ABSTRACT
<p><b>OBJECTIVE</b>To test possible antioxidant activity of n-hexane extract of Podophyllum hexandrum under in vitro and in vivo conditions.</p><p><b>METHODS</b>The in vitro antioxidant activity was evaluated by the ability of the extract to interact with the stable free radical DPPH, Superoxide (O2-), Hydroxyl (OH-), Hydrogen peroxide (H2O2) radicals, and reducing power ability of the extract was also evaluated. Under in vivo conditions the extract was evaluated for its hepatoprotective activity by measuring different biochemical parameters, such as serum alanine aminotransaminase, serum aspartate aminotransaminase and serum lactate dehydrogenase and antioxidant enzymes. Antioxidant status was estimated by determining the activities of antioxidative enzymes, glutathione reductase (GR), glutathione peroxidase (GPx), glutathione-S-transferase (GST) and superoxide dismutase (SOD), and by determining the levels of reduced glutathione (GSH) and thiobarbituric acid reactive substances (TBARS).</p><p><b>RESULTS</b>Hexane extract of P. hexandrum exhibited good radical scavenging capacity in neutralization of DPPH, O2-, OH-, and H2O2 radicals in a dose dependent manner. n-hexane extract of Podophyllum hexandrum at the doses of 20, 30, and 50 mg/kg-day produced hepatoprotective effect by decreasing the activity of serum marker enzymes, while it significantly increased the levels of glutathione (GSH), glutathione peroxidase (GPx), glutathione reductase (GR), super oxide dismutase (SOD), and glutathione-S-transferase (GST) in a dose dependant manner. The effect of n-hexane extract was comparable to that of standard antioxidant vitamin E.</p><p><b>CONCLUSION</b>The extract of Podophyllum hexandrum possess free radical scavenging activity under in vitro conditions and could protect the liver tissue against CCl(4) induced oxidative stress probably by increasing antioxidant defense activities.</p>
Subject(s)
Animals , Male , Rats , Antioxidants , Pharmacology , Biphenyl Compounds , Metabolism , Carbon Tetrachloride , Pharmacology , Glutathione Peroxidase , Metabolism , Glutathione Reductase , Metabolism , Lipid Peroxidation , Liver , Metabolism , Oxidation-Reduction , Oxidative Stress , Picrates , Metabolism , Plant Extracts , Pharmacology , Podophyllum , Chemistry , Rats, Wistar , Superoxide Dismutase , Metabolism , Superoxides , Metabolism , Thiobarbituric Acid Reactive Substances , MetabolismABSTRACT
Mushrooms are considered rich in proteins, carbohydrates and other nutrients. The present study was carried out to evaluate some edible mushrooms of Kashmir valley for their protein, carbohydrate and lipid contents. The highest protein content was found in Boletus edulis [2.20g] followed by Agaricus bisporus [1.80g], Pleurotus ostreatus [1.68g], Morchella esculenta [1.62g] and Pleurotus sajor caju [1.6g]. Carbohydrate content also showed variation in all the five tested edible mushroom species, the highest carbohydrate content observed in Boletus edulis [6.0g] followed by Agaricus bisporus [4.85g], Pleurotus ostreatus [4.30g], Morchella esculenta [4.25g] and Pleurotus sajor caju [3.35g] respectively. Similar results were observed for lipid content. The present study was also investigated for the antioxidant potential of aqueous extract of mushroom species by the methods of DPPH radical scavenging activity, hydroxyl radical scavenging activity and superoxide radical scavenging activity. All these in vitro antioxidant activities were concentration dependent, which were compared with standard antioxidant Catechin