Effects of 6-mercaptopurine in pressure overload induced right heart failure

PLoS One. 2019 Nov 12;14(11):e0225122. doi: 10.1371/journal.pone.0225122. eCollection 2019.

Abstract

Background: Several antineoplastic drugs have been proposed as new compounds for pulmonary arterial hypertension treatment but many have cardiotoxic side effects. The chemotherapeutic agent 6-mercaptopurine may have an effect in treatment of pulmonary arterial hypertension but at the same time, its effects on the afterload adaption of the right ventricle is unpredictable due to interaction with multiple downstream signalling pathways in the cardiomyocytes. We investigated the direct cardiac effects of 6-mercaptopurine in rats with isolated right heart failure caused by pulmonary trunk banding (PTB).

Methods: Male Wistar rat weanlings (112±2 g) were randomized to sham operation (sham, n = 10) or PTB. The PTB animals were randomized to placebo (PTB-control, n = 10) and 6-mercaptopurine (7.5 mg/kg/day) groups with treatment start before the PTB procedure (PTB-prevention, n = 10) or two weeks after (PTB-reversal, n = 10). Right ventricular effects were evaluated by echocardiography, cardiac MRI, invasive pressure-volume measurements, and histological and molecular analyses.

Results: PTB increased right ventricular afterload and caused right ventricular hypertrophy and failure. 6-mercaptopurine did not improve right ventricular function nor reduce right ventricular remodelling in both prevention and reversal studies compared with placebo-treated rats.

Conclusion: Treatment with 6-mercaptopurine did not have any beneficial or detrimental effects on right ventricular function or remodelling. Our data suggest that treatment of pulmonary arterial hypertension with 6-mercaptopurine is not harmful to the failing right ventricle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Blood Pressure
  • Disease Models, Animal
  • Heart Failure / drug therapy
  • Heart Failure / etiology*
  • Heart Failure / pathology
  • Heart Failure / physiopathology*
  • Heart Ventricles
  • Hemodynamics
  • Hypertension, Pulmonary / complications*
  • Male
  • Mercaptopurine / pharmacology*
  • Rats, Wistar
  • Ventricular Function, Right
  • Ventricular Remodeling

Substances

  • Mercaptopurine

Grants and funding

JBA was generously supported by Aarhus Universitets forskningsfond (http://auff.au.dk/), Helga og Peter Kornings Fond grant 274023-9 (https://health.au.dk/om-health/fonde-og-legater-ved-health/helga-og-peter-kornings-fond/), Ingeniør August Frederik Wedell Erichsens Legat grant 13655, Fonden til lægevidenskabens fremme grant 17-L-0099 (https://www.apmollerfonde.dk/ansoegning/laegefonden/), Simon Spies Fonden (http://spiesfonden.dk/), and The Danish Medical Research Grant 2017-1064/96 (https://www.laeger.dk/laegeforeningens-forskningsfond). We acknowledge support from the Netherlands CardioVascular Research Initiative: the Dutch Heart Foundation, Dutch Federation of University Medical Centers, the Netherlands Organization for Health Research and Development, and the Royal Netherlands Academy of Sciences Grant 2012-08 awarded to the Phaedra consortium (http://www.phaedraresearch.nl) (XQS, KK, MJG, FSDM, HJB). We also acknowledge support for KK by the Dutch Lung Foundation (Longfonds) grant number-5.2.17.198J0. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.