Department of Biomedical Engineering, Michigan State University, East Lansing, MI 48824, United States of America. Electronic address: jnbazil@msu.edu.

Funding

Elucidation of the Genuine Impact of Calcium Overload on MitochondriaR01HL183792 · NHLBI · HENRY FORD HEALTH + MICHIGAN STATE UNIVERSITY HEALTH SCIENCES · PI Jason N Bazil · 2026 to 2026
$466k
NHLBI NIH HHS R01 HL183792
6 · The paper itself

Abstract

This mini-review and perspective article goes over a brief history of mitochondria and their role in calcium overload and oxidative stress. Altogether, oxidative stress, calcium overload, and mitochondrial dysfunction form a pathophysiological triad, and most of the explanatory power of this triad relies on invoking the mitochondrial permeability transition pore (mPTP) as driving the pathophysiology. As such, many studies claim that calcium overload triggers oxidative stress and acts as the upstream event in mitochondrial dysfunction to explain experimental results. However, recent findings shed new light on this triad and how it affects living tissue. While the mPTP hypothesis has dominated curated explanations, emerging functional and structural data supports a distinct stable overloaded state that better accounts for graded dysfunction in the presence of low intensity chronic oxidative stress. In this stable calcium overload state, mitochondrial dysfunction is evident from the reduced oxidative metabolism impairments accompanying suppressed free radical emission rates, distinct from the effects of opening the mPTP. This refined framework has direct implications for SR/ER-mitochondrial crosstalk in disease and tunes mechanistic models that better align with the available data. While mitochondria absolutely play an important role in various pathologies, they primarily respond to exogenous driving forces that move them into compromised functional states, which in turn amplify cellular disorder. Ideally, this perspective will help refine the intriguing and complex aspects of mitochondrial function in cell death and disease.

Indexed as

Calcium overloadFree radicalMitochondriaMitochondria permeability transitionOxidative stressPathophysiological triad

Identifiers

PMID42838474
PMCPMC13689492

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.