Kitamura Y, Hayashi S, Nomura Y
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Jpn J Pharmacol. 1990 Apr;52(4):597-607. doi: 10.1254/jjp.52.597.
Effects of 4-aminomethyl-1-benzylpyrrolidin-2-one-hemifumarate (WEB 1881 FU), a novel pyrrolidinone nootropic, on acetylcholine (ACh) receptors and adrenoceptors were investigated using crude membranes of the rat brain. The affinity order of WEB 1881 FU was: M1-muscarinic (m) ACh receptor greater than M2-mACh receptor greater than alpha 2-adrenoceptor greater than beta-adrenoceptor greater than alpha 1-adrenoceptor greater than nicotinic ACh receptor. The WEB 1881 FU-competition curve for [3H]pirenzepine binding in hippocampal membranes was rightward-shifted by GTP gamma S; such behavior was also observed in the case of oxotremorine but not with scopolamine. The effects of long-term administration of WEB 1881 FU (30 mg/kg/day, i.p.) for 21 days resulted in a significant decrease in the Bmax of [3H]quinuclidinyl benzilate binding in the cerebral cortex, hippocampus and striatum. In addition, the Bmax of [3H]pirenzepine binding to hippocampal and striatal membranes and that of [3H]AF-DX 116 binding to cerebellar membranes were significantly decreased as well. From these results, WEB 1881 FU seems to act on M1-mACh receptors, and its long-term administration probably induces the down-regulation of mACh receptors, mainly M1-mACh receptors in the hippocampus and striatum and M2-mACh receptors in the cerebellum.
使用大鼠脑粗膜研究了新型吡咯烷酮类促智药4-氨甲基-1-苄基吡咯烷-2-酮半富马酸盐(WEB 1881 FU)对乙酰胆碱(ACh)受体和肾上腺素能受体的影响。WEB 1881 FU的亲和力顺序为:M1型毒蕈碱(m)ACh受体>M2型mACh受体>α2-肾上腺素能受体>β-肾上腺素能受体>α1-肾上腺素能受体>烟碱型ACh受体。GTPγS使海马膜中[3H]哌仑西平结合的WEB 1881 FU竞争曲线右移;在氧化震颤素的情况下也观察到这种行为,但东莨菪碱则没有。长期给予WEB 1881 FU(30 mg/kg/天,腹腔注射)21天导致大脑皮层、海马和纹状体中[3H]奎宁环基苯甲酸酯结合的Bmax显著降低。此外,海马和纹状体膜中[3H]哌仑西平结合的Bmax以及小脑膜中[3H]AF-DX 116结合的Bmax也显著降低。从这些结果来看,WEB 1881 FU似乎作用于M1型mACh受体,其长期给药可能会诱导mACh受体的下调,主要是海马和纹状体中的M1型mACh受体以及小脑中的M2型mACh受体。