Evidence map›Paper›PMID 30175269›Full record

ArticleJACC. Basic to translational science2018

Red Blood Cells in Type 2 Diabetes Impair Cardiac Post-Ischemic Recovery Through an Arginase-Dependent Modulation of Nitric Oxide Synthase and Reactive Oxygen Species.

Jiangning Yang, Xiaowei Zheng, Ali Mahdi, Zhichao Zhou, Yahor Tratsiakovich, Tong Jiao, Attila Kiss, Oskar Kövamees, Michael Alvarsson, Sergiu-Bogdan Catrina and 3 more

Open access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-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

35 citing papers in PubMed, 62 citations in OpenAlex.

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  9. African walnut (Frontiers in nutrition · 2025
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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

13 authors at 2 institutions in 1 country.

Jiangning YangDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Xiaowei ZhengDivision of Endocrinology and Diabetology, Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Ali MahdiDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Zhichao ZhouDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Yahor TratsiakovichDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Tong JiaoDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Attila KissDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Oskar KövameesDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Michael AlvarssonDivision of Endocrinology and Diabetology, Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Sergiu-Bogdan CatrinaDivision of Endocrinology and Diabetology, Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Jon O LundbergDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Kerstin BrismarDivision of Endocrinology and Diabetology, Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
John PernowDivision of Cardiology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockhom, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study tested the hypothesis that red blood cell (RBC) arginase represents a potential therapeutic target in ischemia-reperfusion in type 2 diabetes. Post-ischemic cardiac recovery was impaired in hearts from db/db mice compared with wild-type hearts. RBCs from mice and patients with type 2 diabetes attenuated post-ischemic cardiac recovery of nondiabetic hearts. This impaired cardiac recovery was reversed by inhibition of RBCs arginase or nitric oxide synthase. The results suggest that RBCs from type 2 diabetics impair cardiac tolerance to ischemia-reperfusion via a pathway involving arginase activity and nitric oxide synthase-dependent oxidative stress.

Indexed as

ABH, 2 (S)-amino-6-boronohexanoic acidarginasedP/dt, the first derivative of left ventricular pressureeNOS, endothelial nitric oxide synthaseiNOS, inducible isoform of nitric oxide synthaseKH, Krebs-HenseleitL-NAME, NG-nitro-L-arginine methyl esterLVDP, left ventricular developed pressureLVEDP, left ventricular end-diastolic pressureNAC, N-acetylcysteinenitric oxide synthaseNO, nitric oxidenor-NOHA, Nω-hydroxy-nor-L-arginineNOS, nitric oxide synthaseRBC, red blood cellreactive oxygen speciesred blood cellsROS, reactive oxygen speciestype 2 diabetesWT, wild type

Identifiers

PMID30175269
PMCPMC6115643
OpenAlexW2883534193

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.