dc.contributor.authors |
Oktar, S; Gokce, A; Aydin, M; Davarci, M; Meydan, S; Ozturk, OH; Koc, A; |
|
dc.date.accessioned |
2020-01-17T11:59:12Z |
|
dc.date.available |
2020-01-17T11:59:12Z |
|
dc.date.issued |
2010 |
|
dc.identifier.citation |
Oktar, S; Gokce, A; Aydin, M; Davarci, M; Meydan, S; Ozturk, OH; Koc, A; (2010). Beneficial effect of erdosteine on methotrexate-induced testicular toxicity in mice. TOXICOLOGY AND INDUSTRIAL HEALTH, 26, 438-433 |
|
dc.identifier.issn |
0748-2337 |
|
dc.identifier.uri |
https://hdl.handle.net/20.500.12619/6973 |
|
dc.identifier.uri |
https://doi.org/10.1177/0748233710369666 |
|
dc.description.abstract |
Methotrexate is used to treat certain types of cancer of the breast, skin, head and neck, or lung. Methotrexate can cause serious or life-threatening side effects on liver, lungs, kidneys, and immune system. Methotrexate chemotherapy causes testicular damage in humans. The aim of this study was to investigate the possible protective role of erdosteine on testicular toxicity of methotrexate in mice. Twenty-six male mice were divided into four groups as follows: group 1, control; group 2, erdosteine-treated; group 3, methotrexate-treated; and group 4, methotrexate + erdosteine treated. On the first day of experiment, a single dose of methotrexate was intraperitoneally administered to groups 3 and 4, although a daily single dose of erdosteine was orally administered to group 2 and 4 for 7 days. At the end of the experiment, the testes of the animals were removed and weighed. The levels of total antioxidant capacity and total oxidative stress, and myeloperoxidase activity in the methotrexate group were higher than the control group (p<0.05). Lipid peroxidation levels were not changed in methotrexate group compared with control group. In conclusion, erdosteine could effectively protect the testes in methotrexate-induced toxicity. |
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dc.language |
English |
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dc.publisher |
SAGE PUBLICATIONS INC |
|
dc.title |
Beneficial effect of erdosteine on methotrexate-induced testicular toxicity in mice |
|
dc.type |
Article |
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dc.identifier.volume |
26 |
|
dc.identifier.startpage |
433 |
|
dc.identifier.endpage |
438 |
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dc.contributor.department |
Sakarya Üniversitesi/Tıp Fakültesi/Cerrahi Tıp Bilimleri Bölümü |
|
dc.contributor.saüauthor |
Gökçe, Ahmet |
|
dc.relation.journal |
TOXICOLOGY AND INDUSTRIAL HEALTH |
|
dc.identifier.wos |
WOS:000280645400005 |
|
dc.identifier.doi |
10.1177/0748233710369666 |
|
dc.contributor.author |
Sueleyman Oktar |
|
dc.contributor.author |
Ahmet Gokce |
|
dc.contributor.author |
Gökçe, Ahmet |
|
dc.contributor.author |
Mehmet Aydin |
|
dc.contributor.author |
Muersel Davarci |
|
dc.contributor.author |
Sedat Meydan |
|
dc.contributor.author |
Oktay Hasan Ozturk |
|
dc.contributor.author |
Ahmet Koc |
|