State key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 210029, China.
Asian J Androl. 2011 Sep;13(5):702-9. doi: 10.1038/aja.2011.76. Epub 2011 Aug 15.
Di-n-butyl phthalate (DBP) is an endocrine-disrupting chemical that has the potential to affect male reproduction. However, the reproductive effects of low-dose DBP are still not well known, especially at the molecular level. In the present study, pubertal male Sprague-Dawley rats were orally administered DBP at a wide range of doses (0.1, 1.0, 10, 100 and 500 mg kg⁻¹ day⁻¹) for 30 days. The selected end points included reproductive organ weights, testicular histopathology and serum hormonal levels. Additionally, proteomic analysis was performed to identify proteins that are differentially expressed as a result of exposure to DBP at low doses (0.1, 1.0 and 10 mg kg⁻¹ day⁻¹). Toxic effects were observed in the high-dose groups, including anomalous development of testes and epididymides, severe atrophy of seminiferous tubules, loss of spermatogenesis and abnormal levels of serum hormones. Treatment with low doses of DBP seemed to exert a 'stimulative effect' on the serum hormones. Proteomics analysis of rat testes showed 20 differentially expressed proteins. Among these proteins, alterations in the expression of HnRNPA2/B1, vimentin and superoxide dismutase 1 (SOD1) were further confirmed by Western blot and immunohistochemistry. Taken together, we conclude that high doses of DBP led to testicular toxicity, and low doses of DBP led to changes in the expression of proteins involved in spermatogenesis as well as changes in the number and function of Sertoli and Leydig cells, although no obvious morphological changes appeared. The identification of these differentially expressed proteins provides important information about the mechanisms underlying the effects of DBP on male rat reproduction.
邻苯二甲酸二正丁酯(DBP)是一种内分泌干扰化学物质,有可能影响男性生殖功能。然而,低剂量 DBP 的生殖毒性作用尚不完全清楚,特别是在分子水平上。在本研究中,青春期雄性 Sprague-Dawley 大鼠经口给予 DBP 不同剂量(0.1、1.0、10、100 和 500mg/kg/d)30 天。选择的终点包括生殖器官重量、睾丸组织病理学和血清激素水平。此外,还进行了蛋白质组学分析,以鉴定由于暴露于低剂量 DBP(0.1、1.0 和 10mg/kg/d)而差异表达的蛋白质。高剂量组观察到毒性作用,包括睾丸和附睾发育异常、生精小管严重萎缩、精子发生丧失和血清激素水平异常。低剂量 DBP 处理似乎对血清激素产生“刺激作用”。大鼠睾丸的蛋白质组学分析显示 20 种差异表达的蛋白质。在这些蛋白质中,hnRNPA2/B1、波形蛋白和超氧化物歧化酶 1(SOD1)的表达变化通过 Western blot 和免疫组化进一步得到证实。综上所述,我们得出结论,高剂量 DBP 导致睾丸毒性,低剂量 DBP 导致参与精子发生的蛋白质表达变化以及 Sertoli 和 Leydig 细胞数量和功能的变化,尽管没有明显的形态学变化。这些差异表达蛋白质的鉴定为 DBP 对雄性大鼠生殖功能的影响机制提供了重要信息。