| 两种保护剂对C离子诱导小鼠急性肝损伤的应答 |
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| 引用本文： | 张录卫,张红,刘阳,郝冀方,赵卫平. 两种保护剂对C离子诱导小鼠急性肝损伤的应答[J]. 原子核物理评论, 2010, 27(2): 192-196. DOI: 10.11804/NuclPhysRev.27.02.192 |
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| 作者姓名： | 张录卫 张红 刘阳 郝冀方 赵卫平 |
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| 作者单位： | 1 中国科学院近代物理研究所, 甘肃 兰州 730000; 2 甘肃省重离子束辐射医学应用基础重点实验室, 甘肃 兰州 730000; 3 中国科学院重离子辐射生物医学重点实验室, 甘肃 兰州 730000; 4 中国科学院研究生院, 北京 100049 |
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| 基金项目： | 国家重点基础研究发展计划(973)资助项目，国家自然科学基金重点项目，甘肃省重大科技专项项目，兰州市-中国科学院科技攻关项目 |
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| 摘 要： | 比较了N-乙酰半胱氨酸(NAC)及乙酰左旋肉毒碱(ALCAR)对12C6+离子照射小鼠的损伤效应,并探讨了其可能的作用机制。利用4Gy剂量的12C6+离子束对预先给予NAC(100mg/kg)和ALCAR(100mg/kg)保护的昆明小鼠进行单次全身照射。随后检测肝组织中总抗氧化能力(TAC)、DNA单链断裂和细胞凋亡率。结果显示,与照射对照组相比,提前给予NAC和ALCAR均极显著地增强了肝组织的抗氧化能力(P0.001),减轻了12C6+离子导致的肝组织中DNA断裂(P0.001)和细胞凋亡(P0.001)。此外,还发现ALCAR组抗重离子辐照损伤的能力显著地高于NAC组(P0.05)。实验结果提示了NAC和ALCAR可通过抵御组织内的氧化胁迫,阻止DNA链的断裂和细胞的凋亡,实现对C离子辐照损伤的保护效应。而且ALCAR比NAC可能更适合成为有潜力、有希望的抗C重离子辐射药物。
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| 关 键 词： | N-乙酰半胱氨酸 乙酰左旋肉毒碱 12C6+离子 小鼠 辐射防护 |
| 收稿时间： | 1900-01-01 |
Response of Two Protective Agents to Acute Injury Induced by 12C6+Ions in Mouse Liver |
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| ZHANG Lu-wei,ZHANG Hong,LIU Yang,HAO Ji-fang,ZHAO Wei-ping. Response of Two Protective Agents to Acute Injury Induced by 12C6+Ions in Mouse Liver[J]. Nuclear Physics Review, 2010, 27(2): 192-196. DOI: 10.11804/NuclPhysRev.27.02.192 |
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| Authors: | ZHANG Lu-wei ZHANG Hong LIU Yang HAO Ji-fang ZHAO Wei-ping |
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| Affiliation: | 1 Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000, China;2 Key Laboratory of Heavy Ion Radiation Medicine of Gansu Province, Lanzhou 730000, China; 3 Key Laboratory of Heavy Ion Radiation Biology and Medicine of Chinese Academy of Sciences, Lanzhou 730000, China; 4 Graduate University of Chinese Academy of Sciences, Beijing 100049, China |
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| Abstract: | The present study was to evaluate the effect and mechanism of N acetylcysteine(NAC) and Acetyl L Carnitine hydrochloride(ALCAR) against 12C6+ ion beams on acute injury in the mouse liver. Pretreated with NAC (100 mg/kg) and ALCAR(100 mg/kg), Kun Ming mice were exposed to whole body irradiation with the dose of 4 Gy. Mice were killed 2 h after irradiation, and then the liver tissues were quickly removed. TAC was measured by using chemical reagent kids, and DNA single strand breaks were determined by single cell gel electrophoresis, and the percentage of cell apoptosis were assayed by flow cytometry method. The results showed that NAC and ALCAR pretreatment significantly enhanced TAC(P<0.001), alleviated DNA single strand breaks(P<0.001) and cell apoptosis(P<0.001) of the liver tissues. Moreover, ALCAR mediated radioprotection induced by 12C6+ ions is stronger than that of NAC (P<0.05). The data suggests that NAC and ALCAR both can ameliorate acute injury caused by 12C6+ ions in mice. In this study, NAC and ALCAR exert their radioprotective effect by virtue of resisting oxidative stress, enhancing TAC, alleviating DNA single strand breaks as well as cell apoptosis. Furthermore, the data imply that NAC and ALCAR may be suitable and promising as radioprotective drug against carbon heavy ions. |
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