GRP-producing nerves control antral somatostatin and gastrin secretion in pigs

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GRP-producing nerves control antral somatostatin and gastrin secretion in pigs. / Holst, J J; Orskov, C; Poulsen, Steen Seier.

In: American Journal of Physiology (Consolidated), Vol. 253, No. 6 Pt 1, 12.1987, p. G767-74.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Holst, JJ, Orskov, C & Poulsen, SS 1987, 'GRP-producing nerves control antral somatostatin and gastrin secretion in pigs', American Journal of Physiology (Consolidated), vol. 253, no. 6 Pt 1, pp. G767-74.

APA

Holst, J. J., Orskov, C., & Poulsen, S. S. (1987). GRP-producing nerves control antral somatostatin and gastrin secretion in pigs. American Journal of Physiology (Consolidated), 253(6 Pt 1), G767-74.

Vancouver

Holst JJ, Orskov C, Poulsen SS. GRP-producing nerves control antral somatostatin and gastrin secretion in pigs. American Journal of Physiology (Consolidated). 1987 Dec;253(6 Pt 1):G767-74.

Author

Holst, J J ; Orskov, C ; Poulsen, Steen Seier. / GRP-producing nerves control antral somatostatin and gastrin secretion in pigs. In: American Journal of Physiology (Consolidated). 1987 ; Vol. 253, No. 6 Pt 1. pp. G767-74.

Bibtex

@article{96146ba2afac4a67896becd3736d7447,
title = "GRP-producing nerves control antral somatostatin and gastrin secretion in pigs",
abstract = "By immunohistochemistry, nerve fibers containing gastrin-releasing polypeptide (GRP)-like immunoreactivity were identified close to the somatostatin (SS)-producing cells of the gastric antral mucosa. We, therefore, studied the possible role of GRP in the control of antral SS secretion by use of isolated perfused pig antrum with intact vagus nerve supply. Electrical stimulation of the vagus nerves at 4 Hz increased the antral release of GRP up to 10-fold and increased SS output 2- to 3-fold. Atropine at 10(-6) M had no effect on these responses. Intra-arterial GRP increased SS secretion significantly at 10(-10) M and eightfold at 10(-8) M, whereas gastrin secretion was stimulated significantly at 10(-11) M and maximally at 10(-10) M and inhibited at 10(-8) M. Preperfusion with a GRP antagonist ([D-Arg1,D-Pro2,D-Trp7,9,Leu11]substance P) or Fab fragments of antibodies against GRP abolished the effects of vagus stimulation on gastrin and somatostatin output. Gastrin in concentrations up to 10(-7) M was without effect on SS secretion. We conclude that electrical stimulation of the vagus nerves increases antral SS gastrin secretion and that GRP is a likely transmitter.",
keywords = "Animals, Atropine, Electric Stimulation, Gastrin-Releasing Peptide, Gastrins, Immunoenzyme Techniques, Immunologic Techniques, Neurotransmitter Agents, Peptides, Perfusion, Secretory Rate, Somatostatin, Stomach, Swine, Vagus Nerve",
author = "Holst, {J J} and C Orskov and Poulsen, {Steen Seier}",
year = "1987",
month = dec,
language = "English",
volume = "253",
pages = "G767--74",
journal = "American Journal of Physiology - Cell Physiology",
issn = "0363-6143",
publisher = "American Physiological Society",
number = "6 Pt 1",

}

RIS

TY - JOUR

T1 - GRP-producing nerves control antral somatostatin and gastrin secretion in pigs

AU - Holst, J J

AU - Orskov, C

AU - Poulsen, Steen Seier

PY - 1987/12

Y1 - 1987/12

N2 - By immunohistochemistry, nerve fibers containing gastrin-releasing polypeptide (GRP)-like immunoreactivity were identified close to the somatostatin (SS)-producing cells of the gastric antral mucosa. We, therefore, studied the possible role of GRP in the control of antral SS secretion by use of isolated perfused pig antrum with intact vagus nerve supply. Electrical stimulation of the vagus nerves at 4 Hz increased the antral release of GRP up to 10-fold and increased SS output 2- to 3-fold. Atropine at 10(-6) M had no effect on these responses. Intra-arterial GRP increased SS secretion significantly at 10(-10) M and eightfold at 10(-8) M, whereas gastrin secretion was stimulated significantly at 10(-11) M and maximally at 10(-10) M and inhibited at 10(-8) M. Preperfusion with a GRP antagonist ([D-Arg1,D-Pro2,D-Trp7,9,Leu11]substance P) or Fab fragments of antibodies against GRP abolished the effects of vagus stimulation on gastrin and somatostatin output. Gastrin in concentrations up to 10(-7) M was without effect on SS secretion. We conclude that electrical stimulation of the vagus nerves increases antral SS gastrin secretion and that GRP is a likely transmitter.

AB - By immunohistochemistry, nerve fibers containing gastrin-releasing polypeptide (GRP)-like immunoreactivity were identified close to the somatostatin (SS)-producing cells of the gastric antral mucosa. We, therefore, studied the possible role of GRP in the control of antral SS secretion by use of isolated perfused pig antrum with intact vagus nerve supply. Electrical stimulation of the vagus nerves at 4 Hz increased the antral release of GRP up to 10-fold and increased SS output 2- to 3-fold. Atropine at 10(-6) M had no effect on these responses. Intra-arterial GRP increased SS secretion significantly at 10(-10) M and eightfold at 10(-8) M, whereas gastrin secretion was stimulated significantly at 10(-11) M and maximally at 10(-10) M and inhibited at 10(-8) M. Preperfusion with a GRP antagonist ([D-Arg1,D-Pro2,D-Trp7,9,Leu11]substance P) or Fab fragments of antibodies against GRP abolished the effects of vagus stimulation on gastrin and somatostatin output. Gastrin in concentrations up to 10(-7) M was without effect on SS secretion. We conclude that electrical stimulation of the vagus nerves increases antral SS gastrin secretion and that GRP is a likely transmitter.

KW - Animals

KW - Atropine

KW - Electric Stimulation

KW - Gastrin-Releasing Peptide

KW - Gastrins

KW - Immunoenzyme Techniques

KW - Immunologic Techniques

KW - Neurotransmitter Agents

KW - Peptides

KW - Perfusion

KW - Secretory Rate

KW - Somatostatin

KW - Stomach

KW - Swine

KW - Vagus Nerve

M3 - Journal article

C2 - 2892416

VL - 253

SP - G767-74

JO - American Journal of Physiology - Cell Physiology

JF - American Journal of Physiology - Cell Physiology

SN - 0363-6143

IS - 6 Pt 1

ER -

ID: 47488455