L-Citrulline ameliorates chronic hypoxia-induced pulmonary hypertension in newborn piglets
Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee Submitted 21 January 2009 ; accepted in final form 9 July 2009 Newborn piglets develop pulmonary hypertension and have diminished pulmonary vascular nitric oxide (NO) production when exposed to chronic hypoxia. NO i...
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creator | Ananthakrishnan, Madhumita Barr, Frederick E Summar, Marshall L Smith, Heidi A Kaplowitz, Mark Cunningham, Gary Magarik, Jordan Zhang, Yongmei Fike, Candice D |
description | Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee
Submitted 21 January 2009
; accepted in final form 9 July 2009
Newborn piglets develop pulmonary hypertension and have diminished pulmonary vascular nitric oxide (NO) production when exposed to chronic hypoxia. NO is produced by endothelial NO synthase (eNOS) in the pulmonary vascular endothelium using L -arginine as a substrate and producing L -citrulline as a byproduct. L -Citrulline is metabolized to L -arginine by two enzymes that are colocated with eNOS in pulmonary vascular endothelial cells. The purpose of this study was to determine whether oral supplementation with L -citrulline during exposure of newborn piglets to 10 days of chronic hypoxia would prevent the development of pulmonary hypertension and increase pulmonary NO production. A total of 17 hypoxic and 17 normoxic control piglets were studied. Six of the 17 hypoxic piglets were supplemented with oral L -citrulline starting on the first day of hypoxia. L -Citrulline supplementation was provided orally twice a day. After 10 days of hypoxia or normoxia, the animals were anesthetized, hemodynamic measurements were performed, and the lungs were perfused in situ. Pulmonary arterial pressure and pulmonary vascular resistance were significantly lower in hypoxic animals treated with L -citrulline compared with untreated hypoxic animals ( P < 0.001). In vivo exhaled NO production ( P = 0.03) and nitrite/nitrate accumulation in the perfusate of isolated lungs ( P = 0.04) were significantly higher in L -citrulline-treated hypoxic animals compared with untreated hypoxic animals. L -Citrulline supplementation ameliorated the development of pulmonary hypertension and increased NO production in piglets exposed to chronic hypoxia. We speculate that L -citrulline may benefit neonates exposed to prolonged periods of hypoxia from cardiac or pulmonary causes.
nitric oxide synthase; nitric oxide; L -arginine recycling
Address for reprint requests and other correspondence: C. D. Fike, Division of Neonatology/Research, 2215 B Garland Ave., 1125 MRB IV/Light Hall, Nashville, TN 37232-0656 (e-mail: candice.fike{at}vanderbilt.edu ) |
doi_str_mv | 10.1152/ajplung.00017.2009 |
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Submitted 21 January 2009
; accepted in final form 9 July 2009
Newborn piglets develop pulmonary hypertension and have diminished pulmonary vascular nitric oxide (NO) production when exposed to chronic hypoxia. NO is produced by endothelial NO synthase (eNOS) in the pulmonary vascular endothelium using L -arginine as a substrate and producing L -citrulline as a byproduct. L -Citrulline is metabolized to L -arginine by two enzymes that are colocated with eNOS in pulmonary vascular endothelial cells. The purpose of this study was to determine whether oral supplementation with L -citrulline during exposure of newborn piglets to 10 days of chronic hypoxia would prevent the development of pulmonary hypertension and increase pulmonary NO production. A total of 17 hypoxic and 17 normoxic control piglets were studied. Six of the 17 hypoxic piglets were supplemented with oral L -citrulline starting on the first day of hypoxia. L -Citrulline supplementation was provided orally twice a day. After 10 days of hypoxia or normoxia, the animals were anesthetized, hemodynamic measurements were performed, and the lungs were perfused in situ. Pulmonary arterial pressure and pulmonary vascular resistance were significantly lower in hypoxic animals treated with L -citrulline compared with untreated hypoxic animals ( P < 0.001). In vivo exhaled NO production ( P = 0.03) and nitrite/nitrate accumulation in the perfusate of isolated lungs ( P = 0.04) were significantly higher in L -citrulline-treated hypoxic animals compared with untreated hypoxic animals. L -Citrulline supplementation ameliorated the development of pulmonary hypertension and increased NO production in piglets exposed to chronic hypoxia. We speculate that L -citrulline may benefit neonates exposed to prolonged periods of hypoxia from cardiac or pulmonary causes.
