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血小板生成素注射用于小鼠肿瘤辅助性治疗的初步研究
引用本文:赵建增,阮杏珍,等.血小板生成素注射用于小鼠肿瘤辅助性治疗的初步研究[J].空军总医院学报,1996,12(4):200-202.
作者姓名:赵建增  阮杏珍
作者单位:临床实验科(赵建增,刘丽,王晓平,谢宝树,芦兴武,王艳华,冷爱军,占志),检验科摘要(阮杏珍)
摘    要:本文利用TPO基因注射治疗接受环磷酰胺化疗后小鼠的血小板及白细胞减少症。将克隆于pcDNA3的TPO质粒按不同剂量注射到试验组27只小鼠后肢内侧肌肉内,其中3只小鼠注射空质粒。三日后其中接受TPO基因注射的12只小鼠每只腹腔内注射环磷酰胺2mg(100mg/kg体重),其余12只不化疗的小鼠作为基因对照组;另设化疗对照组动物15只,按相同剂量注射环磷酰胺。每周尾静脉采血,检测白细胞和血小板水平。结果基因+化疗组的两项血液指标在化疗后两周内明显优于单纯化疗组,无毛发脱落;化疗组和注射空质粒组动物绝大多数发生脱毛现象,并有7只动物死亡。两周后进行第二次环磷酰胺攻击,结果化疗组的死亡数达8只,存活动物体况很差,基因+化疗组动物尚无任何不良表现。此时两组的血液指标已无明显差异,提示在基因注射后TPO的有效表达期在2-3周。本研究发现TPO基因注射后,不但动物血小板和白细胞水平提高,而且其它化疗后的不良症状也得到改善,提示TPO有着更为广泛的作用

关 键 词:血小板生成素,基因疗法,环磷酰胺,血小板减少症,白细胞,减少症,动物疾病模型

Mice Resistant to Cyclophosphomide Toxicity by TPO Gene Injection
Zhao Jianzeng,Liu Li,Wang Xiaoping,et al..Mice Resistant to Cyclophosphomide Toxicity by TPO Gene Injection[J].Journal of General Hospital of Air Force,PLA,1996,12(4):200-202.
Authors:Zhao Jianzeng  Liu Li  Wang Xiaoping  
Institution:Zhao Jianzeng,Liu Li,Wang Xiaoping,et al .
Abstract:We first report that TPO gene injection could prevent mice from leukocytepenia,thrombpenia and alopecia after cyclophosphomide treatment.TPO gene cloned in pcDNA3 was injected 12 mice hind leg muscle,3 mice injected wild pcDNA3 plasmid ,followed with cyclophosphomide treatment(100mg/kg/day,3times) three days later.The number of leukocyte and platelet in gene-injected mice remained higher than controls,and no other symptoms were observed,Meanwhile,most of the controls and these received wild plasmid were hair loss(15/18)and in low spirit ,8 of them died in the second week of cyclophosphomide administer.The hematopoietic activity was independent upon the dose of TPO gene in the range of 20ug to 100ug.In addition ,TPO gene injection seems no harm to mice reproduction.Second cyclophosphomide challenge was made in the 18th day post gene injection,and then no more hemalogical difference was detected between the trials and controls .It suggested that effectiveness fo TPO expression of single injection is about 2to 3 weeks .TPO gene therapy could reduce the toxicity of cyclophosphomide to blood and pevent mice from chemotherapy-induced alopecia.It has great value in cancer accessary treatment.
Keywords:TPO Gene therapy Cyclophosphomide Thrombocytopenia Leukopenia  
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