Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage

Chronic production of reactive oxygen and nitrogen species is an underlying mechanism of irradiation (IR)-induced lung injury. The purpose of this study was to determine the optimum time of delivery of an antioxidant and redox-modulating Mn porphyrin, MnTE-2-PyP5+, to mitigate and/or treat IR-induce...

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Main Authors: Gauter-Fleckenstein, Benjamin (Author) , Fleckenstein, Katharina (Author) , Owzar, Kouros (Author) , Jiang, Chen (Author) , Rebouças, Júlio S. (Author) , Batinic-Haberle, Ines (Author) , Vujaskovic, Zeljko (Author)
Format: Article (Journal)
Language:English
Published: 15 April 2010
In: Free radical biology and medicine
Year: 2010, Volume: 48, Issue: 8, Pages: 1034-1043
ISSN:1873-4596
DOI:10.1016/j.freeradbiomed.2010.01.020
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.freeradbiomed.2010.01.020
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0891584910000390
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Author Notes:Benjamin Gauter-Fleckenstein, Katharina Fleckenstein, Kouros Owzar, Chen Jiang, Júlio S. Rebouças, Ines Batinic-Haberle, Zeljko Vujaskovic
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Summary:Chronic production of reactive oxygen and nitrogen species is an underlying mechanism of irradiation (IR)-induced lung injury. The purpose of this study was to determine the optimum time of delivery of an antioxidant and redox-modulating Mn porphyrin, MnTE-2-PyP5+, to mitigate and/or treat IR-induced lung damage. Female Fischer-344 rats were irradiated to their right hemithorax (28 Gy). Irradiated animals were treated with PBS or MnTE-2-PyP5+ (6 mg /kg/24 h) delivered for 2 weeks by sc-implanted osmotic pumps (beginning after 2, 6, 12, 24, or 72 h or 8 weeks). Animals were sacrificed 10 weeks post-IR. Endpoints were body weight, breathing frequency, histopathology, and immunohistochemistry (8-OHdG, ED-1, TGF-β, HIF-1α, VEGF A). A significant radioprotective effect on functional injury, measured by breathing frequency, was observed for all animals treated with MnTE-2-PyP5+. Treatment with MnTE-2-PyP5+ starting 2, 6, and 12 h but not after 24 or 72 h resulted in a significant decrease in immunostaining for 8-OHdG, HIF-1α, TGF-β, and VEGF A. A significant decrease in HIF-1α, TGF-β, and VEGF A, as well as an overall reduction in lung damage (histopathology), was observed in animals beginning treatment at the time of fully developed lung injury (8 weeks post-IR). The catalytic manganese porphyrin antioxidant and modulator of redox-based signaling pathways MnTE-2-PyP5+ mitigates radiation-induced lung injury when given within the first 12 h after IR. More importantly, this is the first study to demonstrate that MnTE-2-PyP5+ can reverse overall lung damage when started at the time of established lung injury 8 weeks post-IR. The radioprotective effects are presumably mediated through its ability both to suppress oxidative stress and to decrease activation of key transcription factors and proangiogenic and profibrogenic cytokines.
Item Description:Online veröffentlicht: 20. Januar 2010
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Physical Description:Online Resource
ISSN:1873-4596
DOI:10.1016/j.freeradbiomed.2010.01.020