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冬凌草甲素及联合柔红霉素对jurkat细胞增殖抑制作用的观察 被引量:4

Growth inhibitory effects of oridonin alone or combined with DNR on jurkat cells
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摘要 目的:探讨冬凌草甲素单用及联合柔红霉素对急性T淋巴细胞白血病jurkat细胞增殖抑制的影响。方法:采用CCK-8法检测单用冬凌草甲素、柔红霉素对jurkat细胞的抑制作用,及两种药物联合应用对jurkat细胞的抑制作用;采用Giemsa法检测冬凌草甲素作用于jurkat细胞48h的凋亡形态学变化;采用流式细胞仪检测单用冬凌草甲素对jur-kat细胞的凋亡率及两药物联合时的凋亡率。结果:单用不同浓度的冬凌草甲素(1、2、4、8和16μg/mL)对jurkat细胞具有增殖抑制作用,且呈时间-浓度依赖性,其中干预48h后的抑制率分别为(10.80±1.58)%、(32.32±7.83)%、(42.27±4.43)%、(55.07±1.65)%和(70.36±4.11)%;当联合小剂量柔红霉素(0.04μg/mL)时对jurkat细胞的抑制作用显著增加。Giemsa染色后,随着药物浓度的增加,镜下可观察到胞体皱缩、染色质浓集和凋亡小体等形态学变化。不同浓度的冬凌草甲素干预jurkat细胞48h后的凋亡率分别为(7.74±0.96)%、(13.26±1.49)%、(17.42±1.24)%、(25.13±2.12)%和(29.07±0.59)%,呈浓度依赖性增加;单用柔红霉素(0.04μg/mL)干预jurkat细胞48h后的凋亡率为(18.19±1.33)%;当冬凌草甲素(4μg/mL)联合柔红霉素(0.04μg/mL)干预jurkat细胞时,其凋亡率为(51.06±2.25)%,与单用两种药物相比差异有统计学意义,P<0.05。结论:冬凌草甲素能够抑制jurkat细胞增殖和诱导凋亡,联合柔红霉素对jurkat细胞的增殖抑制作用显著增强,具有协同抑制效应。 OBJECTIVE: To investigate the proliferation and apoptotic effects of oridonin alone or combined with DNR on jurkat cells. METHODS:CCK-8 was used to detect the proliferation inhibitory effects of oridonin alone or combined with DNR on jurkat cells and to observe the apoptotic morphologic changes of jurkat cells treated with different concentrations of oridonin for 48 h. FCM was used to exam the apoptotic rate of jurkat cells. RESULTS: The proliferation inhibitory effects of different concentrations of oridonin on jurkat cells were in a dose and time dependent manner and the inhibitory rates of oridonin treated for 48 hour were (10.80±1.58)%,(32. 32±7.83)%,(42.27±4.43)%, (55.07± 1.65)%, (70. 36± 4. 11)% respectively. The inhibitory effects markedly enhanced when combined with DNR (0.04 μg/mL);the morphologic changes such as cell body shrinkage, neuclear condensation, apoptotic bodies were observed by Giemsa stain with the condensation increasing ; the apoptotic rate of different concentrations of oridonin on jurkat cells for 48 h were (7.74±0.96) %,(13.26±1.49)%,(17.42±1.24)%,(25.13±2.12)%, (29.07±0.59)% respectively increased in a dose-dependent manner. When jurkat cells were incubated with oridonin(4 μg/mL) and DNR (0.04 μg/mL) in combination, the apoptotic rate was (51. 06 ± 2. 25)%, which was higher than that of oridonin (4 μg/mL)and DNR(0.04 μg/mL) each alone and there was a significant difference (P〈0.05). CONCLUSION: Orido- nin can inhibit jurkat cells proliferation and induce apoptosis in a does-dependent manner and the inhibitory effects markedly enhanced when combined with DNR,which has collaborative inhibition effect.
作者 张晓芬 周丽
出处 《中华肿瘤防治杂志》 CAS 北大核心 2012年第16期1227-1230,共4页 Chinese Journal of Cancer Prevention and Treatment
关键词 白血病 T淋巴细胞 急性 冬凌草甲素 柔红霉素jurkat细胞 细胞凋亡 leukemia,T lymphocytic,acute oridonin DNR jurkat cell apoptosis
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  • 1Batliva|a SP. Focus on diagnosis: the erythrocyte sedimentation rate and the C-reactive protein test[J]. Pediatr Rev, 2009, 30(2) :72-74.
  • 2Willemse MJ,Seriu T, Hettingger K, et al. Detection of minimal residual disease identifies differences in treatment response be- tween T-ALL and precursor B-ALL[J]. Blood, 2002, 99 (12) : 4386-4393.
  • 3Hirt A,Leibundgut K, Luthy AR, et al. Cell birth and death in childhood acute lymphoblastic leukemia how fast does the neo plastic cell clone expand? [J]. Br J Haematol,1977,98(4):999 1001.
  • 4Hickman JA. Apoptosis induced by anticancer drugs[J]. Cancer Metast Rev, 1992,11(2) : 121-139.
  • 5戴体俊.合并用药的定量分析[J].中国药理学通报,1998,14(5):479-480. 被引量:136
  • 6Lee KH. Anticancer drug design based on plant-derived natural produets[J]. J Biomed Science, 1999,6(4) : 236-250.
  • 7左海军,李丹,吴斌,高慧媛,吴立军,池岛乔.冬凌草的化学成分及其抗肿瘤活性[J].沈阳药科大学学报,2005,22(4):258-262. 被引量:44
  • 8樊惠远 孙汉董 晁金华 等.冬凌草乙素的化学研究[J].河南医学院学报,1979,(1):14-14.
  • 9Liu JJ,Wu XY,Pan XL,et al. Antiproliferation effects of orido- nin on HL-60 cells[J]. Ann Haematol,2004,83(11);691-695.
  • 10Gao F, Tang Q, Yang P. Apoptosis inducing and differentiation enhancement effect of oridonin on the all-trans-retinoic-acid-sen- sitive an&resistant acute promyelocytic leukemia cells[J]. Int J Lab Hematol,2010,32(1 Ptl) :e114-e122.

