Evidence map›Paper›PMID 23241318›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Enhanced resistance to permeability transition in interfibrillar cardiac mitochondria in dogs: effects of aging and long-term aldosterone infusion.

Girma Asemu, Kelly A O'Connell, James W Cox, Erinne R Dabkowski, Wenhong Xu, Rogerio F Ribeiro, Kadambari C Shekar, Peter A Hecker, Sharad Rastogi, Hani N Sabbah and 2 more

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2013. 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
1.3field-weighted citation impact, top 20% 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, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Pharmacological modulation of mitochondrial ion channels.British journal of pharmacology · 2019
    Review
  5. AP39, a mitochondria-targeting hydrogen sulfide (HBritish journal of pharmacology · 2017
    Article
  6. Review
  7. Article
  8. Review
  9. Myofibroblast secretome and its auto-/paracrine signaling.Expert review of cardiovascular therapy · 2016
    Review
  10. Article
  11. Review
  12. Effect of a high-protein diet on development of heart failure in response to pressure overload.Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme · 2014
    Article
  13. Article
  14. Article
  15. Role of mitochondrial oxidative stress in hypertension.American journal of physiology. Heart and circulatory physiology · 2013
    Review
  16. Article
  17. Article
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 3 institutions in 1 country.

Girma AsemuDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Kelly A O'Connell
James W Cox
Erinne R Dabkowski
Wenhong Xu
Rogerio F Ribeiro
Kadambari C Shekar
Peter A Hecker
Sharad Rastogi
Hani N Sabbah
Charles L Hoppel
William C Stanley
University of Maryland, Baltimore · USHenry Ford Hospital · USUniversity School · US

Funding

Substrate Selection and Oxidative Stress in Heart FailureP01HL074237 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI STANLEY, WILLIAM C · 2003 to 2013
$19.9M
Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI AHIMA, REXFORD S. · 2013 to 2017
$9.7M
Docosahexaenoic Acid, Mitochondrial Dysfunction and Cardiac Reperfusion InjuryR21HL110731 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI STANLEY, WILLIAM C · 2011 to 2012
$422k
NHLBI NIH HHS HL-074237NHLBI NIH HHS HL-110731NIAMS NIH HHS T32 AR007592NIDDK NIH HHS P30 DK079637
6 · The paper itself

Abstract

Functional differences between subsarcolemmal and interfibrillar cardiac mitochondria (SSM and IFM) have been observed with aging and pathological conditions in rodents. Results are contradictory, and there is little information from large animal models. We assessed the respiratory function and resistance to mitochondrial permeability transition (MPT) in SSM and IFM from healthy young (1 yr) and old (8 yr) female beagles and in old beagles with hypertension and left ventricular (LV) wall thickening induced by 16 wk of aldosterone infusion. MPT was assessed in SSM and IFM by Ca(2+) retention and swelling. Healthy young and old beagles had similar mitochondrial structure, respiratory function, and Ca(2+)-induced MPT within SSM and IFM subpopulations. On the other hand, oxidative capacity and resistance to Ca(2+)-induced MPT were significantly greater in IFM compared with SSM in all groups. Old beagles treated with aldosterone had greater LV wall thickness and worse diastolic filling but normal LV chamber volume and systolic function. Treatment with aldosterone did not alter mitochondrial respiratory function but accelerated Ca(2+)-induced MPT in SSM, but not IFM, compared with healthy old and young beagles. In conclusion, in a large animal model, oxidative capacity and resistance to MPT were greater in IFM than in SSM. Furthermore, aldosterone infusion increased susceptibility to MPT in SSM, but not IFM. Together this suggests that SSM are less resilient to acute stress than IFM in the healthy heart and are more susceptible to the development of pathology with chronic stress.

Indexed as

AgingAldosteroneAnimalsCell Membrane PermeabilityDogsFemaleHypertensionHypertrophy, Left VentricularIntracellular MembranesMitochondria, HeartAldosterone

Identifiers

PMID23241318
PMCPMC3566488
OpenAlexW2464481106

What OpenQuestion holds

Textmetadata
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.