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β-淀粉样肽作为直接胆碱能神经调节剂:一个缺失的环节?

Beta-amyloid peptides as direct cholinergic neuromodulators: a missing link?

作者信息

Auld D S, Kar S, Quirion R

机构信息

Douglas Hospital Research Center and the Dept of Neurology, McGill University, Montréal, Québec, Canada.

出版信息

Trends Neurosci. 1998 Jan;21(1):43-9. doi: 10.1016/s0166-2236(97)01144-2.

Abstract

Beta-Amyloid peptide (Abeta) is found in diffuse and focal deposits throughout the brain from Alzheimer's disease (AD) patients. Another feature of AD is the widespread degeneration and dysfunction of the basal-forebrain cholinergic system. Until now, it has been unclear how these features of AD might be related. Recent reports, however, suggest that Abeta can potently inhibit various cholinergic neurotransmitter functions independently of apparent neurotoxicity. This capacity of Abeta might contribute to the vulnerability of selected cholinergic neuronal populations in AD. Moreover, the high potency (picomolar to nanomolar concentrations) of these effects and the secretion of Abeta by brain cells indicate that Abeta-induced cholinergic hypoactivity might have physiological in addition to pathological significance.

摘要

β-淀粉样肽(Aβ)存在于阿尔茨海默病(AD)患者大脑中弥漫性和局灶性沉积物中。AD的另一个特征是基底前脑胆碱能系统广泛退化和功能障碍。到目前为止,尚不清楚AD的这些特征之间可能存在何种关联。然而,最近的报告表明,Aβ可以在不产生明显神经毒性的情况下有效抑制各种胆碱能神经递质功能。Aβ的这种能力可能导致AD中特定胆碱能神经元群体的易损性。此外,这些效应的高效力(皮摩尔至纳摩尔浓度)以及脑细胞分泌Aβ表明,Aβ诱导的胆碱能活动减退除了具有病理意义外,可能还具有生理意义。

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