Chandrasekharan Dhanya K, Kagiya Tsutomu V, Nair Cherupally Krishnan Krishnan
Amala Cancer Research Centre, Thrissur, Kerala, India.
J Radiat Res. 2009 May;50(3):203-12. doi: 10.1269/jrr.08090. Epub 2009 Apr 22.
A palmitoyl derivative of ascorbic acid 2-glucoside, 6-palmitoyl ascorbic acid-2-glucoside (PAsAG), which possess good antioxidant properties, is examined for radioprotection in vitro, ex vivo and in vivo models. PAsAG protected plasmid DNA from gamma-radiation induced damages under in vitro conditions. Presence of 1.6 mM PAsAG inhibited the disappearance of ccc (covalently closed circular) form of plasmid pBR322 with a dose modifying factor of 1.5. Comet assay studies on mouse spleen cells exposed to 6 Gy gamma-radiation (ex vivo) in presence and absence of PAsAG revealed that cellular DNA was effectively protected by this compound from radiation induced damages. Oral administration of 80 mg/kg body weight of PAsAG to mice 1 hour prior to 6 Gy whole body gamma-radiation exposure, efficiently protected cellular DNA in tissues such as spleen, bone marrow and blood, from radiation induced damages as indicated by alkaline comet assay. Oxidative stress in tissues such as liver and brain of mice, following whole body exposure to various doses of gamma-radiation (2-8 Gy), monitored as levels of GSH and peroxidation of lipids, were found considerably reduced when PAsAG was orally administered (80 mg/kg body weight) to the mice one hour prior to the radiation exposure. PAsAG administration improved the per cent survival of mice following exposure to 10 Gy whole body gamma-radiation. Thus PAsAG could act as a radioprotector under in vitro, ex vivo and in vivo conditions of ionizing-radiation exposure.
抗坏血酸2 - 葡糖苷的棕榈酰衍生物,即6 - 棕榈酰抗坏血酸 - 2 - 葡糖苷(PAsAG),具有良好的抗氧化性能,已在体外、离体和体内模型中进行了辐射防护研究。在体外条件下,PAsAG保护质粒DNA免受γ射线诱导的损伤。1.6 mM的PAsAG存在时,抑制了质粒pBR322共价闭合环状(ccc)形式的消失,剂量修正因子为1.5。对在有和没有PAsAG存在的情况下暴露于6 Gy γ射线(离体)的小鼠脾细胞进行彗星试验研究表明,该化合物能有效保护细胞DNA免受辐射诱导的损伤。在6 Gy全身γ射线照射前1小时给小鼠口服80 mg/kg体重的PAsAG,碱性彗星试验表明,该化合物能有效保护脾脏、骨髓和血液等组织中的细胞DNA免受辐射诱导的损伤。在全身暴露于不同剂量γ射线(2 - 8 Gy)后,监测小鼠肝脏和脑组织中的氧化应激,以谷胱甘肽水平和脂质过氧化水平衡量,发现当在辐射暴露前1小时给小鼠口服(80 mg/kg体重)PAsAG时,氧化应激显著降低。PAsAG给药提高了小鼠在暴露于10 Gy全身γ射线后的存活率。因此,在电离辐射暴露的体外、离体和体内条件下,PAsAG可作为一种辐射防护剂。