Department of Pharmacology and Medical Formulation with Course of Normal Physiology, Zaporizhzhia State Medical and Pharmaceutical University, 69035 Zaporizhzhia, Ukraine.
Department of Clinical Laboratory Diagnostics, Zaporizhzhia State Medical and Pharmaceutical University, 69035 Zaporizhzhia, Ukraine.
Int J Mol Sci. 2024 Sep 28;25(19):10475. doi: 10.3390/ijms251910475.
The authors propose a novel approach to a comprehensive evaluation of neuroprotective effects using both in vitro and in vivo methods. This approach allows for the initial screening of numerous newly synthesized chemical compounds and substances from plant and animal sources while saving animal life by reducing the number of animals used in research. In vitro techniques, including mitochondrial suspensions and neuronal cell cultures, enable the assessment of neuroprotective activity, which can be challenging in intact organisms. The preliminary methods help outline the neuroprotection mechanism depending on the neurodestruction agent. The authors have validated a model of acute cerebrovascular accident, which simulates key cerebrovascular phenomena such as reduced cerebral blood flow, energy deficit, glutamate-calcium excitotoxicity, oxidative stress, and early gene expression. A significant advantage of this model is its ability to reproduce the clinical picture of cerebral ischemia: impaired motor activity; signs of neurological deficits (paresis, paralysis, etc.); as well as disturbances in attention, learning, and memory. Crucial to this approach is the selection of biochemical, molecular, and cellular markers to evaluate nerve tissue damage and characterize potential neuroprotective agents. Additionally, a comprehensive set of molecular, biochemical, histological, and immunohistochemical methods is proposed for evaluating neuroprotective effects and underlying mechanisms of potential pharmaceutical compounds.
作者提出了一种新的方法,通过体外和体内方法综合评估神经保护作用。这种方法允许对大量新合成的化学化合物和来自植物和动物来源的物质进行初步筛选,同时通过减少研究中使用的动物数量来节省动物生命。体外技术,包括线粒体悬浮液和神经元细胞培养物,能够评估神经保护活性,而在完整的生物体中评估神经保护活性可能具有挑战性。初步方法有助于根据神经破坏剂来概述神经保护机制。作者已经验证了一种急性脑血管意外模型,该模型模拟了关键的脑血管现象,如脑血流减少、能量不足、谷氨酸-钙兴奋毒性、氧化应激和早期基因表达。该模型的一个显著优势是它能够再现脑缺血的临床图像:运动活动受损;神经功能缺损的迹象(偏瘫、瘫痪等);以及注意力、学习和记忆障碍。这种方法的关键是选择生化、分子和细胞标记物来评估神经组织损伤,并描述潜在的神经保护剂。此外,还提出了一套综合的分子、生化、组织学和免疫组织化学方法,用于评估潜在药物化合物的神经保护作用和潜在机制。