Baba H, Fujimura M, Toda N
Department of Pharmacology, Shiga University of Medical Sciences, Ohtsu, Japan.
Regul Pept. 1990 Feb 4;27(2):227-35. doi: 10.1016/0167-0115(90)90041-t.
In isolated canine ileal longitudinal muscle preparations, cholecystokinin-octapeptide (CCK-8) produced a concentration-dependent contraction, which was suppressed by peptide YY (PYY) and was abolished by tetrodotoxin and atropine. PYY was approximately 2200-times as potent as CR1505, a CCK-receptor antagonist. PYY opposed the action of CCK-8 to a greater extent than that of nicotine and transmural electrical stimulation. Acetylcholine-induced contractions were not influenced by PYY. It seems likely that the CCK-8-induced ileal muscle contraction is associated with an activation of CCK receptors in cholinergic nerves, which generates nerve action potentials and releases acetylcholine, whereas CCK-8 acts on CCK receptors in gallbladder smooth muscle, producing contractions. It may be concluded that PYY inhibits the action of CCK-8 on ileal muscle strips, by inhibiting the release of acetylcholine from cholinergic nerve terminals. On the other hand, in the gallbladder, PYY does not appear to block cholinergic nerve function.
在离体犬回肠纵肌标本中,胆囊收缩素八肽(CCK - 8)产生浓度依赖性收缩,该收缩被肽YY(PYY)抑制,并被河豚毒素和阿托品消除。PYY的效力约为CCK受体拮抗剂CR1505的2200倍。PYY比尼古丁和跨壁电刺激更能对抗CCK - 8的作用。乙酰胆碱诱导的收缩不受PYY影响。CCK - 8诱导的回肠肌肉收缩似乎与胆碱能神经中CCK受体的激活有关,这会产生神经动作电位并释放乙酰胆碱,而CCK - 8作用于胆囊平滑肌中的CCK受体,产生收缩。可以得出结论,PYY通过抑制胆碱能神经末梢乙酰胆碱的释放来抑制CCK - 8对回肠肌条的作用。另一方面,在胆囊中,PYY似乎并不阻断胆碱能神经功能。