Inhibitory effect of PYY on vagally stimulated acid secretion is mediated predominantly by Y1 receptors

Kevin C K Lloyd, D. Grandt, K. Aurang, V. E. Eysselein, M. Schimiczek, J. R. Reeve

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Two molecular forms of peptide YY (PYY), PYY-(1-36) and PYY-(3-36), are abundant in rabbit intestine and blood. We have previously shown that PYY- (1-36) (PYY I) activates equipotently Y1 and Y2 receptors and PYY-(3-36) (PYY II) is a highly selective agonist for Y2 receptors. In the present study, we examined the effect of exogenous infusion of PYY on vagally stimulated gastric acid secretion in awake rabbits with chronic gastric fistula. To determine the specific PYY receptor(s) that mediates this effect, we used a highly selective Y1 agonist, Pro34-PYY, a synthetic PYY, and a Y2-selective agonist, PYY II. Vagal stimulation of acid secretion was elicited by an intravenous bolus injection of insulin (0.125 U/kg) 30 min after beginning a 180-min intravenous infusion of either PYY I, PYY II, or [Pro34]-PYY after a 50 μg/kg iv bolus of atropine followed immediately by a 500 μg/kg sc injection. During infusion of 200 pmol · kg-1 · h-1 PYY I, acid output was significantly inhibited to 45 ± 13% of maximum acid output 60 min after injection of insulin. Similarly, acid output during infusion of 200 pmol · kg-1 · h-1 [Pro34]-PYY was significantly inhibited to 52 ± 12% of maximum. In contrast, acid output during infusion of 200 pmol · kg-1 · h-1 of PYY II was not significantly inhibited (101 ± 18% of maximum). Infusion of double the dose (400 pmol · kg-1 · h- 1) of PYY II resulted in acid inhibition (51 ± 15% of maximum), whereas infusion of the same dose did not significantly enhance acid inhibition by infusion of either PYY I or [Pro34]-PYY (28 ± 11 and 42 ± 15% of maximum). These results indicate that PYY, acting predominantly at Y1 receptors, is a potent inhibitor of vagally stimulated acid secretion in adult rabbits.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Gastrointestinal and Liver Physiology
Volume270
Issue number1 33-1
StatePublished - 1996

Fingerprint

Peptide YY
Acids
Rabbits
Gastric Fistula
Insulin
Injections

Keywords

  • cephalic phase
  • gastric acid secretion
  • insulin-induced hypoglycemia
  • peptide tyrosine tyrosine

ASJC Scopus subject areas

  • Gastroenterology
  • Physiology
  • Physiology (medical)

Cite this

Inhibitory effect of PYY on vagally stimulated acid secretion is mediated predominantly by Y1 receptors. / Lloyd, Kevin C K; Grandt, D.; Aurang, K.; Eysselein, V. E.; Schimiczek, M.; Reeve, J. R.

In: American Journal of Physiology - Gastrointestinal and Liver Physiology, Vol. 270, No. 1 33-1, 1996.

Research output: Contribution to journalArticle

@article{1b789968c6e14a5ab6a26ab13f6ea42d,
title = "Inhibitory effect of PYY on vagally stimulated acid secretion is mediated predominantly by Y1 receptors",
abstract = "Two molecular forms of peptide YY (PYY), PYY-(1-36) and PYY-(3-36), are abundant in rabbit intestine and blood. We have previously shown that PYY- (1-36) (PYY I) activates equipotently Y1 and Y2 receptors and PYY-(3-36) (PYY II) is a highly selective agonist for Y2 receptors. In the present study, we examined the effect of exogenous infusion of PYY on vagally stimulated gastric acid secretion in awake rabbits with chronic gastric fistula. To determine the specific PYY receptor(s) that mediates this effect, we used a highly selective Y1 agonist, Pro34-PYY, a synthetic PYY, and a Y2-selective agonist, PYY II. Vagal stimulation of acid secretion was elicited by an intravenous bolus injection of insulin (0.125 U/kg) 30 min after beginning a 180-min intravenous infusion of either PYY I, PYY II, or [Pro34]-PYY after a 50 μg/kg iv bolus of atropine followed immediately by a 500 μg/kg sc injection. During infusion of 200 pmol · kg-1 · h-1 PYY I, acid output was significantly inhibited to 45 ± 13{\%} of maximum acid output 60 min after injection of insulin. Similarly, acid output during infusion of 200 pmol · kg-1 · h-1 [Pro34]-PYY was significantly inhibited to 52 ± 12{\%} of maximum. In contrast, acid output during infusion of 200 pmol · kg-1 · h-1 of PYY II was not significantly inhibited (101 ± 18{\%} of maximum). Infusion of double the dose (400 pmol · kg-1 · h- 1) of PYY II resulted in acid inhibition (51 ± 15{\%} of maximum), whereas infusion of the same dose did not significantly enhance acid inhibition by infusion of either PYY I or [Pro34]-PYY (28 ± 11 and 42 ± 15{\%} of maximum). These results indicate that PYY, acting predominantly at Y1 receptors, is a potent inhibitor of vagally stimulated acid secretion in adult rabbits.",
keywords = "cephalic phase, gastric acid secretion, insulin-induced hypoglycemia, peptide tyrosine tyrosine",
author = "Lloyd, {Kevin C K} and D. Grandt and K. Aurang and Eysselein, {V. E.} and M. Schimiczek and Reeve, {J. R.}",
year = "1996",
language = "English (US)",
volume = "270",
journal = "American Journal of Physiology - Renal Fluid and Electrolyte Physiology",
issn = "1931-857X",
publisher = "American Physiological Society",
number = "1 33-1",

}

TY - JOUR

T1 - Inhibitory effect of PYY on vagally stimulated acid secretion is mediated predominantly by Y1 receptors

AU - Lloyd, Kevin C K

AU - Grandt, D.

