A small molecular weight catalytic metalloporphyrin antioxidant with superoxide dismutase (SOD) mimetic properties protects lungs from radiation-induced injury

被引:166
作者
Vujaskovic, Z
Batinic-Haberle, I
Rabbani, ZN
Feng, QF
Kang, SK
Spasojevic, I
Samulski, TV
Fridovich, I
Dewhirst, MW
Anscher, MS
机构
[1] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
[3] Canc Hosp, Chinese Acad Med Sci, Dept Radiat Oncol, Beijing, Peoples R China
关键词
radiation; pulmonary toxicity; superoxide dismutase mimetics; transforming growth factor-beta; rat; free radicals;
D O I
10.1016/S0891-5849(02)00980-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Radiation therapy (RT) is an important therapeutic modality in the treatment of thoracic tumors. The maximum doses to these tumors are often limited by the radiation tolerance of lung tissues. Lung injury from ionizing radiation is believed to be a consequence of oxidative stress and a cascade of cytokine activity. Superoxide dismutase (SOD) is a key enzyme in cellular defenses against oxidative damage. The objective of this study was to determine whether the SOD mimetic AEOL 10 113 [manganese (111) mesotetrakis (N-ethylpyridinium-2-yl) porphyrin (MnTE-2-pyp(5+))] increases the tolerance of lung to ionizing radiation. AEOL 10113 was able to significantly reduce the severity of RT-induced lung injury. This was strongly supported with histopathology results and measurements of collagen deposition (hydroxyproline content). There was a significant reduction in the plasma level of the profibrogenic cytokine transforming growth factor-beta (TGF-beta) in the group of rats receiving RT + AEOL 10113. In conclusion, the novel SOD mimetic, AEOL 10113, demonstrates a significant protective effect from radiation-induced lung injury. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:857 / 863
页数:7
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