Hou Qiuling, Gao Xiang, Zhang Xuehan, Kong Lingwei, Wang Xinming, Bian Wei, Tu Yanyang, Jin Meilei, Zhao Guoping, Li Baoming, Jing Naihe, Yu Lei
Laboratory of Higher Brain Functions, Institute of Neurobiology, Fudan University, Shanghai, China.
Eur J Neurosci. 2004 Sep;20(6):1593-603. doi: 10.1111/j.1460-9568.2004.03600.x.
As a synaptosomal protein, SNAP-25 plays a role in a number of neuronal functions including axonal growth, dendrite formation, fusion of synaptic vesicles with membrane and the expression of long-term potentiation (LTP) in the hippocampus. Using a learning/memory behavior screening, we identified SNAP-25 as one of the differentially expressed genes in the hippocampus upon behavioral training. The inhibition of SNAP-25 with intracerebroventricular antisense oligonucleotide caused a deficit in long- but not short-term memory for step-down inhibitory avoidance. Intra-CA1 infusion of the SNAP-25 antisense oligonucleotide impaired long-term contextual fear memory and spatial memory and interfered with the LTP of synaptic transmission in the CA1 region. The inhibitory effect on LTP was not mediated by a pre-synaptic mechanism because paired pulse facilitation of synaptic transmission was not affected after administration of the antisense oligonucleotide. Together, the results suggest that SNAP-25 in the CA1 region is involved in memory consolidation.
作为一种突触体蛋白,SNAP-25在许多神经元功能中发挥作用,包括轴突生长、树突形成、突触小泡与膜的融合以及海马体中长时程增强(LTP)的表达。通过学习/记忆行为筛选,我们确定SNAP-25是行为训练后海马体中差异表达的基因之一。脑室内注射反义寡核苷酸抑制SNAP-25会导致被动回避抑制试验中的长时记忆而非短时记忆出现缺陷。向CA1区注射SNAP-25反义寡核苷酸会损害长时情境恐惧记忆和空间记忆,并干扰CA1区突触传递的LTP。对LTP的抑制作用不是由突触前机制介导的,因为注射反义寡核苷酸后突触传递的双脉冲易化不受影响。总之,结果表明CA1区的SNAP-25参与记忆巩固。