Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines

1 Department of Medicine, University of New Mexico Health Sciences Center, and 3 Division of Rheumatology, University of New Mexico, Albuquerque 87131; 2 Albuquerque Academy, Albuquerque, New Mexico 87109; and 4 Department of Surgery, University of Texas Medical Branch, Galveston, Texas 77550 Submit...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of physiology: endocrinology and metabolism 2004-04, Vol.286 (4), p.E658-E664
Hauptverfasser: Raj, Dominic S. C, Dominic, Elizabeth A, Wolfe, Robert, Shah, Vallabh O, Bankhurst, Arthur, Zager, Philip G, Ferrando, Arny
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page E664
container_issue 4
container_start_page E658
container_title American journal of physiology: endocrinology and metabolism
container_volume 286
creator Raj, Dominic S. C
Dominic, Elizabeth A
Wolfe, Robert
Shah, Vallabh O
Bankhurst, Arthur
Zager, Philip G
Ferrando, Arny
description 1 Department of Medicine, University of New Mexico Health Sciences Center, and 3 Division of Rheumatology, University of New Mexico, Albuquerque 87131; 2 Albuquerque Academy, Albuquerque, New Mexico 87109; and 4 Department of Surgery, University of Texas Medical Branch, Galveston, Texas 77550 Submitted 2 October 2003 ; accepted in final form 17 December 2003 Serum albumin, fibrinogen levels, and lean body mass are important predictors of outcome in end-stage renal disease (ESRD). We estimated the fractional synthesis rates of albumin (FSR-A), fibrinogen (FSR-F), and muscle protein (FSR-M) in nine ESRD patients and eight controls, using primed constant infusion of L -[ ring - 13 C 6 ]phenylalanine. Cytokine profile and arteriovenous balance of amino acids were also measured. ESRD patients were studied before (Pre-HD) and during hemodialysis (HD). Plasma IL-6, IL-10, and C-reactive protein increased significantly during HD. Despite a decrease in the delivery of amino acids to the leg, the outflow of the amino acids increased during HD. The net balance of amino acids became more negative during HD, indicating release from the muscle. HD increased leg muscle protein synthesis (45%) and catabolism (108%) but decreased whole body proteolysis (15%). FSR-A during HD (9.7 ± 0.9%/day) was higher than pre-HD (6.5 ± 0.9%/day) and controls (5.8 ± 0.5%/day, P < 0.01). FSR-F increased during HD (19.7 ± 2.6%/day vs. 11.8 ± 0.6%/day, P < 0.01), but it was not significantly different from that of controls (14.4 ± 1.4%/day). FSR-M intradialysis (1.77 ± 0.19%/day) was higher than pre-HD (1.21 ± 0.25%/day) and controls (1.30 ± 0.32%/day, P < 0.001). Pre-HD FSR-A, FSR-F, and FSR-M values were comparable to those of controls. There was a significant and positive correlation between plasma IL-6 and the FSRs. Thus, in ESRD patients without metabolic acidosis, the fractional synthesis rates of albumin, fibrinogen, and muscle protein are not decreased pre-HD. However, HD increases the synthesis of albumin, fibrinogen, and muscle protein. The coordinated increase in the FSRs is facilitated by constant delivery of amino acids derived from the muscle catabolism and intradialytic increase in IL-6. protein catabolism; protein turnover; inflammation; amino acid; endstage renal disease Address for reprint requests and other correspondence: D. S. C. Raj, Div. of Nephrology, ACC 5th Floor, Univ. of New Mexico Health Sciences Center, 2211 Lomas Blvd. NE, Albuquerque, NM 87131 (E-mail: draj{at
doi_str_mv 10.1152/ajpendo.00444.2003
format Article
