Abstract
The purpose of this study is to investigate the effect of peptide YY (PYY) on pentagastrin-, histamine-, and bethanechol-stimulated gastric acid secretion and the possible mechanisms by which PYY inhibits gastric acid secretion. Six mongrel dogs with chronic gastric and duodenal fistulas were given an intravenous infusion of pentagastrin (0.5 μg·kg-1·h-1), histamine (18 μg·kg-1·h-1) either alone or simultaneously with intravenous PYY (100, 200, 400, pmol·kg-1·h-1). PYY (100, 200, 400 pmol·kg-1·h-1) inhibited pentagastrin-stimulated gastric acid secretion in a dose-dependent manner. PYY (400 pmol·kg-1·h-1) did not depress bethanechol-stimulated gastric acid secretion. PYY (400 pmol·kg-1·h-1) also failed to inhibit histamine-stimulated gastric acid secretion. Furthermore, PYY inhibited pentagastrin-stimulated gastric acid secretion in the face of atropine, vagotomy, or indomethacin treatment. These findings indicate that the inhibitory action of PYY on gastric acid secretion is in part independent of long and short cholinergic pathways. These findings also indicate that the inhibitory mechanism of PYY is independent of prostaglandin synthesis. Our findings are discussed in relation to previous reports regarding the effects of PYY on gastric acid secretion.
| Original language | English (US) |
|---|---|
| Journal | American Journal of Physiology - Gastrointestinal and Liver Physiology |
| Volume | 253 |
| Issue number | 3 |
| State | Published - 1987 |
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ASJC Scopus subject areas
- Physiology
- Gastroenterology
Cite this
Inhibitory action of peptide YY on gastric acid secretion. / Guo, Y. S.; Fujimura, M.; Lluis, F.; Tsong, Y.; Greeley, G. H.; Thompson, J. C.
In: American Journal of Physiology - Gastrointestinal and Liver Physiology, Vol. 253, No. 3, 1987.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Inhibitory action of peptide YY on gastric acid secretion
AU - Guo, Y. S.
AU - Fujimura, M.
AU - Lluis, F.
AU - Tsong, Y.
AU - Greeley, G. H.
AU - Thompson, J. C.
PY - 1987
Y1 - 1987
N2 - The purpose of this study is to investigate the effect of peptide YY (PYY) on pentagastrin-, histamine-, and bethanechol-stimulated gastric acid secretion and the possible mechanisms by which PYY inhibits gastric acid secretion. Six mongrel dogs with chronic gastric and duodenal fistulas were given an intravenous infusion of pentagastrin (0.5 μg·kg-1·h-1), histamine (18 μg·kg-1·h-1) either alone or simultaneously with intravenous PYY (100, 200, 400, pmol·kg-1·h-1). PYY (100, 200, 400 pmol·kg-1·h-1) inhibited pentagastrin-stimulated gastric acid secretion in a dose-dependent manner. PYY (400 pmol·kg-1·h-1) did not depress bethanechol-stimulated gastric acid secretion. PYY (400 pmol·kg-1·h-1) also failed to inhibit histamine-stimulated gastric acid secretion. Furthermore, PYY inhibited pentagastrin-stimulated gastric acid secretion in the face of atropine, vagotomy, or indomethacin treatment. These findings indicate that the inhibitory action of PYY on gastric acid secretion is in part independent of long and short cholinergic pathways. These findings also indicate that the inhibitory mechanism of PYY is independent of prostaglandin synthesis. Our findings are discussed in relation to previous reports regarding the effects of PYY on gastric acid secretion.
AB - The purpose of this study is to investigate the effect of peptide YY (PYY) on pentagastrin-, histamine-, and bethanechol-stimulated gastric acid secretion and the possible mechanisms by which PYY inhibits gastric acid secretion. Six mongrel dogs with chronic gastric and duodenal fistulas were given an intravenous infusion of pentagastrin (0.5 μg·kg-1·h-1), histamine (18 μg·kg-1·h-1) either alone or simultaneously with intravenous PYY (100, 200, 400, pmol·kg-1·h-1). PYY (100, 200, 400 pmol·kg-1·h-1) inhibited pentagastrin-stimulated gastric acid secretion in a dose-dependent manner. PYY (400 pmol·kg-1·h-1) did not depress bethanechol-stimulated gastric acid secretion. PYY (400 pmol·kg-1·h-1) also failed to inhibit histamine-stimulated gastric acid secretion. Furthermore, PYY inhibited pentagastrin-stimulated gastric acid secretion in the face of atropine, vagotomy, or indomethacin treatment. These findings indicate that the inhibitory action of PYY on gastric acid secretion is in part independent of long and short cholinergic pathways. These findings also indicate that the inhibitory mechanism of PYY is independent of prostaglandin synthesis. Our findings are discussed in relation to previous reports regarding the effects of PYY on gastric acid secretion.
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UR - http://www.scopus.com/inward/citedby.url?scp=0023253291&partnerID=8YFLogxK
M3 - Article
VL - 253
JO - American Journal of Physiology - Endocrinology and Metabolism
JF - American Journal of Physiology - Endocrinology and Metabolism
SN - 0193-1849
IS - 3
ER -