Dai Jun, Gao Yi, Wang Jian, Zhang Shuyu, Liu Pengfei
( 214400) Jiangyin Clinical College, Xuzhou Medical University, Wuxi 214400, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2024 Sep 20;55(5):1195-1201. doi: 10.12182/20240960403.
Radioactive intestinal injury is a common complication during radiotherapy of tumors. The aim of this study is to observe the effect of ionizing radiation on short-term changes in intestinal bile acids and to investigate the radioprotective effect of bile acids on intestinal cells.
A rat model of small intestinal injury was constructed by exposing the abdomen of the rats to daily irradiation at 2 Gy for 4 d in succession. The bile acids were quantified using metabolomics analysis. IEC-6 cells, a small intestinal epithelial cell line, were divided into a dimethyl sulfoxide (DMSO) control group receiving DMSO and 0 Gy irradiation, a glycoursodeoxycholic acid (GUDCA) experimental group receiving GUDCA and 0 Gy irradiation, a DMSO irradiation group receiving DMSO and 10 Gy irradiation, and a GUDCA irradiation group receiving GUDCA and 10 Gy irradiation. Cell viability and cytotoxicity was assessed by CCK-8 assay test. The apoptosis rate of cells was determined by flow cytometry. The colony formation rate and the radiosensitivity of the cells were determined by colony formation assay on solid media. The expression levels of proteins associated with cell death were determined using Western blot.
After exposure to irradiation, the small intestine tissues of the rats showed typical radioactive intestinal injury. In addition, various bile acids showed fluctuation before and after irradiation. Among the bile acids, GUDCA increased significantly at 3 d after irradiation, but returned to the pre-irradiation level at 7 d after irradiation. Compared with the control group, after GUDCA treatment at 20 μmol/L for 24 h, the cell viability rate after irradiation was significantly higher than that of the DMSO group (<0.05); the expression levels of the proteins, including PARP, caspase-3, RIP, and GSDMD, were significantly lower than those in the control group (<0.05). After GUDCA treatment at 20 μmol/L for 24 h and 48 h, the cell apoptosis rate of the cells after irradiation was lower than that of the DMSO group (<0.05). Compared with the DMSO control group, the colony formation ability of the GUDCA experimental group was stronger than that of the DMSO group after irradiation at 0, 2, 4, and 6 Gy (<0.05). D, or the mean lethal dose, of the GUDCA group was 6.374, while that of the DMSO group was 4.572. Compared with the DMSO control group, the D value of the GUDCA treatment group increased, and the sensitization enhancement ratio (SER) was 0.717.
After exposing the abdomen of rats to irradiation, the intestinal bile acid metabolism of the rats will change significantly, and GUDCA can produce radioprotective effects on intestinal cells to a certain extent.
放射性肠损伤是肿瘤放疗过程中常见的并发症。本研究旨在观察电离辐射对肠道胆汁酸短期变化的影响,并探讨胆汁酸对肠细胞的辐射防护作用。
通过连续4天每天对大鼠腹部进行2 Gy照射构建大鼠小肠损伤模型。采用代谢组学分析对胆汁酸进行定量。将小肠上皮细胞系IEC-6细胞分为接受二甲基亚砜(DMSO)和0 Gy照射的DMSO对照组、接受甘氨熊去氧胆酸(GUDCA)和0 Gy照射的GUDCA实验组、接受DMSO和10 Gy照射的DMSO照射组以及接受GUDCA和10 Gy照射的GUDCA照射组。通过CCK-8检测法评估细胞活力和细胞毒性。采用流式细胞术测定细胞凋亡率。通过固体培养基上的集落形成试验测定细胞的集落形成率和放射敏感性。使用蛋白质印迹法测定与细胞死亡相关的蛋白质表达水平。
照射后,大鼠小肠组织出现典型的放射性肠损伤。此外,各种胆汁酸在照射前后呈现波动。在胆汁酸中,GUDCA在照射后3天显著增加,但在照射后7天恢复到照射前水平。与对照组相比,20 μmol/L GUDCA处理24 h后,照射后细胞活力率显著高于DMSO组(<0.05);包括PARP、caspase-3、RIP和GSDMD在内蛋白质的表达水平显著低于对照组(<0.05)。20 μmol/L GUDCA处理24 h和48 h后,照射后细胞的凋亡率低于DMSO组(<0.05)。与DMSO对照组相比,在0、2、4和6 Gy照射后,GUDCA实验组的集落形成能力强于DMSO组(<0.05)。GUDCA组的平均致死剂量D为6.374,而DMSO组为4.572。与DMSO对照组相比,GUDCA处理组的D值增加,增敏增强比(SER)为0.717。
大鼠腹部照射后,大鼠肠道胆汁酸代谢会发生显著变化,GUDCA可在一定程度上对肠细胞产生辐射防护作用。