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• W2045244498 abstract "PurposeThis study was performed to evaluate the protective benefit of amifostine against esophageal injury from fractionated radiation in a rodent model.MethodsFractionated or sham esophageal irradiation was administered to Fisher-344 rats for 5 consecutive daily fractions of 9 Gy using 150 kV X-rays. Animals received an intraperitoneal injection of amifostine or placebo 30 min before each fraction. Histopathologic analyses for mucosal thickness, submucosal collagen deposition, activation of macrophages, oxidative stress and expression/activation of integrinαvβ6 and transforming growth factor (TGF)–β were performed 5 days and 10 weeks after irradiation.ResultsPre-RT mean mucosal thickness was 35 μm in both the placebo and the amifostine groups. Five days post-RT, mean mucosal thicknesses were 30 μm in the placebo group versus 37 μm in the amifostine group (p = 0.024). At 10 weeks post-RT, the group receiving amifostine experienced a significant decrease in tunica muscularis damage (p = 0.002), submucosal collagen deposition (p = 0.027), and macrophage accumulation (p = 0.026) when compared with the placebo group. The levels of immunoreactivity for oxidative stress, TGF-β, and integrinαvβ6 were significantly decreased 10 weeks post-RT in the group receiving amifostine treatment compared with placebo group.ConclusionsThis study demonstrates that amifostine given before each radiation fraction protects against acute and chronic esophageal injury in a rodent model. Protection of the mucosal epithelium integrity by amifostine prevents integrinαvβ6 expression which reduces TGF-β activation and subsequent development of chronic esophageal injury in this model. Further investigation is necessary to determine the clinical relevance of these findings. This study was performed to evaluate the protective benefit of amifostine against esophageal injury from fractionated radiation in a rodent model. Fractionated or sham esophageal irradiation was administered to Fisher-344 rats for 5 consecutive daily fractions of 9 Gy using 150 kV X-rays. Animals received an intraperitoneal injection of amifostine or placebo 30 min before each fraction. Histopathologic analyses for mucosal thickness, submucosal collagen deposition, activation of macrophages, oxidative stress and expression/activation of integrinαvβ6 and transforming growth factor (TGF)–β were performed 5 days and 10 weeks after irradiation. Pre-RT mean mucosal thickness was 35 μm in both the placebo and the amifostine groups. Five days post-RT, mean mucosal thicknesses were 30 μm in the placebo group versus 37 μm in the amifostine group (p = 0.024). At 10 weeks post-RT, the group receiving amifostine experienced a significant decrease in tunica muscularis damage (p = 0.002), submucosal collagen deposition (p = 0.027), and macrophage accumulation (p = 0.026) when compared with the placebo group. The levels of immunoreactivity for oxidative stress, TGF-β, and integrinαvβ6 were significantly decreased 10 weeks post-RT in the group receiving amifostine treatment compared with placebo group. This study demonstrates that amifostine given before each radiation fraction protects against acute and chronic esophageal injury in a rodent model. Protection of the mucosal epithelium integrity by amifostine prevents integrinαvβ6 expression which reduces TGF-β activation and subsequent development of chronic esophageal injury in this model. Further investigation is necessary to determine the clinical relevance of these findings." @default.
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• W2045244498 date "2007-10-01" @default.
• W2045244498 modified "2023-09-26" @default.
• W2045244498 title "Radioprotective Effects of Amifostine on Acute and Chronic Esophageal Injury in Rodents" @default.
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• W2045244498 doi "https://doi.org/10.1016/j.ijrobp.2007.05.062" @default.
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