Literature DB >> 25489640

Phytoextract of Indian mustard seeds acts by suppressing the generation of ROS against acetaminophen-induced hepatotoxicity in HepG2 cells.

Harita Parikh1, Nancy Pandita, Aparna Khanna.   

Abstract

CONTEXT: Indian mustard [Brassica juncea (L.) Czern. & Coss. (Brassicaceae)] is reported to possess diverse pharmacological properties. However, limited information is available concerning its hepatoprotective activity and mechanism of action.
OBJECTIVE: To study the protective mechanism of mustard seed extract against acetaminophen (APAP) toxicity in a hepatocellular carcinoma (HepG2) cell line.
MATERIALS AND METHODS: Hepatotoxicity models were established using APAP (2.5-22.5 mM) based on the cytotoxicity profile. An antioxidant-rich fraction from mustard seeds was extracted and evaluated for its hepatoprotective potential. The mechanism of action was elucidated using various in vitro antioxidant assays, the detection of intracellular generation of reactive oxygen species (ROS), and cell cycle analysis. The phytoconstituents isolated via HPLC-DAD were also evaluated for hepatoprotective activity.
RESULTS: Hydromethanolic seed extract exhibited hepatoprotective activity in post- and pre-treatment models of 20 mM APAP toxicity and restored the elevated levels of liver indices to normal values (p < 0.05). Post-treatment suppressed the generation of ROS by 58.37% and pre-treatment effectively prevented the generation of ROS by 90.5%. The mechanism of ROS suppression was further supported by antioxidant activity (IC50) data from DPPH (103.37 ± 4.2 µg AAE/mg), FRAP (83.26 ± 1.1 µg AAE/mg), ORAC (1115 µM GAE/ml), ABTS (83.05 µg GAE/ml), and superoxide (345.22 ± 5.15 µg AAE/mg) scavenging assays and by the restoration of cell cycle alterations. HPLC-DAD analysis revealed the presence quercetin, vitamin E, and catechin, which exhibited hepatoprotective activity. DISCUSSION AND
CONCLUSIONS: A phytoextract of mustard seeds acts by suppressing the generation of ROS in response to APAP toxicity.

Entities:  

Keywords:  Antioxidant; Brassica juncea; HPLC-DAD; cell cycle; hepatoprotective; liver enzymes; oxidative stress

Mesh:

Substances:

Year:  2014        PMID: 25489640     DOI: 10.3109/13880209.2014.950675

Source DB:  PubMed          Journal:  Pharm Biol        ISSN: 1388-0209            Impact factor:   3.503


  5 in total

1.  Physiologically relevant oxygen tensions differentially regulate hepatotoxic responses in HepG2 cells.

Authors:  Thomas J DiProspero; Erin Dalrymple; Matthew R Lockett
Journal:  Toxicol In Vitro       Date:  2021-03-31       Impact factor: 3.685

2.  In vitro assessment of hepatoprotective agents against damage induced by acetaminophen and CCl4.

Authors:  Liliana Torres González; Noemí Waksman Minsky; Linda Elsa Muñoz Espinosa; Ricardo Salazar Aranda; Jonathan Pérez Meseguer; Paula Cordero Pérez
Journal:  BMC Complement Altern Med       Date:  2017-01-13       Impact factor: 3.659

Review 3.  Brassicaceae Mustards: Traditional and Agronomic Uses in Australia and New Zealand.

Authors:  Mahmudur Rahman; Amina Khatun; Lei Liu; Bronwyn J Barkla
Journal:  Molecules       Date:  2018-01-21       Impact factor: 4.411

4.  Brassica juncea L. (Mustard) Extract Silver NanoParticles and Knocking off Oxidative Stress, ProInflammatory Cytokine and Reverse DNA Genotoxicity.

Authors:  Sohair Aly Hassan; Ali Mohamed El Hagrassi; Olfat Hammam; Abdelmohsen M Soliman; Essam Ezzeldin; Wessam Magdi Aziz
Journal:  Biomolecules       Date:  2020-12-09

5.  The potential protective role of folic acid against acetaminophen-induced hepatotoxicity and nephrotoxicity in rats.

Authors:  Emrah Akgun; Murat Boyacioglu; Sadiye Kum
Journal:  Exp Anim       Date:  2020-09-21
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.