Abstract j. Crews, D., J. Godwin, V. Hartman, M. Grammer, E. Prediger, R. Shepperd. (1996). Intrasexual variation in behavioral sensitivity to progesterone in male whiptail lizards and correlations with brain steroid hormone receptor mRNA expression. J. Neuroscience 16(22): 7347-7352.
A primary tenet of behavioral neuroendocrinology is that gonadal
steroid hormones act on limbic nuclei to activate mating behavior in vertebrates.
Traditionally, research has focused on the regulation of male-typical sexual
behavior by testicular androgens and female-typical sexual behavior by
ovarian estrogen and progesterone. Indeed, progesterone generally is regarded
as an antiandrogen, acting centrally to inhibit sexual behavior in males.
However, experiments with lizards, and more recently with rats, have challenged
this paradigm. For example, exogenous progesterone induces mating behavior
in some, but not all, castrated male whiptail lizards. The present study
determined that implantation of progesterone into the anterior hypothalamus
preoptic area of castrated, progesterone-sensitive males completely restored
sexual behavior but failed to elicit sexual activity in castrated, progesterone-insensitive
males. Further, androgen receptor -and progesterone receptor-mRNA expression
in specific brain regions was significantly different in progesterone-sensitive
versus progesterone-insensitive animals. Progesterone-sensitive males showed
significantly higher relative abundance of androgen receptor-mRNA in the
preoptic area, amygdala, and lateral septum, as compared with progesterone-insensitive
animals receiving the same treatment. In contrast, progesterone receptor-mRNA
abundance was lower in preoptic area of progesterone-sensitive males than
in progesterone-insensitive males. No differences were found in the baseline
abundance of androgen receptor-or progesterone receptor-mRNA in these nuclei
between control groups of progesterone-sensitive and progesterone-insensitive
males who were castrated but not implanted. This suggests that progesterone
differentially regulates its own receptor as well as androgen receptor
in areas of the brain involved in the control of sexual behavior of males
and that the nature of this regulation shows individual variability.