4.6 Article

In Vitro and In Vivo Protective Effects of Lentil (Lens culinaris) Extract against Oxidative Stress-Induced Hepatotoxicity

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MOLECULES
卷 27, 期 1, 页码 -

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MDPI
DOI: 10.3390/molecules27010059

关键词

lentil; hepatoprotective effect; oxidative stress; Nrf2

资金

  1. Bisa Research Grant of Keimyung University, Republic of Korea [20180771]

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This study found that the phenolic extract of beluga lentil (BLE) has protective effects against oxidative stress-induced hepatotoxicity. BLE can reduce intracellular reactive oxygen species (ROS) levels and enhance the expression of antioxidant genes. In animal experiments, pretreatment with BLE also significantly reduced liver injury markers and increased the activity of intracellular antioxidant enzymes. Therefore, BLE may be a potential source of nutraceuticals with hepatoprotective effects.
Excessive oxidative stress plays a role in hepatotoxicity and the pathogenesis of hepatic diseases. In our previous study, the phenolic extract of beluga lentil (BLE) showed the most potent in vitro antioxidant activity among extracts of four common varieties of lentils; thus, we hypothesized that BLE might protect liver cells against oxidative stress-induced cytotoxicity. BLE was evaluated for its protective effects against oxidative stress-induced hepatotoxicity in AML12 mouse hepatocytes and BALB/c mice. H2O2 treatment caused a marked decrease in cell viability; however, pretreatment with BLE (25-100 mu g/mL) for 24 h significantly preserved the viability of H2O2-treated cells up to about 50% at 100 mu g/mL. As expected, BLE dramatically reduced intracellular reactive oxygen species (ROS) levels in a dose-dependent manner in H2O2-treated cells. Further mechanistic studies demonstrated that BLE reduced cellular ROS levels, partly by increasing expression of antioxidant genes. Furthermore, pretreatment with BLE (400 mg/kg) for 2 weeks significantly reduced serum levels of alanine transaminase and triglyceride by about 49% and 40%, respectively, and increased the expression and activity of glutathione peroxidase in CCl4-treated BALB/c mice. These results suggest that BLE protects liver cells against oxidative stress, partly by inducing cellular antioxidant system; thus, it represents a potential source of nutraceuticals with hepatoprotective effects.

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