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Effects of Lutein on the Growth and Migration of Bovine Lens Epithelial Cells In Vitro 被引量:1

Effects of Lutein on the Growth and Migration of Bovine Lens Epithelial Cells In Vitro
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摘要 The effects of lutein on the growth and migration of bovine lens epithelial cells (BLECs) in vitro were observed in an attempt to find a drug that can prevent after-cataract. BLECs were cultured in vitro and different concentrations of lutein were added to the BLECs cultures of the second and third generations. The effects of lutein on the proliferation of BLECs in vitro were examined by the MTT method, and the migration of BLECs was evaluated by a scratch wound assay. The results showed that: (1) Lutein at concentrations of 1 to 16 μmol/L could inhibit the proliferation of BLECs in a dose-and time-dependent manner (P〈0.01); (2) The migration of BLECs was evaluated by wound healing rate. As compared with the control group, the wound healing rate in the experimental groups was decreased from 0.672±0.164 to -0.234±0.144 and -0.597±0.063 (P〈0.01) at 1 and 2 μmol/L lutein, respectively. It was concluded that lutein at concentration of 〉1 μmol/L inhibited the proliferation and migration of BLECs in vitro, Lutein may become an effective drug to prevent after-cataract. The effects of lutein on the growth and migration of bovine lens epithelial cells (BLECs) in vitro were observed in an attempt to find a drug that can prevent after-cataract. BLECs were cultured in vitro and different concentrations of lutein were added to the BLECs cultures of the second and third generations. The effects of lutein on the proliferation of BLECs in vitro were examined by the MTT method, and the migration of BLECs was evaluated by a scratch wound assay. The results showed that: (1) Lutein at concentrations of 1 to 16 μmol/L could inhibit the proliferation of BLECs in a dose-and time-dependent manner (P〈0.01); (2) The migration of BLECs was evaluated by wound healing rate. As compared with the control group, the wound healing rate in the experimental groups was decreased from 0.672±0.164 to -0.234±0.144 and -0.597±0.063 (P〈0.01) at 1 and 2 μmol/L lutein, respectively. It was concluded that lutein at concentration of 〉1 μmol/L inhibited the proliferation and migration of BLECs in vitro, Lutein may become an effective drug to prevent after-cataract.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2008年第3期360-363,共4页 华中科技大学学报(医学英德文版)
关键词 LUTEIN bovine lens epithelial cells MIGRATION PROLIFERATION AFTER-CATARACT lutein bovine lens epithelial cells migration proliferation after-cataract
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参考文献12

  • 1刘涛,金岩,王新文,黄沙,姜玲,温宁.成纤维细胞上清提取物对成纤维细胞增殖迁移的影响[J].牙体牙髓牙周病学杂志,2006,16(3):129-132. 被引量:2
  • 2张敏,张效房,高晓东,张义国.MTT比色法测定药物对晶体上皮细胞增殖的影响[J].眼科研究,1997,15(4):233-235. 被引量:10
  • 3Itagaki S,,Ogura W,Sato Y et al.Characterization of the disposition of lutein after i.v. administration to rats[].Boil Pharm Bull.2006
  • 4Santosa S,Jones P J.Oxidative stress in ocular disease:Does lutein play a protective role[].Canadian Medical Association Journal.2005
  • 5McDevitt TM,Tchao R,Harrison EH,et al.Carotenoids nor-mally present in serum inhibit proliferation and induce differ-entiation of a human monocyte/macrophage cell line(U937)[].Nutrition.2005
  • 6Zhang Min,Zhang Xiaofang,Gao Xiaodong,et al.Department of Ophthalmology,First AffiliatedHospital,Henan Medical University,Zhengzhou 450052.Drug Effects on Lens Epithelial Cell Proliferation Using the MTTColorimetric Assay[].Chinese Ophthalmic Research.1997
  • 7LIU Tao,JIN Yan,WANG Xin-wen,HUANG Sha,JIANG Ling,WEN Ning(College of Stomatolody,The Fourth Military Medical University,Xi′an 710032 China).Effect of available components in culture supernatants of fibroblasts on fibroblasts[].Chinese Journal of Conservative Dentistry.2006
  • 8Wang E,,Zhao M,Forrester JV,et al.Electric Fields and MAP Kinase Signaling Can RegulateEarly Wound Healing in Lens Epithelium[].Investigative Ophthalmology.2003
  • 9Chew B P,Brown C M,Park J S,et al.Dietary lutein inhibits mouse mammary tumor growth by regulating angiogenesis and apoptosis[].Anticancer Research.2003
  • 10Gross MD,Bishop TD,Belcher JD,et al.Induction of HL-60cell differentiation by carotenoids[].Nutrition and Cancer.1997

二级参考文献13

  • 1陈天瑞.双氯灭痛的药理和临床使用近况[J].医药导报,1993,12(1):18-20. 被引量:4
  • 2周建军,乐秀芳,韩家娴,杨蔚怡,许承辉.影响MTT方法测定结果的一些因素[J].肿瘤,1994,14(2):93-94. 被引量:16
  • 3夏小平,陆道炎,王丽天,陈才根,吴念祖.肝素抑制后发性白内障形成的细胞学研究[J].中华眼科杂志,1994,30(5):363-365. 被引量:21
  • 4Langer R,Vacanti JP.Tissue engineering[J].Science,1993,260(5110):920-926
  • 5Whtke W,Sharpe AH,Hartwig JH,et al.Hemostatic inflammatory and fibroblast responses are blunted in mice backing gelsolin[J].Cell,1995,81(7):41-51
  • 6Ishibashi H,Nakagawa K,Nakashima Y,et al.Conditioned media of carcinoma cells cultured in hypoxic microenvironment stimulate angiogenesis in vitro;relationship to basic fibroblast growth factor[J].Virchows Arch,1995,425(6):561-568
  • 7Coltrini D.Biochemical bases of the interaction of human basic fibroblast growth factor with glycosamine-glycans[J].Eur J Biochem,1993,214(1):51-58
  • 8Breuing K,Andrce C,Helo G,et al.Growth factors in the repair of partial thickness porcine skin wounds[J].Plast Reconstr Surg,1997,100(3):657-664
  • 9Sanz G,Santos H,Izquierdo H,et al.Experimental model for local application of growth factors in skin re-epithelialization[J].Scand J Plast Reconstr Surg,2000,34(3):199-206
  • 10梁谋,吴波,赵明伦.MTT法检测抗癌药物敏感性的探讨[J]中国药理学通报,1993(03).

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