Sex and species differences in tyrosine hydroxylase‐synthesizing cells of the rodent olfactory extended amygdala

Abstract

The bed nucleus of the stria terminalis (BST) and the medial amygdala (MeA) are anatomically connected sites necessary for chemosensory regulation of social behaviors in rodents. Prairie voles (Microtus ochrogaster) are a valuable model for studying the neural regulation of social behaviors because, unlike many other rodents, they are gregarious, pair bond after copulating, and are biparental. We herein describe sex and species differences in immunoreactivity for tyrosine hydroxylase (TH), the rate-limiting enzyme for catecholamine synthesis, in the BST and MeA. Virgin male prairie voles had a large number of TH-immunoreactive cells in areas analogous to the rat principal nucleus of the BST (pBST) and the posterodorsal medial amygdala (MeAPd). Virgin female prairie voles had far fewer TH-immunoreactive cells in these sites ( approximately 17% of the number of cells as males in the pBST, approximately 35% of the number of cells in the MeAPd). A few TH-immunoreactive cells were found in the BST of male and female hamsters and meadow voles, but not in rats. The MeApd also contained a few TH-immunoreactive cells in male and female hamsters and male meadow voles, but not rats. Castration greatly reduced the number of TH-immunoreactive cells in the male prairie vole pBST and MeAPd, an effect that could be reversed with testosterone. Furthermore, treating ovariectomized females with testosterone substantially increased TH-immunoreactive cells in both sites. Therefore, a species-specific sex difference in TH expression is found in a chemosensory pathway in prairie voles. Expression of TH in these sites is influenced by circulating gonadal hormones in adults, which may be related to changes in their display of social behaviors across the reproductive cycle.