Petkova-Kirova Polina, Anastassova Neda, Minchev Borislav, Uzunova Diamara, Grigorova Valya, Tsvetanova Elina, Georgieva Almira, Alexandrova Albena, Stefanova Miroslava, Yancheva Denitsa, Kalfin Reni, Tancheva Lyubka
Institute of Neurobiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., bl. 23, 1113 Sofia, Bulgaria.
Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Building 9, 1113 Sofia, Bulgaria.
Molecules. 2024 Dec 3;29(23):5711. doi: 10.3390/molecules29235711.
Alzheimer's disease (AD) has long proven to be a complex neurodegenerative disorder, with cholinergic dysfunction, oxidative stress, and neuroinflammation being just a few of its pathological features. The complexity of the disease requires a multitargeted treatment covering its many aspects. In the present investigation, an arylhydrazone derivative of 5-methoxyindole-2-carboxylic acid (5MeO), with in vitro strong antioxidant, neuroprotective and monoamine oxidase B-inhibiting effects, was studied in a scopolamine-induced Alzheimer-type dementia in rats. Using behavioral and biochemical methods, we evaluated the effects of 5MeO on learning and memory, and elucidated the mechanisms of these effects. Our experiments demonstrated that 5MeO had a beneficial effect on different types of memory as assessed by the step-through and the Barnes maze tasks. It efficiently restored the decreased by scopolamine brain-derived neurotrophic factor and acetylcholine levels and normalized the increased by scopolamine acetylcholine esterase activity in hippocampus. Most effective 5MeO was in counteracting the induced by scopolamine oxidative stress by decreasing the increased by scopolamine levels of lipid peroxidation and by increasing the reduced by scopolamine catalase activity. Blood biochemical analyses demonstrated a favorable safety profile of 5MeO, prompting further pharmacological studies suggesting 5MeO as a safe and efficient candidate in a multitargeted treatment of AD.
长期以来,阿尔茨海默病(AD)一直被证明是一种复杂的神经退行性疾病,胆碱能功能障碍、氧化应激和神经炎症只是其病理特征中的一部分。该疾病的复杂性需要涵盖其多个方面的多靶点治疗。在本研究中,对一种5-甲氧基吲哚-2-羧酸(5MeO)的芳腙衍生物进行了研究,该衍生物在体外具有较强的抗氧化、神经保护和单胺氧化酶B抑制作用,实验采用东莨菪碱诱导的大鼠阿尔茨海默型痴呆模型。我们运用行为学和生物化学方法评估了5MeO对学习和记忆的影响,并阐明了这些影响的机制。我们的实验表明,通过穿梭箱试验和巴恩斯迷宫试验评估,5MeO对不同类型的记忆均有有益作用。它能有效恢复被东莨菪碱降低的脑源性神经营养因子和乙酰胆碱水平,并使被东莨菪碱升高的海马乙酰胆碱酯酶活性恢复正常。5MeO最有效的作用是通过降低被东莨菪碱升高的脂质过氧化水平以及增加被东莨菪碱降低的过氧化氢酶活性,来对抗东莨菪碱诱导的氧化应激。血液生化分析表明5MeO具有良好的安全性,这促使进一步的药理学研究将5MeO作为AD多靶点治疗中安全有效的候选药物。