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Study · Animal study (in vivo) · rat · 2014

6 results

Central vagal afferent endings mediate reduction of food intake by melanocortin-3/4 receptor agonist.

Campos CA, Shiina H, Ritter RC

The Journal of neuroscience : the official journal of the Society for Neuroscience1 Sept 2014Cited by 22 (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 study6

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In rats, MTII increased PKA-catalyzed phosphorylation of synapsin I in vagal afferent endings in the nucleus of the solitary tract.

    In plain wordsIn rats, melanotan II increased a signal (synapsin I phosphorylation) in vagal nerve endings of the hindbrain.

    Outcome
    IncreasePKA-catalyzed synapsin I phosphorylation in vagal afferent endings
    Study

    ratn: not reported in source

    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Furthermore, MTII and endogenous MC4R agonists increased protein kinase A (PKA)-catalyzed phosphorylation of synapsin I in vagal afferent endings

Studies that did not test the peptide alone5

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. 02AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Efficacy outcome

    In rats, hindbrain injection of the PKA inhibitor KT5720 significantly attenuated the MTII-induced reduction of food intake.

    In plain wordsIn rats, a drug blocking PKA in the hindbrain weakened the food-intake reduction caused by melanotan II.

    Outcome
    DecreaseMTII-induced reduction of food intake with PKA inhibitor
    Study

    ratn: not reported in source

    Outcome group
    Appetite and food intake · Nervous system and cognition

    Source sentences

    Summary
    Hindbrain injection of a PKA inhibitor, KT5720, significantly attenuated MTII-induced reduction of food intake

    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. 03AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Mechanism

    In rats, the PKA inhibitor KT5720 attenuated the MTII-induced increase in synapsin I phosphorylation.

    In plain wordsIn rats, a PKA-blocking drug reduced the nerve-ending signal that melanotan II normally increases.

    Outcome
    DecreaseMTII-induced synapsin I phosphorylation with PKA inhibitor
    Study

    ratn: not reported in source

    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Source sentences

    Summary
    Hindbrain injection of a PKA inhibitor, KT5720, significantly attenuated MTII-induced reduction of food intake and the increase in synapsin I phosphorylation

    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. 04AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Mechanism

    In rats, unilateral nodose ganglion removal abolished MTII-induced synapsin I phosphorylation on the same side.

    In plain wordsIn rats, removing the vagal nodose ganglion on one side abolished the melanotan II nerve-ending signal on that side.

    Outcome
    DecreaseMTII-induced synapsin I phosphorylation after nodose ganglion removal
    Study

    ratn: not reported in source

    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Source sentences

    Summary
    Finally, unilateral nodose ganglion removal, resulting in degeneration of vagal afferent endings in the ipsilateral NTS, abolished MTII-induced synapsin I phosphorylation ipsilateral to nodose ganglion removal.

    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.

  4. 05AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Efficacy outcome

    In rats, the reduction of food intake after MTII injection into the NTS on the side of nodose ganglion removal was significantly attenuated.

    In plain wordsIn rats, melanotan II cut food intake less when injected on the side where the vagal ganglion had been removed.

    Outcome
    DecreaseFood intake after MTII into NTS ipsilateral to nodose ganglion removal
    Study

    ratn: not reported in source

    Outcome group
    Appetite and food intake · Nervous system and cognition

    Source sentences

    Summary
    Moreover, reduction of food intake following MTII injection into the NTS ipsilateral to nodose ganglion removal was significantly attenuated

    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.

  5. 06AnimalNot a test of Melanotan II aloneAnimal study (in vivo)Efficacy outcome

    In rats, the response to MTII was not diminished when it was injected into the NTS on the side opposite to nodose ganglion removal.

    In plain wordsIn rats, melanotan II still worked normally when injected on the side opposite the removed vagal ganglion.

    Outcome
    No significant changeFood intake after MTII into NTS contralateral to nodose ganglion removal
    Study

    ratn: not reported in source

    Outcome group
    Appetite and food intake · Nervous system and cognition

    Source sentences

    Summary
    whereas the response to MTII was not diminished when injected into the contralateral NTS.

    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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