Seidel H J, Kreja L
Exp Hematol. 1982 Feb;10(2):151-60.
DBA/2 mice, 12 days after infection with the polycythemia-inducing Friend virus (F-MulV-P), were treated with a single dose of BCNU. The effect of 35 mg/kg and lower doses on the different stem cell pools (CFUS, CFUC, CFUE) and the F-MulV-P specific ICPC (infectious centers producing cells) and Ep-independent CFUE was studied in detail. The depression of CFUS and CFUC was comparable in normal and F-MuLV-P infected mice. The CFUE population of virus infected mice, which had been completely Ep independent before treatment, showed only some normal Ep dependent colony growth thereafter. This finding was in contrast to the effect of multiple doses of Hydroxyurea, studied previously, which had given the same quantitative depression of CFUS and CFUC. Possible reasons for this failure are discussed; they may be the more proliferation independent mode of action of BCNU and the delayed hemopoietic regeneration.
用诱导红细胞增多的Friend病毒(F-MulV-P)感染12天后的DBA/2小鼠,用单剂量的卡莫司汀(BCNU)进行治疗。详细研究了35mg/kg及更低剂量对不同干细胞池(CFUS、CFUC、CFUE)以及F-MulV-P特异性ICPC(产生感染中心的细胞)和不依赖促红细胞生成素的CFUE的影响。正常小鼠和感染F-MuLV-P的小鼠中CFUS和CFUC的降低情况相当。病毒感染小鼠的CFUE群体在治疗前完全不依赖促红细胞生成素,此后仅表现出一些正常的依赖促红细胞生成素的集落生长。这一发现与先前研究的多次剂量羟基脲的效果形成对比,多次剂量羟基脲对CFUS和CFUC产生了相同程度的降低。讨论了这种失败的可能原因;可能是卡莫司汀更具增殖非依赖性的作用方式以及造血再生延迟。