Abstract

The threat of nuclear exposure is heightened and it is imperative to identify potential countermeasures for acute radiation syndrome. Currently no countermeasures have been approved for prophylactic administration. Effective countermeasures should function to increase survival in the short term as well as to increase the overall prognosis of an exposed individual long term. Here we describe the use of a promising radiation countermeasure, BBT-059, and the results of a long term mouse study (up to 12 months) in the male CD2F1 strain using 60Co gamma irradiation (~0.6 Gy/min, 7.5–12.5 Gy). We report the dose reduction factor of 1.28 for BBT-059 (0.3 mg/kg) compared to control administered 24 h prior to irradiation. In the long term study animals showed accelerated recovery in peripheral blood cell counts, bone marrow colony forming units, sternal cellularity and megakaryocyte numbers in drug treated mice compared to formulation buffer. In addition, increased senescence was observed in the kidneys of animals administered control or drug and exposed to the highest doses of radiation. Decreased levels of E-cadherin, LaminB1 and increased levels of Cyc-D and p21 in spleen lysates were observed in animals administered control. Taken together the results indicate a high level of protection following BBT-059 administration in mice exposed to lethal and supralethal doses of total body gamma-radiation.

Details

Title
Delayed effects of acute whole body lethal radiation exposure in mice pre-treated with BBT-059
Author
Sharma, Neel K 1 ; Holmes-Hampton, Gregory P 1   VIAFID ORCID Logo  ; Kumar, Vidya P 1 ; Biswas Shukla 1 ; Kefale, Wuddie 1 ; Stone, Sasha 1 ; Zemenu, Aschenake 1 ; Wilkins, William L 1 ; Fam, Christine M 2 ; Cox, George N 2 ; Ghosh, Sanchita P 1 

 Uniformed Services University of the Health Sciences, Armed Forces Radiobiology Research Institute, Bethesda, USA (GRID:grid.265436.0) (ISNI:0000 0001 0421 5525) 
 Bolder Biotechnology, Boulder, USA (GRID:grid.281350.d) 
Publication year
2020
Publication date
2020
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2393623610
Copyright
© The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.