Abstract

Araloside A is a pentacyclic triterpenoid saponin, and L-ascorbic acid is a globally recognized antioxidant. In this study, coadministered araloside A and L-ascorbic acid were found to have a strong synergistic antioxidant effect, and correlations between cellular antioxidant indexes and free radical scavenging ability were found. Individual and combined pretreatment with araloside A and L-ascorbic acid increased both cell viability and antioxidant enzyme activity and inhibited the release of lactate dehydrogenase (LDH); the accumulation of malondialdehyde (MDA), lipid peroxidation (LPO) products, and H2O2; and the production of intracellular reactive oxygen species (ROS), protein carbonyls, and 8-hydroxy-2-deoxy guanosine (8-OHdG). Free radical scavenging ability was positively correlated with superoxide dismutase (SOD) and catalase (CAT) activity, the glutathione (GSH)/oxidized glutathione (GSSG) ratio, and total antioxidant capacity (T-AOC). Our study is the first investigation of araloside A and L-ascorbic acid coadministration for the treatment of diseases caused by oxidative stress. The synergistic antioxidant effects of araloside A and L-ascorbic acid support their potential as functional food ingredients for the elimination of oxidative stress-induced adverse reactions.

Highlights

  • IntroductionOxidative stress is essentially caused by an imbalance between excessive free radicals, reactive oxygen species (ROS), reactive nitrogen species (RNS), and weakened antioxidant defence systems [2, 3]

  • Selye first proposed the concept of oxidative stress in 1936 [1]

  • HEK293 cells were treated with 100-800 μM H2O2 for 4 h, and cell viability was measured using the MTS method

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Summary

Introduction

Oxidative stress is essentially caused by an imbalance between excessive free radicals, reactive oxygen species (ROS), reactive nitrogen species (RNS), and weakened antioxidant defence systems [2, 3]. The H2O2-induced cellular oxidative stress model is commonly used to study the functions of various biologically active materials [6, 7]. The antioxidant capacities of araloside A, L-ascorbic acid, and their combination were investigated in a human embryonic kidney cell line (HEK293 cells) using H2O2-induced oxidative stress, which has been utilized in a large number of previous studies. The present study is the first investigation of the in vitro and intracellular antioxidant activities of araloside A and L-ascorbic acid and the correlation between these compounds

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