IN VITRO EXPERIMENTAL STUDY OF TISSUE AND CELLULAR TOXICITY OF DRUGS

Dagar E.A., Mazov Y.A., B. E.V., S. E.V., Eliseikina E.V., Revina N.V., T. S.P., B. D.S.
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Abstract

Abstract. We studied the neurotoxic/neurotropic effects of a new derivative of dimethylacetamide and benzoic acid LHT-5-01 in a mixed neuroglial culture to determine both the effect of various concentrations of the compound on cell survival and their interaction with the glutamate noncainate receptor. To do this, a mixed neuroglial culture of the hippocampus of linear newborn (P 1-3) Sprague Dawley rats was resuspended in a neurobasal medium containing 0.5 mmol glutamine, 2% Supplement B27 and 15 μg/ml gentamicin. The cytoplasmic concentration of calcium in the ionized form [Ca2+]i was determined using a Fura-2 fluorescent probe (USA). The viability of culture cells—neurons and glial cells—was determined by the immunocytochemical method. Experimental studies were performed on cultures aged from 7 to 9 days, to which the test compound of dimethylacetamide LHT-5-01 was added at various concentrations in the laboratory of intracellular signaling of the Institute of Cell Biophysics of the Russian Academy of Sciences - a separate division of the Federal State Budgetary Scientific Institution Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences" (Pushchino) in strict accordance with the literary descriptions. Incubation of the culture with 10 μM of the LHT-5-01 compound completely suppresses the first phase of receptor activity, but does not prevent the formation of the second phase of NMDA receptor excitation. The established activity can be considered in the aspect of the prevention of glutamate-mediated excitotoxicity of the test compound.
药物组织和细胞毒性的体外实验研究
摘要我们研究了一种新的二甲基乙酰胺和苯甲酸衍生物LHT-5-01在混合神经胶质培养中的神经毒性/嗜神经效应,以确定不同浓度的化合物对细胞存活的影响及其与谷氨酸非盐受体的相互作用。为此,将线性新生儿(P 1-3) Sprague Dawley大鼠海马混合神经胶质培养物重悬在含有0.5 mmol谷氨酰胺、2%补充B27和15 μg/ml庆大霉素的神经基础培养基中。使用Fura-2荧光探针(美国)测定离子形式[Ca2+]i的细胞质钙浓度。免疫细胞化学法测定培养细胞神经元和神经胶质细胞的活力。实验研究在7 ~ 9天的培养物上进行,其中二甲乙酰胺LHT-5-01的测试化合物在俄罗斯科学院细胞生物物理研究所的细胞内信号实验室中以各种浓度添加,该实验室是联邦国家预算科学机构联邦研究中心“俄罗斯科学院普什奇诺生物研究科学中心”(普什奇诺)的一个独立部门,严格按照文献描述。10 μM的LHT-5-01化合物完全抑制第一期受体活性,但不阻止第二期NMDA受体激发的形成。所建立的活性可以考虑在预防试验化合物的谷氨酸介导的兴奋性毒性方面。
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