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攀登安第斯石衣酸:一种用于阿尔茨海默病的新型神经保护剂。

Scaling the Andean Shilajit: A Novel Neuroprotective Agent for Alzheimer's Disease.

作者信息

Andrade Víctor, Wong-Guerra Maylin, Cortés Nicole, Pastor Gabriela, González Andrea, Calfío Camila, Guzmán-Martínez Leonardo, Navarrete Leonardo P, Ramos-Escobar Nicolas, Morales Inelia, Santander Rocío, Andrades-Lagos Juan, Bacho Mitchell, Rojo Leonel E, Maccioni Ricardo Benjamín

机构信息

Laboratory of Neuroscience and Functional Medicine, International Center for Biomedicine, Faculty of Sciences, University of Chile, Santiago 7800003, Chile.

Division of Neurogenetics and Molecular Psychiatry, Department of Psychiatry and Psychotherapy, Medical Faculty, University of Cologne, 50923 Köln, Germany.

出版信息

Pharmaceuticals (Basel). 2023 Jul 4;16(7):960. doi: 10.3390/ph16070960.

Abstract

Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder without a cure, despite the enormous number of investigations and therapeutic approaches. AD is a consequence of microglial responses to "damage signals", such as aggregated tau oligomers, which trigger a neuro-inflammatory reaction, promoting the misfolding of cytoskeleton structure. Since AD is the most prevalent cause of dementia in the elderly (>60 years old), new treatments are essential to improve the well-being of affected subjects. The pharmaceutical industry has not developed new drugs with efficacy for controlling AD. In this context, major attention has been given to nutraceuticals and novel bioactive compounds, such as molecules from the Andean Shilajit (AnSh), obtained from the Andes of Chile. Primary cultures of rat hippocampal neurons and mouse neuroblastoma cells were evaluated to examine the functional and neuroprotective role of different AnSh fractions. Our findings show that AnSh fractions increase the number and length of neuronal processes at a differential dose. All fractions were viable in neurons. The AnSh fractions inhibit tau self-aggregation after 10 days of treatment. Finally, we identified two candidate molecules in M3 fractions assayed by UPLC/MS. Our research points to a novel AnSh-derived fraction that is helpful in AD. Intensive work toward elucidation of the molecular mechanisms is being carried out. AnSh is an alternative for AD treatment or as a coadjuvant for an effective treatment.

摘要

阿尔茨海默病(AD)是一种多因素神经退行性疾病,尽管进行了大量研究并采取了多种治疗方法,但仍无法治愈。AD是小胶质细胞对“损伤信号”(如聚集的tau寡聚体)作出反应的结果,这些信号会引发神经炎症反应,促使细胞骨架结构错误折叠。由于AD是老年人(>60岁)痴呆最常见的病因,因此新的治疗方法对于改善患者的生活质量至关重要。制药行业尚未研发出有效控制AD的新药。在此背景下,营养保健品和新型生物活性化合物受到了广泛关注,例如从智利安第斯山脉获取的安第斯希拉季特(AnSh)中的分子。对大鼠海马神经元和小鼠神经母细胞瘤细胞的原代培养物进行了评估,以研究不同AnSh组分的功能和神经保护作用。我们的研究结果表明,AnSh组分在不同剂量下可增加神经元突起的数量和长度。所有组分在神经元中均具有活性。AnSh组分在处理10天后可抑制tau蛋白的自我聚集。最后,我们通过超高效液相色谱/质谱联用(UPLC/MS)分析在M3组分中鉴定出两种候选分子。我们的研究指出了一种新型的源自AnSh的组分,它对AD有帮助。目前正在深入研究其分子机制。AnSh可作为AD治疗的替代品或有效治疗的辅助药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4756/10383824/52d8be486ece/pharmaceuticals-16-00960-g001.jpg

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