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2-取代的5-硝基咪唑类药物在治疗伴有中枢神经系统受累的慢性鼠布氏锥虫感染中的应用。

The use of 2-substituted 5-nitroimidazoles in the treatment of chronic murine Trypanosoma brucei infections with central nervous system involvement.

作者信息

Jennings F W, Urquhart G M, Murray P K, Miller B M

出版信息

Z Parasitenkd. 1984;70(6):691-7. doi: 10.1007/BF00927120.

DOI:10.1007/BF00927120
PMID:6524019
Abstract

Chronic infections of Trypanosoma brucei GVR 35/2 in mice, normally relapse after conventional chemotherapy because infective trypanosomes in the brain escape the action of the drug and are able to multiply and eventually re-establish a parasitaemia. However, if treatment consists of a single dose of 1 x 20 mg/kg suramin followed 3 or 4 days later by a 2-substituted 5-nitroimidazole, given intraperitoneally, either as a single dose or as a course of daily injections, relapses rarely occur and the majority of the mice are permanently cured. The minimum effective levels for the three 5-nitroimidazole compounds (Merck Sharp and Dohme, Rahway, NJ, USA) were two doses of 10 mg/kg of L611,744; four doses of 10 mg/kg of MK 436; and three doses of 10 mg/kg of L634,549. Generally it was more effective to divide a given total dose into two or more daily doses, rather than to give the 4-nitroimidazole as a single treatment. The effective dose levels are low enough to be of practical significance and, if the 5-nitroimidazoles were ever licensed for humans, might well prove to be an alternative to melarsoprol treatment for the elimination of trypanosomes from the central nervous system.

摘要

小鼠感染布氏锥虫GVR 35/2后的慢性感染,在传统化疗后通常会复发,因为大脑中的感染性锥虫会逃避药物作用,能够繁殖并最终重新建立寄生虫血症。然而,如果治疗方案为单剂量1×20mg/kg苏拉明,3或4天后腹腔注射2-取代5-硝基咪唑,无论是单剂量还是每日注射疗程,很少会复发,大多数小鼠会被永久治愈。三种5-硝基咪唑化合物(美国新泽西州拉威市默克夏普多贺美公司生产)的最低有效剂量分别为:两剂10mg/kg的L611,744;四剂10mg/kg的MK 436;以及三剂10mg/kg的L634,549。一般来说,将给定的总剂量分成两个或更多个每日剂量比单次给予4-硝基咪唑更有效。有效剂量水平足够低,具有实际意义,如果5-硝基咪唑类药物获得用于人类的许可,很可能被证明是一种替代美拉胂醇治疗以从中枢神经系统清除锥虫的方法。

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本文引用的文献

1
'Berenil' and nitroimidazole combinations in the treatment of Trypanosoma brucei infection with central nervous system involvement.“贝尼尔”与硝基咪唑类药物联合治疗布氏锥虫感染合并中枢神经系统受累
Int J Parasitol. 1980 Feb;10(1):27-32. doi: 10.1016/0020-7519(80)90060-0.
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Present status of chemotherapy and chemopropylaxis of human trypanosomiasis in the Eastern Hemisphere.
Pharmacol Ther. 1980;11(2):391-413. doi: 10.1016/0163-7258(80)90035-2.
3
Relapsed parasitaemia following chemotherapy of chronic T. brucei infections in mice and its relation to cerebral trypanosomes.小鼠慢性布氏锥虫感染化疗后的寄生虫血症复发及其与脑内锥虫的关系。
Contrib Microbiol Immunol. 1983;7:147-54.
4
Treatment with suramin and 2-substituted 5-nitroimidazoles of chronic murine Trypanosoma brucei infections with central nervous system involvement.用苏拉明和2-取代的5-硝基咪唑治疗伴有中枢神经系统受累的慢性小鼠布氏锥虫感染。
Trans R Soc Trop Med Hyg. 1983;77(5):693-8. doi: 10.1016/0035-9203(83)90207-9.
5
The use of the 2 substituted 5-nitroimidazole, Fexinidazole (Hoe 239) in the treatment of chronic T. brucei infections in mice.2-取代的5-硝基咪唑类药物非昔硝唑(Hoe 239)在治疗小鼠慢性布氏锥虫感染中的应用。
Z Parasitenkd. 1983;69(5):577-81. doi: 10.1007/BF00926669.
6
The activity of fexinidazole (HOE 239) against experimental infections with Trypanosoma cruzi, trichomonads and Entamoeba histolytica.非昔硝唑(HOE 239)对克氏锥虫、毛滴虫和溶组织内阿米巴实验性感染的活性。
Ann Trop Med Parasitol. 1983 Feb;77(1):13-26. doi: 10.1080/00034983.1983.11811668.
7
Difference of effective antitrypanosomal dosages of benznidazole in mice and man. Chemotherapeutic and pharmacokinetic results.小鼠与人中苯硝唑有效抗锥虫剂量的差异。化疗及药代动力学结果。
Acta Trop. 1980 Sep;37(3):257-61.
8
The relationship between duration of infection with Trypanosoma brucei in mice and the efficacy of chemotherapy.小鼠感染布氏锥虫的持续时间与化疗疗效之间的关系。
Parasitology. 1977 Oct;75(2):143-53. doi: 10.1017/s0031182000062284.
9
The brain as a source of relapsing Trypanosoma brucei infection in mice after chemotherapy.
Int J Parasitol. 1979 Aug;9(4):381-4. doi: 10.1016/0020-7519(79)90089-4.