Habert René, Muczynski Vincent, Lehraiki Abdelali, Lambrot Romain, Lécureuil Charlotte, Levacher Christine, Coffigny Hervé, Pairault Catherine, Moison Delphine, Frydman René, Rouiller-Fabre Virginie
Laboratory of Differentiation and Radiobiology of the Gonads, CEA - DSV / iRCM / SCSR, F-92265 Fontenay aux Roses, France Université Paris, Diderot-Paris7, F-92265, Fontenay aux Roses, France INSERM, Unité 967, F-92265, Fontenay aux Roses, France.
Folia Histochem Cytobiol. 2009;47(5):S67-74. doi: 10.2478/v10042-009-0056-5.
There are great concerns about the increasing incidence of abnormalities in male reproductive function. Human sperm counts have markedly dropped and the rate of testicular cancer has clearly augmented over the past four decades. Moreover, the prevalence rates of cryptorchidism and hypospadias are also probably increasing. It has been hypothesized that all these adverse trends in male reproduction result from abnormalities in the development of the testis during foetal and neonatal life. Furthermore, many recent epidemiological, clinical and experimental data suggest that these male reproductive disorders could be due to the effects of xenobiotics termed endocrine disruptors, which are becoming more and more concentrated and prevalent in our environment. Among these endocrine disruptors, we chose to focus this review on the phthalates for different reasons: 1) they are widespread in the environment; 2) their concentrations in many human biological fluids have been measured; 3) the experimental data using rodent models suggesting a reprotoxicity are numerous and are the most convincing; 4) their deleterious effects on the in vivo and in vitro development and function of the rat foetal testis have been largely studied; 5) some epidemiological data in humans suggest a reprotoxic effect at environmental concentrations at least during neonatal life. However, the direct effects of phthalates on human foetal testis have never been explored. Thus, as we did for the rat in the 1990s, we recently developed and validated an organ culture system which allows maintenance of the development of the different cell types of human foetal testis. In this system, addition of 10-4 M MEHP (mono-2-ethylhexyl phthalate), the most produced phthalate, had no effect on basal or LH-stimulated production of testosterone, but it reduced the number of germ cells by increasing their apoptosis, without modification of their proliferation. This is the first experimental demonstration that phthalates alter the development of the foetal testis in humans. Using our organotypic culture system, we and others are currently investigating the effect of MEHP in the mouse and the rat, and it will be interesting to compare the results between these species to analyse the relevance of toxicological tests based on rodent models.
男性生殖功能异常的发生率不断上升,引发了人们的高度关注。在过去的四十年里,人类精子数量显著下降,睾丸癌的发病率也明显增加。此外,隐睾症和尿道下裂的患病率可能也在上升。据推测,男性生殖领域所有这些不良趋势都是由胎儿期和新生儿期睾丸发育异常导致的。此外,最近许多流行病学、临床和实验数据表明,这些男性生殖障碍可能是由于被称为内分泌干扰物的外源性物质的影响,这些物质在我们的环境中越来越集中和普遍。在这些内分泌干扰物中,出于不同原因,我们选择在本综述中重点关注邻苯二甲酸盐:1)它们在环境中广泛存在;2)已测量了它们在许多人体生物体液中的浓度;3)使用啮齿动物模型表明具有生殖毒性的实验数据众多且最具说服力;4)已对它们对大鼠胎儿睾丸体内和体外发育及功能的有害影响进行了大量研究;5)一些人类流行病学数据表明,至少在新生儿期,环境浓度的邻苯二甲酸盐具有生殖毒性作用。然而,邻苯二甲酸盐对人类胎儿睾丸的直接影响从未被探究过。因此,正如我们在20世纪90年代对大鼠所做的那样,我们最近开发并验证了一种器官培养系统,该系统能够维持人类胎儿睾丸不同细胞类型的发育。在这个系统中,添加10-4 M的MEHP(单-2-乙基己基邻苯二甲酸盐),这种产量最高的邻苯二甲酸盐,对基础或促黄体生成素刺激的睾酮分泌没有影响,但它通过增加生殖细胞的凋亡来减少生殖细胞数量,而不改变其增殖。这是邻苯二甲酸盐改变人类胎儿睾丸发育的首个实验证明。利用我们的器官型培养系统,我们和其他人目前正在研究MEHP对小鼠和大鼠的影响,比较这些物种之间的结果以分析基于啮齿动物模型的毒理学测试的相关性将会很有趣。