Ranitidine fails to suppress the growth in vitro of haemopoietic progenitors from human peripheral blood or bone marrow.

C D Reid, A Kirk
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引用次数: 3

Abstract

Ranitidine was added in various concentrations (25-1600 ng/ml) to clonal assays of haemopoietic progenitors of normal human peripheral blood or bone marrow. Although a significant reduction in colonies forming from granulocyte-macrophage progenitors (CFU-GM) was demonstrated at the lowest drug concentration, no significant growth suppression was seen at higher concentrations. There was no evidence for growth inhibition of either erythroid progenitors (BFU-E) or pluripotent progenitors (CFU-mix) at any of the drug concentrations studied. A direct toxic effect of ranitidine on normal haemopoietic progenitors thus appears an unlikely cause of cytopenias observed during treatment.

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雷尼替丁不能抑制体外人外周血或骨髓造血祖细胞的生长。
将不同浓度的雷尼替丁(25-1600 ng/ml)加入到正常人外周血或骨髓造血祖细胞的克隆测定中。尽管在最低药物浓度下,粒细胞-巨噬细胞祖细胞(CFU-GM)形成的菌落明显减少,但在较高浓度下,没有发现明显的生长抑制。在研究的任何药物浓度下,没有证据表明红细胞祖细胞(BFU-E)或多能祖细胞(CFU-mix)的生长受到抑制。因此,雷尼替丁对正常造血祖细胞的直接毒性作用似乎不太可能是治疗期间观察到的细胞减少的原因。
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