Antiferroptotic properties of allicin and related organosulfur compounds—diallyl disulfide and diallyl trisulfide—from Garlic
Allicin (diallyl thiosulfinate) is an abundant bioactive compound in garlic (Allium sativum L.) with broad-spectrum antiinflammatory, antifungal, antioxidant, and antitumor properties. The bioactive compounds of garlic including allicin may also help reduce the incidence of various diseases, althoug...
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creator | Hirata, Yoko Nagase, Haruna Satoh, Keitaro Takemori, Hiroshi Furuta, Kyoji Kamatari, Yuji O. |
description | Allicin (diallyl thiosulfinate) is an abundant bioactive compound in garlic (Allium sativum L.) with broad-spectrum antiinflammatory, antifungal, antioxidant, and antitumor properties. The bioactive compounds of garlic including allicin may also help reduce the incidence of various diseases, although the individual contributions and precise mechanisms are still largely unknown. In this study, we reveal that allicin and the closely related compounds diallyl disulfide and diallyl trisulfide (all containing more than one disulfide bond) protect mouse hippocampal HT22 cells against chemically induced ferroptosis, a newly defined form of cell death characterized by iron-dependent lipid peroxidation. In contrast, these organosulfur compounds did not prevent chemically induced apoptosis. The antiferroptotic efficacies of these compounds were strongly associated with prevention of lipid peroxidation and reactive oxygen species production but independent of glutathione upregulation, ferrous iron chelation, and modulation of the nuclear factor erythroid 2 (NF-E2)-related factor-2-antioxidant element response pathway. Additional studies are warranted on the therapeutic potential of allicin and related compounds in garlic for neurodegenerative diseases associated with ferroptosis.
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•Allicin, diallyl disulfide, and diallyl trisulfide suppress chemically induced ferroptosis.•These garlic-derived organosulfur compounds have no effect on chemically induced apoptosis.•The antiferroptotic properties are independent of iron chelation.•The antiferroptotic properties are associated with reduced ROS and lipid peroxide accumulation. |
doi_str_mv | 10.1016/j.fct.2024.115124 |
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[Display omitted]
•Allicin, diallyl disulfide, and diallyl trisulfide suppress chemically induced ferroptosis.•These garlic-derived organosulfur compounds have no effect on chemically induced apoptosis.•The antiferroptotic properties are independent of iron chelation.•The antiferroptotic properties are associated with reduced ROS and lipid peroxide accumulation.</description><identifier>ISSN: 0278-6915</identifier><identifier>ISSN: 1873-6351</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/j.fct.2024.115124</identifier><identifier>PMID: 39580015</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Allicin ; Allium sativum ; Allyl Compounds - pharmacology ; Animals ; apoptosis ; Apoptosis - drug effects ; bioactive compounds ; Cell Line ; chelation ; diallyl disulfide ; disulfide bonds ; disulfides ; Disulfides - pharmacology ; Ferroptosis ; Ferroptosis - drug effects ; Garlic ; Garlic - chemistry ; Glutathione ; iron ; Lipid peroxidation ; Lipid Peroxidation - drug effects ; Mice ; reactive oxygen species ; Reactive Oxygen Species - metabolism ; Sulfides - pharmacology ; Sulfinic Acids - pharmacology ; therapeutics</subject><ispartof>Food and chemical toxicology, 2025-01, Vol.195, p.115124, Article 115124</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c268t-9ea40ee07b9fe3d3692209191a0a07604a29ec76c1e89dc909ad546536d58bbf3</cites><orcidid>0000-0002-7081-4937</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0278691524006902$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39580015$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hirata, Yoko</creatorcontrib><creatorcontrib>Nagase, Haruna</creatorcontrib><creatorcontrib>Satoh, Keitaro</creatorcontrib><creatorcontrib>Takemori, Hiroshi</creatorcontrib><creatorcontrib>Furuta, Kyoji</creatorcontrib><creatorcontrib>Kamatari, Yuji O.</creatorcontrib><title>Antiferroptotic properties of allicin and related organosulfur compounds—diallyl disulfide and diallyl trisulfide—from Garlic</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><description>Allicin (diallyl thiosulfinate) is an abundant bioactive compound in garlic (Allium sativum L.) with broad-spectrum antiinflammatory, antifungal, antioxidant, and antitumor properties. The bioactive compounds of garlic including allicin may also help reduce the incidence of various diseases, although the individual contributions and precise mechanisms are still largely unknown. In this study, we reveal that allicin and the closely related compounds diallyl disulfide and diallyl trisulfide (all containing more than one disulfide bond) protect mouse hippocampal HT22 cells against chemically induced ferroptosis, a newly defined form of cell death characterized by iron-dependent lipid peroxidation. In contrast, these organosulfur compounds did not prevent chemically induced apoptosis. The antiferroptotic efficacies of these compounds were strongly associated with prevention of lipid peroxidation and reactive oxygen species production but independent of glutathione upregulation, ferrous iron chelation, and modulation of the nuclear factor erythroid 2 (NF-E2)-related factor-2-antioxidant element response pathway. Additional studies are warranted on the therapeutic potential of allicin and related compounds in garlic for neurodegenerative diseases associated with ferroptosis.
