Farnesol induces protection against murine CNS inflammatory demyelination and modifies gut microbiome
Farnesol is a 15‑carbon organic isoprenol synthesized by plants and mammals with anti-oxidant, anti-inflammatory, and neuroprotective activities. We sought to determine whether farnesol treatment would result in protection against murine experimental autoimmune encephalomyelitis (EAE), a well-establ...
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Veröffentlicht in: | Clinical immunology (Orlando, Fla.) Fla.), 2022-02, Vol.235, p.108766-108766, Article 108766 |
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creator | Sell, Lacey B. Ramelow, Christina C. Kohl, Hannah M. Hoffman, Kristina Bains, Jasleen K. Doyle, William J. Strawn, Kevin D. Hevrin, Theresa Kirby, Trevor O. Gibson, K. Michael Roullet, Jean-Baptiste Ochoa-Repáraz, Javier |
description | Farnesol is a 15‑carbon organic isoprenol synthesized by plants and mammals with anti-oxidant, anti-inflammatory, and neuroprotective activities. We sought to determine whether farnesol treatment would result in protection against murine experimental autoimmune encephalomyelitis (EAE), a well-established model of multiple sclerosis (MS). We compared disease progression and severity in C57BL/6 mice treated orally with 100 mg/kg/day farnesol solubilized in corn oil to corn-oil treated and untreated EAE mice. Farnesol significantly delayed the onset of EAE (by ~2 days) and dramatically decreased disease severity (~80%) compared to controls. Disease protection by farnesol was associated with a significant reduction in spinal cord infiltration by monocytes-macrophages, dendritic cells, CD4+ T cells, and a significant change in gut microbiota composition, including a decrease in the Firmicutes:Bacteroidetes ratio. The study suggests FOL could protect MS patients against CNS inflammatory demyelination by partially modulating the gut microbiome composition.
•Oral treatment with farnesol protects against a CNS inflammatory demyelination model of multiple sclerosis.•Treatment with farnesol reduces significantly the infiltration of immune cells into the CNS.•Farnesol treatment modifies the composition of gut microbiome. |
doi_str_mv | 10.1016/j.clim.2021.108766 |
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•Oral treatment with farnesol protects against a CNS inflammatory demyelination model of multiple sclerosis.•Treatment with farnesol reduces significantly the infiltration of immune cells into the CNS.•Farnesol treatment modifies the composition of gut microbiome.</description><identifier>ISSN: 1521-6616</identifier><identifier>EISSN: 1521-7035</identifier><identifier>DOI: 10.1016/j.clim.2021.108766</identifier><identifier>PMID: 34091018</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Administration, Oral ; Animals ; CNS inflammatory demyelination ; EAE ; Encephalomyelitis, Autoimmune, Experimental - chemically induced ; Encephalomyelitis, Autoimmune, Experimental - prevention & control ; Farnesol ; Farnesol - pharmacology ; Female ; Gastrointestinal Microbiome - drug effects ; Gut microbiome ; Isoprenols ; Mice</subject><ispartof>Clinical immunology (Orlando, Fla.), 2022-02, Vol.235, p.108766-108766, Article 108766</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-16b2accb9552a6f797bf6f035782e7d7570ac9ea856cf2d3439801b2aec3c3313</citedby><cites>FETCH-LOGICAL-c455t-16b2accb9552a6f797bf6f035782e7d7570ac9ea856cf2d3439801b2aec3c3313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1521661621001030$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34091018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sell, Lacey B.</creatorcontrib><creatorcontrib>Ramelow, Christina C.</creatorcontrib><creatorcontrib>Kohl, Hannah M.</creatorcontrib><creatorcontrib>Hoffman, Kristina</creatorcontrib><creatorcontrib>Bains, Jasleen K.</creatorcontrib><creatorcontrib>Doyle, William J.</creatorcontrib><creatorcontrib>Strawn, Kevin D.