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α-生育酚琥珀酸酯通过诱导粒细胞集落刺激因子保护小鼠免受γ辐射。

Alpha-tocopherol succinate protects mice from gamma-radiation by induction of granulocyte-colony stimulating factor.

机构信息

Radiation Countermeasures Program, Armed Forces Radiobiology Research Institute, Bethesda, Maryland 20889-5603, USA.

出版信息

Int J Radiat Biol. 2010 Jan;86(1):12-21. doi: 10.3109/09553000903264515.

Abstract

PURPOSE

The purpose of this study was to further elucidate the role of granulocyte-colony stimulating factor (G-CSF)-induced in response to alpha-tocopherol succinate (TS) administration in protecting mice from total body irradiation (TBI).

MATERIAL AND METHODS

The dose, route, and schedule of TS administration for optimal G-CSF induction were determined by giving TS through subcutaneous (sc) and oral routes to male CD2F1 mice. The level of cytokine in serum was determined by multiplex Luminex. The role of G-CSF on survival after TBI was determined by first treating mice with a protective dose (400 mg/kg) of TS 24 h before exposure to a lethal dose (9.2 Gy, 0.6 Gy/min) of cobalt-60 gamma-irradiation. The treated mice were then given neutralising antibody to G-CSF 16 h before TBI to abrogate the radioprotective efficacy of TS. The efficacy of whole blood samples obtained from TS-treated mice was evaluated to protect naïve lethally irradiated mice. The hematopoietic stem cells in blood from TS-treated mice were analysed by fluorescence-activated cell sorting (FACS).

RESULTS

Maximal levels of G-CSF were observed in peripheral blood 24 h after sc administration of TS. When TS-treated mice were given neutralising antibody to G-CSF, TS failed to protect against TBI. After being challenged with an LD90/30 (lethal dose causing 90% mortality over 30 days) dose of gamma-radiation, mice infused with whole blood from TS- and AMD3100 (1,1'-{1,4-phenylenebis(methylene)}bis-1,4,8,11-tetraazacyclotetradecane octahydrochloride)-treated mice exhibited significantly higher survival compared with those infused with whole blood from vehicle-injected mice. FACS data revealed that hematopoietic stem cells were mobilised into the peripheral blood.

CONCLUSIONS

The results indicate that G-CSF-induced by the administration of TS, mobilises hematopoietic stem cells and is responsible for the protection from ionising radiation.

摘要

目的

本研究旨在进一步阐明α-生育酚琥珀酸酯(TS)给药诱导粒细胞集落刺激因子(G-CSF)在保护小鼠免受全身辐射(TBI)中的作用。

材料与方法

通过皮下(sc)和口服途径给予 TS,确定 TS 给药的最佳剂量、途径和方案,以诱导最佳 G-CSF 水平。通过多指标 Luminex 测定血清细胞因子水平。通过先用保护性剂量(400mg/kg)TS 处理小鼠,24 小时后再用钴-60γ射线照射致死剂量(9.2Gy,0.6Gy/min),确定 G-CSF 对 TBI 后存活的作用。然后在 TBI 前 16 小时用中和 G-CSF 的抗体处理经 TS 治疗的小鼠,以消除 TS 的放射保护作用。评估来自 TS 处理的小鼠的全血样本以保护致死照射的幼稚小鼠的功效。通过荧光激活细胞分选(FACS)分析来自 TS 处理的小鼠的血液中的造血干细胞。

结果

sc 给予 TS 后 24 小时,外周血中观察到最大水平的 G-CSF。当给予 TS 治疗的小鼠中和 G-CSF 的抗体时,TS 未能保护免受 TBI。在用 LD90/30(引起 90%死亡率的致死剂量超过 30 天)剂量的γ射线攻击后,用来自 TS 和 AMD3100(1,1'-{1,4-亚苯基双(亚甲基)}双-1,4,8,11-四氮杂环十四烷八盐酸盐)处理的小鼠的全血输注的小鼠与用载体注射的小鼠的全血输注的小鼠相比,显示出显著更高的存活率。FACS 数据显示造血干细胞被动员到外周血中。

结论

结果表明,TS 给药诱导的 G-CSF 动员造血干细胞,并负责防止电离辐射。

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