Kaisho Y, Miyamoto M, Shiho O, Onoue H, Kitamura Y, Nomura S
Discovery Res. Labs., Takeda Chem. Ind. Ltd., Osaka, Japan.
Brain Res. 1994 May 30;647(1):139-44. doi: 10.1016/0006-8993(94)91408-7.
We compared the expression patterns of neurotrophin genes in the brain of senescence-accelerated mouse (SAMP8) which shows age-related impairment of learning behavior, with SAMR1 control which shows normal aging. By Northern blot analysis, NT-3 mRNA levels in the cortex were higher in SAMP8 than in SAMR1 mice during development, whereas in the midbrain, hippocampus and forebrain, NT-3 expression levels in SAMP8 were lower than those in SAMR1. At early stages, although NGF mRNA levels in SAMP8 were lower than those in SAMR1, BDNF mRNA levels were almost equivalent in both strains. By in situ hybridization analysis, NT-3 mRNA signals in the CA1 and CA2 regions in SAMP8 were shown to be reduced at early stages. However, BDNF mRNA signals were almost equivalent in both SAMR1 and SAMP8.
我们比较了表现出与年龄相关学习行为受损的衰老加速小鼠(SAMP8)大脑中神经营养因子基因的表达模式,以及表现出正常衰老的SAMR1对照小鼠。通过Northern印迹分析,在发育过程中,SAMP8小鼠皮质中的NT-3 mRNA水平高于SAMR1小鼠,而在中脑、海马体和前脑,SAMP8中的NT-3表达水平低于SAMR1。在早期阶段,虽然SAMP8中的NGF mRNA水平低于SAMR1,但两种品系中的BDNF mRNA水平几乎相当。通过原位杂交分析,显示SAMP8中CA1和CA2区域的NT-3 mRNA信号在早期阶段减少。然而,SAMR1和SAMP8中的BDNF mRNA信号几乎相当。