nitric oxide synthase; nitric oxide; L -arginine recycling
Address for reprint requests and other correspondence: C. D. Fike, Division of Neonatology/Research, 2215 B Garland Ave., 1125 MRB IV/Light Hall, Nashville, TN 37232-0656 (e-mail: candice.fike{at}vanderbilt.edu )</description><identifier>ISSN: 1040-0605</identifier><identifier>EISSN: 1522-1504</identifier><identifier>DOI: 10.1152/ajplung.00017.2009</identifier><identifier>PMID: 19617312</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Amino Acids - blood ; Animals ; Animals, Newborn ; Blotting, Western ; Chronic Disease ; Citrulline - pharmacology ; Enzymes ; Exhalation - drug effects ; Hemodynamics - drug effects ; Hogs ; Hypertension ; Hypertension, Pulmonary - blood ; Hypertension, Pulmonary - etiology ; Hypertension, Pulmonary - physiopathology ; Hypoxia ; Hypoxia - blood ; Hypoxia - complications ; Hypoxia - physiopathology ; In Vitro Techniques ; Lung - drug effects ; Lung - enzymology ; Lung - physiopathology ; Nitrates - metabolism ; Nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase Type I - metabolism ; Nitric Oxide Synthase Type III - metabolism ; Perfusion ; Pressure ; Pulmonary Artery - drug effects ; Pulmonary Artery - physiopathology ; Sus scrofa</subject><ispartof>American journal of physiology. Lung cellular and molecular physiology, 2009-09, Vol.297 (3), p.L506-L511</ispartof><rights>Copyright American Physiological Society Sep 2009</rights><rights>Copyright © 2009 the American Physiological Society 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-a31713fdb7b13aa7dbc57fed5b7dbf89bcc5939828b69a9c08be0c167100b3a03</citedby><cites>FETCH-LOGICAL-c531t-a31713fdb7b13aa7dbc57fed5b7dbf89bcc5939828b69a9c08be0c167100b3a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19617312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ananthakrishnan, Madhumita</creatorcontrib><creatorcontrib>Barr, Frederick E</creatorcontrib><creatorcontrib>Summar, Marshall L</creatorcontrib><creatorcontrib>Smith, Heidi A</creatorcontrib><creatorcontrib>Kaplowitz, Mark</creatorcontrib><creatorcontrib>Cunningham, Gary</creatorcontrib><creatorcontrib>Magarik, Jordan</creatorcontrib><creatorcontrib>Zhang, Yongmei</creatorcontrib><creatorcontrib>Fike, Candice D</creatorcontrib><title>L-Citrulline ameliorates chronic hypoxia-induced pulmonary hypertension in newborn piglets</title><title>American journal of physiology. Lung cellular and molecular physiology</title><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><description>Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee
Submitted 21 January 2009
; accepted in final form 9 July 2009
Newborn piglets develop pulmonary hypertension and have diminished pulmonary vascular nitric oxide (NO) production when exposed to chronic hypoxia. NO is produced by endothelial NO synthase (eNOS) in the pulmonary vascular endothelium using L -arginine as a substrate and producing L -citrulline as a byproduct. L -Citrulline is metabolized to L -arginine by two enzymes that are colocated with eNOS in pulmonary vascular endothelial cells. The purpose of this study was to determine whether oral supplementation with L -citrulline during exposure of newborn piglets to 10 days of chronic hypoxia would prevent the development of pulmonary hypertension and increase pulmonary NO production. A total of 17 hypoxic and 17 normoxic control piglets were studied. Six of the 17 hypoxic piglets were supplemented with oral L -citrulline starting on the first day of hypoxia. L -Citrulline supplementation was provided orally twice a day. After 10 days of hypoxia or normoxia, the animals were anesthetized, hemodynamic measurements were performed, and the lungs were perfused in situ. Pulmonary arterial pressure and pulmonary vascular resistance were significantly lower in hypoxic animals treated with L -citrulline compared with untreated hypoxic animals ( P < 0.001). In vivo exhaled NO production ( P = 0.03) and nitrite/nitrate accumulation in the perfusate of isolated lungs ( P = 0.04) were significantly higher in L -citrulline-treated hypoxic animals compared with untreated hypoxic animals. L -Citrulline supplementation ameliorated the development of pulmonary hypertension and increased NO production in piglets exposed to chronic hypoxia. We speculate that L -citrulline may benefit neonates exposed to prolonged periods of hypoxia from cardiac or pulmonary causes.