[Display omitted]
•Allicin, diallyl disulfide, and diallyl trisulfide suppress chemically induced ferroptosis.•These garlic-derived organosulfur compounds have no effect on chemically induced apoptosis.•The antiferroptotic properties are independent of iron chelation.•The antiferroptotic properties are associated with reduced ROS and lipid peroxide accumulation.</description><subject>Allicin</subject><subject>Allium sativum</subject><subject>Allyl Compounds - pharmacology</subject><subject>Animals</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>bioactive compounds</subject><subject>Cell Line</subject><subject>chelation</subject><subject>diallyl disulfide</subject><subject>disulfide bonds</subject><subject>disulfides</subject><subject>Disulfides - pharmacology</subject><subject>Ferroptosis</subject><subject>Ferroptosis - drug effects</subject><subject>Garlic</subject><subject>Garlic - chemistry</subject><subject>Glutathione</subject><subject>iron</subject><subject>Lipid peroxidation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Mice</subject><subject>reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Sulfides - pharmacology</subject><subject>Sulfinic Acids - pharmacology</subject><subject>therapeutics</subject><issn>0278-6915</issn><issn>1873-6351</issn><issn>1873-6351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcGOFCEURYnROO3oB7gxtXRT7QMKKOJqMhlHk0nc6JrQ8DB0qooWKJPZ6T_4hX6JtD3t0riCPM49yeMS8pLClgKVb_bb4OqWARu2lArKhkdkQ0fFe8kFfUw2wNTYS03FBXlWyh4AFFXyKbngWowAVGzIj6ulxoA5p0NNNbru0G6Ya8TSpdDZaYouLp1dfJdxshV9l_IXu6SyTmHNnUvzIa2LL7--__Sx4fdT5-PxMXr8EztPaz6PGxpymrtbm5v9OXkS7FTwxcN5ST6_u_l0_b6_-3j74frqrndMjrXXaAdABLXTAbnnUjMGmmpqwYKSMFim0SnpKI7aOw3aejFIwaUX424X-CV5ffK2Db-uWKqZY3E4TXbBtBbDqRgYV3TU_4FyxqUCOKL0hLqcSskYzCHH2eZ7Q8EcSzJ700oyx5LMqaSWefWgX3cz-r-JcysNeHsCsP3Ht4jZFBdxcehjxibzKf5D_xsAIaab</recordid><startdate>202501</startdate><enddate>202501</enddate><creator>Hirata, Yoko</creator><creator>Nagase, Haruna</creator><creator>Satoh, Keitaro</creator><creator>Takemori, Hiroshi</creator><creator>Furuta, Kyoji</creator><creator>Kamatari, Yuji O.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-7081-4937</orcidid></search><sort><creationdate>202501</creationdate><title>Antiferroptotic properties of allicin and related organosulfur compounds—diallyl disulfide and diallyl trisulfide—from Garlic</title><author>Hirata, Yoko ; Nagase, Haruna ; Satoh, Keitaro ; Takemori, Hiroshi ; Furuta, Kyoji ; Kamatari, Yuji O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c268t-9ea40ee07b9fe3d3692209191a0a07604a29ec76c1e89dc909ad546536d58bbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Allicin</topic><topic>Allium sativum</topic><topic>Allyl Compounds - pharmacology</topic><topic>Animals</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>bioactive compounds</topic><topic>Cell Line</topic><topic>chelation</topic><topic>diallyl disulfide</topic><topic>disulfide bonds</topic><topic>disulfides</topic><topic>Disulfides - pharmacology</topic><topic>Ferroptosis</topic><topic>Ferroptosis - drug effects</topic><topic>Garlic</topic><topic>Garlic - chemistry</topic><topic>Glutathione</topic><topic>iron</topic><topic>Lipid peroxidation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Mice</topic><topic>reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Sulfides - pharmacology</topic><topic>Sulfinic Acids - pharmacology</topic><topic>therapeutics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirata, Yoko</creatorcontrib><creatorcontrib>Nagase, Haruna</creatorcontrib><creatorcontrib>Satoh, Keitaro</creatorcontrib><creatorcontrib>Takemori, Hiroshi</creatorcontrib><creatorcontrib>Furuta, Kyoji</creatorcontrib><creatorcontrib>Kamatari, Yuji O.