Evidence map›Paper›PMID 20060879›Full record

ReviewBiochimica et biophysica acta2010

Diversity of mechanisms involved in aromatase regulation and estrogen action in the brain.

Thierry D Charlier, Charlotte A Cornil, Gregory F Ball, Jacques Balthazart

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. The Roles of Androgens in Humans: Biology, Metabolic Regulation and Health.International journal of molecular sciences · 2022
    Review
  3. Enhancing Cytotoxicity of Tamoxifen UsingEvidence-based complementary and alternative medicine : eCAM · 2022
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Cell-Based High-Throughput Screening for Aromatase Inhibitors in the Tox21 10K Library.Toxicological sciences : an official journal of the Society of Toxicology · 2015
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Low doses of 17β-estradiol rapidly improve learning and increase hippocampal dendritic spines.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Article
  16. Review
  17. Article
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

4 authors at 2 institutions in 2 countries.

Thierry D CharlierGIGA Neurosciences, University of Liège, 4000 Liège, Belgium.
Charlotte A Cornil
Gregory F Ball
Jacques Balthazart
University of Liège · BEJohns Hopkins University · US

Funding

STEROID-CATECHOLAMINE INTERACTIONS AND SEX BEHAVIORR01MH050388 · NIMH · UNIV OF MARYLAND, COLLEGE PARK · PI BALL, GREGORY F · 1993 to 2017
$5.1M
NIMH NIH HHS R01 MH050388NIMH NIH HHS R01 MH 50388
6 · The paper itself

Abstract

backgroundThe mechanisms through which estrogens modulate neuronal physiology, brain morphology, and behavior in recent years have proven to be far more complex than previously thought. For example, a second nuclear estrogen receptor has been identified, a new family of coregulatory proteins regulating steroid-dependent gene transcriptions was discovered and, finally, it has become clear that estrogens have surprisingly rapid effects based on their actions on cell membranes, which in turn result in the modulation of intracellular signaling cascades. SCOPE OF REVIEW: This paper presents a selective review of new findings in this area related to work in our laboratories, focusing on the role of estrogens in the activation of male sexual behavior. Two separate topics are considered. We first discuss functions of the steroid receptor coactivator-1 (SRC-1) that has emerged as a key limiting factor for behavioral effects of estradiol. Knocking-down its expression by antisense oligonucleotides drastically inhibits male-typical sexual behaviors. Secondly, we describe rapid regulations of brain estradiol production by calcium-dependent phosphorylations of the aromatase enzyme, themselves under the control of neurotransmitter activity. MAJOR

conclusionsThese rapid changes in estrogen bioavailability have clear behavioral consequences. Increases or decreases in estradiol concentrations respectively obtained by an acute injection of estradiol itself or of an aromatase inhibitor lead within 15-30 min to parallel changes in sexual behavior frequencies. GENERAL SIGNIFICANCE: These new controls of estrogen action offer a vast array of possibilities for discrete local controls of estrogen action. They also represent a formidable challenge for neuroendocrinologists trying to obtain an integrated view of brain function in relation to behavior.

Indexed as

AnimalsAromataseAromatase InhibitorsBrainCalciumEstradiolEstrogensFemaleGene Knockdown TechniquesHumansMaleNeurotransmitter AgentsNuclear Receptor Coactivator 1PhosphorylationReceptors, EstrogenSexual BehaviorAromataseAromatase InhibitorsCalciumEstradiolEstrogensNCOA1 protein, humanNeurotransmitter AgentsNuclear Receptor Coactivator 1Receptors, Estrogen

Identifiers

PMID20060879
PMCPMC2888630
OpenAlexW2069954636

What OpenQuestion holds

Textmetadata
LicenceTDM
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.