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评价奥沙尼喹、吡喹酮及两药联用对曼氏血吸虫螺内期的影响。

Evaluation of the effect of oxamniquine, praziquantel and a combination of both drugs on the intramolluscan phase of Schistosoma mansoni.

作者信息

Mattos A C A, Pereira G C, Jannotti-Passos L K, Kusel J R, Coelho P M Z

机构信息

Laboratório de Esquistossomose, Centro de Pesquisas René Rachou/Fiocruz, Av. Augusto de Lima 1715, Barro Preto, 30.090-002 Belo Horizonte, MG, Brazil.

出版信息

Acta Trop. 2007 May;102(2):84-91. doi: 10.1016/j.actatropica.2007.04.002. Epub 2007 Apr 6.

Abstract

The activity of oxamniquine (OXA), praziquantel (PZQ), and a combination of both drugs was evaluated at the intramolluscan phase of Schistosoma mansoni. Biomphalaria glabrata snails infected with S. mansoni were treated with 500 mg/kg OXA, 1000 mg/kg PZQ or with 250 mg/kg OXA and 500 mg/kg PZQ, in association, at the pre-patent and patent phases of infection. The results showed that either treatments with OXA or PZQ, alone, at the pre-patent period, delayed the parasite's development, increasing the pre-patent period by approximately 10 days. At the same pre-patent period, treatment with a combination of OXA/PZQ delayed the parasite's development even more, extending the pre-patent period up to 56 days. At the patent period, treatment with OXA and PZQ, alone, interrupted cercarial shedding. When the snails were treated with 1000 mg/kg PZQ, the cercarial production was re-established 15 days after treatment, but in lower numbers than those obtained before treatment, whereas the snails treated with 500 mg/kg OXA were able to shed cercariae in similar quantities to those observed before treatment. The association 250 mg/kg OXA+500 mg/kg PZQ, at the patent period, not only discontinued cercarial shedding, but also led to the "cure" of the snails, showing a synergistic effect of this combination of drugs. These results suggest that this model will be useful for selection of resistant parasites, as well as for screening new antischistosomal drugs.

摘要

在曼氏血吸虫的螺内期评估了奥沙尼喹(OXA)、吡喹酮(PZQ)以及两种药物联合使用的活性。用500mg/kg奥沙尼喹、1000mg/kg吡喹酮或250mg/kg奥沙尼喹与500mg/kg吡喹酮联合,在感染的潜伏期和发病期对感染曼氏血吸虫的光滑双脐螺进行治疗。结果显示,在潜伏期单独使用奥沙尼喹或吡喹酮治疗均会延迟寄生虫的发育,使潜伏期延长约10天。在相同的潜伏期,奥沙尼喹/吡喹酮联合治疗使寄生虫发育延迟得更多,将潜伏期延长至56天。在发病期,单独使用奥沙尼喹和吡喹酮治疗可中断尾蚴排放。当用1000mg/kg吡喹酮治疗螺时,治疗后15天尾蚴产量重新恢复,但数量低于治疗前,而用500mg/kg奥沙尼喹治疗的螺能够排出与治疗前观察到的数量相似的尾蚴。在发病期,250mg/kg奥沙尼喹 + 500mg/kg吡喹酮联合使用不仅停止了尾蚴排放,还导致螺“治愈”,显示出这种药物组合的协同作用。这些结果表明,该模型将有助于选择耐药寄生虫以及筛选新的抗血吸虫药物。

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