Dr SAM COOPER SAM.COOPER@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
Long‐term cardiovascular effects of vandetanib and pazopanib in normotensive rats
Cooper, Samantha L.; Carter, Joanne J.; March, Julie; Woolard, Jeanette
Authors
Joanne J. Carter
Julie March
Professor JEANETTE WOOLARD Jeanette.Woolard@nottingham.ac.uk
PROFESSOR OF CARDIOVASCULAR PHYSIOLOGY AND PHARMACOLOGY
Abstract
Vandetanib and pazopanib are clinically available, multi‐targeted inhibitors of vascular endothelial growth factor (VEGF) and platelet‐derived growth factor (PDGF) receptor tyrosine kinases. Short‐term VEGF receptor inhibition is associated with hypertension in 15%‐60% of patients, which may limit the use of these anticancer therapies over the longer term. To evaluate the longer‐term cardiovascular implications of treatment, we investigated the “on”‐treatment (21 days) and “off”‐treatment (10 days) effects following daily administration of vandetanib, pazopanib, or vehicle, in conscious rats. Cardiovascular variables were monitored in unrestrained Sprague‐Dawley rats instrumented with radiotelemetric devices. In Study 1, rats were randomly assigned to receive either daily intraperitoneal injections of vehicle (volume 0.5 mL; n = 5) or vandetanib 25 mg/kg/day (volume 0.5 mL; n = 6). In Study 2, rats received either vehicle (volume 0.5 mL; n = 4) or pazopanib 30 mg/kg/day (volume 0.5 mL; n = 7), dosed once every 24 hours for 21 days. All solutions were in 2% Tween, 5% propylene glycol in 0.9% saline solution. Vandetanib caused sustained increases in mean arterial pressure (MAP), systolic blood pressure (SBP), and diastolic blood pressure (DBP) compared to baseline and vehicle. Vandetanib also significantly altered the circadian cycling of MAP, SBP, and DBP. Elevations in SBP were detectable 162 hours after the last dose of vandetanib. Pazopanib also caused increases in MAP, SBP, and DBP. However, compared to vandetanib, these increases were of slower onset and a smaller magnitude. These data suggest that the cardiovascular consequences of vandetanib and pazopanib treatment are sustained, even after prolonged cessation of drug treatment.
Citation
Cooper, S. L., Carter, J. J., March, J., & Woolard, J. (2019). Long‐term cardiovascular effects of vandetanib and pazopanib in normotensive rats. Pharmacology Research and Perspectives, 7(3), Article e00477. https://doi.org/10.1002/prp2.477
Journal Article Type | Article |
---|---|
Acceptance Date | Apr 8, 2019 |
Online Publication Date | May 31, 2019 |
Publication Date | 2019-06 |
Deposit Date | Jan 8, 2020 |
Publicly Available Date | Jan 13, 2020 |
Journal | Pharmacology Research & Perspectives |
Print ISSN | 2052-1707 |
Electronic ISSN | 2052-1707 |
Publisher | Wiley Open Access |
Peer Reviewed | Peer Reviewed |
Volume | 7 |
Issue | 3 |
Article Number | e00477 |
DOI | https://doi.org/10.1002/prp2.477 |
Public URL | https://nottingham-repository.worktribe.com/output/2469954 |
Publisher URL | https://bpspubs.onlinelibrary.wiley.com/doi/full/10.1002/prp2.477 |
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Long- term cardiovascular effects of vandetanib and pazopanib
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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