TY - JOUR
T1 - Effects of 6-mercaptopurine in pressure overload induced right heart failure
AU - Axelsen, Julie Birkmose
AU - Andersen, Stine
AU - Sun, Xiao-Qing
AU - Ringgaard, Steffen
AU - Hyldebrandt, Janus Adler
AU - Kurakula, Kondababu
AU - Goumans, Marie-José
AU - de Man, Frances S.
AU - Nielsen-Kudsk, Jens Erik
AU - Bogaard, Harm-Jan
AU - Andersen, Asger
N1 - Funding Information:
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-legaterved-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.
Publisher Copyright:
© 2019 Axelsen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2019
Y1 - 2019
N2 - 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-mercapto-purine (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.
AB - 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-mercapto-purine (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.
UR - https://www.scopus.com/pages/publications/85074942854
UR - https://www.ncbi.nlm.nih.gov/pubmed/31714926
U2 - 10.1371/journal.pone.0225122
DO - 10.1371/journal.pone.0225122
M3 - Article
C2 - 31714926
SN - 1932-6203
VL - 14
JO - PLoS ONE
JF - PLoS ONE
IS - 11
M1 - e0225122
ER -