Adolescent Neurochemical Plasticity of Oxytocin Receptors in the Bed Nucleus of the Stria Terminalis

Adolescence has become an intriguing key period in neurodevelopment when different types of neuroplasticity occur. The bed nucleus of the stria terminalis (BNST) is a part of the limbic system involved in the generation of anxiety, control of social behaviour, and aggression. Because of the increasing frequency of these conditions in adolescence, we set it as a goal to investigate the BNST for neurochemical plasticity during that period. The oxytocin receptor was studied due to its known function in neurodevelopment, anxiety-related behaviours, and social activity. Its expression in preadolescent 20-days-old rats both male and female was compared with adult 60-days-old rats from both sexes too. We found that during adolescence there was a significant down-regulation of these receptors in some subnuclei of BNST. The expression of oxytocin receptors did not differ between sexes. Our results suggest that such a down-regulation in the pubertal period could have effects on the aggressive behaviour and the shifts in the social conduct. The observed neuroplasticity can serve as a fundamental paradigm for further pharmacological research.

Authors

Institutions

Publication Details

Journal
Proceedings of the Bulgarian Academy of Sciences
Published
2025-09-29
DOI
https://doi.org/10.7546/crabs.2025.09.14
Primary Topic
Neuroendocrine regulation and behavior
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Adolescent Neurochemical Plasticity of Oxytocin Receptors in the Bed Nucleus of the Stria Terminalis

Nikolai Lazarov, Pavel Rashev, Albert Gradev, A. Dandov et al.
Proceedings of the Bulgarian Academy of Sciences
Neuroendocrine regulation and behavior
article

Adolescent Neurochemical Plasticity of Oxytocin Receptors in the Bed Nucleus of the Stria Terminalis

Nikolai Lazarov, Pavel Rashev, Albert Gradev, A. Dandov, Vasil Iliev, Lazar Jelev
article en

Abstract

Adolescence has become an intriguing key period in neurodevelopment when different types of neuroplasticity occur. The bed nucleus of the stria terminalis (BNST) is a part of the limbic system involved in the generation of anxiety, control of social behaviour, and aggression. Because of the increasing frequency of these conditions in adolescence, we set it as a goal to investigate the BNST for neurochemical plasticity during that period. The oxytocin receptor was studied due to its known function in neurodevelopment, anxiety-related behaviours, and social activity. Its expression in preadolescent 20-days-old rats both male and female was compared with adult 60-days-old rats from both sexes too. We found that during adolescence there was a significant down-regulation of these receptors in some subnuclei of BNST. The expression of oxytocin receptors did not differ between sexes. Our results suggest that such a down-regulation in the pubertal period could have effects on the aggressive behaviour and the shifts in the social conduct. The observed neuroplasticity can serve as a fundamental paradigm for further pharmacological research.

Proceedings of the Bulgarian Academy of SciencesVol. 78(9)
Bulgarian Academy of Sciences (BG), Medical University of Sofia (BG)
Openalex Percentile: Top 69%
Neuroendocrine regulation and behavior
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Adolescent Neurochemical Plasticity of Oxytocin Receptors in the Bed Nucleus of the Stria Terminalis — Nikolai Lazarov, Pavel Rashev, et al. · Proceedings of the Bulgarian Academy of Sciences (2025) | TGRS Research Map | TGRS