Journal
FRONTIERS IN NUTRITION
Volume 9, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2022.991524
Keywords
nanomaterials; oxidative stress; inflammation; alpha-lipoic acid; meta-analysis
Categories
Funding
- National Key Research and Development Program of China
- China Postdoctoral Science Foundation
- [2017YFA0204600]
- [2017M621322]
- [2018T110324]
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Extensive exposure to nanomaterials can cause oxidative stress and inflammation, increasing the risk of adverse health outcomes. Alpha-lipoic acid (ALA) has shown antioxidant and anti-inflammatory activities, suggesting its potential effectiveness in preventing nanomaterial-induced toxicity. A meta-analysis of multiple studies found that ALA supplementation significantly affected oxidative stress, inflammation, apoptosis, DNA damage, and organ damage caused by nanomaterials. In vitro studies also demonstrated that ALA intervention increased cell viability, decreased ROS levels, inhibited cell apoptosis, and chelated metal ions. These findings suggest that ALA supplementation may be a potential strategy for preventing nanomaterial-induced toxicity.
Extensive exposure to nanomaterials causes oxidative stress and inflammation in various organs and leads to an increased risk of adverse health outcomes; therefore, how to prevent the toxic effects are of great concern to human. Alpha-lipoic acid (ALA) has anti-oxidant and anti-inflammatory activities, suggesting it may be effective to prevent nanomaterial-induced toxicity. However, the results obtained in individual studies remained controversial. We aimed to comprehensively evaluate the effects of ALA supplementation on nanomaterial-induced toxicity by performing a meta-analysis. Databases of PubMed, EMBASE, and Cochrane Library were searched up to May 2022. STATA 15.0 software was used for statistical analysis. Twelve studies were included. Meta-analysis of eight in vivo studies showed ALA supplementation could exert significant effects on nanomaterial-induced oxidative stress (by reducing MDA, ROS and increasing GSH, CAT, GPx, and SOD), inflammation (by downregulating NO, IgG, TNF-alpha, IL-6, and CRP), apoptosis (by activation of pro-apoptotic caspase-3), DNA damage (by a reduction in the tail length) and organ damage (by a decrease in the liver biomarker ALT and increases in brain neuron biomarker AChE and heart biomarker CPK). Pooled analysis of four in vitro studies indicated ALA intervention increased cell viability, decreased ROS levels, inhibited cell apoptosis and chelated metal ions. Subgroup analyses revealed changing the levels of GSH, IL-6, and metal ions were the main protective mechanisms of ALA supplementation because they were not changed by any subgroup factors. In conclusion, ALA supplementation may represent a potential strategy for the prevention of the toxicity induced by nanomaterials.
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