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Study · Ex vivo tissue · mouse · 2008

5 results

Agouti-related peptide and MC3/4 receptor agonists both inhibit excitatory hypothalamic ventromedial nucleus neurons.

Fu LY, van den Pol AN

The Journal of neuroscience : the official journal of the Society for Neuroscience1 May 2008Cited by 65 (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: CC BY-NC. Results still quote short attributed sentences.

Results from this study5

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

  1. 01LabEx vivo tissueMechanism

    In mouse hypothalamic slices, MTII reduced the spontaneous firing rate of VMH vGluT2 neurons.

    In plain wordsIn mouse brain slices, melanotan II slowed the firing of nerve cells in a brain area called the VMH.

    Outcome
    DecreaseSpontaneous firing rate of VMH vGluT2 neurons
    Study

    mousen: not reported in source

    Hypothalamic slices, VMH vGluT2-GFP neurons
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    alpha-MSH, melanotan II (MTII), and selective MC3R or MC4R agonists were all inhibitory, reducing the spontaneous firing rate and hyperpolarizing vGluT2 neurons.
    1 context sentence
    Summary · context
    A total of 370 hypothalamic ventromedial nucleus (VMH) glutamatergic neurons was studied using whole-cell recording in hypothalamic slices from a novel mouse expressing green fluorescent protein (GFP) under control of the vesicular glutamate transporter 2 (vGluT2) promoter.
  2. 02LabEx vivo tissueMechanism

    In mouse hypothalamic slices, MTII hyperpolarized VMH vGluT2 neurons.

    In plain wordsIn mouse brain slices, melanotan II made VMH nerve cells less electrically excitable.

    Outcome
    DecreaseMembrane potential of VMH vGluT2 neurons
    Study

    mousen: not reported in source

    Hypothalamic slices, VMH vGluT2-GFP neurons
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    alpha-MSH, melanotan II (MTII), and selective MC3R or MC4R agonists were all inhibitory, reducing the spontaneous firing rate and hyperpolarizing vGluT2 neurons.
    1 context sentence
    Summary · context
    A total of 370 hypothalamic ventromedial nucleus (VMH) glutamatergic neurons was studied using whole-cell recording in hypothalamic slices from a novel mouse expressing green fluorescent protein (GFP) under control of the vesicular glutamate transporter 2 (vGluT2) promoter.
  3. 03LabEx vivo tissueMechanism

    In mouse hypothalamic slices without synaptic activity, MTII evoked no hyperpolarization or change in input resistance, which suggests an indirect action.

    In plain wordsIn mouse brain slices with synaptic signalling blocked, melanotan II did not change the nerve cells' electrical state.

    Outcome
    No significant changeHyperpolarization and input resistance without synaptic activity
    Study

    mousen: not reported in source

    Hypothalamic slices, VMH vGluT2-GFP neurons
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In the absence of synaptic activity, no hyperpolarization or change in input resistance was evoked by either MTII or AgRP, suggesting indirect actions.
    1 context sentence
    Summary · context
    A total of 370 hypothalamic ventromedial nucleus (VMH) glutamatergic neurons was studied using whole-cell recording in hypothalamic slices from a novel mouse expressing green fluorescent protein (GFP) under control of the vesicular glutamate transporter 2 (vGluT2) promoter.
  4. 04LabEx vivo tissueMechanism

    In mouse hypothalamic slices, MTII increased the frequency of spontaneous and miniature IPSCs in VMH neurons.

    In plain wordsIn mouse brain slices, melanotan II increased inhibitory input signals to VMH nerve cells.

    Outcome
    IncreaseSpontaneous and miniature IPSC frequency
    Study

    mousen: not reported in source

    Hypothalamic slices, VMH vGluT2-GFP neurons
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Consistent with this view, MTII increased the frequency of spontaneous and miniature IPSCs.
    1 context sentence
    Summary · context
    A total of 370 hypothalamic ventromedial nucleus (VMH) glutamatergic neurons was studied using whole-cell recording in hypothalamic slices from a novel mouse expressing green fluorescent protein (GFP) under control of the vesicular glutamate transporter 2 (vGluT2) promoter.

Studies that did not test the peptide alone1

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. 05LabNot a test of Melanotan II aloneEx vivo tissueMechanism

    In mouse hypothalamic slices, AgRP did not attenuate the inhibitory action of MTII on VMH neurons; the two compounds showed an additive inhibitory effect.

    In plain wordsIn mouse brain slices, AgRP did not weaken melanotan II's slowing of nerve cells; together they slowed the cells more.

    Outcome
    DecreaseCombined MTII and AgRP effect on VMH neurons
    Study

    mousen: not reported in source

    Hypothalamic slices, VMH vGluT2-GFP neurons
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Source sentences

    Summary
    Unexpectedly, AgRP did not attenuate MTII actions on these neurons; instead, these two compounds showed an additive inhibitory effect.
    1 context sentence
    Summary · context
    A total of 370 hypothalamic ventromedial nucleus (VMH) glutamatergic neurons was studied using whole-cell recording in hypothalamic slices from a novel mouse expressing green fluorescent protein (GFP) under control of the vesicular glutamate transporter 2 (vGluT2) promoter.

    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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