Pospíŝil M, Hofer M, Znojil V, Vácha J, Netíková J, Holá J
Institute of Biophysics, Academy of Sciences of the Czech Republic, Brno, Czech Republic.
Blood. 1995 Nov 15;86(10):3692-7.
Experimental evidence suggests that the activation of purinoceptors by extracellular adenosine can modulate proliferation and/or differentiation of hematopoietic cells. The present study was undertaken to investigate the potential interactions of this system of intercellular signaling with the effects of granulocyte colony-stimulating factor (G-CSF) on granulopoiesis in vivo. Elevation of extracellular adenosine in normal mice was induced by the joined administration of dipyridamole, a drug inhibiting the cellular uptake of adenosine, and adenosine monophosphate (AMP), an adenosine prodrug. The effects of dipyridamole, AMP, and G-CSF, administered either alone or in combinations, were evaluated. The agents were injected to mice in a 4-day regimen, and the hematologic endpoints were determined 24 hours after the completion of the treatment. It was shown that the effects of G-CSF, ie, increases in peripheral blood neutrophils, granulocyte-macrophage progenitor cells (GM-CFC), and morphologically determined granulocytic cells in femoral marrow and a decrease in the marrow erythroid cells, can be enhanced by the combination of dipyridamole plus AMP administered 30 minutes before G-CSF. Furthermore, it was ascertained that the stimulatory action of dipyridamole plus AMP was expressed particularly at lower doses of G-CSF (1.5, 3, and 4.5 micrograms/d). At higher doses of G-CSF (6 and 9 micrograms/d), the interactions were no more evident. When combining dipyridamole, AMP, and 3 micrograms of G-CSF, peripheral neutrophils increased approximately 3.9- to 4.5-fold compared with an approximate 2.2-fold increase induced by G-CSF alone. The results indicate the possible therapeutic potential of combination therapy with G-CSF and drugs increasing extracellular adenosine.
实验证据表明,细胞外腺苷激活嘌呤受体可调节造血细胞的增殖和/或分化。本研究旨在探讨这种细胞间信号系统与粒细胞集落刺激因子(G-CSF)对体内粒细胞生成的影响之间的潜在相互作用。通过联合给予双嘧达莫(一种抑制腺苷细胞摄取的药物)和腺苷前体药物单磷酸腺苷(AMP),诱导正常小鼠细胞外腺苷水平升高。评估了双嘧达莫、AMP和G-CSF单独或联合给药的效果。将这些药物以4天的方案注射到小鼠体内,并在治疗完成后24小时测定血液学终点指标。结果表明,在G-CSF给药前30分钟联合给予双嘧达莫加AMP,可增强G-CSF的作用,即外周血中性粒细胞、粒细胞-巨噬细胞祖细胞(GM-CFC)增加,股骨骨髓中形态学确定的粒细胞增加,骨髓红细胞减少。此外,还确定双嘧达莫加AMP的刺激作用在较低剂量的G-CSF(1.5、3和4.5微克/天)时尤为明显。在较高剂量的G-CSF(6和9微克/天)时,这种相互作用不再明显。当联合使用双嘧达莫、AMP和3微克G-CSF时,外周血中性粒细胞增加约3.9至4.5倍,而单独使用G-CSF时增加约2.2倍。结果表明G-CSF与增加细胞外腺苷的药物联合治疗可能具有治疗潜力。