Effects of Trans-resveratrol in Peanut Red Coat on Antioxidant in HEK293T Cells
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(1.Institute of Agro-food Technology, Jilin Academy of Agricultural Sciences, Changchun 130033;2.Baotou Light Industry Vocational Technical College, Baotou 014035, Inner Mongolia;3.China International Engineering Consulting Corporation, Beijing 100048)

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    Abstract:

    Objective: This experiment analyzed the resveratrol composition in peanut red coat to investigate the antioxidant effects of its main component trans-resveratrol (RES) on human embryonic kidney cell 293 (HEK293T) and its potential molecular mechanism. Methods: The resveratrol in peanut red coat was extracted by ultrasonic-assisted enzymatic method, and the constituents of the crude extract of resveratrol in peanut red coat were analyzed by high performance liquid chromatography-mass spectrometry (HPLC-MS). The highest toxicity of RES on HEK293T cells was detected by cell viability assay, its effects of Keap1-Nrf2-ARE antioxidant signaling pathway was detected by luciferase reporter gene assay and Western blot assay, and its in vitro antioxidant capacity was determined by DPPH free radical clearance. Results: The results of HPLC-MS showed that resveratrol glycosides, paclitaxel and RES were contained in peanut red coat. Since resveratrol mainly exists in the form of trans-resveratrol in nature, RES was selected for the subsequent experiments. The results of cell viability assay showed that the highest non-toxic concentration of RES on HEK293T cells was 50 μmol/L, and the in vitro antioxidant effects was concentration-dependent. Western blot results showed that RES induced Nrf2-mediated expression of three target proteins heme oxygenase 1 (HO-1), quinone oxidoreductase 1 (NQO1) and glutamate cysteine ligase (GCLM). In addition, the results of the DPPH radical scavenging assay showed that RES could effectively scavenge DPPH radicals and had in vitro antioxidant capacity. Conclusion: The major components of resveratrol in peanut red coat have antioxidant effects on HEK293T cells and can activate a potential antioxidant activity through the Keap1-Nrf2-ARE signaling pathway.

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  • Received:May 20,2023
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  • Online: June 20,2024
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