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Study · Animal study (in vivo) · horse · 2015

11 results

Pharmacokinetics and pharmacodynamics of dermorphin in the horse.

Robinson MA, Guan F, McDonnell S, Uboh CE, Soma LR

Journal of veterinary pharmacology and therapeutics5 Nov 2014Cited by 10 (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 study11

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

  1. 01AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, dermorphin bioavailability after intramuscular administration ranged from 47-100%.

    In plain wordsIn horses, dermorphin bioavailability after muscle injection ranged from 47-100%.

    Peptide
    Dermorphin
    Outcome
    Not applicableIntramuscular bioavailability
    Study

    horsen = 3

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kg · intramuscularAs given in this study (horse).

    Measurements

    Bioavailability
    47 to 100%
    intramuscular dermorphin

    Source sentences

    Summary
    Bioavailability following intramuscular administration was variable (47-100%, n = 3).
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  2. 02AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, intravenous dermorphin had a distribution half-life of 0.09 ± 0.02 h.

    In plain wordsIn horses, intravenous dermorphin had a distribution half-life of 0.09 ± 0.02 h.

    Peptide
    Dermorphin
    Outcome
    Not applicableIntravenous distribution half-life
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kg · intravenousAs given in this study (horse).

    Measurements

    Distribution half-life
    0.09 h
    intravenous dermorphin

    Source sentences

    Summary
    Data from intravenous administrations fit a 2-compartment model best with distribution and elimination half-lives (harmonic mean ± pseudo SD) of 0.09 ± 0.02 and 0.76 ± 0.22 h, respectively.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  3. 03AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, intravenous dermorphin had an elimination half-life of 0.76 ± 0.22 h.

    In plain wordsIn horses, intravenous dermorphin had an elimination half-life of 0.76 ± 0.22 h.

    Peptide
    Dermorphin
    Outcome
    Not applicableIntravenous elimination half-life
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kg · intravenousAs given in this study (horse).

    Measurements

    Elimination half-life
    0.76 h
    intravenous dermorphin

    Source sentences

    Summary
    Data from intravenous administrations fit a 2-compartment model best with distribution and elimination half-lives (harmonic mean ± pseudo SD) of 0.09 ± 0.02 and 0.76 ± 0.22 h, respectively.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  4. 04AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, intramuscular dermorphin had a terminal elimination half-life of 0.68 ± 0.24 h.

    In plain wordsIn horses, intramuscular dermorphin had a terminal elimination half-life of 0.68 ± 0.24 h.

    Peptide
    Dermorphin
    Outcome
    Not applicableIntramuscular terminal elimination half-life
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kg · intramuscularAs given in this study (horse).

    Measurements

    Terminal elimination half-life
    0.68 h
    intramuscular dermorphin

    Source sentences

    Summary
    Data from intramuscular administrations fit a noncompartmental model best with a terminal elimination half-life of 0.68 ± 0.24 (h).
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  5. 05AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, urinary dermorphin excretion was 5.0 (3.7-10.6) %.

    In plain wordsIn horses, urinary dermorphin excretion was 5.0 (3.7-10.6) %.

    Peptide
    Dermorphin
    Outcome
    Not applicableUrinary excretion
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kgAs given in this study (horse).

    Measurements

    Urinary excretion
    5%
    dermorphin

    Source sentences

    Summary
    The percentage of dermorphin excreted in urine was 5.0 (3.7-10.6) %.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  6. 06AnimalAnimal study (in vivo)Safety outcome

    In horses, excitation occurred only after intravenous dermorphin and subsided after 5 min.

    In plain wordsIn horses, excitation occurred only after intravenous dermorphin and subsided after 5 min.

    Peptide
    Dermorphin
    Outcome
    IncreaseExcitation
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Adverse events · Nervous system and cognition
    Studied dose
    9.3 ± 1.0 μg/kg · intravenousAs given in this study (horse).

    Source sentences

    Summary
    Excitation accompanied by an increased heart rate followed intravenous administration only and subsided after 5 min.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  7. 07AnimalAnimal study (in vivo)Safety outcome

    In horses, increased heart rate accompanied excitation only after intravenous dermorphin and subsided after 5 min.

    In plain wordsIn horses, heart rate increased with excitation only after intravenous dermorphin, then recovered after 5 min.

    Peptide
    Dermorphin
    Outcome
    IncreaseHeart rate increase
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    9.3 ± 1.0 μg/kg · intravenousAs given in this study (horse).

    Source sentences

    Summary
    Excitation accompanied by an increased heart rate followed intravenous administration only and subsided after 5 min.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  8. 08AnimalAnimal study (in vivo)Activity measurement

    In horses, the dermorphin concentration-response model for heart rate yielded an EC(50) of 21.1 ± 8.8 ng/mL.

    In plain wordsIn horses, dermorphin's modeled half-maximal heart rate effect occurred at 21.1 ± 8.8 ng/mL.

    Peptide
    Dermorphin
    Outcome
    Not applicableHeart rate concentration-response EC50
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kgAs given in this study (horse).

    Measurements

    EC50
    21.1 ng/mL
    heart rate response

    Source sentences

    Summary
    A plot of the mean change in heart rate vs. the plasma concentration of dermorphin fit a hyperbolic equation (simple Emax model), and an EC(50) of 21.1 ± 8.8 ng/mL was calculated.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  9. 09AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, dermorphin remained detectable in plasma for 12 h after intravenous or intramuscular administration.

    In plain wordsIn horses, dermorphin remained detectable in blood plasma for 12 h after intravenous or muscle injection.

    Peptide
    Dermorphin
    Outcome
    Not applicablePlasma detection duration
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kgAs given in this study (horse).

    Measurements

    Plasma detection duration
    12 h
    intravenous or intramuscular

    Source sentences

    Summary
    Dermorphin was detected in plasma for 12 h and in urine for 48 or 72 h following intravenous or intramuscular administration, respectively.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  10. 10AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, dermorphin remained detectable in urine for 48 h after intravenous administration.

    In plain wordsIn horses, dermorphin remained detectable in urine for 48 h after intravenous injection.

    Peptide
    Dermorphin
    Outcome
    Not applicableUrine detection duration after intravenous administration
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kg · intravenousAs given in this study (horse).

    Measurements

    Urine detection duration
    48 h
    intravenous

    Source sentences

    Summary
    Dermorphin was detected in plasma for 12 h and in urine for 48 or 72 h following intravenous or intramuscular administration, respectively.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.
  11. 11AnimalAnimal study (in vivo)Pharmacokinetics

    In horses, dermorphin remained detectable in urine for 72 h after intramuscular administration.

    In plain wordsIn horses, dermorphin remained detectable in urine for 72 h after muscle injection.

    Peptide
    Dermorphin
    Outcome
    Not applicableUrine detection duration after intramuscular administration
    Study

    horsen: not reported in source

    Horses
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    9.3 ± 1.0 μg/kg · intramuscularAs given in this study (horse).

    Measurements

    Urine detection duration
    72 h
    intramuscular

    Source sentences

    Summary
    Dermorphin was detected in plasma for 12 h and in urine for 48 or 72 h following intravenous or intramuscular administration, respectively.
    1 context sentence
    Summary · context
    Ten horses were intravenously and/or intramuscularly administered dermorphin (9.3 ± 1.0 μg/kg), and plasma concentration vs. time data were evaluated using compartmental and noncompartmental analyses.

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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

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