Gene Knockout and Metabolome Analysis of Carnitine/Organic Cation Transporter OCTN1

Purpose Solute carrier OCTN1 (SLC22A4) is an orphan transporter, the physiologically important substrate of which is still unidentified. The aim of the present study was to examine physiological roles of OCTN1. Methods We first constructed octn1 gene knockout (octn1 ⁻/⁻ ) mice. Metabolome analysis w...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pharmaceutical research 2010-05, Vol.27 (5), p.832-840
Hauptverfasser: Kato, Yukio, Kubo, Yoshiyuki, Iwata, Daisuke, Kato, Sayaka, Sudo, Tomohisa, Sugiura, Tomoko, Kagaya, Takashi, Wakayama, Tomohiko, Hirayama, Akiyoshi, Sugimoto, Masahiro, Sugihara, Kazushi, Kaneko, Shuichi, Soga, Tomoyoshi, Asano, Masahide, Tomita, Masaru, Matsui, Toshiyuki, Wada, Morimasa, Tsuji, Akira
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 840
container_issue 5
container_start_page 832
container_title Pharmaceutical research
container_volume 27
creator Kato, Yukio
Kubo, Yoshiyuki
Iwata, Daisuke
Kato, Sayaka
Sudo, Tomohisa
Sugiura, Tomoko
Kagaya, Takashi
Wakayama, Tomohiko
Hirayama, Akiyoshi
Sugimoto, Masahiro
Sugihara, Kazushi
Kaneko, Shuichi
Soga, Tomoyoshi
Asano, Masahide
Tomita, Masaru
Matsui, Toshiyuki
Wada, Morimasa
Tsuji, Akira
description Purpose Solute carrier OCTN1 (SLC22A4) is an orphan transporter, the physiologically important substrate of which is still unidentified. The aim of the present study was to examine physiological roles of OCTN1. Methods We first constructed octn1 gene knockout (octn1 ⁻/⁻ ) mice. Metabolome analysis was then performed to identify substrates in vivo. The possible association of the substrate identified with diseased conditions was further examined. Results The metabolome analysis of blood and several organs indicated complete deficiency of a naturally occurring potent antioxidant ergothioneine in octn1 ⁻/⁻ mice among 112 metabolites examined. Pharmacokinetic analyses after oral administration revealed the highest distribution to small intestines and extensive renal reabsorption of [³H]ergothioneine, both of which were much reduced in octn1 ⁻/⁻ mice. The octn1 ⁻/⁻ mice exhibited greater susceptibility to intestinal inflammation under the ischemia and reperfusion model. The blood ergothioneine concentration was also much reduced in Japanese patients with Crohn's disease, compared with healthy volunteers and patients with another inflammatory bowel disease, ulcerative colitis. Conclusions These results indicate that OCTN1 plays a pivotal role for maintenance of systemic and intestinal exposure of ergothioneine, which could be important for protective effects against intestinal tissue injuries, providing a possible diagnostic tool to distinguish the inflammatory bowel diseases.
doi_str_mv 10.1007/s11095-010-0076-z
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_733871575</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2006942161</sourcerecordid><originalsourceid>FETCH-LOGICAL-c563t-b15908aad24f9ec94e9f8a109b13882659d50c4b49706126cadd5e3e3f8738883</originalsourceid><addsrcrecordid>eNp9kEFPHCEYhkljo1vbH9CLTkyanqZ-HzADHM3G2qa2e3BNeiMMw2xGZ2GFmYP--mJmq0kPPRHgeV_4HkI-InxBAHGeEEFVJSCUeVuXT2_IAivBSgX89wFZgKC8lILjEXmX0h0ASFT8kBxRoJQrhQtyc-W8K374YO_DNBbGt8VPN5omDGHrigtvhsfUpyJ0xdJE34-9d-eruDG-t_lk7IMv1tH4tAtxdLFYLde_8D1525khuQ_79Zjcfr1cL7-V16ur78uL69JWNRvLBisF0piW8k45q7hTnTR5ogaZlLSuVFuB5Q1XAmqktTVtWznmWCdFBiQ7Jp_n3l0MD5NLo972ybphMN6FKWnBmBTZR5XJs3_IuzDFPFzSlFIBlEnMEM6QjSGl6Dq9i_3WxEeNoJ9969m3zr71s2_9lDMn--Kp2br2JfFXcAY-7QGTrBm67Mr26ZWjQnGh6szRmUv5ym9cfP3h_14_nUOdCdpsYi6-vaGADFBSxTiwP_5Mn5E</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>222702381</pqid></control><display><type>article</type><title>Gene Knockout and Metabolome Analysis of Carnitine/Organic Cation Transporter OCTN1</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Kato, Yukio ; Kubo, Yoshiyuki ; Iwata, Daisuke ; Kato, Sayaka ; Sudo, Tomohisa ; Sugiura, Tomoko ; Kagaya, Takashi ; Wakayama, Tomohiko ; Hirayama, Akiyoshi ; Sugimoto, Masahiro ; Sugihara, Kazushi ; Kaneko, Shuichi ; Soga, Tomoyoshi ; Asano, Masahide ; Tomita, Masaru ; Matsui, Toshiyuki ; Wada, Morimasa ; Tsuji, Akira</creator><creatorcontrib>Kato, Yukio ; Kubo, Yoshiyuki ; Iwata, Daisuke ; Kato, Sayaka ; Sudo, Tomohisa ; Sugiura, Tomoko ; Kagaya, Takashi ; Wakayama, Tomohiko ; Hirayama, Akiyoshi ; Sugimoto, Masahiro ; Sugihara, Kazushi ; Kaneko, Shuichi ; Soga, Tomoyoshi ; Asano, Masahide ; Tomita, Masaru ; Matsui, Toshiyuki ; Wada, Morimasa ; Tsuji, Akira</creatorcontrib><description>Purpose Solute carrier OCTN1 (SLC22A4) is an orphan transporter, the physiologically important substrate of which is still unidentified. The aim of the present study was to examine physiological roles of OCTN1. Methods We first constructed octn1 gene knockout (octn1 ⁻/⁻ ) mice. Metabolome analysis was then performed to identify substrates in vivo. The possible association of the substrate identified with diseased conditions was further examined. Results The metabolome analysis of blood and several organs indicated complete deficiency of a naturally occurring potent antioxidant ergothioneine in octn1 ⁻/⁻ mice among 112 metabolites examined. Pharmacokinetic analyses after oral administration revealed the highest distribution to small intestines and extensive renal reabsorption of [³H]ergothioneine, both of which were much reduced in octn1 ⁻/⁻ mice. The octn1 ⁻/⁻ mice exhibited greater susceptibility to intestinal inflammation under the ischemia and reperfusion model. The blood ergothioneine concentration was also much reduced in Japanese patients with Crohn's disease, compared with healthy volunteers and patients with another inflammatory bowel disease, ulcerative colitis. Conclusions These results indicate that OCTN1 plays a pivotal role for maintenance of systemic and intestinal exposure of ergothioneine, which could be important for protective effects against intestinal tissue injuries, providing a possible diagnostic tool to distinguish the inflammatory bowel diseases.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-010-0076-z</identifier><identifier>PMID: 20224991</identifier><identifier>CODEN: PHREEB</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Adolescent ; Adult ; Aged ; Animals ; Antioxidants - metabolism ; Biochemistry ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Blotting, Southern ; Blotting, Western ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; Chemical compounds ; Chromatography, High Pressure Liquid ; Crohn Disease - genetics ; Crohn Disease - metabolism ; Crohn's disease ; Ergothioneine - blood ; Ergothioneine - pharmacokinetics ; Female ; General pharmacology ; Genetic engineering ; Genotype ; Humans ; Intestinal Absorption - genetics ; Intestinal Absorption - physiology ; Intestines - blood supply ; Ischemia - pathology ; Japan ; Male ; Medical Law ; Medical sciences ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Metabolites ; Metabolomics ; Mice ; Mice, Knockout ; Microvilli - metabolism ; Middle Aged ; Molecular biology ; Organic Cation Transport Proteins - genetics ; Organic Cation Transport Proteins - metabolism ; Oxidative Stress - physiology ; Pharmaceutical sciences ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Pharmacy ; Reperfusion Injury - pathology ; Research Paper ; Spectrophotometry, Ultraviolet ; Young Adult</subject><ispartof>Pharmaceutical research, 2010-05, Vol.27 (5), p.832-840</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-b15908aad24f9ec94e9f8a109b13882659d50c4b49706126cadd5e3e3f8738883</citedby><cites>FETCH-LOGICAL-c563t-b15908aad24f9ec94e9f8a109b13882659d50c4b49706126cadd5e3e3f8738883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11095-010-0076-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11095-010-0076-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22794796$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20224991$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kato, Yukio</creatorcontrib><creatorcontrib>Kubo, Yoshiyuki</creatorcontrib><creatorcontrib>Iwata, Daisuke</creatorcontrib><creatorcontrib>Kato, Sayaka</creatorcontrib><creatorcontrib>Sudo, Tomohisa</creatorcontrib><creatorcontrib>Sugiura, Tomoko</creatorcontrib><creatorcontrib>Kagaya, Takashi</creatorcontrib><creatorcontrib>Wakayama, Tomohiko</creatorcontrib><creatorcontrib>Hirayama, Akiyoshi</creatorcontrib><creatorcontrib>Sugimoto, Masahiro</creatorcontrib><creatorcontrib>Sugihara, Kazushi</creatorcontrib><creatorcontrib>Kaneko, Shuichi</creatorcontrib><creatorcontrib>Soga, Tomoyoshi</creatorcontrib><creatorcontrib>Asano, Masahide</creatorcontrib><creatorcontrib>Tomita, Masaru</creatorcontrib><creatorcontrib>Matsui, Toshiyuki</creatorcontrib><creatorcontrib>Wada, Morimasa</creatorcontrib><creatorcontrib>Tsuji, Akira</creatorcontrib><title>Gene