Endocrine Disruptors and Leydig Cell Function

被引:92
作者
Svechnikov, K. [1 ]
Izzo, G.
Landreh, L.
Weisser, J.
Soder, O.
机构
[1] Karolinska Inst, Dept Womens & Childrens Hlth, Pediat Endocrinol Unit, SE-17176 Stockholm, Sweden
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2010年
基金
瑞典研究理事会;
关键词
LUTEINIZING-HORMONE RECEPTOR; HUMAN CHORIONIC-GONADOTROPIN; ACUTE REGULATORY PROTEIN; SPRAGUE-DAWLEY RATS; SOY FORMULA MILK; ANDROGEN RECEPTOR; SEXUAL-DIFFERENTIATION; BISPHENOL-A; FETAL-RAT; GENE-EXPRESSION;
D O I
10.1155/2010/684504
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
During the past decades, a large body of information concerning the effects of endocrine disrupting compounds (EDCs) on animals and humans has been accumulated. EDCs are of synthetic or natural origin and certain groups are known to disrupt the action of androgens and to impair the development of the male reproductive tract and external genitalia. The present overview describes the effects of the different classes of EDCs, such as pesticides, phthalates, dioxins, and phytoestrogens, including newly synthesized resveratrol analogs on steroidogenesis in Leydig cells. The potential impact of these compounds on androgen production by Leydig cells during fetal development and in the adult age is discussed. In addition, the possible role of EDCs in connection with the increasing frequency of abnormalities in reproductive development in animals and humans is discussed.
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页数:10
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