Research article

Hypericum alpestre extract affects the activity of the key antioxidant enzymes in microglial BV-2 cellular models

  • Received: 11 May 2022 Revised: 09 June 2022 Accepted: 15 June 2022 Published: 20 June 2022
  • In the presented work, we aimed to investigate the antioxidant and possible neuroprotective capacity of extract of the aerial parts of Hypericum alpestre, found in high altitude Armenian landscape. The neuroprotective activity was evaluated using BV-2 wild type (WT) cells and acyl-CoA oxidase 1 (ACOX1) deficient (Acox1-/-) microglial cell lines. In the chemical-based tests, H. alpestre extract showed high antioxidant activity, which was maintained even after heat treatment at 121 °C for 30 min. MTT test showed that the sub-cytotoxic concentration of investigated extracts for both microglial cell lines was 40 µg/mL. There were no significant changes in catalase activity during all period of treatment in both cell lines, meanwhile, SOD activity increased (up to 30%) in WT cells during the 48 h treatment. Increase of SOD activity (up to 50%) in Acox-/- cells was observed under the 24 h treatment. Significant modulation in activity of palmitoyl-CoA oxidase 1 was noticed only during the 48 h treatment of WT microglial cells. These results evidenced the pro-oxidant activity of the investigated extract. This finding can serve as a basis for further evaluation of plant extracts influence on cancer cell lines.

    Citation: Mikayel Ginovyan, Pierre Andreoletti, Mustapha Cherkaoui-Malki, Naira Sahakyan. Hypericum alpestre extract affects the activity of the key antioxidant enzymes in microglial BV-2 cellular models[J]. AIMS Biophysics, 2022, 9(2): 161-171. doi: 10.3934/biophy.2022014

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  • In the presented work, we aimed to investigate the antioxidant and possible neuroprotective capacity of extract of the aerial parts of Hypericum alpestre, found in high altitude Armenian landscape. The neuroprotective activity was evaluated using BV-2 wild type (WT) cells and acyl-CoA oxidase 1 (ACOX1) deficient (Acox1-/-) microglial cell lines. In the chemical-based tests, H. alpestre extract showed high antioxidant activity, which was maintained even after heat treatment at 121 °C for 30 min. MTT test showed that the sub-cytotoxic concentration of investigated extracts for both microglial cell lines was 40 µg/mL. There were no significant changes in catalase activity during all period of treatment in both cell lines, meanwhile, SOD activity increased (up to 30%) in WT cells during the 48 h treatment. Increase of SOD activity (up to 50%) in Acox-/- cells was observed under the 24 h treatment. Significant modulation in activity of palmitoyl-CoA oxidase 1 was noticed only during the 48 h treatment of WT microglial cells. These results evidenced the pro-oxidant activity of the investigated extract. This finding can serve as a basis for further evaluation of plant extracts influence on cancer cell lines.


    Abbreviations

    ACOX1

    acyl-CoA oxidase 1

    HE

    Hypericum alpestre extract

    DMEM

    Dulbecco's modified Eagle medium

    DMSO

    dimethyl sulfoxide

    DPPH

    1,1-diphenyl-2-picrylhydrazyl

    EDTA

    ethylenediamine tetraacetic acid

    EO

    essential oil

    FBS

    fetal bovine serum

    MTT

    3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

    PBS

    Phosphate-buffered saline

    RIPA

    radioimmunoprecipitation

    ROS

    reactive oxygen species

    SOD

    superoxide dismutase

    VLCFA

    very-long-chain fatty acids

    WT

    wild type

    GA

    gallic acid

    加载中

    Acknowledgments



    This work was supported by the Science Committee of RA, in the frames of the research project № 21AG-4D027 as well as is based upon work from COST Action NutRedOx-CA16112 supported by COST (European Cooperation in Science and Technology) in the frames of STSM programs. The authors would like to acknowledge Ms. Ashkhen Abrahamyan (Russian-Armenian University) for re-editing the manuscript and improving English.

    Conflict of interest



    The authors declare no conflict of interest.

    Author contributions



    All authors contributed to the study's conception and design. NS and MG have carried out the investigations and analyzed the outcomes. NS and MG wrote the manuscript. All authors edited the manuscript. All authors revised and accepted the final version of the manuscript.

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