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阿尔茨海默病病理学的小鼠非转基因模型:关注风险因素。

Murine Non-Transgenic Models of Alzheimer's Disease Pathology: Focus on Risk Factors.

作者信息

Hernández-Rodríguez Maricarmen, Vega López Juan Manuel, Martínez-Rosas Martín, Nicolás-Vázquez María Inés, Mera Jiménez Elvia

机构信息

Laboratorio de Cultivo Celular, Neurofarmacología y Conducta, Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón s/n, Mexico City 11340, Mexico.

Departamento de Química Inórgánica, Escuela Nacional de Ciencias Biológicas, Prolongación de Carpio y Plan de Ayala s/n, Mexico City 11340, Mexico.

出版信息

Brain Sci. 2025 Mar 19;15(3):322. doi: 10.3390/brainsci15030322.

Abstract

Alzheimer's disease (AD) represents a significant challenge among neurodegenerative disorders, as effective treatments and therapies remain largely undeveloped. Despite extensive research efforts employing various methodologies and diverse genetic models focused on amyloid-β (Aβ) pathology, the research for effective therapeutic strategies remains inconclusive. The key pathological features of AD include Aβ senile plaques, neurofibrillary tangles (NFTs), and the activation of neuroinflammatory pathways. Presently, investigations into AD and assessing potential treatments predominantly utilize Aβ transgenic models. Conversely, non-transgenic models may provide valuable insights into the multifaceted pathological states associated with AD. Thus, these models may serve as practical complementary tools for evaluating therapeutic and intervention strategies, since the primary AD risk factors are most frequently modeled. This review aims to critically assess the existing literature on AD non-transgenic models induced by streptozotocin, scopolamine, aging, mechanical stress, metals, and dietary patterns to enhance their application in AD research.

摘要

阿尔茨海默病(AD)是神经退行性疾病中的一项重大挑战,因为有效的治疗方法在很大程度上仍未得到开发。尽管运用了各种方法并采用了多种聚焦于淀粉样β(Aβ)病理的遗传模型进行了广泛研究,但有效治疗策略的研究仍无定论。AD的关键病理特征包括Aβ老年斑、神经原纤维缠结(NFTs)以及神经炎症途径的激活。目前,对AD的研究和潜在治疗方法的评估主要利用Aβ转基因模型。相反,非转基因模型可能为与AD相关的多方面病理状态提供有价值的见解。因此,由于AD的主要危险因素最常被建模,这些模型可作为评估治疗和干预策略的实用补充工具。本综述旨在批判性地评估现有关于由链脲佐菌素、东莨菪碱、衰老、机械应激、金属和饮食模式诱导的AD非转基因模型的文献,以加强其在AD研究中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e916/11940003/129b74a1b5de/brainsci-15-00322-g001.jpg

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