Evidence map›Paper›PMID 21150913›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2011

Angiotensin II AT1 receptor blockade ameliorates brain inflammation.

Julius Benicky, Enrique Sánchez-Lemus, Masaru Honda, Tao Pang, Martina Orecna, Juan Wang, Yan Leng, De-Maw Chuang, Juan M Saavedra

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 9% 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

135 citing papers in PubMed, 2 syntheses or guidelines pooled it, 259 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Ang II-mediated effects on BBB integrity in psychiatric and neurological disorders.Progress in neuro-psychopharmacology & biological psychiatry · 2026
    Review
  8. Article
  9. Current updates on latest basic research of scientific relevance in hypertensive dementia.Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Review
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75 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Julius BenickySection on Pharmacology, Division of Intramural Research Programs, Department of Health and Human Services, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA. benickyj@mail.nih.gov
Enrique Sánchez-Lemus
Masaru Honda
Tao Pang
Martina Orecna
Juan Wang
Yan Leng
De-Maw Chuang
Juan M Saavedra
National Institutes of Health · USNational Institute of Mental Health · USNational Institute of Mental Health · CZ

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
Intramural NIH HHS ZIA MH002762
6 · The paper itself

Abstract

Brain inflammation has a critical role in the pathophysiology of brain diseases of high prevalence and economic impact, such as major depression, schizophrenia, post-traumatic stress disorder, Parkinson's and Alzheimer's disease, and traumatic brain injury. Our results demonstrate that systemic administration of the centrally acting angiotensin II AT(1) receptor blocker (ARB) candesartan to normotensive rats decreases the acute brain inflammatory response to administration of the bacterial endotoxin lipopolysaccharide (LPS), a model of brain inflammation. The broad anti-inflammatory effects of candesartan were seen across the entire inflammatory cascade, including decreased production and release to the circulation of centrally acting proinflammatory cytokines, repression of nuclear transcription factors activation in the brain, reduction of gene expression of brain proinflammatory cytokines, cytokine and prostanoid receptors, adhesion molecules, proinflammatory inducible enzymes, and reduced microglia activation. These effects are widespread, occurring not only in well-known brain target areas for circulating proinflammatory factors and LPS, that is, hypothalamic paraventricular nucleus and the subfornical organ, but also in the prefrontal cortex, hippocampus, and amygdala. Candesartan reduced the associated anorexic effects, and ameliorated associated body weight loss and anxiety. Direct anti-inflammatory effects of candesartan were also documented in cultured rat microglia, cerebellar granule cells, and cerebral microvascular endothelial cells. ARBs are widely used in the treatment of hypertension and stroke, and their anti-inflammatory effects contribute to reduce renal and cardiac failure. Our results indicate that these compounds may offer a novel and safe therapeutic approach for the treatment of brain disorders.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsAnimals, NewbornBenzimidazolesBiphenyl CompoundsBrainFemaleInflammationLipopolysaccharidesMaleRatsRats, Inbred SHRRats, Sprague-DawleyRats, WistarReceptor, Angiotensin, Type 1TetrazolesAngiotensin II Type 1 Receptor BlockersBenzimidazolesBiphenyl CompoundscandesartanLipopolysaccharidesReceptor, Angiotensin, Type 1Tetrazoles

Identifiers

PMID21150913
PMCPMC3055735
OpenAlexW2120778240

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.