| Literature DB >> 35024692 |
Samantha A Blankers1,2, Liisa A M Galea1,2,3.
Abstract
Adult neurogenesis in the hippocampus is modulated by steroid hormones, including androgens, in male rodents. In this review, we summarize research showing that chronic exposure to androgens, such as testosterone and dihydrotestosterone, enhances the survival of new neurons in the dentate gyrus of male, but not female, rodents, via the androgen receptor. However, the neurogenesis promoting the effect of androgens in the dentate gyrus may be limited to younger adulthood as it is not evident in middle-aged male rodents. Although direct exposure to androgens in adult or middle age does not significantly influence neurogenesis in female rodents, the aromatase inhibitor letrozole enhances neurogenesis in the hippocampus of middle-aged female mice. Unlike other androgens, androgenic anabolic steroids reduce neurogenesis in the hippocampus of male rodents. Collectively, the research indicates that the ability of androgens to enhance hippocampal neurogenesis in adult rodents is dependent on dose, androgen type, sex, duration, and age. We discuss these findings and how androgens may be influencing neuroprotection, via neurogenesis in the hippocampus, in the context of health and disease. © Samantha A. Blankers and Liisa A.M. Galea 2021; Published by Mary Ann Liebert, Inc.Entities:
Keywords: aging; cognition; dentate gyrus; dihydrotestosterone; sex differences; testosterone
Year: 2021 PMID: 35024692 PMCID: PMC8744005 DOI: 10.1089/andro.2021.0016
Source DB: PubMed Journal: Androg Clin Res Ther ISSN: 2689-4645