fullrecord <record><control><sourceid>proquest_highw</sourceid><recordid>TN_cdi_highwire_physiology_ajpendo_286_4_E658</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71714608</sourcerecordid><originalsourceid>FETCH-LOGICAL-c387t-1674b1f5cc2e35b388686d6614da20fbb3032073b476bf15cf10c3b97a7f1af3</originalsourceid><addsrcrecordid>eNp1kM1u1DAUhS0EotPCC7BAWbEig3_jDDs0ailSJTazt_xzPXFJ4mAnonl7PMxAV6x85fudo6sPoXcEbwkR9JN-nGB0cYsx53xLMWYv0KYsaE2EEC_RBpMdq0nLd1foOudHjLEUnL5GV4RLSjHlGzTtY0wujHoGV4XRJtAZylDp3ixDGD9WPpgUxniEMuvRVcOSbQ_VlOIMhcvrOHeQQ67cUrhj1cEQXdD9Wv4-VykWNvrKrnP8EUbIb9Arr_sMby_vDTrc3R729_XD96_f9l8eastaOdekkdwQL6ylwIRhbdu0jWsawp2m2BvDMKNYMsNlYzwR1hNsmdlJLT3Rnt2gD-facufPBfKshpAt9L0eIS5ZSSIJb3BbQHoGbYo5J_BqSmHQaVUEq5NmddGs_mhWJ80l9P7SvpgB3HPk4rUA9RnowrH7FRKoqStCYh-P679C2jaKq9tGnK7Y_Z-_W_r-AE_z3-BzTk3Os9-BraGU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71714608</pqid></control><display><type>article</type><title>Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines</title><source>MEDLINE</source><source>American Physiological Society Paid</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Raj, Dominic S. C ; Dominic, Elizabeth A ; Wolfe, Robert ; Shah, Vallabh O ; Bankhurst, Arthur ; Zager, Philip G ; Ferrando, Arny</creator><creatorcontrib>Raj, Dominic S. C ; Dominic, Elizabeth A ; Wolfe, Robert ; Shah, Vallabh O ; Bankhurst, Arthur ; Zager, Philip G ; Ferrando, Arny</creatorcontrib><description>1 Department of Medicine, University of New Mexico Health Sciences Center, and 3 Division of Rheumatology, University of New Mexico, Albuquerque 87131; 2 Albuquerque Academy, Albuquerque, New Mexico 87109; and 4 Department of Surgery, University of Texas Medical Branch, Galveston, Texas 77550 Submitted 2 October 2003 ; accepted in final form 17 December 2003 Serum albumin, fibrinogen levels, and lean body mass are important predictors of outcome in end-stage renal disease (ESRD). We estimated the fractional synthesis rates of albumin (FSR-A), fibrinogen (FSR-F), and muscle protein (FSR-M) in nine ESRD patients and eight controls, using primed constant infusion of L -[ ring - 13 C 6 ]phenylalanine. Cytokine profile and arteriovenous balance of amino acids were also measured. ESRD patients were studied before (Pre-HD) and during hemodialysis (HD). Plasma IL-6, IL-10, and C-reactive protein increased significantly during HD. Despite a decrease in the delivery of amino acids to the leg, the outflow of the amino acids increased during HD. The net balance of amino acids became more negative during HD, indicating release from the muscle. HD increased leg muscle protein synthesis (45%) and catabolism (108%) but decreased whole body proteolysis (15%). FSR-A during HD (9.7 ± 0.9%/day) was higher than pre-HD (6.5 ± 0.9%/day) and controls (5.8 ± 0.5%/day, P &lt; 0.01). FSR-F increased during HD (19.7 ± 2.6%/day vs. 11.8 ± 0.6%/day, P &lt; 0.01), but it was not significantly different from that of controls (14.4 ± 1.4%/day). FSR-M intradialysis (1.77 ± 0.19%/day) was higher than pre-HD (1.21 ± 0.25%/day) and controls (1.30 ± 0.32%/day, P &lt; 0.001). Pre-HD FSR-A, FSR-F, and FSR-M values were comparable to those of controls. There was a significant and positive correlation between plasma IL-6 and the FSRs. Thus, in ESRD patients without metabolic acidosis, the fractional synthesis rates of albumin, fibrinogen, and muscle protein are not decreased pre-HD. However, HD increases the synthesis of albumin, fibrinogen, and muscle protein. The coordinated increase in the FSRs is facilitated by constant delivery of amino acids derived from the muscle catabolism and intradialytic increase in IL-6. protein catabolism; protein turnover; inflammation; amino acid; endstage renal disease Address for reprint requests and other correspondence: D. S. C. Raj, Div. of Nephrology, ACC 5th Floor, Univ. of New Mexico Health Sciences Center, 2211 Lomas Blvd. NE, Albuquerque, NM 87131 (E-mail: draj{at}salud.unm.edu ).