Yu R K, Manuelidis E E
J Neurol Sci. 1978 Jan;35(1):15-23. doi: 10.1016/0022-510x(78)90098-9.
Gangliosides were isolated from guinea pig brains at the end stages of experimental Creutzfeldt-Jakob disease. Quantitative analyses revealed marked decreases of ganglioside levels in pathologically devastated tissues such as cerebral cortex (-21%), basal ganglia and thalamus (-18%), and brain stem (-23%). The cerebellum revealed only minor pathological abnormalities and its ganglioside level remained unchanged. Thin-layer chromatography of the Creutzfeldt-Jakob brain gangliosides showed aberrant ganglioside patterns in all regions studied, including the cerebellum. With some exceptions, a trend in ganglioside pattern changes was detected which consisted of proliferation of GM3, GD3, GD2 and loss of GM1, GD1a, GD1b and GT1b.
在实验性克雅氏病末期,从豚鼠大脑中分离出神经节苷脂。定量分析显示,在病理受损组织如大脑皮层(-21%)、基底神经节和丘脑(-18%)以及脑干(-23%)中,神经节苷脂水平显著降低。小脑仅显示轻微病理异常,其神经节苷脂水平保持不变。克雅氏病大脑神经节苷脂的薄层色谱分析显示,在所有研究区域包括小脑中,神经节苷脂模式均异常。除了一些例外情况,检测到神经节苷脂模式变化的趋势,包括GM3、GD3、GD2增多以及GM1、GD1a、GD1b和GT1b减少。