nitric oxide synthase; nitric oxide; L -arginine recycling
Address for reprint requests and other correspondence: C. D. Fike, Division of Neonatology/Research, 2215 B Garland Ave., 1125 MRB IV/Light Hall, Nashville, TN 37232-0656 (e-mail: candice.fike{at}vanderbilt.edu )</description><subject>Amino Acids - blood</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Blotting, Western</subject><subject>Chronic Disease</subject><subject>Citrulline - pharmacology</subject><subject>Enzymes</subject><subject>Exhalation - drug effects</subject><subject>Hemodynamics - drug effects</subject><subject>Hogs</subject><subject>Hypertension</subject><subject>Hypertension, Pulmonary - blood</subject><subject>Hypertension, Pulmonary - etiology</subject><subject>Hypertension, Pulmonary - physiopathology</subject><subject>Hypoxia</subject><subject>Hypoxia - blood</subject><subject>Hypoxia - complications</subject><subject>Hypoxia - physiopathology</subject><subject>In Vitro Techniques</subject><subject>Lung - drug effects</subject><subject>Lung - enzymology</subject><subject>Lung - physiopathology</subject><subject>Nitrates - metabolism</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type I - metabolism</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Perfusion</subject><subject>Pressure</subject><subject>Pulmonary Artery - drug effects</subject><subject>Pulmonary Artery - physiopathology</subject><subject>Sus scrofa</subject><issn>1040-0605</issn><issn>1522-1504</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU-P0zAQxS0EYpeFL8ABRRy4pYztOo4vSKiCBakSF7hwsWzHSVw5drATln573G21_Dl5pPeb55l5CL3EsMGYkbfqMPs1DBsAwHxDAMQjdF0EUmMG28elhi3U0AC7Qs9yPhSOATRP0RUWDeYUk2v0fV_v3JJW712wlZqsdzGpxebKjCkGZ6rxOMdfTtUudKuxXTWvfopBpeNJsWmxIbsYKheqYO90TKGa3eDtkp-jJ73y2b64vDfo28cPX3ef6v2X28-79_vaMIqXWlHMMe07zTWmSvFOG8Z72zFdyr4V2hgmqGhJqxuhhIFWWzC44RhAUwX0Br07-86rnmxnbFiS8nJObipTyqic_FcJbpRD_CnLt4RCWwzeXAxS_LHavMjJZWO9V8HGNcuGM8FhewJf_wce4ppCWU4SDK1ot1wUiJwhk2LOyfYPk2CQp9zkJTd5n5s85VaaXv29w5-WS1AFqM_A6IbxziUr5_FYDu_jcHwwJIJLKvcMGvobHz2pKg</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Ananthakrishnan, Madhumita</creator><creator>Barr, Frederick E</creator><creator>Summar, Marshall L</creator><creator>Smith, Heidi A</creator><creator>Kaplowitz, Mark</creator><creator>Cunningham, Gary</creator><creator>Magarik, Jordan</creator><creator>Zhang, Yongmei</creator><creator>Fike, Candice D</creator><general>American Physiological Society</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>7QP</scope><scope>7TS</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090901</creationdate><title>L-Citrulline ameliorates chronic hypoxia-induced pulmonary hypertension in newborn piglets</title><author>Ananthakrishnan, Madhumita ; Barr, Frederick E ; Summar, Marshall L ; Smith, Heidi A ; Kaplowitz, Mark ; Cunningham, Gary ; Magarik, Jordan ; Zhang, Yongmei ; Fike, Candice D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-a31713fdb7b13aa7dbc57fed5b7dbf89bcc5939828b69a9c08be0c167100b3a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Amino Acids - blood</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Blotting, Western</topic><topic>Chronic Disease</topic><topic>Citrulline - pharmacology</topic><topic>Enzymes</topic><topic>Exhalation - drug effects</topic><topic>Hemodynamics - drug effects</topic><topic>Hogs</topic><topic>Hypertension</topic><topic>Hypertension, Pulmonary - blood</topic><topic>Hypertension, Pulmonary - etiology</topic><topic>Hypertension, Pulmonary - physiopathology</topic><topic>Hypoxia</topic><topic>Hypoxia - blood</topic><topic>Hypoxia - complications</topic><topic>Hypoxia - physiopathology</topic><topic>In Vitro Techniques</topic><topic>Lung - drug effects</topic><topic>Lung - enzymology</topic><topic>Lung - physiopathology</topic><topic>Nitrates - metabolism</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase Type I - metabolism</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Perfusion</topic><topic>Pressure</topic><topic>Pulmonary Artery - drug effects</topic><topic>Pulmonary Artery - physiopathology</topic><topic>Sus scrofa</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ananthakrishnan, Madhumita</creatorcontrib><creatorcontrib>Barr, Frederick