Nakajo Yukako, Miyamoto Susumu, Nakano Yoshikazu, Xue Jing-Hui, Hori Takuya, Yanamoto Hiroji
Laboratory for Cerebrovascular Disorders, Research Institute of National Cardio-Vascular Center, Suita, Osaka 565-8565, Japan.
Brain Res. 2008 Nov 19;1241:103-9. doi: 10.1016/j.brainres.2008.08.080. Epub 2008 Sep 9.
Brain-derived neurotrophic factor (BDNF), a neurotrophin, is known to promote neuronal differentiation stimulating neurite outgrowth in the developing CNS, and is also known to modulate synaptic plasticity, thereby contributing to learning and memory in the mature brain. Here, we investigated the role of increased levels of intracerebral BDNF in learning and memory function. Using genetically engineered transgenic BDNF overexpressing mice (RTG-BDNF), young adult, homozygous (+/+), heterozygous (+/-), or wild-type (-/-) littermates, we analyzed escape latency to a hidden-platform and swimming velocity in the Morris Water Maze test (MWM) with modifications for the mice. The MWM comprised 4 trials per day over 5 consecutive days (sessions) without prior or subsequent training. In a separate set of animals, BDNF protein levels in the cortex, thalamostriatum and the hippocampus were measured quantitatively using ELISA. In the BDNF (+/-) mice, the BDNF levels in the cortex, the thalamostriatum and the hippocampus were significantly high, compared to the wild-type littermates; 238%, 158%, and 171%, respectively (P<0.01, one-way ANOVA and a post-hoc test in each region). The BDNF levels in the BDNF (+/+) mice were not elevated. The BDNF (+/-), but not the (+/+) mice, demonstrated significantly shorter escape latency, shorter total path length in the MWM, and more frequent arrivals at the location where the platform had been placed previously in the probe trial, compared with the wild-type littermates (P<0.05, at each time pint). Because the maximum swimming velocity was not affected in the BDNF-transgenic mice, increased BDNF levels in the brain were found to enhance spatial learning and memory function. Although it has been postulated that excessive BDNF is deteriorating for neuronal survival or neurite outgrowth, further investigations are needed to clarify the mechanism of paradoxical lack of increase in BDNF levels in the (+/+) mouse brain.
脑源性神经营养因子(BDNF)作为一种神经营养素,已知其可促进神经元分化,刺激发育中的中枢神经系统(CNS)中的神经突生长,并且还已知其可调节突触可塑性,从而有助于成熟大脑的学习和记忆。在此,我们研究了脑内BDNF水平升高在学习和记忆功能中的作用。我们使用基因工程构建的BDNF过表达转基因小鼠(RTG-BDNF)、成年幼鼠、纯合子(+/+)、杂合子(+/-)或野生型(-/-)同窝小鼠,在对小鼠进行改良的莫里斯水迷宫试验(MWM)中分析了到达隐藏平台的逃避潜伏期和游泳速度。MWM在连续5天(试验期)内每天进行4次试验,无需事先或事后训练。在另一组动物中,使用酶联免疫吸附测定法(ELISA)定量测量皮质、丘脑纹状体和海马体中的BDNF蛋白水平。与野生型同窝小鼠相比,BDNF(+/-)小鼠的皮质、丘脑纹状体和海马体中的BDNF水平显著升高,分别为238%、158%和171%(P<0.01,各区域进行单因素方差分析和事后检验)。BDNF(+/+)小鼠的BDNF水平未升高。与野生型同窝小鼠相比,BDNF(+/-)小鼠(而非(+/+)小鼠)在MWM中表现出显著缩短的逃避潜伏期、更短的总路径长度,并且在探索试验中更频繁地到达先前放置平台的位置(每次时间点P<0.05)。由于BDNF转基因小鼠的最大游泳速度未受影响,因此发现脑内BDNF水平升高可增强空间学习和记忆功能。尽管据推测过量的BDNF会对神经元存活或神经突生长产生不利影响,但仍需要进一步研究以阐明(+/+)小鼠脑中BDNF水平未升高这一矛盾现象的机制。