Born G V, Kratzer M A
J Physiol. 1984 Sep;354:419-29. doi: 10.1113/jphysiol.1984.sp015385.
A new technique was developed for the measurement of extracellular free ATP in very small samples of whole blood using the luciferin-luciferase enzyme system. The method had a very low background corresponding to approximately 10(-16) mol ATP. ATP was measured in blood as it emerged during haemostasis following precise puncture of rat and rabbit arteries and after standardized incisions of human skin by the Simplate device. The initial concentration of free ATP in blood emerging 2-4 s after vascular injury was about 2 X 10(-7) M in rats and rabbits and about 2 X 10(-6) M in humans. The free-ATP concentration increased to 2 X 10(-5) M 3-5 min after injury and these increases could be prevented by heparin (20 u./ml). The source of the initial free ATP was identified as damaged cells in the injured vessel wall. Sufficient ADP, both released as such with ATP and generated by enzymic dephosphorylation of ATP, would be present at the site of injury to initiate haemostatic aggregation of platelets.
利用荧光素 - 荧光素酶酶系统开发了一种新技术,用于测量极少量全血样本中的细胞外游离ATP。该方法具有非常低的背景,相当于约10(-16)摩尔ATP。在大鼠和兔动脉精确穿刺止血过程中以及通过Simplate装置对人皮肤进行标准化切口后,对血液中的ATP进行了测量。血管损伤后2 - 4秒出现的血液中游离ATP的初始浓度在大鼠和兔中约为2×10(-7)M,在人中约为2×10(-6)M。损伤后3 - 5分钟,游离ATP浓度增加到2×10(-5)M,这些增加可被肝素(20单位/毫升)阻止。初始游离ATP的来源被确定为受损血管壁中的受损细胞。在损伤部位会存在足够的ADP,它既与ATP一起释放,又由ATP的酶促去磷酸化产生,从而启动血小板的止血聚集。