TY - JOUR
T1 - Gamma-tocotrienol, a tocol antioxidant as a potent radioprotector
AU - Ghosh, Sanchita P.
AU - Kulkarni, Shilpa
AU - Hieber, Kevin
AU - Toles, Raymond
AU - Romanyukha, Lyudmila
AU - Kao, Tzu Cheg
AU - Hauer-Jensen, Martin
AU - Kumar, K. Sree
N1 - Funding Information:
This work was supported by the U.S. Department of Defense Threat Reduction Agency grant H.10027_07_AR_R (KSK), administered by The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. and HDTRA 1-07-C-0028 (MH-J). SPG, SK, KH, and LR are affiliated with The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., 1401 Rockville pike, Rockville, MD 20852, USA.
PY - 2009/7
Y1 - 2009/7
N2 - Purpose: To assess the radioprotective potential of gamma-tocotrienol. Materials and methods: To optimise its dose and time regimen, gamma-tocotrienol (GT3) was injected subcutaneously (SC) at different doses into male CD2F1 mice [LD50/30 (lethal radiation dose that results in the mortality of 50% mice in 30 days) radiation dose of 8.6 Gy with vehicle]. The mice were given 10.5, 11 and 11.5 Gy cobalt-60 radiation, and 30-day survival-protection was determined. Time optimisation was done by SC administration of GT3 at different intervals before irradiation. Dose reduction factor (DRF) was determined by probit analysis using mortality as the end point at six radiation doses. Protection from radiation induced pancytopenia was determined by enumerating peripheral blood cells from mice given GT3 and irradiated at 7 Gy. Results: At an optimal dose of 200 mg/kg given SC 24h before irradiation, GT3 had a DRF of 1.29. GT3 accelerated the recovery of total white blood cells, neutrophils, monocytes, platelets, and reticulocytes in irradiated mice, compared to vehicle-injected, irradiated controls. Conclusion: GT3 is a radioprotectant having a higher DRF than any other tocols. The protection it provides close to the gastro-intestinal range indicate that GT3 can be considered as an ideal radioprotectant meriting further drug development stages for the ultimate use in humans.
AB - Purpose: To assess the radioprotective potential of gamma-tocotrienol. Materials and methods: To optimise its dose and time regimen, gamma-tocotrienol (GT3) was injected subcutaneously (SC) at different doses into male CD2F1 mice [LD50/30 (lethal radiation dose that results in the mortality of 50% mice in 30 days) radiation dose of 8.6 Gy with vehicle]. The mice were given 10.5, 11 and 11.5 Gy cobalt-60 radiation, and 30-day survival-protection was determined. Time optimisation was done by SC administration of GT3 at different intervals before irradiation. Dose reduction factor (DRF) was determined by probit analysis using mortality as the end point at six radiation doses. Protection from radiation induced pancytopenia was determined by enumerating peripheral blood cells from mice given GT3 and irradiated at 7 Gy. Results: At an optimal dose of 200 mg/kg given SC 24h before irradiation, GT3 had a DRF of 1.29. GT3 accelerated the recovery of total white blood cells, neutrophils, monocytes, platelets, and reticulocytes in irradiated mice, compared to vehicle-injected, irradiated controls. Conclusion: GT3 is a radioprotectant having a higher DRF than any other tocols. The protection it provides close to the gastro-intestinal range indicate that GT3 can be considered as an ideal radioprotectant meriting further drug development stages for the ultimate use in humans.
KW - Anti-oxidant
KW - Gamma tocotrienol
KW - Ionising radiation
KW - Mice
KW - Radioprotectant
UR - http://www.scopus.com/inward/record.url?scp=67651162024&partnerID=8YFLogxK
U2 - 10.1080/09553000902985128
DO - 10.1080/09553000902985128
M3 - Article
C2 - 19557601
AN - SCOPUS:67651162024
SN - 0955-3002
VL - 85
SP - 598
EP - 606
JO - International Journal of Radiation Biology
JF - International Journal of Radiation Biology
IS - 7
ER -