Maroni M, Bleecker M L
J Appl Toxicol. 1986 Feb;6(1):1-7. doi: 10.1002/jat.2550060102.
The target enzyme in organophosphorous-induced delayed neuropathy (OPIDN) has been designated neuropathy target esterase or neurotoxic esterase (NTE). NTE activity can be measured in blood lymphocytes and platelets, which could be of use as biomonitors in man at risk for the development of OPIDN. Separation of lymphocytes and platelets from whole blood, recovery, purity, storage and expression of data were examined. A substantial amount of the NTE activity of a human lymphocyte preparation made using Ficoll/Pacque was due to contamination by platelets; further purification was achieved by sucrose-gradient centrifugation. In an easily prepared sample of human platelets less than 10% of NTE was associated with contaminating white cells. We were unable to preserve NTE activity of platelets or lymphocytes at -80 degrees C either 'dry' or with added buffer and glycerol. In 68 male subjects, NTE activity in platelets averaged 8.36 +/- 1.54 nmol min-1 mg protein-1 and NTE activity in lymphocytes, obtained from blood after removal of platelets, 13.34 +/- 2.42 nmol min-1 mg protein-1. A good correlation was found between platelet and lymphocyte NTE activity. NTE activity in platelets may be a preferable method for measuring exposure to axonopathic organophosphorous compounds because of the ease and purity of separation. No correlation with other neuropathic risk factors such as age, smoking and alcohol intake was noted.
有机磷诱导的迟发性神经病(OPIDN)中的靶酶已被命名为神经病靶酯酶或神经毒性酯酶(NTE)。NTE活性可在血液淋巴细胞和血小板中检测,这可作为有OPIDN发病风险人群的生物监测指标。研究了从全血中分离淋巴细胞和血小板、回收率、纯度、储存及数据表达情况。用Ficoll/Pacque制备的人淋巴细胞制剂中,大量的NTE活性是由血小板污染所致;通过蔗糖梯度离心进一步纯化。在一份易于制备的人血小板样本中,不到10%的NTE与污染的白细胞有关。无论是“干燥”状态还是添加缓冲液和甘油后,我们都无法在-80℃保存血小板或淋巴细胞的NTE活性。在68名男性受试者中,血小板中的NTE活性平均为8.36±1.54 nmol min-1 mg蛋白-1,从去除血小板后的血液中获得的淋巴细胞中的NTE活性为13.34±2.42 nmol min-1 mg蛋白-1。血小板和淋巴细胞的NTE活性之间存在良好的相关性。由于分离简便且纯度高,血小板中的NTE活性可能是一种更优的测量轴索性有机磷化合物暴露的方法。未发现与年龄、吸烟和饮酒等其他神经病风险因素存在相关性。