Author/Authors :
Oguz, Fatih Inonu University - School of Medicine - Department of Urology - Malatya, Turkey , Beytur, Ali Inonu University - School of Medicine - Department of Urology - Malatya, Turkey , Taslidere, Elif Inonu University - School of Medicine - Department of Histology and Embryology - Malatya, Turkey , Parlakpinar, Hakan Inonu University - School of Medicine - Department of Pharmacology - Malatya, Turkey , Kurnaz Oguz, Hilal Malatya State Hospital - Department of Internal Medicine - Malatya, Turkey , Polat, Alaaddin Inonu University - School of Medicine - Department of Physiology - Malatya, Turkey , Topcu, İbrahim Inonu University - School of Medicine - Department of Urology - Malatya, Turkey , Vardi, Nigar Inonu University - School of Medicine - Department of Histology and Embryology - Malatya, Turkey , Burak Selcuk, Engin Inonu University - School of Medicine - Department of Family Medicine - Malatya, Turkey
Abstract :
Objective(s): Varenicline is a selective partial agonist for the nicotinic acetylcholine receptor a4b2
subtype, which is widely used to treat smoking addiction. However, there is still no data about its
potential toxic effects on tissues. In this study, we aimed to determine the varenicline-induced toxicity
on reproductive and renal tissues in rats.
Materials and Methods: Rats were randomly divided into two groups: control (n=10) and varenicline
(n=24). Then, rats in each group were sub-divided equally as acute and chronic groups. The control
rats were orally given distilled water only. Varenicline was administrated orally as follows: 1st–3rd days
9 μg/kg/day, 4th–7th days 9 μg/kg twice daily, and 8th–90th days 18 μg/kg twice daily. The rats of acute
and chronic groups were sacrificed on the 45th and 90th days, respectively. Some tissue markers related
to oxidative stress were measured, and sperm characteristics were observed.
Results: In the acute group, varenicline led to a significant decrease in SOD activities in both kidney
and testis tissues. In the chronic group, varenicline significantly increased MDA and MPO production,
and reduced CAT and GPx levels in the kidneys and testes. Also, SOD and GSH levels significantly
decreased in the testes. Moreover, sperm characteristics were negatively affected; histopathological
deformation was observed in the testes and kidneys in all groups.
Conclusion: This study showed that varenicline could detrimentally affect the kidneys and testes in
both acute and chronic term usage. Further studies will provide more insights into the molecular
dynamics of this damage.
Keywords :
Kidney , Rat , Testis , Toxicity , Varenicline