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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >DMAPT is an Effective Radioprotector from Long-Term Radiation-Induced Damage to Normal Mouse Tissues In Vivo
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DMAPT is an Effective Radioprotector from Long-Term Radiation-Induced Damage to Normal Mouse Tissues In Vivo

机译:Dmapt是一种有效的辐射防护剂,从长期辐射诱导的常规小鼠组织损伤

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While radiotherapy is widely used in cancer treatment, the benefits can be limited by radiation-induced damage to neighboring healthy tissues. We previously demonstrated in mice that the anti-inflammatory compound dimethylamino-parthenolide (DMAPT) selectively induces radiosensitivity in prostate tumor tissue from transgenic adenocarcinoma of mouse prostate (TRAMP) mice, while simultaneously protecting healthy tissues from 6 Gy whole-body radiation-induced apoptosis. Here, we examined the radioprotective effect of DMAPT on fibrosis in normal tissues after a partial-body fractionated radiation protocol that more closely mimics the image-guided fractionated radiotherapy protocols used clinically. Male C57BL/6J mice, 16 weeks old, received 20 Gy fractionated doses of X rays (2 Gy daily fractions, five days/week for two weeks) or sham irradiation to the lower abdomen, with or without a prior 20 mGy dose to mimic an image dose. In addition, mice received thrice weekly DMAPT (100 mg/kg by oral gavage) or vehicle control from 15 weeks of age until time of analysis at 6 weeks postirradiation. In the absence of exposure to radiation, there were no significant differences observed in the tissues of DMAPT and vehicle-treated mice (P > 0.05). DMAPT treatment significantly reduced radiation-induced testis weight loss by 60.9% (P < 0.0001), protected against a decrease in the seminiferous tubule diameter by 42.1% (P < 0.0001) and largely preserved testis morphology. Inclusion of the image dose had no significant effect on testis mass, seminiferous tubule diameter or testis morphology. DMAPT reduced radiation-induced fibrosis in the corpus cavernous region of the penis (98.1% reduction, P = 0.009) and in the muscle layer around the bladder (80.1% reduction, P = 0.0001). There was also a trend towards reduced collagen infiltration into the submucosal and muscle layers in the rectum. These results suggest that DMAPT could be useful in providing protection from the radiation-induced
机译:虽然放射疗法广泛用于癌症治疗,但受益可能受到对邻近健康组织的辐射造成的损伤的限制。我们之前在小鼠中证明了抗炎化合物二甲基氨基 - 嘌呤(DMAPT)从小鼠前列腺(Tramp)小鼠的转基因腺癌​​中选择性地诱导前列腺肿瘤组织中的放射敏感性,同时保护6 Gy全体辐射诱导的细胞凋亡的健康组织。在这里,我们在部分体分级辐射方案之后检查了DMAPT对正常组织纤维化的放射性应对作用,从临床上更紧密地模仿图像引导的分级放疗方案。男性C57BL / 6J小鼠,16周龄,接受了20种分级的X射线(2 Gy每日分数,五天/周为两周)或假辐射到下腹部,有或没有预先的20 MGY剂量以模拟图像剂量。此外,小鼠每周接受每周一次DMAPT(100mg / kg的口服饲养)或从15周的载体控制直到分析时间,在接收6周后分析。在没有暴露于辐射的情况下,在DMAPT和载体处理的小鼠的组织中没有观察到显着差异(P> 0.05)。 DMAPT治疗显着降低了辐射诱导的睾丸体重减轻60.9%(P <0.0001),免受嗜聚细胞小管直径的降低42.1%(p <0.0001)和大量保留的睾丸形态。包含图像剂量对睾丸质量,嗜聚小管直径或睾丸形态没有显着影响。 DMAPT降低了阴茎的肠道区域中的辐射诱导的纤维化(减少98.1%,p = 0.009),并在膀胱周围的肌肉层中(减少80.1%,p = 0.0001)。还存在将胶原蛋白浸润降低到直肠中的粘膜和肌肉层中。这些结果表明,DMAPT可能有助于提供辐射诱导的保护

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