用青蒿琥酯和/或醋酸二硝基萘治疗的布氏锥虫感染大鼠的体内和体外变化

KO Jolayemi, M. Mamman, D. Sani, M. Okoronkwo, J. Amaje
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引用次数: 4

摘要

摘要本研究评价了青蒿琥酯和/或乙酸地咪那烯对实验性感染布鲁氏锥虫的Wistar大鼠的体内外抗锥虫作用。以0.2、2、20 μg/μl的青蒿琥酯50 μl为试药,分3组进行体外筛选;96孔微滴板,37℃孵育5分钟,取醋酸萘、生理盐水和锥虫感染的血液作为对照。在60分钟内观察到减少或完全固定锥虫的疗效。结果显示,与对照组相比,青蒿琥酯能显著(p < 0.001)诱导浓度依赖性的锥虫体运动停止。选取体重190 ~ 210 g的雄性和雌性Wistar大鼠70只,随机分为7组(雄性5只,雌性5只)进行体内研究。ⅰ组为正常对照组,ⅱ组为模型对照组。III ~ VII组腹腔感染勃氏锥虫(10只/ml)。在寄生虫病高峰期(感染后8 d), III组给予醋酸地咪那烯(3.5 mg/kg)肌注1次,IV、V、VI组给予青蒿琥酯(200、100、50)mg/kg口服,连续5 d, VII组给予青蒿琥酯(50 mg/kg)口服和醋酸地咪那烯(1.75 mg/kg)肌注,连续5 d。结果表明,接种前潜伏期为4 d,接种后寄生虫血症水平升高。第0 ~ 8天,ⅱ~ⅶ组PCV、Hb浓度、RBC计数、MCV、MCHC、总白细胞计数均显著降低(p < 0.05)。治疗后,除II、IV、V、VI组大鼠死亡外,其余各组均显著升高(p < 0.05)。因此,青蒿琥酯(50 mg/kg)和一半标准剂量的醋酸地咪那烯联合使用能够减少寄生虫病,改善锥虫引起的贫血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro and in vivo changes observed in Trypanosoma brucei brucei-infected rats treated with artesunate and/or diminazene aceturate
Publication History: Received: 02-09-2020 Accepted: 14-10-2020 Abstract This study evaluated in vitro and in vivo antitrypanosomal effect of artesunate and/or diminazene aceturate in Wistar rats experimentally infected with Trypanosoma brucei brucei. In vitro screening was carried out in triplicates using 50 μl of 0.2, 2 and 20 μg/μl of artesunate as test drug; diminazene aceturate, normal saline and trypanosome-infected blood served as controls in a 96-well microtitre plate, incubated at 37 ̊C for 5 minutes. Efficacy was observed over a period of 60 minutes for reduced or complete trypanosomal immobilization. Results showed concentration-dependent cessation of trypanosomal motility was significantly (p < 0.001) induced by artesunate when compared to the controls. Seventy Wistar rats of both sexes weighing between 190 and 210 g were randomly divided into 7 groups (5 males and 5 females) are used for in vivo study. Groups I and II served as normal control and model control respectively. Groups III to VII were infected with Trypanosoma brucei brucei (10 trypanosomes/ml) intraperitoneally. At peak parasitaemia (8 days post-infection), group III was treated with diminazene aceturate (3.5 mg/kg) intramuscularly once while groups IV, V, VI were treated with artesunate (200, 100, 50) mg/kg orally for 5 consecutive days and group VII was treated with combination of artesunate (50 mg/kg) orally and diminazene aceturate (1.75 mg/kg) intramuscularly for 5 days. Results indicated pre-patent period of 4 days and increase in levels of parasitaemia post-inoculation. PCV, Hb concentration, RBC count, MCV, MCHC and total leucocyte count decreased significantly (p < 0.05) between days 0 and 8 in groups II to VII. Following treatment, significant increases (p < 0.05) were recorded except for groups II, IV, V and VI where the rats died. Thus, combination of artesunate (50 mg/kg) and half the standard dose of diminazene aceturate was able to reduce parasitaemia and ameliorate the anaemia elicited by the trypanosomes.
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