Gamma tocotrienol, a potent radioprotector, preferentially upregulates expression of anti-apoptotic genes to promote intestinal cell survival

被引:38
作者
Suman, Shubhankar [1 ,2 ]
Datta, Kamal [1 ,2 ]
Chakraborty, Kushal [3 ]
Kulkarni, Shilpa S. [3 ]
Doiron, Kathryn [1 ,2 ]
Fornace, Albert J., Jr. [1 ,2 ,4 ]
Kumar, K. Sree [3 ]
Hauer-Jensen, Martin [5 ,6 ]
Ghosh, Sanchita P. [4 ]
机构
[1] Georgetown Univ, Dept Biochem & Mol & Cellular Biol, Med Ctr, Washington, DC 20057 USA
[2] Georgetown Univ, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[3] Armed Forces Radiobiol Res Inst, Bethesda, MD 20892 USA
[4] King Abdulaziz Univ, CEGMR, Jeddah 21413, Saudi Arabia
[5] Univ Arkansas Med Sci, Coll Pharm, Div Radiat Hlth, Little Rock, AR 72205 USA
[6] Cent Arkansas Vet Healthcare Syst, Surg Serv, Little Rock, AR USA
基金
美国国家航空航天局;
关键词
Radiation; Gamma tocotrienol; Apoptosis; Gastrointestinal toxicity; Radioprotection; RADIATION-INDUCED APOPTOSIS; TOTAL-BODY IRRADIATION; DNA-DAMAGE; OXIDATIVE STRESS; STEM-CELLS; MICE; PROTECTS; INJURY; MOUSE; P53;
D O I
10.1016/j.fct.2013.08.011
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Gamma tocotrienol (GT3) has been reported as a potent ameliorator of radiation-induced gastrointestinal (GI) toxicity when administered prophylactically. This study aimed to evaluate the role of GT3 mediated pro- and anti-apoptotic gene regulation in protecting mice from radiation-induced GI damage. Male 10- to 12-weeks-old CD2F1 mice were administered with a single dose of 200 mg/kg of GT3 or equal volume of vehicle (5% Tween-80) 24 h before exposure to 11 Gy of whole-body gamma-radiation. Mouse jejunum was surgically removed 4 and 24 h after radiation exposure, and was used for PCR array, histology, immunohistochemistry, and immunoblot analysis. Results were compared among vehicle pre-treated no radiation, vehicle pre-treated irradiated, and GT3 pre-treated irradiated groups. GT3 pretreated irradiated groups, both 4 h and 24 h after radiation, showed greater upregulation of anti-apoptotic gene expression than vehicle pretreated irradiated groups. TUNEL staining and intestinal crypt analysis showed protection of jejunum after GT3 pre-treatment and immunoblot results were supportive of PCR data. Our study demonstrated that GT3-mediated protection of intestinal cells from a GI-toxic dose of radiation occurred via upregulation of antiapoptotic and downregulation of pro-apoptotic factors, both at the transcript as well as at the protein levels. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:488 / 496
页数:9
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