Section of Neurotoxicology and Neuroendocrinology, Department of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161 Rome, Italy.
Behav Brain Res. 2011 Aug 10;221(2):623-9. doi: 10.1016/j.bbr.2011.03.051. Epub 2011 Mar 30.
We studied the long-term effects of a postnatal choline supplementation (from birth till weaning) in the truncated MeCP2-308 mouse model of Rett syndrome. Adult male mutant hemizygous (hz) mice showed a reduction of locomotor activity compared to wild type (wt) littermates. Early choline treatment restored wt-like locomotor activity levels in hz mice. Reduced striatal choline acetyl transferase (ChAT) activity and decreased levels of cortical mRNA NGF were found in hz mice. Choline supplementation increased striatal ChAT activity and also enhanced NGF and BDNF expression in cortical and hippocampal regions. As a whole, postnatal choline supplementation attenuates some of the behavioural and neurobiological abnormalities of the Mecp2-308 phenotype.
我们研究了产后胆碱补充(从出生到断奶)对 Rett 综合征截断 MeCP2-308 小鼠模型的长期影响。成年雄性突变杂合(hz)小鼠的运动活性较野生型(wt)同窝仔鼠降低。早期胆碱治疗可使 hz 小鼠恢复类似 wt 的运动活性水平。hz 小鼠纹状体胆碱乙酰转移酶(ChAT)活性降低,皮质 NGFmRNA 水平降低。胆碱补充增加了纹状体 ChAT 活性,也增强了皮质和海马区的 NGF 和 BDNF 表达。总之,产后胆碱补充可减轻 Mecp2-308 表型的一些行为和神经生物学异常。