Dygaĭ A M, Zhdanov V V, Khlusov I A, Liubavina P A, Gol'dberg E D
Gematol Transfuziol. 1995 Sep-Oct;40(5):11-5.
The study of bone marrow hemopoiesis, the count of hemopoietic precursor cells, bone marrow structural and functional organization, the level of humoral stimulators and secretion by hemopoiesis-inducing microenvironment (HIM) cells following a single injection of 5-fluorouracil, cyclophosphamide or adriamycin has found out that cytostatic-related changes in hemopoiesis recovery depend primarily on relationships between proliferation and differentiation of hemopoietic cells. These relationships are dictated by the state of HIM cells. Enhanced functional activity of HIM elements in response to hemopoietic tissue damage caused by adriamycin or cyclophosphamide promotes rapid hemopoiesis regeneration. At the same time, 5-fluorouracil gave rise to prolonged bone marrow hypoplasia, severe disorder of microenvironment cell function.
对骨髓造血、造血前体细胞计数、骨髓结构和功能组织、单次注射5-氟尿嘧啶、环磷酰胺或阿霉素后体液刺激因子水平以及造血诱导微环境(HIM)细胞分泌情况的研究发现,与细胞生长抑制剂相关的造血恢复变化主要取决于造血细胞增殖与分化之间的关系。这些关系由HIM细胞的状态决定。阿霉素或环磷酰胺引起造血组织损伤后,HIM成分功能活性增强,促进造血快速再生。与此同时,5-氟尿嘧啶导致骨髓发育不全持续时间延长,微环境细胞功能严重紊乱。