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Am J Physiol Gastrointest Liver Physiol 244: G392-G396, 1983;
0193-1857/83 $5.00
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AJP - Gastrointestinal and Liver Physiology, Vol 244, Issue 4 392-G396, Copyright © 1983 by American Physiological Society


ARTICLES

Pepsinogen secretion from dispersed glands from rabbit stomach

D. K. Kasbekar, R. T. Jensen and J. D. Gardner

In dispersed glands from rabbit stomach, pepsinogen secretion was stimulated by carbamylcholine, the C-terminal octapeptide of cholecystokinin (CCK-8), and structurally related peptides physalaemin and A23187 but not by bombesin or histamine. Reducing the incubation temperature from 37 degrees to 4 degrees C or adding carbonyl cyanide m-chlorophenylhydrazone reduced basal as well as stimulated pepsinogen secretion. Dibutyryl cGMP inhibited the stimulation of pepsinogen secretion caused by cholecystokinin but not that caused by carbamylcholine; atropine inhibited the stimulation of pepsinogen secretion caused by carbamylcholine but not that caused by cholecystokinin. Each cholecystokinin-related peptide had the same efficacy for stimulating pepsinogen secretion. In terms of the concentration that caused half-maximal stimulation of pepsinogen secretion, the relative potencies of cholecystokinin-related peptides were caerulein greater than CCK-8 greater than [desSO3]CCK-8 greater than gastrin. Removing extracellular calcium did not alter basal or cholecystokinin-stimulated pepsinogen secretion. These results illustrate that dispersed glands from rabbit stomach constitute a suitable preparation for examining the actions of various agents on pepsinogen secretion in vitro.





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