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寻找咀嚼与认知脑系统之间未知的神经联系,以阐明其损伤在阿尔茨海默病发病机制中的作用。

Search for unknown neural link between the masticatory and cognitive brain systems to clarify the involvement of its impairment in the pathogenesis of Alzheimer's disease.

作者信息

Kang Youngnam, Toyoda Hiroki, Saito Mitsuru

机构信息

Department of Behavioral Physiology, Osaka University Graduate School of Human Sciences, Osaka, Japan.

Department of Oral Physiology, Osaka University Graduate School of Dentistry, Osaka, Japan.

出版信息

Front Cell Neurosci. 2024 Jun 27;18:1425645. doi: 10.3389/fncel.2024.1425645. eCollection 2024.

Abstract

Brain degenerations in sporadic Alzheimer's disease (AD) are observed earliest in the locus coeruleus (LC), a population of noradrenergic neurons, in which hyperphosphorylated tau protein expression and β-amyloid (Aβ) accumulation begin. Along with this, similar changes occur in the basal forebrain cholinergic neurons, such as the nucleus basalis of Meynert. Neuronal degeneration of the two neuronal nuclei leads to a decrease in neurotrophic factors such as brain-derived neurotrophic factor (BDNF) in the hippocampus and cerebral cortex, which results in the accumulation of Aβ and hyperphosphorylated tau protein and ultimately causes neuronal cell death in those cortices. On the other hand, a large number of epidemiological studies have shown that tooth loss or masticatory dysfunction is a risk factor for dementia including AD, and numerous studies using experimental animals have also shown that masticatory dysfunction causes brain degeneration in the basal forebrain, hippocampus, and cerebral cortex similar to those observed in human AD, and that learning and memory functions are impaired accordingly. However, it remains unclear how masticatory dysfunction can induce such brain degeneration similar to AD, and the neural mechanism linking the trigeminal nervous system responsible for mastication and the cognitive and memory brain system remains unknown. In this review paper, we provide clues to the search for such "missing link" by discussing the embryological, anatomical, and physiological relationship between LC and its laterally adjoining mesencephalic trigeminal nucleus which plays a central role in the masticatory functions.

摘要

散发性阿尔茨海默病(AD)中的脑退化最早在蓝斑(LC)中被观察到,蓝斑是一群去甲肾上腺素能神经元,其中开始出现tau蛋白过度磷酸化表达和β-淀粉样蛋白(Aβ)积累。与此同时,基底前脑胆碱能神经元,如Meynert基底核,也会发生类似变化。这两个神经核的神经元退化导致海马体和大脑皮层中脑源性神经营养因子(BDNF)等神经营养因子减少,进而导致Aβ和tau蛋白过度磷酸化积累,最终导致这些皮层中的神经元细胞死亡。另一方面,大量流行病学研究表明,牙齿缺失或咀嚼功能障碍是包括AD在内的痴呆症的危险因素,许多使用实验动物的研究也表明,咀嚼功能障碍会导致基底前脑、海马体和大脑皮层发生与人类AD中观察到的类似的脑退化,相应地学习和记忆功能也会受损。然而,目前尚不清楚咀嚼功能障碍如何诱发这种类似于AD的脑退化,连接负责咀嚼的三叉神经系统与大脑认知和记忆系统的神经机制仍然未知。在这篇综述文章中,我们通过讨论LC与其在咀嚼功能中起核心作用的外侧相邻的中脑三叉神经核之间的胚胎学、解剖学和生理学关系,为寻找这种“缺失环节”提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6975/11236757/c90bc0ec5f63/fncel-18-1425645-g001.jpg

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