Evidence map›Paper›PMID 29059347›Full record

ArticleEndocrinology2018

Sim1 Neurons Are Sufficient for MC4R-Mediated Sexual Function in Male Mice.

Erin Semple, Jennifer W Hill

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Reply to Liu et al.: Tissue specificity ofProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  10. Article
  11. Genetic variation in theProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  12. Review
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Erin SempleDepartment of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio 43606.
Jennifer W HillDepartment of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio 43606.
University of Toledo · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Defective melanocortin signaling underlying T2D-associated erectile dysfunctionR01HD081792 · NICHD · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI HILL, JENNIFER WOOTTON · 2015 to 2019
$1.6M
NICHD NIH HHS R01 HD081792NIDDK NIH HHS P30 DK020572
6 · The paper itself

Abstract

Sexual dysfunction is a poorly understood condition that affects up to one-third of men around the world. Existing treatments that target the periphery do not work for all men. Previous studies have shown that central melanocortins, which are released by pro-opiomelanocortin neurons in the arcuate nucleus of the hypothalamus, can lead to male erection and increased libido. Several studies specifically implicate the melanocortin 4 receptor (MC4R) in the central control of sexual function, but the specific neural circuitry involved is unknown. We hypothesized that single-minded homolog 1 (Sim1) neurons play an important role in the melanocortin-mediated regulation of male sexual behavior. To test this hypothesis, we examined the sexual behavior of mice expressing MC4R only on Sim1-positive neurons (tbMC4Rsim1 mice) in comparison with tbMC4R null mice and wild-type controls. In tbMC4Rsim1 mice, MC4R reexpression was found in the medial amygdala and paraventricular nucleus of the hypothalamus. These mice were paired with sexually experienced females, and their sexual function and behavior was scored based on mounting, intromission, and ejaculation. tbMC4R null mice showed a longer latency to mount, a reduced intromission efficiency, and an inability to reach ejaculation. Expression of MC4R only on Sim1 neurons reversed the sexual deficits seen in tbMC4R null mice. This study implicates melanocortin signaling via the MC4R on Sim1 neurons in the central control of male sexual behavior.

Indexed as

alpha-MSHAmygdalaAnimalsArcuate Nucleus of HypothalamusBasic Helix-Loop-Helix ProteinsCopulationCrosses, GeneticFertility Agents, MaleHeterozygoteInfertility, MaleInjections, IntraventricularMaleMice, KnockoutNerve Tissue ProteinsNeuronsOrgan Specificityalpha-MSHBasic Helix-Loop-Helix ProteinsFertility Agents, MaleMC4R protein, mouseNerve Tissue ProteinsReceptor, Melanocortin, Type 4Repressor ProteinsSim1 protein, mouse

Identifiers

PMID29059347
PMCPMC5761591
OpenAlexW2766913903

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.