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Secretagogue-induced [14C]aminopyrine uptake in isolated equine parietal cells.

Abstract: Equine oxyntic mucosal cells were obtained by sequential exposure to pronase and collagenase. Acid production by parietal cells was assessed by uptake of [14C]aminopyrine (AP), a weak base that accumulates in intracellular acidic spaces. Incubation for various times revealed a maximal AP uptake at 10 minutes for histamine and carbachol. Similar secretagogue responses were observed for parietal cells from the mucosal cell preparation or after enrichment by elutriation. Histamine and isobutyl-methylxanthine (IBMX) stimulated AP uptake with a dose-dependent response and maximal effective concentration of 100 microM. Carbachol, 1 to 100 microM, and pentagastrin (PG), 1 to 1,000 nM, were ineffective stimulants of AP uptake. The AP uptake values for 100 microM IBMX, 1 microM carbachol, or 100 nM PG were 77 +/- 6%, 50 +/- 3.2%, and 40 +/- 4.5%, respectively, of that observed with maximal stimulation by 100 microM histamine (mean +/- SEM, n = 4 to 14). Uptake of AP by nonstimulated control cells was 36 +/- 3.6% of maximal histamine stimulation. The AP accumulations during control conditions and after stimulation with 100 microM histamine and IBMX, 1 microM carbachol, or 100 nM PG were 1.18 +/- 0.39, 2.81 +/- 0.85, 1.93 +/- 0.48, 1.44 +/- 0.36, and 1.23 +/- 0.33 pmol of AP/10(5) parietal cells, respectively. Individual histamine dose-response curves were shifted to the right by increasing ranitidine and cimetidine concentrations (0.1 to 50 microM). These results indicate that isolated equine parietal cells are maximally stimulated by histamine and minimally stimulated by carbachol and PG.
Publication Date: 1994-01-01 PubMed ID: 7511358
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  • Comparative Study
  • Journal Article

Summary

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This research aimed to study acid production and secretagogue response in isolated equine parietal cells using [14C]aminopyrine, and found histamine to be the most effective stimulant. However, carbachol and pentagastrin were less effective.

Research Methodology

  • Equine oxyntic mucosal cells were isolated using pronase and collagenase.
  • Acid production by these cells was measured using [14C]aminopyrine (AP) which is a weak base that accumulates in acidic spaces within the cells.
  • Cells were incubated for different periods of time, and it was discovered that AP uptake was maximized at 10 minutes for histamine and carbachol.
  • Different chemical stimulants (secretagogues) such as IBMX, carbachol, and pentagastrin (PG) were used on the cells.

Key Findings

  • Histamine and isobutyl-methylxanthine (IBMX) induced a dose-dependent response in AP uptake, showing maximum efficacy at a concentration of 100 microM.
  • Carbachol and PG, however, didn’t significantly stimulate AP uptake even at increased concentrations.
  • The research shows uptake values for different substances in comparison to that by 100 microM histamine.
  • Cells not stimulated (i.e., control cells) had an AP uptake of 36 +/- 3.6% of the maximal stimulation by histamine.
  • The AP accumulation in control conditions, and in the presence of histamine, IBMX, carbachol, or PG were all calculated showing histamine had by far the greatest impact.

Conclusions

  • The shift in individual histamine dose-response curves to the right by increasing ranitidine and cimetidine concentrations indicates histamine was most effective in stimulating the cells.
  • The study concludes that equine parietal cells are maximally stimulated by histamine and minimally stimulated by carbachol and PG.

Cite This Article

APA
Campbell-Thompson M. (1994). Secretagogue-induced [14C]aminopyrine uptake in isolated equine parietal cells. Am J Vet Res, 55(1), 132-137.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 55
Issue: 1
Pages: 132-137

Researcher Affiliations

Campbell-Thompson, M
  • Department of Medicine, College of Medicine, University of Florida, Gainesville 32610.

MeSH Terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • Aminopyrine / metabolism
  • Animals
  • Biological Transport / drug effects
  • Carbachol / pharmacology
  • Carbon Radioisotopes
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Female
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / metabolism
  • Histamine / pharmacology
  • Horses
  • Humans
  • Kinetics
  • Male
  • Parietal Cells, Gastric / drug effects
  • Parietal Cells, Gastric / metabolism
  • Pentagastrin / pharmacology
  • Rats
  • Species Specificity
  • Swine
  • Time Factors

Citations

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