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Study · Animal study (in vivo) · rat · 2004

7 results

Role of adrenergic activity in pressor responses to chronic melanocortin receptor activation.

Kuo JJ, da Silva AA, Tallam LS, Hall JE

Hypertension (Dallas, Tex. : 1979)5 Jan 2004Cited by 61 (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 study7

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In rats, chronic intracerebroventricular MTII decreased food intake from 21 to 8 g/d by day 3.

    In plain wordsIn rats, MTII infused into the brain cut daily food intake sharply by day 3.

    Outcome
    DecreaseFood intake
    Study

    ratn: not reported in source

    Chronically instrumented rats
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    10 ng/h · intracerebroventricular · 11 daysAs given in this study (rat).

    Measurements

    Food intake
    21 g/d
    before MTII
    Food intake
    8 g/d
    day 3 of MTII

    Source sentences

    Summary
    MC3/4-R activation decreased food intake from 21+/-1 to 8+/-2 g/d by day 3 of MC3/4-R activation
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In rats, chronic intracerebroventricular MTII increased mean arterial pressure by an average of 8 mm Hg.

    In plain wordsIn rats, MTII infused into the brain raised blood pressure by about 8 mm Hg on average.

    Outcome
    IncreaseMean arterial pressure
    Study

    ratn: not reported in source

    Chronically instrumented rats
    Outcome group
    Blood pressure · Cardiovascular
    Studied dose
    10 ng/h · intracerebroventricular · 11 daysAs given in this study (rat).

    Measurements

    Mean arterial pressure change
    8 mm Hg
    MTII

    Source sentences

    Summary
    and increased MAP and HR by an average of 8+/-2 mm Hg and 9+/-5 bpm, respectively.
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In rats, chronic intracerebroventricular MTII increased heart rate by an average of 9 bpm.

    In plain wordsIn rats, MTII infused into the brain raised heart rate by about 9 beats per minute on average.

    Outcome
    IncreaseHeart rate
    Study

    ratn: not reported in source

    Chronically instrumented rats
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    10 ng/h · intracerebroventricular · 11 daysAs given in this study (rat).

    Measurements

    Heart rate change
    9 bpm
    MTII

    Source sentences

    Summary
    and increased MAP and HR by an average of 8+/-2 mm Hg and 9+/-5 bpm, respectively.
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In rats, glomerular filtration rate was unchanged during MTII infusion, both with vehicle and with adrenergic blockade.

    In plain wordsIn rats, kidney filtration rate did not change during MTII infusion, with or without adrenergic blockers.

    Outcome
    No significant changeGlomerular filtration rate
    Study

    ratn: not reported in source

    Chronically instrumented rats
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    10 ng/h · intracerebroventricular · 11 daysAs given in this study (rat).

    Source sentences

    Summary
    Glomerular filtration rate was unchanged in both the vehicle-infused and adrenergic blocked rats during MC3/4-R activation.
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.

Studies that did not test the peptide alone3

In this study, Melanotan II 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 Melanotan II.

  1. 05AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Efficacy outcome

    In rats, adrenergic blockade did not alter the decrease in food intake caused by MTII.

    In plain wordsIn rats, blocking adrenergic signals did not change the food intake drop caused by MTII.

    Outcome
    No significant changeMTII-induced decrease in food intake under adrenergic blockade
    Study

    ratn = 6

    Chronically instrumented rats
    Comparator
    Vehicle (no blockade)
    Outcome group
    Appetite and food intake · Metabolic and weight

    Source sentences

    Summary
    Adrenergic blockade did not alter the MC3/4-R-mediated decrease in food intake but abolished the increases in MAP and HR (1+/-2 mm Hg and -12+/-5 bpm, respectively, compared with control).
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.

    In this study, Melanotan II 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 Melanotan II.

  2. 06AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Efficacy outcome

    In rats, adrenergic blockade abolished the MTII-induced increase in mean arterial pressure.

    In plain wordsIn rats, blocking adrenergic signals removed the blood pressure rise caused by MTII.

    Outcome
    DecreaseMTII-induced rise in mean arterial pressure under adrenergic blockade
    Study

    ratn = 6

    Chronically instrumented rats
    Comparator
    Vehicle (no blockade)
    Outcome group
    Blood pressure · Cardiovascular

    Source sentences

    Summary
    Adrenergic blockade did not alter the MC3/4-R-mediated decrease in food intake but abolished the increases in MAP and HR (1+/-2 mm Hg and -12+/-5 bpm, respectively, compared with control).
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.

    In this study, Melanotan II 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 Melanotan II.

  3. 07AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Efficacy outcome

    In rats, adrenergic blockade abolished the MTII-induced increase in heart rate.

    In plain wordsIn rats, blocking adrenergic signals removed the heart rate rise caused by MTII.

    Outcome
    DecreaseMTII-induced rise in heart rate under adrenergic blockade
    Study

    ratn = 6

    Chronically instrumented rats
    Comparator
    Vehicle (no blockade)
    Outcome group
    Heart function · Cardiovascular

    Source sentences

    Summary
    Adrenergic blockade did not alter the MC3/4-R-mediated decrease in food intake but abolished the increases in MAP and HR (1+/-2 mm Hg and -12+/-5 bpm, respectively, compared with control).
    1 context sentence
    Summary · context
    Five days after starting the vehicle or adrenergic blockade, the MC3/4-R agonist, MTII (10 ng/h), was infused ICV for 11 days followed by a 5-day recovery period.

    In this study, Melanotan II 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 Melanotan II.

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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