Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5559664 | Environmental Toxicology and Pharmacology | 2017 | 29 Pages |
Abstract
Glutathione (GSH) protects cells against oxidative stress. Redox modifiers induce GSH biosynthesis and recycling to maintain reduced environment inside cells. Cadmium (Cd2+) is a heavy metal that activates redox-sensitive transcriptional factors. The antioxidant α-lipoic acid (ALA) has shown to modulate GSH pathways. This study aimed to investigate de novo synthesis and recycling pathways for GSH balance by different Cd2+ concentrations and ALA in HepG2 cells. ALA activates Nrf2 pathway leading to GSH increment. Pre-treatment with 1 μM Cd2+ or ALA produces tolerance to 5 μM Cd2+ toxic effects. 5 μM Cd2+ exposure significantly augmented nuclear Nrf2, GSH and GCLC, GCLM, HMOX1, TNFα and IL-6 mRNA expression but not GSR, however these upsurges were significantly abrogated by ALA or 1 μM Cd2+ pre-treatments. Exposure to low Cd2+ concentration generate timely protective responses, similar to that elicited by ALA, maintaining a normal redox balance inside the cell due to GSH replenishment.
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Authors
Jose Macias-Barragan, Selene G. Huerta-Olvera, Ivan Hernandez-Cañaveral, Ana Laura Pereira-Suarez, Margarita Montoya-Buelna,