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Study · Animal study (in vivo) · rat · 2005

15 results

Gene expression profiling reveals multiple protective influences of the peptide alpha-melanocyte-stimulating hormone in experimental heart transplantation.

Colombo G, Gatti S, Turcatti F, Sordi A, Fassati LR, Bonino F, Lipton JM, Catania A

Journal of immunology (Baltimore, Md. : 1950)1 Sept 2005Cited by 18 (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 study15

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts on postoperative day 1, NDP-alpha-MSH induced expression of cytoskeleton proteins.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH raised the activity of genes for cell structure proteins.

    Outcome
    IncreaseCytoskeleton protein expression, day 1
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    On postoperative day 1, the peptide induced expression of cytoskeleton proteins, intracellular kinases, transcription regulators, metallopeptidases, and protease inhibitors.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts on postoperative day 1, NDP-alpha-MSH induced expression of intracellular kinases.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH raised the activity of genes for signaling enzymes.

    Outcome
    IncreaseIntracellular kinase expression, day 1
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    On postoperative day 1, the peptide induced expression of cytoskeleton proteins, intracellular kinases, transcription regulators, metallopeptidases, and protease inhibitors.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts on postoperative day 1, NDP-alpha-MSH induced expression of transcription regulators.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH raised the activity of genes that control other genes.

    Outcome
    IncreaseTranscription regulator expression, day 1
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    On postoperative day 1, the peptide induced expression of cytoskeleton proteins, intracellular kinases, transcription regulators, metallopeptidases, and protease inhibitors.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts on postoperative day 1, NDP-alpha-MSH induced expression of metallopeptidases.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH raised the activity of genes for protein-cutting enzymes.

    Outcome
    IncreaseMetallopeptidase expression, day 1
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    On postoperative day 1, the peptide induced expression of cytoskeleton proteins, intracellular kinases, transcription regulators, metallopeptidases, and protease inhibitors.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts on postoperative day 1, NDP-alpha-MSH induced expression of protease inhibitors.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH raised the activity of genes for protease inhibitors.

    Outcome
    IncreaseProtease inhibitor expression, day 1
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    On postoperative day 1, the peptide induced expression of cytoskeleton proteins, intracellular kinases, transcription regulators, metallopeptidases, and protease inhibitors.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, NDP-alpha-MSH repressed expression of immune mediators.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH lowered the activity of immune genes.

    Outcome
    DecreaseImmune mediator expression, day 1
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Conversely, NDP-alpha-MSH repressed immune, inflammatory, cell cycle, and protein turnover mediators.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, NDP-alpha-MSH repressed expression of inflammatory mediators.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH lowered the activity of inflammation genes.

    Outcome
    DecreaseInflammatory mediator expression
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Conversely, NDP-alpha-MSH repressed immune, inflammatory, cell cycle, and protein turnover mediators.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  8. 08AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, NDP-alpha-MSH repressed expression of cell cycle mediators.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH lowered the activity of cell cycle genes.

    Outcome
    DecreaseCell cycle mediator expression
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Conversely, NDP-alpha-MSH repressed immune, inflammatory, cell cycle, and protein turnover mediators.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  9. 09AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, NDP-alpha-MSH repressed expression of protein turnover mediators.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH lowered the activity of protein turnover genes.

    Outcome
    DecreaseProtein turnover mediator expression
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Conversely, NDP-alpha-MSH repressed immune, inflammatory, cell cycle, and protein turnover mediators.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  10. 10AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, later effects of alpha-MSH treatment included down-regulation of the oxidative stress response.

    In plain wordsIn rats with heart grafts, later treatment lowered the activity of oxidative stress response genes.

    Outcome
    DecreaseOxidative stress response, later time point
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Later effects of alpha-MSH treatment included down-regulation of oxidative stress response and up-regulation of ion channels, calcium regulation proteins, phosphatidylinositol signaling system, and glycolipidic metabolism.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  11. 11AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, later effects of alpha-MSH treatment included up-regulation of ion channels.

    In plain wordsIn rats with heart grafts, later treatment raised the activity of ion channel genes.

    Outcome
    IncreaseIon channel expression, later time point
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Later effects of alpha-MSH treatment included down-regulation of oxidative stress response and up-regulation of ion channels, calcium regulation proteins, phosphatidylinositol signaling system, and glycolipidic metabolism.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  12. 12AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, later effects of alpha-MSH treatment included up-regulation of calcium regulation proteins.

    In plain wordsIn rats with heart grafts, later treatment raised the activity of calcium control genes.

    Outcome
    IncreaseCalcium regulation protein expression, later time point
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Later effects of alpha-MSH treatment included down-regulation of oxidative stress response and up-regulation of ion channels, calcium regulation proteins, phosphatidylinositol signaling system, and glycolipidic metabolism.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  13. 13AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, later effects of alpha-MSH treatment included up-regulation of the phosphatidylinositol signaling system.

    In plain wordsIn rats with heart grafts, later treatment raised the activity of genes in a cell signaling system.

    Outcome
    IncreasePhosphatidylinositol signaling system, later time point
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Later effects of alpha-MSH treatment included down-regulation of oxidative stress response and up-regulation of ion channels, calcium regulation proteins, phosphatidylinositol signaling system, and glycolipidic metabolism.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  14. 14AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, later effects of alpha-MSH treatment included up-regulation of glycolipidic metabolism.

    In plain wordsIn rats with heart grafts, later treatment raised the activity of genes for sugar-fat metabolism.

    Outcome
    IncreaseGlycolipidic metabolism, later time point
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Later effects of alpha-MSH treatment included down-regulation of oxidative stress response and up-regulation of ion channels, calcium regulation proteins, phosphatidylinositol signaling system, and glycolipidic metabolism.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.
  15. 15AnimalAnimal study (in vivo)Mechanism

    In rat heart grafts, NDP-alpha-MSH exerted its effects on both antigen-dependent and antigen-independent injury.

    In plain wordsIn rats with heart grafts, NDP-alpha-MSH acted on both immune-driven and non-immune injury.

    Outcome
    Not applicableEffect on antigen-dependent and independent injury
    Study

    ratn: not reported in source

    heart transplantation
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    NDP-alpha-MSH exerted its effects on both Ag-dependent and -independent injury.
    1 context sentence
    Summary · context
    Gene expression profile was examined in heart grafts removed on postoperative days 1 and 4 from rats treated with saline or the synthetic alpha-MSH analog Nle4DPhe7 (NDP)-alpha-MSH.

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

    13 Oct 2026, 21:44 UTC

    Study results updated

  2. Version 1

    13 Oct 2026, 16:31 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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