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Evaluation of the cardiovascular effects of varenicline in rats

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dc.contributor.author Selcuk, EB
dc.contributor.author Sungu, M
dc.contributor.author Parlakpinar, H
dc.contributor.author Ermis, N
dc.contributor.author Taslidere, E
dc.contributor.author Vardi, N
dc.contributor.author Yalcinsoy, M
dc.contributor.author Sagir, M
dc.contributor.author Polat, A
dc.contributor.author Karatas, M
dc.contributor.author Kayhan-Tetik, B
dc.date.accessioned 2022-03-24T13:17:22Z
dc.date.available 2022-03-24T13:17:22Z
dc.date.issued 2015
dc.identifier.uri http://hdl.handle.net/11616/57799
dc.description.abstract Background: Cardiovascular disease is an important cause of morbidity and mortality among tobacco users. Varenicline is widely used worldwide to help smoking cessation, but some published studies have reported associated cardiovascular events.
dc.description.abstract Objective: To determine the cardiovascular toxicity induced by varenicline in rats.
dc.description.abstract Materials and methods: We randomly separated 34 rats into two groups: 1) the control group (given only distilled water orally, n=10) and the varenicline group (given 9 mu g/kg/day varenicline on days 1-3, 9 mu g/kg twice daily on days 4-7, and 18 mu g/kg twice daily on days 8-90 [total 83 days], n=24). Each group was then subdivided equally into acute and chronic subgroups, and all rats in these groups were euthanized with anesthesia overdose on days 45 and 90, respectively. Body and heart weights, hemodynamic (mean oxygen saturation, mean blood pressure, and heart rate, electrocardiographic (PR, QRS, and QT intervals) biochemical (oxidants and antioxidants), and histopathological analyses (including immunostaining) were performed.
dc.description.abstract Results: Acute varenicline exposure resulted in loss of body weight, while chronic varenicline exposure caused heart weight loss and decreased mean blood pressure, induced lipid peroxidation, and reduced antioxidant activity. Both acute and chronic varenicline exposure caused impairment of mean oxygen saturation. QT interval was prolonged in the chronic varenicline group, while PR interval prolongation was statistically significant in both the control and acute varenicline groups. Caspase-9 activity was also significantly increased by chronic exposure. Moreover, histopathological observations revealed severe morphological heart damage in both groups.
dc.description.abstract Conclusion: Adverse effects of chronic varenicline exposure on cardiovascular tissue were confirmed by our electrocardiographic, biochemical, and histopathological analyses. This issue needs to be investigated with new experimental and clinical studies to evaluate the exact mechanism(s) of the detrimental effects of varenicline. Physicians should bear in mind the toxic effects of varenicline on the cardiovascular system when prescribing it for smoking cessation.
dc.source DRUG DESIGN DEVELOPMENT AND THERAPY
dc.title Evaluation of the cardiovascular effects of varenicline in rats


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