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Acta cir. bras ; 35(1): e202000104, 2020. graf
Artigo em Inglês | LILACS | ID: biblio-1088525

RESUMO

Abstract Purpose Glutamine, as an essential part of enteral nutrition and parenteral nutrition agent, has been widely recognized to be a kind of important intestinal mucosa protectant in clinical practice and experimental research. However, the mechanisms of its protective effects are still not fully understand. Consequently, this study aimed to explore the potential mechanism of glutamine on ischemia-reperfusion (I/R) injury induced endoplasmic reticulum (ER) stress in intestine. Methods An experimental model of intestinal I/R in rats was established by 1 hour occlusion of the superior mesenteric artery followed by 3 hours of reperfusion. Morphologic changes of intestinal mucosa, apoptosis of epithelial cells, and expression of intestinal Grp78, Gadd153, Caspase-12, ATF4, PERK phosphorylation (P-PERK) and elF2αphosphorylation(P-elF2α) were determined. Results After I/R, the apoptotic index of intestinal mucosa epithelial cells observably increased with notable necrosis of intestinal mucosa, and the expressions of Grp78, Gadd153, Caspase-12, ATF4, P-PERK and P-elF2αall were increased. However, treatment with glutamine could significantly relieve intestinal I/R injury and apoptosis index. Moreover, glutamine could clearly up-regulate the expression of Grp78, restrain P-PERK and P-elF2α, and reduce ATF4, Gadd153 and Caspase-12 expressions. Conclusion Glutamine may be involved in alleviating ER stress induced intestinal mucosa cells apoptosis.


Assuntos
Animais , Masculino , Traumatismo por Reperfusão/prevenção & controle , Apoptose/efeitos dos fármacos , Substâncias Protetoras/farmacologia , Estresse do Retículo Endoplasmático/efeitos dos fármacos , Glutamina/farmacologia , Mucosa Intestinal/efeitos dos fármacos , RNA Mensageiro/efeitos dos fármacos , Ratos Sprague-Dawley , Artéria Mesentérica Superior/lesões , eIF-2 Quinase/efeitos dos fármacos , Modelos Animais , Fator 4 Ativador da Transcrição/efeitos dos fármacos , Fator de Transcrição CHOP/efeitos dos fármacos , Caspase 12/efeitos dos fármacos , Proteínas de Choque Térmico/efeitos dos fármacos , Mucosa Intestinal , Mucosa Intestinal/ultraestrutura
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