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Study · Animal study (in vivo) · rat · 2002

8 results

Central melanocortin receptor agonist reduces spontaneous and scheduled meal size but does not augment duodenal preload-induced feeding inhibition.

Azzara AV, Sokolnicki JP, Schwartz GJ

Physiology & behavior1 Nov 2002Cited by 54 (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)Efficacy outcome

    In male rats, central MTII reduced subsequent glucose intake during scheduled access to liquid glucose.

    In plain wordsIn rats, MTII given in the brain reduced how much glucose solution they drank.

    Outcome
    DecreaseGlucose intake during scheduled access
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.01-1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    and MTII reduced subsequent glucose intake.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In male rats, no dose of MTII augmented the reduction in food intake produced by duodenal glucose alone.

    In plain wordsIn rats, MTII did not add to the intake-lowering effect of glucose placed in the gut.

    Outcome
    No significant changeInteraction of MTII with duodenal glucose preload on intake
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.01-1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    However, no dose of MTII augmented the reductions in food intake produced by duodenal glucose alone.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In male rats with overnight chow access, MTII at 0.1 and 1.0 nmol reduced food intake.

    In plain wordsIn rats, MTII reduced overnight chow intake.

    Outcome
    DecreaseOvernight chow intake
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.1 and 1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    During overnight access to pelleted chow, the 0.1- and 1.0-nmol doses of MTII reduced food intake, meal size, meal duration, and body weight, and increased the satiety ratio (duration of intermeal interval/preceding meal size) but did not change meal frequency.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In male rats with overnight chow access, MTII at 0.1 and 1.0 nmol reduced meal size.

    In plain wordsIn rats, MTII made meals smaller.

    Outcome
    DecreaseMeal size
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.1 and 1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    During overnight access to pelleted chow, the 0.1- and 1.0-nmol doses of MTII reduced food intake, meal size, meal duration, and body weight, and increased the satiety ratio (duration of intermeal interval/preceding meal size) but did not change meal frequency.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In male rats with overnight chow access, MTII at 0.1 and 1.0 nmol reduced meal duration.

    In plain wordsIn rats, MTII made meals shorter.

    Outcome
    DecreaseMeal duration
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.1 and 1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    During overnight access to pelleted chow, the 0.1- and 1.0-nmol doses of MTII reduced food intake, meal size, meal duration, and body weight, and increased the satiety ratio (duration of intermeal interval/preceding meal size) but did not change meal frequency.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  6. 06AnimalAnimal study (in vivo)Efficacy outcome

    In male rats with overnight chow access, MTII at 0.1 and 1.0 nmol reduced body weight.

    In plain wordsIn rats, MTII lowered body weight.

    Outcome
    DecreaseBody weight
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    0.1 and 1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    During overnight access to pelleted chow, the 0.1- and 1.0-nmol doses of MTII reduced food intake, meal size, meal duration, and body weight, and increased the satiety ratio (duration of intermeal interval/preceding meal size) but did not change meal frequency.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  7. 07AnimalAnimal study (in vivo)Efficacy outcome

    In male rats with overnight chow access, MTII at 0.1 and 1.0 nmol increased the satiety ratio (intermeal interval divided by preceding meal size).

    In plain wordsIn rats, MTII made the gap between meals longer relative to meal size.

    Outcome
    IncreaseSatiety ratio
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.1 and 1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    During overnight access to pelleted chow, the 0.1- and 1.0-nmol doses of MTII reduced food intake, meal size, meal duration, and body weight, and increased the satiety ratio (duration of intermeal interval/preceding meal size) but did not change meal frequency.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)
  8. 08AnimalAnimal study (in vivo)Efficacy outcome

    In male rats with overnight chow access, MTII did not change meal frequency.

    In plain wordsIn rats, MTII did not change how often they ate.

    Outcome
    No significant changeMeal frequency
    Study

    ratn: not reported in source

    Male Sprague-Dawley rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    0.1 and 1.0 nmol · intracerebroventricularAs given in this study (rat).

    Source sentences

    Summary
    but did not change meal frequency.
    1 context sentence
    Summary · context
    We examined meal patterns and intake in male Sprague-Dawley rats following central intracerebroventricular administration of MTII (0.01-1.0 nmol)

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

    10 Oct 2026, 09:43 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:04 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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