Comte L, Lorgeot V, Volkov L, Allegraud A, Aldigier J C, Praloran V
Laboratoire d'Hématologie Expérimentale, Faculté de Médicine, Limoges, France.
Eur J Clin Invest. 1997 Sep;27(9):788-90. doi: 10.1046/j.1365-2362.1997.1980737.x.
Acetyl-N-Ser-Asp-Lys-Pro (AcSDKP) is a physiological inhibitor of the proliferation of haematopoietic stem cells. In 12 healthy volunteers treated with the angiotensin-converting enzyme (ACE) inhibitor enalapril (20 mg day-1 for 15 days), we studied plasma and urinary AcSDKP levels, the in vitro degradation of AcSDKP by plasma ACE and the numbers of circulating haematopoietic progenitors (granulocyte-monocytic colony forming unit: CFU-GM; burst forming unit-erythroid: BFU-E; and mixed colony forming unit: CFU-mixed). During treatment, plasma and urinary AcSDKP concentrations increased 2- to 5-fold, degradation of AcSDKP was reduced, and CFU-mixed significantly increased by 100% while BFU-E and CFU-GM significantly decreased by 16% and 26%, respectively. These results indicate that ACE inhibitors may be of value during chemotherapy or radiotherapy, warranting further study.
乙酰 - N - 丝氨酸 - 天冬氨酸 - 赖氨酸 - 脯氨酸(AcSDKP)是造血干细胞增殖的一种生理抑制剂。在12名接受血管紧张素转换酶(ACE)抑制剂依那普利(每天20毫克,共15天)治疗的健康志愿者中,我们研究了血浆和尿液中AcSDKP的水平、血浆ACE对AcSDKP的体外降解以及循环造血祖细胞的数量(粒细胞 - 单核细胞集落形成单位:CFU - GM;红系爆式集落形成单位:BFU - E;混合集落形成单位:CFU - 混合)。治疗期间,血浆和尿液中AcSDKP浓度增加了2至5倍,AcSDKP的降解减少,CFU - 混合显著增加了100%,而BFU - E和CFU - GM分别显著减少了16%和26%。这些结果表明,ACE抑制剂在化疗或放疗期间可能具有价值,值得进一步研究。