Clinical Efficacy and Molecular Mechanism of Nourishing Shen and Supplementing Marrow Principle in Treating β Thalassemia

被引:6
作者
吴志奎
方素萍
张新华
蔡辉国
王蕾
易杰
柴立民
吕鑫霞
陈玉英
黄有文
王荣新
陈佩珍
机构
[1] China Academy of Traditional Chinese Medicine
[2] Chinese Academy of Medical Sciences
[3] Chinese Academy of Medical Sciences BeiJing (100053)
[4] Department of Molecular Biology
[5] Guang’anmen Hospital
[6] Institute of Hematology
[7] The 303 Hospitol of PLA
关键词
nourishing Shen and supplementing marrow principle; Shen producing marrow; β-thalassemia; gene analysis; mRNA gene ex pression; molecular mechanism;
D O I
暂无
中图分类号
R55 [血液及淋巴系疾病];
学科分类号
1002 ; 100201 ;
摘要
Objective: To explore the possibility of using traditional Chinese medicine (TCM) in treating β thalassemia, its clinical effect and molecular mechanism of the action.Methods: According to the TCM theory of“Shen producing marrow”, the composite recipe, Yisui Shenxueling Granule (YSSXL), consisting of Chinese drugs for nourishing Shen and supplementing marrow (NS&SM) was given orally to 7 8 patients with β thalassemia (49 of the severe type and 29 of moderate type ), 3 times a day, 10 g each time (for children, the dose would be reduced proper ly), with 3 months as one therapeutic course, and no blood transfusion used in t he course. The clinical therapeutic efficacy and hematologic parameters in patie nts were observed, and systemic gene analysis was conducted with PAGE, PCR, PCR SSCP, RT PCR and DNA sequences analysis and mRNA detection, in order to s tudy the molecular mechanism from the relationships between genetic mutation and clinical efficacy, gene expression and its regulation. Results: YSSXL showed obvious therapeutic effect in treating β thalassemia. Gene analysis revealed that it did not change the genetic mutatio n type, but could obviously increase hemoglobin, fetal hemoglobin (HbF), γ/(β+ γ) globin ratio, γ globin mRNA expression and GM CSF mRNA expression in patients, as well as the GM CSFmRMA in marrow of mice after 60 Co radia tion. Conclusion: YSSXL has a remarkable therapeutic effect on β tha lassemia, and its possible mechanism is its action in unlocking γ gene, in creasing the γ globin expression and enhancing HbF synthesis so as to compe nsate for the gene defect. This study has opened a new path for the treatment of β thalassemia with TCM.
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页码:248 / 253
页数:6
相关论文
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[1]  
Treatment of severeβthalassemia ( patient ) with Myleran. LIU DP,LIANG ZQ,AO ZH,et al. American Journal of Hematology . 1990