在硅胶G板上,以正丁醉-26%氨水-无水乙醇(30:3:1)为展开剂,用薄层扫描法分离测定了中国姜黄属植物毛郁金Curcuma aromatica Salisb.,温郁金C. wenyujin Y. H. Chen et C.Ling(or C. aromatica cv. Wenyujin),莪术C. aeruginosa Roxb.,...在硅胶G板上,以正丁醉-26%氨水-无水乙醇(30:3:1)为展开剂,用薄层扫描法分离测定了中国姜黄属植物毛郁金Curcuma aromatica Salisb.,温郁金C. wenyujin Y. H. Chen et C.Ling(or C. aromatica cv. Wenyujin),莪术C. aeruginosa Roxb.,黄莪术C. zedoaria (Christm.)Rosc.,桂莪术C. kwangsiensis S. G. Lee et C. F. Liang,川郁金C. chuanyujin C. K. Hsich et H.Zhang,姜黄C. longa L.根茎中姜黄素(curcumin),去甲氧基姜黄素(demethoxycurcumin),双去甲氧基姜黄素(bisdemethoxycurcumin)和总姜黄素(curcuminoids)的含量,回收率97.07%～102.0%(n=6),变异系数为3.1%～5.0%。展开更多
AIM To reveal the inhibitory effects ofCurcuma aromatica oil(CAO)on cellproliferation of hepatoma in mice.METHODS Two tumor inhibitory experimentsof CAO on hepatoma in mice were conducted.The inhibitory effects of CAO...AIM To reveal the inhibitory effects ofCurcuma aromatica oil(CAO)on cellproliferation of hepatoma in mice.METHODS Two tumor inhibitory experimentsof CAO on hepatoma in mice were conducted.The inhibitory effects of CAO on proliferation ofhepatoma in mice were evaluated by DNA imagecytometry and immunohistochemical staining ofproliferating cell nuclear antigen(PCNA).RESULTS The tumor inhibitory rates of CAOwere 52% and 51% in two experiments,respectively.Compared with those of the saline-treated control groups,both differences werestatistically significant(P【0.01).In the groupof mice treated with CAO,the cellular nuclearDNA OD value(249±70),areas(623 μm^2±228 μm^2)and DNA(2.38±0.67)index of hepaticcarcinomas were significantly lower than thoseof the control group(430±160,1073 μm^2±101 μm^2 and 4.48±0.71).CAO also couldincrease diploidy cell rates(29.00%±9.34% vs2.97%±5.69%,P【0.01)and decreasepentaploidy cell exceeding rate(30.04%±15.10% vs 70.89%±14.94%,P【0.01).In thegroup of mice treated with CAO,the labelingindexes of proliferating cell nuclear antigen (PCNA-LI)were 30%±4%,which weresignificantly lower than 40%±6% of the controlgroup(P【0.01).CONCLUSION The inhibition of CAO on thegrowth of hepatoma in mice might be associatedwith its depression on cellular proliferativeactivity.展开更多
文摘在硅胶G板上,以正丁醉-26%氨水-无水乙醇(30:3:1)为展开剂,用薄层扫描法分离测定了中国姜黄属植物毛郁金Curcuma aromatica Salisb.,温郁金C. wenyujin Y. H. Chen et C.Ling(or C. aromatica cv. Wenyujin),莪术C. aeruginosa Roxb.,黄莪术C. zedoaria (Christm.)Rosc.,桂莪术C. kwangsiensis S. G. Lee et C. F. Liang,川郁金C. chuanyujin C. K. Hsich et H.Zhang,姜黄C. longa L.根茎中姜黄素(curcumin),去甲氧基姜黄素(demethoxycurcumin),双去甲氧基姜黄素(bisdemethoxycurcumin)和总姜黄素(curcuminoids)的含量,回收率97.07%～102.0%(n=6),变异系数为3.1%～5.0%。
基金National key project of the 9~(th) 5-year Plan for Medicine and Health,No.96-906-07-04Guangdong provincial natural scientific grants,No.980663.
文摘AIM To reveal the inhibitory effects ofCurcuma aromatica oil(CAO)on cellproliferation of hepatoma in mice.METHODS Two tumor inhibitory experimentsof CAO on hepatoma in mice were conducted.The inhibitory effects of CAO on proliferation ofhepatoma in mice were evaluated by DNA imagecytometry and immunohistochemical staining ofproliferating cell nuclear antigen(PCNA).RESULTS The tumor inhibitory rates of CAOwere 52% and 51% in two experiments,respectively.Compared with those of the saline-treated control groups,both differences werestatistically significant(P【0.01).In the groupof mice treated with CAO,the cellular nuclearDNA OD value(249±70),areas(623 μm^2±228 μm^2)and DNA(2.38±0.67)index of hepaticcarcinomas were significantly lower than thoseof the control group(430±160,1073 μm^2±101 μm^2 and 4.48±0.71).CAO also couldincrease diploidy cell rates(29.00%±9.34% vs2.97%±5.69%,P【0.01)and decreasepentaploidy cell exceeding rate(30.04%±15.10% vs 70.89%±14.94%,P【0.01).In thegroup of mice treated with CAO,the labelingindexes of proliferating cell nuclear antigen (PCNA-LI)were 30%±4%,which weresignificantly lower than 40%±6% of the controlgroup(P【0.01).CONCLUSION The inhibition of CAO on thegrowth of hepatoma in mice might be associatedwith its depression on cellular proliferativeactivity.
