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体内二氢青蒿素抗曼氏血吸虫感染的活性。

Effect of the in vivo activity of dihydroartemisinin against Schistosoma mansoni infection in mice.

机构信息

Jiangsu Institute of Parasitic Diseases, 117 Yangxiang, Meiyuan, Wuxi, 214064, Jiangsu Province, People's Republic of China.

出版信息

Parasitol Res. 2012 May;110(5):1727-32. doi: 10.1007/s00436-011-2692-x. Epub 2011 Oct 18.

Abstract

Dihydroartemisinin, formerly known as an antimalarial drug, is the main metabolite of the mother compound artemisinins, as well as of artemether and artesunate. It has been shown that the drug exhibits antischistosomal efficacy against Schistosoma japonicum. The purpose of the current study was to assess the in vivo effect of dihydroartemisinin against Schistosoma mansoni infection in mice. Drugs at a single oral dose of 300 mg/kg were given to mice to assess the efficacy against different developmental stages of the parasite; juvenile and adult S. mansoni were treated with single doses of dihydroarteminisin with different regimens (at 200, 300, 400 or 600 mg/kg) in the stage of drug sensitivity, and the dose-response relationship was assessed; and the effect of multiple doses (at 200, 300 or 400 mg/kg) on juvenile and adult S. mansoni was also observed. The results showed that a single oral dose (300 mg/kg) of dihydroartemisinin reduced total worm burdens by 13.8-82.1% and female worm burdens by 13-82.8%, and the greatest reductions were seen when treatment was given on day 21 post-infection, with total and female worm burden reductions of 82.1% and 82.8%. Administration of a single oral dose of dihydroartemisinin on day 21 post-infection with different drug dosage (at 200, 300, 400 or 600 mg/kg) reduced total worm burdens by 70.3-87.3% and female worm burdens by 73.5-92.4%, depending on dosage. Similar treatments given on day 49 post-infection reduced total worm burdens by 48.7-68.73% and female worm burdens by 63.25-94.6%. There was obvious dose-response relationship of dihydroartemisinin against the schistosomula and adult worms of S. mansoni observed. Administration with dihydroartemisinin at oral doses of 200, 300 and 400 mg/kg, given once on each of days 20-22 post-infection of three successive days, reduced total worm burdens by 88.5-90.1% and female worm burdens by 89.2-92.1%, depending on dosage. Similar treatments given once on each of days 48-50 post-infection reduced total worm burdens by 60-70.3% and female worm burdens by 77.5-94.9%. It is concluded that dihydroartemisinin exhibits in vivo activity against various developmental stages of S. mansoni, particularly the 21-day schistosomula, and there is obvious dose-response relationship of dihydroartemisinin against the schistosomula and adult worms of S. mansoni observed.

摘要

双氢青蒿素,以前被称为抗疟药物,是母体化合物青蒿素的主要代谢物,也是青蒿琥酯和蒿甲醚的主要代谢物。已经表明该药物对日本血吸虫具有抗血吸虫病的功效。本研究的目的是评估双氢青蒿素对感染曼氏血吸虫的小鼠体内的作用。给小鼠口服 300mg/kg 的单剂量药物,以评估对寄生虫不同发育阶段的疗效;用不同方案(200、300、400 或 600mg/kg)的双氢青蒿素单次剂量治疗曼氏血吸虫的幼体和成虫,并评估剂量-反应关系;还观察了多次剂量(200、300 或 400mg/kg)对幼体和成虫的影响。结果表明,口服单剂量(300mg/kg)双氢青蒿素可使总虫荷减少 13.8-82.1%,雌虫荷减少 13-82.8%,在感染后第 21 天治疗时效果最大,总虫荷和雌虫荷减少 82.1%和 82.8%。在感染后第 21 天给予不同剂量(200、300、400 或 600mg/kg)的单次口服双氢青蒿素可使总虫荷减少 70.3-87.3%,雌虫荷减少 73.5-92.4%,这取决于剂量。在感染后第 49 天进行类似的治疗可使总虫荷减少 48.7-68.73%,雌虫荷减少 63.25-94.6%。观察到双氢青蒿素对曼氏血吸虫的尾蚴和成虫有明显的剂量反应关系。在感染后连续 3 天的第 20-22 天每天口服 200、300 和 400mg/kg 的双氢青蒿素,可使总虫荷减少 88.5-90.1%,雌虫荷减少 89.2-92.1%,这取决于剂量。在感染后第 48-50 天进行类似的治疗可使总虫荷减少 60-70.3%,雌虫荷减少 77.5-94.9%。综上所述,双氢青蒿素对曼氏血吸虫的各个发育阶段具有体内活性,特别是 21 天的尾蚴,并且观察到双氢青蒿素对曼氏血吸虫的尾蚴和成虫有明显的剂量反应关系。

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