Fernández-Gil Beatriz, Moneim Ahmed E Abdel, Ortiz Francisco, Shen Ying-Qiang, Soto-Mercado Viviana, Mendivil-Perez Miguel, Guerra-Librero Ana, Acuña-Castroviejo Darío, Molina-Navarro María M, García-Verdugo José M, Sayed Ramy K A, Florido Javier, Luna Juan D, López Luis Carlos, Escames Germaine
Instituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt.
PLoS One. 2017 Apr 12;12(4):e0174474. doi: 10.1371/journal.pone.0174474. eCollection 2017.
Radiotherapy-induced gut toxicity is among the most prevalent dose-limiting toxicities following radiotherapy. Prevention of radiation enteropathy requires protection of the small intestine. However, despite the prevalence and burden of this pathology, there are currently no effective treatments for radiotherapy-induced gut toxicity, and this pathology remains unclear. The present study aimed to investigate the changes induced in the rat small intestine after external irradiation of the tongue, and to explore the potential radio-protective effects of melatonin gel. Male Wistar rats were subjected to irradiation of their tongues with an X-Ray YXLON Y.Tu 320-D03 irradiator, receiving a dose of 7.5 Gy/day for 5 days. For 21 days post-irradiation, rats were treated with 45 mg/day melatonin gel or vehicle, by local application into their mouths. Our results showed that mitochondrial oxidative stress, bioenergetic impairment, and subsequent NLRP3 inflammasome activation were involved in the development of radiotherapy-induced gut toxicity. Oral treatment with melatonin gel had a protective effect in the small intestine, which was associated with mitochondrial protection and, consequently, with a reduced inflammatory response, blunting the NF-κB/NLRP3 inflammasome signaling activation. Thus, rats treated with melatonin gel showed reduced intestinal apoptosis, relieving mucosal dysfunction and facilitating intestinal mucosa recovery. Our findings suggest that oral treatment with melatonin gel may be a potential preventive therapy for radiotherapy-induced gut toxicity in cancer patients.
放疗引起的肠道毒性是放疗后最常见的剂量限制性毒性之一。预防放射性肠炎需要保护小肠。然而,尽管这种病理情况普遍存在且负担沉重,但目前尚无针对放疗引起的肠道毒性的有效治疗方法,而且这种病理情况仍不清楚。本研究旨在调查舌部外照射后大鼠小肠所诱导的变化,并探索褪黑素凝胶的潜在放射保护作用。雄性Wistar大鼠用X射线YXLON Y.Tu 320 - D03辐照器对其舌部进行照射,每天接受7.5 Gy的剂量,持续5天。在照射后21天内,通过经口局部给药,用45 mg/天的褪黑素凝胶或赋形剂对大鼠进行治疗。我们的结果表明,线粒体氧化应激、生物能量损害以及随后的NLRP3炎性小体激活参与了放疗引起的肠道毒性的发展。口服褪黑素凝胶在小肠中具有保护作用,这与线粒体保护相关,因此与炎症反应减轻、NF-κB/NLRP3炎性小体信号激活减弱有关。因此,用褪黑素凝胶治疗的大鼠肠道凋亡减少,缓解了黏膜功能障碍并促进了肠黏膜恢复。我们的研究结果表明,口服褪黑素凝胶可能是癌症患者放疗引起的肠道毒性的一种潜在预防疗法。