Oguz Fatih, Beytur Ali, Taslidere Elif, Parlakpinar Hakan, Oguz Hilal Kurnaz, Polat Alaaddin, Topcu İbrahim, Vardi Nigar, Selcuk Engin Burak
Inonu University, School of Medicine, Department of Urology, Malatya, Turkey.
Inonu University, School of Medicine, Department of Histology and Embryology, Malatya, Turkey.
Iran J Basic Med Sci. 2019 Dec;22(12):1392-1399. doi: 10.22038/IJBMS.2019.13986.
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.
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: 1-3 days 9 µg/kg/day, 4-7 days 9 µg/kg twice daily, and 8-90 days 18 µg/kg twice daily. The rats of acute and chronic groups were sacrificed on the 45 and 90 days, respectively. Some tissue markers related to oxidative stress were measured, and sperm characteristics were observed.
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.
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.
伐尼克兰是烟碱型乙酰胆碱受体α4β2亚型的选择性部分激动剂,广泛用于治疗吸烟成瘾。然而,关于其对组织潜在毒性作用的数据仍然缺乏。在本研究中,我们旨在确定伐尼克兰对大鼠生殖和肾脏组织的毒性作用。
将大鼠随机分为两组:对照组(n = 10)和伐尼克兰组(n = 24)。然后,每组大鼠再平均分为急性组和慢性组。对照组大鼠仅口服蒸馏水。伐尼克兰的给药方式如下:第1 - 3天,9 μg/kg/天;第4 - 7天,9 μg/kg,每日两次;第8 - 90天,18 μg/kg,每日两次。急性组和慢性组大鼠分别在第45天和第90天处死。检测了一些与氧化应激相关的组织标志物,并观察了精子特征。
在急性组中,伐尼克兰导致肾脏和睾丸组织中的超氧化物歧化酶(SOD)活性显著降低。在慢性组中,伐尼克兰显著增加了肾脏和睾丸中丙二醛(MDA)和髓过氧化物酶(MPO)的生成,并降低了过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)的水平。此外,睾丸中的SOD和谷胱甘肽(GSH)水平也显著降低。而且,精子特征受到负面影响;所有组的睾丸和肾脏均观察到组织病理学变形。
本研究表明,急性和长期使用伐尼克兰均可对肾脏和睾丸产生有害影响。进一步的研究将为这种损伤的分子动力学提供更多见解。