INHIBITORY EFFECTS OF KW-5092, A NOVEL GASTROPROKINETIC AGENT, ON THE ACTIVITY OF ACETYLCHOLINESTERASE IN GUINEA-PIG ILEUM

被引:16
作者
KISHIBAYASHI, N
ISHII, A
KARASAWA, A
机构
[1] Department of Pharmacology, Pharmaceutical Research Laboratories, Kyo wa Hakko Kogyo Co., Ltd., Shizuoka 411, 1188 Simotogari, Sunto-gun
关键词
KW-5092; NEOSTIGMINE; ANTICHOLINESTERASE ACTIVITY; ILEUM (GUINEA PIG);
D O I
10.1254/jjp.66.397
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
KW-5092 ({1-[2-[[[5-(piperidinomethyl)-2-furanyl]methyl]amino]ethyl]-2-imidazolidinylidene} propanedinitrile fumarate) is a novel gastroprokinetic agent with acetylcholinesterase (AChE) inhibitory activity and acetylcholine release facilitatory activity. The present study used guinea pig ileal homogenates to examine the inhibitory effects of KW-5092 on the activities of AChE and butyrylcholinesterase (BuChE). KW-5099 inhibited AChE and BuChE with the IC50 values of 6.8 x 10(-8) M and 2.4 x 10(-5) M, respectively. The IC50 values of neostigmine for AChE and BuChE were 3.6 x 10(-8) M and 1.9 x 10(-7) M, respectively. HSR-803 (N-[4-[2-(dimethylamino)ethoxy]benzyl]-3 hydrochloride), a gastroprokinetic agent, inhibited AChE and BuChE with the IC50 values of 8.6 x 10(-6) M and 6.0 x 10(-4) M, respectively. The AChE inhibition by KW-5092 was reversible and noncompetitive, whereas that by HSR-803 was reversible and uncompetitive. On the other hand, the AChE inhibition by neostigmine was noncompetitive when the enzyme was preincubated with this inhibitor for 2 min prior to the addition of the substrate, and it was nearly competitive when the enzyme, the inhibitor and the substrate were incubated simultaneously. The present results demonstrate that KW-5092 is a selective, reversible and noncompetitive inhibitor of AChE with different characteristics from those of neostigmine and HSR-803. The AChE inhibitory action may contribute to its gastroprokinetic effect.
引用
收藏
页码:397 / 403
页数:7
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