Evidence map›Paper›PMID 35505637›Full record

ArticlePharmacology research & perspectives2022

Inhibitory role of recombinant neorudin on canine coronary artery thrombosis.

Yu-Bin Liu, Xing-Chen Zhou, Yun Liu, Lin Zhang, Ying Zhou, Xiao Xu, Can Zheng, Zhuan-You Zhao, Chu-Tse Wu, Ji-de Jin

Abstract read
In one paragraph

Article in Pharmacology research & perspectives, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

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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

10 authors.

Yu-Bin LiuBeijing Institute of Radiation Medicine, Beijing, China.ORCID 0000-0001-9479-8727
Xing-Chen ZhouBeijing Institute of Radiation Medicine, Beijing, China.
Yun LiuBeijing Institute of Radiation Medicine, Beijing, China.
Lin ZhangBeijing Institute of Radiation Medicine, Beijing, China.
Ying ZhouBeijing Institute of Radiation Medicine, Beijing, China.
Xiao XuBeijing Institute of Radiation Medicine, Beijing, China.
Can ZhengBeijing Institute of Radiation Medicine, Beijing, China.
Zhuan-You ZhaoCenter for Pharmacodynamic Research, Tianjin Institute of Pharmaceutical Research, Tianjin, China.
Chu-Tse WuBeijing Institute of Radiation Medicine, Beijing, China.
Ji-de JinBeijing Institute of Radiation Medicine, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The anticoagulant application is an effective treatment modality for cardiovascular diseases such as coronary heart disease, unstable angina pectoris, and myocardial infarction. In this study, the antithrombotic effect of recombinant neorudin (EPR-hirudin, EH) was evaluated using a canine model of coronary artery thrombosis. A canine model with platelet thrombosis in the left circumferent branch of the coronary artery was designed using Folt's method, and the anti-thrombus activity of EH was investigated. Femoral administration of EH intravenously had a significant dose-dependent inhibitory effect on canine coronary artery thrombosis and the effective rates were 66.7% (p < .05), 83.3% (p < .05), and 100% (p < .01) after injection of 0.3, 1.0, and 3.0 mg/kg EH, respectively. Furthermore, EH demonstrated lower bleeding, with shorter bleeding time and less bleeding loss than low molecular weight heparin (LMWH). Under the similar effect intensity of EH and LMWH (85 IU/kg), the bleeding time of the EH group at 30 min was shorter, and the blood loss at 30-120 min was less than that of LMWH (p < .05 and p < .05-.001, respectively). EH had a significant dose-dependent inhibitory effect in the dose range of 0.3-3.0 mg/kg on the coronary artery thrombosis and lower bleeding side effects than LMWH with a similar antithrombosis effect.

Indexed as

Coronary ThrombosisMyocardial InfarctionAnimalsCoronary VesselsDogsHemorrhageHeparin, Low-Molecular-WeightHeparin, Low-Molecular-Weightanimal model validationblood pharmacologyin vivopharmacodynamics

Identifiers

PMID35505637
PMCPMC9065819

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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.