Oestrogens and puberty

被引:62
作者
Alonso, LC
Rosenfield, RL
机构
[1] Univ Chicago, Pritzker Sch Med, Dept Pediat, Chicago, IL 60637 USA
[2] Univ Chicago, Pritzker Sch Med, Dept Med, Chicago, IL 60637 USA
[3] Univ Chicago Hosp & Clin, Dept Med, Endocrinol Sect, Chicago, IL 60637 USA
关键词
aromatase; endocrine disrupters; 17 beta-hydroxysteroid dehydrogenase; neuroendocrinology; receptors; oestrogen; signalling;
D O I
10.1053/beem.2002.0177
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oestrogens induce the development of female reproductive tissues. Endogenous human oestrogens include oestradiol, oestrone and oestriol. Oestrogen signalling in target tissues is dependent on the tissue concentration of oestrogen and the interaction of oestrogen receptors with an array of cell-specific co-regulator proteins. The diverse mechanisms of oestrogen signalling are complex and incompletely understood. In puberty, oestrogen is derived from both gonadal and peripheral sources. Originally, oestrogen was only thought to drive feminization in females; now, oestrogen is known to be important for pubertal development of males as well. Oestrogen is required for normal maturation of the neuroendocrine-gonadal axis and bone in both sexes, and a variety of other tissues are also responsive to oestrogen. Abnormal puberty can be associated with either excessive or inadequate oestrogen production. Girls deficient in oestrogen should receive replacement in physiological doses. Aromatase inhibitors and anti-oestrogens may prove to be useful therapeutic tools in some types of abnormal puberty.
引用
收藏
页码:13 / 30
页数:18
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