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首页> 外文期刊>Parasitology International >Combination chemotherapy with a substance P receptor antagonist (aprepitant) and melarsoprol in a mouse model of human African trypanosomiasis
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Combination chemotherapy with a substance P receptor antagonist (aprepitant) and melarsoprol in a mouse model of human African trypanosomiasis

机译:在非洲非洲锥虫病小鼠模型中,将P物质拮抗剂(阿瑞匹坦)和美拉索洛联合化疗

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摘要

Drug therapy for late-stage (encephalitic) human African trypanosomiasis (HAT) is currently very unsatisfactory with the most commonly used drug, melarsoprol, having a 5% overall mortality. There is evidence in a mouse model of HAT that Substance P (SP) receptor antagonism reduces the neuroinflammatory reaction to CNS trypanosome infection. In this study we investigated the effects of combination chemotherapy with melarsoprol and a humanised SP receptor antagonist aprepitant (EMEND) in this mouse model. The melarsoprol/aprepitant drug combination did not produce any clinical signs of illness in mice with CNS trypanosome infection. This lack of any additional or unexpected CNS toxicity in the mouse model of CNS HAT provides valuable safety data for the future possible use of this drug combination in patients with late-stage HAT.
机译:目前,对于晚期(脑炎性)人类非洲锥虫病(HAT)的药物治疗非常不满意,而最常用的药物美拉索洛的总死亡率为5%。在HAT的小鼠模型中,有证据表明P物质(SP)受体拮抗作用可减轻对CNS锥虫感染的神经炎症反应。在这项研究中,我们调查了美拉莫洛和人源化SP受体拮抗剂阿瑞匹坦(EMEND)联合化疗的效果。在患有中枢神经系统锥虫感染的小鼠中,美拉莫普尔/阿瑞匹坦的药物组合未产生任何临床疾病迹象。在CNS HAT小鼠模型中缺乏任何其他或未预期的CNS毒性,为该药物组合在晚期HAT患者中的未来可能使用提供了宝贵的安全性数据。

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