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中国临床药理学与治疗学 ›› 2006, Vol. 11 ›› Issue (11): 1243-1247.

• 研究原著 • 上一篇    下一篇

异十三基二乙胺体内外抗肿瘤作用研究

王瑞幸, 黄循铷1, 吴枝娟, 林菁2, 方秋娟   

  1. 福建医科大学生理学与病理生理学系, 福州 350004, 福建;
    1福建医科大学附属第一医院消化内科, 福州 350005, 福建;
    2福建医科大学药理学系, 福州 350004, 福建
  • 收稿日期:2006-09-21 修回日期:2006-10-17 出版日期:2006-11-26 发布日期:2020-11-06
  • 作者简介:王瑞幸, 男, 医学硕士, 讲师, 研究方向:肿瘤药理。Tel:0591-87113656 ;13075905660  E-mail:wrx530@163.com

Study on antitumor activity of allotri-tridecyl diethylamine in vitro and in vitro

WANG Rui-xing, HUANG Xun-ru1, WU Zhi-juan, LIN Jing2, FANG Qiu-juan   

  1. Department of Physiology and Pathophysiology, Fujian Medical University , Fuzhou 350004, Fujian, China;
    1Department of Gastroenterology , the Affilicated First Hospital , Fujian Medical University , Fuzhou 350004, Fujian, China;
    2Department of Pharmacology , Fujian Medical University , Fuzhou 350004 , Fujian, China
  • Received:2006-09-21 Revised:2006-10-17 Online:2006-11-26 Published:2020-11-06

摘要: 目的 探讨异十三基二乙胺( D-108) 体内外抗肿瘤作用。方法 应用台盼蓝排染法、MTT 法检测D-108 对多种体外培养肿瘤细胞、人牙龈成纤维细胞( HGF) 及Beagle 犬骨髓基质干细胞(MSC) 的细胞毒作用;Bliss 法观察小鼠灌胃( i.g.) D-108 急性毒性实验;在可耐受剂量下观察D-108 对小鼠移植性实体瘤U14 的抑制率。Giemsa 染色法观察在D-108 影响下, HL 60 细胞的形态学变化。结果 D-108 对肿瘤细胞的体外细胞毒作用( IC50:0.22 ~2.19 mg·L-1) 强于HGF 及MSC ( IC50 分别为5.55 、3.57 mg·L-1) 。LD50 为36.49 mg·kg-1 ( i.g.) 。D-108 有效抑制U14 在小鼠体内的生长,100 mg·kg-1 ·d-1 i.g.瘤质量抑制率为45.27 %。HL60 细胞经D-108 处理后呈典型凋亡形态学改变。结论 D-108 有较强的体内外抗肿瘤活性且毒性较小,并能诱导HL60 细胞凋亡。

关键词: 抗肿瘤药, 异十三基二乙胺, 肿瘤细胞, 肿瘤移植

Abstract: AIM: To investigate antitumor effect of allotri-tridecyl diethylamine ( D-108) in vivo and in vitro.METHODS: The cytotoxic effects of D-108 on various tumor cell lines, human gingival fibroblast and marrow stromal cell cultured in vitro were determined with trypan blue dye exclusion test and MTT method.The acute toxicity of mice by administration of D-108 was evaluated by Bliss method.At a tolerable dose level, D-108 was administrated to treat transplanted solid tumor U14, and tumor weight inhibition was observed.Apoptosis morphological transformation of HL 60 cell induced by D-108 was detected by the Giemsa staining.RESULTS: The cytotoxic effects in vitro of D-108 on various tumor cell lines ( IC50:0.22 to 2.19 mg·L-1) were more powerful than both human gingival fibroblast and marrow stromal cell ( IC50:5.55 and 3.57 mg·L-1).LD50 of D-108 was 36.49 mg·kg-1 ( mice, i.g.).D-108 inhibited in vivo growth of implanted solid tumor U14 of mice effectually.The inhibition rate of tumor weight of D-108 ( 100mg·kg-1 ·d-1 i.g.) was 45.27 %.HL 60 cell appearance typical apoptosis morphological transformation induced by D-108.CONCLUSION: D-108 had obvious antitumor activity in vivo and in vitro and little toxicity.D-108 could induce the apoptosis of HL 60 cell.

Key words: antineoplastic agents, allotri-tridecyl diethylamine, tumor cells, cultured, neoplasms transplantation

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