检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李民英[1,2] 雷风[2] 尤玮[3] 谭宇静[2] 陆小军[2] 陈龙华[1] 张积仁[3]
机构地区:[1]南方医科大学南方医院放疗科,广东广州510515 [2]中山市人民医院放射治疗科,广东中山528403 [3]南方医科大学珠江医院肿瘤中心,广东广州510282
出 处:《南方医科大学学报》2010年第8期1787-1789,共3页Journal of Southern Medical University
基 金:国家自然科学基金(30772530)
摘 要:目的探讨氧化型辅酶Ⅰ(NAD^+)抗辐射损伤作用及其量效关系。方法L02人正常肝细胞株加入含10%胎牛血清的RPMl 1640培养基中常规方法培养,X线照射后和在照射后即刻加入NAD^+,采用MTT法检测细胞活性,TUNEL法检测细胞凋亡,观察X线照射对L02人正常肝细胞的辐射损伤,并观察NAD+对受照射L02肝细胞辐射损伤的影响作用及其与NAD^+浓度的关系。结果L02人正常肝细胞受X线照射后细胞损伤随照射吸收剂量的增大而加重,受照射后24h细胞抑制作用最显著,细胞损伤多表现为细胞凋亡;加入NAD^+可提高受照射细胞存活率,其作用在NAD^+终浓度为100-1000μg/ml范围内与浓度呈正相关,在浓度大于1000μg/ml后,加大浓度并不再显著增加受照射细胞的存活率。结论NAD^+具有一定的抗细胞辐射损伤作用,其作用在一定范围内与其浓度呈正相关关系。Objective To explore the effect ofNAD+ against radiation injury and its dose-effect relationship. Methods L02 liver cells cultured in RPMI 1640 medium containing 10% fetal calf serum were exposed to X-ray irradiation followed by immediate application of NAD+. The cellular viability was analyzed by MTT assay and the apoptotic cells were detected by TUNEL methods to observe the damages of L02 liver cells induced by X-ray exposure and analyze the dose-effect relationship of NAD+. Results The viability of L02 liver cells was decreased with increasing dose of X-ray irradiation. The most obvious growth inhibition of L02 cells occurred 24 h after the irradiation. NAD+ significantly increased the cell survival rate alter irradiation, and this effect was gradually increased within the concentration range of 100-1000 μg/ml; at higher concentrations, the survival rate of the irradiated L02 cells showed no significant increase. Conclusion NAD+ provides partial protection of the liver cells against radiation injury, and the effect is positively correlated to NAD+ concentration within a certain range.
关 键 词:肝细胞 辐射损伤 凋亡 烟酰胺腺嘌呤二核苷酸
分 类 号:R144[医药卫生—公共卫生与预防医学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.201