Melanin-concentrating hormone receptor 1

Last updated
MCHR1
Identifiers
Aliases MCHR1 , GPR24, MCH-1R, MCH1R, SLC-1, SLC1, melanin concentrating hormone receptor 1
External IDs OMIM: 601751 MGI: 2180756 HomoloGene: 21097 GeneCards: MCHR1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005297

NM_145132

RefSeq (protein)

NP_005288

NP_660114

Location (UCSC) Chr 22: 40.68 – 40.68 Mb Chr 15: 81.12 – 81.12 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Melanin-concentrating hormone receptor 1, also known as MCH1, is one of the melanin-concentrating hormone receptors found in all mammals. [5]

Contents

The protein encoded by this gene, a member of the G protein-coupled receptor family 1, is an integral plasma membrane protein which binds melanin-concentrating hormone. The encoded protein can inhibit cAMP accumulation and stimulate intracellular calcium flux, and is probably involved in the neuronal regulation of food consumption. Although structurally similar to somatostatin receptors, this protein does not seem to bind somatostatin. [5]

Function

MCH1 is thought to have a number of functions including in the regulation of appetite, [6] [7] and in stress, anxiety and depression. [8] [9] [10] [11] [12] [13]

Selective ligands

Agonists

Antagonists

See also

Related Research Articles

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Two Melanin-concentrating hormone receptors (MCHR) have recently been characterized: MCH-R1 and MCH-R2. These two receptors share approximately 38% homology.

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<span class="mw-page-title-main">ATC-0175</span> Chemical compound

ATC-0175 is a drug used in scientific research, which is a selective, non-peptide antagonist at the melanin concentrating hormone receptor MCH1. In animal studies it has been shown to produce both anxiolytic and antidepressant actions, but without sedative or ataxic side effects.

<span class="mw-page-title-main">SNAP-94847</span> Chemical compound

SNAP-94847 is a drug used in scientific research, which is a selective, non-peptide antagonist at the melanin concentrating hormone receptor MCH1. In animal studies it has been shown to produce both anxiolytic and antidepressant effects, and also reduces food consumption suggesting a possible anorectic effect.

GW-803430 (GW-3430) is a drug used in scientific research and is a selective non-peptide antagonist at the melanin concentrating hormone receptor MCH1. In animal studies it has anxiolytic, antidepressant and anorectic effects.

<span class="mw-page-title-main">SNAP-7941</span> Chemical compound

SNAP-7941 is a drug used in scientific research, which is a selective, non-peptide antagonist at the melanin concentrating hormone receptor MCH1. In initial animal studies it had promising anxiolytic, antidepressant and anorectic effects, but subsequent trial results were disappointing, and the main significance of SNAP-7941 is as the lead compound from which more potent and selective antagonists such as SNAP-94847 were developed, although it continues to be used for research into the function of the MCH1 receptor.

<span class="mw-page-title-main">NGD-4715</span> Chemical compound

NGD-4715 is a drug developed by Neurogen, which acts as a selective, non-peptide antagonist at the melanin concentrating hormone receptor MCH1. In animal models it has anxiolytic, antidepressant, and anorectic effects, and it has successfully passed Phase I clinical trials in humans.

References

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  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.