Jing H, Lin K W, Mei M H
Department of Physiology, Dalian Medical University.
Sheng Li Xue Bao. 1995 Jun;47(3):245-52.
Our previous study showed that microinjection of substance P (SP) into caudate nucleus inhibits gastric myoelectric fast wave and gastric motility, an effect mediated by muscarinic receptor. The present investigation showed that this effects of SP could be blocked by coinjected SP antiserum or SP antagonist [Arg6, D-Trip7,9, MePhe8]-SP6-11 or D2 dopamine antagonist haloperidol. In addition, microinjection of dopamine (DA) into caudate nucleus could also inhibit gastric fast wave and motility, an effect again being blockable by coinjected DA antagonist haloperidol or atropine. Thus, it appears that the muscarinergic inhibitory effect of SP on gastric fast wave and motility is mediated by D2 dopamine receptor.
我们先前的研究表明,向尾状核微量注射P物质(SP)会抑制胃肌电快波和胃动力,这一效应由毒蕈碱受体介导。目前的研究表明,SP的这种效应可被共同注射的SP抗血清或SP拮抗剂[Arg6,D-Trip7,9,MePhe8]-SP6-11或D2多巴胺拮抗剂氟哌啶醇阻断。此外,向尾状核微量注射多巴胺(DA)也会抑制胃快波和动力,这一效应同样可被共同注射的DA拮抗剂氟哌啶醇或阿托品阻断。因此,似乎SP对胃快波和动力的毒蕈碱能抑制作用是由D2多巴胺受体介导的。