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Biomedical and Environmental Sciences ; (12): 623-631, 2017.
Article in English | WPRIM | ID: wpr-311369

ABSTRACT

<p><b>OBJECTIVE</b>In the present study, we investigated the antioxidant and anti-aging effects of Silybum marianum protein hydrolysate (SMPH) in D-galactose-treated mice.</p><p><b>METHODS</b>D-galactose (500 mg/kg body weight) was intraperitoneally injected daily for 7 weeks to accelerate aging, and SMPH (400, 800, 1,200 mg/kg body weight, respectively) was simultaneously administered orally. The antioxidant and anti-aging effects of SMPH in the liver and brain were measured by biochemical assays. Transmission electron microscopy (TEM) was performed to study the ultrastructure of liver mitochondri.</p><p><b>RESULTS</b>SMPH decreased triglyceride and cholesterol levels in the D-galactose-treated mice. It significantly elevated the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), and total antioxidant capacity (T-AOC), which were suppressed by D-galactose. Monoamine oxidase (MAO) and malondialdehyde (MDA) levels as well as the concentrations of caspase-3 and 8-OHdG in the liver and brain were significantly reduced by SMPH. Moreover, it increased Bcl-2 levels in the liver and brain. Furthermore, SMPH significantly attenuated D-galactose-induced liver mitochondrial dysfunction by improving the activities of Na+-K+-ATPase and Ca2+-Mg2+-ATPase as well as mitochondrial membrane potential (ΔΨm) and fluidity. TEM showed that the degree of liver mitochondrial damage was significantly decreased by SMPH.</p><p><b>CONCLUSION</b>The results indicated that SMPH protects against D-galactose-induced accelerated aging in mice through its antioxidant and anti-aging activities.</p>


Subject(s)
Animals , Male , Mice , Aging , Antioxidants , Pharmacology , Brain , Caspase 3 , Metabolism , Galactose , Toxicity , Gene Expression Regulation, Enzymologic , Glutathione Peroxidase , Metabolism , Malondialdehyde , Metabolism , Maze Learning , Milk Thistle , Chemistry , Mitochondria, Liver , Oxidative Stress , Plant Proteins , Chemistry , Pharmacology , Protective Agents , Pharmacology , Protein Hydrolysates , Chemistry , Pharmacology , Superoxide Dismutase , Metabolism
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