Evidence map›Paper›PMID 18609298›Full record

ArticleStress (Amsterdam, Netherlands)2008

Angiotensin II AT(1) receptor blockade selectively enhances brain AT(2) receptor expression, and abolishes the cold-restraint stress-induced increase in tyrosine hydroxylase mRNA in the locus coeruleus of spontaneously hypertensive rats.

C Bregonzio, A Seltzer, I Armando, J Pavel, J M Saavedra

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Stress (Amsterdam, Netherlands), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-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

23 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Prostaglandin EThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  3. Enhancing Fear Extinction: Pharmacological Approaches.Current topics in behavioral neurosciences · 2023
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Ontogeny of angiotensin type 2 and type 1 receptor expression in mice.Journal of the renin-angiotensin-aldosterone system : JRAAS · 2012
    Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

C BregonzioDepartment of Pharmacology, Faculty of Chemical Sciences, National University of Cordoba, Cordoba, Argentina.
A Seltzer
I Armando
J Pavel
J M Saavedra
Universidad Nacional de Córdoba · ARNational Institutes of Health · US

Funding

Role Of Neuropeptides And Biogenic Amines In Stress and Brain InflammationZIAMH002762 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI SAAVEDRA, JUAN M · 2009 to 2013
$5.2M
ROLE OF NEUROPEPTIDES AND BIOGENIC AMINES IN STRESS AND BRAIN ISCHEMIAZ01MH002762 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI SAAVEDRA, JUAN M · 1997 to 2008
$4.6M
Intramural NIH HHS Z01 MH002762Intramural NIH HHS Z99 MH999999
6 · The paper itself

Abstract

Spontaneously hypertensive rats, a stress-sensitive strain, were pretreated orally for 14 days with the AT(1) receptor antagonist candesartan before submission to 2 h of cold-restraint stress. In non-treated rats, stress decreased AT(1) receptor binding in the median eminence and basolateral amygdala, increased AT(2) receptor binding in the medial subnucleus of the inferior olive, decreased AT(2) binding in the ventrolateral thalamic nucleus and increased tyrosine hydroxylase mRNA level in the locus coeruleus. In non-stressed rats, AT(1) receptor blockade reduced AT(1) receptor binding in all areas studied and enhanced AT(2) receptor binding in the medial subnucleus of the inferior olive. Candesartan pretreatment produced a similar decrease in brain AT(1) binding after stress, and prevented the stress-induced AT(2) receptor binding decrease in the ventrolateral thalamic nucleus. In the locus coeruleus and adrenal medulla, AT(1) blockade abolished the stress-induced increase in tyrosine hydroxylase mRNA level. Our results demonstrate that oral administration of candesartan effectively blocked brain AT(1) receptors, selectively increased central AT(2) receptor expression and prevented the stress-induced central stimulation of tyrosine hydroxylase transcription. The present results support a role of brain AT(1) and AT(2) receptors in the regulation of the stress response, and the hypothesis that AT(1) receptor antagonists may be considered as potential therapeutic compounds in stress related disorders in addition to their anti-hypertensive properties.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsBenzimidazolesBiphenyl CompoundsBrainCold TemperatureGene ExpressionLocus CoeruleusMaleRatsRats, Inbred SHRReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Restraint, PhysicalRNA, MessengerStress, PhysiologicalAngiotensin II Type 1 Receptor BlockersBenzimidazolesBiphenyl Compoundscandesartan cilexetilReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2RNA, MessengerTetrazolesTyrosine 3-Monooxygenase

Identifiers

PMID18609298
PMCPMC2742314
OpenAlexW1677147117

What OpenQuestion holds

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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.