Establishing Pediatric Mouse Models of the Hematopoietic Acute Radiation Syndrome and the Delayed Effects of Acute Radiation Exposure.


Journal

Radiation research
ISSN: 1938-5404
Titre abrégé: Radiat Res
Pays: United States
ID NLM: 0401245

Informations de publication

Date de publication:
01 04 2021
Historique:
received: 20 11 2020
accepted: 19 01 2021
pubmed: 13 2 2021
medline: 24 4 2021
entrez: 12 2 2021
Statut: ppublish

Résumé

Medical countermeasures (MCMs) for hematopoietic acute radiation syndrome (H-ARS) should be evaluated in well-characterized animal models, with consideration of at-risk populations such as pediatrics. We have developed pediatric mouse models of H-ARS and delayed effects of acute radiation exposure (DEARE) for efficacy testing of MCMs against radiation. Male and female C57BL/6J mice aged 3, 4, 5, 6, 7 and 8 weeks old (±1 day) were characterized for baseline hematopoietic and gastrointestinal parameters, radiation response, efficacy of a known MCM, and DEARE at six and 12 months after total-body irradiation (TBI). Weanlings (age 3 weeks) were the most radiosensitive age group with an estimated LD50/30 of 712 cGy, while mice aged 4 to 8 weeks were more radioresistant with an estimated LD50/30 of 767-787 cGy. Female weanlings were more radiosensitive than males at 3 and 4 weeks old but became significantly more radioresistant after the pubertal age of 5 weeks. The most dramatic increase in body weight, RBC counts and intestinal circumference length occurred from 3 to 5 weeks of age. The established radiomitigator Neulasta® (pegfilgrastim) significantly increased 30-day survival in all age groups, validating these models for MCM efficacy testing. Analyses of DEARE among pediatric survivors revealed depressed weight gain in males six months post-TBI, and increased blood urea nitrogen at 12 months post-TBI which was more severe in females. Hematopoietic DEARE at six months post-TBI appeared to be less severe in survivors from the 3- and 4-week-old groups but was equally severe in all age groups by 12 months of age. Similar to our other acute radiation mouse models, there was no appreciable effect of Neulasta used as an H-ARS MCM on the severity of DEARE. In summary, these data characterize a pediatric mouse model useful for assessing the efficacy of MCMs against ARS and DEARE in children.

Identifiants

pubmed: 33577641
pii: 461407
doi: 10.1667/RADE-20-00259.1
doi:

Substances chimiques

pegfilgrastim 3A58010674
Polyethylene Glycols 3WJQ0SDW1A
Filgrastim PVI5M0M1GW

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

307-323

Subventions

Organisme : NIAID NIH HHS
ID : HHSN266200500030C
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201000046C
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA082709
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK090948
Pays : United States

Informations de copyright

©2021 by Radiation Research Society. All rights of reproduction in any form reserved.

Auteurs

Andrea M Patterson (AM)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Rajendran Sellamuthu (R)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

P Artur Plett (PA)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Carol H Sampson (CH)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Hui Lin Chua (HL)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Alexa Fisher (A)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Sasidhar Vemula (S)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Hailin Feng (H)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Barry P Katz (BP)

Department of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana.

Gregory Tudor (G)

Epistem, Ltd., Manchester, United Kingdom.

Steven J Miller (SJ)

Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.

Thomas J MacVittie (TJ)

Department of Radiation Oncology, University of Maryland School of Medicine, Baltimore, Maryland.

Catherine Booth (C)

Epistem, Ltd., Manchester, United Kingdom.

Christie M Orschell (CM)

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

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Classifications MeSH