E</creatorcontrib><creatorcontrib>Summar, Marshall L</creatorcontrib><creatorcontrib>Smith, Heidi A</creatorcontrib><creatorcontrib>Kaplowitz, Mark</creatorcontrib><creatorcontrib>Cunningham, Gary</creatorcontrib><creatorcontrib>Magarik, Jordan</creatorcontrib><creatorcontrib>Zhang, Yongmei</creatorcontrib><creatorcontrib>Fike, Candice D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ananthakrishnan, Madhumita</au><au>Barr, Frederick E</au><au>Summar, Marshall L</au><au>Smith, Heidi A</au><au>Kaplowitz, Mark</au><au>Cunningham, Gary</au><au>Magarik, Jordan</au><au>Zhang, Yongmei</au><au>Fike, Candice D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>L-Citrulline ameliorates chronic hypoxia-induced pulmonary hypertension in newborn piglets</atitle><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>297</volume><issue>3</issue><spage>L506</spage><epage>L511</epage><pages>L506-L511</pages><issn>1040-0605</issn><eissn>1522-1504</eissn><abstract>Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee
Submitted 21 January 2009
; accepted in final form 9 July 2009
Newborn piglets develop pulmonary hypertension and have diminished pulmonary vascular nitric oxide (NO) production when exposed to chronic hypoxia. NO is produced by endothelial NO synthase (eNOS) in the pulmonary vascular endothelium using L -arginine as a substrate and producing L -citrulline as a byproduct. L -Citrulline is metabolized to L -arginine by two enzymes that are colocated with eNOS in pulmonary vascular endothelial cells. The purpose of this study was to determine whether oral supplementation with L -citrulline during exposure of newborn piglets to 10 days of chronic hypoxia would prevent the development of pulmonary hypertension and increase pulmonary NO production. A total of 17 hypoxic and 17 normoxic control piglets were studied. Six of the 17 hypoxic piglets were supplemented with oral L -citrulline starting on the first day of hypoxia. L -Citrulline supplementation was provided orally twice a day. After 10 days of hypoxia or normoxia, the animals were anesthetized, hemodynamic measurements were performed, and the lungs were perfused in situ. Pulmonary arterial pressure and pulmonary vascular resistance were significantly lower in hypoxic animals treated with L -citrulline compared with untreated hypoxic animals ( P < 0.001). In vivo exhaled NO production ( P = 0.03) and nitrite/nitrate accumulation in the perfusate of isolated lungs ( P = 0.04) were significantly higher in L -citrulline-treated hypoxic animals compared with untreated hypoxic animals. L -Citrulline supplementation ameliorated the development of pulmonary hypertension and increased NO production in piglets exposed to chronic hypoxia. We speculate that L -citrulline may benefit neonates exposed to prolonged periods of hypoxia from cardiac or pulmonary causes.
nitric oxide synthase; nitric oxide; L -arginine recycling
Address for reprint requests and other correspondence: C. D. Fike, Division of Neonatology/Research, 2215 B Garland Ave., 1125 MRB IV/Light Hall, Nashville, TN 37232-0656 (e-mail: candice.fike{at}vanderbilt.edu )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>19617312</pmid><doi>10.1152/ajplung.00017.2009</doi><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Amino Acids - blood Animals Animals, Newborn Blotting, Western Chronic Disease Citrulline - pharmacology Enzymes Exhalation - drug effects Hemodynamics - drug effects Hogs Hypertension Hypertension, Pulmonary - blood Hypertension, Pulmonary - etiology Hypertension, Pulmonary - physiopathology Hypoxia Hypoxia - blood Hypoxia - complications Hypoxia - physiopathology In Vitro Techniques Lung - drug effects Lung - enzymology Lung - physiopathology Nitrates - metabolism Nitric oxide Nitric Oxide - metabolism Nitric Oxide Synthase Type I - metabolism Nitric Oxide Synthase Type III - metabolism Perfusion Pressure Pulmonary Artery - drug effects Pulmonary Artery - physiopathology Sus scrofa |
title | L-Citrulline ameliorates chronic hypoxia-induced pulmonary hypertension in newborn piglets |
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