Evidence map›Paper›PMID 19650122›Full record

ArticleHippocampus2010

Chronic 17beta-estradiol or cholesterol prevents stress-induced hippocampal CA3 dendritic retraction in ovariectomized female rats: possible correspondence between CA1 spine properties and spatial acquisition.

Katie J McLaughlin, Jessica O Wilson, James Harman, Ryan L Wright, Lindsay Wieczorek, Juan Gomez, Donna L Korol, Cheryl D Conrad

Open access · greenAbstract read
In one paragraph

Article in Hippocampus, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed, 77 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Katie J McLaughlinDepartment of Psychology, Arizona State University, Tempe, Arizona 85287-1104, USA. mclaughlin@loras.edu
Jessica O Wilson
James Harman
Ryan L Wright
Lindsay Wieczorek
Juan Gomez
Donna L Korol
Cheryl D Conrad
Arizona State University · USUniversity of Illinois Urbana-Champaign · USHunter College · USLoras College · USWashington University in St. Louis · US

Funding

Significance of Stress-Induced Hippocampal AtrophyR01MH064727 · NIMH · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CONRAD, CHERYL D · 2002 to 2006
$1.0M
NIMH NIH HHS MH64727NIMH NIH HHS R01 MH064727
6 · The paper itself

Abstract

Chronic stress may have different effects on hippocampal CA3 and CA1 neuronal morphology and function depending upon hormonal status, but rarely are manipulations of stress and gonadal steroids combined. Experiment 1 investigated the effects of chronic restraint and 17beta-estradiol replacement on CA3 and CA1 dendritic morphology and spatial learning in ovariectomized (OVX) female Sprague-Dawley rats. OVX rats were implanted with 25% 17beta-estradiol, 100% cholesterol, or blank silastic capsules and then chronically restrained (6h/d/21d) or kept in home cages. 17beta-Estradiol or cholesterol prevented stress-induced CA3 dendritic retraction, increased CA1 apical spine density, and altered CA1 spine shape. The combination of chronic stress and 17beta-estradiol facilitated water maze acquisition compared to chronic stress + blank implants and nonstressed controls + 17beta-estradiol. To further investigate the interaction between 17beta-estradiol and stress on hippocampal morphology, experiment 2 was conducted on gonadally intact, cycling female rats that were chronically restrained (6h/d/21d), and then euthanized at proestrus (high ovarian hormones) or estrus (low ovarian hormones). Cycling female rats failed to show chronic stress-induced CA3 dendritic retraction at either estrous phase. Chronic stress enhanced the ratio of CA1 basal spine heads to headless spines as found in experiment 1. In addition, proestrous rats displayed increased CA1 spine density regardless of stress history. These results show that 17beta-estradiol or cholesterol protect against chronic stress-induced CA3 dendritic retraction in females. These stress- and 17beta-estradiol-induced morphological changes may provide insight into how dendritic complexity and spine properties contribute to spatial ability.

Indexed as

AnimalsCholesterolDendritic SpinesEstradiolFemaleHippocampusMaze LearningNeuronsNeuroprotective AgentsOvariectomyRatsRats, Sprague-DawleySpatial BehaviorStress, PsychologicalCholesterolEstradiolNeuroprotective Agents

Identifiers

PMID19650122
PMCPMC2878912
OpenAlexW2108527426

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.