</description><identifier>ISSN: 0193-1849</identifier><identifier>EISSN: 1522-1555</identifier><identifier>DOI: 10.1152/ajpendo.00444.2003</identifier><identifier>PMID: 14722024</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Albumins - biosynthesis ; Algorithms ; Amino Acids - metabolism ; Cytokines - physiology ; Female ; Fibrinogen - biosynthesis ; Hormones - blood ; Humans ; Kidney Failure, Chronic - metabolism ; Kidney Failure, Chronic - therapy ; Kinetics ; Male ; Middle Aged ; Muscle Proteins - biosynthesis ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - physiology ; Phenylalanine - metabolism ; Renal Dialysis</subject><ispartof>American journal of physiology: endocrinology and metabolism, 2004-04, Vol.286 (4), p.E658-E664</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-1674b1f5cc2e35b388686d6614da20fbb3032073b476bf15cf10c3b97a7f1af3</citedby><cites>FETCH-LOGICAL-c387t-1674b1f5cc2e35b388686d6614da20fbb3032073b476bf15cf10c3b97a7f1af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14722024$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raj, Dominic S. C</creatorcontrib><creatorcontrib>Dominic, Elizabeth A</creatorcontrib><creatorcontrib>Wolfe, Robert</creatorcontrib><creatorcontrib>Shah, Vallabh O</creatorcontrib><creatorcontrib>Bankhurst, Arthur</creatorcontrib><creatorcontrib>Zager, Philip G</creatorcontrib><creatorcontrib>Ferrando, Arny</creatorcontrib><title>Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol Endocrinol Metab</addtitle><description>1 Department of Medicine, University of New Mexico Health Sciences Center, and 3 Division of Rheumatology, University of New Mexico, Albuquerque 87131; 2 Albuquerque Academy, Albuquerque, New Mexico 87109; and 4 Department of Surgery, University of Texas Medical Branch, Galveston, Texas 77550 Submitted 2 October 2003 ; accepted in final form 17 December 2003 Serum albumin, fibrinogen levels, and lean body mass are important predictors of outcome in end-stage renal disease (ESRD). We estimated the fractional synthesis rates of albumin (FSR-A), fibrinogen (FSR-F), and muscle protein (FSR-M) in nine ESRD patients and eight controls, using primed constant infusion of L -[ ring - 13 C 6 ]phenylalanine. Cytokine profile and arteriovenous balance of amino acids were also measured. ESRD patients were studied before (Pre-HD) and during hemodialysis (HD). Plasma IL-6, IL-10, and C-reactive protein increased significantly during HD. Despite a decrease in the delivery of amino acids to the leg, the outflow of the amino acids increased during HD. The net balance of amino acids became more negative during HD, indicating release from the muscle. HD increased leg muscle protein synthesis (45%) and catabolism (108%) but decreased whole body proteolysis (15%). FSR-A during HD (9.7 ± 0.9%/day) was higher than pre-HD (6.5 ± 0.9%/day) and controls (5.8 ± 0.5%/day, P &lt; 0.01). FSR-F increased during HD (19.7 ± 2.6%/day vs. 11.8 ± 0.6%/day, P &lt; 0.01), but it was not significantly different from that of controls (14.4 ± 1.4%/day). FSR-M intradialysis (1.77 ± 0.19%/day) was higher than pre-HD (1.21 ± 0.25%/day) and controls (1.30 ± 0.32%/day, P &lt; 0.001). Pre-HD FSR-A, FSR-F, and FSR-M values were comparable to those of controls. There was a significant and positive correlation between plasma IL-6 and the FSRs. Thus, in ESRD patients without metabolic acidosis, the fractional synthesis rates of albumin, fibrinogen, and muscle protein are not decreased pre-HD. However, HD increases the synthesis of albumin, fibrinogen, and muscle protein. The coordinated increase in the FSRs is facilitated by constant delivery of amino acids derived from the muscle catabolism and intradialytic increase in IL-6. protein catabolism; protein turnover; inflammation; amino acid; endstage renal disease Address for reprint requests and other correspondence: D. S. C. Raj, Div. of Nephrology, ACC 5th Floor, Univ. of New Mexico Health Sciences Center, 2211 Lomas Blvd. NE, Albuquerque, NM 87131 (E-mail: draj{at}salud.unm.edu ).