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirata, Yoko</au><au>Nagase, Haruna</au><au>Satoh, Keitaro</au><au>Takemori, Hiroshi</au><au>Furuta, Kyoji</au><au>Kamatari, Yuji O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antiferroptotic properties of allicin and related organosulfur compounds—diallyl disulfide and diallyl trisulfide—from Garlic</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2025-01</date><risdate>2025</risdate><volume>195</volume><spage>115124</spage><pages>115124-</pages><artnum>115124</artnum><issn>0278-6915</issn><issn>1873-6351</issn><eissn>1873-6351</eissn><abstract>Allicin (diallyl thiosulfinate) is an abundant bioactive compound in garlic (Allium sativum L.) with broad-spectrum antiinflammatory, antifungal, antioxidant, and antitumor properties. The bioactive compounds of garlic including allicin may also help reduce the incidence of various diseases, although the individual contributions and precise mechanisms are still largely unknown. In this study, we reveal that allicin and the closely related compounds diallyl disulfide and diallyl trisulfide (all containing more than one disulfide bond) protect mouse hippocampal HT22 cells against chemically induced ferroptosis, a newly defined form of cell death characterized by iron-dependent lipid peroxidation. In contrast, these organosulfur compounds did not prevent chemically induced apoptosis. The antiferroptotic efficacies of these compounds were strongly associated with prevention of lipid peroxidation and reactive oxygen species production but independent of glutathione upregulation, ferrous iron chelation, and modulation of the nuclear factor erythroid 2 (NF-E2)-related factor-2-antioxidant element response pathway. Additional studies are warranted on the therapeutic potential of allicin and related compounds in garlic for neurodegenerative diseases associated with ferroptosis.
[Display omitted]
•Allicin, diallyl disulfide, and diallyl trisulfide suppress chemically induced ferroptosis.•These garlic-derived organosulfur compounds have no effect on chemically induced apoptosis.•The antiferroptotic properties are independent of iron chelation.•The antiferroptotic properties are associated with reduced ROS and lipid peroxide accumulation.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39580015</pmid><doi>10.1016/j.fct.2024.115124</doi><orcidid>https://orcid.org/0000-0002-7081-4937</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Allicin Allium sativum Allyl Compounds - pharmacology Animals apoptosis Apoptosis - drug effects bioactive compounds Cell Line chelation diallyl disulfide disulfide bonds disulfides Disulfides - pharmacology Ferroptosis Ferroptosis - drug effects Garlic Garlic - chemistry Glutathione iron Lipid peroxidation Lipid Peroxidation - drug effects Mice reactive oxygen species Reactive Oxygen Species - metabolism Sulfides - pharmacology Sulfinic Acids - pharmacology therapeutics |
title | Antiferroptotic properties of allicin and related organosulfur compounds—diallyl disulfide and diallyl trisulfide—from Garlic |
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