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Study · Animal study (in vivo) · mouse · 1992

14 results

Radioprotective effects of serum thymic factor in mice.

Kobayashi H, Abe H, Ueyama T, Awaya A, Shikita M

Radiation research1 Mar 1992Cited by 4 (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 study14

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In mice after total-body irradiation, daily FTS reduced mortality at radioprotective doses.

    In plain wordsIn mice after irradiation, daily FTS reduced deaths.

    Outcome
    DecreaseMortality after irradiation
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Mortality · Whole body
    Studied dose
    3-100 micrograms daily · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Serum thymic factor (FTS) reduced mortality of mice after total-body irradiation with 7.56 Gy X rays.
    1 context sentence
    Summary · context
    The radioprotective effect was achieved by daily repeated subcutaneous injections of 3-100 micrograms FTS, while doses higher than 300 micrograms/day/mouse were neither radioprotective nor toxic.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, FTS doses higher than 300 micrograms/day/mouse were not radioprotective.

    In plain wordsIn irradiated mice, FTS doses higher than 300 micrograms/day/mouse did not provide radioprotection.

    Outcome
    No significant changeRadioprotection at high doses
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Mortality · Whole body
    Studied dose
    >300 micrograms/day/mouse · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The radioprotective effect was achieved by daily repeated subcutaneous injections of 3-100 micrograms FTS, while doses higher than 300 micrograms/day/mouse were neither radioprotective nor toxic.
  3. 03AnimalAnimal study (in vivo)Safety outcome

    In mice, FTS doses higher than 300 micrograms/day/mouse were not toxic.

    In plain wordsIn mice, FTS doses higher than 300 micrograms/day/mouse were not toxic.

    Outcome
    No significant changeHigh-dose toxicity
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Adverse events · Whole body
    Studied dose
    >300 micrograms/day/mouse · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The radioprotective effect was achieved by daily repeated subcutaneous injections of 3-100 micrograms FTS, while doses higher than 300 micrograms/day/mouse were neither radioprotective nor toxic.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In sublethally irradiated mice, FTS moderated spleen degeneration at 3-100 micrograms.

    In plain wordsIn sublethally irradiated mice, FTS reduced spleen degeneration at 3-100 micrograms.

    Outcome
    DecreaseSpleen degeneration at lower doses
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    3-100 micrograms · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Similarly, degeneration of the spleen was moderated by 3-100 micrograms FTS but not by 500 micrograms FTS in sublethally (3.78 Gy) irradiated mice.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In sublethally irradiated mice, 500 micrograms FTS did not moderate spleen degeneration.

    In plain wordsIn sublethally irradiated mice, 500 micrograms FTS did not reduce spleen degeneration.

    Outcome
    No significant changeSpleen degeneration at high dose
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    500 micrograms · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Similarly, degeneration of the spleen was moderated by 3-100 micrograms FTS but not by 500 micrograms FTS in sublethally (3.78 Gy) irradiated mice.
  6. 06AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, daily FTS enhanced splenic hematopoiesis.

    In plain wordsIn irradiated mice, daily FTS increased blood-cell production in the spleen.

    Outcome
    IncreaseSplenic hematopoiesis
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    10 micrograms daily · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Histological examination showed that hematopoiesis was enhanced in the spleen by daily injections of 10 micrograms FTS.
  7. 07AnimalAnimal study (in vivo)Efficacy outcome

    Spleen cells from FTS-treated mice incorporated more thymidine in culture with or without concanavalin A.

    In plain wordsIn mice, FTS treatment increased subsequent thymidine incorporation by spleen cells in cultures with or without concanavalin A.

    Outcome
    IncreaseSplenic cell thymidine incorporation
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Spleen cells from the FTS-treated mice incorporated more [3H]thymidine in culture with or without concanavalin A.
  8. 08AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, FTS increased colony-stimulating factor production in the spleen.

    In plain wordsIn irradiated mice, FTS increased colony-stimulating factor production in the spleen.

    Outcome
    IncreaseSplenic colony-stimulating factor production
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The treatment with FTS increased the production of colony-stimulating factor in the spleen as well as in peritoneal macrophage-like cells, and caused a significant increase in the number of granulocyte-macrophage colony-forming cells both in the spleen and in the femoral bone marrow.
  9. 09AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, FTS increased colony-stimulating factor production in peritoneal macrophage-like cells.

    In plain wordsIn irradiated mice, FTS increased colony-stimulating factor production in peritoneal macrophage-like cells.

    Outcome
    IncreasePeritoneal colony-stimulating factor production
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The treatment with FTS increased the production of colony-stimulating factor in the spleen as well as in peritoneal macrophage-like cells, and caused a significant increase in the number of granulocyte-macrophage colony-forming cells both in the spleen and in the femoral bone marrow.
  10. 10AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, FTS significantly increased splenic granulocyte-macrophage colony-forming cell numbers.

    In plain wordsIn irradiated mice, FTS increased granulocyte-macrophage colony-forming cells in the spleen.

    Outcome
    IncreaseSplenic granulocyte-macrophage colony-forming cells
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The treatment with FTS increased the production of colony-stimulating factor in the spleen as well as in peritoneal macrophage-like cells, and caused a significant increase in the number of granulocyte-macrophage colony-forming cells both in the spleen and in the femoral bone marrow.
  11. 11AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, FTS significantly increased granulocyte-macrophage colony-forming cells in femoral bone marrow.

    In plain wordsIn irradiated mice, FTS increased granulocyte-macrophage colony-forming cells in bone marrow.

    Outcome
    IncreaseBone marrow granulocyte-macrophage colony-forming cells
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The treatment with FTS increased the production of colony-stimulating factor in the spleen as well as in peritoneal macrophage-like cells, and caused a significant increase in the number of granulocyte-macrophage colony-forming cells both in the spleen and in the femoral bone marrow.
  12. 12AnimalAnimal study (in vivo)Efficacy outcome

    In sublethally irradiated mice, FTS prevented the decrease in circulating neutrophils.

    In plain wordsIn sublethally irradiated mice, FTS prevented a decrease in circulating neutrophils.

    Outcome
    IncreaseCirculating neutrophil decrease
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, FTS prevented a decrease in circulating neutrophils in the sublethally irradiated mice.
  13. 13AnimalAnimal study (in vivo)Efficacy outcome

    In sublethally irradiated mice, occasional prominent myelopoiesis overshoot recovery did not occur with FTS treatment.

    In plain wordsIn sublethally irradiated mice, FTS-treated animals did not show the occasional overshoot in blood-cell production.

    Outcome
    DecreaseMyelopoiesis overshoot recovery
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    Prominent overshoot recovery of myelopoiesis, which occurred occasionally in sublethally irradiated mice, did not occur in the FTS-treated mice.
  14. 14AnimalAnimal study (in vivo)Efficacy outcome

    In irradiated mice, FTS significantly reduced the decrease in blood erythrocytes.

    In plain wordsIn irradiated mice, FTS reduced the loss of red blood cells.

    Outcome
    IncreaseBlood erythrocyte decrease
    Study

    mousen: not reported in source

    Total-body X-irradiated mice
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The decrease in blood erythrocytes was also significantly reduced.

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

    21 Oct 2026, 15:58 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 12:50 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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