RENIN-ANGIOTENSIN SYSTEM SUPPRESSION MITIGATES EXPERIMENTAL RADIATION PNEUMONITIS

被引:115
作者
Ghosh, Swarajit N. [1 ]
Zhang, Rong [3 ]
Fish, Brian L. [2 ]
Semenenko, Vladmir A. [2 ]
Li, X. Allen [2 ]
Moulder, John E. [2 ]
Jacobs, Elizabeth R.
Medhora, Meetha
机构
[1] Med Coll Wisconsin, Ctr Cardiovasc, Dept Med, Div Pulm & Crit Care, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Radiat Oncol, Milwaukee, WI 53226 USA
[3] Harbin Med Univ, Coll Pharm, Dept Pharmacol, Harbin, Peoples R China
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2009年 / 75卷 / 05期
基金
美国国家卫生研究院;
关键词
Radiation injury; mitigation; lung function; angiotensin-converting enzyme inhibitors; ACE; CONVERTING-ENZYME-INHIBITORS; BRADYKININ B-1 RECEPTOR; INDUCED LUNG INJURY; ACE-INHIBITORS; ENDOTHELIAL DYSFUNCTION; INDUCED PNEUMONOPATHY; II TYPE-1; IRRADIATION; RAT; NEPHROPATHY;
D O I
10.1016/j.ijrobp.2009.07.1743
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: To find the mitigators of pneumonitis induced by moderate doses of thoracic radiation (10-15 Gy). Methods and Materials: Unanesthetized WAG/RijCmcr female rats received a single dose of X-irradiation (10, 12, or 15 Gy at 1.615 Gy/min) to the thorax. Captopril (an angiotensin-converting enzyme inhibitor) or losartan (an angiotensin receptor blocker) was administered in the drinking water after irradiation. Pulmonary structure and function were assessed after 8 weeks in randomly selected rats by evaluating the breathing rate, ex vivo vascular reactivity, and histopathologic findings. Survival analysis was undertaken on all animals, except those scheduled for death. Results: Survival after a dose of 10 Gy to the thorax was not different from that of unirradiated rats for <= 1 year. Survival decreased to <50% by 45 weeks after 12 Gy and by 8-9 weeks after 15 Gy. Captopril (17-56mg/kg/d) improved survival and reduced radiation-induced increases in breathing rate, changes in vascular reactivity, and histopathologic evidence of injury. Radiation-induced increases in the breathing rate were prevented even if captopril was started I week after irradiation or if it was discontinued after 5 weeks. Losartan, although effective in reducing mortality, was not as efficacious as captopril in mitigating radiation-induced increases in the breathing rate or altered vasoreactivity. Conclusion: In rats, a moderate thoracic radiation dose induced pneumonitis and morbidity. These injuries were mitigated by captopril even when it was begun 1 week after radiation or if discontinued 5 weeks after exposure. Losartan was less effective in protecting against radiation-induced changes in vascular reactivity or tachypnea. (C) 2009 Elsevier Inc.
引用
收藏
页码:1528 / 1536
页数:9
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