Evidence map›Paper›PMID 33436885›Full record

ArticleScientific reports2021

Angiotensin-(1-7) treatment blocks lipopolysaccharide-induced organ damage, platelet dysfunction, and IL-6 and nitric oxide production in rats.

Hsin-Jung Tsai, Chih-Chin Shih, Kuang-Yi Chang, Mei-Hui Liao, Wen-Jinn Liaw, Chin-Chen Wu, Cheng-Ming Tsao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Observational
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  4. Review
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  7. Article
  8. Angiotensin 1-7 in an experimental septic shock model.Critical care (London, England) · 2023
    Article
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  10. Article
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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

7 authors at 5 institutions in 1 country.

Hsin-Jung TsaiDepartment of Anesthesiology, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Rd., Beitou District, Taipei, 112, Taiwan.
Chih-Chin ShihDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Kuang-Yi ChangDepartment of Anesthesiology, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Rd., Beitou District, Taipei, 112, Taiwan.
Mei-Hui LiaoDepartment of Nursing, Oriental Institute of Technology, New Taipei City, Taiwan.
Wen-Jinn LiawDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Chin-Chen WuDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Cheng-Ming TsaoDepartment of Anesthesiology, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Rd., Beitou District, Taipei, 112, Taiwan. cm.cmtsao@gmail.com.
National Defense Medical Center · TWTaipei Veterans General Hospital · TWChung Shan Medical University Hospital · TWNational Yang Ming Chiao Tung University · TWOriental Institute of Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis can lead to shock, multiple organ failure, and even death. Platelets play an active role in the pathogenesis of sepsis-induced multiple organ failure. Angiotensin (Ang)-(1-7), a biologically active peptide, counteracts various effects of Ang II and attenuates inflammatory responses, reactive oxygen species production, and apoptosis. We evaluated the effects of Ang-(1-7) on organ injury and platelet dysfunction in rats with endotoxaemia. We treated male Wistar rats with saline or lipopolysaccharide (LPS, 10 mg, intravenously) then Ang-(1-7) (1 mg/kg, intravenous infusion for 3 h beginning 30 min after LPS administration). We analysed several haemodynamic, biochemical, and inflammatory parameters, as well as platelet counts and aggregation. Ang-(1-7) improved hypotension and organ dysfunction, and attenuated plasma interleukin-6, chemokines and nitric oxide production in rats after LPS administration. The LPS-induced reduction in platelet aggregation, but not the decreased platelet count, was restored after Ang-(1-7) treatment. The protein expression of iNOS and IκB, but not phosphorylated ERK1/2 and p38, was diminished in Ang-(1-7)-treated LPS rats. The histological changes in liver and lung were significantly attenuated in Ang-(1-7)-treated LPS rats. Our results suggest that Ang-(1-7) ameliorates endotoxaemic-induced organ injury and platelet dysfunction, likely through the inhibition of the inflammatory response and nitric oxide production.

Indexed as

Angiotensin IAnimalsBlood PlateletsEndotoxemiaHypotensionInterleukin-6LipopolysaccharidesMaleMultiple Organ FailurePeptide FragmentsRatsRats, WistarSepsisVasodilator AgentsAngiotensin Iangiotensin I (1-7)Interleukin-6LipopolysaccharidesPeptide FragmentsVasodilator Agents

Identifiers

PMID33436885
PMCPMC7804205
OpenAlexW3118825091

What OpenQuestion holds

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LicenceCC BY
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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.