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Study · Animal study (in vivo) · mouse · 1985

5 results

Oxytocin and a C-terminal derivative (Z-prolyl-D-leucine) attenuate tolerance to and dependence on morphine and interact with dopaminergic neurotransmission in the mouse brain.

Kovács GL, Horváth Z, Sarnyai Z, Faludi M, Telegdy G

Neuropharmacology1 May 1985Cited by 64 (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 study5

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In mice, oxytocin attenuated the development of acute tolerance to the antinociceptive effect of morphine.

    In plain wordsIn mice, oxytocin reduced the build-up of acute tolerance to the pain-relieving effect of morphine.

    Peptide
    Oxytocin
    Outcome
    DecreaseAcute tolerance to morphine antinociception
    Study

    mousen: not reported in source

    Morphine tolerance and dependence
    Outcome group
    Pain · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Oxytocin and the dipeptides attenuated the development of acute and chronic tolerance to the antinociceptive effect of morphine and delayed the onset of the naloxone-precipitated withdrawal syndrome.
    1 context sentence
    Summary · context
    The effects of oxytocin (OXT) and of dipeptides derived from the C-terminal portion of oxytocin (Z-prolyl-leucine and Z-prolyl-D-leucine) on the development of acute and chronic tolerance to, and dependence on morphine were tested in the mouse.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In mice, oxytocin attenuated the development of chronic tolerance to the antinociceptive effect of morphine.

    In plain wordsIn mice, oxytocin reduced the build-up of chronic tolerance to the pain-relieving effect of morphine.

    Peptide
    Oxytocin
    Outcome
    DecreaseChronic tolerance to morphine antinociception
    Study

    mousen: not reported in source

    Morphine tolerance and dependence
    Outcome group
    Pain · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Oxytocin and the dipeptides attenuated the development of acute and chronic tolerance to the antinociceptive effect of morphine and delayed the onset of the naloxone-precipitated withdrawal syndrome.
    1 context sentence
    Summary · context
    The effects of oxytocin (OXT) and of dipeptides derived from the C-terminal portion of oxytocin (Z-prolyl-leucine and Z-prolyl-D-leucine) on the development of acute and chronic tolerance to, and dependence on morphine were tested in the mouse.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In mice, oxytocin delayed the onset of the naloxone-precipitated morphine withdrawal syndrome.

    In plain wordsIn mice, oxytocin delayed the start of withdrawal signs after naloxone in morphine-treated animals.

    Peptide
    Oxytocin
    Outcome
    IncreaseOnset latency of naloxone-precipitated withdrawal syndrome
    Study

    mousen: not reported in source

    Morphine tolerance and dependence
    Outcome group
    Pain · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Oxytocin and the dipeptides attenuated the development of acute and chronic tolerance to the antinociceptive effect of morphine and delayed the onset of the naloxone-precipitated withdrawal syndrome.
    1 context sentence
    Summary · context
    The effects of oxytocin (OXT) and of dipeptides derived from the C-terminal portion of oxytocin (Z-prolyl-leucine and Z-prolyl-D-leucine) on the development of acute and chronic tolerance to, and dependence on morphine were tested in the mouse.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In mice, oxytocin potentiated the hypermotility induced by a large dose of apomorphine.

    In plain wordsIn mice, oxytocin increased the extra movement caused by a large dose of apomorphine.

    Peptide
    Oxytocin
    Outcome
    IncreaseApomorphine-induced hypermotility
    Study

    mousen: not reported in source

    Drug-induced behavioural responses related to dopamine in the brain
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Thus, oxytocin potentiated the hypermotility induced by a large dose of apomorphine and decreased the supersensitivity of the DA receptors.
    1 context sentence
    Summary · context
    The effects of oxytocin (OXT) and of dipeptides derived from the C-terminal portion of oxytocin (Z-prolyl-leucine and Z-prolyl-D-leucine) on the development of acute and chronic tolerance to, and dependence on morphine were tested in the mouse.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In mice, oxytocin decreased the supersensitivity of dopamine receptors.

    In plain wordsIn mice, oxytocin reduced the over-sensitivity of dopamine receptors.

    Peptide
    Oxytocin
    Outcome
    DecreaseDopamine receptor supersensitivity
    Study

    mousen: not reported in source

    Drug-induced behavioural responses related to dopamine in the brain
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Thus, oxytocin potentiated the hypermotility induced by a large dose of apomorphine and decreased the supersensitivity of the DA receptors.
    1 context sentence
    Summary · context
    The effects of oxytocin (OXT) and of dipeptides derived from the C-terminal portion of oxytocin (Z-prolyl-leucine and Z-prolyl-D-leucine) on the development of acute and chronic tolerance to, and dependence on morphine were tested in the mouse.

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

    11 Oct 2026, 20:03 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:52 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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