期刊文献+

建立大鼠C6/SD脑胶质瘤放射剂量效应模型的实验研究 被引量:4

Experimental study of radiation on C6 glioma rats model
下载PDF
导出
摘要 目的本研究通过对大鼠C6/SD脑胶质瘤模型分不同剂量单次全脑放疗后,观察大鼠生存状态及生存期改变,为胶质瘤模型施行综合治疗提供动物实验基础。方法雌性SD大鼠,随机分为假照射荷瘤鼠组和5、10、15、20 Gy4个荷瘤鼠照射组,采用立体定向法在大鼠右侧尾状核接种C6细胞建立大鼠C6胶质瘤模型,于建模后第17天行相应剂量单次全脑放疗,观察各组大鼠生存状态及生存期改变的实验研究。结果①SD大鼠右侧尾状核立体定向方法建立的C6脑胶质瘤模型确切可靠,未见远处及颅外转移。②荷瘤大鼠受照射后第1周内出现体重增加,全身营养状况改善;2周后大鼠自发活动明显减少,饮食量减少,体重下降,照射剂量越低生存期越短,恶液质出现越早;而且3周时15、20 Gy照射组大鼠脑照射区皮肤有脱毛反应,为不全脱毛,无明显充血。③各组大鼠的生存时间:假照射组、5、10、15、20 Gy组的MeST分别为24、30.5、37.5、49、63 d。四个照射组的生存期与假照射组比较差异均具有统计学意义(P<0.05)。结论①脑内接种1×106个C6细胞建立的模型用于治疗实验研究时,治疗处理时间以细胞接种后第2~3周为宜。②荷瘤鼠全脑放疗后,首先出现较短的兴奋亢进过程,然后转入长时间的抑制过程,随着放射剂量的增加,荷瘤鼠生存期延长,说明放射线具有治疗脑胶质瘤作用。 Objective To investigate the C6 glioma rats model and observe the survival states and overall survival days after single whole-brain irradiation with different doses in rats,and establish a basis for glioma combined-therapy from animal experiment.Methods Female SD rats were randomly divided into sham irradiation group and brain-baring C6 glioma groups with radiation by 5,10,15 and 20 Gy.The models of C6 glioma were established by stereotaxical injection of C6 glioma cells into the right caudate nuclei in female SD rats.The rats with brain-baring C6 glioma were radiotherapied with whole brain at 17th day,and then observed the survival status and recorded the survival time of all groups.Results ① Using stereotactic methods to establish the C6 glioma model was exact and reliable without distant and extracranial metastasis.② The weight and nutritional status of tumor-bearing rats gained general improvement within 1 week after irradiation.The spontaneous activity,eating and drinking of rats was significantly reduced,and the weight gradually decreased after 2 weeks.The lower the radiation dose,the shorter survival time and sooner cachexia occurred.At 3 weeks,brain irradiation area were incompletely shed reaction in 15 Gy and 20 Gy irradiated groups,which hadn't obvious hyperemia.③ The MeST of sham irradiation group,5 Gy group,10 Gy group,15 Gy group and 20 Gy group was 24 d,30.5 d,37.5 d,49 d and 63 d,respective.The survival time of the four exposure groups were significantly different from the sham exposure group(P 0.05).Conclusion The model implanted with 1×106 C6 gliomaous cells sterotactically into intracerebral was used for the treatment of experimental studies,and the appropriate time to the treatment was 2 to 3 weeks after cells inoculation.After whole-brain radiotherapy,rats expressed an exited graduation for a few time firstly,then turn to a long time with depressed status.With the role of radiation to treat cancer,with the development of irradiation doses can extend survival time of rats,which in
出处 《解剖学研究》 CAS 2011年第1期4-8,F0003,共6页 Anatomy Research
关键词 C6细胞 脑胶质瘤 放射治疗 C6 cell Glioma Irradiation/radiotherapy
  • 相关文献

