4.3 Article

Low molecular weight catalytic metalloporphyrin antioxidant AEOL 10150 protects lungs from fractionated radiation

Journal

FREE RADICAL RESEARCH
Volume 41, Issue 11, Pages 1273-1282

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10715760701689550

Keywords

radiation; pulmonary toxicity; hypoxia; oxidative stress; superoxide dismutase metalloporphyrin mimetic

Funding

  1. NCI NIH HHS [R44 CA96245, R01 CA098452] Funding Source: Medline

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The objective of this study was to determine whether administration of a catalytic antioxidant, Mn(III) tetrakis(N-N'-diethylimidazolium-2-yl) porphyrin, AEOL10150, reduces the severity of long-term lung injury induced by fractionated radiation (RT). Fisher 344 rats were randomized into five groups: RT+AEOL10150 (2.5 mg/kg BID), AEOL10150 (2.5 mg/kg BID) alone, RT+AEOL10150 (5 mg/kg BID), AEOL10150 (5 mg/kg BID) alone and RT alone. Animals received five 8 Gy fractions of RT to the right hemithorax. AEOL10150 was administered 15 min before RT and 8 h later during the period of RT treatment (5 days), followed by subcutaneous injections for 30 days, twice daily. Lung histology at 26 weeks revealed a significant decrease in lung structural damage and collagen deposition in RT+AEOL10150 (5 mg/kg BID) group, in comparison to RT alone. Immunohistochemistry studies revealed a significant reduction in tissue hypoxia (HIF1 alpha, CAIX), angiogenic response (VEGF, CD-31), inflammation (ED-1), oxidative stress (8-OHdG, 3-nitrotyrosine) and fibrosis pathway (TGF beta 1, Smad3, p-Smad2/3), in animals receiving RT + AEOL10150 (5 mg/kg BID). Administration of AEOL10150 at 5 mg/kg BID during and after RT results in a significant protective effect from long-term RT-induced lung injury. Low dose (2.5 mg/kg BID) delivery of AEOL10150 has no beneficial radioprotective effects.

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