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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >Safety assessment of methanolic extract of Terminalia chebula fruit, Terminalia arjuna bark and its bioactive constituent 7-methyl gallic acid: In vitro and in vivo studies
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Safety assessment of methanolic extract of Terminalia chebula fruit, Terminalia arjuna bark and its bioactive constituent 7-methyl gallic acid: In vitro and in vivo studies

机译:常年枯草水果,末端Arjuna Bark及其生物活性成分7-甲基食品的安全评估:体外和体内研究

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摘要

Terminalia chebula and Terminalia arjuna were widely used in traditional medicine for the treatment of memory impairment, inflammatory disorders and as an anti-aging agent. However, reports regarding their safety aspects are lacking. Hence, the present study was carried out to investigate the toxicity of methanolic extracts of Terminalia chebula fruit (TCF), Terminalia arjuna bark (TAB) and its bioactive constituent 7- Methyl gallic acid (7MG) under in vitro and in vivo conditions. In vitro toxicity profile of TCF, TAB and 7MG (250-2000 mu g/ml) were assessed through cytotoxicity, hemolytic activity, mutagenicity and genotoxicity assays. Results of Ames test, comet assay, MTT and hemolytic assays illustrated that TCF, TAB and 7MG exhibited neither cytotoxic and genotoxic effect in PBMC nor hemolytic activity in ABC and no mutagenic effect in TA 98 and TA 100 up to a limited dose of 2000 mu g/ml. Acute and subacute toxicity studies showed no significant change in body weight, behavior, hematology, biochemical parameters, organ weight and histopathology. Over all the results of acute and subacute toxicity studies conclude that oral administration of TCF, TAB and 7MG were observed to be relatively non-toxic and affords practical guidance for selecting safe dose for further clinical trials.
机译:恒定的Chebula和Termancia Arjuna广泛用于传统医学中,用于治疗内存损伤,炎症疾病和抗衰老剂。但是,缺乏关于其安全方面的报告。因此,对本研究进行了探讨了在体外和体内条件下探讨了终端亚洲混苯果(TCF),末端Arjuna Bark(Tab)及其生物活性成分7-甲基食小酸(7mg)的毒性。通过细胞毒性,溶血活性,突变性和遗传毒性测定评估TCF,突片和7mg(250-2000μmg/ ml)的体外毒性分布。 AMES试验的结果,COMET测定,MTT和溶血测定表明,TCF,突片和7mg在ABC中的PBMC和溶血活性既没有表现出细胞毒性和遗传毒性作用,在TA 98和TA 100中没有致致致突变作用,直至2000亩的有限剂量g / ml。急性和亚急性毒性研究表明,体重,行为,血液学,生化参数,器官体重和组织病理学没有显着变化。在急性和亚急性毒性研究的所有结果得出结论中,观察到TCF,突片和7mg的口服给药是相对无毒的,并为进一步的临床试验选择安全剂量提供实际指导。

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