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

Publication ,  Journal Article
Gauter-Fleckenstein, B; Fleckenstein, K; Owzar, K; Jiang, C; Rebouças, JS; Batinic-Haberle, I; Vujaskovic, Z
Published in: Free Radic Biol Med
April 15, 2010

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-PyP(5+), 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-PyP(5+) (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-beta, HIF-1alpha, VEGF A). A significant radioprotective effect on functional injury, measured by breathing frequency, was observed for all animals treated with MnTE-2-PyP(5+). Treatment with MnTE-2-PyP(5+) starting 2, 6, and 12 h but not after 24 or 72 h resulted in a significant decrease in immunostaining for 8-OHdG, HIF-1alpha, TGF-beta, and VEGF A. A significant decrease in HIF-1alpha, TGF-beta, 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-PyP(5+) 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-PyP(5+) 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.

Duke Scholars

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Published In

Free Radic Biol Med

DOI

EISSN

1873-4596

Publication Date

April 15, 2010

Volume

48

Issue

8

Start / End Page

1034 / 1043

Location

United States

Related Subject Headings

  • Time Factors
  • Respiration
  • Rats, Inbred F344
  • Rats
  • Radiation-Protective Agents
  • Radiation Pneumonitis
  • Metalloporphyrins
  • Female
  • Biochemistry & Molecular Biology
  • Antioxidants
 

Citation

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Gauter-Fleckenstein, B., Fleckenstein, K., Owzar, K., Jiang, C., Rebouças, J. S., Batinic-Haberle, I., & Vujaskovic, Z. (2010). Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage. Free Radic Biol Med, 48(8), 1034–1043. https://doi.org/10.1016/j.freeradbiomed.2010.01.020
Gauter-Fleckenstein, Benjamin, Katharina Fleckenstein, Kouros Owzar, Chen Jiang, Júlio S. Rebouças, Ines Batinic-Haberle, and Zeljko Vujaskovic. “Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage.Free Radic Biol Med 48, no. 8 (April 15, 2010): 1034–43. https://doi.org/10.1016/j.freeradbiomed.2010.01.020.
Gauter-Fleckenstein B, Fleckenstein K, Owzar K, Jiang C, Rebouças JS, Batinic-Haberle I, et al. Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage. Free Radic Biol Med. 2010 Apr 15;48(8):1034–43.
Gauter-Fleckenstein, Benjamin, et al. “Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage.Free Radic Biol Med, vol. 48, no. 8, Apr. 2010, pp. 1034–43. Pubmed, doi:10.1016/j.freeradbiomed.2010.01.020.
Gauter-Fleckenstein B, Fleckenstein K, Owzar K, Jiang C, Rebouças JS, Batinic-Haberle I, Vujaskovic Z. Early and late administration of MnTE-2-PyP5+ in mitigation and treatment of radiation-induced lung damage. Free Radic Biol Med. 2010 Apr 15;48(8):1034–1043.
Journal cover image

Published In

Free Radic Biol Med

DOI

EISSN

1873-4596

Publication Date

April 15, 2010

Volume

48

Issue

8

Start / End Page

1034 / 1043

Location

United States

Related Subject Headings

  • Time Factors
  • Respiration
  • Rats, Inbred F344
  • Rats
  • Radiation-Protective Agents
  • Radiation Pneumonitis
  • Metalloporphyrins
  • Female
  • Biochemistry & Molecular Biology
  • Antioxidants