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体外正常体温和低温缺血期间大鼠肝细胞线粒体絮状密度的定量分析。

Quantitative analysis of mitochondrial flocculent densities in rat hepatocytes during normothermic and hypothermic ischemia in vitro.

作者信息

Myagkaya G L, van Veen H, James J

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1985;49(1):61-72. doi: 10.1007/BF02912085.

Abstract

The development of flocculent densities in mitochondria as a sign of irreversible cell injury in rat hepatocytes has been studied by quantitative electron microscopy during in vitro ischemia under both normothermic (37 degrees C) and hypothermic (4 degrees C) conditions. At 37 degrees C flocculent densities first appear after 1 h ischemia; at this stage they are small in diameter (170 nm) and occur in only 8% of mitochondria. After 1.5 hour ischemia, flocculent densities increase in diameter (207 nm) and are seen in 37% of mitochondria. Death of the majority of hepatocytes seems to occur between 1.5 and 2 h ischemia since at this stage the percentage of mitochondria containing flocculent densities reaches a maximum (48%). However, flocculent densities continue to increase in size (to 337 nm diam.) up to between 2 and 4 h ischemia (the prenecrotic phase). In contrast, at 4 degrees C signs of ischemic damage to hepatocytes are considerably delayed. Flocculent densities of comparable size and frequency to those observed after 1 h ischemia at 37 degrees C are not seen till as late as 4 days at 4 degrees C. At the latter temperature, only after 7 days ischemia a substantial rise (to about 25%) in the proportion of mitochondria containing flocculent densities occurs. A further slow increase in size and in the percentage of mitochondria containing densities occurs up to 14 days ischemia at 4 degrees C. It is concluded that the development of flocculent densities may be used only as a parameter of irreversible damage in cells with a sufficient number of mitochondria, such as hepatocytes, under normothermic conditions. With ischemia at 4 degrees C, possibly due to a different protein denaturation pattern, the development of flocculent densities is of much less value as an indication of irreversible cell damage and cannot, therefore, be considered as a reliable sign of cellular damage in organs stored at 4 degrees C for transplantation purposes.

摘要

通过定量电子显微镜研究了在正常体温(37摄氏度)和低温(4摄氏度)条件下体外缺血期间,大鼠肝细胞线粒体中絮状密度的发展,以此作为不可逆细胞损伤的标志。在37摄氏度时,缺血1小时后絮状密度首次出现;此时它们直径较小(170纳米),仅出现在8%的线粒体中。缺血1.5小时后,絮状密度直径增大(207纳米),出现在37%的线粒体中。大多数肝细胞的死亡似乎发生在缺血1.5至2小时之间,因为在此阶段含有絮状密度的线粒体百分比达到最大值(48%)。然而,絮状密度的大小继续增加(至直径337纳米),直至缺血2至4小时(坏死前期)。相比之下,在4摄氏度时,肝细胞缺血损伤的迹象明显延迟。在4摄氏度下,直到4天后才出现与37摄氏度缺血1小时后观察到的大小和频率相当的絮状密度。在后者温度下,仅在缺血7天后,含有絮状密度的线粒体比例才大幅上升(至约25%)。在4摄氏度下,缺血长达14天,含有密度的线粒体的大小和百分比进一步缓慢增加。结论是,在正常体温条件下,絮状密度的发展仅可作为具有足够数量线粒体的细胞(如肝细胞)中不可逆损伤的一个参数。在4摄氏度缺血时,可能由于不同的蛋白质变性模式,絮状密度的发展作为不可逆细胞损伤的指标价值要小得多,因此不能被视为用于移植目的而在4摄氏度下储存的器官中细胞损伤的可靠标志。

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