Hohmann Christine F
Department of Biology, Morgan State University, Cold Spring Lane and Hillen Road, 1700 E. Cold Spring Lane, Baltimore, MD 21251, USA.
Neurosci Biobehav Rev. 2003 Sep;27(4):351-63. doi: 10.1016/s0149-7634(03)00066-6.
Recently, cholinergic afferents to cerebral cortex have met renewed attention regarding the regulation of plasticity as well as cognitive processing. My laboratory has developed a mouse neonatal basal forebrain lesion paradigm that has contributed considerably to the understanding of cholinergic mechanisms in cortical development. We have shown that transient cholinergic deafferentation, beginning at birth, precipitates alterations in neuronal differentiation and synaptic connectivity that persist into maturity, and contribute to altered cognitive behavior. These data are in general agreement with studies in rats in which the cholinergic basal forebrain is lesioned very early in development but contrast with effects of later developmental lesions. Moreover, in mouse, both morphological and behavioral consequences of the lesion are sex dependent. Studies of receptors and secondary messengers that are instrumental in morphogenesis and plasticity suggest that sex dependent molecular alterations occur within days if not hours following cortical cholinergic deafferentation.
最近,大脑皮质的胆碱能传入神经在可塑性调节以及认知加工方面重新受到关注。我的实验室开发了一种小鼠新生儿基底前脑损伤模型,该模型对理解皮质发育中的胆碱能机制有很大帮助。我们已经表明,从出生开始的短暂胆碱能脱失会引发神经元分化和突触连接的改变,这些改变会持续到成熟,并导致认知行为改变。这些数据总体上与大鼠研究一致,在大鼠研究中,胆碱能基底前脑在发育早期就受到损伤,但与后期发育损伤的影响形成对比。此外,在小鼠中,损伤的形态学和行为学后果都具有性别依赖性。对形态发生和可塑性起重要作用的受体和第二信使的研究表明,皮质胆碱能脱失后,如果不是在数小时内,也会在数天内发生性别依赖性分子改变。