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溶酶体在慢性铜中毒绵羊肝损伤发病机制中的作用:超微结构和形态计量学研究

Lysosomes in the pathogenesis of liver injury in chronic copper poisoned sheep: an ultrastructural and morphometric study.

作者信息

Kumaratilake J S, Howell J M

机构信息

School of Veterinary Studies, Murdoch University, Western Australia.

出版信息

J Comp Pathol. 1989 May;100(4):381-90. doi: 10.1016/0021-9975(89)90003-0.

Abstract

Chronic copper poisoning was induced in sheep by oral dosing with CuSO4. The distribution of copper between hepatocytes was unequal and, with increasing liver copper concentration, isolated hepatocytes packed with electron-dense lysosomes were seen. These cells underwent degeneration and necrosis. During the pre-haemolytic period, the concentration of Cu in the liver increased and the volume density, numerical density and mean volume of hepatocyte lysosomes increased in a linear fashion, indicating that there was proliferation as well as increase in the size of lysosomes. However, in animals killed during haemolysis, the numerical density had decreased but the volume density was little changed which indicates that lysosomal production may have diminished. It is postulated that the necrosis of hepatocytes packed with electron-dense lysosomes may be due to the accumulation of toxic amounts of copper in the cytosol, resulting from a reduced uptake of copper into the lysosomal system of these cells, and that the susceptibility of liver cells to Cu-induced damage may be increased if lysosome production is diminished.

摘要

通过口服硫酸铜在绵羊中诱发慢性铜中毒。肝细胞之间铜的分布不均,随着肝脏铜浓度的增加,可见充满电子致密溶酶体的分离肝细胞。这些细胞发生变性和坏死。在溶血前期,肝脏中铜的浓度增加,肝细胞溶酶体的体积密度、数量密度和平均体积呈线性增加,表明溶酶体有增殖以及大小增加。然而,在溶血期间处死的动物中,数量密度降低但体积密度变化不大,这表明溶酶体的产生可能减少。据推测,充满电子致密溶酶体的肝细胞坏死可能是由于这些细胞的溶酶体系统对铜的摄取减少,导致胞质溶胶中有毒量铜的积累,并且如果溶酶体产生减少,肝细胞对铜诱导损伤的易感性可能会增加。

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