Evidence map›Paper›PMID 23997103›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Imatinib attenuates monocrotaline pulmonary hypertension and has potent vasodilator activity in pulmonary and systemic vascular beds in the rat.

Edward A Pankey, Supat Thammasiboon, George F Lasker, Syed Baber, Joseph A Lasky, Philip J Kadowitz

Open access · greenAbstract 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 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Positioning Imatinib for Pulmonary Arterial Hypertension: A Dose-Finding Phase 2 Study.American journal of respiratory and critical care medicine · 2025
    Trial
  3. Article
  4. Growth factors involved in vascular remodeling in pulmonary arterial hypertension.Journal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi · 2025
    Review
  5. Article
  6. Receptor Tyrosine Kinase: Still an Interesting Target to Inhibit the Proliferation of Vascular Smooth Muscle Cells.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Analysis of erectile responses to H2S donors in the anesthetized rat.American journal of physiology. Heart and circulatory physiology · 2015
    Article
  17. Analysis of cardiovascular responses to the H2S donors Na2S and NaHS in the rat.American journal of physiology. Heart and circulatory physiology · 2015
    Article
  18. Deficiency of Akt1, but not Akt2, attenuates the development of pulmonary hypertension.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Edward A PankeyDepartments of Pharmacology and Medicine (Pulmonary Diseases, Critical Care and Environmental Medicine Tulane University School of Medicine, New Orleans, Louisiana.
Supat Thammasiboon
George F Lasker
Syed Baber
Joseph A Lasky
Philip J Kadowitz
Tulane University · US

Funding

CARDIOPULMONARY SURGERY RESEARCHR01HL062000 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI KADOWITZ, PHILIP J · 2000 to 2008
$2.5M
Stem Cell Therapy for Pulmonary HypertensionR01HL077421 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI KADOWITZ, PHILIP J · 2005 to 2008
$1.9M
NHLBI NIH HHS HL-62000NHLBI NIH HHS HL-77421
6 · The paper itself

Abstract

Cardiovascular responses to the tyrosine kinase inhibitor imatinib were investigated in the rat. Intravenous injections of 0.3-30 mg/kg imatinib produced small decreases in pulmonary arterial pressure, larger dose-dependent decreases in systemic arterial pressure, and no change or small increases in cardiac output, suggesting that the systemic vasodilator response is more pronounced under baseline conditions. When pulmonary arterial pressure was increased with U-46619 or N(ω)-nitro-L-arginine methyl ester (L-NAME), intravenous injections of imatinib produced larger dose-dependent decreases in pulmonary arterial pressure. Imatinib attenuated the acute hypoxic pulmonary vasoconstrictor response. Vasodilator responses to imatinib were not inhibited by meclofenamate, glybenclamide, or rolipram, suggesting that cyclooxygenase, ATP-sensitive K(+) (KATP) channels, and cAMP were not involved in mediating the response. In a 21-day prevention study, imatinib treatment (50 mg/kg ip) attenuated the increase in pulmonary arterial pressure, right ventricular hypertrophy, and small vessel remodeling induced by monocrotaline. Imatinib reduced PDGF receptor phosphorylation and PDGF-stimulated thymidine incorporation in rat pulmonary artery smooth muscle cells. These data suggest that the beneficial effect of imatinib in pulmonary hypertension may involve inhibition of PDGF tyrosine kinase receptor-mediated effects on smooth muscle cell proliferation and on vasoconstrictor tone. These results indicate that imatinib has nonselective vasodilator activity in the pulmonary and systemic vascular beds similar to the Rho kinase inhibitor fasudil and the calcium entry antagonist isradipine. The present results are consistent with the hypothesis that imatinib may inhibit a constitutively active tyrosine kinase vasoconstrictor pathway in the pulmonary and systemic vascular beds in the rat.

Indexed as

MonocrotalineAnimalsAntihypertensive AgentsArterial PressureBenzamidesCyclooxygenase InhibitorsDisease Models, AnimalDose-Response Relationship, DrugHypertension, PulmonaryHypertrophy, Right VentricularImatinib MesylateMaleMuscle, Smooth, VascularPhosphodiesterase 4 InhibitorsPiperazinesPotassium Channel BlockersAntihypertensive AgentsBenzamidesCyclooxygenase InhibitorsImatinib MesylateMonocrotalinePDGF receptor tyrosine kinasePhosphodiesterase 4 InhibitorsPiperazinesPotassium Channel BlockersProtein Kinase InhibitorsPyrimidinesReceptors, Platelet-Derived Growth FactorVasodilator AgentsimatinibPDGFpulmonary vascular bedtyrosine kinase inhibitorvasodilation

Identifiers

PMID23997103
PMCPMC3840242
OpenAlexW2132324778

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.