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Fontes, A. ; Jauch, A.T.* ; Sailer, J.* ; Engler, J.* ; Azul, A.M.* ; Zischka, H.

Metabolic derangement of essential transition metals and potential antioxidant therapies.

Int. J. Mol. Sci. 25:7880 (2024)
Verlagsversion DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Essential transition metals have key roles in oxygen transport, neurotransmitter synthesis, nucleic acid repair, cellular structure maintenance and stability, oxidative phosphorylation, and metabolism. The balance between metal deficiency and excess is typically ensured by several extracellular and intracellular mechanisms involved in uptake, distribution, and excretion. However, provoked by either intrinsic or extrinsic factors, excess iron, zinc, copper, or manganese can lead to cellular damage upon chronic or acute exposure, frequently attributed to oxidative stress. Intracellularly, mitochondria are the organelles that require the tightest control concerning reactive oxygen species production, which inevitably leaves them to be one of the most vulnerable targets of metal toxicity. Current therapies to counteract metal overload are focused on chelators, which often cause secondary effects decreasing patients' quality of life. New therapeutic options based on synthetic or natural antioxidants have proven positive effects against metal intoxication. In this review, we briefly address the cellular metabolism of transition metals, consequences of their overload, and current therapies, followed by their potential role in inducing oxidative stress and remedies thereof.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Antioxidants ; Copper ; Iron ; Manganese ; Oxidative Stress ; Transition Metals ; Zinc; Induced Oxidative Stress; Iron-metabolism; Acute Hepatitis; Wilson-disease; Cortical Iron; Human Health; Mouse Model; Manganese; Copper; Zinc
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 1661-6596
e-ISSN 1422-0067
Zeitschrift International Journal of Molecular Sciences
Quellenangaben Band: 25, Heft: 14, Seiten: , Artikelnummer: 7880 Supplement: ,
Verlag MDPI
Verlagsort Basel
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Molecular Toxicology and Pharmacology (TOX)
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-505200-003
Förderungen European Union
Deutsche Forschungsgemeinschaft (DFG)
Bundesministerium fur Bildung und Forschung (BMBF) (Project "WilsonMed-Multimolecular Targeting of Copper Overload in Wilson's Disease")
DOI 10.3390/ijms25147880
WOS ID 001277113800001
Scopus ID 85199779251
PubMed ID 39063122
Erfassungsdatum 2024-07-30
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