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Study · Animal study (in vivo) · rat · 2011

5 results

Systemic but not central nervous system nitric oxide synthase inhibition exacerbates the hypertensive effects of chronic melanocortin-3/4 receptor activation.

do Carmo JM, Bassi M, da Silva AA, Hall JE

Hypertension (Dallas, Tex. : 1979)24 Jan 2011Cited by 15 (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 rats given intravenous L-NAME, central melanocortin 3/4 receptor activation by MTII caused a greater rise in mean arterial pressure than L-NAME plus vehicle or MTII alone.

    In plain wordsIn rats, brain MTII raised blood pressure more when nitric oxide synthase was blocked in the body than with MTII alone.

    Outcome
    IncreaseMean arterial pressure with intravenous L-NAME
    Study

    ratn: not reported in source

    Sprague-Dawley rats with telemetry and ICV cannulae
    Outcome group
    Blood pressure · Cardiovascular
    Studied dose
    10 ng/hr · intracerebroventricular infusion · 10 daysAs given in this study (rat).

    Measurements

    MAP increase
    35 mm Hg
    MTII with intravenous L-NAME

    Source sentences

    Summary
    Melanocortin 3/4 receptor activation caused a greater increase in mean arterial pressure (MAP) and heart rate in rats treated with intravenous L-NAME (35 ± 6 mm Hg and 56 ± 8 bpm) than L-NAME plus vehicle or MTII alone (22 ± 5 and 9 ± 2 mm Hg, and 26 ± 14 and 27 ± 5 bpm), despite a 58% and 50% reduc…
    1 context sentence
    Summary · context
    After control measurements, the NO synthase inhibitor L-NAME was infused (10 μg/kg/min intravenous) for 17 days and, starting on day 7 of L-NAME infusion, the melanocortin 3/4 receptor agonist melanotan II (MTII; 10 ng/hr; group 1) or saline vehicle (group 2) was infused ICV for 10 days.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In rats given intravenous L-NAME, central MTII caused a greater rise in heart rate than L-NAME plus vehicle or MTII alone.

    In plain wordsIn rats, brain MTII raised heart rate more when nitric oxide synthase was blocked in the body than with MTII alone.

    Outcome
    IncreaseHeart rate with intravenous L-NAME
    Study

    ratn: not reported in source

    Sprague-Dawley rats with telemetry and ICV cannulae
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    10 ng/hr · intracerebroventricular infusion · 10 daysAs given in this study (rat).

    Measurements

    Heart rate increase
    56 bpm
    MTII with intravenous L-NAME

    Source sentences

    Summary
    Melanocortin 3/4 receptor activation caused a greater increase in mean arterial pressure (MAP) and heart rate in rats treated with intravenous L-NAME (35 ± 6 mm Hg and 56 ± 8 bpm) than L-NAME plus vehicle or MTII alone (22 ± 5 and 9 ± 2 mm Hg, and 26 ± 14 and 27 ± 5 bpm), despite a 58% and 50% reduc…
    1 context sentence
    Summary · context
    After control measurements, the NO synthase inhibitor L-NAME was infused (10 μg/kg/min intravenous) for 17 days and, starting on day 7 of L-NAME infusion, the melanocortin 3/4 receptor agonist melanotan II (MTII; 10 ng/hr; group 1) or saline vehicle (group 2) was infused ICV for 10 days.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In rats, central MTII infusion reduced food intake by 58% and 50% during the first 6 days.

    In plain wordsIn rats, MTII infused into the brain reduced food intake during the first 6 days.

    Outcome
    DecreaseFood intake during first 6 days of MTII
    Study

    ratn: not reported in source

    Sprague-Dawley rats with telemetry and ICV cannulae
    Outcome group
    Appetite and food intake · Metabolic and weight
    Studied dose
    10 ng/hr · intracerebroventricular infusion · 10 daysAs given in this study (rat).

    Measurements

    Food intake reduction
    58%
    first 6 days of MTII infusion
    Food intake reduction
    50%
    first 6 days of MTII infusion

    Source sentences

    Summary
    despite a 58% and 50% reduction in food intake during the first 6 days of MTII infusion.
    1 context sentence
    Summary · context
    After control measurements, the NO synthase inhibitor L-NAME was infused (10 μg/kg/min intravenous) for 17 days and, starting on day 7 of L-NAME infusion, the melanocortin 3/4 receptor agonist melanotan II (MTII; 10 ng/hr; group 1) or saline vehicle (group 2) was infused ICV for 10 days.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In rats, ICV MTII given with the challenge drug L-NAME caused about a 10 mm Hg rise in mean arterial pressure, similar to ICV MTII alone.

    In plain wordsIn rats, brain MTII given with L-NAME raised blood pressure about as much as MTII alone.

    Outcome
    IncreaseMean arterial pressure with ICV L-NAME plus MTII
    Study

    ratn: not reported in source

    Sprague-Dawley rats with telemetry and ICV cannulae
    Outcome group
    Blood pressure · Cardiovascular
    Studied dose
    10 ng/hr · intracerebroventricular infusion · 10 daysAs given in this study (rat).

    Measurements

    MAP increase
    ≈ 10 mm Hg
    ICV L-NAME plus MTII

    Source sentences

    Summary
    ICV infusion of L-NAME plus MTII caused only ≈ 10 mm Hg increase in MAP with no change in heart rate, similar to the effects of ICV infusion of MTII alone
    1 context sentence
    Summary · context
    After control measurements, the NO synthase inhibitor L-NAME was infused (10 μg/kg/min intravenous) for 17 days and, starting on day 7 of L-NAME infusion, the melanocortin 3/4 receptor agonist melanotan II (MTII; 10 ng/hr; group 1) or saline vehicle (group 2) was infused ICV for 10 days.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In rats, ICV MTII given with the challenge drug L-NAME caused no change in heart rate, similar to ICV MTII alone.

    In plain wordsIn rats, brain MTII given with L-NAME did not change heart rate, like MTII alone.

    Outcome
    No significant changeHeart rate with ICV L-NAME plus MTII
    Study

    ratn: not reported in source

    Sprague-Dawley rats with telemetry and ICV cannulae
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    10 ng/hr · intracerebroventricular infusion · 10 daysAs given in this study (rat).

    Source sentences

    Summary
    ICV infusion of L-NAME plus MTII caused only ≈ 10 mm Hg increase in MAP with no change in heart rate, similar to the effects of ICV infusion of MTII alone
    1 context sentence
    Summary · context
    After control measurements, the NO synthase inhibitor L-NAME was infused (10 μg/kg/min intravenous) for 17 days and, starting on day 7 of L-NAME infusion, the melanocortin 3/4 receptor agonist melanotan II (MTII; 10 ng/hr; group 1) or saline vehicle (group 2) was infused ICV for 10 days.

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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