Evidence map›Paper›PMID 41238093›Full record

ArticleMitochondrion2026

Assessment of mitochondrial viability under calcium Stress: Insights for mitochondrial transplantation.

Melody Toosky, Arash Kheradvar

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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
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

2 authors.

Melody TooskyDepartment of Biomedical Engineering, University of California, Irvine, Irvine, CA, USA.
Arash KheradvarDepartment of Biomedical Engineering, University of California, Irvine, Irvine, CA, USA; Department of Radiological Sciences, University of California, Irvine, Irvine, CA, USA. Electronic address: arashkh@uci.edu.

Funding

Volumetric Echocardiographic Particle Image Velocimetry for Grading the Severity of Mitral Valve RegurgitationR01HL153724 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Arash Kheradvar · 2022 to 2026
$3.9M
Computational and Experimental Modeling of Subclinical Leaflet Thrombosis in Bioprosthetic Aortic ValvesR01HL157631 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FOGELSON, AARON L, GRIFFITH, BOYCE EUGENE · 2022 to 2025
$2.7M
Reciprocal effects between scaffold geometry and ventricular vortex flow on viability and performance of tissue-engineered mitral valveR01HL162687 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Arash Kheradvar · 2023 to 2026
$2.3M
High-speed 4D echocardiography system with adjustable multi-planar acquisitionR56HL173809 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KHERADVAR, ARASH, YEN, JESSE T-P · 2024 to 2024
$678k
NHLBI NIH HHS R01 HL153724NHLBI NIH HHS R01 HL157631NHLBI NIH HHS R01 HL162687NHLBI NIH HHS R56 HL173809
6 · The paper itself

Abstract

Mitochondrial transplantation has emerged as a promising cardioprotective strategy for ischemia-reperfusion injury, aiming to restore bioenergetic function by delivering healthy mitochondria to damaged tissue. However, conflicting reports exist regarding whether mitochondria can survive exposure to the calcium-rich extracellular environment, such as the bloodstream, prior to cellular uptake. Resolving this question is essential for advancing the therapeutic use of mitochondria in clinical settings. Isolated mitochondria from L6 rat skeletal muscle cells were incubated with physiologic (1.3  mM), sub-physiologic (0.65  mM), and supraphysiologic (2.6  mM) concentrations of calcium. Mitochondrial membrane potential was assessed using MitoTracker™ Red FM fluorescence, and structural integrity was evaluated using impedance-based Coulter counter analysis over a 12-hour time course. Mitochondria exposed to 1.3  mM calcium retained 90-95 % membrane potential by 12 h, while 2.6  mM calcium caused progressive loss of function and integrity, approaching levels seen in freeze-thawed controls. Coulter counter measurements revealed more extensive mitochondrial loss across all calcium-treated groups than fluorescence assays alone, suggesting that dye-based methods may underestimate structural damage. Nonetheless, a substantial proportion of mitochondria remained both structurally and functionally intact at physiologically relevant calcium levels. These findings demonstrate that a substantial number of mitochondria can retain membrane potential and structural integrity after exposure to extracellular calcium concentrations approximating those found in blood. This supports the feasibility of intracoronary mitochondrial transplantation and underscores the need for further in vivo studies to optimize survival and efficacy of mitochondria delivered in calcium-rich environments.

Indexed as

CalciumMitochondriaStress, PhysiologicalAnimalsMembrane Potential, MitochondrialRatsCalciumCalcium overloadCardioprotectionExtracellular mitochondriaIntracoronary DeliveryIschemia-reperfusion injuryMitochondrial membrane potentialMitochondrial transplantation

Identifiers

PMID41238093
PMCPMC12746765

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Registered trials

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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.