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Mitogen Activated Protein Kinases in Steatotic and Non-Steatotic Livers Submitted to Ischemia-Reperfusion.
Jiménez-Castro, Mónica B; Cornide-Petronio, María Eugenia; Gracia-Sancho, Jordi; Casillas-Ramírez, Araní; Peralta, Carmen.
Afiliación
  • Jiménez-Castro MB; Transplant Biomedicals S.L., Barcelona 08042, Spain. monicabjimenez@hotmail.com.
  • Cornide-Petronio ME; Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona 08036, Spain. cornide@clinic.ub.es.
  • Gracia-Sancho J; Liver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory IDIBAPS, 08036 Barcelona, Spain. jgracia@clinic.ub.es.
  • Casillas-Ramírez A; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), 08036 Barcelona, Spain. jgracia@clinic.ub.es.
  • Peralta C; Hospital Regional de Alta Especialidad de Ciudad Vitoria, Ciudad Victoria 87087, Mexico. cperalta@clinic.ub.es.
Int J Mol Sci ; 20(7)2019 Apr 10.
Article en En | MEDLINE | ID: mdl-30974915
ABSTRACT
We analyzed the participation of mitogen-activated protein kinases (MAPKs), namely p38, JNK and ERK 1/2 in steatotic and non-steatotic livers undergoing ischemia-reperfusion (I-R), an unresolved problem in clinical practice. Hepatic steatosis is a major risk factor in liver surgery because these types of liver tolerate poorly to I-R injury. Also, a further increase in the prevalence of steatosis in liver surgery is to be expected. The possible therapies based on MAPK regulation aimed at reducing hepatic I-R injury will be discussed. Moreover, we reviewed the relevance of MAPK in ischemic preconditioning (PC) and evaluated whether MAPK regulators could mimic its benefits. Clinical studies indicated that this surgical strategy could be appropriate for liver surgery in both steatotic and non-steatotic livers undergoing I-R. The data presented herein suggest that further investigations are required to elucidate more extensively the mechanisms by which these kinases work in hepatic I-R. Also, further researchers based in the development of drugs that regulate MAPKs selectively are required before such approaches can be translated into clinical liver surgery.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Daño por Reperfusión / Precondicionamiento Isquémico / Proteínas Quinasas Activadas por Mitógenos / Sistema de Señalización de MAP Quinasas / Hígado Graso / Hígado Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2019 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Daño por Reperfusión / Precondicionamiento Isquémico / Proteínas Quinasas Activadas por Mitógenos / Sistema de Señalización de MAP Quinasas / Hígado Graso / Hígado Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2019 Tipo del documento: Article País de afiliación: España