二级参考文献13

  • 1杨延武,姬昂,何炳林,许肖龙,裘鉴卿,王德华,钱保功,赵清治,张雁冰,薛华珍.2D NMR方法研究抗癌药物冬凌草乙素的结构与谱线归属[J].高等学校化学学报,1993,14(5):733-737. 被引量:7
  • 2吴斌,吴立军,张磊,金哲史.麻叶千里光抗菌化学成分的研究(Ⅰ)[J].沈阳药科大学学报,2004,21(5):341-345. 被引量:69
  • 3Francisco T, Federico F, Antonio G. 5, 3′, 4′-trihydroxy-6, 7, 8-trimethoxyflavone from Sideritis leucantha [J]. Phytochemistry, 1979, 18:185 - 186.
  • 4Wu SH, Zhang HJ, Chen YP, et al. Diterpenoids from Isodon wikstroemioides [J]. Phytochemistry, 1993,34:1099 - 1102.
  • 5Sun HD, Chao JH, Lin ZW, et al. The structure of rubescensin C: a new minor diterpenoid isolated from Isodon rubescens [J]. Chem Pharm Bull, 1982, 30(1):341 - 343.
  • 6Liu HM, Yan XB, Kiuchi FY, et al. A new diterpene glycoside from Rabdosia rubescens [J]. Chem Pharm Bull, 2000, 48(1): 148 - 149.
  • 7Fei XF, Wang BX, Li TJ, et al. Evodiamine, a constituent of Evodiae fructus, induces anti-proliferating effects in tumor cells [J]. Cancer Sci, 2003, 94:92 -98.
  • 8戴体俊.协同、拮抗等定义亟待统一[J]生理科学进展,1997(04).
  • 9江明性.药理学[M]人民卫生出版社,1989.
  • 10刘晨江,赵志鸿.冬凌草的研究进展[J].中国药学杂志,1998,33(10):577-581. 被引量:80

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