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复方斑蝥制剂对直肠癌微淋巴管生成影响的实验研究 被引量:4

Effect of Fufangbanmao on lymphangiogenesis in rectal cancer
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摘要 目的通过建立未分化人直肠癌HR8348原位移植裸鼠模型,应用复方斑蝥制剂治疗,观察其对裸鼠原位移植人直肠癌微淋巴管生成的影响。方法建立人直肠癌HR8348原位种植BALB/C裸鼠模型80只,随机分为两组,每组40只,分别腹腔内注射0.9%氯化钠溶液、复方斑蝥制剂8 mg/kg,2次/周。8周后处死裸鼠,采用定量免疫组化染色检测肾小球足突细胞膜黏蛋白;计数微淋巴管密度(LM-VD)值。结果复方斑蝥制剂组肾小球足突细胞黏蛋白值较0.9%氯化钠溶液组显著下降(P<0.05)。复方斑蝥制剂组LMVD值为3.98±0.42,较0.9%氯化钠溶液组显著下降(7.52±1.25,P<0.05)。结论复方斑蝥制剂能抑制直肠癌微淋巴管生成,抑制肿瘤的生长和转移。 Objective To evaluate the inhibitory effect of Fofangbanmao on lymphangiogenesis in rectal cancer using orthotopic implantated tumor models of BALB/C nude mice. Methods A BALB/C nude mouse model of transplanted in situ human rectal cancer was established. Eighty nude mice were divided into two groups with 40 each: normal saline or 8 mg/kg of Fufangbanmao were injected in, repectively,twice a week for 8 weeks. At the end.of the 8th week, all mice were sacrificed for detection of lymphatic microvessel density ( LMVD), and podoplanin was detected by immunohistoehemical staining. Results In comparison with control group, the concentrations of podoplanin in Fufangbanmao group decreased significantly than those in control group (P 〈 0. 05 ). The number of LMVD in Fufangbanmao group was 3.98 ± 0. 42, which was significantly lower than that in control group(7.52 ± 1.25,P 〈 0.05). Conclusion Fufangbanmao can inhibit the growth of rectal cancer by interfering lymphangiogenesis.
出处 《哈尔滨医科大学学报》 CAS 北大核心 2011年第4期327-329,共3页 Journal of Harbin Medical University
基金 黑龙江省教育厅课题(11541244)
关键词 直肠癌 复方斑蝥制剂 淋巴管 rectal neoplasms Fufangbanmao lymphatic vessels
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  • 1杨军,丁敏,张太君,郭渝,宋自阆,曹永艳.血清药理学方法观察复方斑蝥胶囊对人肝癌细胞SMMC-7721增殖的影响[J].中国药房,2005,16(4):262-264. 被引量:15
  • 2邹箴蕾,吴启南.半枝莲的化学成分及药理作用研究进展[J].时珍国医国药,2005,16(2):149-150. 被引量:48
  • 3江洪,张太君,邓晓玲.复方斑蝥胶囊治疗原发性肺癌临床总结[J].实用中医药杂志,2006,22(3):166-167. 被引量:10
  • 4王海南.人参皂苷药理研究进展[J].中国临床药理学与治疗学,2006,11(11):1201-1206. 被引量:113
  • 5[12]Seok Choi,Hyun-Ju Kim,Yoo-Seung Ko,Seong-Woo Jeong,Yang In Kim,William F.Simonds,et al.Gαq/11 coupled to mammalian phospholipase C β3-like enzyme mediates the ginsenoside effect on Ca2+-activated Cl-current in the Xenopus oocyte[J].J Biol Chem,2001;276:48797-802
  • 6[13]Dou DQ,Zhang YW,Zhang L,Chen YJ,Yao XS.The inhibitory effects of ginsenosides on protein tyrosine kinase activated by hypoxia/reoxygenation in cultured human umbilical vein endothelial cells[J].Planta Med,2001;67:19-23
  • 7[14]Choi SS,Lee JK,Han EJ,Han KJ,Lee HK,Lee J,et al.Effect of ginsenoside Rd on nitric oxide system induced by lipopolysaccharide plus TNF-alpha in C6 rat glioma cells[J].Arch Pharm Res,2003;26:375-82
  • 8[15]Choi SE,Choi S,Lee JH,Whiting PJ,Lee SM,Nah SY.Effects of ginsenosides on GABA(A)receptor channels expressed in Xenopus oocytes[J].Arch Pharm Res,2003;26:28-33
  • 9[16]Noh JH,Choi S,Lee JH,Betz H,Kim JI,Park CS,et al.Effects of ginsenosides on glycine receptor α1 channels expressed in Xenopus oocytes[J].Molecules and Cells,2003;15:34-9
  • 10[17]Choi S,Rho SH,Jung SY,Kim SC,Park CS,Nah SY.A novel activation of Ca2+-activated Cl-channel in Xenopus oocytes by Ginseng saponins:evidence for the involvement of phospholipase C and intracellular Ca2+ mobilization[J].Br J Pharmacol,2001;132:641-8

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