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铜锌超氧化物歧化酶对四氧嘧啶诱导糖尿病的保护作用:形态学方面

The protective role of copper-zinc superoxide dismutase against alloxan-induced diabetes: morphological aspects.

作者信息

Thaete L G, Crouch R K, Buse M G, Spicer S S

出版信息

Diabetologia. 1985 Sep;28(9):677-82. doi: 10.1007/BF00291975.

DOI:10.1007/BF00291975
PMID:3905479
Abstract

Copper-zinc superoxide dismutase is known to protect pancreatic beta-cell function from the damage of alloxan. A morphological investigation of copper-zinc superoxide dismutase prophylaxis against alloxan was undertaken in rats to investigate the mechanism of this protective action. Exogenous copper-zinc superoxide dismutase reproducibly protected the morphological features of pancreatic beta cells against damage by alloxan as determined by light microscopic immunostaining for insulin and by ultrastructural examination. By the same criteria, alpha and delta cells appeared unaffected by administration of a combination of alloxan and copper-zinc superoxide dismutase or either agent alone. Autoradiography after injection of 125I labelled copper-zinc superoxide dismutase into normal rats showed no evidence that the enzyme enters viable islet cells, suggesting an extracellular site of protection against alloxan.

摘要

已知铜锌超氧化物歧化酶可保护胰腺β细胞功能免受四氧嘧啶的损害。为研究这种保护作用的机制,对大鼠进行了铜锌超氧化物歧化酶预防四氧嘧啶损伤的形态学研究。通过胰岛素的光镜免疫染色和超微结构检查确定,外源性铜锌超氧化物歧化酶可重复性地保护胰腺β细胞的形态特征免受四氧嘧啶的损伤。根据相同标准,α细胞和δ细胞在注射四氧嘧啶和铜锌超氧化物歧化酶的组合或单独使用任何一种试剂后似乎未受影响。向正常大鼠注射125I标记的铜锌超氧化物歧化酶后的放射自显影显示,没有证据表明该酶进入活的胰岛细胞,这表明存在针对四氧嘧啶的细胞外保护位点。

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1
The protective role of copper-zinc superoxide dismutase against alloxan-induced diabetes: morphological aspects.铜锌超氧化物歧化酶对四氧嘧啶诱导糖尿病的保护作用:形态学方面
Diabetologia. 1985 Sep;28(9):677-82. doi: 10.1007/BF00291975.
2
[Nickel chloride and alloxan. I. Determination of glucose, insulin and superoxide dismutase in blood and pancreas of rats].[氯化镍与四氧嘧啶。I. 大鼠血液及胰腺中葡萄糖、胰岛素和超氧化物歧化酶的测定]
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Res Commun Chem Pathol Pharmacol. 1989 Jan;63(1):27-44.
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Effect of superoxide dismutase, catalase, chelating agents, and free radical scavengers on the toxicity of alloxan to isolated pancreatic islets in vitro.超氧化物歧化酶、过氧化氢酶、螯合剂和自由基清除剂对四氧嘧啶体外对分离胰岛毒性的影响。
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Physiol Chem Phys Med NMR. 1995;27(3):149-59.

引用本文的文献

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Maternal zinc intake of Wistar rats has a protective effect in the alloxan-induced diabetic offspring.母鼠摄入锌对丙烯醛诱导的糖尿病子代具有保护作用。
J Physiol Biochem. 2013 Mar;69(1):35-43. doi: 10.1007/s13105-012-0185-8. Epub 2012 Jun 23.
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Alloxan cytotoxicity is highly potentiated by plasma membrane- and lysosomal-associated iron--a study on a model system of cultured J-774 cells.四氧嘧啶的细胞毒性因质膜和溶酶体相关铁而显著增强——一项关于培养的J-774细胞模型系统的研究。
Diabetologia. 1993 Aug;36(8):707-15. doi: 10.1007/BF00401140.

本文引用的文献

1
FINE STRUCTURE OF RABBIT PANCREATIC B CELLS IN CORTISONE-ALLOXAN INDUCED SUBDIABETES.可的松-四氧嘧啶诱导的亚糖尿病状态下兔胰腺B细胞的精细结构
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Electron microscopy of islet cells in alloxan-treated rabbits.
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Superoxide dismutase is a prophylactic against alloxan diabetes.超氧化物歧化酶是一种预防四氧嘧啶糖尿病的药物。
Nature. 1981 Nov 12;294(5837):158-60. doi: 10.1038/294158a0.
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CuZn-superoxide dismutase, Mn-superoxide dismutase, catalase and glutathione peroxidase in pancreatic islets and other tissues in the mouse.小鼠胰岛及其他组织中的铜锌超氧化物歧化酶、锰超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶
Biochem J. 1981 Nov 1;199(2):393-8. doi: 10.1042/bj1990393.
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Superoxide dismutase in human islets of Langerhans.人胰岛中的超氧化物歧化酶
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Inhibition of alloxan action in isolated pancreatic islets by superoxide dismutase, catalase, and a metal chelator.超氧化物歧化酶、过氧化氢酶和金属螯合剂对分离的胰岛中四氧嘧啶作用的抑制
Diabetes. 1980 Mar;29(3):213-6. doi: 10.2337/diab.29.3.213.
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Alloxan toxicity to the pancreatic B-cell. A new hypothesis.四氧嘧啶对胰腺β细胞的毒性作用。一种新假说。
Biochem Pharmacol. 1982 Nov 15;31(22):3527-34. doi: 10.1016/0006-2952(82)90571-8.
8
Extracellular superoxide dismutase in human tissues and human cell lines.人体组织和人细胞系中的细胞外超氧化物歧化酶
J Clin Invest. 1984 Oct;74(4):1398-403. doi: 10.1172/JCI111550.
9
The inhibition of islet superoxide dismutase by diabetogenic drugs.致糖尿病药物对胰岛超氧化物歧化酶的抑制作用。
Diabetes. 1981 Mar;30(3):235-41. doi: 10.2337/diab.30.3.235.
10
Chemically induced (streptozotocin-alloxan) diabetes mellitus in the dog. Biochemical and ultrastructural studies.化学诱导(链脲佐菌素-四氧嘧啶)犬糖尿病。生化及超微结构研究。
Am J Pathol. 1980 Feb;98(2):295-310.