Abstract
The transient actions of gonadal steroids on the adult brain facilitate social behaviors, including reproduction. In male rodents, testosterone acts in the posterior medial amygdala (MeP) and medial preoptic area (MPOA) to promote mating. Adult neurogenesis occurs in both regions. The current study determined if testosterone and/or sexual behavior promote cell proliferation and survival in MeP and MPOA. Two experiments were conducted using the thymidine analog BrdU. First, gonad-intact and castrated male hamsters (n=6/group) were compared 24 h or 7 weeks after BrdU. In MeP, testosterone-stimulated cell proliferation 24 h after BrdU (intact: 22.8+/-3.9 cells/mm(2), castrate: 13.2+/-1.4 cells/mm(2)). Testosterone did not promote cell proliferation in MPOA. Seven weeks after BrdU, cell survival was sparse in both regions (MeP: 2.5+/-0.6 and MPOA: 1.7+/-0.2 cells/mm(2)), and was not enhanced by testosterone. In Experiment 2, gonad-intact sexually-experienced animals were mated weekly to determine if regular neural activation enhances cell survival 7 weeks after BrdU in MeP and MPOA. Weekly mating failed to increase cell survival in MeP (8.1+/-1.6 vs. 9.9+/-3.2 cells/mm(2)) or MPOA (3.9+/-0.7 vs. 3.4+/-0.3 cells/mm(2)). Furthermore, mating at the time of BrdU injection did not stimulate cell proliferation in MeP (8.9+/-1.7 vs. 8.1+/-1.6 cells/mm(2)) or MPOA (3.6+/-0.5 vs. 3.9+/-0.7 cells/mm(2)). Taken together, our results demonstrate a limited capacity for neurogenesis in the mating circuitry. Specifically, cell proliferation in MeP and MPOA are differentially influenced by testosterone, and the birth and survival of new cells in either region are not enhanced by reproductive activity.