0/G1期向S、G2/M期轉(zhuǎn)化(P<0.05);能一定程度上緩解化療導(dǎo)致的成纖維細(xì)胞集落生成單位(CFU-F)形成減少(P<0.05);能上調(diào)抗凋亡基因Bcl-2 mRNA的表達(dá)((P<0.05)。結(jié)論 消巖湯能夠促進(jìn)骨髓細(xì)胞向增殖周期轉(zhuǎn)化,上調(diào)Bcl-2 mRNA表達(dá),改善造血微環(huán)境,從而緩解Lewis肺癌骨髓抑制對小鼠造血功能的影響。;Objective To observe the effects of Xiaoyan Decoction on hemopoietic microenvironment in Lewis lung cancer mice with myelosuppression induced by cyclophosphamide, and discuss the improvement on hemopoietic microenvironment in Lewis lung cancer mice with myelosuppression and to explore its mechanism. Methods SPF Lewis lung cancer mice were randomly divided into control, model, recombinant human granulocyte colony-stimulating factor (rhG-CSF), and Xiaoyan Decoction groups, and each group had 10 mice. Mice in the control and model groups were ig normal saline 0.02 mL/g. Mice in the rhG-CSF group were sc Recombinant Human Granulocyte Colony-Stimulating Factor Injection 15 ng/g after be established myelosuppression models, once daily, and be treated for 7 d. Mice in the Xiaoyan Decoction group were ig Xiaoyan Decoction 2.9 g/mL afterbe established myelosuppression models, twice daily, 0.2 mL/time, and be treated for 7 d. The cell cycles were analyzed by flow cytometry, differentiation of stromal cell were determined by cell culture technique, and express levels on Bcl-2 mRNA and Bax mRNA of bone marrow cells were checked by qRT-PCR method. Results Compared with the model group, Xiaoyan decoction could promote the bone marrow cells from G0/G1 phase to S and G2 /M phase transformation in the cell cycle (P < 0.05), could inhibit the reduction of fibroblast colony forming unit (CFU-F) formation induced by chemotherapy to a certain extent(P < 0.05), and could up-regulate the expression of anti apoptotic gene Bcl-2 mRNA (P < 0.05). Conclusion Xiaoyan Decoction can promote the transformation of bone marrow cells to proliferation cycles, up-regulate the expression of Bcl-2 mRNA gene, improve hemopoietic microenvironment, and relieve the effect of hematopoietic function in Lewis lung cancer mice with myelosuppression."/>