Knockout and Metabolome Analysis of Carnitine/Organic Cation Transporter OCTN1</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Purpose Solute carrier OCTN1 (SLC22A4) is an orphan transporter, the physiologically important substrate of which is still unidentified. The aim of the present study was to examine physiological roles of OCTN1. Methods We first constructed octn1 gene knockout (octn1 ⁻/⁻ ) mice. Metabolome analysis was then performed to identify substrates in vivo. The possible association of the substrate identified with diseased conditions was further examined. Results The metabolome analysis of blood and several organs indicated complete deficiency of a naturally occurring potent antioxidant ergothioneine in octn1 ⁻/⁻ mice among 112 metabolites examined. Pharmacokinetic analyses after oral administration revealed the highest distribution to small intestines and extensive renal reabsorption of [³H]ergothioneine, both of which were much reduced in octn1 ⁻/⁻ mice. The octn1 ⁻/⁻ mice exhibited greater susceptibility to intestinal inflammation under the ischemia and reperfusion model. The blood ergothioneine concentration was also much reduced in Japanese patients with Crohn's disease, compared with healthy volunteers and patients with another inflammatory bowel disease, ulcerative colitis. Conclusions These results indicate that OCTN1 plays a pivotal role for maintenance of systemic and intestinal exposure of ergothioneine, which could be important for protective effects against intestinal tissue injuries, providing a possible diagnostic tool to distinguish the inflammatory bowel diseases.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Animals</subject><subject>Antioxidants - metabolism</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Blotting, Southern</subject><subject>Blotting, Western</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Chemical compounds</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Crohn Disease - genetics</subject><subject>Crohn Disease - metabolism</subject><subject>Crohn's disease</subject><subject>Ergothioneine - blood</subject><subject>Ergothioneine - pharmacokinetics</subject><subject>Female</subject><subject>General pharmacology</subject><subject>Genetic engineering</subject><subject>Genotype</subject><subject>Humans</subject><subject>Intestinal Absorption - genetics</subject><subject>Intestinal Absorption - physiology</subject><subject>Intestines - blood supply</subject><subject>Ischemia - pathology</subject><subject>Japan</subject><subject>Male</subject><subject>Medical Law</subject><subject>Medical sciences</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Microvilli - metabolism</subject><subject>Middle Aged</subject><subject>Molecular biology</subject><subject>Organic Cation Transport Proteins - genetics</subject><subject>Organic Cation Transport Proteins - metabolism</subject><subject>Oxidative Stress - physiology</subject><subject>Pharmaceutical sciences</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Reperfusion Injury - pathology</subject><subject>Research Paper</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Young