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肽YY对胆囊收缩素诱导的离体犬回肠收缩的抑制作用机制。

Mechanism of inhibitory action of peptide YY on cholecystokinin-induced contractions of isolated dog ileum.

作者信息

Baba H, Fujimura M, Toda N

机构信息

Department of Pharmacology, Shiga University of Medical Sciences, Ohtsu, Japan.

出版信息

Regul Pept. 1990 Feb 4;27(2):227-35. doi: 10.1016/0167-0115(90)90041-t.

Abstract

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.

摘要

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。

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