Abstract

Neurodegenerative diseases pose a major health problem for developed countries, and stress has been identified as one of the main risk factors in the development of these disorders. Here, we have examined the protective properties against oxidative stress of several bioactive natural food supplements. We found that MecobalActive®, Olews®, and red and white grape seed polyphenol extracts may have a neuroprotective effect in vitro, both in the SH-SY 5Y cell line and in hippocampal neuron cultures, mainly by reducing reactive oxygen species levels and decreasing caspase-3 activity. In vivo, we demonstrated that oral administration of the supplements reduces the expression of genes involved in inflammation and oxidation mechanisms, whereas it increments the expression of genes related to protection against oxidative stress. Furthermore, we found that preventive treatment with these natural extracts increases the activity of antioxidant enzymes and prevents lipid peroxidation in the brain of stressed mice. Thus, our results indicate that some natural bioactive supplements may have important protective properties against oxidative stress processes occurring in the brain.

Highlights

  • The increasing population lifespan in developed countries is leading to a higher incidence of age-related illnesses, including neurodegenerative diseases (ND) [1]

  • We tested the activity of the chosen supplements (Cardiose®, Olews®, citicoline, MecobalActive®, and red and white grape extracts) on the SH-SY 5Y cell line to study their potential toxicity

  • We demonstrated that oral administration of the supplements for just five days reduces the expression of genes involved in inflammation and oxidation mechanisms, whereas it increments the expression of genes related to protection against oxidative stress

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Summary

Introduction

The increasing population lifespan in developed countries is leading to a higher incidence of age-related illnesses, including neurodegenerative diseases (ND) [1]. NDs encompass a heterogeneous group of chronic disorders that include, among others, Alzheimer’s disease (AD) and other dementias, Huntingtons disease, Parkinsons disease, multiple sclerosis, human prion, and motoneuron diseases [3,4,5,6] All these diseases are untreatable at the moment, and, in terms of human suffering and economic and social costs, they represent the fourth cause of global disease burden in developed countries [1]. There is evidence that mitochondrial damage resulting in an increased production of ROS contributes to the early stages of the disease prior to the onset of clinical symptoms [9,13]. For these reasons, numerous scientific studies suggest

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