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有证据表明,两种胆囊收缩素受体介导豚鼠离体回肠纵行肌肌间神经丛的收缩。

Evidence for two cholecystokinin receptors mediating the contraction of the guinea pig isolated ileum longitudinal muscle myenteric plexus.

作者信息

Dal Forno G, Pietra C, Urciuoli M, van Amsterdam F T, Toson G, Gaviraghi G, Trist D

机构信息

Glaxo Research Laboratories, Verona, Italy.

出版信息

J Pharmacol Exp Ther. 1992 Jun;261(3):1056-63.

PMID:1602372
Abstract

In guinea pig isolated ileum longitudinal muscle myenteric plexus, cholecystokinin octapeptide (CCK-8S) produced a rapid (phasic) contraction followed by a slower tonic phase. The tetrapeptide derivative CCK-4 and pentagastrin elicited only the phasic response up to 10(-6) M, whereas the tonic phase was also apparent at higher concentrations. The rank order of potency for the effect of agonists on the tonic and phasic responses were CCK-8S much greater than gastrin greater than CCK-8US congruent to pentagastrin greater than CCK-4 and CCK-8S greater than gastrin congruent to pentagastrin greater than CCK-4 greater than CCK-8US, respectively. Phasic responses of CCK-8S and CCK-4 were sensitive to atropine, whereas the tonic response could be completely abolished with the neurokinin-1 antagonist GR82334. The CCK-A receptor antagonist L-364,718 up to 10(-7) M had little effect on the phasic contracture of CCK-4. The CCK-B/gastrin receptor antagonist L-365,260 had no effect on the CCK-8S phasic response up to 10(-7) M, but antagonized the phasic response induced by low concentrations of CCK-4 in a competitive manner with an estimated pKB of 8.51. This value is close to that of 8.53 found in a guinea pig cortical binding assay. Both the second phase of the CCK-4 phasic concentration response curve (CRC) and the tonic contraction were insensitive to L-365,260.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在豚鼠离体回肠纵行肌肌间神经丛中,八肽胆囊收缩素(CCK - 8S)产生快速(相性)收缩,随后是较慢的紧张性收缩阶段。四肽衍生物CCK - 4和五肽胃泌素在浓度高达10⁻⁶ M时仅引起相性反应,而在更高浓度时紧张性收缩阶段也很明显。激动剂对紧张性和相性反应作用的效价顺序分别为:CCK - 8S远大于胃泌素大于CCK - 8US等同于五肽胃泌素大于CCK - 4,以及CCK - 8S大于胃泌素等同于五肽胃泌素大于CCK - 4大于CCK - 8US。CCK - 8S和CCK - 4的相性反应对阿托品敏感,而紧张性反应可被神经激肽-1拮抗剂GR82334完全消除。高达10⁻⁷ M的CCK - A受体拮抗剂L - 364,718对CCK - 4的相性挛缩几乎没有影响。CCK - B/胃泌素受体拮抗剂L - 365,260在浓度高达10⁻⁷ M时对CCK - 8S的相性反应没有影响,但以竞争性方式拮抗低浓度CCK - 4诱导的相性反应,估计pKB为8.51。该值与豚鼠皮质结合试验中测得的8.53接近。CCK - 4相性浓度反应曲线(CRC)的第二阶段和紧张性收缩对L - 365,260均不敏感。(摘要截断于250字)

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