Traina Maria Elsa, Rescia Michele, Urbani Elisabetta, Mantovani Alberto, Macrì Caterina, Ricciardi Claudio, Stazi Anna Velia, Fazzi Paola, Cordelli Eugenia, Eleuteri Patrizia, Leter Giorgio, Spanò Marcello
Laboratory of Environmental Hygiene, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Reprod Toxicol. 2003 Jan-Feb;17(1):25-35. doi: 10.1016/s0890-6238(02)00101-6.
Long-lasting effects on mouse spermatogenesis induced by prenatal exposure to the insecticide lindane have been investigated by conventional reproductive endpoints complemented by the flow cytometric (FCM) DNA content analysis of testis cells and by the Sperm Chromatin Structure Assay (SCSA). Two lindane dose levels, 15 and 25 mg/kg bw, and diethylstilboestrol (DES, 10 microg/kg bw) as positive control, were administered daily by gavage to pregnant CD1 mice on gestation days (GD) 9-16. Reproductive endpoints were evaluated on F1 male mice on postnatal day (PND) 60; additionally, animals treated with lindane 25 mg/kg per day and DES were examined on PND 100 to evaluate the possible reversibility of the effects. On PND 60, lindane and DES caused a reduction in the sperm head count and concentration, with recovery in older lindane 25 mg/kg per day animals (PND 100). By contrast, the DES group exhibited a greater reduction in the sperm head count on PND 100 than on PND 60. Changes in biochemical parameters in the testes, lactate dehydrogenase-C(4) (LDH-C(4)), and sorbitol dehydrogenase (SDH) activities, were also observed in adult treated F1 mice. Furthermore on PND 60, the FCM analysis revealed changes in the pattern of testicular germ cell distribution, especially in the haploid subcompartment, in the lindane 25 mg/kg per day group. A dose-dependent increase in chromatin abnormalities of the epididymal sperm was also shown by SCSA. These changes recovered on PND 100. Preliminary qualitative examination did not reveal any significant difference in the structure of testicular tissue; however, there were suggestions of a moderate increase in number and size of Leydig cells in both DES- and lindane-treated animals. The partial reversibility of these effects and the lack of structural modification of the testicular tissue as evidenced by histopathologic assessment suggest a functional impairment of sperm production and maturation, possibly associated with changes induced by lindane on factors affecting intratesticular steroidogenesis.
通过传统生殖终点指标,并辅以睾丸细胞的流式细胞术(FCM)DNA含量分析和精子染色质结构分析(SCSA),研究了产前暴露于杀虫剂林丹对小鼠精子发生的长期影响。在妊娠第9至16天,通过灌胃法每天给怀孕的CD1小鼠施用两种林丹剂量水平,即15和25 mg/kg体重,以及作为阳性对照的己烯雌酚(DES,10 μg/kg体重)。在出生后第60天(PND 60)对F1雄性小鼠的生殖终点指标进行评估;此外,对每天用25 mg/kg林丹和DES处理的动物在PND 100进行检查,以评估这些影响的可能可逆性。在PND 60时,林丹和DES导致精子头部数量和浓度减少,每天用25 mg/kg林丹处理的老年动物(PND 100)有所恢复。相比之下,DES组在PND 100时精子头部数量的减少比PND 60时更大。在成年受处理的F1小鼠中,还观察到睾丸中生化参数的变化,即乳酸脱氢酶-C(4)(LDH-C(4))和山梨醇脱氢酶(SDH)活性的变化。此外,在PND 60时,FCM分析显示每天用25 mg/kg林丹处理的组中睾丸生殖细胞分布模式发生变化,特别是在单倍体亚群中。SCSA还显示附睾精子的染色质异常呈剂量依赖性增加。这些变化在PND 100时恢复。初步定性检查未发现睾丸组织结构有任何显著差异;然而,有迹象表明,在DES和林丹处理的动物中,睾丸间质细胞的数量和大小适度增加。这些影响的部分可逆性以及组织病理学评估所证明的睾丸组织无结构改变,表明精子产生和成熟存在功能障碍,可能与林丹对影响睾丸内类固醇生成的因素所诱导的变化有关。