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Study · Animal study (in vivo) · mouse · 1988

8 results

Toxicologic studies of a superpotent alpha-melanotropin, [Nle4, D-Phe7]alpha-MSH.

Dorr RT, Dawson BV, al-Obeidi F, Hadley ME, Levine N, Hruby VJ

Investigational new drugs1 Dec 1988Cited by 17 (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 study8

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

  1. 01AnimalAnimal study (in vivo)Safety outcome

    In mice given NDP-MSH up to 2 mg/kg for 4 or 12 weeks, no toxic effects were observed in various organs.

    In plain wordsIn mice, NDP-MSH given for 4 or 12 weeks caused no toxic effects in organs.

    Outcome
    No significant changeOrgan toxicity
    Study

    mousen: not reported in source

    mice
    Outcome group
    Adverse events · Whole body
    Studied dose
    up to 2 mg/kg daily or weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 4 or 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    Mice were administered up to 2 mg/kg of the analog daily and weekly over 4 or 12 weeks by both topical application (in 90% DMSO) or by IP injections (in physiologic saline).
    1 context sentence
    Summary · context
    no toxic effects were observed in various organs, on hematologic indices, or on weight gain.
  2. 02AnimalAnimal study (in vivo)Safety outcome

    In mice given NDP-MSH, no toxic effects were observed on hematologic indices.

    In plain wordsIn mice, NDP-MSH caused no toxic effects on blood counts.

    Outcome
    No significant changeHematologic indices
    Study

    mousen: not reported in source

    mice
    Outcome group
    Adverse events · Whole body
    Studied dose
    up to 2 mg/kg daily or weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 4 or 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    At the end of this period, no toxic effects were observed in various organs, on hematologic indices, or on weight gain.
    2 context sentences
    Summary · context
    A toxicology study was performed in mice given a superpotent alpha melanocyte stimulating hormone (MSH) analog.
    Summary · context
    This 13 amino acid derivative, [Nle4, D-Phe7]alpha-MSH or NDP-MSH, is a melanotropin which is very slowly biodegraded in vivo and is active at 1/1,000 the concentration of natural alpha-MSH.
  3. 03AnimalAnimal study (in vivo)Safety outcome

    In mice given NDP-MSH, no toxic effects were observed on weight gain.

    In plain wordsIn mice, NDP-MSH did not affect weight gain.

    Outcome
    No significant changeWeight gain
    Study

    mousen: not reported in source

    mice
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    up to 2 mg/kg daily or weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 4 or 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    At the end of this period, no toxic effects were observed in various organs, on hematologic indices, or on weight gain.
    2 context sentences
    Summary · context
    A toxicology study was performed in mice given a superpotent alpha melanocyte stimulating hormone (MSH) analog.
    Summary · context
    This 13 amino acid derivative, [Nle4, D-Phe7]alpha-MSH or NDP-MSH, is a melanotropin which is very slowly biodegraded in vivo and is active at 1/1,000 the concentration of natural alpha-MSH.
  4. 04AnimalAnimal study (in vivo)Safety outcome

    A slight increase in triglyceride levels was noted in mice given NDP-MSH weekly for 12 weeks.

    In plain wordsIn mice, weekly NDP-MSH for 12 weeks slightly raised triglyceride levels.

    Outcome
    IncreaseSerum triglyceride level
    Study

    mousen: not reported in source

    mice
    Outcome group
    Lipids · Metabolic and weight
    Studied dose
    up to 2 mg/kg weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    A slight increase in triglyceride and platelet levels were noted in mice given the analog weekly for 12 weeks.
    2 context sentences
    Summary · context
    A toxicology study was performed in mice given a superpotent alpha melanocyte stimulating hormone (MSH) analog.
    Summary · context
    This 13 amino acid derivative, [Nle4, D-Phe7]alpha-MSH or NDP-MSH, is a melanotropin which is very slowly biodegraded in vivo and is active at 1/1,000 the concentration of natural alpha-MSH.
  5. 05AnimalAnimal study (in vivo)Safety outcome

    A slight increase in platelet levels was noted in mice given NDP-MSH weekly for 12 weeks.

