Hu Jing-Yi, Wang Xin-Ru
Nanjing Maternity and Child Health Care Hospital, Nanjing Medical University, Nanjing, Jiangsu 210004, China.
Zhonghua Nan Ke Xue. 2008 Nov;14(11):968-72.
To assess the joint toxicity of phoxim (Pho) and fenvalerate (Fen) on the spermatogenesis of male rats and to clarify its mechanism.
Based on the three administrative levels of factorial analysis (3 x 3) of Pho and Fen, i. e. their half lethal dose (LD50) 1/250 LD50 (5.9, 2.4 mg/kg) and 1/50 LD50 (29.4, 12.0 mg/kg) and the control, 135 adult male SD rats were randomly assigned to9 groups, the control (0.0 mg/kg), Pho (5.9, 29.4 mg/kg), Fen (2.4, 12.0 mg/kg), Pho + Fen (5.9 + 2.4, 5.9 + 12.0, 29.4 + 2.4, 29.4 + 12.0 mg/kg), and treated intragastrically with different doses of Pho, Fen and Pho + Fen for 15 and 30 days. The levels of serum follicle stimulating hormone (FSH), luteinizing hormone (LH), testosterone (T) and testis homogenate T were determined by radioimmunoassay (RIA), the activity of testicular marker enzymes such as acid phosphatases (ACP) and gamma-glutamyl transpeptidase (gamma-GT) examined, and the sperm head count measured for the changes of daily sperm production (Spr).
At 15 days, obvious interaction was observed between Pho and Fen in both serum LH and FSH (P < 0.05), as well as between their reproductive toxicities. With the increase in doses, the joint action was synergistic in LH (P < 0.05) and antagonistic in FSH (P < 0.01) at a high dose ( 29.4 + 12.0 mg/kg). At 30 days, marked interaction between Pho and Fen was noted in the content of homogenate T (P < 0.05) , with a joint synergistic effect. At 15 and 30 days, with the increase of doses, both Pho and Fen reduced Spr and the activity of ACP and gamma-GT, but Pho + Fen showed no obvious interaction in them (P > 0.05) , and their joint action was an additive effect.
Pho and Fen jointly impaired spermatogenesis in a dose- and time-dependent manner. Their joint action exhibited mainly as a synergistic effect, an additive effect and increased toxicity.
评估辛硫磷(Pho)和氰戊菊酯(Fen)对雄性大鼠精子发生的联合毒性,并阐明其作用机制。
根据Pho和Fen的三水平析因分析(3×3),即它们的半数致死剂量(LD50)的1/250(5.9、2.4mg/kg)和1/50(29.4、12.0mg/kg)以及对照组,将135只成年雄性SD大鼠随机分为9组,即对照组(0.0mg/kg)、Pho组(5.9、29.4mg/kg)、Fen组(2.4、12.0mg/kg)、Pho+Fen组(5.9+2.4、5.9+12.0、29.4+2.4、29.4+12.0mg/kg),分别给予不同剂量的Pho、Fen及Pho+Fen灌胃15天和30天。采用放射免疫分析法(RIA)测定血清卵泡刺激素(FSH)、黄体生成素(LH)、睾酮(T)及睾丸匀浆T水平,检测睾丸酸性磷酸酶(ACP)和γ-谷氨酰转肽酶(γ-GT)等标志酶活性,计数精子头数观察每日精子生成量(Spr)的变化。
15天时,Pho与Fen在血清LH和FSH方面存在明显交互作用(P<0.05),在生殖毒性方面也有交互作用。随着剂量增加,高剂量(29.4+12.0mg/kg)时联合作用在LH上呈协同效应(P<0.05),在FSH上呈拮抗效应(P<0.01)。30天时,Pho与Fen在匀浆T含量上有显著交互作用(P<0.05),呈联合协同效应。15天和30天时,随着剂量增加,Pho和Fen均降低了Spr以及ACP和γ-GT的活性,但Pho+Fen组在这些指标上无明显交互作用(P>0.05),其联合作用为相加效应。
Pho和Fen联合以剂量和时间依赖方式损害精子发生。它们的联合作用主要表现为协同效应、相加效应和毒性增加。