Wenk G L, Naidu S, Casanova M F, Kitt C A, Moser H
Department of Psychology, Johns Hopkins University, Baltimore, MD.
Neurology. 1991 Nov;41(11):1753-6. doi: 10.1212/wnl.41.11.1753.
Rett's syndrome (RS) is a neurologic disorder associated with severe mental deficiency and neurologic manifestations of cortical and extrapyramidal origin. The present report is a preliminary postmortem brain study that compares the levels of endogenous biogenic amines and selected neurotransmitter receptors in five cases with RS and six normal controls of similar age. The level of choline acetyltransferase activity was reduced in several cortical and subcortical regions. Endogenous levels of dopamine in the superior frontal and superior temporal gyri, occipital cortex, and putamen were reduced. The changes in specific neurotransmitter markers, particularly those associated with the basal ganglia and cortex, may underlie the progressive deterioration in motor and cognitive function characteristic of this progressive disorder.
雷特综合征(RS)是一种与严重智力缺陷以及皮质和锥体外系起源的神经学表现相关的神经障碍。本报告是一项初步的死后脑部研究,比较了5例雷特综合征患者和6例年龄相仿的正常对照者体内内源性生物胺和选定神经递质受体的水平。胆碱乙酰转移酶活性水平在几个皮质和皮质下区域有所降低。额上回、颞上回、枕叶皮质和壳核中的内源性多巴胺水平降低。特定神经递质标志物的变化,尤其是与基底神经节和皮质相关的变化,可能是这种进行性疾病运动和认知功能逐渐恶化的基础。