    In plain wordsIn mice, weekly NDP-MSH for 12 weeks slightly raised platelet levels.

    Outcome
    IncreasePlatelet level
    Study

    mousen: not reported in source

    mice
    Outcome group
    Adverse events · Whole body
    Studied dose
    up to 2 mg/kg weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    A slight increase in triglyceride and platelet levels were noted in mice given the analog weekly for 12 weeks.
    2 context sentences
    Summary · context
    A toxicology study was performed in mice given a superpotent alpha melanocyte stimulating hormone (MSH) analog.
    Summary · context
    This 13 amino acid derivative, [Nle4, D-Phe7]alpha-MSH or NDP-MSH, is a melanotropin which is very slowly biodegraded in vivo and is active at 1/1,000 the concentration of natural alpha-MSH.
  6. 06AnimalAnimal study (in vivo)Safety outcome

    In mice given NDP-MSH, there was no evidence of an effect on behavior.

    In plain wordsIn mice, NDP-MSH had no sign of an effect on behavior.

    Outcome
    No significant changeBehavior
    Study

    mousen: not reported in source

    mice
    Outcome group
    Adverse events · Nervous system and cognition
    Studied dose
    up to 2 mg/kg daily or weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 4 or 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    There was no evidence of an effect on behavior nor ACTH-like endocrine actions such as elevated serum cortisol levels.
    2 context sentences
    Summary · context
    A toxicology study was performed in mice given a superpotent alpha melanocyte stimulating hormone (MSH) analog.
    Summary · context
    This 13 amino acid derivative, [Nle4, D-Phe7]alpha-MSH or NDP-MSH, is a melanotropin which is very slowly biodegraded in vivo and is active at 1/1,000 the concentration of natural alpha-MSH.
  7. 07AnimalAnimal study (in vivo)Safety outcome

    In mice given NDP-MSH, there was no evidence of ACTH-like endocrine actions such as elevated serum cortisol.

    In plain wordsIn mice, NDP-MSH did not raise cortisol or cause other ACTH-like hormone effects.

    Outcome
    No significant changeACTH-like endocrine actions (serum cortisol)
    Study

    mousen: not reported in source

    mice
    Outcome group
    Adverse events · Endocrine and hormones
    Studied dose
    up to 2 mg/kg daily or weekly · topical (in 90% DMSO) or intraperitoneal (in saline) · 4 or 12 weeksAs given in this study (mouse).

    Source sentences

    Summary
    There was no evidence of an effect on behavior nor ACTH-like endocrine actions such as elevated serum cortisol levels.
    2 context sentences
    Summary · context
    A toxicology study was performed in mice given a superpotent alpha melanocyte stimulating hormone (MSH) analog.
    Summary · context
    This 13 amino acid derivative, [Nle4, D-Phe7]alpha-MSH or NDP-MSH, is a melanotropin which is very slowly biodegraded in vivo and is active at 1/1,000 the concentration of natural alpha-MSH.
  8. 08LabEx vivo tissuePharmacokinetics

    In diffusion studies with full-thickness mouse skin, NDP-MSH diffused reproducibly: about 0.002% of a 10(-4) M preparation in DMSO/water and 0.05% in a PEG/alcohol cream base was delivered.

    In plain wordsIn lab tests on mouse skin, a small share of NDP-MSH crossed the skin, from about 0.002% to 0.05% depending on the base.

    Outcome
    Not applicableTransdermal delivery through mouse skin in vitro
    Study

    mousen: not reported in source

    full-thickness mouse skin in diffusion studies
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    10(-4) M preparation · transdermalAs given in this study (mouse).

    Measurements

    Transdermal delivery
    0.002 % of 10(-4) M preparation
    DMSO/water solution
    Transdermal delivery
    0.05 % of 10(-4) M preparation
    PEG/alcohol cream base

    Source sentences

    Summary
    Transdermal drug delivery studies performed in vitro showed reproducible diffusion of the NDP-MSH analog through full-thickness mouse skin.
    1 context sentence
    Summary · context
    Approximately 0.002% to 0.05% of a 10(-4) M preparation was transdermally delivered using a DMSO/water solution or a PEG/alcohol cream base, respectively.

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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