Brain-Derived Neurotrophic Factor (BDNF) in the Frontal Cortex Enhances Social Interest in the BTBR Mouse Model of Autism

• Published in: Biochemistry (Moscow) 2024-08, Vol.89 (8), p.1509-1518
• Main Authors: Kaminskaya, Yana P., Ilchibaeva, Tatiana V., Shcherbakova, Alexandra I., Allayarova, Elina R., Popova, Nina K., Naumenko, Vladimir S., Tsybko, Anton S.
• Format: Article
• Language: English
• Subjects: Adenoviruses; Animal models; Animals; Anxiety; Autism; Autistic Disorder - genetics; Autistic Disorder - metabolism; Behavior, Animal; Biochemistry; Biomedical and Life Sciences; Biomedicine; Bioorganic Chemistry; Brain; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Brain-Derived Neurotrophic Factor - metabolism; Cortex (frontal); Disease Models, Animal; Exploratory behavior; Frontal Lobe - metabolism; Hippocampus; Life Sciences; Male; Mice; Mice, Inbred C57BL; Microbiology; Object recognition; Pathogenesis; Pattern recognition; Social Behavior; Social interactions; Stereotyped behavior
• ISSN: 0006-2979; 1608-3040; 1608-3040
• DOI: 10.1134/S0006297924080091

A large body of evidence implies the involvement of brain-derived neurotrophic factor (BDNF) in the pathogenesis of autism spectrum disorders (ASDs). A deficiency of BDNF in the hippocampus and frontal cortex of BTBR mice (a model of autism) has been noted in a number of studies. Earlier, we showed that induction of BDNF overexpression in the hippocampus of BTBR mice reduced anxiety and severity of stereotyped behavior, but did not affect social interest. Here, we induced BDNF overexpression in the frontal cortex neurons of BTBR mice using an adeno-associated viral vector, which resulted in a significant increase in the social interest in the three-chamber social test. At the same time, the stereotypy, exploratory behavior, anxiety-like behavior, and novel object recognition were not affected. Therefore, we have shown for the first time that the presence of BDNF in the frontal cortex is critical for the expression of social interest in BTBR mice, since compensation for its deficiency in this structure eliminated the autism-like deficiencies in the social behavior characteristic for these animals.