山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2015年
8期
1-3
,共3页
黄颖%梁晓燕%李骋进%胡军%康晓莉
黃穎%樑曉燕%李騁進%鬍軍%康曉莉
황영%량효연%리빙진%호군%강효리
人参皂苷%造血干细胞%电离辐射%活性氧%半胱氨酸蛋白酶%Nrf-2
人參皂苷%造血榦細胞%電離輻射%活性氧%半胱氨痠蛋白酶%Nrf-2
인삼조감%조혈간세포%전리복사%활성양%반광안산단백매%Nrf-2
ginsenoside%hematopoietic progenitor cells%ionizing radiation%reactive oxygen species%cysteine protein-ase%Nrf-2
目的:观察人参总皂苷预处理对电离辐射下人造血干细胞( HPCs )的保护作用,并探讨其作用机制。方法将HPCs随机分为对照组和观察组,对照组不处理,观察组予以人参皂苷5.0μmol/L培养24 h,分别用剂量为0、1、2、5 Gy的X线对两组细胞进行照射。 MTT法测算细胞存活率,流式细胞仪测定辐射后24 h细胞内的活性氧( ROS),Western blot 法测定细胞内的Caspase-3和Nrf-2。结果随着辐射剂量的增加,两组细胞存活率均逐渐下降(P均<0.05),细胞内ROS活性增强、Caspase-3表达增加、Nrf-2表达减少(P均<0.05);与相同照射剂量对照组比较,观察组细胞存活率增加(P均<0.05),细胞内ROS活性减弱、Caspase-3表达减少、Nrf-2表达增加(P均<0.05)。结论人参皂苷对电离辐射下的HPCs具有保护作用,该作用与其抗凋亡和抑制氧化应激有关。
目的:觀察人參總皂苷預處理對電離輻射下人造血榦細胞( HPCs )的保護作用,併探討其作用機製。方法將HPCs隨機分為對照組和觀察組,對照組不處理,觀察組予以人參皂苷5.0μmol/L培養24 h,分彆用劑量為0、1、2、5 Gy的X線對兩組細胞進行照射。 MTT法測算細胞存活率,流式細胞儀測定輻射後24 h細胞內的活性氧( ROS),Western blot 法測定細胞內的Caspase-3和Nrf-2。結果隨著輻射劑量的增加,兩組細胞存活率均逐漸下降(P均<0.05),細胞內ROS活性增彊、Caspase-3錶達增加、Nrf-2錶達減少(P均<0.05);與相同照射劑量對照組比較,觀察組細胞存活率增加(P均<0.05),細胞內ROS活性減弱、Caspase-3錶達減少、Nrf-2錶達增加(P均<0.05)。結論人參皂苷對電離輻射下的HPCs具有保護作用,該作用與其抗凋亡和抑製氧化應激有關。
목적:관찰인삼총조감예처리대전리복사하인조혈간세포( HPCs )적보호작용,병탐토기작용궤제。방법장HPCs수궤분위대조조화관찰조,대조조불처리,관찰조여이인삼조감5.0μmol/L배양24 h,분별용제량위0、1、2、5 Gy적X선대량조세포진행조사。 MTT법측산세포존활솔,류식세포의측정복사후24 h세포내적활성양( ROS),Western blot 법측정세포내적Caspase-3화Nrf-2。결과수착복사제량적증가,량조세포존활솔균축점하강(P균<0.05),세포내ROS활성증강、Caspase-3표체증가、Nrf-2표체감소(P균<0.05);여상동조사제량대조조비교,관찰조세포존활솔증가(P균<0.05),세포내ROS활성감약、Caspase-3표체감소、Nrf-2표체증가(P균<0.05)。결론인삼조감대전리복사하적HPCs구유보호작용,해작용여기항조망화억제양화응격유관。
Objective To investigate the protective effect of ginsenoside on hematopoietic progenitor cells ( HPCs ) under different intensity of ionizing radiations .Methods The HPCs were divided into the control group and the observe group, then to add ginsenoside into the observe group and cultivated for 24 hours.Respectively exposed under X-ray irradi-ations on 1, 2, 5 Gy.Cell viability was studied by MTT method .The generation of reactive oxygen species ( ROS) after 24 hours, the expression of caspase-3 mRNA and Nrf-2 mRNA were measured by means of flow cytometry and Western blot , respectively .Results With the increase of radiation dose , cell viability reduced , the generation of ROS increased , the ex-pression of caspase-3 mRNA enhanced and the Nrf-2 mRNA decreased, gradually, all P<0.05.Compared with control group with the same radiation dose , cell viability in the observe group increased , the generation of ROS and the expression of caspase-3 mRNA decreased, the Nrf-2 mRNA increased, all P<0.05.Conclusion Ginsenoside could protect HPCs from radiation effects , which was correlated with anti-apoptosis and inhibition of oxidation stress .