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...
Gespeichert in:
| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
15 April 2010
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| In: |
Free radical biology and medicine
Year: 2010, Jahrgang: 48, Heft: 8, Pages: 1034-1043 |
| ISSN: | 1873-4596 |
| DOI: | 10.1016/j.freeradbiomed.2010.01.020 |
| Online-Zugang: | 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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| Verfasserangaben: | Benjamin Gauter-Fleckenstein, Katharina Fleckenstein, Kouros Owzar, Chen Jiang, Júlio S. Rebouças, Ines Batinic-Haberle, Zeljko Vujaskovic |
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| 245 | 1 | 0 | |a Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage |c Benjamin Gauter-Fleckenstein, Katharina Fleckenstein, Kouros Owzar, Chen Jiang, Júlio S. Rebouças, Ines Batinic-Haberle, Zeljko Vujaskovic |
| 246 | 1 | |i Abweichender Titel |a MnTE-2-PyP 5 + | |
| 246 | 3 | 3 | |a Early and late administration of MnTE-2-PyP 5+ in mitigation and treatment of radiation-induced lung damage |
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| 520 | |a 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. | ||
| 650 | 4 | |a Free radicals | |
| 650 | 4 | |a Lung injury | |
| 650 | 4 | |a Manganese porphyrin | |
| 650 | 4 | |a MnTE-2-PyP | |
| 650 | 4 | |a Oxidative stress | |
| 650 | 4 | |a Radiation | |
| 650 | 4 | |a Radioprotector | |
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| 700 | 1 | |a Jiang, Chen |e VerfasserIn |4 aut | |
| 700 | 1 | |a Rebouças, Júlio S. |e VerfasserIn |4 aut | |
| 700 | 1 | |a Batinic-Haberle, Ines |e VerfasserIn |4 aut | |
| 700 | 1 | |a Vujaskovic, Zeljko |e VerfasserIn |4 aut | |
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