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预先低剂量X射线照射对大鼠铁(Ⅲ)-亚氮三乙酸诱导的肝病的抑制作用

Inhibitory effects of prior low dose X-ray irradiation on Fe(3+)-NTA-induced hepatopathy in rats.

作者信息

Yamaoka K, Nomura T, Iriyama K, Kojima S

机构信息

Bio-Science Department Komae Branch, Abiko Research Laboratory, Tokyo, Japan.

出版信息

Physiol Chem Phys Med NMR. 1998;30(1):15-23.

PMID:9807233
Abstract

Blood activities of hepatocellular enzymes such as lactate dehydrogenase (LDH), glutamic pyruvic transaminase (GPT) and glutamic oxalacetic transaminase (GOT) peaked at 12 hours after a single intraabdominal injection of ferric nitrilotriacetate (Fe(3+)-NTA) in rats. Enzymes such as alkaline phosphatase (ALP) and leucin amino peptidase (LAP) originating in the capillary bile ducts or bile secretory liver cells were also released into the blood between 6-24 hours after intraabdominal injection of Fe(3+)-NTA in rats. Furthermore, hyperoxidation of lipids occurred in rat hepatic cell membranes, reaching a peak 6 hours after intraabdominal injection of Fe(3+)-NTA. It was found that a single prior 0.5 Gy whole body X-ray irradiation significantly increased superoxide dismutase (SOD) activities and suppressed above-mentioned symptoms of transient hepatopathy in rats.

摘要

在大鼠腹腔内单次注射次氮基三乙酸铁(Fe(3+)-NTA)后,肝细胞酶如乳酸脱氢酶(LDH)、谷丙转氨酶(GPT)和谷草转氨酶(GOT)的血液活性在12小时达到峰值。源自胆小管或胆汁分泌肝细胞的碱性磷酸酶(ALP)和亮氨酸氨基肽酶(LAP)等酶,在大鼠腹腔内注射Fe(3+)-NTA后6至24小时也释放入血。此外,大鼠肝细胞膜发生脂质过氧化,在腹腔内注射Fe(3+)-NTA后6小时达到峰值。研究发现,预先单次全身0.5 Gy X射线照射可显著提高超氧化物歧化酶(SOD)活性,并抑制大鼠上述短暂性肝病症状。

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