Sex-Dependent Actions of Prenatal Stress on the Activity of the Hypothalamo-Hypophyseal-Adrenocortical System in Rats: The Role of Corticosteroid Receptors in the Brain

Prenatal stress is regarded as a risk factor for the development of diseases such as mental, cardiovascular, and metabolic disorders in later life. Dysregulation of the activity of the hypothalamo-hypophyseal-adrenocortical system (HHAS) is one of the mechanisms producing these disorders. Regulation of the HHAS is mediated by two types of receptor – mineralocorticoid (MR) and glucocorticoid receptors (GR) – in the corticolimbic structures of the brain. The link between prenatal stress, sex, and HHAS activity, as well as the role of central MR and GR in this interaction, has received insufficient study. We have investigated the effects of prenatal stress on HHAS activity in adult male and female rats and the expression of GR and MR in the hippocampus and medial prefrontal cortex (mPFC). Prenatal stress was modeled by subjecting pregnant female Wistar rats to 1-h restraint from days 15 to 19 of pregnancy. Basal HHAS activity and stress corticosterone levels in response to 30-min restraint were studied in their adult offspring. GR and MR expression was assessed by western blotting and also, in the hippocampus, by an immunohistochemical method. Prenatally stressed males displayed prolonged stress responses, while females showed increases in basal and stress reactivity, along with increases in the sensitivity of the HHAS to feedback signals. In males, changes in HHAS activity were accompanied by decreases in GR and MR content in the hippocampus and mPFC with an unaltered GR:MR ratio. Prenatally stressed females showed increased expression of GR protein and decreased quantities of MR protein in the hippocampus and an increased GR:MR ratio in both areas of the brain. The hippocampus of male and female animals showed changes in GR and MR content in field CA3 and the dentate gyrus. These data indicate that sex-dependent changes in GR and MR protein expression in the hippocampus and mPFC contribute to modifications of HHAS activity due to prenatal stress. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.