Abstract

Liver fibrosis is the common response to chronic liver injury, ultimately leading to cirrhosis and its complications: portal hypertension, liver failure, hepatic encephalopathy, and hepatocellular carcinoma and others. Efficient and well-tolerated antifibrotic drugs are still lacking, and current treatment of hepatic fibrosis is limited to withdrawal of the noxious agent. Efforts over the past decade have mainly focused on fibrogenic cells generating the scarring response, although promising data on inhibition of parenchymal injury or reduction of liver inflammation have also been obtained. A large number of approaches have been validated in culture studies and in animal models, and several clinical trials are underway or anticipated for a growing number of molecules. This review highlight recent advances in the molecular mechanisms of liver fibrosis and discusses mechanistically based strategies that have recently emerged.

Highlights

  • El daño hepático crónico induce fibrosis en el hígado y en sus estados finales cirrosis, que se presenta como uno de los mayores problemas de salud pública a nivel mundial

  • Liver fibrosis is the common response to chronic liver injury

  • current treatment of hepatic fibrosis is limited to withdrawal of the noxious agent

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Summary

Therapeutical targets for revert liver fibrosis

Liver fibrosis is the common response to chronic liver injury, leading to cirrhosis and its complications: portal hypertension, liver failure, hepatic encephalopathy, and hepatocellular carcinoma and others. Principales eventos moleculares que conducen a la cirrosis hepática y que deben ser corregidos para el tratamiento de la enfermedad. La activación de las HSC presentes en el espacio subendotelial (espacio de Disse) que inducen una exacerbada expresión de proteínas fibrilares (principalmente colágena tipo I, III y VI) y una disminución en la actividad de enzimas (conocidas como metaloproteasas) que degradan dichas proteínas colagénicas, ocasionan una alteración en el intercambio de sustancias entre el sinusoide y los hepatocitos para ser metabolizadas son sólo algunos de los mecanismos involucrados durante el desarrollo de la cirrosis en el hígado. BLANCOS TERAPÉUTICOS POTENCIALES PARA REVERTIR LA CIRROSIS HEPÁTICA - L García et al su efectividad en procesos fibróticos experimentales que afectan a otros órganos

CÉLULAS FIBROGÉNICAS DEL HÍGADO
MODELOS EXPERIMENTALES
ESTRATEGIAS ANTIFIBRÓTICAS
BLANCOS TERAPÉUTICOS
VANGUARDIA EN INVESTIGACIÓN TERAPÉUTICA
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