首页   按字顺浏览 期刊浏览 卷期浏览 Changes of Xanthine Oxidase, Lipid Peroxide and Superoxide Dismutase in Mouse Acute Pan...
Changes of Xanthine Oxidase, Lipid Peroxide and Superoxide Dismutase in Mouse Acute Pancreatitis

 

作者: Atsushi Nonaka,   Tadao Manabe,   Kohichiro Tamura,   Noboru Asano,   Katsuhiro Imanishi,   Takayoshi Tobe,  

 

期刊: Digestion  (Karger Available online 1989)
卷期: Volume 43, issue 1-2  

页码: 41-46

 

ISSN:0012-2823

 

年代: 1989

 

DOI:10.1159/000199859

 

出版商: S. Karger AG

 

关键词: Pancreatitis;CDE pancreatitis;Xanthine oxidase;Lipid peroxide;Superoxide dismutase;Nitroblue tetrazolium

 

数据来源: Karger

 

摘要:

The role of free radicals in the development of pancreatitis was evaluated by measuring the level of activities of xanthine oxidase (XOD), lipid peroxide (LPO) and superoxide dismutase (SOD). Acute pancreatitis was induced in female mice fed a choline-deficient meal containing 0.5 % DL-ethionine (CDE meal). Acute pancreatitis was confirmed by the changes in serum amylase level and other typical features observed microscopically 24 h after the meal was taken. Activity of XOD was elevated significantly (p < 0.05) from the baseline of 1.13 ± 0.19 U/g tissue to 2.34 ± 0.46, 2.59 ± 0.33 and 3.46 ± 0.70 U/g tissue, 8, 12 and 24 h, respectively, after the CDE meal. The LPO level was also increased from an undetectable amount to 1.10 ± 0.47 nmol/ml (p < 0.05), 1.03 ± 0.18 (p < 0.01) at 6 and 8 h, respectively, and then returned to an undetectable amount at 12 h. The peak level of LPO was shown at 24 h, 1.76 ± 0.40 nmol/ml (p < 0.01) and gradually decreased until 48 h, 1.17 ± 0.37 nmol/ml (p < 0.01) after the CDE meal. Changes of LPO took a biphasic pattern. SOD was decreased significantly from 47.1 ± 3.4 mU/g tissue to 30.7 ± 2.5, 24.8 ± 1.7 and 20.6 ± 1.1 mU/g tissue at 8 (p < 0.01), 12 (p < 0.01), and 24 (p < 0.01) h, respectively. These results indicate that oxygen-derived free radicals play an important role in the development of acute pancreatitis and that the imbalance of the offense system represented by XOD and LPO and the defense system reflected by SOD in the tissue might be an important cause of tissue damage induced by oxygen-derived fr

 

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