首页> 外文期刊>International Journal of Andrology >The endocrine disruptors dibutyl phthalate (DBP) and diethylstilbestrol (DES) influence Leydig cell regeneration following ethane dimethane sulphonate treatment of adult male rats
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The endocrine disruptors dibutyl phthalate (DBP) and diethylstilbestrol (DES) influence Leydig cell regeneration following ethane dimethane sulphonate treatment of adult male rats

机译:内分泌干​​扰物邻苯二甲酸二丁酯(DBP)和己烯雌酚(DES)影响乙烷二甲烷磺酸盐处理成年雄性大鼠后的Leydig细胞再生

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摘要

The manner by which endocrine-disrupting xenobiotics, such as phthalates, can induce changes in the development of the male reproductive system still remains largely unknown. Herein, we have explored the application of ethane dimethane sulphonate (EDS) to eliminate adult-type Leydig cells in the mature rat testis, leading to their regeneration from resident stem cells, as a novel system to investigate the effects of dibutyl phthalate (DBP) and diethylstilbestrol (DES) on adult-type Leydig cell differentiation. The advantage of this model is that one can study adult-type Leydig cell differentiation in vivo divorced from the concomitant endocrine development of puberty. In these preliminary studies, we show that both DBP and/or DES, given for 2 or 4days following EDS application, indeed affect Leydig cell differentiation in the adult testis, largely by increasing early Leydig cell proliferation and possibly thereby delaying early differentiation. In particular, on day 27 post-EDS, a time-point when the differentiation trajectory appears to be most discriminating, we observe that both DBP and/or DES cause a fourfold increase in Leydig cell density, and a significant increase in the expression of the Leydig cell-specific marker transcripts INSL3, LH receptor, Cyp17a1 and Cyp 11a1. In conclusion, both DBP and DES are able to affect adult-type Leydig cells during their differentiation to cause a significant perturbation in their ultimate functional capacity.
机译:破坏内分泌的异源生物(如邻苯二甲酸酯)可以诱导男性生殖系统发育变化的方式仍然很大程度上未知。在这里,我们已经探索了应用乙烷二甲磺酸盐(EDS)消除成熟大鼠睾丸中成年型Leydig细胞,从而使其从驻留干细胞再生的方法,作为研究邻苯二甲酸二丁酯(DBP)作用的新型系统和己烯雌酚(DES)对成年型Leydig细胞分化的影响。该模型的优势在于,可以研究与青春期伴随的内分泌发育分开的体内成年型Leydig细胞分化。在这些初步研究中,我们表明,应用EDS后2天或4天给予的DBP和/或DES确实确实影响了成年睾丸中Leydig细胞的分化,主要是通过增加早期Leydig细胞的增殖并可能因此延迟了早期分化。特别是在EDS后第27天,这是分化轨迹似乎最能区分的时间点,我们观察到DBP和/或DES均导致Leydig细胞密度增加了四倍,并且Lydig的表达显着增加。 Leydig细胞特异性标记物转录物INSL3,LH受体,Cyp17a1和Cyp 11a1。总之,DBP和DES都能够在分化过程中影响成年型Leydig细胞,从而对其最终功能产生重大干扰。

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