Journal
HORMONES AND BEHAVIOR
Volume 48, Issue 5, Pages 512-521Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yhbeh.2005.07.011
Keywords
masculinization; defeminization; prostaglandin-E-2; sexual behavior; maternal behavior; sexually dimorphic nucleus
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The preoptic area of the mammalian forebrain is a critical substrate for the development and maintenance of many sexually dimorphic behaviors relevant to reproduction. Normal development of the male rodent brain requires completion of two processes: (1) masculinization-induction of the male phenotype, and (2) deferninization-removal of the female phenotype. Both processes, although distinct, are largely directed by the same steroid, estradiol. Whether estradiol achieves both ends via the same or separate mechanisms has been unknown. Here, we report that prostaglandin-E-2 (PGE(2)) acting downstream of estradiol, is necessary and sufficient to masculinize sexual behavior but does not affect deferninization of sexual behavior or maternal behavior. Moreover, the volume of the sexually dimorphic nucleus of the preoptic area predicts deferninization of sexual behavior, but not masculinization of sexual behavior. Another sexually dimorphic cellular endpoint regulated by estradiol, spinophilin protein expression in the mediobasal hypothalamus, was not affected by PGE(2). Thus, PGE(2) is a key divergence point in the downstream actions of estradiol to simultaneously masculinize and deferninize sexual behavior. (c) 2005 Elsevier Inc. All rights reserved.
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