El extracto de Ginkgo biloba L. y la flunixina meglumina atenúan la lesión hepática, el estrés oxidativo, la inflamación y la apoptosis asociados a la sepsis en ratas
Resumen
El lipopolisacárido (LPS), conocido como un estimulante de la inflamación, causa daño hepático agudo al inducir la producción de mediadores inflamatorios y estrés oxidativo. El propósito de este estudio es determinar si un fármaco antiinflamatorio no esteroide (AINE) Flunixin meglumine (FM) y un agente natural extracto de Ginkgo biloba L. (GBE) muestran efectos antioxidantes, antiinflamatorios o antiapoptóticos en el tejido hepático en la hepatotoxicidad inducida por LPS. Los animales se separaron en 6 grupos como control, sepsis (1 mg·kg-1, dosis única el séptimo día, intraperitoneal (ip)), sepsis + FM (1 mg·kg-1, dosis única el séptimo día, ip + 2,2 mg·kg-1 día, ip), sepsis + GBE (1 mg·kg-1, dosis única el séptimo día, ip + 50 mg·kg-1 día, sonda), FM y GBE y el estudio continuó durante 7 días. Los tejidos hepáticos extraídos de ratas sacrificadas se analizaron bioquímicamente, histológicamente e inmunohistoquímicamente. En consecuencia, el LPS provocó alteración de los marcadores de la función hepática, inflamación, estrés oxidativo y apoptosis, así como cambios histopatológicos en el tejido hepático. Sin embargo, se observó que los cambios inducidos por LPS fueron regulados por la aplicación de FM y GBE. Se demostró que FM y GBE tienen propiedades antioxidantes, antiinflamatorias y antiapoptóticas en la hepatotoxicidad inducida por LPS.
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Derechos de autor 2024 Tuba Parlak Ak, Burcu Gul, Mine Yaman, Ismail Seven, Gurdal Dagoglu, Huseyin Fatih Gul
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