实用肿瘤学杂志 ›› 2009, Vol. 23 ›› Issue (2): 139-141.doi: 10.3969/j.issn.1002-3070.2009.02.010

• 论著 • 上一篇    下一篇

吉西他滨和顺铂联合化疗对大鼠脊髓损伤的实验研究

邹丽娟1, 徐晓颖1, 王若雨2, 邵淑娟3   

  1. 1.大连医科大学附属第二医院肿瘤放疗科(大连 116027);
    2.大连大学附属中心医院肿瘤科;
    3.大连医科大学组胚教研室
  • 收稿日期:2009-02-27 出版日期:2009-04-20 发布日期:2012-02-21
  • 作者简介:邹丽娟, 女, (1963-), 博士, 教授, 从事肿瘤放射生物学研究
  • 基金资助:
    辽宁省科技攻关资助项目(2005225003-12), 大连市科技局科研项目[编号:2003B3Ns218]

Experimental study on the injury of rat spinal cord made by gemcitabine and cisplatin combined chemotherapy

ZOU Lijuan1, XU Xiaoying1, WANG Ruoyu2, SHAO Shujuan3   

  1. 1.The second-affiaiated hospital of Dalian Medical University, Dalian 116027;
    2.Department of Oncology, Affiliated Zhongshan Hospital of Dalian University;
    3.Dalian Medical University
  • Received:2009-02-27 Online:2009-04-20 Published:2012-02-21

摘要: 目的观察吉西他滨和顺铂对脊髓损伤的影响, 为放化同步治疗减低毒副作用提供理论依据。方法 通过大鼠腹腔注射化疗药物, 吉西他滨30mg/kg、顺铂5mg/kg, 两药间隔时间为30分钟。自然饲养20周。通过光镜、电镜观察脊髓的形态学改变;免疫组化方法检测引起脊髓损伤凋亡基因Bax及caspase-3蛋白的表达。结果 吉西他滨或吉西他滨联合顺铂均可引起脊髓的损伤, 吉西他滨联合顺铂对脊髓的损伤要重于单用吉西他滨。HE染色表现为白质近中央管处脱髓鞘、变性、炎性细胞浸润, 灰质结构疏松、血管增多;超微结构显示白质内部分有髓神经纤维脱髓鞘改变, 髓板增厚、扭曲、皱缩。其凋亡基因Bax及caspase-3在脊髓损伤各组均有过表达, 且联合治疗组明显高于单药组(P<0.05)。结论 不论吉西他滨单药还是吉西他滨联合顺铂均能引起脊髓损伤, 其损伤机制与凋亡相关基因Bax, caspase-3蛋白过表达有关。

Abstract: Objective We researched the injury of rats spinal cord made by gemcitabine and cisplatin combined chemotherapy in order to provide important academic guidance for synchronous chemoradiotherapy.Methods The dose of GEM and DDP is one-off 30mg/kg and 5mg/kg respectively.We observed spinal cord morphological change by light microscope and transmission electron microscope;detected the protein expression of apoptosis associated genes:bax and caspase-3 by immunohistochemistry.Results Gemcitabine or gemcitabine+cisplatin all caused spinal cord injury, and the injury caused by gemcitabine+cisplatin was more severe than gemcitabine alone.The spinal cord showed partial demyelination, denaturation of the white matter close to central canal, infiltration of flammatory cell, rarefaction of cinerea structure, and increase of veins by H-E staining;and demyelination of partial nerve fiber within the white matter, incrassation, twisting, and shrinkage of neural plate of spinal cord by transmission electron microscope.The apoptosis associated gene-bax and caspase-3 all had high-expression in all groups, moreover the expression of combined treatment group was obviously higher than gemcitabinealone(P<0.05).Conclusion Not only gemcitabine alone can cause spinal cord injury, but also gemcitabine+cisplatin can cause it.The injury mechanism is associated with the high-expression of Bax and caspase-3.

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