Evidence map›Paper›PMID 24963034›Full record

ArticlePhysiological reports2014

A new twist on an old idea part 2: cyclosporine preserves normal mitochondrial but not cardiomyocyte function in mini-swine with compensated heart failure.

Jessica A Hiemstra, Manuel Gutiérrez-Aguilar, Kurt D Marshall, Kyle S McCommis, Pamela J Zgoda, Noelany Cruz-Rivera, Nathan T Jenkins, Maike Krenz, Timothy L Domeier, Christopher P Baines and 1 more

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  6. ER stress and calcium-dependent arrhythmias.Frontiers in physiology · 2022
    Review
  7. Cardiovascular effects of immunosuppression agents.Frontiers in cardiovascular medicine · 2022
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  13. Review
  14. Chronic interval exercise training prevents BKJournal of applied physiology (Bethesda, Md. : 1985) · 2018
    Article
  15. Article
  16. Review
  17. Article
  18. Regulation of sarcoplasmic reticulum CaJournal of molecular and cellular cardiology · 2016
    Review
  19. Article
  20. Review
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

11 authors at 2 institutions in 1 country.

Jessica A HiemstraDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Manuel Gutiérrez-AguilarDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri Dalton Cardiovascular Research Center, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Kurt D MarshallDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri Dalton Cardiovascular Research Center, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Kyle S McCommisDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri Dalton Cardiovascular Research Center, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Pamela J ZgodaDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Noelany Cruz-RiveraDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Nathan T JenkinsDepartment of Kinesiology, University of Georgia, Athens, Georgia.
Maike KrenzDalton Cardiovascular Research Center, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri Department of Medical Pharmacology and Physiology, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Timothy L DomeierDepartment of Medical Pharmacology and Physiology, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Christopher P BainesDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri Dalton Cardiovascular Research Center, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
Craig A EmterDepartment of Biomedical Science, University of Missouri- Columbia, 1600 E. RollinsW160 Veterinary Medicine, Columbia, Missouri.
University of Missouri · USUniversity of Georgia · US

Funding

TRAINING: MUSCLE BLOOD FLOW &CAPILLARY DYNAMICSR01HL036088 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI LAUGHLIN, M HAROLD · 1985 to 2013
$4.0M
Exercise &Health: Integration from Molecule to PatientT32AR048523 · NIAMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI TERJUNG, RONALD L · 2003 to 2013
$2.5M
SHP2 controls cardiac stress adaptationR01HL116525 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI KRENZ, MAIKE · 2013 to 2016
$1.4M
Cardiomyocyte stretch and intracellular calcium release with advancing ageK01AG041208 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI DOMEIER, TIMOTHY LEE · 2012 to 2016
$545k
NHLBI NIH HHS R01 HL036088NHLBI NIH HHS R01 HL116525NIAMS NIH HHS T32 AR048523NIA NIH HHS K01 AG041208
6 · The paper itself

Abstract

We recently developed a clinically relevant mini-swine model of heart failure with preserved ejection fraction (HFpEF), in which diastolic dysfunction was associated with increased mitochondrial permeability transition (MPT). Early diastolic function is ATP and Ca(2+)-dependent, thus, we hypothesized chronic low doses of cyclosporine (CsA) would preserve mitochondrial function via inhibition of MPT and subsequently maintain normal cardiomyocyte Ca(2+) handling and contractile characteristics. Left ventricular cardiomyocytes were isolated from aortic-banded Yucatan mini-swine divided into three groups; control nonbanded (CON), HFpEF nontreated (HF), and HFpEF treated with CsA (HF-CsA). CsA mitigated the deterioration of mitochondrial function observed in HF animals, including functional uncoupling of Complex I-dependent mitochondrial respiration and increased susceptibility to MPT. Attenuation of mitochondrial dysfunction in the HF-CsA group was not associated with commensurate improvement in cardiomyocyte Ca(2+) handling or contractility. Ca(2+) transient amplitude was reduced and transient time to peak and recovery (tau) prolonged in HF and HF-CsA groups compared to CON. Alterations in Ca(2+) transient parameters observed in the HF and HF-CsA groups were associated with decreased cardiomyocyte shortening and shortening rate. Cellular function was consistent with impaired in vivo systolic and diastolic whole heart function. A significant systemic hypertensive response to CsA was observed in HF-CsA animals, and may have played a role in the accelerated the development of heart failure at both the whole heart and cellular levels. Given the significant detriment to cardiac function observed in response to CsA, our findings suggest chronic CsA treatment is not a viable therapeutic option for HFpEF.

Indexed as

CalciumcardiomyocytecyclosporineHFpEFmitochondria

Identifiers

PMID24963034
PMCPMC4208639
OpenAlexW2157034749

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.