Fujimiya M, Miyazaki M, Fujimura M, Kimura H
Department of Anatomy, Shiga University of Medical Science, Japan.
Peptides. 1995;16(5):939-44. doi: 10.1016/0196-9781(95)00062-o.
Possible cholinergic control on the release of PYY from intestine into the lumen or blood vessel was studied by radioimmunoassay in the isolated perfused rat ileum. The basal release of PYY into the lumen was 43.1 +/- 8.9 pg/min, which was comparable with that into the vasculature (35.2 +/- 2.6 pg/min). The administration of 1 microM carbachol into the vascular perfusate resulted in a more than 40-fold increase of the luminal release but only a twofold increase of the vascular release. Carbachol-induced release of PYY into both lumen and vasculature was completely blocked by atropine, but not by hexamethonium. Tetrodotoxin abolished carbachol-induced release of PYY into lumen and vasculature. These data suggest that the ileal PYY release, into either lumen or vasculature, is under the control of postganglionic cholinergic neurons via muscarinic receptors.
通过放射免疫分析法,在离体灌注的大鼠回肠中研究了胆碱能对肠道中PYY释放至肠腔或血管的可能控制作用。PYY向肠腔的基础释放量为43.1±8.9 pg/分钟,这与向血管系统的释放量(35.2±2.6 pg/分钟)相当。向血管灌流液中加入1 microM卡巴胆碱,导致肠腔释放增加40多倍,但血管释放仅增加两倍。卡巴胆碱诱导的PYY向肠腔和血管系统的释放被阿托品完全阻断,但六甲铵未阻断。河豚毒素消除了卡巴胆碱诱导的PYY向肠腔和血管系统的释放。这些数据表明,回肠中PYY向肠腔或血管系统的释放受节后胆碱能神经元通过毒蕈碱受体的控制。