Can Iron and Polyunsaturated Fatty Acid Supplementation Induce Ferroptosis?

Autor:	Delesderrier E; Institute of Nutrition, State University of Rio de Janeiro, Rio de Janeiroe, Brazil, emiliadeles@gmail.com., Monteiro JDC; Institute of Nutrition, State University of Rio de Janeiro, Rio de Janeiroe, Brazil., Freitas S; Institute of Nutrition, State University of Rio de Janeiro, Rio de Janeiroe, Brazil., Pinheiro IC; Institute of Nutrition, State University of Rio de Janeiro, Rio de Janeiroe, Brazil., Batista MS; Institute of Nutrition, State University of Rio de Janeiro, Rio de Janeiroe, Brazil., Citelli M; Institute of Nutrition, State University of Rio de Janeiro, Rio de Janeiroe, Brazil.
Jazyk:	angličtina
Zdroj:	Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology [Cell Physiol Biochem] 2023 Apr 15; Vol. 57 (S1), pp. 24-41.
DOI:	10.33594/000000620
Abstrakt:	Ferroptosis is a regulated non-apoptotic cell death process triggered by excessive iron-induced lipid peroxidation. Excess intracellular iron promotes lipid peroxidation by increasing reactive oxygen species formation through the Fenton reaction. Thus, iron and polyunsaturated fatty acid intake may trigger ferroptosis under certain conditions. The aims of this review were to compile and examine evidence in the literature for the effects of iron and polyunsaturated fatty acid supplementation on ferroptosis. Omega-6 polyunsaturated fatty acids have relatively greater susceptibility to lipid peroxidation and could, therefore, participate in ferroptosis. By contrast, omega-3 polyunsaturated fatty acids promote intracellular antioxidants synthesis and reduce the formation of hydroperoxides that induce ferroptosis. As intestinal iron absorption is regulated by iron nutritional status, individuals with normal functioning of the hepcidin-ferroportin axis are at low risk of developing iron overload in response to ingestion of iron-rich foods. Therefore, iron supplementation is potentially toxic mainly for the intestinal epithelium and the microbiota. In animal models, iron-rich diets increased oxidative damage, lowered the glutathione concentration within hepatocytes, and downregulated desaturases that synthesize long-chain polyunsaturated fatty acids. These adverse effects of iron supplementation were prevented by omega-3 fatty acid co-supplementation. The impact of food and supplement intake on ferroptosis has seldom been investigated. Scientific evidence still does not allow us to know for sure whether iron and PUFA supplementation are capable of inducing ferroptosis. As the mechanisms that control ferroptosis can determine whether cells proliferate or die, future studies should directly investigate the effects of nutrient supplementation and food intake on the ferroptosis process in different types of cells and tissues. Competing Interests: No potential Disclosure Statement was reported by the authors. (© Copyright by the Author(s). Published by Cell Physiol Biochem Press.)
Databáze:	MEDLINE
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