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...
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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 |
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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&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 & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & 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> |
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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 |
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