Abstract:
:CCK-octapeptide (CCK-8) (EC50 = 0.5 nM), in the presence of Li+, increased 3H-inositol phosphate (IP) accumulation in guinea pig gastric glands prelabeled with 3H-inositol. CCK-8 desulfate, human gastrin I and pentagastrin were much less potent than CCK-8. Antagonists of CCK receptors such as proglumide, dibutyryl-c-GMP and CBZ-Tyr (SO3H)-Met-Gly-Trp-Met-AspNH2 shifted the CCK dose response curve to the right. However, histamine (H1 and H2), cholinergic, substance P and alpha- and beta-adrenergic receptor antagonists had no effect on 3H-IP accumulation induced by CCK. The results suggest that CCK receptor activation in gastric glands leads to an enhanced breakdown of inositol phospholipids which may relate to calcium mobilization and pepsinogen secretion.
journal_name
Life Scijournal_title
Life sciencesauthors
Chang RS,Lotti VJ,Chen TBdoi
10.1016/0024-3205(85)90392-3subject
Has Abstractpub_date
1985-03-11 00:00:00pages
965-71issue
10eissn
0024-3205issn
1879-0631pii
0024-3205(85)90392-3journal_volume
36pub_type
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