A study of the activity of 2-(alkylamino)-1-phenyl-1-ethanethiosulfuric acids against infection by Schistosoma mansoni in a murine model

被引:15
作者
Alves Moreira, Liliani Salum
Pilo-Veloso, Dorila
de Mello, Romulo Teixeira
Zech Coelho, Paulo Marcos
Nelson, David Lee [1 ]
机构
[1] Univ Fed Minas Gerais, Fac Farm, Dept Alimentos, BR-31270901 Belo Horizonte, MG, Brazil
[2] Santa Casa Misericordia Belo Horizonte, Belo Horizonte, MG, Brazil
[3] Fdn Osvaldo Cruz, Ctr Pesquisas Rene Rachou, Belo Horizonte, MG, Brazil
[4] Univ Fed Minas Gerais, Fac Farm, Dept Anal Clin & Toxicol, Belo Horizonte, MG, Brazil
[5] Univ Fed Minas Gerais, Inst Ciencias Exatas, Dept Quim, Belo Horizonte, MG, Brazil
关键词
schistosomiasis; Schistosoma mansoni; aminoalkanethiosulfuric acid; preclinical drug evaluation; drug resistance; toxicity;
D O I
10.1016/j.trstmh.2006.06.006
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The schistosomicidal. activities of seven 2-(alkytamino)-1-phenyl-1-ethanethiosulfuric acids (1a-g) (R = propyl, isopropyl, butyl, isobutyl, t-butyl, sec-butyl, cyclohexyl, respectively) were determined in female Swiss mice infected with Schistosoma mansoni. The compounds were administered in a single oral dose of 800 mg/kg to groups of 15 mice infected with 50 cercariae each. All the compounds were found to be active, a high animal mortality being observed with 1e. These compounds have a high specificity against female worms (64-100% reduction vs. 33-61% reduction in mate worms). The test was repeated, a 400-mg/kg sub-dose of 1f also being tested, and similar results were observed. A 94% reduction in the number of female worms was observed when compound 1c was administered in a single 800-mg/kg dose to animals infected with 80 cercariae. Finally, the test was repeated with single 800 mg/kg oral doses of compounds 1e (highly purified) and 1f and a 400-mg/kg sub-dose of 1c. The toxicity of le was confirmed, while the animals that received 1c and 1f presented reductions in the worm Loads corresponding to 45.9% (male worms) and 84.8% (female worms) for 1c and 50.4% (male worms) and 94.2% (female worms) for 1f. (C) 2006 Royal Society of Tropical Medicine and Hygiene. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:385 / 390
页数:6
相关论文
共 33 条
[1]  
Araujo N, 1996, Rev Soc Bras Med Trop, V29, P467, DOI 10.1590/S0037-86821996000500010
[2]  
BATZINGER RP, 1977, J PHARMACOL EXP THER, V200, P221
[3]   Altered response of strain of Schistosoma mansoni to oxamniquine and praziquantel [J].
Bonesso-Sabadini, PIP ;
de Souza Dias, LC .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2002, 97 (03) :381-385
[4]  
Coelho P. M. Z., 1997, Revista do Instituto de Medicina Tropical de Sao Paulo, V39, P101, DOI 10.1590/S0036-46651997000200007
[5]   Activity of oxamniquine at skin, pulmonary and sexual maturation phases, on a Schistosoma mansoni strain (R1) previously reported as resistant at the adult phase [J].
Coelho, PMZ ;
Ribeiro, F ;
Mello, RT ;
Silva, FCLE ;
Nogueira-Machado, JA .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1998, 93 :267-268
[6]   Study of Schistosoma mansoni isolates from patients with failure of treatment with oxamniquine [J].
Conceiçao, MJ ;
Argento, CA ;
Corrêa, A .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2000, 95 (03) :375-380
[7]  
Dias L C, 1978, Rev Saude Publica, V12, P110, DOI 10.1590/S0034-89101978000100013
[8]   RESPONSE OF DRUG-RESISTANT ISOLATES OF SCHISTOSOMA-MANSONI TO ANTISCHISTOSOMAL AGENTS [J].
DRESCHER, KM ;
ROGERS, EJ ;
BRUCE, JI ;
KATZ, N ;
DIAS, LCD ;
COLES, GC .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1993, 88 (01) :89-95
[9]   The global epidemiological situation of schistosomiasis and new approaches to control and research [J].
Engels, D ;
Chitsulo, L ;
Montresor, A ;
Savioli, L .
ACTA TROPICA, 2002, 82 (02) :139-146
[10]   DRUG-RESISTANT SCHISTOSOMIASIS - RESISTANCE TO PRAZIQUANTEL AND OXAMNIQUINE INDUCED IN SCHISTOSOMA-MANSONI IN MICE IS DRUG-SPECIFIC [J].
FALLON, PG ;
DOENHOFF, MJ .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1994, 51 (01) :83-88