Department of Molecular Biology and Genetics, Erzurum Technical University, Erzurum, Turkey.
Department of Medical Pharmacology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
Biomed Res Int. 2022 Oct 15;2022:5467498. doi: 10.1155/2022/5467498. eCollection 2022.
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by behavioral and psychological symptoms in addition to cognitive impairment and loss of memory. The exact pathogenesis and genetic background of AD are unclear and there remains no effective treatment option. Sarcosine, an n-methyl derivative of glycine, showed a promising therapeutic strategy for some cognitive disorders. To our knowledge, the impacts of sarcosine supplementation against AD have not yet been elucidated. Therefore, we aimed to determine the neuroprotective potential of sarcosine in and AD model. studies have demonstrated that sarcosine increased the percentage of viable cells against aluminum induced neurotoxicity. In AlCl-induced rat model of AD, the level of antioxidant capacity was significantly decreased and expression levels of , , , and genes were elevated compared to the control group. Additionally, histopathological examinations of the hippocampus of AlCl-induced rat brains showed the presence of neurofibrillary tangles (NFTs). However, the administration of sarcosine produced marked improvement and protection of AD-associated pathologies induced by AlCl in experimental rats. Therefore, this investigation may contribute to design novel therapeutic strategies using sarcosine for the management of AD pathologies.
阿尔茨海默病(AD)是一种神经退行性疾病,其特征除了认知障碍和记忆力丧失外,还伴有行为和心理症状。AD 的确切发病机制和遗传背景尚不清楚,目前仍没有有效的治疗方法。肌氨酸,甘氨酸的 N-甲基衍生物,在一些认知障碍的治疗中显示出了有希望的治疗策略。据我们所知,肌氨酸补充对 AD 的影响尚未阐明。因此,我们旨在确定肌氨酸对 AD 模型的神经保护潜力。研究表明,肌氨酸可提高铝诱导神经毒性后存活细胞的百分比。在 AD 的 AlCl3 诱导的大鼠模型中,与对照组相比,抗氧化能力水平显著降低,和 基因的表达水平升高。此外,AlCl3 诱导的大鼠海马的组织病理学检查显示存在神经纤维缠结(NFTs)。然而,肌氨酸的给药对 AlCl 诱导的 AD 相关病理学有明显的改善和保护作用。因此,这项研究可能有助于设计使用肌氨酸治疗 AD 病理的新治疗策略。