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补髓生血颗粒对慢性再障患者骨髓影响的实验研究 被引量:5

The study of the effects and mechanism of the soluble granules of Busui shengxue to Chrouic aplastic anemia
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摘要 目的 :探讨补髓生血颗粒对慢性再生障碍性贫血 (CAA)患者CD34 +细胞及CD34 +C -myc细胞表达影响及疗效机理。方法 :应用免疫组化技术和双染法标记 ,检测 36例CAA患者治疗前后骨髓CD34 +细胞及CD34 +C -myc细胞表达水平。结果 :CAA患者CD34 +细胞表达疗前和疗后均低于正常组 (P <0 .0 5 ) ,疗后与疗前相比差异显著 (P <0 .0 5 ) ;CD34 +C -myc细胞表达疗前和疗后均高于正常组 (P <0 .0 5 ) ,疗后与疗前相比差异显著 (P <0 .0 5 ) ;且实验组疗效优于对照组 (P <0 .0 5 )。结论 :补髓生血颗粒作用机制之一可能是通过降低C -myc蛋白表达 ,从而提高CAA患者骨髓造血干细胞水平的。 Objective:To observe the effects and the mechanism of the soluble granules of Busui Shengxue(补髓生血冲剂)to Chronic Aplastic Anemia(CAA).Methods:Doublelabel immunohistochemical method to observe the level of CD + 34 and CD 34 + C-MYC BEFORE AND AFTER TREATMENT IN 36 CAA patients.Result:CD + 34 of CAA patients showed lower level before and after treatment than normal groups ( P< 0.05 ),CD + 34 showed higher level after treatment than before( P< 0.05 );CD 34 +C-myc of CAA patients showed higher level before and after treatmen than normal groups( P< 0.05 ),CD 34 +C-myc showed lower leve after treatment than before ( P< 0.05 );Experimental groups showed better effect than opposite groups( P< 0.05 ).Conclusion:One of the mechanism of the soluble granules of Busui Shengxue(补髓生血冲剂)probably increased the level of CAA patients'bone marrow hemopoietic stem cell by decreasing the level of C-myc. Author's address:The 210 Hospital of Dalian,Dalian 163515,China
出处 《中医药信息》 2005年第2期54-55,共2页 Information on Traditional Chinese Medicine
基金 国家自然科学基金资助项目 (30 2 71 62 1 )
关键词 再生障碍性贫血 补髓生血颗粒 慢性 CD34^+、CD34^+C—myc 实验研究 The soluble granules of Busui Shengxue Aplastic Anemia Chronic CD_(34)^+ CD_(34)^+ CD_(34)^+C-myc
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  • 1朱振宇,李惠玲,王盛巍,李树浓.免疫介导再障小鼠脾淋巴细胞诱导骨髓造血细胞凋亡[J].中国病理生理杂志,1997,13(5):465-469. 被引量:9
  • 2Koopman G, Reutelingsperger CP, kuijiten GA, et al. Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptisis[ J]. Blood, 1994,84(5): 1415 - 1420.
  • 3Maciejewski JP, Anderson S, Katevas P, et al. Phenotypic and functional analysis of bone marrow progenitor cell compatment in bone marrow failure [J]. Br J . Haematol, 1994(87) :227.

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