Davison J S, Najafi-Farashah A
Life Sci. 1982 Jul 26;31(4):355-61. doi: 10.1016/0024-3205(82)90415-5.
Dibutyryl cyclic guanosine monophosphate (dbcGMP), a specific competitive inhibitor of the gastrin, cholecystokinin-pancreozymin (CCK-PZ) family of peptides in pancreas, gallbladder and ileum, had no effect on basal acid secretion in the isolated mouse stomach nor on secretion stimulated by bethanechol or histamine. Secretion evoked by low doses of pentagastrin were likewise unaffected by dbcGMP but responses to high doses of pentagastrin were augmented. CCK-PZ and glucagon each inhibited acid secretion evoked by pentagastrin. DbcGMP blocked CCK-PZ-mediated inhibition but was without effect on inhibition by glucagon. These observations suggest that in the gastric glands there exist two receptors with different affinities for gastrin and CCK-PZ which mediate excitation and inhibition respectively.
二丁酰环磷酸鸟苷(dbcGMP)是胃泌素、胆囊收缩素-促胰酶素(CCK-PZ)肽家族在胰腺、胆囊和回肠中的特异性竞争性抑制剂,对离体小鼠胃的基础胃酸分泌以及由氨甲酰甲胆碱或组胺刺激引起的分泌均无影响。低剂量五肽胃泌素引起的分泌同样不受dbcGMP影响,但对高剂量五肽胃泌素的反应增强。CCK-PZ和胰高血糖素均可抑制五肽胃泌素引起的胃酸分泌。dbcGMP可阻断CCK-PZ介导的抑制作用,但对胰高血糖素的抑制作用无影响。这些观察结果表明,胃腺中存在两种对胃泌素和CCK-PZ具有不同亲和力的受体,它们分别介导兴奋和抑制作用。