Effects of 3-chloro-phenyl-1,4-dihydropyridine derivatives on Trypanosome cruzi epimastigotes

被引:24
作者
Maya, JD
Morello, A
Repetto, Y
Tellez, R
Rodriguez, A
Zelada, U
Puebla, P
Caballero, E
Medarde, M
Núñez-Vergara, LJ
Squella, JA
Bontá, M
Bollo, S
San Feliciano, A
机构
[1] Univ Chile, Fac Med, Inst Biomed Sci, Program Clin & Mol Pharmacol, Santiago 7, Chile
[2] Univ Salamanca, Fac Pharm, Dept Pharmaceut Chem, E-37008 Salamanca, Spain
[3] Univ Chile, Fac Chem & Pharmaceut Sci, Lab Bioelectrochem, Santiago, Chile
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY | 2000年 / 125卷 / 01期
关键词
3-chloro-phenyl-1,4-dihydropyridine; parasite growth; Trypanosoma cruzi; felodipine; nicardipine;
D O I
10.1016/S0742-8413(99)00096-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of 3-chloro-phenyl-1,4-dihydropyridine derivatives produced different degrees of inhibition of parasite growth and respiration on clone Brener, LQ and Tulahuen strains of Trypanosome cruzi epimastigotes. Respiratory chain inhibition appears to be a posible determinant of the trypanosomicidal activity of this compounds. No difference in the action of these derivatives was found among the different parasite strains. For comparative purposes, the inhibitory effects of felodipine and nicardipine are also reported. A good correlation between toxic effects and the easiness of oxidation of the dihydripyridine ring was found. The presence of a fused ring on the dihydropyridine moiety significantly diminished the inhibitory effects. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:103 / 109
页数:7
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