Evidence map›Paper›PMID 19829100›Full record

ArticleCritical care medicine2010

Cardioprotection, attenuated systemic inflammation, and survival benefit of beta1-adrenoceptor blockade in severe sepsis in rats.

Gareth L Ackland, Song T Yao, Alain Rudiger, Alex Dyson, Ray Stidwill, Dmitry Poputnikov, Mervyn Singer, Alexander V Gourine

Abstract read
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In one paragraph

Article in Critical care medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 144 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Observational
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  12. Observational
  13. Blockade of sympathetic ganglia improves vascular dysfunction in septic shock.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Article
  14. Article
  15. Current Perspectives of Mitochondria in Sepsis-Induced Cardiomyopathy.International journal of molecular sciences · 2024
    Review
  16. Ivabradine in Septic Shock: A Narrative Review.Journal of clinical medicine · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Gareth L AcklandCentre for Anaesthesia, Critical Care and Pain Medicine, University College London, UK. g.ackland@ucl.ac.uk
Song T Yao
Alain Rudiger
Alex Dyson
Ray Stidwill
Dmitry Poputnikov
Mervyn Singer
Alexander V Gourine
University College London · GB

Funding

Department of HealthMedical Research CouncilWellcome Trust
6 · The paper itself

Abstract

objectiveTo explore the hypothesis that beta-1 adrenoreceptor blockade may be protective through the attenuation of sympathetic hyperactivity and catecholaminergic inflammatory effects on cardiac and hepatic function.

designProspective, randomized, controlled study.

settingAnimal laboratory in a university medical center. SUBJECTS: Male adult Wistar rats.

interventionsPeripheral beta1-adrenoceptor blockade through daily intraperitoneal injection (metoprolol, 100 mg x kg(-1); atenolol, 6 mg x kg(-1)) or central nervous system beta1-adrenoceptor blockade (intracerebroventricular metoprolol, 25 microg) to achieve approximately 20% heart rate reduction in rats for 2 days before or after the induction of lethal endotoxemia, cecal ligation and puncture, or fecal peritonitis. MEASUREMENTS AND MAIN

resultsPeripheral beta1-adrenoceptor blockade established for 2 days before lethal endotoxemia markedly improved survival in both metoprolol-treated (n = 16; log rank test, p = .002) and atenolol-treated (n = 15; p = .03) rats. Overall mortality in cecal ligation and puncture was similar between metoprolol (40%; n = 10) and saline (50%; n = 10) pretreatment (p = .56), but the median time to death was increased by 33 hrs in metoprolol-treated rats (p = .03). Metoprolol pretreatment reduced hepatic expression of proinflammatory cytokines and lowered plasma interleukin-6 (both p < .05). Myocardial protein expression of interleukin-18 and monocyte chemoattractant protein-1, key mediators of cardiac dysfunction in sepsis, were also reduced (p < .05). Peripheral beta1-adrenoceptor blockade commenced 6 hrs after lethal endotoxemia or fecal peritonitis did not improve survival. However, arterial blood pressure was preserved and left ventricular contractility restored similar to that found in nonseptic controls. Central nervous system beta1-adrenoceptor blockade (metoprolol) did not reduce plasma cytokines or mortality, despite enhancing parasympathetic tone.

conclusionsPeripheral beta1-adrenoceptor blockade offers anti-inflammatory and cardioprotective effects, with mortality reduction if commenced before a septic insult. Its role in sepsis should be explored further.

Indexed as

Adrenergic beta-1 Receptor AntagonistsAdrenergic beta-AntagonistsAnimalsAtenololCytokinesHeartHeart RateInflammationInjections, IntraperitonealLiverMaleMetoprololRatsRats, WistarReceptors, Adrenergic, beta-1SepsisAdrenergic beta-1 Receptor AntagonistsAdrenergic beta-AntagonistsAtenololCytokinesMetoprololReceptors, Adrenergic, beta-1

Identifiers

PMID19829100
OpenAlexW1997456213

What OpenQuestion holds

Textmetadata
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.