Shaikh Ammara, Ahmad Fairus, Teoh Seong Lin, Kumar Jaya, Yahaya Mohamad Fairuz
Department of Anatomy, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Department of Physiology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Front Mol Neurosci. 2025 Apr 1;18:1518868. doi: 10.3389/fnmol.2025.1518868. eCollection 2025.
Alzheimer's disease (AD) is the leading cause of dementia, accounting for 60-80% of all cases globally. Hallmark pathologies of AD include the accumulation of amyloid peptide and phosphorylated tau, leading to neuronal circuit dysfunction, defective axonal transport, and neurotransmitter system (NTS) abnormalities. Disruptions in acetylcholine, GABA, dopamine, serotonin, and glutamate levels, as well as the loss of cholinergic, GABAergic, and monoaminergic neurons, contribute to the progression of AD. Additionally, neurotrophic factors like brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) are significantly reduced in AD, impacting neuronal health and synaptic integrity. This review highlights the emerging role of neurotrophic factor alpha 1 (NF-α1), also known as carboxypeptidase E, in AD. NF-α1 shows neuroprotective and neurogenesis-promoting properties, offering potential for therapeutic interventions. The review compares NF-α1 gene therapy with other neurotrophin-based treatments, providing insights into its efficacy in AD management.
阿尔茨海默病(AD)是痴呆症的主要病因,占全球所有病例的60 - 80%。AD的标志性病理特征包括淀粉样肽的积累和tau蛋白磷酸化,导致神经回路功能障碍、轴突运输缺陷和神经递质系统(NTS)异常。乙酰胆碱、γ-氨基丁酸、多巴胺、血清素和谷氨酸水平的紊乱,以及胆碱能、γ-氨基丁酸能和单胺能神经元的丧失,都促进了AD的进展。此外,在AD中,脑源性神经营养因子(BDNF)和神经生长因子(NGF)等神经营养因子显著减少,影响神经元健康和突触完整性。本综述强调了神经营养因子α1(NF-α1),也称为羧肽酶E,在AD中的新作用。NF-α1具有神经保护和促进神经发生的特性,为治疗干预提供了潜力。该综述将NF-α1基因治疗与其他基于神经营养因子的治疗方法进行了比较,为其在AD管理中的疗效提供了见解。