Hodgkins P S, Prasher V, Farrar G, Armstrong R, Sturman S, Corbett J, Blair J A
MRC Radiobiology Unit, Chilton, Didcot, UK.
Neuroreport. 1993 Oct 25;5(1):21-4. doi: 10.1097/00001756-199310000-00005.
Plasma transferrin binding in Down syndrome and Alzheimer's disease is significantly reduced compared with age matched controls and it was thought this may help elucidate a pathological time sequence for the onset of dementia in Down syndrome. In Down syndrome, there was a reduction in gallium and aluminium transferrin binding both with age and the onset of dementia. Non-transferrin bound gallium species were identified as non-transportable phosphate or silicate. Thus, the route of entry of metals into the brain must be via a transferrin mediated complex only. A clear sequence of pathological events has been demonstrated in Down syndrome which shows the pathway to development of plaques and dementia and this is believed to have an immunological origin.
与年龄匹配的对照组相比,唐氏综合征和阿尔茨海默病患者的血浆转铁蛋白结合显著降低,人们认为这可能有助于阐明唐氏综合征痴呆症发病的病理时间顺序。在唐氏综合征中,随着年龄增长和痴呆症的发作,镓和铝与转铁蛋白的结合减少。未与转铁蛋白结合的镓物种被鉴定为不可运输的磷酸盐或硅酸盐。因此,金属进入大脑的途径必定仅通过转铁蛋白介导的复合物。唐氏综合征中已证明了明确的病理事件序列,该序列显示了斑块和痴呆症的发展途径,并且认为这具有免疫起源。