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Evaluation of reproductive and renal toxicity of varenicline in male rats
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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043878/ https://www.ncbi.nlm.nih.gov/pubmed/32133056 http://dx.doi.org/10.22038/IJBMS.2019.13986 |
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author | Oguz, Fatih Beytur, Ali Taslidere, Elif Parlakpinar, Hakan Oguz, Hilal Kurnaz Polat, Alaaddin Topcu, İbrahim Vardi, Nigar Selcuk, Engin Burak |
author_facet | Oguz, Fatih Beytur, Ali Taslidere, Elif Parlakpinar, Hakan Oguz, Hilal Kurnaz Polat, Alaaddin Topcu, İbrahim Vardi, Nigar Selcuk, Engin Burak |
author_sort | Oguz, Fatih |
collection | PubMed |
description | 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: 1(st)–3(rd) days 9 µg/kg/day, 4(th)–7(th) days 9 µg/kg twice daily, and 8(th)–90(th) days 18 µg/kg twice daily. The rats of acute and chronic groups were sacrificed on the 45(th) and 90(th) 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. |
format | Online Article Text |
id | pubmed-7043878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-70438782020-03-04 Evaluation of reproductive and renal toxicity of varenicline in male rats Oguz, Fatih Beytur, Ali Taslidere, Elif Parlakpinar, Hakan Oguz, Hilal Kurnaz Polat, Alaaddin Topcu, İbrahim Vardi, Nigar Selcuk, Engin Burak Iran J Basic Med Sci Original Article 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: 1(st)–3(rd) days 9 µg/kg/day, 4(th)–7(th) days 9 µg/kg twice daily, and 8(th)–90(th) days 18 µg/kg twice daily. The rats of acute and chronic groups were sacrificed on the 45(th) and 90(th) 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. Mashhad University of Medical Sciences 2019-12 /pmc/articles/PMC7043878/ /pubmed/32133056 http://dx.doi.org/10.22038/IJBMS.2019.13986 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Oguz, Fatih Beytur, Ali Taslidere, Elif Parlakpinar, Hakan Oguz, Hilal Kurnaz Polat, Alaaddin Topcu, İbrahim Vardi, Nigar Selcuk, Engin Burak Evaluation of reproductive and renal toxicity of varenicline in male rats |
title | Evaluation of reproductive and renal toxicity of varenicline in male rats |
title_full | Evaluation of reproductive and renal toxicity of varenicline in male rats |
title_fullStr | Evaluation of reproductive and renal toxicity of varenicline in male rats |
title_full_unstemmed | Evaluation of reproductive and renal toxicity of varenicline in male rats |
title_short | Evaluation of reproductive and renal toxicity of varenicline in male rats |
title_sort | evaluation of reproductive and renal toxicity of varenicline in male rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043878/ https://www.ncbi.nlm.nih.gov/pubmed/32133056 http://dx.doi.org/10.22038/IJBMS.2019.13986 |
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