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Esculetin, a Coumarin Derivative, Inhibits Aldose Reductase Activity in vitro and Cataractogenesis in Galactose-Fed Rats
Article en En | WPRIM | ID: wpr-177272
Biblioteca responsable: WPRO
ABSTRACT
Naturally occurring coumarin compounds have received substantial attention due to their pharmaceutical effects. Esculetin is a coumarin derivative and a polyphenol compound that is used in a variety of therapeutic and pharmacological strategies. However, its effect on aldose reductase activity remains poorly understood. In this study, the potential beneficial effects of esculetin on lenticular aldose reductase were investigated in galactose-fed (GAL) rats, an animal model of sugar cataracts. Cataracts were induced in Sprague-Dawley (SD) rats via a 50% galactose diet for 2 weeks, and groups of GAL rats were orally treated with esculetin (10 or 50 mg/kg body weight). In vehicle-treated GAL rats, lens opacification was observed, and swelling and membrane rupture of the lens fiber cells were increased. Additionally, aldose reductase was highly expressed in the lens epithelium and superficial cortical fibers during cataract development in the GAL rats. Esculetin reduced rat lens aldose reductase (RLAR) activity in vitro, and esculetin treatment significantly inhibited lens opacity, as well as morphological alterations, such as swelling, vacuolation and liquefaction of lens fibers, via the inhibition of aldose reductase in the GAL rats. These results indicate that esculetin is a useful treatment for galactose-induced cataracts.
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Texto completo: 1 Base de datos: WPRIM Asunto principal: Rotura / Catarata / Aldehído Reductasa / Ratas Sprague-Dawley / Modelos Animales / Dieta / Epitelio / Galactosa / Membranas Límite: Animals Idioma: En Revista: Biomolecules & Therapeutics Año: 2016 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Rotura / Catarata / Aldehído Reductasa / Ratas Sprague-Dawley / Modelos Animales / Dieta / Epitelio / Galactosa / Membranas Límite: Animals Idioma: En Revista: Biomolecules & Therapeutics Año: 2016 Tipo del documento: Article