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Acute and subacute toxicological evaluation of scutellarin in rodents.

机译:黄cut素在啮齿动物中的急性和亚急性毒理学评价。

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Acute and subacute investigations were carried out to evaluate the safety of scutellarin, an active flavone glycoside that has been used to treating cardiocerebral vascular diseases and cerebral infarction in rodents. For the acute study, scutellarin was administered to mice by gavage at different dose levels. Scutellarin caused dose-dependent general behavior adverse effects, but the LD values could not be detected, and the maximum tolerated dose was more than 10 g/kg. In the subacute study, scutellarin was administered orally at doses of 100 and 500 mg/kg daily for 30 days to rats. Body weight, heart rate, blood pressure, biochemical, hematological and urine parameters were determined at the end of the experimental day. Daily oral administration for up to 30 days did not result in death or significant changes in hematology, blood chemistries or urinalysis. However, a 30 day regimen of scutellarin at doses of 100 or 500 mg/kg led to non-dose related decreases in BUN and triglyceride levels. Scutellarin was found to be minimally toxic or non-toxic in rodents. In view of the doses of the components used, the results from acute and subacute toxicity studies suggest that this component has a sufficient margin of safety for therapeutic use.
机译:进行了急性和亚急性研究以评估黄苷的活性,黄av苷是一种活性黄酮苷,已被用于治疗啮齿动物的心脑血管疾病和脑梗塞。对于急性研究,以不同剂量水平通过管饲法向小鼠施用黄rin苷。黄cut苷可引起剂量依赖性的一般行为不良反应,但无法检测到LD值,最大耐受剂量超过10 g / kg。在亚急性研究中,黄cut素每天以100和500 mg / kg的剂量口服给予大鼠30天。在实验结束时确定体重,心率,血压,生化,血液学和尿液参数。每天口服最多30天不会导致死亡或血液学,血液化学或尿液分析的显着变化。然而,以100或500 mg / kg的剂量服用30天的黄cut苷可导致BUN和甘油三酯水平与剂量无关。发现黄cut苷对啮齿动物的毒性最小或无毒。鉴于所用成分的剂量,急性和亚急性毒性研究的结果表明,该成分具有足够的安全性可用于治疗。

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