Literature DB >> 2783534

Effects of hCGRP I and II on gastric blood flow and acid secretion in anesthetized rabbits.

P Bauerfeind1, R Hof, A Hof, M Cucala, S Siegrist, C von Ritter, J A Fischer, A L Blum.   

Abstract

Effects of intravenously administered human calcitonin gene-related peptides (hCGRP) I and II on regional blood flow and gastric acid secretion were examined in barbiturate-anesthetized rabbits. Blood flow was measured by injection of radioactively labeled microspheres at 0, 10, 20, 30, and 60 min. hCGRP I and II and vehicle were infused intravenously in five rabbits in rising doses of 0.01 (0-10th min), 0.03 (11-20th min), and 0.1 microgram.kg-1.min-1 (21-30th min). hCGRP I and II increased gastric blood flow dose dependently. Moreover, hCGRP I raised regional conductance (inverse of vascular resistance) in the stomach, duodenum, heart, brain, and skeletal muscle. As a result of the increased total peripheral conductance the mean arterial pressure was reduced, but the cardiac output remained unchanged. hCGRP II increased blood flow and conductance selectively in the stomach and the pancreas. The total peripheral conductance and mean arterial pressure remained unchanged. Apparently, hCGRP II exerts a more localized effect on the stomach than hCGRP I. hCGRP I and II did not affect basal gastric acid secretion. Pentagastrin-stimulated acid secretion was increased by 28% with hCGRP I (0.025 micrograms.kg-1.min-1) and decreased by 27% with hCGRP II (0.025 micrograms.kg-1.min-1). The inverse effect of hCGRP I and II and the parallel stimulation of blood flow brought about with hCGRP I and II indicate a different mode of action of the peptides on gastric blood flow and gastric acid secretion.

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Year:  1989        PMID: 2783534     DOI: 10.1152/ajpgi.1989.256.1.G145

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  7 in total

Review 1.  Thirteenth Gaddum Memorial Lecture. Neuronal and endothelium-derived mediators in the modulation of the gastric microcirculation: integrity in the balance.

Authors:  B J Whittle
Journal:  Br J Pharmacol       Date:  1993-09       Impact factor: 8.739

2.  Visceral vasodilatation and somatic vasoconstriction evoked by acid challenge of the rat gastric mucosa: diversity of mechanisms.

Authors:  C Wachter; A Heinemann; M Jocic; P Holzer
Journal:  J Physiol       Date:  1995-07-15       Impact factor: 5.182

3.  Nitric oxide-dependent and -independent hyperaemia due to calcitonin gene-related peptide in the rat stomach.

Authors:  P Holzer; I T Lippe; M Jocic; C Wachter; R Erb; A Heinemann
Journal:  Br J Pharmacol       Date:  1993-09       Impact factor: 8.739

4.  The paradoxical vascular interactions between endothelin-1 and calcitonin gene-related peptide in the rat gastric mucosal microcirculation.

Authors:  J Lopez-Belmonte; B J Whittle
Journal:  Br J Pharmacol       Date:  1993-09       Impact factor: 8.739

5.  Interactions between the vascular peptide endothelin-1 and sensory neuropeptides in gastric mucosal injury.

Authors:  B J Whittle; J Lopez-Belmonte
Journal:  Br J Pharmacol       Date:  1991-04       Impact factor: 8.739

6.  Vascular bed-dependent roles of the peptide CGRP and nitric oxide in acid-evoked hyperaemia of the rat stomach.

Authors:  P Holzer; C Wachter; M Jocic; A Heinemann
Journal:  J Physiol       Date:  1994-11-01       Impact factor: 5.182

Review 7.  Calcitonin gene products and the kidney.

Authors:  A Kurtz; R Muff; J A Fischer
Journal:  Klin Wochenschr       Date:  1989-09-01
  7 in total

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