Inhibition effects of benactyzine and drofenine on human serum butyrylcholinesterase

被引:20
作者
Bodur, E [1 ]
Çokugras, AN [1 ]
Tezcan, EF [1 ]
机构
[1] Hacettepe Univ, Fac Med, Dept Biochem, TR-06100 Ankara, Turkey
关键词
butyrylcholinesterase; benactyzine; drofenine; inhibition; serum; human;
D O I
10.1006/abbi.2000.2188
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Benactyzine and drofenine are widely used anticholinergic drugs. Benactyzine is used to treat organophosphate poisoning and drofenine acts on smooth muscle to stop muscle spasms. Both of these drugs are esters, After they enter the bloodstream, they will interact with butyrylcholinesterase (BChE; acylcholine acyl hydrolase: EC 3.1.1.8), which has an ability to hydrolyze a wide variety of esters, Therefore, the kinetic analysis of their inhibitory effects on human serum BChE was examined using butyrylthiocholine as substrate. Both drugs were competitive inhibitors of BChE and the gi values of benactyzine and drofenine were calculated to be 0.010 +/- 0.001 and 0.003 +/- 0.000 mM, respectively, using the Systat (version 5.03, 1991) nonlinear regression analysis software package. According to these parameters, drofenine is a more potent competitive inhibitor of BChE than benactyzine, (C) 2001 Academic Press.
引用
收藏
页码:25 / 29
页数:5
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