THE CHALLENGE OF CHAGAS-DISEASE CHEMOTHERAPY - AN UPDATE OF DRUGS ASSAYED AGAINST TRYPANOSOMA-CRUZI

被引:135
作者
DECASTRO, SL
机构
[1] Departamento de Ultraestrutura e Biologia Celular, Instituto Oswaldo Cruz, Fundaçào Oswaldo Cruz, Rio de Janeiro
关键词
TRYPANOSOMA-CRUZI; CHAGAS DISEASE; CHEMOTHERAPY; DRUGS;
D O I
10.1016/0001-706X(93)90021-3
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The chemotherapy of Chagas' disease remains an unsolved problem, and the search for alternative drugs continues. Only two nitroheterocyclic drugs are in clinical use at the present time, and these have severely restricted applicability for chronic patients, as well as being highly toxic. This review covers drugs tested in the last 12 years. A large number of different compounds have been assayed in a variety of ways, most commonly in terms of their capacity to inhibit epimastigote proliferation. Allopurinol has emerged for the treatment of chronic cases. However, only with greater knowledge of the biochemistry of the parasite and in particular of its peculiarities, will it be possible to shift the emphasis of drug research away from random screenings onto a more rational footing. This is exemplified by recent studies carried out using purine derivatives and trypanothione reductase inhibitors.
引用
收藏
页码:83 / 98
页数:16
相关论文
共 93 条
[1]  
ABITBOL H, 1964, Bol Chil Parasitol, V19, P132
[2]  
ABITBOL H, 1961, ACTA PHYSL LATINOAM, V11, P47
[3]   THE AEROBIC METABOLISM OF METRONIDAZOLE BY TRYPANOSOMA-CRUZI EPIMASTIGOTES [J].
AGOSIN, M .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1983, 75 (02) :311-315
[4]   ACTIVITY OF P536, A UDP-GLUCOSE ANALOG, AGAINST TRYPANOSOMA-CRUZI [J].
ALCINA, A ;
FRESNO, M ;
ALARCON, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (09) :1412-1415
[5]   DESTRUCTION OF INTRACELLULAR TRYPANOSOMA-CRUZI AFTER TREATMENT OF INFECTED MACROPHAGES WITH CATIONIC ELECTRON CARRIERS [J].
ALVES, MJM ;
RABINOVITCH, M .
INFECTION AND IMMUNITY, 1983, 39 (01) :435-438
[6]  
ANDRADE SG, 1989, B WORLD HEALTH ORGAN, V67, P509
[7]   LYSIS OF TRYPANOSOMES BY PEPTIDYL FLUOROMETHYL KETONES [J].
ASHALL, F ;
ANGLIKER, H ;
SHAW, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (02) :923-929
[8]   DIFFERENCES IN ALLOPURINOL AND 4-AMINOPYRAZOLO(3,4-D) PYRIMIDINE METABOLISM IN DRUG-SENSITIVE AND INSENSITIVE STRAINS OF TRYPANOSOMA-CRUZI [J].
AVILA, JL ;
AVILA, A ;
MONZON, H .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1984, 11 (APR) :51-60
[9]   BIOLOGICAL ACTION OF PYRAZOLOPYRIMIDINE DERIVATIVES AGAINST TRYPANOSOMA-CRUZI - STUDIES INVITRO AND INVIVO [J].
AVILA, JL ;
POLEGRE, MA ;
ROBINS, RK .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1987, 86 (01) :49-54
[10]   THE EFFICACY OF A NOVEL COMPOUND, (E)-1-(4'-BROMO-4-BIPHENYLYL)-1-(4-CHLOROPHENYL)-3-DIMETHYLAMINOPROP-1-ENE AGAINST TRYPANOSOMA-CRUZI IN MICE [J].
BARRETT, PA ;
BEVERIDGE, E ;
BULL, D ;
CALDWELL, IC ;
ISLIP, PJ ;
NEAL, RA ;
WOODS, NC .
EXPERIENTIA, 1982, 38 (03) :338-339