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The Effects of Amanitin Poisoning on Mouse Kidney

机译:蚕豆素中毒对小鼠肾脏的影响

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摘要

The effect of α- and β-amanitin on mouse kidney and rat kidney have been studied.The experiments on adult male mice show that (1) an MLD of α- or β-amanitin always produces necrosis in the kidneys but never in the liver; (2) with the doses used (up to 3 MLD) necrosis of the kidneys never appears less than 3 days after injection; (3) necrosis of the liver only appears with doses above MLD and generally within 2 days.No lesions were found in rat kidney after injection of amanitin.Mice injected with the conjugate of β-amanitin with albumin from rabbit serum all died from necrosis of the liver without any lesions in the kidney, 3 days after i.p. injection. It has been deduced that amanitin poisoning in mouse kidney depends on reabsorption in the tubules, that either the liver or the kidney can be the target organ of amanitin (depending on the dose) and that in rats nephrosis is prevented because there is no reabsorption of amanitin in the kidney tubules.The earliest ultrastructural changes occur in nuclei. First there is fragmentation of nucleoli and segregation of its granular and fibrillar components. At a second stage these fragments fall in number and then tend to disappear. At the same time there is a temporary increase in the number of perichromatin granules. Chromatin condensates at the borders of the nucleus and there is a big increase in numbers of interchromatin granules at the centre.Changes in the cytoplasm appear just before necrosis sets in.
机译:研究了α-和β-amanitin对小鼠肾脏和大鼠肾脏的影响。对成年雄性小鼠的实验表明:(1)α-或β-amanitin的MLD总是在肾脏中产生坏死,但在肝脏中却没有。 ; (2)所用剂量(最多3个MLD)在注射后3天之内不会出现肾脏坏死; (3)肝坏死仅在高于MLD的剂量下出现,一般在2天之内出现。注射金黄色素后大鼠肾脏未见病变;注射β-amanitin与兔血清白蛋白结合物的小鼠均因死于肝坏死而死亡。腹腔注射后3天,肝脏在肾脏中没有任何病变注射。已经推论出,小鼠肾脏中的甘露素中毒取决于细管中的重吸收,肝脏或肾脏都可能是甘露素的靶器官(取决于剂量),并且在大鼠中可以预防肾病,因为它没有重吸收。最早的超微结构改变发生在细胞核中。首先是核仁碎裂,其颗粒状和纤维状成分分离。在第二阶段,这些碎片的数量下降,然后趋于消失。同时,外周染色质颗粒的数量暂时增加。染色质在细胞核边缘凝结,中心的染色质间颗粒数量大大增加,细胞质的变化在坏死发生之前就出现了。

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