LIPOSOME-ENTRAPPED PGE(1) POSTTREATMENT DECREASES IL-1-ALPHA-INDUCED NEUTROPHIL ACCUMULATION AND LUNG LEAK IN RATS

被引:25
作者
LEFF, JA
BAER, JW
KIRKMAN, JM
BODMAN, ME
SHANLEY, PF
CHO, OJ
OSTRO, MJ
REPINE, JE
机构
[1] UNIV COLORADO,HLTH SCI CTR,DEPT MED,DENVER,CO 80262
[2] LIPOSOME CO,PRINCETON,NJ 08540
关键词
ADULT RESPIRATORY DISTRESS SYNDROME; ACUTE LUNG INJURY; CYTOKINES; OXYGEN RADICALS;
D O I
10.1152/jappl.1994.76.1.151
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We found that treatment with liposome-entrapped prostaglandin E(1) (Lip-PGE(1)), but not with empty liposomes and/or free PGE(1), decreased the leak of intravascularly administered I-125-labeled albumin into lungs of rats given interleukin-1 alpha (IL-1 alpha) intratracheally. Lip-PGE(1) treatment also decreased lung myeloperoxidase activity, lung lavage neutrophil increases, and lung histological abnormalities found in rats given IL-1 alpha intratracheally. Interestingly, decreased lung leak and lung neutrophil accumulation occurred when Lip-PGE(1) was given intravenously 2.5 h after, but not immediately before, intratracheal IL-1 alpha administration. When Lip-PGE(1) treatment was given both before and 2.5 h after IL-1 alpha administration, lung leak was decreased to baseline levels. Lip-PGE(1) treatment given 2.5 h after IL-1 alpha administration also decreased lung oxidized glutathione levels, which increased in rats given IL-1 alpha intratracheally. We conclude that postinsult treatment with Lip-PGE(1) decreases lung leak, neutrophil recruitment, and oxidative responses in lungs of rats given IL-1 alpha intratracheally.
引用
收藏
页码:151 / 157
页数:7
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