| Literature DB >> 25416742 |
Sarah Atwi1, Dallan McMahon1, Helen Scharfman2, Neil J MacLusky3.
Abstract
Androgens have profound effects on hippocampal structure and function, including induction of spines and spine synapses on the dendrites of CA1 pyramidal neurons, as well as alterations in long-term synaptic plasticity (LTP) and hippocampally dependent cognitive behaviors. How these effects occur remains largely unknown. Emerging evidence, however, suggests that one of the key elements in the response mechanism may be modulation of brain-derived neurotrophic factor (BDNF) in the mossy fiber (MF) system. In male rats, orchidectomy increases synaptic transmission and excitability in the MF pathway. Testosterone reverses these effects, suggesting that testosterone exerts tonic suppression on MF BDNF levels. These findings suggest that changes in hippocampal function resulting from declining androgen levels may reflect the outcome of responses mediated through normally balanced, but opposing, mechanisms: loss of androgen effects on the hippocampal circuitry may be compensated, at least in part, by an increase in BDNF-dependent MF plasticity.Entities:
Keywords: BDNF; CA3; hippocampus; mossy fibers; testosterone
Mesh:
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Year: 2014 PMID: 25416742 PMCID: PMC5002217 DOI: 10.1177/1073858414558065
Source DB: PubMed Journal: Neuroscientist ISSN: 1073-8584 Impact factor: 7.519