[Effects of phalloidin in liver cells: binding, morphological changes, and elimination (author's transl)].

Cytobiologie Pub Date : 1978-06-01
H Schimassek, D Jeckel
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Abstract

1. The uptake, binding and elimination of phalloidin in liver is compared in adult (180 to 240 g) and "baby" (17 to 19 days old) rats in vivo and in vitro. 2. In both groups there is no relation between the concentration of the poison in the liver and the toxicity. 3. Although baby rats show a significantly higher tolerance against phalloidin than the adult animals, the concentration of the poison in the liver of baby rats is higher, and the elimination is significantly slower than in adult rats. 4. The very tight binding and concentration of phalloidin in the liver is explained by an extremely low dissociation constant. 5. Furthermore, the morphological differences between the poisoning of the liver cells in the entire organ and of isolated liver cells are discussed.

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[phalloidin在肝细胞中的作用:结合、形态改变和消除[作者译]。
1. 在体内和体外比较成年大鼠(180 ~ 240 g)和“婴儿”大鼠(17 ~ 19日龄)对phalloidin在肝脏中的摄取、结合和消除。2. 在两组中,肝脏中毒素的浓度与毒性之间没有关系。3.虽然幼鼠对phalloidin的耐受性明显高于成年动物,但幼鼠肝脏中的毒性浓度更高,消除速度明显慢于成年大鼠。4. 极低的解离常数解释了phalloidin在肝脏中的紧密结合和浓度。5. 此外,还讨论了肝细胞全器官中毒与分离肝细胞中毒的形态学差异。
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