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阿尔茨海默病和帕金森病中Meynert核的病理变化。

Pathological changes in the nucleus of Meynert in Alzheimer's and Parkinson's diseases.

作者信息

Candy J M, Perry R H, Perry E K, Irving D, Blessed G, Fairbairn A F, Tomlinson B E

出版信息

J Neurol Sci. 1983 May;59(2):277-89. doi: 10.1016/0022-510x(83)90045-x.

Abstract

Combined neuropathological and neurochemical assessment of the nucleus of Meynert in senile dementia of Alzheimer type (SDAT) have demonstrated that the cholinergic biochemical activity, choline acetyltransferase, is more extensively reduced in the nucleus (over 90%) than the loss of putative cholinergic perikarya (35%). Acetylcholinesterase histochemical activity was however substantially retained in individual neurones in the nucleus although virtually absent from the neocortex in SDAT. These abnormalities are consistent with a primary degeneration of cholinergic axons projecting to the cortex and secondary loss of perikarya from the subcortical nucleus. In contrast, preliminary observations on cases of Parkinson's disease suggest that the neuronal loss from the nucleus of Meynert may be greater in this disease than in SDAT, and previous studies have not consistently demonstrated a reduction in cortical choline acetyltransferase activities in Parkinson's disease. These observations, together with major differences in the neuropathology of the nucleus in SDAT and Parkinson's disease (neurofibrillary tangle and Lewy body formation, respectively) suggest that the involvement of the cholinergic system may differ in the two disease processes.

摘要

对阿尔茨海默型老年痴呆症(SDAT)患者的迈内特核进行神经病理学和神经化学联合评估发现,胆碱能生化活性即胆碱乙酰转移酶在该核中的降低程度(超过90%)比假定的胆碱能神经元胞体丢失(35%)更为广泛。然而,乙酰胆碱酯酶组织化学活性在该核的单个神经元中基本保留,而在SDAT患者的新皮质中则几乎不存在。这些异常情况与投射到皮质的胆碱能轴突原发性变性以及皮质下核中神经元胞体继发性丢失是一致的。相比之下,对帕金森病病例的初步观察表明,迈内特核的神经元丢失在这种疾病中可能比在SDAT中更严重,并且先前的研究并未一致证明帕金森病患者皮质胆碱乙酰转移酶活性降低。这些观察结果,连同SDAT和帕金森病中该核神经病理学的主要差异(分别为神经原纤维缠结和路易小体形成)表明,胆碱能系统在这两种疾病过程中的受累情况可能不同。

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