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作 者:张森[1] 万德森[2] 肖锡宾[2] 潘志忠[2] 高枫[1]
机构地区:[1]广西医科大学第一附属医院大肠肛门病外科,南宁530021 [2]中山大学肿瘤医院腹科,广州510060
出 处:《大肠肛门病外科杂志》2005年第4期257-259,共3页Journal of Coloproctological Surgery
摘 要:目的:体外实验明确大蒜油是否能增强枯否细胞(KupfferCell,KC)的抗肿瘤活性。方法:酶消化法提取小鼠肝脏枯否细胞,分别以含大蒜油浓度为1200、600、300、150、75、37·5μg/mL的培养液培养枯否细胞24h。换洗培养液后,按10∶1效靶比加入小鼠结肠癌细胞CT26,共同培养24h。用MTT法测定活细胞数量。以未加药的KC/CT26共同培养和KC、CT26单独培养为对照组。结果:KC的杀癌率为10·49%。经一定浓度大蒜油激活后,KC的杀癌率明显增强,并且杀癌率随大蒜油浓度的升高而增强,大蒜油浓度分别为1200、600、300、150、75、37·5μg/mL的杀癌率分别为91·91%、75·92%、73·71%、42·38%、37·94%和18·07%。300μg/mL组与600μg/mL组差异不明显,37·5μg/mL组与不用大蒜油激活组亦无差异。结论:大蒜油能激活枯否细胞,从而增强其抗癌活性。300μg/mL的大蒜油浓度可能是一个恰当的选择。Objective:Kupffer Cell (KC) in liver is the maximum part of macrophage in vivo. This study is to determine the antineoplastic activity of KC strengthened by garlic extract in vitro. Methods:Kupffer cell of mouse abstracted by enzyme digestion were cultured with garlic oil contain 1200,600,300,150,75,37.5 μg/mL respectively. Mouse colon cancer cells (CT26) were joined together according to effect target ratiol of 10:1 after changing culture fluid. Viable cell were assayed with MTT and control groups were KC/ CT26 culture together and KC, CT26 culture alone. Results: The repress/ kill carcinoma rate of KC were 10.49% and could be enhanced by a certainty density of garlic oil distinctly. The repress/kill carcinoma rate came along with the garlic oil density as follows:91.91%,75.92% ,73.71%,42. 38% ,37. 94% and 18. 07 % with 1200,600,300,150,75 and 37.5μ g/mL respectively. No difference were found between 300μ g / mL group with 600μ g/mL group and 37. 5μg /mL group with no-medicine KC/CT26 culture together group. Conclusion:Garlic oil can activate Kupffer cell and enhance its anticancer activity. 300 μg/mL may be a correct select.
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