Neuropsychopharmacology and Toxicology Program, College of Pharmacy, Kangwon National University, Chunchon, 24341, Republic of Korea.
Department of Anatomy, College of Medicine, Chung-Ang University, Seoul, 06974, Republic of Korea.
Chem Biol Interact. 2019 Jul 1;307:136-146. doi: 10.1016/j.cbi.2019.05.001. Epub 2019 May 3.
Since reproductive toxicity is associated with oxidative stress, nuclear factor κB (NFκB), a redox-sensitive transcription factor, may be involved in the reproductive dysfunction induced by the abusive drug, such as cocaine. In the present study, we investigated whether NFκB mediates cocaine-induced reproductive dysfunction in male mice, and whether glutathione peroxidase (GPx)-1, a well-known enzymatic antioxidant, modulates NFκB activity to affect this reproductive dysfunction. Cocaine treatment significantly increased nuclear translocation of NFκB and its DNA binding activity in the testis of mice. Treatment with cocaine resulted in a significant increase in sperm abnormality, and in significant decreases in the sperm viability and sperm level. Furthermore, cocaine significantly reduced hypothalamic gonadotropin-releasing-hormone expression and plasma testosterone level. These alterations were more pronounced in the GPx-1 knockout (GPx-1 KO) than wild type (WT) mice, and they were less pronounced in GPx-1 overexpressing transgenic (GPx-1 TG) than in non-transgenic (non-TG) mice. Pyrrolidine dithiocarbamate (PDTC), an NFκB inhibitor, was more effective in attenuating cocaine-induced reproductive toxicity in GPx-1 KO than in WT mice. Although PDTC treatment was also significantly protective against the reproductive toxicity in non-TG mice, PDTC did not show additional positive effects against the protective potential mediated by GPx-1 overexpression in mice. Therefore, our results suggest that GPx-1 gene is a protective factor in response to reproductive dysfunction induced by cocaine in male mice, and that NFκB is a critical mediator of protective activity of GPx-1 gene in our experimental conditions.
由于生殖毒性与氧化应激有关,核因子 κB(NFκB)作为一种氧化还原敏感的转录因子,可能参与了滥用药物如可卡因引起的生殖功能障碍。在本研究中,我们研究了 NFκB 是否介导了可卡因诱导的雄性小鼠生殖功能障碍,以及谷胱甘肽过氧化物酶-1(GPx-1),一种众所周知的酶抗氧化剂,是否调节 NFκB 活性来影响这种生殖功能障碍。可卡因处理显著增加了 NFκB 的核转位及其在小鼠睾丸中的 DNA 结合活性。可卡因处理导致精子畸形显著增加,精子活力和精子水平显著降低。此外,可卡因显著降低了下丘脑促性腺激素释放激素的表达和血浆睾酮水平。这些改变在 GPx-1 基因敲除(GPx-1 KO)小鼠中比野生型(WT)小鼠更为明显,而在 GPx-1 过表达转基因(GPx-1 TG)小鼠中比非转基因(non-TG)小鼠更为明显。吡咯烷二硫代氨基甲酸盐(PDTC),一种 NFκB 抑制剂,在减轻 GPx-1 KO 小鼠可卡因诱导的生殖毒性方面比 WT 小鼠更为有效。尽管 PDTC 治疗对非 TG 小鼠的生殖毒性也有显著的保护作用,但 PDTC 并没有显示出对 GPx-1 过表达介导的保护潜力的额外积极影响。因此,我们的结果表明,GPx-1 基因是雄性小鼠可卡因诱导生殖功能障碍的一种保护因子,NFκB 是 GPx-1 基因在我们实验条件下保护活性的关键介质。