天津医药
天津醫藥
천진의약
Tianjin Medical Journal
2015年
11期
1278-1280,1281
,共4页
黄挺章%李远辉%郭圣奇%卢善善%齐梁煜%冯雪萍%黄锁义
黃挺章%李遠輝%郭聖奇%盧善善%齊樑煜%馮雪萍%黃鎖義
황정장%리원휘%곽골기%로선선%제량욱%풍설평%황쇄의
抗肿瘤药(中药)%薏苡%薏苡茎%醇提取物%H22%体内抗肿瘤%环磷酰胺
抗腫瘤藥(中藥)%薏苡%薏苡莖%醇提取物%H22%體內抗腫瘤%環燐酰胺
항종류약(중약)%의이%의이경%순제취물%H22%체내항종류%배린선알
Antineoplastic Drugs (TCD)%COIX LACRYMA-JOBI L%Coix stalk%alcohol extract%H22%anti tumor in vivo%cyclophosphamide
目的:研究薏苡茎醇提取物对荷H22小鼠体内抗肿瘤作用。方法采用小鼠肝癌H22腹水型瘤细胞建立荷瘤小鼠动物模型,将84只模型小鼠随机均分为薏苡茎醇提取物剂量1~5组、模型对照组、环磷酰胺组,分别灌胃薏苡茎醇提取液10、8、6、4、2 g/kg,等体积生理盐水和环磷酰胺0.02 g/kg,每日1次,连续8 d。观察小鼠的活动能力、腹部膨隆大小及出现的时间、毛发和摄食、饮水量变化等情况。测量荷H22小鼠的实体瘤质量,计算抑瘤率,并计算肝脏指数、脾脏指数和胸腺指数。结果模型对照组最先出现腋下肿瘤鼓起且生长最快,自主活动减少、食欲下降、毛色开始暗淡等反应,剂量1、2组次之,剂量5组和环磷酰胺组最慢。薏苡茎醇提取物剂量1~5组瘤质量[分别为(0.47±0.18)、(0.37±0.13)、(0.34±0.10)、(0.30±0.11)、(0.28±0.09)mg]均低于模型对照组(0.60±0.21)mg[F=5.700,P<0.05],薏苡茎醇提取物剂量1~5组、环磷酰胺组抑瘤率依次升高(分别是21.67%、38.33%、43.33%、50.00%、53.33%和60.00%)。环磷酰胺组和薏苡茎醇提取物组的肝脏指数、脾脏指数和胸腺指数均低于模型对照组(剂量1组脾脏指数除外);薏苡茎醇提取物各剂量组的肝脏指数低于环磷酰胺组,脾脏指数、胸腺指数与环磷酰胺组差异无统计学意义。结论薏苡茎醇提取物对荷H22小鼠体内肿瘤和肝脏损害有抑制作用。
目的:研究薏苡莖醇提取物對荷H22小鼠體內抗腫瘤作用。方法採用小鼠肝癌H22腹水型瘤細胞建立荷瘤小鼠動物模型,將84隻模型小鼠隨機均分為薏苡莖醇提取物劑量1~5組、模型對照組、環燐酰胺組,分彆灌胃薏苡莖醇提取液10、8、6、4、2 g/kg,等體積生理鹽水和環燐酰胺0.02 g/kg,每日1次,連續8 d。觀察小鼠的活動能力、腹部膨隆大小及齣現的時間、毛髮和攝食、飲水量變化等情況。測量荷H22小鼠的實體瘤質量,計算抑瘤率,併計算肝髒指數、脾髒指數和胸腺指數。結果模型對照組最先齣現腋下腫瘤鼓起且生長最快,自主活動減少、食欲下降、毛色開始暗淡等反應,劑量1、2組次之,劑量5組和環燐酰胺組最慢。薏苡莖醇提取物劑量1~5組瘤質量[分彆為(0.47±0.18)、(0.37±0.13)、(0.34±0.10)、(0.30±0.11)、(0.28±0.09)mg]均低于模型對照組(0.60±0.21)mg[F=5.700,P<0.05],薏苡莖醇提取物劑量1~5組、環燐酰胺組抑瘤率依次升高(分彆是21.67%、38.33%、43.33%、50.00%、53.33%和60.00%)。環燐酰胺組和薏苡莖醇提取物組的肝髒指數、脾髒指數和胸腺指數均低于模型對照組(劑量1組脾髒指數除外);薏苡莖醇提取物各劑量組的肝髒指數低于環燐酰胺組,脾髒指數、胸腺指數與環燐酰胺組差異無統計學意義。結論薏苡莖醇提取物對荷H22小鼠體內腫瘤和肝髒損害有抑製作用。
목적:연구의이경순제취물대하H22소서체내항종류작용。방법채용소서간암H22복수형류세포건립하류소서동물모형,장84지모형소서수궤균분위의이경순제취물제량1~5조、모형대조조、배린선알조,분별관위의이경순제취액10、8、6、4、2 g/kg,등체적생리염수화배린선알0.02 g/kg,매일1차,련속8 d。관찰소서적활동능력、복부팽륭대소급출현적시간、모발화섭식、음수량변화등정황。측량하H22소서적실체류질량,계산억류솔,병계산간장지수、비장지수화흉선지수。결과모형대조조최선출현액하종류고기차생장최쾌,자주활동감소、식욕하강、모색개시암담등반응,제량1、2조차지,제량5조화배린선알조최만。의이경순제취물제량1~5조류질량[분별위(0.47±0.18)、(0.37±0.13)、(0.34±0.10)、(0.30±0.11)、(0.28±0.09)mg]균저우모형대조조(0.60±0.21)mg[F=5.700,P<0.05],의이경순제취물제량1~5조、배린선알조억류솔의차승고(분별시21.67%、38.33%、43.33%、50.00%、53.33%화60.00%)。배린선알조화의이경순제취물조적간장지수、비장지수화흉선지수균저우모형대조조(제량1조비장지수제외);의이경순제취물각제량조적간장지수저우배린선알조,비장지수、흉선지수여배린선알조차이무통계학의의。결론의이경순제취물대하H22소서체내종류화간장손해유억제작용。
