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Ischemic Preconditioning Preserves Liver Energy Charge and Function on Hepatic Ischemia/Reperfusion Injury in Rats.
Rodríguez-Reynoso, Sergio; Leal-Cortés, Caridad; Portilla-de Buen, Eliseo; López-De la Torre, Selene Paulina.
Afiliación
  • Rodríguez-Reynoso S; División de Investigación Quirúrgica, Centro de Investigación Biomédica de Occidente, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México. Electronic address: galeno@mail.udg.mx.
  • Leal-Cortés C; División de Investigación Quirúrgica, Centro de Investigación Biomédica de Occidente, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.
  • Portilla-de Buen E; División de Investigación Quirúrgica, Centro de Investigación Biomédica de Occidente, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.
  • López-De la Torre SP; División de Investigación Quirúrgica, Centro de Investigación Biomédica de Occidente, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México; Farmacología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco,
Arch Med Res ; 49(6): 373-380, 2018 08.
Article en En | MEDLINE | ID: mdl-30554858
ABSTRACT

BACKGROUND:

Cell energy during ischemia/reperfusion depends on mechanisms including adenosine diphosphate degradation, oxygen species and cytokine liberation, neutrophil infiltration, and endothelial dysfunction. Preconditioning-a brief ischemic episode that confers a state of protection against subsequent ischemia-reperfusion injury-involves NO and adenosine production, reduction in oxygen species liberation, and preservation of microcirculation. During hypoxia, constitutive NO production assures adequate oxygen delivery and reduced energy loss. The aim was to determine the role of ischemic preconditioning in the stimulation of constitutive endothelial nitric oxide (NO) production and its effect on energy charge, radical oxygen species generation, cytokine liberation, and neutrophil infiltration during reperfusion. MATERIALS AND

METHODS:

Rats were assigned to one of four groups depending on the preconditioning protocol hepatic ischemia/reperfusion, or hepatic ischemia/reperfusion and ischemic preconditioning, for 5, 10, or 20 min. A portosystemic shunt was established between the portal and left jugular veins during ischemia.

RESULTS:

Preconditioning produced rises in plasma nitrites, but no rise in inducible nitric oxide synthase gene expression. A 5 or 10 min preconditioning period allowed for higher energy charge, bile production, and glutathione levels, with less lipoperoxide, alanine aminotransferase, tumor necrosis factor-α, and interleukin-1 production and neutrophil infiltration, compared with 20 min or control. Survival was 80% in the G10 group, 70 in G5, 10 in GC, and 0% in the G20 group.

CONCLUSIONS:

Ten-min liver preconditioning improves survival and prevents energy loss during hepatic ischemia/reperfusion by stimulating constitutive NO production, maintaining glutathione concentrations and reducing oxygen species and proinflammatory cytokine generation as well as neutrophil infiltration.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Daño por Reperfusión / Adenosina / Especies Reactivas de Oxígeno / Precondicionamiento Isquémico / Óxido Nítrico Límite: Animals Idioma: En Revista: Arch Med Res Asunto de la revista: MEDICINA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Daño por Reperfusión / Adenosina / Especies Reactivas de Oxígeno / Precondicionamiento Isquémico / Óxido Nítrico Límite: Animals Idioma: En Revista: Arch Med Res Asunto de la revista: MEDICINA Año: 2018 Tipo del documento: Article
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