Abass Kasim Sakran
Department of Basic Nursing Sciences, College of Nursing, University of Kirkuk, Kirkuk, Iraq.
Biomed Res Int. 2014;2014:451982. doi: 10.1155/2014/451982. Epub 2014 Apr 22.
Organophosphate compounds can bind to carboxylesterase, which may lower the concentration of organophosphate pesticides at the target site enzyme, cholinesterase. It is unclear from the literature whether it is the carboxylesterase affinity for the organophosphate and/or the number of carboxylesterase molecules that is the dominant factor in determining the protective potential of carboxylesterase. The fundamental dilutions and kinetic effects of esterase enzyme are still poorly understood. This study aims to confirm and extend our current knowledge about the effects of dilutions on esterases activities in the blood for birds with respect to protecting the enzyme from organophosphate inhibition. There was significantly higher esterases activities in dilution 1 : 10 in the all blood samples from quail, duck, and chick compared to other dilutions (1 : 5, 1 : 15, 1 : 20, and 1 : 25) in all cases. Furthermore, our results also pointed to the importance of estimating different dilutions effects prior to using in birds as biomarker tools of environmental exposure. Concentration-inhibition curves were determined for the inhibitor in the presence of dilutions 1 : 5, 1 : 10, plus 1 : 15 (to stimulate carboxylesterase). Point estimates (concentrations calculated to produce 20, 50, and 80% inhibition) were compared across conditions and served as a measure of esterase-mediated detoxification. Results with well-known inhibitors (malathion) were in agreement with the literature, serving to support the use of this assay. Among the thiol-esters dilution 1 : 5 was observed to have the highest specificity constant (k(cat)/K(m)), and the K m and k cat values were 176 μM and 16,765 s(-1), respectively, for S-phenyl thioacetate ester, while detected in dilution 1: 15 was the lowest specificity constant (k(cat)/K(m)), and the Km and k cat values were 943 μM and 1154 s(-1), respectively, for acetylthiocholine iodide ester.
有机磷酸酯化合物可与羧酸酯酶结合,这可能会降低目标位点酶(胆碱酯酶)处有机磷酸酯农药的浓度。从文献中尚不清楚是羧酸酯酶对有机磷酸酯的亲和力和/或羧酸酯酶分子的数量是决定羧酸酯酶保护潜力的主导因素。酯酶的基本稀释和动力学效应仍知之甚少。本研究旨在确认并扩展我们目前关于稀释对鸟类血液中酯酶活性的影响的知识,以保护该酶免受有机磷酸酯抑制。在所有情况下,鹌鹑、鸭和小鸡的所有血液样本中,1:10稀释度下的酯酶活性显著高于其他稀释度(1:5、1:15、1:20和1:25)。此外,我们的结果还指出了在将其用作环境暴露生物标志物工具之前估计不同稀释效应的重要性。在1:5、1:10和1:15稀释度(以刺激羧酸酯酶)存在的情况下测定抑制剂的浓度-抑制曲线。比较不同条件下的点估计值(计算得出产生20%、50%和80%抑制的浓度),并将其作为酯酶介导的解毒作用的一种衡量指标。使用知名抑制剂(马拉硫磷)的结果与文献一致,有助于支持该检测方法的应用。在硫醇酯中,观察到1:5稀释度具有最高的特异性常数(k(cat)/K(m)),对于S-苯基硫代乙酸酯,Km和k cat值分别为176μM和16765 s(-1),而在1:15稀释度下检测到的乙酰硫代胆碱碘化物酯的特异性常数(k(cat)/K(m))最低,Km和k cat值分别为943μM和1154 s(-1)。