Kondaurova Elena M, Belokopytova Irina I, Kulikova Elisabeth A, Khotskin Nikita V, Ilchibaeva Tatiana V, Tsybko Anton S, Popova Nina K, Naumenko Vladimir S
Federal research center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Akad. Lavrentyeva Ave. 10, Novosibirsk 630090, Russia.
Federal research center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Akad. Lavrentyeva Ave. 10, Novosibirsk 630090, Russia.
Behav Brain Res. 2023 Feb 13;438:114168. doi: 10.1016/j.bbr.2022.114168. Epub 2022 Oct 21.
Autism spectrum disorders (ASDs) are some of the most common neurodevelopmental disorders; however, the mechanisms underlying ASDs are still poorly understood. Serotonin (5-HT) and brain-derived neurotrophic factor (BDNF) are known as key players in brain and behavioral plasticity and interact with each other. 5-HT receptor is a principal regulator of the brain 5-HT system, which modulates normal and pathological behavior. Here we investigated effects of adeno-associated-virus-based 5-HT receptor overexpression in the hippocampus of BTBR mice (which are a model of autism) on various types of behavior and on the expression of 5-HT receptor, proBDNF, mature BDNF, and BDNF receptors (TrkB and p75). The 5-HT receptor overexpression in BTBR mice reduced stereotyped behavior in the marble-burying test and extended the time spent in the center in the open field test. Meanwhile, this overexpression failed to affect social behavior in the three-chambered test, immobility time in the tail suspension test, locomotor activity in the open field test, and associative learning within the "operant wall" paradigm. The 5-HT receptor overexpression in the hippocampus raised hippocampal 5-HT receptor mRNA and protein levels. Additionally, the 5-HT receptor overexpression lowered both mRNA and protein levels of TrkB receptor but failed to affect proBDNF, mature BDNF, and p75 receptor expression in the hippocampus of BTBR mice. Thus, obtained results suggest the involvement of the 5-HT and BDNF systems' interaction mediated by 5-HT and TrkB receptors in the mechanisms underlying autistic-like behavior in BTBR mice.
自闭症谱系障碍(ASD)是一些最常见的神经发育障碍;然而,ASD背后的机制仍知之甚少。血清素(5-羟色胺,5-HT)和脑源性神经营养因子(BDNF)是大脑和行为可塑性的关键参与者,并且它们相互作用。5-HT受体是大脑5-HT系统的主要调节因子,该系统调节正常和病理行为。在这里,我们研究了基于腺相关病毒的5-HT受体在BTBR小鼠(一种自闭症模型)海马体中的过表达对各种行为类型以及对5-HT受体、前体BDNF、成熟BDNF和BDNF受体(TrkB和p75)表达的影响。BTBR小鼠中5-HT受体的过表达减少了埋珠试验中的刻板行为,并延长了旷场试验中在中央区域停留的时间。同时,这种过表达未能影响三室试验中的社交行为、悬尾试验中的不动时间、旷场试验中的运动活动以及“操作墙”范式中的联想学习。海马体中5-HT受体的过表达提高了海马体中5-HT受体的mRNA和蛋白质水平。此外,5-HT受体的过表达降低了TrkB受体的mRNA和蛋白质水平,但未能影响BTBR小鼠海马体中前体BDNF、成熟BDNF和p75受体的表达。因此,所得结果表明5-HT和BDNF系统通过5-HT和TrkB受体介导的相互作用参与了BTBR小鼠自闭症样行为的潜在机制。