Of mice and men: the evolving phenotype of aromatase deficiency

被引:146
作者
Jones, MEE
Boon, WC
Proietto, J
Simpson, ER
机构
[1] Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
[2] Univ Melbourne, Repatriat Hosp, Dept Med, Heidelberg, Vic 3081, Australia
关键词
D O I
10.1016/j.tem.2006.01.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We are rapidly becoming aware of the importance of estrogen in maintaining virtually all facets of male health. In order for estrogens to be synthesized endogenously, the enzyme responsible for their synthesis from androgens, aromatase, must be functional. The seven known men in whom aromatase is nonfunctional all have a mutation in either exon V or IX of the CYP19 gene, which encodes aromatase. Collectively, these men are reported to have undetectable estrogen; normal to high levels of testosterone and gonadotropins; tall stature with delayed skeletal maturation and epiphyseal closure; osteoporosis; impaired lipid and insulin metabolism; and impaired reproductive function. The aromatase knockout mouse presents with a phenotype that is similar in many aspects and provides a valuable tool with which to examine and manipulate the actions of estrogen. By studying the naturally occurring aromatase-deficient humans, together with studies of the aromatase-knockout mouse, we are expanding our understanding of the essential role of estrogen in male physiology.
引用
收藏
页码:53 / 62
页数:10
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