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用免疫抑制大鼠模型筛选抗隐孢子虫药物活性。

Anti-cryptosporidial drug activity screened with an immunosuppressed rat model.

作者信息

Brasseur P, Lemeteil D, Ballet J J

机构信息

Laboratoire de Parasitologie, C.H.R.U., Rouen, France.

出版信息

J Protozool. 1991 Nov-Dec;38(6):230S-231S.

PMID:1818183
Abstract

Cryptosporidium parvum, a coccidian parasite can cause mild or severe self-limiting diarrhea in immunocompetent humans, but chronic and life-threatening in immunocompromised individuals. An immunosuppressed rat model with persistent cryptosporidiosis was used to investigate the anti-cryptosporidial activity of drugs. Using curative procedures, no activity was found with 6 antibiotics assayed, including spiramycin (31-100%). Mepacrine at a dose of 100 mg/kg had mild activity (19%), while lasalocid (10 mg/kg) and sulfadimethoxine (60 mg/kg) exhibited a 0.1% and 13%, activity respectively. This experimental immuno-suppressed rat model appears suitable for screening candidate drugs either for preventive or curative treatment of cryptosporidiosis.

摘要

微小隐孢子虫是一种球虫寄生虫,可在免疫功能正常的人群中引起轻度或重度自限性腹泻,但在免疫功能低下的个体中会导致慢性且危及生命的腹泻。使用患有持续性隐孢子虫病的免疫抑制大鼠模型来研究药物的抗隐孢子虫活性。采用治疗程序,对所检测的6种抗生素(包括螺旋霉素,31%-100%)未发现活性。剂量为100mg/kg的米帕林有轻度活性(19%),而拉沙洛西(10mg/kg)和磺胺二甲氧嘧啶(60mg/kg)的活性分别为0.1%和13%。这种实验性免疫抑制大鼠模型似乎适用于筛选用于隐孢子虫病预防或治疗的候选药物。

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