Altered androgen regulation of differentiated ventral prostate function during aging of the AXC rat

We have examined testosterone regulation of differentiated androgen responsive ventral prostate function in aging AXC rats as a possible means of identifying age-related changes in prostate gene function. Concerning cellular content of functional macromolecules, we identified three categories of age-related change in ventral prostate: (1) diminutions completely reversible by short-term chronic testosterone treatment, as exemplified by androgen receptor content; (2) diminutions partially reversible by testosterone treatment, as exemplified by prolactin receptor content and L-ornithine-decarboxylase (ODC) activity; and (3) diminutions not reversed by exogenous testosterone treatment, as exemplified by S-adenosyl-L-methionine decarboxylase (AMDC) activity. A fourth category of alteration revealed apparent age-related changes in polyamine homeostasis. The anabolic products of ODC and AMDC activities, putrescine, spermidine and spermine, showed an age-related diminished dependence between the activities of ODC and AMDC and ventral prostate polyamine content. The possibility that these changes reflect age-related alterations in ventral prostate gene activity is under investigation.