Adult</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kEFPHCEYhkljo1vbH9CLTkyanqZ-HzADHM3G2qa2e3BNeiMMw2xGZ2GFmYP--mJmq0kPPRHgeV_4HkI-InxBAHGeEEFVJSCUeVuXT2_IAivBSgX89wFZgKC8lILjEXmX0h0ASFT8kBxRoJQrhQtyc-W8K374YO_DNBbGt8VPN5omDGHrigtvhsfUpyJ0xdJE34-9d-eruDG-t_lk7IMv1tH4tAtxdLFYLde_8D1525khuQ_79Zjcfr1cL7-V16ur78uL69JWNRvLBisF0piW8k45q7hTnTR5ogaZlLSuVFuB5Q1XAmqktTVtWznmWCdFBiQ7Jp_n3l0MD5NLo972ybphMN6FKWnBmBTZR5XJs3_IuzDFPFzSlFIBlEnMEM6QjSGl6Dq9i_3WxEeNoJ9969m3zr71s2_9lDMn--Kp2br2JfFXcAY-7QGTrBm67Mr26ZWjQnGh6szRmUv5ym9cfP3h_14_nUOdCdpsYi6-vaGADFBSxTiwP_5Mn5E</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Kato, Yukio</creator><creator>Kubo, Yoshiyuki</creator><creator>Iwata, Daisuke</creator><creator>Kato, Sayaka</creator><creator>Sudo, Tomohisa</creator><creator>Sugiura, Tomoko</creator><creator>Kagaya, Takashi</creator><creator>Wakayama, Tomohiko</creator><creator>Hirayama, Akiyoshi</creator><creator>Sugimoto, Masahiro</creator><creator>Sugihara, Kazushi</creator><creator>Kaneko, Shuichi</creator><creator>Soga, Tomoyoshi</creator><creator>Asano, Masahide</creator><creator>Tomita, Masaru</creator><creator>Matsui, Toshiyuki</creator><creator>Wada, Morimasa</creator><creator>Tsuji, Akira</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20100501</creationdate><title>Gene Knockout and Metabolome Analysis of Carnitine/Organic Cation Transporter OCTN1</title><author>Kato, Yukio ; Kubo, Yoshiyuki ; Iwata, Daisuke ; Kato, Sayaka ; Sudo, Tomohisa ; Sugiura, Tomoko ; Kagaya, Takashi ; Wakayama, Tomohiko ; Hirayama, Akiyoshi ; Sugimoto, Masahiro ; Sugihara, Kazushi ; Kaneko, Shuichi ; Soga, Tomoyoshi ; Asano, Masahide ; Tomita, Masaru ; Matsui, Toshiyuki ; Wada, Morimasa ; Tsuji, Akira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-b15908aad24f9ec94e9f8a109b13882659d50c4b49706126cadd5e3e3f8738883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Animals</topic><topic>Antioxidants - metabolism</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Blotting, Southern</topic><topic>Blotting, Western</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>Chemical compounds</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Crohn Disease - genetics</topic><topic>Crohn Disease - metabolism</topic><topic>Crohn's disease</topic><topic>Ergothioneine - blood</topic><topic>Ergothioneine - pharmacokinetics</topic><topic>Female</topic><topic>General pharmacology</topic><topic>Genetic engineering</topic><topic>Genotype</topic><topic>Humans</topic><topic>Intestinal Absorption - genetics</topic><topic>Intestinal Absorption - physiology</topic><topic>Intestines - blood supply</topic><topic>Ischemia - pathology</topic><topic>Japan</topic><topic>Male</topic><topic>Medical Law</topic><topic>Medical sciences</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Microvilli - metabolism</topic><topic>Middle Aged</topic><topic>Molecular biology</topic><topic>Organic Cation Transport Proteins - genetics</topic><topic>Organic Cation Transport Proteins - metabolism</topic><topic>Oxidative Stress - physiology</topic><topic>Pharmaceutical sciences</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Reperfusion Injury - pathology</topic><topic>Research Paper</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kato, Yukio</creatorcontrib><creatorcontrib>Kubo, Yoshiyuki</creatorcontrib><creatorcontrib>Iwata, Daisuke</creatorcontrib><creatorcontrib>Kato, Sayaka</creatorcontrib><creatorcontrib>Sudo, Tomohisa</creatorcontrib><creatorcontrib>Sugiura, Tomoko</creatorcontrib><creatorcontrib>Kagaya, Takashi</creatorcontrib><creatorcontrib>Wakayama, Tomohiko</creatorcontrib><creatorcontrib>Hirayama, Akiyoshi</creatorcontrib><creatorcontrib>Sugimoto, Masahiro</creatorcontrib><creatorcontrib>Sugihara, Kazushi</creatorcontrib><creatorcontrib>Kaneko, Shuichi</creatorcontrib><creatorcontrib>Soga, Tomoyoshi</creatorcontrib><creatorcontrib>Asano, Masahide</creatorcontrib><creatorcontrib>Tomita, Masaru</creatorcontrib><creatorcontrib>Matsui, Toshiyuki</creatorcontrib><creatorcontrib>Wada, Morimasa</creatorcontrib><creatorcontrib>Tsuji, Akira</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kato, Yukio</au><au>Kubo, Yoshiyuki</au><au>Iwata, Daisuke</au><au>Kato, Sayaka</au><au>Sudo, Tomohisa</au><au>Sugiura, Tomoko</au><au>Kagaya, Takashi</au><au>Wakayama, Tomohiko</au><au>Hirayama, Akiyoshi</au><au>Sugimoto, Masahiro</au><au>Sugihara, Kazushi</au><au>Kaneko, Shuichi</au><au>Soga, Tomoyoshi</au><au>Asano, Masahide</au><au>Tomita, Masaru</au><au>Matsui, Toshiyuki</au><au>Wada, Morimasa</au><au>Tsuji, Akira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene