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Study · Animal study (in vivo) · 2026

6 results

Breaking a mitochondrial danger-STING feed-forward amplifier preserves alveolar-capillary architecture and dampens interferon-chemokine signaling in acute lung injury.

Elmorsy EA, Amer MM, Hamad RS, Abdel-Hamed MR, Farrag AA, Alorini M, Khodeir MM, Ali MAM, Alhowail AH, Mohamed EA, Alsalloom AA, Alsaykhan H and 5 more

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Alsoqih NS, Ata HS, Sameh A, Chaudhary AA, Saber S

Tissue & cell2 Apr 2026Cited by 1 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study6

2 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In experimental acute lung injury after lipopolysaccharide, elamipretide predominantly improved redox status.

    In plain wordsIn an animal lung injury model, elamipretide mainly improved the balance of oxidative stress.

    Outcome
    Not applicableRedox status
    Study

    n: not reported in source

    LPS-induced acute lung injury
    Outcome group
    Inflammation markers · Respiratory
    Studied dose
    Dose not stated

    Source sentences

    Summary
    ELM predominantly improved redox status
    1 context sentence
    Summary · context
    At 24 h post intratracheal lipopolysaccharide, lung architecture was assessed histologically, and BALF and lung tissue were analyzed for barrier and cytolytic injury
  2. 02AnimalAnimal study (in vivo)Mechanism

    In experimental acute lung injury after lipopolysaccharide, elamipretide reduced mitochondrial leak.

    In plain wordsIn an animal lung injury model, elamipretide reduced the leak of mitochondrial material.

    Outcome
    DecreaseMitochondrial leak
    Study

    n: not reported in source

    LPS-induced acute lung injury
    Outcome group
    Mitochondrial function · Respiratory
    Studied dose
    Dose not stated

    Source sentences

    Summary
    ELM predominantly improved redox status and reduced mitochondrial leak
    1 context sentence
    Summary · context
    At 24 h post intratracheal lipopolysaccharide, lung architecture was assessed histologically, and BALF and lung tissue were analyzed for barrier and cytolytic injury

Studies that did not test the peptide alone4

In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Elamipretide (SS-31).

  1. 03AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In experimental acute lung injury, combined elamipretide and H151 gave the greatest improvement in lung histology.

    In plain wordsIn an animal lung injury model, elamipretide with H151 gave the best improvement in lung tissue structure.

    Outcome
    Not applicableLung histology
    Study

    n: not reported in source

    LPS-induced acute lung injury
    Outcome group
    Inflammation markers · Respiratory

    Source sentences

    Summary
    Notably, combined ELM+H151 produced the most comprehensive protection, yielding the greatest improvement in lung histology together with reductions in barrier disruption, inflammatory cellular infiltration, and downstream signaling outputs.
    1 context sentence
    Summary · context
    At 24 h post intratracheal lipopolysaccharide, lung architecture was assessed histologically, and BALF and lung tissue were analyzed for barrier and cytolytic injury

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  2. 04AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In experimental acute lung injury, combined elamipretide and H151 reduced barrier disruption.

    In plain wordsIn an animal lung injury model, elamipretide with H151 reduced damage to the lung barrier.

    Outcome
    DecreaseBarrier disruption
    Study

    n: not reported in source

    LPS-induced acute lung injury
    Outcome group
    Inflammation markers · Respiratory

    Source sentences

    Summary
    Notably, combined ELM+H151 produced the most comprehensive protection, yielding the greatest improvement in lung histology together with reductions in barrier disruption, inflammatory cellular infiltration, and downstream signaling outputs.
    1 context sentence
    Summary · context
    At 24 h post intratracheal lipopolysaccharide, lung architecture was assessed histologically, and BALF and lung tissue were analyzed for barrier and cytolytic injury

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  3. 05AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In experimental acute lung injury, combined elamipretide and H151 reduced inflammatory cellular infiltration.

    In plain wordsIn an animal lung injury model, elamipretide with H151 reduced the inflammatory cells in the lung.

    Outcome
    DecreaseInflammatory cellular infiltration
    Study

    n: not reported in source

    LPS-induced acute lung injury
    Outcome group
    Inflammation markers · Respiratory

    Source sentences

    Summary
    Notably, combined ELM+H151 produced the most comprehensive protection, yielding the greatest improvement in lung histology together with reductions in barrier disruption, inflammatory cellular infiltration, and downstream signaling outputs.
    1 context sentence
    Summary · context
    At 24 h post intratracheal lipopolysaccharide, lung architecture was assessed histologically, and BALF and lung tissue were analyzed for barrier and cytolytic injury

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  4. 06AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Mechanism

    In experimental acute lung injury, combined elamipretide and H151 reduced downstream signaling outputs.

    In plain wordsIn an animal lung injury model, elamipretide with H151 reduced inflammation signals.

    Outcome
    DecreaseDownstream signaling outputs
    Study

    n: not reported in source

    LPS-induced acute lung injury
    Outcome group
    Inflammation markers · Respiratory

    Source sentences

    Summary
    Notably, combined ELM+H151 produced the most comprehensive protection, yielding the greatest improvement in lung histology together with reductions in barrier disruption, inflammatory cellular infiltration, and downstream signaling outputs.
    1 context sentence
    Summary · context
    At 24 h post intratracheal lipopolysaccharide, lung architecture was assessed histologically, and BALF and lung tissue were analyzed for barrier and cytolytic injury

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    10 Oct 2026, 08:19 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:47 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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