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

5 results

Electrophysiological studies on the spinal effects of dermorphin, an endogenous mu-opioid agonist.

Sullivan AF, Dickenson AH

Brain research1 Sept 1988Cited by 7 (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

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

  1. 01AnimalAnimal study (in vivo)Activity measurement

    In rats, intrathecal dermorphin dose-dependently inhibited C fibre-evoked dorsal horn neuronal responses, with an ED50 of 0.11 micrograms.

    In plain wordsIn rats, intrathecal dermorphin dose-dependently inhibited pain-related C fibre-evoked neuronal responses.

    Peptide
    Dermorphin
    Outcome
    DecreaseC fibre-evoked neuronal responses
    Study

    ratn: not reported in source

    Dorsal horn nociceptive neurons
    Outcome group
    Pain · Nervous system and cognition
    Studied dose
    Dose not stated · intrathecalAs given in this study (rat).

    Measurements

    ED50
    0.11 micrograms
    C fibre-evoked response inhibition

    Source sentences

    Summary
    The intrathecal administration of dermorphin, an endogenous heptopeptide first discovered in amphibia, produces dose-dependent selective inhibitions of C fibre-evoked responses in rat dorsal horn nociceptive neurones (ED50 0.11 micrograms).
  2. 02AnimalAnimal study (in vivo)Activity measurement

    In rats, A beta-fibre-evoked activity remained relatively unaffected by dermorphin.

    In plain wordsIn rats, dermorphin left A beta-fibre-evoked activity relatively unaffected.

    Peptide
    Dermorphin
    Outcome
    No significant changeA beta-fibre-evoked activity
    Study

    ratn: not reported in source

    Dorsal horn nociceptive neurons
    Outcome group
    Pain · Nervous system and cognition
    Studied dose
    Dose not stated · intrathecalAs given in this study (rat).

    Source sentences

    Summary
    A beta-fibre-evoked activity was relatively unaffected.
    1 context sentence
    Summary · context
    The intrathecal administration of dermorphin, an endogenous heptopeptide first discovered in amphibia, produces dose-dependent selective inhibitions of C fibre-evoked responses in rat dorsal horn nociceptive neurones (ED50 0.11 micrograms).
  3. 03AnimalAnimal study (in vivo)Activity measurement

    In rats, dermorphin was approximately 40 times more potent than morphine in this spinal preparation.

    In plain wordsIn rats, dermorphin was more potent than morphine in this spinal preparation.

    Peptide
    Dermorphin
    Outcome
    IncreaseRelative potency versus morphine
    Study

    ratn: not reported in source

    Dorsal horn nociceptive neurons
    Comparator
    Morphine
    Outcome group
    Pain · Nervous system and cognition
    Studied dose
    Dose not stated · intrathecalAs given in this study (rat).

    Measurements

    Relative potency
    ≈ 40 times
    Versus morphine

    Source sentences

    Summary
    Thus dermorphin can profoundly inhibit nociceptive afferent input in the spinal cord, and in this preparation is more potent (approximately 40X) than morphine.

Studies that did not test the peptide alone2

In this study, Dermorphin was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Dermorphin.

  1. 04AnimalNot a test of Dermorphin aloneAnimal study (in vivo)Mechanism

    In rats, naloxone antagonised dermorphin's spinal effects.

    In plain wordsIn rats, naloxone antagonised dermorphin's spinal effects.

    Peptide
    Dermorphin
    Outcome
    Not applicableNaloxone antagonism
    Study

    ratn: not reported in source

    Dorsal horn nociceptive neurons
    Outcome group
    Pain · Nervous system and cognition

    Source sentences

    Summary
    Naloxone (10 micrograms) but not ICI 174,864 (125 micrograms) antagonised the effects of the peptide.
    1 context sentence
    Summary · context
    The intrathecal administration of dermorphin, an endogenous heptopeptide first discovered in amphibia, produces dose-dependent selective inhibitions of C fibre-evoked responses in rat dorsal horn nociceptive neurones (ED50 0.11 micrograms).

    In this study, Dermorphin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dermorphin.

  2. 05AnimalNot a test of Dermorphin aloneAnimal study (in vivo)Mechanism

    In rats, ICI 174,864 did not antagonise dermorphin's spinal effects.

    In plain wordsIn rats, ICI 174,864 did not antagonise dermorphin's spinal effects.

    Peptide
    Dermorphin
    Outcome
    Not applicableICI 174,864 antagonism
    Study

    ratn: not reported in source

    Dorsal horn nociceptive neurons
    Outcome group
    Pain · Nervous system and cognition

    Source sentences

    Summary
    Naloxone (10 micrograms) but not ICI 174,864 (125 micrograms) antagonised the effects of the peptide.
    1 context sentence
    Summary · context
    The intrathecal administration of dermorphin, an endogenous heptopeptide first discovered in amphibia, produces dose-dependent selective inhibitions of C fibre-evoked responses in rat dorsal horn nociceptive neurones (ED50 0.11 micrograms).

    In this study, Dermorphin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dermorphin.

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

    27 Oct 2026, 18:20 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:32 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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