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Nutrients ; 16(12)2024 Jun 17.
Artículo en Inglés | MEDLINE | ID: mdl-38931268

RESUMEN

Obesity is acknowledged as a significant risk factor for cardiovascular disease, often accompanied by increased inflammation and diabetes. Bioactive peptides derived from marine animal proteins show promise as safe and effective anti-obesity agents by regulating adipocyte differentiation through the AMPK signaling pathway. Therefore, this study aims to investigate the anti-obesity and anti-diabetic effects of bioactive compounds derived from a Meretrix lusoria Protamex enzymatic hydrolysate (MLP) fraction (≤1 kDa) through a 6-week treatment (150 mg/kg or 300 mg/kg, administered once daily) in leptin receptor-deficient db/db mice. The MLP treatment significantly decreased the body weight, serum total cholesterol, triglycerides, and LDL-cholesterol levels while also exhibiting a beneficial effect on hepatic and serum marker parameters in db/db mice. A histological analysis revealed a reduction in hepatic steatosis and epididymal fat following MLP treatment. Furthermore, poor glucose tolerance was improved, and hepatic antioxidant enzyme activities were elevated in MLP-treated mice compared to db/db control mice. Western blot analysis showed an increased expression of the AMPK protein after MLP treatment. In addition, the expression of lipogenic genes decreased in db/db mice. These findings indicate that bioactive peptides, which are known to regulate blood glucose levels, lipid metabolism, and adipogenesis, could be beneficial functional food additives and pharmaceuticals.


Asunto(s)
Fármacos Antiobesidad , Obesidad , Péptidos , Animales , Obesidad/tratamiento farmacológico , Ratones , Masculino , Péptidos/farmacología , Fármacos Antiobesidad/farmacología , Hidrolisados de Proteína/farmacología , Hígado/efectos de los fármacos , Hígado/metabolismo , Glucemia/efectos de los fármacos , Glucemia/metabolismo , Hipoglucemiantes/farmacología , Metabolismo de los Lípidos/efectos de los fármacos , Proteínas Quinasas Activadas por AMP/metabolismo , Ratones Endogámicos C57BL , Receptores de Leptina/metabolismo , Receptores de Leptina/genética , Adipogénesis/efectos de los fármacos , Peso Corporal/efectos de los fármacos
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