Hosseinimehr Seyed Jalal
Department of Medicinal Chemistry, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Drug Discov Today. 2007 Oct;12(19-20):794-805. doi: 10.1016/j.drudis.2007.07.017. Epub 2007 Sep 10.
People may be exposed to ionizing radiation during radiotherapy or following exposure to radionuclides in nuclear medicine. Radioprotective agents have been used to reduce morbidity or mortality produced by ionizing irradiation. Early developments of such agents focused on thiol synthetic compounds, such as amifostine. This compound reduced mortality; however, there were difficulties in administering aminothiols that led to adverse effects. Hence, the development of radioprotective agents with lower toxicity and an extended window of protection has attracted much attention. Natural compounds have been evaluated as radioprotectants and they seem to exert their effect through antioxidant and immunostimulant activities. Although recent agents have lower efficacy, they have lower toxicity, more favourable administration routes and improved pharmacokinetics compared to the older thiol compounds.
人们在放射治疗期间或接触核医学中的放射性核素后可能会受到电离辐射。辐射防护剂已被用于降低电离辐射产生的发病率或死亡率。此类药物的早期研发集中在硫醇合成化合物上,比如氨磷汀。这种化合物降低了死亡率;然而,氨基硫醇的给药存在困难,会导致不良反应。因此,开发毒性更低、保护窗口更长的辐射防护剂备受关注。天然化合物已被评估为辐射防护剂,它们似乎通过抗氧化和免疫刺激活性发挥作用。尽管近期的药物疗效较低,但与旧的硫醇化合物相比,它们具有更低的毒性、更有利的给药途径和更好的药代动力学。