中国中西医结合杂志
中國中西醫結閤雜誌
중국중서의결합잡지
CHINESE JOURNAL OF INTEGRATED TRADITIONAL AND WESTERN MEDICINE
2001年
2期
123-125
,共3页
许勇钢%麻柔%胡乃平%刘锋%杨经敏%马玲%胡晓梅
許勇鋼%痳柔%鬍迺平%劉鋒%楊經敏%馬玲%鬍曉梅
허용강%마유%호내평%류봉%양경민%마령%호효매
扶正抗白冲剂%微小残留白血病%免疫功能
扶正抗白遲劑%微小殘留白血病%免疫功能
부정항백충제%미소잔류백혈병%면역공능
目的:研究扶正抗白冲剂(FZKBG)对实验小鼠免疫功能及生存期的影响,探讨FZKBG治疗微小残留白血病(MRL)的机理。方法:接种L7212细胞1×106/只,接种后第3天腹腔注射环磷酰胺250mg/kg,造成MRL模型小鼠,分成模型对照组、模型给药组,另设正常对照组、正常给药组,分别观察各组小鼠淋巴细胞亚群(CD3+、CD4+、CD8+)改变,免疫器官病理变化和生存期。结果:与模型组比较,FZKBG能明显提高正常小鼠和MRL模型小鼠CD3+、CD4+、CD8+的百分比和绝对值(P<0.05,P<0.01)。且明显延长MRL模型小鼠存活期,延长生命率29.6%~60.4%。结论:FZKBG能明显延长MRL模型小鼠存活期,其机理可能是通过提高MRL模型小鼠的免疫功能,抑制体内白血病细胞而实现的。
目的:研究扶正抗白遲劑(FZKBG)對實驗小鼠免疫功能及生存期的影響,探討FZKBG治療微小殘留白血病(MRL)的機理。方法:接種L7212細胞1×106/隻,接種後第3天腹腔註射環燐酰胺250mg/kg,造成MRL模型小鼠,分成模型對照組、模型給藥組,另設正常對照組、正常給藥組,分彆觀察各組小鼠淋巴細胞亞群(CD3+、CD4+、CD8+)改變,免疫器官病理變化和生存期。結果:與模型組比較,FZKBG能明顯提高正常小鼠和MRL模型小鼠CD3+、CD4+、CD8+的百分比和絕對值(P<0.05,P<0.01)。且明顯延長MRL模型小鼠存活期,延長生命率29.6%~60.4%。結論:FZKBG能明顯延長MRL模型小鼠存活期,其機理可能是通過提高MRL模型小鼠的免疫功能,抑製體內白血病細胞而實現的。
목적:연구부정항백충제(FZKBG)대실험소서면역공능급생존기적영향,탐토FZKBG치료미소잔류백혈병(MRL)적궤리。방법:접충L7212세포1×106/지,접충후제3천복강주사배린선알250mg/kg,조성MRL모형소서,분성모형대조조、모형급약조,령설정상대조조、정상급약조,분별관찰각조소서림파세포아군(CD3+、CD4+、CD8+)개변,면역기관병리변화화생존기。결과:여모형조비교,FZKBG능명현제고정상소서화MRL모형소서CD3+、CD4+、CD8+적백분비화절대치(P<0.05,P<0.01)。차명현연장MRL모형소서존활기,연장생명솔29.6%~60.4%。결론:FZKBG능명현연장MRL모형소서존활기,기궤리가능시통과제고MRL모형소서적면역공능,억제체내백혈병세포이실현적。
Objective: To observe the effects of Fuzheng Kangbai Granule(FZKBG) on immune function and survival time in minimal residual leukemia (MRL) model mice and study its mechanism. Methods: MRL model mice were established by hypodermic inoculation with L7212 cells following intraperitoneal injection of cytoxan (CTX)25 mg/kg 3 days later, and divided into the control group and FZKBG group. The changes of T-lymphocyte subsets, including CD3+、CD4+ and CD8+, and the survival time in model mice were observed. Results: Comparing with the control group, FZKBG could obviously increase both the percentage and absolute value of CD3+and CD4+ lymphocytes and prolong the survival time of model mice, the prolongation rate being 29.6%-60.4%. Conclusion: FZKBG could markedly prolong the survival time of MRL mice, its mechanism might be through elevating the immune function and inhibiting the leukemic cells in model mice.