AU - Aurang, K.

AU - Eysselein, V. E.

AU - Schimiczek, M.

AU - Reeve, J. R.

PY - 1996

Y1 - 1996

N2 - Two molecular forms of peptide YY (PYY), PYY-(1-36) and PYY-(3-36), are abundant in rabbit intestine and blood. We have previously shown that PYY- (1-36) (PYY I) activates equipotently Y1 and Y2 receptors and PYY-(3-36) (PYY II) is a highly selective agonist for Y2 receptors. In the present study, we examined the effect of exogenous infusion of PYY on vagally stimulated gastric acid secretion in awake rabbits with chronic gastric fistula. To determine the specific PYY receptor(s) that mediates this effect, we used a highly selective Y1 agonist, Pro34-PYY, a synthetic PYY, and a Y2-selective agonist, PYY II. Vagal stimulation of acid secretion was elicited by an intravenous bolus injection of insulin (0.125 U/kg) 30 min after beginning a 180-min intravenous infusion of either PYY I, PYY II, or [Pro34]-PYY after a 50 μg/kg iv bolus of atropine followed immediately by a 500 μg/kg sc injection. During infusion of 200 pmol · kg-1 · h-1 PYY I, acid output was significantly inhibited to 45 ± 13% of maximum acid output 60 min after injection of insulin. Similarly, acid output during infusion of 200 pmol · kg-1 · h-1 [Pro34]-PYY was significantly inhibited to 52 ± 12% of maximum. In contrast, acid output during infusion of 200 pmol · kg-1 · h-1 of PYY II was not significantly inhibited (101 ± 18% of maximum). Infusion of double the dose (400 pmol · kg-1 · h- 1) of PYY II resulted in acid inhibition (51 ± 15% of maximum), whereas infusion of the same dose did not significantly enhance acid inhibition by infusion of either PYY I or [Pro34]-PYY (28 ± 11 and 42 ± 15% of maximum). These results indicate that PYY, acting predominantly at Y1 receptors, is a potent inhibitor of vagally stimulated acid secretion in adult rabbits.

AB - Two molecular forms of peptide YY (PYY), PYY-(1-36) and PYY-(3-36), are abundant in rabbit intestine and blood. We have previously shown that PYY- (1-36) (PYY I) activates equipotently Y1 and Y2 receptors and PYY-(3-36) (PYY II) is a highly selective agonist for Y2 receptors. In the present study, we examined the effect of exogenous infusion of PYY on vagally stimulated gastric acid secretion in awake rabbits with chronic gastric fistula. To determine the specific PYY receptor(s) that mediates this effect, we used a highly selective Y1 agonist, Pro34-PYY, a synthetic PYY, and a Y2-selective agonist, PYY II. Vagal stimulation of acid secretion was elicited by an intravenous bolus injection of insulin (0.125 U/kg) 30 min after beginning a 180-min intravenous infusion of either PYY I, PYY II, or [Pro34]-PYY after a 50 μg/kg iv bolus of atropine followed immediately by a 500 μg/kg sc injection. During infusion of 200 pmol · kg-1 · h-1 PYY I, acid output was significantly inhibited to 45 ± 13% of maximum acid output 60 min after injection of insulin. Similarly, acid output during infusion of 200 pmol · kg-1 · h-1 [Pro34]-PYY was significantly inhibited to 52 ± 12% of maximum. In contrast, acid output during infusion of 200 pmol · kg-1 · h-1 of PYY II was not significantly inhibited (101 ± 18% of maximum). Infusion of double the dose (400 pmol · kg-1 · h- 1) of PYY II resulted in acid inhibition (51 ± 15% of maximum), whereas infusion of the same dose did not significantly enhance acid inhibition by infusion of either PYY I or [Pro34]-PYY (28 ± 11 and 42 ± 15% of maximum). These results indicate that PYY, acting predominantly at Y1 receptors, is a potent inhibitor of vagally stimulated acid secretion in adult rabbits.

KW - cephalic phase

KW - gastric acid secretion

KW - insulin-induced hypoglycemia

KW - peptide tyrosine tyrosine

UR - http://www.scopus.com/inward/record.url?scp=0030060667&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0030060667&partnerID=8YFLogxK

M3 - Article

C2 - 8772509

AN - SCOPUS:0030060667

VL - 270

JO - American Journal of Physiology - Renal Fluid and Electrolyte Physiology

JF - American Journal of Physiology - Renal Fluid and Electrolyte Physiology

SN - 1931-857X

IS - 1 33-1

ER -