首页> 外文期刊>Japanese Journal of Pharmacology >Inhibitory Effects of KW-5092, a Novel Gastroprokinetic Agent, on the Activity of Acetylcholinesterase in Guinea Pig Ileum
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Inhibitory Effects of KW-5092, a Novel Gastroprokinetic Agent, on the Activity of Acetylcholinesterase in Guinea Pig Ileum

机译:新型胃肠动力药KW-5092对豚鼠回肠乙酰胆碱酯酶活性的抑制作用

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References(19) Cited-By(10) 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-5092 inhibited AChE and BuChE with the IC50 values of 6.8 × 10-8 M and 2.4 × 10-5 M, respectively. The IC50 values of neostigmine for AChE and BuChE were 3.6 × 10-8 M and 1.9 × 10-7 M, respectively. HSR-803 (N-[4-[2-(dimethylamino)ethoxy]benzyl]-3, 4-dimethoxybenzamide hydrochloride), a gastroprokinetic agent, inhibited AChE and BuChE with the IC50 values of 8.6 × 10-6 M and 6.0 × 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 non-competitive 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.
机译:参考文献(19)被引用的By(10)KW-5092({1- [2-[[[5-(哌啶子基甲基-2-呋喃基]甲基]氨基]乙基] -2-咪唑啉亚基}丙烷富马酸酯)胃肠动力剂具有乙酰胆碱酯酶(AChE)抑制活性和乙酰胆碱释放促进活性。本研究使用豚鼠回肠匀浆检查KW-5092对AChE和丁酰胆碱酯酶(BuChE)的抑制作用。 KW-5092抑制AChE和BuChE,IC50值分别为6.8×10-8 M和2.4×10-5M。新斯的明对AChE和BuChE的IC50值分别为3.6×10-8 M和1.9×10-7M。胃动力药HSR-803(N- [4- [2-(二甲基氨基)乙氧基]苄基] -3,4-二甲氧基苯甲酰胺盐酸盐)抑制AChE和BuChE,IC50值为8.6×10-6 M和6.0× 10-4M。 KW-5092对AChE的抑制作用是可逆且非竞争性的,而HSR-803对AChE的抑制则具有可逆性和非竞争性。另一方面,在加入底物之前将酶与该抑制剂预孵育2分钟时,新斯的明对AChE的抑制作用是非竞争性的,而在同时孵育酶,抑制剂和底物时,该酶几乎具有竞争性。 。目前的结果表明,KW-5092是一种选择性,可逆和非竞争性的AChE抑制剂,具有与新斯的明和HSR-803不同的特征。 AChE抑制作用可能有助于其胃肠动力作用。

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