Cholecystokinin receptor mediated hydrolysis of inositol phospholipids in guinea pig gastric glands.

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 Sci

journal_title

Life sciences

authors

Chang RS,Lotti VJ,Chen TB

doi

10.1016/0024-3205(85)90392-3

subject

Has Abstract

pub_date

1985-03-11 00:00:00

pages

965-71

issue

10

eissn

0024-3205

issn

1879-0631

pii

0024-3205(85)90392-3

journal_volume

36

pub_type

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