</creatorcontrib><creatorcontrib>Hevrin, Theresa</creatorcontrib><creatorcontrib>Kirby, Trevor O.</creatorcontrib><creatorcontrib>Gibson, K. Michael</creatorcontrib><creatorcontrib>Roullet, Jean-Baptiste</creatorcontrib><creatorcontrib>Ochoa-Repáraz, Javier</creatorcontrib><title>Farnesol induces protection against murine CNS inflammatory demyelination and modifies gut microbiome</title><title>Clinical immunology (Orlando, Fla.)</title><addtitle>Clin Immunol</addtitle><description>Farnesol is a 15‑carbon organic isoprenol synthesized by plants and mammals with anti-oxidant, anti-inflammatory, and neuroprotective activities. We sought to determine whether farnesol treatment would result in protection against murine experimental autoimmune encephalomyelitis (EAE), a well-established model of multiple sclerosis (MS). We compared disease progression and severity in C57BL/6 mice treated orally with 100 mg/kg/day farnesol solubilized in corn oil to corn-oil treated and untreated EAE mice. Farnesol significantly delayed the onset of EAE (by ~2 days) and dramatically decreased disease severity (~80%) compared to controls. Disease protection by farnesol was associated with a significant reduction in spinal cord infiltration by monocytes-macrophages, dendritic cells, CD4+ T cells, and a significant change in gut microbiota composition, including a decrease in the Firmicutes:Bacteroidetes ratio. The study suggests FOL could protect MS patients against CNS inflammatory demyelination by partially modulating the gut microbiome composition.
•Oral treatment with farnesol protects against a CNS inflammatory demyelination model of multiple sclerosis.•Treatment with farnesol reduces significantly the infiltration of immune cells into the CNS.•Farnesol treatment modifies the composition of gut microbiome.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>CNS inflammatory demyelination</subject><subject>EAE</subject><subject>Encephalomyelitis, Autoimmune, Experimental - chemically induced</subject><subject>Encephalomyelitis, Autoimmune, Experimental - prevention & control</subject><subject>Farnesol</subject><subject>Farnesol - pharmacology</subject><subject>Female</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>Gut microbiome</subject><subject>Isoprenols</subject><subject>Mice</subject><issn>1521-6616</issn><issn>1521-7035</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1LBCEUhiWKvv9AFzF_YDd1VmcGIoilL4i6qK7F0TPbWUZddDbYf5_LVNRNV4q-73P0IeSM0SmjTF4sp6ZHN-WUs3xQV1LukEMmOJtUtBS7X3spmTwgRyktKaWCc7lPDsoZbTKiPiRwq6OHFPoCvV0bSMUqhgHMgMEXeqHRp6Fw64geivnTS051vXZODyFuCgtuAz16Paa9LVyw2GGmLNa5hiaGFoODE7LX6T7B6dd6TN5ub17n95PH57uH-fXjxMyEGCZMtlwb0zZCcC27qqnaTnb5L1XNobKVqKg2DehaSNNxW87KpqYsd8CUpixZeUyuRu5q3TqwBvwQda9WEZ2OGxU0qr83Ht_VInyoWkqap2YAHwH55SlF6H66jKqtdLVUW-lqK12N0nPp_PfUn8q35Ry4HAOQ__6BEFUyCN6AxZhVKxvwP_4nFgiWrQ</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Sell, Lacey B.</creator><creator>Ramelow, Christina C.</creator><creator>Kohl, Hannah M.</creator><creator>Hoffman, Kristina</creator><creator>Bains, Jasleen K.</creator><creator>Doyle, William J.</creator><creator>Strawn, Kevin D.</creator><creator>Hevrin, Theresa</creator><creator>Kirby, Trevor O.</creator><creator>Gibson, K. Michael</creator><creator>Roullet, Jean-Baptiste</creator><creator>Ochoa-Repáraz, Javier</creator><general>Elsevier Inc</general><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>5PM</scope></search><sort><creationdate>20220201</creationdate><title>Farnesol induces protection against murine CNS inflammatory demyelination and modifies gut microbiome</title><author>Sell, Lacey B. ; Ramelow, Christina C. ; Kohl, Hannah M. ; Hoffman, Kristina ; Bains, Jasleen K. ; Doyle, William J. ; Strawn, Kevin D. ; Hevrin, Theresa ; Kirby, Trevor O. ; Gibson, K. Michael ; Roullet, Jean-Baptiste ; Ochoa-Repáraz, Javier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-16b2accb9552a6f797bf6f035782e7d7570ac9ea856cf2d3439801b2aec3c3313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>CNS inflammatory demyelination</topic><topic>EAE</topic><topic>Encephalomyelitis, Autoimmune, Experimental - chemically induced</topic><topic>Encephalomyelitis, Autoimmune, Experimental - prevention & control</topic><topic>Farnesol</topic><topic>Farnesol - pharmacology</topic><topic>Female</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Gut microbiome</topic><topic>Isoprenols</topic><topic>Mice</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sell, Lacey B.