Wu, Shu-JingShu-JingWuLEAN-TEIK HUANG2018-09-102018-09-102007-06https://www.scopus.com/pages/publications/34347213440?inwardhttp://scholars.lib.ntu.edu.tw/handle/123456789/330510Palm oil extract (POE) at different concentrations (0.1-500 μg/mL) was evaluated for antioxidant and antihepatoma activities. Results showed that POE exhibited a greater antioxidant activity than α-tocopherol in all model systems tested. At concentrations of 0.1-100 μg/mL, POE showed a superoxide radical scavenging activity ranging from 50.6 to 100%, with an IC50 value (0.09 μg/mL) lower than α-tocopherol (0.51 μg/mL). In the xanthine oxidase inhibition test, POE (IC50 = 0.67 μg/mL) also exhibited a stronger inhibitory effect on xanthine oxidase activity than α-tocopherol (IC50 = 0.83 μg/mL). At concentrations of 0.1 μg/mL and above, POE showed significant ability in inhibiting the oxidative damage to lipids induced by ascorbate-Fe2+ than α-tocopherol in rat liver (IC50 = 0.53 μg/mL versus 0.94 μg/mL), brain (IC50 = 0.10 μg/mL versus 52.52 μg/mL) and plasma (IC50 = 77.17 μg/mL versus 190.81 μg/mL). In the antihepatoma studies, POE showed a greater potency than α-tocopherol in inhibiting Hep G2, Hep 3B and PLC/PRF/5 cells. The antiproliferative effect of POE against these human hepatoma cells was dose-dependent, with IC50 values varying from 4.86 to 68.44 μg/mL. The present results demonstrate that POE is an effective natural antioxidant supplement for protecting cellular membranes against oxidative damage and inhibiting hepatoma cell proliferation.RattusAntioxidant and antihepatoma activities of palm oil extractjournal article10.1111/j.1745-4522.2007.00075.x2-s2.0-34347213440