Doi Hiroshi, Matsumoto Seiji, Odawara Soichi, Shikata Toshiyuki, Kitajima Kazuhiro, Tanooka Masao, Takada Yasuhiro, Tsujimura Tohru, Kamikonya Norihiko, Hirota Shozo
Department of Radiology, Hyogo College of Medicine, Nishinomiya, Hyogo 663-8501, Japan.
Department of Thoracic Surgery, Hyogo College of Medicine, Nishinomiya, Hyogo 663-8501, Japan.
Exp Ther Med. 2017 May;13(5):1765-1772. doi: 10.3892/etm.2017.4192. Epub 2017 Mar 8.
Pravastatin is an inhibitor of 3-hydroxy-3-methyl- glutaryl-coenzyme A reductase that has been reported to have therapeutic applications in a range of inflammatory conditions. The aim of the present study was to assess the radioprotective effects of pravastatin in an experimental animal model. Mice were divided into two groups: The control group received ionizing radiation with no prior medication, while the pravastatin group received pravastatin prior to ionizing radiation. Pravastatin was administered orally at 30 mg/kg body weight in drinking water at 24 and 4 h before irradiation. Intestinal crypt epithelial cell survival and the incidence of apoptosis in the intestine and lung were measured post-irradiation. The effect of pravastatin on intestinal DNA damage was determined by immunohistochemistry. Finally, the effect of pravastatin on tumor response to radiotherapy was examined in a mouse mesothelioma xenograft model. Pravastatin increased the number of viable intestinal crypts and this effect was statistically significant in the ileum (P<0.0001). The pravastatin group showed significantly lower apoptotic indices in all examined parts of the intestine (P<0.0001) and tended to show reduced apoptosis in the lung. Pravastatin reduced the intestinal expression of ataxia-telangiectasia mutated and gamma-H2AX after irradiation. No apparent pravastatin-related differences were observed in the response of xenograft tumors to irradiation. In conclusion, pravastatin had radioprotective effects on the intestine and lung and reduced radiation-induced DNA double-strand breaks. Pravastatin may increase the therapeutic index of radiotherapy.
普伐他汀是3-羟基-3-甲基戊二酰辅酶A还原酶的抑制剂,据报道在一系列炎症性疾病中具有治疗应用。本研究的目的是评估普伐他汀在实验动物模型中的辐射防护作用。将小鼠分为两组:对照组在未预先用药的情况下接受电离辐射,而普伐他汀组在电离辐射前接受普伐他汀。在照射前24小时和4小时,以30mg/kg体重的剂量通过饮水口服给予普伐他汀。照射后测量肠道隐窝上皮细胞存活率以及肠道和肺部的凋亡发生率。通过免疫组织化学确定普伐他汀对肠道DNA损伤的影响。最后,在小鼠间皮瘤异种移植模型中研究普伐他汀对肿瘤放疗反应的影响。普伐他汀增加了存活肠道隐窝的数量,并且在回肠中这种作用具有统计学意义(P<0.0001)。普伐他汀组在肠道所有检查部位的凋亡指数均显著降低(P<0.0001),并且在肺部凋亡倾向于减少。普伐他汀降低了照射后肠道中共济失调毛细血管扩张突变蛋白和γ-H2AX的表达。在异种移植肿瘤对照射的反应中未观察到明显的与普伐他汀相关的差异。总之,普伐他汀对肠道和肺部具有辐射防护作用,并减少了辐射诱导的DNA双链断裂。普伐他汀可能会提高放疗的治疗指数。