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铜负荷绵羊肝脏中铜的细胞内分布——亚细胞分级分离研究

Intracellular distribution of copper in the liver of copper-loaded sheep--a subcellular fractionation 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 Aug;101(2):161-76. doi: 10.1016/0021-9975(89)90064-9.

Abstract

Eighteen ewes in two groups were dosed orally with CuSO4 to induce chronic Cu toxicity. Copper dosing was stopped at the first rise of acid AP activity in the serum in group 1 sheep and on the first day of haemolysis in group 2 sheep. Liver samples were obtained 1 week prior to the start of Cu dosing, at the first rise of acid phosphatase (AP) activity in serum and on the first day of haemolysis. These liver samples were homogenized and were separated into nuclear (N), heavy mitochondrial (MH), light mitochondrial (ML), microsomal (MI) and cytosolic (CY) fractions by centrifugation. The Cu concentration and specific activities of AP were determined in the liver, LH and subcellular fractions. The composition of the fractions was studied by light and electron microscopy. In the predosing biopsies, the concentration and percentage of Cu and the total specific activity of AP were highest in the ML fractions. With increasing Cu loading, the concentration of Cu in all fractions increased; the percentage of Cu increased in the N and MH fractions, decreased in the ML and MI fractions and was maintained at a constant level in the CY fractions. The total specific activities of AP in LH, N, MH, MI and CY fractions were increased and the activity was highest in the MH fraction. The results indicate that the increase in the concentration of Cu in liver cells was predominantly in lysosomes and cytosol. Furthermore, it is suggested that the necrosis of isolated hepatocytes observed in chronic Cu-poisoned sheep may be due to a saturation of the uptake of Cu into the lysosomal system of the cell, leading to the accumulation of toxic levels of Cu in the cytosol.

摘要

将两组共18只母羊经口给予硫酸铜以诱导慢性铜中毒。在第1组绵羊血清酸性酸性磷酸酶(AP)活性首次升高时以及第2组绵羊溶血的第一天停止铜给药。在开始铜给药前1周、血清酸性磷酸酶(AP)活性首次升高时以及溶血的第一天采集肝脏样本。将这些肝脏样本匀浆,通过离心分离为核(N)、重线粒体(MH)、轻线粒体(ML)、微粒体(MI)和胞质(CY)组分。测定肝脏、肝脏匀浆和亚细胞组分中铜的浓度和AP的比活性。通过光学显微镜和电子显微镜研究各组分的组成。在给药前的活检中,ML组分中铜的浓度、百分比以及AP的总比活性最高。随着铜负荷的增加,所有组分中铜的浓度均升高;N和MH组分中铜的百分比增加,ML和MI组分中铜的百分比降低,CY组分中铜的百分比保持恒定水平。LH、N、MH、MI和CY组分中AP的总比活性增加,且MH组分中的活性最高。结果表明,肝细胞中铜浓度的增加主要发生在溶酶体和胞质溶胶中。此外,提示在慢性铜中毒绵羊中观察到的孤立肝细胞坏死可能是由于细胞溶酶体系统对铜的摄取饱和,导致胞质溶胶中有毒水平的铜积累所致。

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