Scott B W, Burnham W M
University of Toronto Epilepsy Research Program, University of Toronto, M5S1A8, Toronto, Canada.
Acta Neuropathol. 2006 Apr;111(4):364-71. doi: 10.1007/s00401-006-0039-y. Epub 2006 Mar 7.
New neurons continue to be generated throughout adulthood in the dentate gyrus of mammals. This process of neurogenesis is believed to play a role in some forms of learning and memory. Hippocampal-dependent learning tasks have been shown to specifically enhance the survival of new granule neurons. The present study examined the effects of kindled seizures in rats on the survival of young neurons born before the kindling began. Kindled seizures within the perforant path input to the dentate gyrus triggered between 1 and 2 weeks following the injection of bromodeoxyuridine (BrdU), were found to increase the number of BrdU and NeuN co-labeled cells in the granule cell layer by 128% 1 month later. The number of co-labeled cells was not correlated with measures of seizure severity. These results demonstrate that kindled seizures enhance the survival of new born neurons in the adult rat dentate gyrus which may reflect the actions of an activity-dependent mechanism normally involved in hippocampal-dependent learning and memory.
在哺乳动物的齿状回中,成年期会持续生成新的神经元。这种神经发生过程被认为在某些形式的学习和记忆中发挥作用。海马体依赖的学习任务已被证明能特异性地提高新颗粒神经元的存活率。本研究考察了大鼠点燃式癫痫发作对点燃开始前出生的年轻神经元存活的影响。发现在注射溴脱氧尿苷(BrdU)后1至2周内,齿状回穿通通路输入处的点燃式癫痫发作,1个月后会使颗粒细胞层中BrdU和NeuN共标记细胞的数量增加128%。共标记细胞的数量与癫痫发作严重程度的指标无关。这些结果表明,点燃式癫痫发作可提高成年大鼠齿状回新生神经元的存活率,这可能反映了一种通常参与海马体依赖的学习和记忆的活动依赖机制的作用。