Evidence map›Paper›PMID 24849208›Full record

ArticlePloS one2014

Nebivolol protects against myocardial infarction injury via stimulation of beta 3-adrenergic receptors and nitric oxide signaling.

Zheng Zhang, Liping Ding, Zhitao Jin, Guojie Gao, Huijun Li, Lijuan Zhang, Lina Zhang, Xin Lu, Lihua Hu, Bingwei Lu and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

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  12. βJournal of the American College of Cardiology · 2017
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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

12 authors at 1 institution in 1 country.

Zheng ZhangDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Liping DingDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Zhitao JinDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Guojie GaoDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Huijun LiDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Lijuan ZhangDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Lina ZhangDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Xin LuDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Lihua HuDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Bingwei LuDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Xiongjun YuDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Taohong HuDepartment of Cardiology, The Second Artillery General Hospital of Chinese People's Liberation Army, Beijing, China.
Second Artillery General Hospital of Chinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nebivolol, third-generation β-blocker, may activate β3-adrenergic receptor (AR), which has been emerged as a novel and potential therapeutic targets for cardiovascular diseases. However, it is not known whether nebivolol administration plays a cardioprotective effect against myocardial infarction (MI) injury. Therefore, the present study was designed to clarify the effects of nebivolol on MI injury and to elucidate the underlying mechanism. MI model was constructed by left anterior descending (LAD) artery ligation. Nebivolol, β3-AR antagonist (SR59230A), Nitro-L-arginine methylester (L-NAME) or vehicle was administered for 4 weeks after MI operation. Cardiac function was monitored by echocardiography. Moreover, the fibrosis and the apoptosis of myocardium were assessed by Masson's trichrome stain and TUNEL assay respectively 4 weeks after MI. Nebivolol administration reduced scar area by 68% compared with MI group (p<0.05). Meanwhile, nebivolol also decreased the myocardial apoptosis and improved the heart function after MI (p<0.05 vs. MI). These effects were associated with increased β3-AR expression. Moreover, nebivolol treatment significantly increased the phosphorylation of endothelial NOS (eNOS) and the expression of neuronal NOS (nNOS). Conversely, the cardiac protective effects of nebivolol were abolished by SR and L-NAME. These results indicate that nebivolol protects against MI injury. Furthermore, the cardioprotective effects of nebivolol may be mediated by β3-AR-eNOS/nNOS pathway.

Indexed as

Adrenergic beta-1 Receptor AntagonistsAnimalsApoptosisArteriesBenzopyransBlood PressureEchocardiographyEthanolaminesHeartHemodynamicsMaleMiceMice, Inbred C57BLMyocardial InfarctionNebivololNG-Nitroarginine Methyl Ester3-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalateAdrenergic beta-1 Receptor AntagonistsBenzopyransEthanolaminesNebivololNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide Synthase Type INitric Oxide Synthase Type IIINos1 protein, mouseNos3 protein, mousePropanolaminesReceptors, Adrenergic, beta-3

Identifiers

PMID24849208
PMCPMC4029889
OpenAlexW2095134785

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.