Metabolomic studies in tissues of mice treated with amifostine and exposed to gamma-radiation

被引:30
作者
Cheema, Amrita K. [1 ,2 ]
Li, Yaoxiang [1 ]
Girgis, Michael [1 ]
Jayatilake, Meth [1 ]
Simas, Madison [3 ,4 ]
Wise, Stephen Y. [3 ,4 ]
Olabisi, Ayodele O. [4 ]
Seed, Thomas M. [5 ]
Singh, Vijay K. [3 ,4 ]
机构
[1] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Dept Oncol, Washington, DC 20007 USA
[2] Georgetown Univ, Dept Biochem Mol & Cellular Biol, Med Ctr, Washington, DC USA
[3] Uniformed Serices Univ Hlth Sci, F Edward Hebert Sch Med, Dept Pharmacol & Mol Therapeut, Div Radioprotectants, Bethesda, MD 20814 USA
[4] Uniformed Serices Univ Hlth Sci, Armed Forces Radiobiol Res Inst, Bethesda, MD 20814 USA
[5] Tech Micro Serv, Bethesda, MD USA
关键词
MYELOID-LEUKEMIA; CHEMOTHERAPY; PROTECTION; WR-2721; COUNTERMEASURES; RADIOPROTECTION; GLUTATHIONE; CISPLATIN; EFFICACY; INJURY;
D O I
10.1038/s41598-019-52120-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although multiple radioprotectors are currently being investigated preclinically for efficacy and safety, few studies have investigated concomitant metabolic changes. This study examines the effects of amifostine on the metabolic profiles in tissues of mice exposed to cobalt-60 total-body gamma-radiation. Global metabolomic and lipidomic changes were analyzed using ultra-performance liquid chromatography (UPLC) quadrupole time-of-flight mass spectrometry (QTOF-MS) in bone marrow, jejunum, and lung samples of amifostine-treated and saline-treated control mice. Results demonstrate that radiation exposure leads to tissue specific metabolic responses that were corrected in part by treatment with amifostine in a drug-dose dependent manner. Bone marrow exhibited robust responses to radiation and was also highly responsive to protective effects of amifostine, while jejunum and lung showed only modest changes. Treatment with amifostine at 200 mg/kg prior to irradiation seemed to impart maximum survival benefit, while the lower dose of 50 mg/kg offered only limited survival benefit. These findings show that the administration of amifostine causes metabolic shifts that would provide an overall benefit to radiation injury and underscore the utility of metabolomics and lipidomics to determine the underlying physiological mechanisms involved in the radioprotective efficacy of amifostine. This approach may be helpful in identifying biomarkers for radioprotective efficacy of amifostine and other countermeasures under development.
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页数:13
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