Hydrogen Sulfide Prevents Ethanol-Induced Gastric Damage in Mice: Role of ATP-Sensitive Potassium Channels and Capsaicin-Sensitive Primary Afferent Neurons


Autoria(s): MEDEIROS, Jand Venes R.; BEZERRA, Victor H.; GOMES, Antoniella S.; BARBOSA, Andre Luiz R.; LIMA-JUNIOR, Roberto Cesar P.; SOARES, Pedro Marcos G.; BRITO, Gerly Anne C.; RIBEIRO, Ronaldo A.; CUNHA, Fernando Q.; SOUZA, Marcellus H. L. P.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

The aim of this study was to evaluate the protective effect of hydrogen sulfide (H(2)S) on ethanol-induced gastric lesions in mice and the influence of ATP-sensitive potassium (K(ATP)) channels, capsaicin-sensitive sensory afferent neurons, and transient receptor potential vanilloid (TRPV) 1 receptors on such an effect. Saline and L-cysteine alone or with propargylglycine, sodium hydrogen sulfide (NaHS), or Lawesson`s reagent were administrated for testing purposes. For other experiments, mice were pretreated with glibenclamide, neurotoxic doses of capsaicin, or capsazepine. Afterward, mice received L-cysteine, NaHS, or Lawesson`s reagent. After 30 min, 50% ethanol was administrated by gavage. After 1 h, mice were sacrificed, and gastric damage was evaluated by macroscopic and microscopic analyses. L-Cysteine, NaHS, and Lawesson`s reagent treatment prevented ethanol-induced macroscopic and microscopic gastric damage in a dose-dependent manner. Administration of propargylglycine, an inhibitor of endogenous H(2)S synthesis, reversed gastric protection induced by L-cysteine. Glibenclamide reversed L-cysteine, NaHS, or Lawesson`s reagent gastroprotective effects against ethanol-induced macroscopic damage in a dose-dependent manner. Chemical ablation of sensory afferent neurons by capsaicin reversed gastroprotective effects of L-cysteine or H(2)S donors (NaHS or Lawesson`s reagent) in ethanol-induced macroscopic gastric damage. Likewise, in the presence of the TRPV1 antagonist capsazepine, the gastroprotective effects of L-cysteine, NaHS, or Lawesson`s reagent were also abolished. Our results suggest that H(2)S prevents ethanol-induced gastric damage. Although there are many mechanisms through which this effect can occur, our data support the hypothesis that the activation of K(ATP) channels and afferent neurons/TRPV1 receptors is of primary importance.

National Counsel of Technological and Scientific Development of Brazil (CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)

Identificador

JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, v.330, n.3, p.764-770, 2009

0022-3565

http://producao.usp.br/handle/BDPI/24363

10.1124/jpet.109.152801

http://dx.doi.org/10.1124/jpet.109.152801

Idioma(s)

eng

Publicador

AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS

Relação

Journal of Pharmacology and Experimental Therapeutics

Direitos

restrictedAccess

Copyright AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS

Palavras-Chave #GASTROINTESTINAL-TRACT #NEUTROPHIL MIGRATION #VANILLOID RECEPTOR #URINARY-BLADDER #K+ CHANNELS #RATS #INFLAMMATION #IMMUNOREACTIVITY #ENHANCEMENT #ACTIVATION #Pharmacology & Pharmacy
Tipo

article

original article

publishedVersion