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Characterization of the dose response relationship for lung injury following acute radiation exposure in three well-established murine strains: developing an interspecies bridge to link animal models with human lung.
Jackson, Isabel L; Xu, Pu-Ting; Nguyen, Giao; Down, Julian D; Johnson, Cynthia S; Katz, Barry P; Hadley, Caroline C; Vujaskovic, Zeljko.
Afiliación
  • Jackson IL; *University of Maryland School of Medicine, Baltimore, MD, 21201; †Duke University Medical Center, Durham, NC 27710; ‡Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA; §Indiana University School of Medicine, Indianapolis, IN; **Baylor University College of Medicine, Houston, TX.
Health Phys ; 106(1): 48-55, 2014 Jan.
Article en En | MEDLINE | ID: mdl-24276549
Approval of radiation countermeasures through the FDA Animal Rule requires pivotal efficacy screening in one or more species that are expected to react with a response similar to humans (21 C.F.R. § 314.610, drugs; § 601.91, biologics). Animal models used in screening studies should reflect the dose response relationship (DRR), clinical presentation, and pathogenesis of lung injury in humans. Over the past 5 y, the authors have characterized systematically the temporal onset, dose-response relationship (DRR), and pathologic outcomes associated with acute, high dose radiation exposure in three diverse mouse strains. In these studies, C57L/J, CBA/J, and C57BL/6J mice received wide field irradiation to the whole thorax with shielding of the head, abdomen, and forelimbs. Doses were delivered at a rate of 69 cGy min using an x-ray source operated at 320 kVp with half-value layer (HVL) of 1 mm Cu. For all strains, radiation dose was associated significantly with 180 d mortality (p < 0.0001). The lethal dose for 50% of animals within the first 180 d (LD50/180) was 11.35 Gy (95% CI 11.1-11.6 Gy) for C57L/J mice, 14.17 Gy (95% CI 13.9-14.5 Gy) for CBA/J mice, and 14.10 Gy (95% CI 12.2-16.4 Gy) for C57BL/6J mice. The LD50/180 in the C57L/J strain was most closely analogous to the DRR for clinical incidence of pneumonitis in non-human primates (10.28 Gy; 95% CI 9.9-10.7 Gy) and humans (10.60 Gy; 95% CI 9.9-12.1 Gy). Furthermore, in the C57L/J strain, there was no gender-specific difference in DRR (p = 0.5578). The reliability of the murine models is demonstrated by the reproducibility of the dose-response and consistency of disease presentation across studies.Health Phys. 106(1):000-000; 2014.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Traumatismos Experimentales por Radiación / Neumonitis por Radiación / Modelos Animales de Enfermedad / Pulmón Tipo de estudio: Etiology_studies Límite: Animals / Female / Humans Idioma: En Revista: Health Phys Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Traumatismos Experimentales por Radiación / Neumonitis por Radiación / Modelos Animales de Enfermedad / Pulmón Tipo de estudio: Etiology_studies Límite: Animals / Female / Humans Idioma: En Revista: Health Phys Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos