Daenen S, Goris H, de Boer F, Halie M R, van der Waaij D
Department of Haematology, University of Groningen, The Netherlands.
Leuk Res. 1991;15(11):1013-8. doi: 10.1016/0145-2126(91)90106-4.
The influence of intestinal flora modulation by oral bacitracin on the recovery of myelopoiesis after Ara-C was studied in C3H/Law mice. Bacitracin resulted in a 3-5 log increase of Gram-negative bacteria and a 10-fold increase of the intestinal endotoxin concentration. Initiation of bacitracin before Ara-C stimulated the initial rebound increase of colony-forming units for granulocytes and macrophages (CFU-GM) from 23.2 +/- 1.3 to 28.4 +/- 1.4 x 10(3) per femur. Starting the bacitracin after Ara-C advanced the second phase of the rebound CFU-GM increase with 6 days. An important role in the recovery of myelopoiesis after cytostatic drugs in C3H/Law mice is suggested for the intestinal Gram-negative microflora, probably mediated by bacterial endotoxin.
在C3H/Law小鼠中研究了口服杆菌肽调节肠道菌群对阿糖胞苷(Ara-C)后骨髓生成恢复的影响。杆菌肽导致革兰氏阴性菌增加3-5个对数,肠道内毒素浓度增加10倍。在Ara-C之前开始使用杆菌肽可刺激粒细胞和巨噬细胞集落形成单位(CFU-GM)的初始反弹增加,从每只股骨23.2±1.3增加到28.4±1.4×10³。在Ara-C之后开始使用杆菌肽可使CFU-GM反弹增加的第二阶段提前6天。提示肠道革兰氏阴性微生物群在C3H/Law小鼠中细胞毒性药物后骨髓生成的恢复中起重要作用,可能由细菌内毒素介导。