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Fimbristylis ovata extract and its ability to encounter AGEs-induced neurotoxicity in SH-SY5Y

  • Sirirattanakul, Suphasarang (Graduate Program in Clinical Biochemistry and Molecular Medicine, Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University) ;
  • Santiyanont, Rachana (Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University)
  • Received : 2019.12.08
  • Accepted : 2020.11.04
  • Published : 2021.07.15

Abstract

Advanced glycation end products (AGEs) upon binding to its receptor (receptor for AGEs, RAGE) trigger several pathological processes involving oxidative stress and inflammatory pathway which play a pivotal role in various degenerative diseases including Alzheimer's disease. Fimbristylis ovata (F. ovata) has long been reported to be used as a traditional herbal medicine; nonetheless, very few studies have been reported. In this study, the protective effects of F. ovata extract on neurotoxicity of hippocampal neuronal cells (SH-SY5Y) was investigated. When compared to normal control, AGEs treatment significantly induced oxidative stress level and enhanced NF-κB translocation to nucleus in the neuronal cells (p<0.05). The increase in NF-κB translocation leads to increase in transcription level of the target genes including RAGE and pro-inflammatory cytokines which include interleukin 1 beta (IL1B), tumor necrosis factor-alpha (TNFA) and interleukin 6 (IL6). Pre-treatment of SH-SY5Y with the extracts of F. ovata shows favorable results by significantly suppressing oxidative stress level (p<0.05) as well transcriptional level of RAGE (p<0.05) and pro-inflammatory cytokines (p<0.05). Chemical analysis of F. ovata extracts using High Resolution Liquid Chromatograph Mass Spectrometer (HR-LCMS) and Gas Chromatograph with high resolution Mass Spectrometer (GC-HRMS) suggested some potential active phytochemical compounds. The results from this study may provide possible alternative treatment for prevention and/or therapy of neurodegenerative disorders by targeting the above-mentioned pathways. The role of the phytochemical active ingredient (s) in inhibiting the AGEs-triggered signaling inflammatory pathway should be investigated in future study.

Keywords

Acknowledgement

We thank Dr. Suporn Sukjamnong for technical support in plant material and extract preparation. This work was granted by Chulalongkorn University Graduate Scholarship to Commemorate the 72nd Anniversary of His Majesty King BhumibolAdulyadej, The 90th Anniversary of Chulalongkorn University Fund (Ratchadaphiseksomphot Endowment Fund), and Asia Research Center, Chulalongkorn University (ARC) (contract no. 005/2560).

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