新型单酚类合成激活剂Keap1/Nrf2/ARE氧化还原敏感信号系统的体外和体内毒性研究

Q4 Biochemistry, Genetics and Molecular Biology
M. Khrapova, S. E. Khrapov, A. Chechushkov, P. Kozhin, L. Romakh, A. E. Serykh, S. Kholshin, N. Kandalintseva, E. Menshchikova
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引用次数: 0

摘要

现代药理学最有前途的领域之一是开发能够激活氧化还原敏感信号系统的“间接抗氧化剂”,主要是Keap1/Nrf2/ARE系统。其化学诱导剂之一是正在开发的亲水单取代单酚(3′-叔丁基-4′-羟基苯基)丙基硫磺酸钠(TS-13)。研究了TS-13对肿瘤细胞系BT-474的体外抗增殖活性和小鼠急性口服毒性。材料和方法。采用MTT法测定TS-13浓度与人乳腺导管癌细胞BT-474增殖活性的关系,计算其IC50并与MCF-7细胞株进行比较;结果与基于基因表达(在硅GSEA)的细胞功能特性相关。用不同剂量的TS-13蒸馏水灌胃50只雌性C57Bl/6J小鼠,研究其体内急性毒性。比较了实验得到的LD50和利用GUSAR web service在计算机上预测的LD50。结果和讨论。TS-13对BT-474细胞的抑制呈浓度依赖性(指数近似,IC50 = 59.5 μM),其毒性是MCF-7细胞的2.2倍。正如GSEA结果所证明的那样,这可能是由于BT-474和MCF-7系之间的功能差异。体内实验中建立的LD50值为936 mg/kg体重,所得值与计算机预测值(561 mg/kg)相吻合,尽管实际上该化合物的毒性比根据其结构可以预期的要小一些。结论。一项对新型水溶性单酚TC-13急性毒性的研究允许将其分类为轻度毒性(毒性等级4)(根据Hodge - Sterner等级)或中度危险(危害等级3)(根据GOST 12.1.007-76)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toxicity of new monophenolic synthetic activator of Keap1/Nrf2/ARE redox-sensitive signaling system in vitro and in vivo
One of the promising areas of modern pharmacology is the development of «indirect antioxidants» capable of activating redox-sensitive signaling systems, primarily the Keap1/Nrf2/ARE system. Among its chemical inductors is the hydrophilic monosubstituted monophenol (3’-tert-butyl-4’-hydroxyphenyl)sodium propylthiosulfonate (TS-13) in development. The aim of the study was to investigate TS-13 antiproliferative activity against tumor cell line BT-474 in vitro and acute oral toxicity in mice in vivo. Material and methods. The relationship between TS-13 concentration and proliferative activity of human breast ductal carcinoma cell line BT-474 was determined using the MTT test, the IC50 was calculated and compared to the previously obtained for MCF-7 line; results were correlated with the functional properties of cells based on gene expression (in silico GSEA). In vivo acute toxicity was studied in 50 female C57Bl/6J mice, who received a TS-13 solution in distilled water at various doses by intragastric gavage. LD50 obtained experimentally and predicted in silico using the GUSAR web service were compared. Results and discussion. TS-13 inhibited the proliferation of BT-474 cells in a concentration-dependent manner (exponential approximation, IC50 = 59.5 μM) and was 2.2 times more toxic than for MCF-7 cells. This may be due to functional differences between the BT-474 and MCF-7 lines, as evidenced by the GSEA results. The LD50 value established in the in vivo experiment was 936 mg/kg body weight, the obtained value satisfactorily corresponds to the predicted in silico (561 mg/kg), although in reality the compound turned out to be somewhat less toxic than could be expected based on its structure. Conclusions. A study of the acute toxicity of the new water-soluble monophenol TC-13 allows the classification of it as slightly toxic (toxicity rating level 4) according to the Hodge – Sterner scale) or as moderately hazardous (hazard class 3) according to GOST 12.1.007-76.
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
54
审稿时长
12 weeks
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