</description><subject>Adult</subject><subject>Albumins - biosynthesis</subject><subject>Algorithms</subject><subject>Amino Acids - metabolism</subject><subject>Cytokines - physiology</subject><subject>Female</subject><subject>Fibrinogen - biosynthesis</subject><subject>Hormones - blood</subject><subject>Humans</subject><subject>Kidney Failure, Chronic - metabolism</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Kinetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Muscle Proteins - biosynthesis</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - physiology</subject><subject>Phenylalanine - metabolism</subject><subject>Renal Dialysis</subject><issn>0193-1849</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1u1DAUhS0EotPCC7BAWbEig3_jDDs0ailSJTazt_xzPXFJ4mAnonl7PMxAV6x85fudo6sPoXcEbwkR9JN-nGB0cYsx53xLMWYv0KYsaE2EEC_RBpMdq0nLd1foOudHjLEUnL5GV4RLSjHlGzTtY0wujHoGV4XRJtAZylDp3ixDGD9WPpgUxniEMuvRVcOSbQ_VlOIMhcvrOHeQQ67cUrhj1cEQXdD9Wv4-VykWNvrKrnP8EUbIb9Arr_sMby_vDTrc3R729_XD96_f9l8eastaOdekkdwQL6ylwIRhbdu0jWsawp2m2BvDMKNYMsNlYzwR1hNsmdlJLT3Rnt2gD-facufPBfKshpAt9L0eIS5ZSSIJb3BbQHoGbYo5J_BqSmHQaVUEq5NmddGs_mhWJ80l9P7SvpgB3HPk4rUA9RnowrH7FRKoqStCYh-P679C2jaKq9tGnK7Y_Z-_W_r-AE_z3-BzTk3Os9-BraGU</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Raj, Dominic S. C</creator><creator>Dominic, Elizabeth A</creator><creator>Wolfe, Robert</creator><creator>Shah, Vallabh O</creator><creator>Bankhurst, Arthur</creator><creator>Zager, Philip G</creator><creator>Ferrando, Arny</creator><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></search><sort><creationdate>20040401</creationdate><title>Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines</title><author>Raj, Dominic S. C ; Dominic, Elizabeth A ; Wolfe, Robert ; Shah, Vallabh O ; Bankhurst, Arthur ; Zager, Philip G ; Ferrando, Arny</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-1674b1f5cc2e35b388686d6614da20fbb3032073b476bf15cf10c3b97a7f1af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Albumins - biosynthesis</topic><topic>Algorithms</topic><topic>Amino Acids - metabolism</topic><topic>Cytokines - physiology</topic><topic>Female</topic><topic>Fibrinogen - biosynthesis</topic><topic>Hormones - blood</topic><topic>Humans</topic><topic>Kidney Failure, Chronic - metabolism</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Kinetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Muscle Proteins - biosynthesis</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - physiology</topic><topic>Phenylalanine - metabolism</topic><topic>Renal Dialysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raj, Dominic S. C</creatorcontrib><creatorcontrib>Dominic, Elizabeth A</creatorcontrib><creatorcontrib>Wolfe, Robert</creatorcontrib><creatorcontrib>Shah, Vallabh O</creatorcontrib><creatorcontrib>Bankhurst, Arthur</creatorcontrib><creatorcontrib>Zager, Philip G</creatorcontrib><creatorcontrib>Ferrando, Arny</creatorcontrib><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><jtitle>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raj, Dominic S. C</au><au>Dominic, Elizabeth A</au><au>Wolfe, Robert</au><au>Shah, Vallabh O</au><au>Bankhurst, Arthur</au><au>Zager, Philip G</au><au>Ferrando, Arny</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>286</volume><issue>4</issue><spage>E658</spage><epage>E664</epage><pages>E658-E664</pages><issn>0193-1849</issn><eissn>1522-1555</eissn><abstract>1 Department of Medicine, University of New Mexico Health Sciences Center, and 3 Division of Rheumatology, University of New Mexico, Albuquerque 87131; 2 Albuquerque Academy, Albuquerque, New Mexico 87109; and 4 Department of Surgery, University of Texas Medical Branch, Galveston, Texas 77550 Submitted 2 October 