Protective role of N-acetylcysteine (NAC) on human sperm exposed to etoposide

被引:9
作者
Baetas, Joao [1 ,2 ]
Rabaca, Ana [1 ]
Goncalves, Ana [3 ]
Barros, Alberto [3 ,4 ,5 ]
Sousa, Mario [1 ,6 ]
Sa, Rosalia [1 ,6 ]
机构
[1] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Lab Cell Biol, Dept Microscopy, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[2] Univ Porto, Fac Sci, P-4169007 Porto, Portugal
[3] Ctr Reprod Genet A Barros CGR, Av Bessa 240,1 Dto Frente, P-4100012 Porto, Portugal
[4] Univ Porto, Fac Med, Dept Genet, Alameda Prof Hernani Monteiro, P-4200319 Porto, Portugal
[5] Univ Porto, Hlth Inst Res & Innovat IPATIMUP i3S, Rua Alfredo Allen 208, P-4200135 Porto, Portugal
[6] Univ Porto, Multidisciplinary Unit Biomed Res UMIB, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
关键词
N-acetylcysteine (NAC); Etoposide; Sperm DNA fragmentation; Sperm oxidative stress; OXIDATIVE STRESS; FERTILITY PRESERVATION; CLINICAL-PHARMACOLOGY; ANTIOXIDANT ACTION; DNA FRAGMENTATION; TUMOR PATIENTS; CANCER; CHEMOTHERAPY; CISPLATIN; MEN;
D O I
10.1186/s12610-018-0082-2
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Background: Although recent progress in cancer treatment has increased patient survival and improved quality of life, reproductive side effects are still for concern. One way to decrease gonadal impairment is to use cytoprotectors. In testicular cancer, etoposide is generally used in combination with other agents, but there are no in-vitro studies of sperm exposure to etoposide and cytoprotectors, namely N-acetylcysteine (NAC). Methods: Twenty semen samples were individually divided into five groups: control, incubation with NAC alone, incubation with etoposide alone, sequential exposure of NAC followed by etoposide (pre-treatment) and sequential exposure of etoposide followed by NAC (post-treatment). Sperm characteristics, chromatin condensation (aniline blue), DNA fragmentation (TUNEL), oxidative stress (OxyDNA labelling) and glutathione quantification were used to evaluate the capabilities of NAC as a prophylactic (pre-treatment) or ameliorator (post-treatment) agent over the effects caused in sperm during in-vitro exposure to etoposide. Results: No deleterious effects were observed on sperm motility or sperm membrane integrity. Results revealed that prophylactic use of NAC (pre-treatment) increased rates of immature sperm chromatin as compared to ameliorator use of NAC (post-treatment), and increased rates of sperm DNA fragmentation in relation to controls. Pre and post-treatment with NAC increased oxidative levels in comparison to controls, but also increased levels of cellular antioxidant glutathione. Conclusions: The results indicate that NAC has the ability to counteract etoposide-induced toxicity rather than preventing the etoposide cytotoxic effects over sperm DNA, suggesting that the administration of NAC to cells formerly exposed to etoposide is preferable to its prophylactic use. As the results evidenced that NAC seems to be more efficient in attenuating sperm etoposide cytotoxic effects instead of being used as a chemoprophylactic agent, this reinforces the idea that there might be a new NAC mechanism over DNA.
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页数:9
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