Evidence map›Paper›PMID 30525078›Full record

ArticleRegenerative therapy2018

Pretreatment with an angiotensin II receptor blocker abolished ameliorating actions of adipose-derived stem cell sheets on cardiac dysfunction and remodeling after myocardial infarction.

Kenshiro Yamamoto, Yasutaka Kurata, Yumiko Inoue, Maya Adachi, Motokazu Tsuneto, Junichiro Miake, Kazuhide Ogino, Haruaki Ninomiya, Akio Yoshida, Yasuaki Shirayoshi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Regenerative therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

15 authors at 3 institutions in 1 country.

Kenshiro YamamotoDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Yasutaka KurataDepartment of Physiology II, Kanazawa Medical University Faculty of Medicine, 1-1 Daigaku, Uchinada-machi, Kahoku-gun, Ishikawa 920-0293, Japan.
Yumiko InoueDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Maya AdachiDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Motokazu TsunetoDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Junichiro MiakeDivision of Cardiovascular Medicine, Department of Molecular Medicine and Therapeutics, Tottori University Faculty of Medicine, Yonago, Japan.
Kazuhide OginoDepartment of Cardiology, Tottori Red Cross Hospital, Tottori, Japan.
Haruaki NinomiyaDepartment of Biological Regulation, Tottori University, Yonago, Japan.
Akio YoshidaDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Yasuaki ShirayoshiDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Yoshiko SuyamaDepartment of Plastic and Reconstructive Surgery, Tottori University Faculty of Medicine, Yonago, Japan.
Shunjiro YagiDepartment of Plastic and Reconstructive Surgery, Tottori University Faculty of Medicine, Yonago, Japan.
Motonobu NishimuraDepartment of Cardiovascular Surgery, Tottori University Faculty of Medicine, Yonago, Japan.
Kazuhiro YamamotoDivision of Cardiovascular Medicine, Department of Molecular Medicine and Therapeutics, Tottori University Faculty of Medicine, Yonago, Japan.
Ichiro HisatomeDivision of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Tottori University Graduate School of Medical Science, 86 Nishi-cho, Yonago 683-8503, Japan.
Tottori University · JPKanazawa Medical University · JPTottori Prefectural Central Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCell sheets using myoblasts have been developed for the treatment of heart failure after myocardial infarction (MI) bridging to heart transplantation. Stem cells are supposed to be better than myoblasts as a source of cells, since they possess a potential to proliferate and differentiate into cardiomyocytes, and also have capacity to secrete angiogenic factors. Adipose-derived stem cells (ASCs) obtained from fat tissues are expected to be a new cell source for ASC sheet therapies. Administration of angiotensin II receptor blockers (ARBs) is a standard therapy for heart failure after MI. However, it is not known whether ARBs affect the cell sheet therapy. This study aimed to examine ameliorating effects of ASC sheets on heart failure and remodeling after MI, and how pretreatment with ARBs prior to the creation of MI and ASC sheet transplantation modifies the effects of ASC sheets.

methodsASCs were isolated from fat tissues of wild-type rats, and ASC sheets were engineered on temperature-responsive dishes. In

resultsIn the

conclusionsASC sheets ameliorated cardiac dysfunctions and remodeling after MI via increasing VEGF expression, which was abolished by pretreatment with irbesartan before the creation of MI and transplantation.

Indexed as

Adipose-derived stem cell sheetAngiotensin IIANP, atrial natriuretic peptideARB, angiotensin receptor blockerASC, adipose-derived stem cellAT1(2)R, angiotensin II receptor type 1(2)CRT, cardiac resynchronization therapyEF, ejection fractionFGF, fibroblast growth factorFS, fractional shorteningHGF, hepatocyte growth factorIrbesartanLVEDD, left ventricular end-diastolic diameterLVESD, left ventricular end-systolic diameterMI, myocardial infarctionMSC, mesenchymal stem cellMyocardial infarctionRAS, renin–angiotensin systemVEGFVEGF, vascular endothelial growth factorvWF, von Willebrand factor

Identifiers

PMID30525078
PMCPMC6223028
OpenAlexW2892323430

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.