Gill D P, Jenkins V K, Kempen R R, Ellis S
Toxicology. 1980;16(2):163-71. doi: 10.1016/0300-483x(80)90046-3.
Several schedules of benzene exposure were evaluated for their effects on peripheral white blood cell counts, bone marrow cellularity and transplantable colony forming units (CFU-S) in male C57 Bl/6 mice. Intermittent exposure to 4000 ppm benzene in air produced leukopenia without altering the bone marrow cellularity. This same treatment, however, decreased the number of CFU-S to 30% of control values. Uninterrupted exposure to lower levels of benzene decreased peripheral cell counts within 24 h, and later decreased marrow cellularity. Exposure of a non-dividing population of stem cells (CFU-S) to benzene for up to 24 h produced no detectable effect on the subsequent development of spleen colonies, suggesting that the effect of benzene on CFU-S occurs only after peripheral cells are depleted. These findings indicate that benzene has affects on both differentiated cells and undifferentiated stem cells. An effect on the pluripotential stem cell is an important aspect of benzene toxicity, but not its exclusive or initial site of action.
对雄性C57 Bl/6小鼠进行了几种苯暴露方案,以评估其对外周血白细胞计数、骨髓细胞密度和可移植集落形成单位(CFU-S)的影响。间歇性暴露于空气中4000 ppm的苯会导致白细胞减少,但不会改变骨髓细胞密度。然而,相同的处理会使CFU-S的数量降至对照值的30%。持续暴露于较低水平的苯会在24小时内降低外周血细胞计数,随后降低骨髓细胞密度。将一群不分裂的干细胞(CFU-S)暴露于苯中长达24小时,对随后脾脏集落的发育没有可检测到的影响,这表明苯对CFU-S的影响仅在外周细胞耗尽后才会出现。这些发现表明苯对分化细胞和未分化干细胞都有影响。对多能干细胞的影响是苯毒性的一个重要方面,但不是其唯一或初始作用部位。