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首页> 外文期刊>Transactions of the Royal Society of Tropical Medicine and Hygiene >Toxicity evaluation of artesunate and artelinate in Plasmodium berghei-infected and uninfected rats.
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Toxicity evaluation of artesunate and artelinate in Plasmodium berghei-infected and uninfected rats.

机译:青蒿琥酯和青蒿琥酯对伯氏疟原虫感染和未感染大鼠的毒性评估。

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摘要

A recent therapeutic index study in rats demonstrated that i.v. artesunate (AS) is safer than artelinate (AL). The present study of acute toxicity illustrated an LD(50) of 177 mg/kg and 488 mg/kg for AL and AS, respectively, following daily i.v. injection for 3 days in Plasmodium berghei-infected rats. In uninfected rats, the LD(50) values were 116 mg/kg and 351 mg/kg after a single dose of AL and AS, respectively. This study showed vascular necrosis in 50% of the animals at 13.5 mg/kg AL and at 42.8 mg/kg AS. Animals also showed moderate signs of renal failure at 40 mg/kg AL and 240 mg/kg AS (100 times higher than the therapeutic dose). Histopathological evaluation demonstrated mild to moderate tubular necrosis in uninfected rats treated with 40 mg/kg AL and 240 mg/kg AS; interestingly, fewer pathological lesions were observed in malaria-infected rats. Renal injury was reversible in all cases by Day 8 after cessation of dosing. No neurotoxicity was seen in any case with all i.v. regimens. In conclusion, AL and AS exhibit less toxic effects in P. berghei-infected rats than in uninfected rats. Both agents caused irreversible vascular irritation, reversible nephrotoxicity and no neurotoxicity at high doses. The data indicate that AS is three times safer than AL in rats.
机译:最近在大鼠中进行的治疗指数研究表明,静脉注射青蒿琥酯(AS)比青蒿琥酯(AL)更安全。本急性毒性研究表明,每日静脉注射后,AL和AS的LD(50)分别为177 mg / kg和488 mg / kg。在伯氏疟原虫感染的大鼠中注射3天。在未感染的大鼠中,单剂AL和AS后的LD(50)值分别为116 mg / kg和351 mg / kg。这项研究显示50%的动物在13.5 mg / kg AL和42.8 mg / kg AS时出现血管坏死。在40 mg / kg的AL和240 mg / kg的AS下,动物还显示出中等程度的肾衰竭迹象(比治疗剂量高100倍)。组织病理学评估显示,未感染的大鼠经40 mg / kg AL和240 mg / kg AS治疗后,轻度至中度肾小管坏死。有趣的是,在感染疟疾的大鼠中观察到的病理病变较少。在所有情况下,在停止给药后第8天,肾损伤是可逆的。在所有情况下,均未见神经毒性。养生方法。总之,AL和AS在感染伯氏疟原虫的大鼠中显示出的毒性作用小于未感染大鼠。两种药物在高剂量时均引起不可逆的血管刺激,可逆的肾毒性和无神经毒性。数据表明,在大鼠中,AS比AL安全三倍。

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