Ferroptosis at the crossroads of manganese-induced neurotoxicity: A retrospective study
Manganese is an essential trace element, but overexposure can cause neurotoxicity and subsequent neurodegenerative diseases. Ferroptosis is a form of cell death characterized by lipid peroxidation and iron overload inside cells, which is closely related to manganese neurotoxicity. Manganese can indu...
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Veröffentlicht in: | Toxicology (Amsterdam) 2024-02, Vol.502, p.153727-153727, Article 153727 |
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creator | Liu, Yaoyang Lv, Shanyu He, Guoguo Wang, Changyong Ou, Chaoyan |
description | Manganese is an essential trace element, but overexposure can cause neurotoxicity and subsequent neurodegenerative diseases. Ferroptosis is a form of cell death characterized by lipid peroxidation and iron overload inside cells, which is closely related to manganese neurotoxicity. Manganese can induce ferroptosis through multiple pathways: causing oxidative stress and increased cellular reactive oxygen species (ROS), resulting in lipid peroxidation; depleting glutathione (GSH) and weakening the antioxidant capacity of cells; disrupting iron metabolism and increasing iron-dependent lipid peroxidation; damaging mitochondrial function and disrupting the electron transport chain, leading to increased ROS production. Oxidative stress, iron metabolism disorders, lipid peroxidation, GSH depletion, and mitochondrial dysfunction, typical features of ferroptosis, have been observed in animal and cell models after manganese exposure. In summary, manganese can participate in the pathogenesis of neurodegenerative diseases by inducing events related to ferroptosis. This provides new insights into studying the mechanism of manganese neurotoxicity and developing therapeutic drugs. |
doi_str_mv | 10.1016/j.tox.2024.153727 |
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Ferroptosis is a form of cell death characterized by lipid peroxidation and iron overload inside cells, which is closely related to manganese neurotoxicity. Manganese can induce ferroptosis through multiple pathways: causing oxidative stress and increased cellular reactive oxygen species (ROS), resulting in lipid peroxidation; depleting glutathione (GSH) and weakening the antioxidant capacity of cells; disrupting iron metabolism and increasing iron-dependent lipid peroxidation; damaging mitochondrial function and disrupting the electron transport chain, leading to increased ROS production. Oxidative stress, iron metabolism disorders, lipid peroxidation, GSH depletion, and mitochondrial dysfunction, typical features of ferroptosis, have been observed in animal and cell models after manganese exposure. In summary, manganese can participate in the pathogenesis of neurodegenerative diseases by inducing events related to ferroptosis. This provides new insights into studying the mechanism of manganese neurotoxicity and developing therapeutic drugs.</description><identifier>ISSN: 0300-483X</identifier><identifier>EISSN: 1879-3185</identifier><identifier>DOI: 10.1016/j.tox.2024.153727</identifier><identifier>PMID: 38216111</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Ferroptosis ; Manganese ; Neurotoxicity</subject><ispartof>Toxicology (Amsterdam), 2024-02, Vol.502, p.153727-153727, Article 153727</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-6ac5c92e89f05b8258d0b30626c65ada2acf431a7e8c775e05d238e6420daee53</citedby><cites>FETCH-LOGICAL-c353t-6ac5c92e89f05b8258d0b30626c65ada2acf431a7e8c775e05d238e6420daee53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0300483X24000088$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38216111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yaoyang</creatorcontrib><creatorcontrib>Lv, Shanyu</creatorcontrib><creatorcontrib>He, Guoguo</creatorcontrib><creatorcontrib>Wang, Changyong</creatorcontrib><creatorcontrib>Ou, Chaoyan</creatorcontrib><title>Ferroptosis at the crossroads of manganese-induced neurotoxicity: A retrospective study</title><title>Toxicology (Amsterdam)</title><addtitle>Toxicology</addtitle><description>Manganese is an essential trace element, but overexposure can cause neurotoxicity and subsequent neurodegenerative diseases. Ferroptosis is a form of cell death characterized by lipid peroxidation and iron overload inside cells, which is closely related to