Evidence map›Paper›PMID 20348154›Full record

ArticleThe Journal of endocrinology2010

Modulation of responses to stress by estradiol benzoate and selective estrogen receptor agonists.

Lidia I Serova, Heather A Harris, Shreekrishna Maharjan, Esther L Sabban

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 25% 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

19 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. D[HisPsychopharmacology · 2026
    Article
  3. Article
  4. Article
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  6. Article
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  9. Aberrant Expression ofDevelopment & reproduction · 2017
    Article
  10. Article
  11. 5α-Reduced neurosteroids sex-dependently reverse central prenatal programming of neuroendocrine stress responses in rats.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Hindbrain noradrenergic A2 neurons: diverse roles in autonomic, endocrine, cognitive, and behavioral functions.American journal of physiology. Regulatory, integrative and comparative physiology · 2011
    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

4 authors at 1 institution in 1 country.

Lidia I SerovaDepartment of Biochemistry and Molecular Biology, New York Medical College, Valhalla, New York 10595, USA.
Heather A Harris
Shreekrishna Maharjan
Esther L Sabban
New York Medical College · US

Funding

MOLECULAR BIOLOGY OF NOREPINEPHRINE BIOSYNTHESISR01NS028869 · NINDS · NEW YORK MEDICAL COLLEGE · PI SABBAN, ESTHER LOUISE · 1990 to 2006
$1.7M
NINDS NIH HHS NS 28869NINDS NIH HHS R01 NS028869
6 · The paper itself

Abstract

Previously, pretreatment with estradiol benzoate (EB) was found to modulate the response of hypothalamic-pituitary-adrenal (HPA) axis and gene expression in several catecholaminergic neuronal locations in ovariectomized (OVX) rats exposed to single immobilization stress (IMO). Here, we investigated the role of estrogen receptor (ER) subtypes, using selective agonists for ERalpha (propyl pyrazole triol, PPT) or ERbeta (WAY-200070) in two major central noradrenergic systems and the HPA axis after exposure to single and repeated IMO. OVX female rats received 21 daily injections of either EB (25 mug/kg), PPT (10 mg/kg), WAY-200070 (10 mg/kg), or vehicle. Injections of EB and PPT, but not WAY-200070, elicited reduced body weight and increased uterine weight, showing their selectivity. Both EB and PPT increased corticosterone levels about two- to threefold, but prevented any further rise with either single or repeated IMO, indicating an ERalpha (ESR1)-, but not ERbeta (ESR2)-, mediated mechanism. In the locus coeruleus (LC), the rise in dopamine-beta-hydroxylase (Dbh) mRNA with both stress paradigms was abrogated in EB- or PPT-injected animals. However, WAY-200070 blocked the response of DBH mRNA to single IMO but not to repeated IMO. In the nucleus of the solitary tract (NTS), the rise in tyrosine hydroxylase and DBH mRNAs with both IMOs was absent, or greatly attenuated, in EB- or PPT-treated rats. In most cases, WAY-200070 inhibited the response to single IMO but not to repeated IMO. The results demonstrate that pretreatment with estradiol, or ER-selective agonists, modulates the stress-triggered induction of gene expression of norepinephrine biosynthetic enzymes in LC and NTS, with ER selectivity depending on duration of the stress.

Indexed as

OvariectomyAdrenal Cortex HormonesAnimalsBody WeightDopamine beta-HydroxylaseEstradiolFemaleLocus CoeruleusOxazolesPhenolsPyrazolesRatsRats, Sprague-DawleyReceptors, EstrogenRestraint, PhysicalSolitary Nucleus4,4',4''-(4-propyl-((1)H)-pyrazole-1,3,5-triyl) tris-phenolAdrenal Cortex HormonesDopamine beta-HydroxylaseEstradiolestradiol 3-benzoateOxazolesPhenolsPyrazolesReceptors, EstrogenTyrosine 3-MonooxygenaseWAY 200070

Identifiers

PMID20348154
PMCPMC2927979
OpenAlexW2118112130

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.