Evidence map›Paper›PMID 24084216›Full record

ArticleJournal of cardiovascular pharmacology2013

Atrophic cardiomyocyte signaling in hypertensive heart disease.

German Kamalov, Wenyuan Zhao, Tieqiang Zhao, Yao Sun, Robert A Ahokas, Tony N Marion, Fahed Al Darazi, Ivan C Gerling, Syamal K Bhattacharya, Karl T Weber

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of cardiovascular pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Myofibroblast secretome and its auto-/paracrine signaling.Expert review of cardiovascular therapy · 2016
    Review
  6. 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

10 authors at 3 institutions in 3 countries.

German Kamalov*Department of Medicine, Division of Cardiovascular Diseases; Departments of †Obstetrics and Gynecology; and ‡Microbiology, Immunology and Biochemistry; and §Department of Medicine, Division of Endocrinology, University of Tennessee Health Science Center, Memphis, TN. G. Kamalov is now with the Division of Cardiovascular Medicine, Ohio State University, Columbus, OH.
Wenyuan Zhao
Tieqiang Zhao
Yao Sun
Robert A Ahokas
Tony N Marion
Fahed Al Darazi
Ivan C Gerling
Syamal K Bhattacharya
Karl T Weber
University of Tennessee Health Science Center · USNational Institute of Cardiovascular Diseases · BDDiabetes Australia · AU

Funding

Aldosteronism: An Immunostimulatory StateR01HL073043 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WEBER, KARL T · 2004 to 2008
$1.8M
Recovery from Cachexia in Heart and Skeletal MuscleR01HL090867 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WEBER, KARL T · 2008 to 2011
$1.5M
NHLBI NIH HHS R01 HL073043NHLBI NIH HHS R01 HL090867NHLBI NIH HHS R01-HL73043NHLBI NIH HHS R01 HL90867
6 · The paper itself

Abstract

Cardinal pathological features of hypertensive heart disease (HHD) include not only hypertrophied cardiomyocytes and foci of scattered microscopic scarring, a footprint of prior necrosis, but also small myocytes ensnared by fibrillar collagen where disuse atrophy with protein degradation would be predicted. Whether atrophic signaling is concordant with the appearance of HHD and involves oxidative and endoplasmic reticulum (ER) stress remains unexplored. Herein, we examine these possibilities focusing on the left ventricle and cardiomyocytes harvested from hypertensive rats receiving 4 weeks aldosterone/salt treatment (ALDOST) alone or together with ZnSO₄, a nonvasoactive antioxidant, with the potential to attenuate atrophy and optimize hypertrophy. Compared with untreated age-/sex-/strain-matched controls, ALDOST was accompanied by (1) left ventricle hypertrophy with preserved systolic function; (2) concordant cardiomyocyte atrophy (<1000 μm²) found at sites bordering on fibrosis where they were reexpressing β-myosin heavy chain; and (3) upregulation of ubiquitin ligases, muscle RING-finger protein-1 and atrogin-1, and elevated 8-isoprostane and unfolded protein ER response with messenger RNA upregulation of stress markers. ZnSO₄ cotreatment reduced lipid peroxidation, fibrosis, and the number of atrophic myocytes, together with a further increase in cell area and width of atrophied and hypertrophied myocytes, and improved systolic function but did not attenuate elevated blood pressure. We conclude that atrophic signaling, concordant with hypertrophy, occurs in the presence of a reparative fibrosis and induction of oxidative and ER stress at sites of scarring where myocytes are atrophied. ZnSO₄ cotreatment in HHD with ALDOST attenuates the number of atrophic myocytes, optimizes size of atrophied and hypertrophied myocytes, and improves systolic function.

Indexed as

Disease Models, AnimalSignal TransductionAnimalsAntihypertensive AgentsAntioxidantsCardiotonic AgentsCells, CulturedCell SizeEndoplasmic Reticulum StressHeart VentriclesHypertensionHypertrophy, Left VentricularMaleMuscle ProteinsMyocytes, CardiacOxidative StressAntihypertensive AgentsAntioxidantsCardiotonic AgentsFbxo32 protein, ratMuscle ProteinsSKP Cullin F-Box Protein LigasesTrim63 protein, ratTripartite Motif ProteinsUbiquitin-Protein Ligases

Identifiers

PMID24084216
PMCPMC3881541
OpenAlexW1970831372

What OpenQuestion holds

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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.