Dias Olivia F M, Valle Nicole M E, Mamani Javier B, Costa Cicero J S, Alves Arielly H, Oliveira Fernando A, Rego Gabriel N A, Galanciak Marta C S, Felix Keithy, Nucci Mariana P, Gamarra Lionel F
Hospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.
LIM44-Hospital das Clínicas da Faculdade Medicina da Universidade de São Paulo, São Paulo 05403-000, SP, Brazil.
Int J Mol Sci. 2025 Apr 12;26(8):3657. doi: 10.3390/ijms26083657.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by the accumulation of β-amyloid (Aβ) and hyperphosphorylated tau, leading to neuroinflammation, oxidative stress, and neuronal death. Early detection of AD remains a challenge, as clinical manifestations only emerge in the advanced stages, limiting therapeutic interventions. Minimally invasive biomarkers are essential for early identification and monitoring of disease progression. This study aims to evaluate the sensitivity of the relationship between serum oligoelement levels as biomarkers and the monitoring of AD progression in the 3xTg-AD model. Transgenic 3xTg-AD mice and C57BL/6 controls were evaluated over 12 months through serum oligoelement quantification using inductively coupled plasma mass spectrometry (ICP-MS), Aβ deposition via immunohistochemistry, and cognitive assessments using memory tests (Morris water maze and novel object recognition test), as well as spontaneous locomotion analysis using the open field test. The results demonstrated that oligoelements (copper, zinc, and selenium) were sensitive in detecting alterations in the AD group, preceding cognitive and motor deficits. Immunohistochemistry was performed for qualitative purposes, confirming the presence of β-amyloid in the CNS of transgenic animals. Up to the third month, labeling was moderate and restricted to neuronal cell bodies; from the fifth month onward, evident extracellular deposits emerged. Behavioral assessment indicated impairments in spatial and episodic memory, as well as altered locomotor patterns in AD mice. These findings reinforce that oligoelement variations may be associated with neurodegenerative processes, including oxidative stress and synaptic dysfunction. Thus, oligoelement analysis emerges as a promising approach for the early diagnosis of AD and the monitoring of disease progression, potentially contributing to the development of new therapeutic strategies.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是β淀粉样蛋白(Aβ)和过度磷酸化的tau蛋白积累,导致神经炎症、氧化应激和神经元死亡。AD的早期检测仍然是一项挑战,因为临床表现仅在疾病晚期才出现,这限制了治疗干预。微创生物标志物对于疾病的早期识别和进展监测至关重要。本研究旨在评估作为生物标志物的血清微量元素水平与3xTg-AD模型中AD进展监测之间关系的敏感性。通过电感耦合等离子体质谱(ICP-MS)对转基因3xTg-AD小鼠和C57BL/6对照小鼠进行了为期12个月的血清微量元素定量评估,通过免疫组织化学评估Aβ沉积,通过记忆测试(莫里斯水迷宫和新物体识别测试)进行认知评估,并通过旷场试验进行自发运动分析。结果表明,微量元素(铜、锌和硒)在检测AD组的变化方面很敏感,早于认知和运动缺陷。进行免疫组织化学是为了定性,证实转基因动物中枢神经系统中存在β淀粉样蛋白。在第三个月之前,标记为中度,仅限于神经元细胞体;从第五个月开始,出现明显的细胞外沉积物。行为评估表明AD小鼠存在空间和情景记忆障碍以及运动模式改变。这些发现强化了微量元素变化可能与神经退行性过程有关,包括氧化应激和突触功能障碍。因此,微量元素分析成为AD早期诊断和疾病进展监测的一种有前景的方法,可能有助于开发新的治疗策略。