Evidence map›Paper›PMID 25322707›Full record

ArticleCardiovascular drugs and therapy2014

Tadalafil prevents acute heart failure with reduced ejection fraction in mice.

Fadi N Salloum, Vinh Q Chau, Nicholas N Hoke, Rakesh C Kukreja

Open access · greenAbstract read
In one paragraph

Article in Cardiovascular drugs and therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Potential beneficial impacts of tadalafil on cardiovascular diseases.Journal of the Chinese Medical Association : JCMA · 2025
    Review
  3. Review
  4. Article
  5. Anti-Apoptosis and Anti-Fibrosis Effects ofInternational journal of molecular sciences · 2018
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

4 authors at 1 institution in 1 country.

Fadi N SalloumPauley Heart Center, Division of Cardiology, Department of Internal Medicine, Virginia Commonwealth University, 1101 East Marshall Street, Room 7-020A, Richmond, VA, 23298-0204, USA, fnsalloum@vcu.edu.
Vinh Q Chau
Nicholas N Hoke
Rakesh C Kukreja
Virginia Commonwealth University · US

Funding

Protection against Doxorubicin-Induced CardiomyopathyR37HL051045 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI KUKREJA, RAKESH C · 2006 to 2015
$3.8M
CARDIOPROTECTIVE EFFECTS OF PDE-5 INHIBITORSR01HL079424 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI KUKREJA, RAKESH C · 2005 to 2013
$3.6M
MOLECULAR MECHANISMS OF DELAYED PRECONDITIONINGR01HL059469 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI KUKREJA, RAKESH C. · 1998 to 2006
$2.4M
Cardioprotective Signaling following Phosphodiesterase-5 InhibitionR01HL093685 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI KUKREJA, RAKESH C · 2008 to 2012
$1.9M
SIGNALING MECHANISMS IN PHARMACOLOGICAL PRECONDITIONINGR01HL051045 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI KUKREJA, RAKESH C. · 1995 to 2004
$1.4M
NHLBI NIH HHS HL-51045NHLBI NIH HHS HL-79424NHLBI NIH HHS HL-93685NHLBI NIH HHS R01 HL051045NHLBI NIH HHS R01 HL059469NHLBI NIH HHS R01 HL079424NHLBI NIH HHS R01 HL093685NHLBI NIH HHS R37 HL051045
6 · The paper itself

Abstract

purposePhosphodiesterase-5 (PDE5) inhibitors were shown to exert powerful protection in various animal models of cardiomyopathy. Tadalafil is a long-acting and highly specific PDE5 inhibitor, which makes it the most attractive in its class for long-term management of patients with heart failure. We studied the effects of tadalafil in attenuating ischemic cardiomyopathy in mice. METHODS AND

resultsAdult male mice underwent myocardial infarction (MI) by permanent left coronary artery ligation and were treated daily with tadalafil (1 mg/kg; ip) or volume-matched 10% DMSO for 4 weeks. Twenty four hours after coronary ligation, infarct size, measured by TTC staining, was reduced from 70.1 ± 3.1% in DMSO-treated group to 49.3 ± 2.6% with tadalafil (P < 0.05). Similarly, tadalafil treatment yielded a smaller fibrotic area (8.8 ± 2.8% of LV), assessed by Masson's trichrome staining, as compared to DMSO group (21.9 ± 3.9%, P < 0.05). Apoptosis, measured by TUNEL assay, also declined with tadalafil (2.1 ± 0.2%) as compared to DMSO (6.7 ± 0.4%, P < 0.05) at 28 days post MI. Tadalafil also attenuated the increase in cardiac hypertrophy and pulmonary edema following infarction. These parameters reflect diminished left ventricular (LV) adverse remodeling and preserved fractional shortening with tadalafil at 7 and 28 days post infarction.

conclusionsTadalafil attenuates ischemic cardiomyopathy in mice and preserves LV function.

Indexed as

AnimalsApoptosisCarbolinesCardiomegalyCardiomyopathiesCoronary VesselsHeart FailureMaleMiceMice, Inbred ICRMyocardial InfarctionPhosphodiesterase InhibitorsPulmonary EdemaTadalafilVentricular Dysfunction, LeftVentricular Function, LeftCarbolinesPhosphodiesterase InhibitorsTadalafil

Identifiers

PMID25322707
PMCPMC8529582
OpenAlexW1968494724

What OpenQuestion holds

Textmetadata
LicenceTDM
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.