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Study · Animal study (in vivo) · mouse · 2011

6 results

Novel mitochondria-targeted antioxidant peptide ameliorates burn-induced apoptosis and endoplasmic reticulum stress in the skeletal muscle of mice.

Lee HY, Kaneki M, Andreas J, Tompkins RG, Martyn JA

Shock (Augusta, Ga.)1 Dec 2011Cited by 37 (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

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In burned mice, SS‑31 peptide prevented the burn-induced increase in caspase 3 activity in skeletal muscle on postburn day 7.

    In plain wordsIn mice with burns, SS‑31 prevented the rise in a cell-death enzyme in muscle.

    Outcome
    DecreaseCaspase 3 activity (postburn day 7)
    Study

    mousen: not reported in source

    Mice with 30% total body surface area burn
    Comparator
    Burned mice without SS-31
    Outcome group
    Muscle injury and repair · Musculoskeletal
    Studied dose
    5 mg/kg body weight dailyAs given in this study (mouse).

    Source sentences

    Summary
    Treatment with SS-31 peptide prevented burn-induced increases in the caspase 3 activity (P < 0.05)
    1 context sentence
    Summary · context
    Following 30% total body surface area burn or sham burn, mice were injected daily with SS-31 peptide (5 mg/kg body weight), and the rectus abdominis muscles collected on postburn days 1, 3, and 7.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In burned mice, SS‑31 peptide prevented the burn-induced increase in apoptosis in skeletal muscle on postburn day 7.

    In plain wordsIn mice with burns, SS‑31 prevented the rise in programmed cell death in muscle.

    Outcome
    DecreaseMuscle apoptosis (postburn day 7)
    Study

    mousen: not reported in source

    Mice with 30% total body surface area burn
    Comparator
    Burned mice without SS-31
    Outcome group
    Muscle injury and repair · Musculoskeletal
    Studied dose
    5 mg/kg body weight dailyAs given in this study (mouse).

    Source sentences

    Summary
    Treatment with SS-31 peptide prevented burn-induced increases in the caspase 3 activity (P < 0.05) and apoptosis (P < 0.01) on postburn day 7
    1 context sentence
    Summary · context
    Following 30% total body surface area burn or sham burn, mice were injected daily with SS-31 peptide (5 mg/kg body weight), and the rectus abdominis muscles collected on postburn days 1, 3, and 7.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In burned mice, SS‑31 peptide prevented the burn-induced increase in phosphatase and tensin homolog expression on postburn days 3 and 7.

    In plain wordsIn mice with burns, SS‑31 prevented the rise in a signalling protein (PTEN) in muscle.

    Outcome
    DecreasePTEN expression (postburn days 3 and 7)
    Study

    mousen: not reported in source

    Mice with 30% total body surface area burn
    Comparator
    Burned mice without SS-31
    Outcome group
    Muscle injury and repair · Musculoskeletal
    Studied dose
    5 mg/kg body weight dailyAs given in this study (mouse).

    Source sentences

    Summary
    The SS-31 peptide treatment also prevented the increase in the expression levels of phosphatase and tensin homolog on postburn days 3 and 7.
    1 context sentence
    Summary · context
    Following 30% total body surface area burn or sham burn, mice were injected daily with SS-31 peptide (5 mg/kg body weight), and the rectus abdominis muscles collected on postburn days 1, 3, and 7.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In burned mice, SS‑31 peptide significantly decreased the burn-induced increase in the endoplasmic reticulum stress marker binding immunoglobulin protein on postburn days 3 and 7.

    In plain wordsIn mice with burns, SS‑31 lowered a stress marker in muscle cells.

    Outcome
    DecreaseBinding immunoglobulin protein (ER stress marker)
    Study

    mousen: not reported in source

    Mice with 30% total body surface area burn
    Comparator
    Burned mice without SS-31
    Outcome group
    Muscle injury and repair · Musculoskeletal
    Studied dose
    5 mg/kg body weight dailyAs given in this study (mouse).

    Source sentences

    Summary
    Burn injury-induced increases in the levels of two endoplasmic reticulum stress markers, binding immunoglobulin protein and protein disulfide isomerase, were significantly decreased by the SS-31 peptide treatments on postburn day 7 and on day 3 for binding immunoglobulin protein as well (P < 0.05).
    1 context sentence
    Summary · context
    Following 30% total body surface area burn or sham burn, mice were injected daily with SS-31 peptide (5 mg/kg body weight), and the rectus abdominis muscles collected on postburn days 1, 3, and 7.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In burned mice, SS‑31 peptide significantly decreased the burn-induced increase in the endoplasmic reticulum stress marker protein disulfide isomerase on postburn day 7.

    In plain wordsIn mice with burns, SS‑31 lowered a second stress marker in muscle cells.

    Outcome
    DecreaseProtein disulfide isomerase (ER stress marker)
    Study

    mousen: not reported in source

    Mice with 30% total body surface area burn
    Comparator
    Burned mice without SS-31
    Outcome group
    Muscle injury and repair · Musculoskeletal
    Studied dose
    5 mg/kg body weight dailyAs given in this study (mouse).

    Source sentences

    Summary
    Burn injury-induced increases in the levels of two endoplasmic reticulum stress markers, binding immunoglobulin protein and protein disulfide isomerase, were significantly decreased by the SS-31 peptide treatments on postburn day 7 and on day 3 for binding immunoglobulin protein as well (P < 0.05).
    1 context sentence
    Summary · context
    Following 30% total body surface area burn or sham burn, mice were injected daily with SS-31 peptide (5 mg/kg body weight), and the rectus abdominis muscles collected on postburn days 1, 3, and 7.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In burned mice, SS‑31 peptide reduced the expression of oxidized proteins in muscle on postburn day 7.

    In plain wordsIn mice with burns, SS‑31 reduced oxidized proteins in muscle.

    Outcome
    DecreaseOxidized protein expression (postburn day 7)
    Study

    mousen: not reported in source

    Mice with 30% total body surface area burn
    Comparator
    Burned mice without SS-31
    Outcome group
    Muscle injury and repair · Musculoskeletal
    Studied dose
    5 mg/kg body weight dailyAs given in this study (mouse).

    Source sentences

    Summary
    The effects of SS-31 appear to be, in part, due to its ability to reduce oxidative stress in burned mice, evidenced by reduced expression of oxidized proteins that were clearly evident on postburn day 7.
    1 context sentence
    Summary · context
    Following 30% total body surface area burn or sham burn, mice were injected daily with SS-31 peptide (5 mg/kg body weight), and the rectus abdominis muscles collected on postburn days 1, 3, and 7.

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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