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过氧亚硝酸盐影响克氏锥虫中的钙离子运输。

Peroxynitrite affects Ca2+ transport in Trypanosoma cruzi.

作者信息

Thomson L, Gadelha F R, Peluffo G, Vercesi A E, Radi R

机构信息

Departamento de Bioquimica, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.

出版信息

Mol Biochem Parasitol. 1999 Jan 5;98(1):81-91. doi: 10.1016/s0166-6851(98)00149-2.

Abstract

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 arsenazo III. Peroxynitrite, at biologically relevant concentrations produced within phagosomes (250-750 microM), 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 Ca(2+)-uptake, concomitant with the inactivation of a Ca(2+)-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 Ca(2+)-transport. We conclude that the disruption of calcium homeostasis by peroxynitrite may contribute to the observed cytotoxic effects of macrophages against T. cruzi.

摘要

巨噬细胞通过产生超氧化物、一氧化氮和过氧亚硝酸盐,在抵抗克氏锥虫感染中发挥重要作用。过氧亚硝酸盐已被证明对克氏锥虫前鞭毛体具有高度细胞毒性。钙参与寄生虫的许多重要功能,其细胞内浓度由多种转运系统控制,涉及线粒体和非线粒体区室。在本文中,我们报告了过氧亚硝酸盐对钙摄取系统的影响,该影响是通过在偶氮胂III存在下用洋地黄皂苷通透化的锥虫进行研究的。在吞噬体中产生的生物学相关浓度(250 - 750 microM)的过氧亚硝酸盐以剂量依赖的方式抑制钙摄取。过氧亚硝酸盐降低了在四甲基对苯二胺(TMPD)/抗坏血酸存在下获得的线粒体膜电位。此外,观察到非线粒体Ca(2+)摄取减少,同时伴有Ca(2+)依赖性ATP酶活性失活。对细胞腺嘌呤核苷酸库的HPLC分析显示,寄生虫的ATP含量和能量电荷随时间下降;然而,相对于ATP依赖性Ca(2+)转运的下降,ATP水平的这种下降明显延迟。我们得出结论,过氧亚硝酸盐破坏钙稳态可能导致观察到的巨噬细胞对克氏锥虫的细胞毒性作用。

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