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局部麻醉药(普鲁卡因和丁卡因)对沙漠眼镜蛇(埃及沃尔特氏蛇)毒液中乙酰胆碱酯酶的抑制动力学

Kinetics of the inhibition of acetylcholinesterase from desert cobra (Walterinnesia aegyptia) venom by local anesthetics: procaine and tetracaine.

作者信息

al-Jafari A A, Kamal M A, Duhaiman A S, Alhomida A S

机构信息

Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.

出版信息

J Enzyme Inhib. 1996 Oct;11(2):123-34. doi: 10.3109/14756369609036539.

Abstract

The kinetic parameters of W. aegyptia venom acetylcholinesterase (AChE) inhibition by procaine and tetracaine hydrochloride were investigated in the present study. Procaine and tetracaine reversibly inhibited the AChE activity in a concentration-dependent manner, the IC50 being about 0.28 and 0.04 mM, respectively. The Michaelis-Menten constant (K(m)) for the hydrolysis of acetylthiocholine iodide was found to be 0.051 mM with Vmax 10.2 mumole/min/mg protein. Both K(m) and Vmax were affected by procaine while only Vmax decreased with tetracaine. A Lineweaver-Burk plot and its secondary replot indicated that the nature of the inhibition is of the linear mixed type for procaine which is considered to be a mixture of competitive and noncompetitive types while the inhibition was noncompetitive for tetracaine. The values of Ki(slope) and K(intercept were estimated as 0.133 mM and 0.451 mM for procaine and 7.2 x 10(-3) mM for tetracaine, respectively, by the secondary replots of the Lineweaver-Burk plot.

摘要

本研究考察了普鲁卡因和盐酸丁卡因对埃及伊蚊毒液乙酰胆碱酯酶(AChE)抑制作用的动力学参数。普鲁卡因和丁卡因以浓度依赖性方式可逆地抑制AChE活性,IC50分别约为0.28和0.04 mM。发现碘化硫代乙酰胆碱水解的米氏常数(K(m))为0.051 mM,Vmax为10.2微摩尔/分钟/毫克蛋白。K(m)和Vmax均受普鲁卡因影响,而丁卡因仅使Vmax降低。双倒数图及其二级重绘图表明,普鲁卡因的抑制性质为线性混合型,被认为是竞争性和非竞争性类型的混合物,而丁卡因的抑制作用为非竞争性。通过双倒数图的二级重绘图,普鲁卡因的Ki(斜率)和K(截距)值分别估计为0.133 mM和0.451 mM,丁卡因的为7.2×10(-3) mM。

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