</creatorcontrib><creatorcontrib>Ramelow, Christina C.</creatorcontrib><creatorcontrib>Kohl, Hannah M.</creatorcontrib><creatorcontrib>Hoffman, Kristina</creatorcontrib><creatorcontrib>Bains, Jasleen K.</creatorcontrib><creatorcontrib>Doyle, William J.</creatorcontrib><creatorcontrib>Strawn, Kevin D.</creatorcontrib><creatorcontrib>Hevrin, Theresa</creatorcontrib><creatorcontrib>Kirby, Trevor O.</creatorcontrib><creatorcontrib>Gibson, K. Michael</creatorcontrib><creatorcontrib>Roullet, Jean-Baptiste</creatorcontrib><creatorcontrib>Ochoa-Repáraz, Javier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical immunology (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sell, Lacey B.</au><au>Ramelow, Christina C.</au><au>Kohl, Hannah M.</au><au>Hoffman, Kristina</au><au>Bains, Jasleen K.</au><au>Doyle, William J.</au><au>Strawn, Kevin D.</au><au>Hevrin, Theresa</au><au>Kirby, Trevor O.</au><au>Gibson, K. Michael</au><au>Roullet, Jean-Baptiste</au><au>Ochoa-Repáraz, Javier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Farnesol induces protection against murine CNS inflammatory demyelination and modifies gut microbiome</atitle><jtitle>Clinical immunology (Orlando, Fla.)</jtitle><addtitle>Clin Immunol</addtitle><date>2022-02-01</date><risdate>2022</risdate><volume>235</volume><spage>108766</spage><epage>108766</epage><pages>108766-108766</pages><artnum>108766</artnum><issn>1521-6616</issn><eissn>1521-7035</eissn><abstract>Farnesol is a 15‑carbon organic isoprenol synthesized by plants and mammals with anti-oxidant, anti-inflammatory, and neuroprotective activities. We sought to determine whether farnesol treatment would result in protection against murine experimental autoimmune encephalomyelitis (EAE), a well-established model of multiple sclerosis (MS). We compared disease progression and severity in C57BL/6 mice treated orally with 100 mg/kg/day farnesol solubilized in corn oil to corn-oil treated and untreated EAE mice. Farnesol significantly delayed the onset of EAE (by ~2 days) and dramatically decreased disease severity (~80%) compared to controls. Disease protection by farnesol was associated with a significant reduction in spinal cord infiltration by monocytes-macrophages, dendritic cells, CD4+ T cells, and a significant change in gut microbiota composition, including a decrease in the Firmicutes:Bacteroidetes ratio. The study suggests FOL could protect MS patients against CNS inflammatory demyelination by partially modulating the gut microbiome composition.
•Oral treatment with farnesol protects against a CNS inflammatory demyelination model of multiple sclerosis.•Treatment with farnesol reduces significantly the infiltration of immune cells into the CNS.•Farnesol treatment modifies the composition of gut microbiome.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34091018</pmid><doi>10.1016/j.clim.2021.108766</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals CNS inflammatory demyelination EAE Encephalomyelitis, Autoimmune, Experimental - chemically induced Encephalomyelitis, Autoimmune, Experimental - prevention & control Farnesol Farnesol - pharmacology Female Gastrointestinal Microbiome - drug effects Gut microbiome Isoprenols Mice |
title | Farnesol induces protection against murine CNS inflammatory demyelination and modifies gut microbiome |
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