Yamada Kiyofumi, Nabeshima Toshitaka
Laboratory of Neuropsychopharmacology, Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa, Japan.
Drug News Perspect. 2004 Sep;17(7):435-8. doi: 10.1358/dnp.2004.17.7.863702.
Brain-derived neurotrophic factor (BDNF) and its receptor TrkB play important roles in learning and memory. Memory acquisition is associated with an increase in BDNF mRNA and TrkB activation in specific brain areas. Pharmacologic and genetic deprivation of BDNF or TrkB results in an impairment of memory. Activation of the mitogen-associated protein kinase and phosphatidylinositol 3-kinase signaling pathways is involved in BDNF-dependent learning and memory. A frequent single nucleotide polymorphism in the targeting region of the human BDNF gene (val66met) is associated with poorer episodic memory and abnormal hippocampal neuronal function in humans. The interaction of BDNF/TrkB signaling with N-methyl-D-aspartate receptors is important for spatial learning and memory, and an Src-family tyrosine kinase Fyn may play a key role in this interaction by linking TrkB with NR2B.
脑源性神经营养因子(BDNF)及其受体TrkB在学习和记忆中发挥着重要作用。记忆形成与特定脑区中BDNF信使核糖核酸(mRNA)的增加以及TrkB的激活相关。BDNF或TrkB的药理学和基因缺失会导致记忆障碍。丝裂原活化蛋白激酶和磷脂酰肌醇3激酶信号通路的激活参与了BDNF依赖的学习和记忆过程。人类BDNF基因靶向区域的常见单核苷酸多态性(val66met)与人类较差的情景记忆和海马神经元功能异常有关。BDNF/TrkB信号与N-甲基-D-天冬氨酸受体的相互作用对空间学习和记忆很重要,Src家族酪氨酸激酶Fyn可能通过将TrkB与NR2B连接在这种相互作用中起关键作用。