农业科学与技术(英文版)
農業科學與技術(英文版)
농업과학여기술(영문판)
AGRICULTURAL SCIENCE & TECHNOLOGY
2014年
11期
1876-1878
,共3页
王晓珊%史秋梅%张艳英%高桂生%沈萍%高光平%梁敬玮%李艳云%卢会朋%郭杨柳%吴楠
王曉珊%史鞦梅%張豔英%高桂生%瀋萍%高光平%樑敬瑋%李豔雲%盧會朋%郭楊柳%吳楠
왕효산%사추매%장염영%고계생%침평%고광평%량경위%리염운%로회붕%곽양류%오남
紫锥菊%多糖%IEC-6细胞株%增殖
紫錐菊%多糖%IEC-6細胞株%增殖
자추국%다당%IEC-6세포주%증식
Echinacea purpurea%Polysaccharide%IEC-6 cel%Proliferation
[目的]研究紫锥菊多糖对大鼠小肠上皮细胞株 IEC-6细胞增殖的影响。[方法]以IEC-6细胞为研究对象,采用 MTT方法检测细胞增殖率,观察紫锥菊多糖对该细胞增殖的影响。[结果]紫锥菊不同剂量与不同的培养时间对 IEC-6细胞的生长均有促进作用,但是随着处理时间的延长,不同浓度的促增殖效果也不尽相同,表现为在浓度为50、200μg/ml 时增殖率随着处理时间的延长先增加后逐渐减弱,但在培养24 h后表现显著促增殖作用;浓度100μg/ml 在72 h、浓度500μg/ml 在48 h表现明显促增殖作用;经48 h处理的EPS其增殖率随浓度提高而增强。[结论]紫锥菊多糖具有促进 IEC-6细胞增殖的作用,通过对小肠上皮细胞增殖的影响而发挥对肠道黏膜吸收和免疫功能的调整作用。
[目的]研究紫錐菊多糖對大鼠小腸上皮細胞株 IEC-6細胞增殖的影響。[方法]以IEC-6細胞為研究對象,採用 MTT方法檢測細胞增殖率,觀察紫錐菊多糖對該細胞增殖的影響。[結果]紫錐菊不同劑量與不同的培養時間對 IEC-6細胞的生長均有促進作用,但是隨著處理時間的延長,不同濃度的促增殖效果也不儘相同,錶現為在濃度為50、200μg/ml 時增殖率隨著處理時間的延長先增加後逐漸減弱,但在培養24 h後錶現顯著促增殖作用;濃度100μg/ml 在72 h、濃度500μg/ml 在48 h錶現明顯促增殖作用;經48 h處理的EPS其增殖率隨濃度提高而增彊。[結論]紫錐菊多糖具有促進 IEC-6細胞增殖的作用,通過對小腸上皮細胞增殖的影響而髮揮對腸道黏膜吸收和免疫功能的調整作用。
[목적]연구자추국다당대대서소장상피세포주 IEC-6세포증식적영향。[방법]이IEC-6세포위연구대상,채용 MTT방법검측세포증식솔,관찰자추국다당대해세포증식적영향。[결과]자추국불동제량여불동적배양시간대 IEC-6세포적생장균유촉진작용,단시수착처리시간적연장,불동농도적촉증식효과야불진상동,표현위재농도위50、200μg/ml 시증식솔수착처리시간적연장선증가후축점감약,단재배양24 h후표현현저촉증식작용;농도100μg/ml 재72 h、농도500μg/ml 재48 h표현명현촉증식작용;경48 h처리적EPS기증식솔수농도제고이증강。[결론]자추국다당구유촉진 IEC-6세포증식적작용,통과대소장상피세포증식적영향이발휘대장도점막흡수화면역공능적조정작용。
Objective] This study was conducted to investigate the effects of Echi-nacea purpurea polysaccharides (EPS) on proliferation of rat intestinal epithelial cel IEC-6. [Method] The proliferation rate of IEC-6 cel s cultured in EPS at different concentrations and for different time was measured by MTT assay and analyzed by statistic methods. [Result] The proliferation rate of IEC-6 cel s cultured in EPS at al the concentrations and for different time was improved by different extents in com-parison with the control. In detail, 50 and 200 μg/ml EPS greatly improved the IEC-6 cel proliferation after 24 h of culture; then, the cel proliferation rate in the two treatments increased from 24 to 48 h, and declined from 48 to 72 h. The cel pro-liferation was also significantly improved by culturing in 100 μg/ml EPS for 72 h and in 500 μg/ml EPS for 48 h. After 48 h of culture, the proliferation rate of IEC-6 cel increased in a EPS dose-dependent manner. [Conclusion] EPS can promote IEC-6 cel proliferation, and thus improve the intestinal mucosal absorption and immune function of rat.