Objective To study the anti-tumor effects of alcohol extraction of Coix stalk objects on H22 tumor-bearing mice. Methods The animal model of tumor bearing mice with H22 ascitic tumor cells was established. Eighty-four model mice were randomly and equally divided into Coix stalk extract groups 1-5 (10, 8, 6, 4 and 2 g/kg), model control group and cyclophosphamide group. Mice were treated orally with Coix stalk alcohol extraction solution (10, 8, 6, 4 and 2 g/kg), cyclophosphamide 0.02 g/kg and normal saline once a day for 8 days for Coix stalk extract group, cyclophosphamide group and model control group. The mouse activity, the size and the appearance of time of abdominal swelling, and changes of hair, feeding and drinking water quantity were observed in groups of mice. The solid tumor mass was measured in H22 tumor-bearing mice. The tumor inhibitory rate, liver index, spleen index and thymus index were calculated. Results The axillary tumor muster was found first in model control group with the fastest growth, reduced independent activity, decreased appetite and dim in hair color, followed by the Coix stalk extract group 1 and group 2. The last was Coix stalk extract group 5 and cyclophosphamide group. The solid tumor mass were (0.47±0.18), (0.37± 0.13), (0.34±0.10), (0.30±0.11) and (0.28±0.09) mg for Coix stalk alcohol extract groups 1-5, which were significantly lower than those of model control group (0.60 mg±0.21 mg, F=5.700,P<0.05). The tumor inhibition rates were 21.67%, 38.33%, 43.33%, 50.00%, 53.33%and 60.00%in Coix stalk extract groups 1-5 and cyclophosphamide group. The liver index, spleen index and thymus index were lower in cyclophosphamide group and Coix stalk alcohol extract groups than those of model control group (except for the spleen index of Coix stalk extract group 1). The liver index was lower in Coix stalk ethanol extract groups than that of cyclophosphamide group. There were no significant differences in the spleen index, thymus index between Coix stalk ethanol extract groups and cyclophosphamide group. Conclusion Coix stalk alcohol extract has inhibitory effects on the tumor and liver damage in H22 mice.