Evidence map›Paper›PMID 19259805›Full record

ReviewCellular and molecular neurobiology2009

Anti-inflammatory effects of angiotensin receptor blockers in the brain and the periphery.

Julius Benicky, Enrique Sánchez-Lemus, Jaroslav Pavel, Juan M Saavedra

Abstract readReview
In one paragraph

Review in Cellular and molecular neurobiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 124 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  5. Review
  6. Article
  7. Article
  8. Article
  9. Genome-wide pleiotropy analysis of longitudinal blood pressure and harmonized cognitive performance measures.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
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  16. The Renin Angiotensin System as a Therapeutic Target in Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
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  18. Review
  19. Article
  20. Article

13 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

4 authors at 2 institutions in 1 country.

Julius BenickyDepartment of Health and Human Services, Division of Intramural Research Programs, Section on Pharmacology, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
Enrique Sánchez-Lemus
Jaroslav Pavel
Juan M Saavedra
National Institute of Mental Health · USNational 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 MH002762
6 · The paper itself

Abstract

In addition to regulating blood pressure, angiotensin II (Ang II) exerts powerful pro-inflammatory effects in hypertension through stimulation of its AT(1) receptors, most clearly demonstrated in peripheral arteries and in the cerebral vasculature. Administration of Ang II receptor blockers (ARBs) decreases hypertension-related vascular inflammation in peripheral organs. In rodent models of genetic hypertension, ARBs reverse the inflammation in the cerebral microcirculation. We hypothesized that ARBs could be effective in inflammatory conditions beyond hypertension. Our more recent studies, summarized here, indicate that this is indeed the case. We used the model of systemic administration of the bacterial endotoxin lipopolysaccharide (LPS). LPS produces a robust initial inflammatory reaction, the innate immune response, in peripheral organs and in the brain. Pretreatment with the ARB candesartan significantly diminishes the response to LPS, including reduction of pro-inflammatory cytokine release to the general circulation and decreased production and release of the pro-inflammatory adrenal hormone aldosterone. In addition, the ARB very significantly decreased the LPS-induced gene expression of pro-inflammatory cytokines and microglia activation in the brain. Our results demonstrate that AT(1) receptor activity is essential for the unrestricted development of full-scale innate immune response in the periphery and in the brain. ARBs, due to their immune response-limiting properties, may be considered as therapeutically useful in a number of inflammatory diseases of the peripheral organs and the brain.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsAnti-Inflammatory Agents, Non-SteroidalArteritisChronic DiseaseEncephalitisHypertensionMicrogliaRenin-Angiotensin SystemAngiotensin II Type 1 Receptor BlockersAnti-Inflammatory Agents, Non-Steroidal

Identifiers

PMID19259805
PMCPMC2718067
OpenAlexW2059864514

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.