Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
Bolder Biotechnology, Boulder, CO, 80301, USA.
Sci Rep. 2020 Apr 22;10(1):6825. doi: 10.1038/s41598-020-63818-7.
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 Co 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.
核辐射的威胁加剧,因此必须确定急性辐射综合征的潜在对策。目前,尚无预防给药的对策获得批准。有效的对策应能在短期内提高生存率,并长期提高受照射个体的总体预后。在这里,我们描述了一种有前途的辐射对策 BBT-059 的使用,以及在雄性 CD2F1 品系中进行的长达 12 个月的长期小鼠研究(使用 Coγ射线照射,约 0.6Gy/min,7.5-12.5Gy)的结果。我们报告了 BBT-059(0.3mg/kg)的剂量减少因子为 1.28,与照射前 24 小时给予对照药物相比。在长期研究中,与制剂缓冲液相比,药物治疗的小鼠在外周血细胞计数、骨髓集落形成单位、胸骨细胞数和巨核细胞数方面的恢复速度更快。此外,在接受最高剂量辐射的动物的肾脏中观察到衰老加速。在给予对照药物的动物的脾脏裂解物中观察到 E-钙黏蛋白、LaminB1 水平降低,Cyc-D 和 p21 水平升高。总的来说,这些结果表明,在接受致死和超致死全身γ射线剂量照射的小鼠中,给予 BBT-059 后具有高水平的保护作用。