Peroxynitrite affects Ca2+ transport in Trypanosoma cruzi

被引:21
|
作者
Thomson, L
Gadelha, FR
Peluffo, G
Vercesi, AE
Radi, R [1 ]
机构
[1] Univ Republ, Fac Med, Dept Bioquim, Montevideo 11800, Uruguay
[2] Univ Republ, Fac Ciencias, Inst Biol, Montevideo 11800, Uruguay
[3] Univ Estadual Campinas, Inst Biol, Dept Bioquim, Sao Paulo, Brazil
[4] Univ Estadual Campinas, NMCE, Dept Patol Clin, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Trypanosoma cruzi; peroxynitrite; calcium; calcium transport systems; Ca2+-ATPase activity;
D O I
10.1016/S0166-6851(98)00149-2
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
Macrophages play an important role against Trypanosoma cruzi infection, via superoxide: nitric oxide, and peroxynitrite production. Peroxynitrite has been shown to be highly cytotoxic against Trypanosoma cruzi epimastigotes. Calcium is involved in many vital functions of the parasites, being its intracellular concentration governed by several transport systems, involving mitochondrial and non-mitochondrial compartments. In this paper: we report the effect of peroxynitrite on the calcium uptake systems, as studied by digitonin-permeabilized trypanosomes in the presence of arsenate III. Peroxynitrite, at biologically relevant concentrations produced within phagosomes (250-750 IJ-M), inhibited calcium uptake in a dose-dependent manner. Peroxynitrite decreased the mitochondrial membrane potential obtained in the presence of tetramethyl-p-phenylenediamine (TMPD)/ascorbate. In addition, a decrease of the non-mitochondrial Ca2+-uptake, concomitant with the inactivation of a Ca2+-dependent ATPase activity, was observed. HPLC analyses of the cellular adenine nucleotide pool showed a time-dependent decrease of ATP content and energy charge of the parasite; however this drop in ATP levels was significantly delayed with respect to decrease of the ATP-dependent Ca2+-transport. We conclude that the disruption of calcium homeostasis by peroxynitrite may contribute to the observed cytotoxic effects of macrophages against T, cruzi. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 91
页数:11
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