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盐酸氨溴索与柠檬酸廓清肺内难溶性贫铀的实验研究

刘坤璐 潘秀颉 杨陟华 徐龙 卢爱民 熊珊珊 李若曦 汪倩君 朱茂祥

军事医学Issue(10):775-779,5.
军事医学Issue(10):775-779,5.DOI:10.7644/j.issn.1674-9960.2014.10.007

盐酸氨溴索与柠檬酸廓清肺内难溶性贫铀的实验研究

Clearance of insoluble depleted uranium particles in lungs by citric acid and ambroxol

刘坤璐 1潘秀颉 1杨陟华 1徐龙 1卢爱民 2熊珊珊 1李若曦 1汪倩君 1朱茂祥1

作者信息

  • 1. 北京放射与辐射医学研究所,北京 100850
  • 2. 武警疾控中心,北京 102613
  • 折叠

摘要

Abstract

Objective To investigate the effect of citric acid and ambroxol on clearing insoluble particles of depleted uranium in rat lungs by establishing a tracheal perfusion model.Methods One hundred and fifty male Wistar rats were randomly divided into model exposure group, normal control group(NC group), depleted uranium exposure group(DU), citric acid treatment group( CA) , ambroxol treatment group( AM) and citric acid+ambroxol treatment group( CA+AM) . The rats were sacrificed on 7, 15 and 30 days.Uranium content in the lungs was detected by microwave digestion method, pathological changes in the lungs were observed, and inflammatory factors of lung homogenates were detected.Results Compared to DU control group, the intrapulmonary uranium deposit amount in experimental groups was significantly reduced on 7 and 15 days (P<0.05).HE stained lung tissue showed that the pathological changes in treatment groups were less significant than in DU control group.The level of IL-1α,IL-1β,and IL-2 was significantly lower than in DU control, but the level of MCP-1 and MIP-1 was observably higher.Conclusion Citric acid and ambroxol can evidently improve the clear-ance of lung uranium and reduce damnification of lung tissues.Drug treatment can reduce the level of pulmonary inflamma-tory cytokines alleviate the chronic inflammation in the lungs, and enhance the capacity of macrophage to recruitment.

关键词

贫铀/柠檬酸/盐酸氨溴索/炎性因子

Key words

depleted uranium/citric acid/ambroxol/inflammatory factor

分类

医药卫生

引用本文复制引用

刘坤璐,潘秀颉,杨陟华,徐龙,卢爱民,熊珊珊,李若曦,汪倩君,朱茂祥..盐酸氨溴索与柠檬酸廓清肺内难溶性贫铀的实验研究[J].军事医学,2014,(10):775-779,5.

基金项目

国家自然科学基金资助项目 ()

军事医学

OA北大核心CSCDCSTPCD

1674-9960

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