manganese neurotoxicity. Manganese can induce ferroptosis through multiple pathways: causing oxidative stress and increased cellular reactive oxygen species (ROS), resulting in lipid peroxidation; depleting glutathione (GSH) and weakening the antioxidant capacity of cells; disrupting iron metabolism and increasing iron-dependent lipid peroxidation; damaging mitochondrial function and disrupting the electron transport chain, leading to increased ROS production. Oxidative stress, iron metabolism disorders, lipid peroxidation, GSH depletion, and mitochondrial dysfunction, typical features of ferroptosis, have been observed in animal and cell models after manganese exposure. In summary, manganese can participate in the pathogenesis of neurodegenerative diseases by inducing events related to ferroptosis. This provides new insights into studying the mechanism of manganese neurotoxicity and developing therapeutic drugs.</description><subject>Ferroptosis</subject><subject>Manganese</subject><subject>Neurotoxicity</subject><issn>0300-483X</issn><issn>1879-3185</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kL1OwzAYRS0EglJ4ABbkkSXFP3HiwFRV_EmVWECwWa79BVy1cbEdRN8eoxRGJi_3ns_3IHRGyYQSWl0uJ8l_TRhh5YQKXrN6D42orJuCUyn20YhwQopS8tcjdBzjkhDCeFkdoiMuGa0opSP0cgsh-E3y0UWsE07vgE3wMQavbcS-xWvdvekOIhSus70Bizvog8-XnXFpe4WnOEDKlQ2Y5D4Bx9Tb7Qk6aPUqwunuHaPn25un2X0xf7x7mE3nheGCp6LSRpiGgWxaIhaSCWnJgpOKVaYS2mqmTVtyqmuQpq4FEGEZl1CVjFgNIPgYXQzcTfAfPcSk1i4aWK3yl30fFWtYzSjLxBylQ3TYB63aBLfWYasoUT8-1VLlVerHpxp85s75Dt8v1mD_Gr8Cc-B6CEAe-ekgqGgcdFmTC9mHst79g_8Gxm-HUw</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Liu, Yaoyang</creator><creator>Lv, Shanyu</creator><creator>He, Guoguo</creator><creator>Wang, Changyong</creator><creator>Ou, Chaoyan</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240201</creationdate><title>Ferroptosis at the crossroads of manganese-induced neurotoxicity: A retrospective study</title><author>Liu, Yaoyang ; Lv, Shanyu ; He, Guoguo ; Wang, Changyong ; Ou, Chaoyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-6ac5c92e89f05b8258d0b30626c65ada2acf431a7e8c775e05d238e6420daee53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Ferroptosis</topic><topic>Manganese</topic><topic>Neurotoxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yaoyang</creatorcontrib><creatorcontrib>Lv, Shanyu</creatorcontrib><creatorcontrib>He, Guoguo</creatorcontrib><creatorcontrib>Wang, Changyong</creatorcontrib><creatorcontrib>Ou, Chaoyan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Toxicology (Amsterdam)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yaoyang</au><au>Lv, Shanyu</au><au>He, Guoguo</au><au>Wang, Changyong</au><au>Ou, Chaoyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ferroptosis at the crossroads of manganese-induced neurotoxicity: A retrospective study</atitle><jtitle>Toxicology (Amsterdam)</jtitle><addtitle>Toxicology</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>502</volume><spage>153727</spage><epage>153727</epage><pages>153727-153727</pages><artnum>153727</artnum><issn>0300-483X</issn><eissn>1879-3185</eissn><abstract>Manganese is an essential trace element, but overexposure can cause neurotoxicity and subsequent neurodegenerative diseases. Ferroptosis is a form of cell death characterized by lipid peroxidation and iron overload inside cells, which is closely related to manganese neurotoxicity. Manganese can induce ferroptosis through multiple pathways: causing oxidative stress and increased cellular reactive oxygen species (ROS), resulting in lipid peroxidation; depleting glutathione (GSH) and weakening the antioxidant capacity of cells; disrupting iron metabolism and increasing iron-dependent lipid peroxidation; damaging mitochondrial function and disrupting the electron transport chain, leading to increased ROS production. Oxidative stress, iron metabolism disorders, lipid peroxidation, GSH depletion, and mitochondrial dysfunction, typical features of ferroptosis, have been observed in animal and cell models after manganese exposure. In summary, manganese can participate in the pathogenesis of neurodegenerative diseases by inducing events related to ferroptosis. 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subjects | Ferroptosis Manganese Neurotoxicity |
title | Ferroptosis at the crossroads of manganese-induced neurotoxicity: A retrospective study |
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