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前脑神经元中过度表达脑源性神经营养因子(BDNF)的小鼠会随着年龄增长出现行为表型改变。

Mice over-expressing BDNF in forebrain neurons develop an altered behavioral phenotype with age.

作者信息

Weidner Kate L, Buenaventura Diego F, Chadman Kathryn K

机构信息

City University of New York, College of Staten Island, Staten Island, NY 10314, USA; New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.

City University of New York, College of Staten Island, Staten Island, NY 10314, USA; New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.

出版信息

Behav Brain Res. 2014 Jul 15;268:222-8. doi: 10.1016/j.bbr.2014.04.025. Epub 2014 Apr 22.

DOI:10.1016/j.bbr.2014.04.025
PMID:24768643
Abstract

Evidence from clinical studies suggests that abnormal activity of brain derived neurotrophic factor (BDNF) contributes to the pathogenesis of autism spectrum disorders (ASDs). A genetically modified line of mice over-expressing a BDNF transgene in forebrain neurons was used to investigate if this mutation leads to changes in behavior consistent with ASD. The mice used in these experiments were behaviorally tested past 5 months of age when spontaneous seizures were evident. These seizures were not observed in age-matched wildtype (WT) mice or younger mice from this transgenic line. The BDNF mice in these experiments weighed less than their WT littermates. The BDNF transgenic (BDNF-tg) mice demonstrated similar levels of sociability in the social approach test. Conversely, the BDNF-tg mice demonstrated less obsessive compulsive-like behavior in the marble burying test, less anxiety-like behavior in the elevated plus maze test, and less depressive-like behavior in the forced swim test. Changes in behavior were found in these older mice that have not been observed in younger mice from this transgenic line, which may be due to the development of seizures as the mice age. These mice do not have an ASD phenotype but may be useful to study adult onset epilepsy.

摘要

临床研究证据表明,脑源性神经营养因子(BDNF)的异常活性促成了自闭症谱系障碍(ASD)的发病机制。利用一种在前脑神经元中过表达BDNF转基因的基因工程小鼠品系,来研究这种突变是否会导致与ASD一致的行为变化。这些实验中使用的小鼠在5个月龄后进行行为测试,此时自发性癫痫明显。在年龄匹配的野生型(WT)小鼠或该转基因品系的幼龄小鼠中未观察到这些癫痫发作。这些实验中的BDNF小鼠比其WT同窝小鼠体重轻。BDNF转基因(BDNF-tg)小鼠在社交接近测试中表现出相似程度的社交能力。相反,BDNF-tg小鼠在大理石掩埋测试中表现出较少的强迫性类似行为,在高架十字迷宫测试中表现出较少的焦虑样行为,在强迫游泳测试中表现出较少的抑郁样行为。在这些老龄小鼠中发现了行为变化,而在该转基因品系的幼龄小鼠中未观察到这种变化,这可能是由于小鼠随着年龄增长癫痫发作的发展。这些小鼠没有ASD表型,但可能有助于研究成年期癫痫。

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