Evidence map›Paper›PMID 17068101›Full record

ArticleThe Journal of physiology2007

Melanocortins and agouti-related protein modulate the excitability of two arcuate nucleus neuron populations by alteration of resting potassium conductances.

Mark A Smith, Kazunari Hisadome, Hind Al-Qassab, Helen Heffron, Dominic J Withers, Michael L J Ashford

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  6. Biased signaling at neural melanocortin receptors in regulation of energy homeostasis.Biochimica et biophysica acta. Molecular basis of disease · 2017
    Review
  7. Melanocortin 3 Receptor Signaling in Midbrain Dopamine Neurons Increases the Motivation for Food Reward.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
  8. Article
  9. Article
  10. Review
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  12. Article
  13. Review
  14. Review
  15. Differential control of metabolic and cardiovascular functions by melanocortin-4 receptors in proopiomelanocortin neurons.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Mark A SmithDivision of Pathology and Neuroscience, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, UK.
Kazunari Hisadome
Hind Al-Qassab
Helen Heffron
Dominic J Withers
Michael L J Ashford
University College London · GBUniversity of Dundee · GB

Funding

Wellcome Trust 068692
6 · The paper itself

Abstract

The hypothalamic melanocortin system is crucial for the control of appetite and body weight. Two of the five melanocortin receptors, MC3R and MC4R are involved in hypothalamic control of energy homeostasis, with the MC4R having the major influence. It is generally thought that the main impact of the melanocortin system on hypothalamic circuits is external to the arcuate nucleus, and that any effect locally in the arcuate nucleus is inhibitory on proopiomelanocortin-expressing (POMC) neurons. In contrast, using current- and voltage-clamp recordings from identified neurons, we demonstrate that MC3R and MC4R agonists depolarize arcuate POMC neurons and a separate arcuate neuronal population identified by the rat insulin 2 promoter (RIPCre) transgene expression. Furthermore, the endogenous MC3R and MC4R antagonist, agouti-related protein (AgRP), hyperpolarizes POMC and RIPCre neurons in the absence of melanocortin agonist, consistent with inverse agonism at the MC4R. A decreased transient outward (I(A)) potassium conductance, and to a lesser extent the inward rectifier (K(IR)) conductance, underlies neuronal depolarization, whereas an increase in I(A) mediates AgRP-induced hyperpolarization. Accordingly, POMC and RIPCre neurons may be targets for peptide transmitters that are possibly released locally from AgRP-expressing and POMC neurons in the arcuate nucleus, adding further previously unappreciated complexity to the arcuate system.

Indexed as

4-AminopyridineAction PotentialsAdenylyl Cyclase InhibitorsAgouti-Related Proteinalpha-MSHAnimalsArcuate Nucleus of HypothalamusBariumGreen Fluorescent ProteinsIntegrasesIntercellular Signaling Peptides and ProteinsMelanocortinsMelanocyte-Stimulating HormonesMiceMice, TransgenicNeurons4-AminopyridineAdenylyl Cyclase InhibitorsAgouti-Related ProteinAgrp protein, mouseAGRP protein, ratalpha-MSHBariumCre recombinaseGreen Fluorescent ProteinsIntegrasesIntercellular Signaling Peptides and ProteinsMc3r protein, mouseMelanocortinsMelanocyte-Stimulating Hormonesmelanotan-IIPeptides, CyclicPotassium Channel BlockersPotassium ChannelsReceptor, Melanocortin, Type 3Receptor, Melanocortin, Type 4SHU 9119

Identifiers

PMID17068101
PMCPMC1864999
OpenAlexW2152483203

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.