Plopper C G, Van Winkle L S, Fanucchi M V, Malburg S R, Nishio S J, Chang A, Buckpitt A R
Department of Anatomy, School of Veterinary Medicine, University of California-Davis, Davis 95616, USA.
Am J Respir Cell Mol Biol. 2001 Mar;24(3):272-81. doi: 10.1165/ajrcmb.24.3.4247.
One of the presumed roles of intracellular glutathione (GSH) is the protection of cells from injury by reactive intermediates produced by the metabolism of xenobiotics. To establish whether GSH depletion is a critical step in the initiation of events that lead to cytotoxicity by P450-activated cytotoxicants, naphthalene, a well-defined Clara cell cytotoxicant, was administered to mice (200 mg/kg) by intraperitoneal injection. Shortly after injection (1, 2, and 3 h), intracellular GSH content was assessed by high performance liquid chromatography or quantitative epifluorescent imaging microscopy and compared with the degree of cytotoxicity as assessed by high resolution histopathology. In highly susceptible airways (distal bronchioles), GSH decreased by 50% in 1 h. Cytoplasmic vacuolization was not visible until 2 h, when GSH had decreased by an additional 50%. By 3 h, cytoplasmic blebbing was extensive. In minimally susceptible airways (lobar and proximal bronchi), GSH depletion varied widely within the population; a small proportion of the cells lost greater than 50% of their GSH by 2 h and a significant percentage of the cells retained most of their GSH throughout the entire 3 h. Cytoplasmic vacuolization was apparent in some of the cells at 2 h but not visible in any cells at 3 h. We conclude that (1) loss of intracellular GSH is an early event that precedes initial signs of cellular damage in Clara cell cytotoxicity; (2) this pattern of loss in relation to early injury is found both in highly susceptible and minimally susceptible airway sites; (3) there is wide cell-to-cell heterogeneity in the response; (4) the heterogeneity in the response profile varies between populations in highly susceptible and minimally susceptible sites; and (5) once the intracellular GSH concentration within the entire cell population drops below a certain threshold, the initial phase of injury becomes irreversible.
细胞内谷胱甘肽(GSH)的一个假定作用是保护细胞免受外源性物质代谢产生的反应性中间体的损伤。为了确定GSH耗竭是否是导致P450激活的细胞毒性剂产生细胞毒性的起始事件中的关键步骤,通过腹腔注射给小鼠(200 mg/kg)施用萘,萘是一种明确的克拉拉细胞细胞毒性剂。注射后不久(1、2和3小时),通过高效液相色谱法或定量落射荧光成像显微镜评估细胞内GSH含量,并与通过高分辨率组织病理学评估的细胞毒性程度进行比较。在高度易感的气道(终末细支气管)中,GSH在1小时内下降了50%。直到2小时,当GSH又下降了50%时,细胞质空泡化才可见。到3小时,细胞质起泡广泛。在低度易感的气道(大叶支气管和近端支气管)中,GSH耗竭在群体中差异很大;一小部分细胞在2小时内GSH损失超过50%,而相当比例的细胞在整个3小时内保留了大部分GSH。细胞质空泡化在2小时时在一些细胞中明显,但在3小时时在任何细胞中都不可见。我们得出以下结论:(1)细胞内GSH的丧失是克拉拉细胞细胞毒性中细胞损伤初始迹象之前的早期事件;(2)这种与早期损伤相关的丧失模式在高度易感和低度易感的气道部位均有发现;(3)反应存在广泛的细胞间异质性;(4)高度易感和低度易感部位群体的反应谱异质性不同;(5)一旦整个细胞群体内的细胞内GSH浓度降至某个阈值以下,损伤的初始阶段就变得不可逆转。