Knockout and Metabolome Analysis of Carnitine/Organic Cation Transporter OCTN1</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2010-05-01</date><risdate>2010</risdate><volume>27</volume><issue>5</issue><spage>832</spage><epage>840</epage><pages>832-840</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><coden>PHREEB</coden><abstract>Purpose Solute carrier OCTN1 (SLC22A4) is an orphan transporter, the physiologically important substrate of which is still unidentified. The aim of the present study was to examine physiological roles of OCTN1. Methods We first constructed octn1 gene knockout (octn1 ⁻/⁻ ) mice. Metabolome analysis was then performed to identify substrates in vivo. The possible association of the substrate identified with diseased conditions was further examined. Results The metabolome analysis of blood and several organs indicated complete deficiency of a naturally occurring potent antioxidant ergothioneine in octn1 ⁻/⁻ mice among 112 metabolites examined. Pharmacokinetic analyses after oral administration revealed the highest distribution to small intestines and extensive renal reabsorption of [³H]ergothioneine, both of which were much reduced in octn1 ⁻/⁻ mice. The octn1 ⁻/⁻ mice exhibited greater susceptibility to intestinal inflammation under the ischemia and reperfusion model. The blood ergothioneine concentration was also much reduced in Japanese patients with Crohn's disease, compared with healthy volunteers and patients with another inflammatory bowel disease, ulcerative colitis. Conclusions These results indicate that OCTN1 plays a pivotal role for maintenance of systemic and intestinal exposure of ergothioneine, which could be important for protective effects against intestinal tissue injuries, providing a possible diagnostic tool to distinguish the inflammatory bowel diseases.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>20224991</pmid><doi>10.1007/s11095-010-0076-z</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0724-8741
ispartof Pharmaceutical research, 2010-05, Vol.27 (5), p.832-840
issn 0724-8741
1573-904X
language eng
recordid cdi_proquest_miscellaneous_733871575
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Adolescent
Adult
Aged
Animals
Antioxidants - metabolism
Biochemistry
Biological and medical sciences
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Biomedicine
Blotting, Southern
Blotting, Western
Carrier Proteins - genetics
Carrier Proteins - metabolism
Chemical compounds
Chromatography, High Pressure Liquid
Crohn Disease - genetics
Crohn Disease - metabolism
Crohn's disease
Ergothioneine - blood
Ergothioneine - pharmacokinetics
Female
General pharmacology
Genetic engineering
Genotype
Humans
Intestinal Absorption - genetics
Intestinal Absorption - physiology
Intestines - blood supply
Ischemia - pathology
Japan
Male
Medical Law
Medical sciences
Membrane Proteins - genetics
Membrane Proteins - metabolism
Metabolites
Metabolomics
Mice
Mice, Knockout
Microvilli - metabolism
Middle Aged
Molecular biology
Organic Cation Transport Proteins - genetics
Organic Cation Transport Proteins - metabolism
Oxidative Stress - physiology
Pharmaceutical sciences
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Pharmacology/Toxicology
Pharmacy
Reperfusion Injury - pathology
Research Paper
Spectrophotometry, Ultraviolet
Young Adult
title Gene Knockout and Metabolome Analysis of Carnitine/Organic Cation Transporter OCTN1
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T16%3A16%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Gene%20Knockout%20and%20Metabolome%20Analysis%20of%20Carnitine/Organic%20Cation%20Transporter%20OCTN1&rft.jtitle=Pharmaceutical%20research&rft.au=Kato,%20Yukio&rft.date=2010-05-01&rft.volume=27&rft.issue=5&rft.spage=832&rft.epage=840&rft.pages=832-840&rft.issn=0724-8741&rft.eissn=1573-904X&rft.coden=PHREEB&rft_id=info:doi/10.1007/s11095-010-0076-z&rft_dat=%3Cproquest_cross%3E2006942161%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=222702381&rft_id=info:pmid/20224991&rfr_iscdi=true