参考文献10

  • 1Behin A, Hoang-xuan K, Carpentier AF, et al. Primary brain tumours in adults. Lancet, 2003,361:323-331. 被引量:1
  • 2Morreale VM, Herman BH, Der-Minassian V, et al. A brain-tumor model utilizing stereotactic implantation of a permanent cannula. J Neurosurg, 1993:78(6):959-965. 被引量:1
  • 3Chicoine MR, Silbergeld DL. Invading C6 glioma cells maintaining tumorigenicity. J Neurosurg, 1995,83 (4) : 665-671. 被引量:1
  • 4陈骏,余永强,钱银锋,张诚,沈玉先,张玲玲.大鼠C6脑胶质瘤生长的动态观察和MR灌注成像可行性研究[J].中华神经医学杂志,2004,3(1):18-21. 被引量:6
  • 5吴波,游潮,黄光富,帅克刚.大鼠C6脑胶质瘤血-脑屏障的硝酸镧示踪电镜研究[J].中国临床神经外科杂志,2007,12(1):28-30. 被引量:7
  • 6Schlegel J, Piontek G, Kuhne C, et al. Molecula genetic characterization of intracerebrally transplanted brain tumors. Exp Toxicol Patho, 1999,51 ( 1 ) : 41-45. 被引量:1
  • 7Barth RF. Rat brain tumor models in experimental neuro-oncology : the 9L, C6, T9, F98, RG2 (D74), RT-2 and CNS-1 gliomas. Neuro Oncol, 1998, (1) :91-102. 被引量:1
  • 8Julia R, Caroline B, Rolf F. Barth, et al. Enhanced survival and cure of F98 glioma bearing rats following intracerebral delivery of carboplatin in combination with photon irradiation. Cancer Therapy: Preclinical Clin Cancer Res, 2007,13 (17) : 5195-5201. 被引量:1
  • 9Marie-Claude B, Aurelie J, Jean-Francois A, et al. Cure of fisher rats bearing radioresistant F98 glioma treated with cis-platinum and irradiated with monochromatic synchrotron X-rays. Cancer Res, 2004,4(64) : 2317-2323. 被引量:1
  • 10Fatome M, Foman V. A study of the mechanism of cerebral hyperexcitability after irradiation. Int J Radiat Biol, 1984,46 : 421-424. 被引量:1

二级参考文献9

  • 1Tator CH. Chemotherapy of brain tumors. Uptake of tritiated methotrexate by a transplantable intracerebral ependymoblastoma in mice [J]. J Neurosurg, 37(1): 1-8. 被引量:1
  • 2Stewart PA, Farrell CL, Del Maestro RF. The effect of cellular mit on vessels in the brain. Part 1: vessel structure in tumour, peritumour and brain from humans with malignant glioma [J]. Int J Radiat Biol, 1991, 60(1-2):125-130. 被引量:1
  • 3Dvorak AM, Kohn S, Morgan ES, et al . The vesiculo-vacuolar organelle (VVO): a distinct endothelial cell structure that provides a transcellular pathway for macromolecular extravasation [J]. J Leukoc Biol, 1996, 59(1): 100-115. 被引量:1
  • 4Hofman P, Blaauwgeers HG, Tolentino M J, et al. VEGF-A induced hyperpermeability of blood-retinal barrier endothelium in vivo is predominantly associated with pinocytotic vesicular transport and not with formation of fenestrations. Vascular endothelial growth factor-A [J]. Curr Eye Res.2000, 21(2): 637-645. 被引量:1
  • 5柴田尚武.脑肿疡の血液脑关门[J].神经进步,1988,32(6):974-984. 被引量:1
  • 6Willis CL, Leach L, Clarke GL, et al . Reversible disruption of tight junction complexes in the rat blood-brain barrier,following transitory focal astrocyte loss [J]. Glia, 2004, 48(1): 1-13. 被引量:1
  • 7Gunnersen JM, Spirkoska V, Smith PE, et al . Growth and migration markers of rat C6 glioma cells identified by serial analysis of gene expression [J]. Glia, 2000, 32 (2): 146 -154. 被引量:1
  • 8Pilkington GJ. The paradox of neoplastic glial cell invasion of the brain and apparent metastatic failure [J]. Anticancer Res, 1997, 17(6B): 4103-4105. 被引量:1
  • 9吴景文,章翔,高大宽,易林华,荆俊杰,刘先珍,梁景文,王煊.建立大鼠C6脑胶质瘤模型与观察颅内肿瘤生长[J].第四军医大学学报,2000,21(3):307-310. 被引量:14

共引文献11

同被引文献42

引证文献4

二级引证文献19

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