Skip to content

Study · Animal study (in vivo) · mouse · 2007

7 results

Mitochondrial targeting with antioxidant peptide SS-31 prevents mitochondrial depolarization, reduces islet cell apoptosis, increases islet cell yield, and improves posttransplantation function.

Thomas DA, Stauffer C, Zhao K, Yang H, Sharma VK, Szeto HH, Suthanthiran M

Journal of the American Society of Nephrology : JASN6 Dec 2006Cited by 70 (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 study7

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In diabetic mice given 200 islets from old donors, SS‑31 treatment was associated with prompt and sustained normoglycemia, whereas recipients of untreated islets remained diabetic.

    In plain wordsIn diabetic mice given a small number of islets, SS‑31 treatment was linked to lasting normal blood sugar, while untreated recipients stayed diabetic.

    Outcome
    IncreaseNormoglycemia after marginal islet mass transplantation
    Study

    mousen: not reported in source

    Marginal islet mass transplantation (200 islets from old donor mice) in syngeneic diabetic mice
    Comparator
    Untreated islet graft recipients
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In a stringent marginal islet cell mass transplantation model (200 mouse islets transplanted under the renal capsule of syngeneic diabetic mice) and using islets that were derived from old mice (>24 wk), SS-31 treatment was associated with prompt and sustained normoglycemia, whereas the untreated is…
  2. 02LabEx vivo tissuePharmacokinetics

    SS‑31 readily penetrated intact mouse islets.

    In plain wordsIn lab tests, SS‑31 easily entered intact mouse pancreatic islets.

    Outcome
    Not applicableSS-31 penetration into intact islets
    Study

    mousen: not reported in source

    Isolated mouse islets
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    Dose not stated

    Source sentences

    Summary
    SS-31 readily penetrates intact mouse islets, preserves mitochondrial polarization, reduces islet cell apoptosis, and increases islet cell yield.
  3. 03LabEx vivo tissueMechanism

    In isolated mouse islets, SS‑31 preserved mitochondrial polarization.

    In plain wordsIn lab tests on mouse islets, SS‑31 kept the electrical balance of mitochondria intact.

    Outcome
    IncreaseIslet mitochondrial polarization
    Study

    mousen: not reported in source

    Isolated mouse islets
    Outcome group
    Mitochondrial function · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    preserves mitochondrial polarization, reduces islet cell apoptosis, and increases islet cell yield.
  4. 04LabEx vivo tissueEfficacy outcome

    In isolated mouse islets, SS‑31 reduced islet cell apoptosis.

    In plain wordsIn lab tests on mouse islets, SS‑31 reduced programmed cell death.

    Outcome
    DecreaseMouse islet cell apoptosis
    Study

    mousen: not reported in source

    Isolated mouse islets
    Outcome group
    Cell viability and death · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    reduces islet cell apoptosis, and increases islet cell yield.
  5. 05LabEx vivo tissueEfficacy outcome

    In isolated mouse islets, SS‑31 increased islet cell yield.

    In plain wordsIn lab tests on mouse islets, SS‑31 increased the number of islet cells recovered.

    Outcome
    IncreaseMouse islet cell yield
    Study

    mousen: not reported in source

    Isolated mouse islets
    Outcome group
    Cell viability and death · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    increases islet cell yield.
  6. 06LabEx vivo tissueEfficacy outcome

    In cultured human islets, supplementing the culture medium with SS‑31 reduced islet cell apoptosis.

    In plain wordsIn lab tests on human islets, adding SS‑31 to the culture medium reduced programmed cell death.

    Outcome
    DecreaseHuman islet apoptosis
    Study

    humann: not reported in source

    Cultured human islets
    Outcome group
    Cell viability and death · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    reduced islet cell apoptosis and increased the viability of human islets
  7. 07LabEx vivo tissueEfficacy outcome

    In cultured human islets, supplementing the culture medium with SS‑31 increased islet viability.

    In plain wordsIn lab tests on human islets, adding SS‑31 to the culture medium increased the share of living cells.

    Outcome
    IncreaseHuman islet viability
    Study

    humann: not reported in source

    Cultured human islets
    Outcome group
    Cell viability and death · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    reduced islet cell apoptosis and increased the viability of human islets

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.

PepBank is a research reference. Talk to a doctor before you use any peptide.