2003 ; accepted in final form 17 December 2003 Serum albumin, fibrinogen levels, and lean body mass are important predictors of outcome in end-stage renal disease (ESRD). We estimated the fractional synthesis rates of albumin (FSR-A), fibrinogen (FSR-F), and muscle protein (FSR-M) in nine ESRD patients and eight controls, using primed constant infusion of L -[ ring - 13 C 6 ]phenylalanine. Cytokine profile and arteriovenous balance of amino acids were also measured. ESRD patients were studied before (Pre-HD) and during hemodialysis (HD). Plasma IL-6, IL-10, and C-reactive protein increased significantly during HD. Despite a decrease in the delivery of amino acids to the leg, the outflow of the amino acids increased during HD. The net balance of amino acids became more negative during HD, indicating release from the muscle. HD increased leg muscle protein synthesis (45%) and catabolism (108%) but decreased whole body proteolysis (15%). FSR-A during HD (9.7 ± 0.9%/day) was higher than pre-HD (6.5 ± 0.9%/day) and controls (5.8 ± 0.5%/day, P &lt; 0.01). FSR-F increased during HD (19.7 ± 2.6%/day vs. 11.8 ± 0.6%/day, P &lt; 0.01), but it was not significantly different from that of controls (14.4 ± 1.4%/day). FSR-M intradialysis (1.77 ± 0.19%/day) was higher than pre-HD (1.21 ± 0.25%/day) and controls (1.30 ± 0.32%/day, P &lt; 0.001). Pre-HD FSR-A, FSR-F, and FSR-M values were comparable to those of controls. There was a significant and positive correlation between plasma IL-6 and the FSRs. Thus, in ESRD patients without metabolic acidosis, the fractional synthesis rates of albumin, fibrinogen, and muscle protein are not decreased pre-HD. However, HD increases the synthesis of albumin, fibrinogen, and muscle protein. The coordinated increase in the FSRs is facilitated by constant delivery of amino acids derived from the muscle catabolism and intradialytic increase in IL-6. protein catabolism; protein turnover; inflammation; amino acid; endstage renal disease Address for reprint requests and other correspondence: D. S. C. Raj, Div. of Nephrology, ACC 5th Floor, Univ. of New Mexico Health Sciences Center, 2211 Lomas Blvd. NE, Albuquerque, NM 87131 (E-mail: draj{at}salud.unm.edu ).</abstract><cop>United States</cop><pmid>14722024</pmid><doi>10.1152/ajpendo.00444.2003</doi></addata></record>
fulltext fulltext
identifier ISSN: 0193-1849
ispartof American journal of physiology: endocrinology and metabolism, 2004-04, Vol.286 (4), p.E658-E664
issn 0193-1849
1522-1555
language eng
recordid cdi_highwire_physiology_ajpendo_286_4_E658
source MEDLINE; American Physiological Society Paid; EZB-FREE-00999 freely available EZB journals
subjects Adult
Albumins - biosynthesis
Algorithms
Amino Acids - metabolism
Cytokines - physiology
Female
Fibrinogen - biosynthesis
Hormones - blood
Humans
Kidney Failure, Chronic - metabolism
Kidney Failure, Chronic - therapy
Kinetics
Male
Middle Aged
Muscle Proteins - biosynthesis
Muscle, Skeletal - metabolism
Muscle, Skeletal - physiology
Phenylalanine - metabolism
Renal Dialysis
title Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T13%3A56%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_highw&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Coordinated%20increase%20in%20albumin,%20fibrinogen,%20and%20muscle%20protein%20synthesis%20during%20hemodialysis:%20role%20of%20cytokines&rft.jtitle=American%20journal%20of%20physiology:%20endocrinology%20and%20metabolism&rft.au=Raj,%20Dominic%20S.%20C&rft.date=2004-04-01&rft.volume=286&rft.issue=4&rft.spage=E658&rft.epage=E664&rft.pages=E658-E664&rft.issn=0193-1849&rft.eissn=1522-1555&rft_id=info:doi/10.1152/ajpendo.00444.2003&rft_dat=%3Cproquest_highw%3E71714608%3C/proquest_highw%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=71714608&rft_id=info:pmid/14722024&rfr_iscdi=true