期刊文献+

皖南蝮蛇毒抑瘤组分Ⅰ对人胃癌细胞SGC-7901荷瘤鼠体内抑制作用的研究 被引量:5

In vivo tumor-inhibitory effects of Agkistrodon halys venom antitumor component Ⅰ on tumor-bearing mice with human gastric cancer cell SGC-7901
暂未订购
导出
摘要 目的:研究皖南蝮蛇毒抑瘤组分Ⅰ(Agkis-trodon halys venom antitumor component Ⅰ,AHVAC-Ⅰ)对人胃癌细胞SGC-7901荷瘤鼠的体内抑制作用及瘤细胞增殖活性变化,并初步探讨其作用机制。方法:取生长状态良好的浓度为1×107个/mL的SGC-7901人胃癌细胞悬液0.1mL接种于裸小鼠右侧腋窝皮下,待其成瘤后随机分为模型组、紫杉醇阳性对照组、AH-VAC-Ⅰ高、中、低剂量组,隔日连续给药5次,定期观察肿瘤生长情况,测量肿瘤体积,绘制肿瘤生长曲线并计算抑瘤率,HE染色观察瘤体形态学变化,免疫组化SP法检测Ki-67增殖指数,原位末端标记技术(TUNEL)法检测细胞凋亡指数。结果:AHVAC-Ⅰ在1.0mg/kg剂量时对SGC-7901细胞有抑制作用,抑瘤率达42.2%;在3.0mg/kg剂量时有显著抑制作用,抑瘤率达78.5%。实验组肿瘤内Ki-67阳性细胞数量下降,凋亡细胞明显增多。结论:AHVAC-Ⅰ能明显抑制裸鼠体内SGC-7901人胃癌细胞的生长,其作用机制可能与诱导胃癌细胞发生凋亡及抑制肿瘤细胞增殖有关。 ABSTRACT AIM: To investigate the in vivo tumor-inhibitory effects of snake venom antttu mot component I(AHVAC-I) from Agkistrodon halys living in south Anhui province on the tumor-bearing mice with human gastric cancer cell SGC-7901 and activities of the cell prolifera- tion as well as its mechanisms. METHODS: Ceil suspension of 0.1 mL was obtained from the well-grown cell SGC-7901 by cell count of 1 ×10^7/mL and incubated subcutaneously into the nude mice via right axillary fossa. After tumor formation, the mice were randomized into groups of model controls, positive paclitaxiel controls, AHVAC-I of low, medium and low dosage in which the animals were managed with AHVAC-I every other day for 5 consecutive times. The tumor growth and its sizes were ob- served and measured for mapping the growth curve and calculating the inhibitory rate. HE staining was performed to examine the morpho-logic change of tumors, and streptavidin-peroxi- dase (SP) immunohistochemical technique was used to detect the proliferation index of Ki-67 and TUNEL method was for examination of the apoptotic index. RESULTS:AHVAC-I at dose of 1.0 mg/kg produced inhibitory effects on SGC- 7901 with inhibition rate of 42.2%, and inhibi- tory effects were significant at close of 3.0 mg/kg with a rate of 78.5%. Ki-67 protein was reduced in the positive cells of treatment groups, leading to increased apoptosis of tumor cells. CONCLUSION= AHVAC-I can effectively inhibit the in vivo growth of gastric cell SGC 7901 in nude mice, and the possible mechanisms may be associated with the induced apoptosis and sup- pressed proliferation of the gastric tumor cells.
出处 《中国临床药理学与治疗学》 CAS CSCD 2012年第5期491-496,共6页 Chinese Journal of Clinical Pharmacology and Therapeutics
基金 安徽省科技厅基金资助项目(10021303009) 芜湖市科技局科研基金项目(09卫生类1-1)
关键词 皖南蝮蛇毒抑瘤组分Ⅰ 胃癌 裸小鼠抑制 增殖 凋亡 AHVAC-I Gastric cancer Nude mice Inhibition Proliferation Apoptosis
  • 相关文献

参考文献11

二级参考文献143

共引文献137

同被引文献33

  • 1Chcn Y, Mestek A, I.iu J, et al. Molecular cloning and functional expression of a l opioid receptorfrom rat brain [J]. Mol Pharmacol, 1993, 44(1):8 -12.
  • 2Benyamin R, Trescot AM, Datta S, et al. Opioid complications and side effects [J]. Pain Physician, 2008,11(2) :S105-S120.
  • 3Smith HS, Elliott JA. Opioid-induced androgen de- ficiency (OPIAD) [J]. Pain Physician, 2012, 15 (3) : 145-156.
  • 4Manglik A, Kruse AC, Kobilka TS, et al. Crystal structure of the opioid receptor bound to a morphi- nan antagonist [J]. Nature,2012,485(7398) :321- 326.
  • 5Diochot S, Baron A, Salinas M, et al. Black mamba venom peptides target acid sensing ion channels to abolish pain[J]. Nature, 2012,490 (7421):552- 555.
  • 6Woolf CJ. Pain: morphine, metabolites, mambas, and mutations[J].Lancet Neurol,2013 12(1): 18- 20.
  • 7David I. Macht Experimental and clinical study of cobra venom as an analgesic[J]. Harmacology, 1936, 22(1): 61-71.
  • 8Chen RZ, Robinson SE, et al. The effect of cholin ergic manipulations on the analgesic response to co bra toxin in mice [J]. Life Sciences, 1990, 47(21) 1949-1954.
  • 9Scholz J, Woolf CJ. The neuropathic pain triad: neurons, immune cells and glia[J]. Nat Neurosci 2007, 10(11) :1361-1368.
  • 10Bertorelli R, Corradini L, Rafiq K, et al. Nocicep tin and the ORL 1 ligand EPhel (CH2-NH)Gly22 nociceptin(1-13)NH2 exert anti-opioid effects in the Freund's adjuvant induced arthritic rat model of chronic pain.[J]. Br J Pharmacol,1999, 128 (6) : 1252-1258.

引证文献5

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部