Saltar al contenido
Merck

Prostaglandin E(2) mediates acid-induced heartburn in healthy volunteers.

American journal of physiology. Gastrointestinal and liver physiology (2013-02-02)
Takashi Kondo, Tadayuki Oshima, Toshihiko Tomita, Hirokazu Fukui, Jiro Watari, Hiroki Okada, Shojiro Kikuchi, Mitsuru Sasako, Takayuki Matsumoto, Charles H Knowles, Hiroto Miwa
RESUMEN

Prostaglandin E(2) (PGE(2)) plays a major role in pain processing and hypersensitivity. This study investigated whether PGE(2) levels are increased in the esophageal mucosa after acid infusion and whether increases in PGE(2) are associated with heartburn. Furthermore, expression of the PGE(2) receptor EP1 was investigated in human esophageal mucosa. Fourteen healthy male volunteers were randomized to 30-min lower esophageal acid (1% HCl) or saline perfusion. Before and after acid perfusion, endoscopic biopsies were taken from the distal esophagus. PGE(2) concentration (pg/mg protein) and EP1 mRNA and protein in biopsy samples were measured by ELISA, RT-PCR, and Western blotting. Symptom status of heartburn was evaluated with a validated categorical rating scale with a higher values corresponding to increasing intensity. PGE(2) levels in the esophageal mucosa significantly increased after acid infusion (before vs. after acid infusion: 23.2 ± 8.6 vs. 68.6 ± 18.3, P < 0.05), but not after saline infusion (before vs. after saline infusion: 9.3 ± 2.5 vs. 9.0 ± 3.2, NS). Time to first sensation (min) after acid infusion was less than after saline (saline vs. acid infusion: 22.1 ± 4.1 vs. 5.4 ± 1.5, P < 0.05). Intensity of heartburn in the acid-infusion group was also significantly greater compared with saline (saline vs. acid infusion: 54.3 ± 13.1 vs. 178.5 ± 22.8, P < 0.01). Changes in PGE(2) levels in the esophagus correlated with symptom intensity score (r = 0.80, P = 0.029). EP1 mRNA and protein expression were observed in the normal human esophageal mucosa. Esophageal PGE(2) expression is associated with mucosal acid exposure and heartburn.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
Ácido clorhídrico, ACS reagent, 37%
Sigma-Aldrich
Ácido clorhídrico, ACS reagent, 37%
Sigma-Aldrich
Cloruro de hidrógeno solution, 4.0 M in dioxane
Sigma-Aldrich
Ácido clorhídrico solution, 1.0 N, BioReagent, suitable for cell culture
Sigma-Aldrich
Ácido clorhídrico, 37 wt. % in H2O, 99.999% trace metals basis
Sigma-Aldrich
Ácido clorhídrico, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., fuming, ≥37%, APHA: ≤10
Sigma-Aldrich
Ácido clorhídrico, 36.5-38.0%, BioReagent, for molecular biology
Sigma-Aldrich
Cloruro de hidrógeno solution, 2.0 M in diethyl ether
Sigma-Aldrich
Ácido clorhídrico, meets analytical specification of Ph. Eur., BP, NF, fuming, 36.5-38%
Supelco
Ácido clorhídrico solution, volumetric, 0.1 M HCl (0.1N), endotoxin free
Sigma-Aldrich
Ácido clorhídrico, SAJ first grade, 35.0-37.0%
Sigma-Aldrich
Cloruro de hidrógeno solution, 1.0 M in diethyl ether
Sigma-Aldrich
Ácido clorhídrico, JIS special grade, 35.0-37.0%
Sigma-Aldrich
Hydrogen chloride, ReagentPlus®, ≥99%
Sigma-Aldrich
Ácido clorhídrico, puriss., 24.5-26.0%
Sigma-Aldrich
Ácido clorhídrico solution, 1 M
Sigma-Aldrich
Ácido clorhídrico solution, ~6 M in H2O, for amino acid analysis
Sigma-Aldrich
Ácido clorhídrico solution, 6 M
Sigma-Aldrich
Ácido clorhídrico solution, 12 M
Sigma-Aldrich
Cloruro de hidrógeno solution, 3 M in cyclopentyl methyl ether (CPME)
Sigma-Aldrich
Ácido clorhídrico solution, 32 wt. % in H2O, FCC
Sigma-Aldrich
Ácido clorhídrico solution, 2 M
Sigma-Aldrich
Cloruro de hidrógeno solution, 1.0 M in acetic acid
Sigma-Aldrich
Ácido clorhídrico solution, 0.5 M
Supelco
Hydrogen chloride - 1-butanol solution, ~3 M in 1-butanol, for GC derivatization, LiChropur
Sigma-Aldrich
Ácido clorhídrico solution, 0.2 M
Supelco
Hydrogen chloride – ethanol solution, ~1.25 M HCl, for GC derivatization, LiChropur
Sigma-Aldrich
Ácido clorhídrico solution, 0.01 M
Sigma-Aldrich
Ácido clorhídrico solution, 0.05 M
Sigma-Aldrich
Ácido clorhídrico solution, 0.02 M