Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats

Exposure to high altitudes is associated with hypoxia and increased vulnerability to oxidative stress. Polycythemia (increased number of circulating erythrocytes) develops to compensate the high altitude associated hypoxia. Iron supplementation is, thus, recommended to meet the demand for the physio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Toxicology and applied pharmacology 2014-01, Vol.274 (1), p.1-6
Hauptverfasser: Salama, Samir A., Omar, Hany A., Maghrabi, Ibrahim A., AlSaeed, Mohammed S., EL-Tarras, Adel E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6
container_issue 1
container_start_page 1
container_title Toxicology and applied pharmacology
container_volume 274
creator Salama, Samir A.
Omar, Hany A.
Maghrabi, Ibrahim A.
AlSaeed, Mohammed S.
EL-Tarras, Adel E.
description Exposure to high altitudes is associated with hypoxia and increased vulnerability to oxidative stress. Polycythemia (increased number of circulating erythrocytes) develops to compensate the high altitude associated hypoxia. Iron supplementation is, thus, recommended to meet the demand for the physiological polycythemia. Iron is a major player in redox reactions and may exacerbate the high altitudes-associated oxidative stress. The aim of this study was to explore the potential iron-induced oxidative lung tissue injury in rats at high altitudes (6000ft above the sea level). Iron supplementation (2mg elemental iron/kg, once daily for 15days) induced histopathological changes to lung tissues that include severe congestion, dilatation of the blood vessels, emphysema in the air alveoli, and peribronchial inflammatory cell infiltration. The levels of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), lipid peroxidation product and protein carbonyl content in lung tissues were significantly elevated. Moreover, the levels of reduced glutathione and total antioxidant capacity were significantly reduced. Co-administration of trolox, a water soluble vitamin E analog (25mg/kg, once daily for the last 7days of iron supplementation), alleviated the lung histological impairments, significantly decreased the pro-inflammatory cytokines, and restored the oxidative stress markers. Together, our findings indicate that iron supplementation at high altitudes induces lung tissue injury in rats. This injury could be mediated through excessive production of reactive oxygen species and induction of inflammatory responses. The study highlights the tissue injury induced by iron supplementation at high altitudes and suggests the co-administration of antioxidants such as trolox as protective measures. [Display omitted] •Iron supplementation at high altitudes induced lung histological changes in rats.•Iron induced oxidative stress in lung tissues of rats at high altitudes.•Iron increased the levels of IL-1β, IL-6 & TNF-α in lung tissues at high altitudes.•Trolox alleviated the iron-induced histological and biochemical changes to the lungs.
doi_str_mv 10.1016/j.taap.2013.10.034
format Article
fullrecord <record><control><sourceid>elsevier_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_22285550</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0041008X13004821</els_id><sourcerecordid>S0041008X13004821</sourcerecordid><originalsourceid>FETCH-LOGICAL-c414t-454526f0f4f03544826016631a7c89f6a48b461e7181157a965d5129649b22033</originalsourceid><addsrcrecordid>eNp9kE1LxDAQhoMouq7-AQ8SEI9dJ5_bghdZ_ALBi4K3kk1TN0ubliQV_femu6vePA0z87zDOy9CZwRmBIi8Ws-iUv2MAmFpMAPG99CEQCEzYIztowkAJxlA_naEjkNYA0DBOTlER5RTIgqWT9Dq0XcOh6HvG9MaF1W0qVcRr-z7Cqsm2jhUJmDrqkFvat2ott1hrsLdp61S92HSaj34Lxw73AzuHUcbwrBRYK9iOEEHtWqCOd3VKXq9u31ZPGRPz_ePi5unTHPCY8YFF1TWUPMamOA8pzK9KhlRc50XtVQ8X3JJzJzkhIi5KqSoBKGF5MWS0vT3FF1s73Yh2jJoG41e6c45o2NJKc2FEJAouqW070Lwpi57b1vlv0oC5RhuuS7HcMsx3HGWwk2i862oH5atqX4lP2km4HIHqKBVU3vltA1_XM4g3Ru56y1nUhAf1vjRp3HaVNaPNqvO_ufjG4nIlxs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Salama, Samir A. ; Omar, Hany A. ; Maghrabi, Ibrahim A. ; AlSaeed, Mohammed S. ; EL-Tarras, Adel E.</creator><creatorcontrib>Salama, Samir A. ; Omar, Hany A. ; Maghrabi, Ibrahim A. ; AlSaeed, Mohammed S. ; EL-Tarras, Adel E.</creatorcontrib><description>Exposure to high altitudes is associated with hypoxia and increased vulnerability to oxidative stress. Polycythemia (increased number of circulating erythrocytes) develops to compensate the high altitude associated hypoxia. Iron supplementation is, thus, recommended to meet the demand for the physiological polycythemia. Iron is a major player in redox reactions and may exacerbate the high altitudes-associated oxidative stress. The aim of this study was to explore the potential iron-induced oxidative lung tissue injury in rats at high altitudes (6000ft above the sea level). Iron supplementation (2mg elemental iron/kg, once daily for 15days) induced histopathological changes to lung tissues that include severe congestion, dilatation of the blood vessels, emphysema in the air alveoli, and peribronchial inflammatory cell infiltration. The levels of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), lipid peroxidation product and protein carbonyl content in lung tissues were significantly elevated. Moreover, the levels of reduced glutathione and total antioxidant capacity were significantly reduced. Co-administration of trolox, a water soluble vitamin E analog (25mg/kg, once daily for the last 7days of iron supplementation), alleviated the lung histological impairments, significantly decreased the pro-inflammatory cytokines, and restored the oxidative stress markers. Together, our findings indicate that iron supplementation at high altitudes induces lung tissue injury in rats. This injury could be mediated through excessive production of reactive oxygen species and induction of inflammatory responses. The study highlights the tissue injury induced by iron supplementation at high altitudes and suggests the co-administration of antioxidants such as trolox as protective measures. [Display omitted] •Iron supplementation at high altitudes induced lung histological changes in rats.•Iron induced oxidative stress in lung tissues of rats at high altitudes.•Iron increased the levels of IL-1β, IL-6 &amp; TNF-α in lung tissues at high altitudes.•Trolox alleviated the iron-induced histological and biochemical changes to the lungs.</description><identifier>ISSN: 0041-008X</identifier><identifier>EISSN: 1096-0333</identifier><identifier>DOI: 10.1016/j.taap.2013.10.034</identifier><identifier>PMID: 24215938</identifier><identifier>CODEN: TXAPA9</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; Altitude ; Animals ; ANOXIA ; ANTIOXIDANTS ; Antioxidants - therapeutic use ; Biological and medical sciences ; BLOOD VESSELS ; Chemical and industrial products toxicology. Toxic occupational diseases ; Chromans - therapeutic use ; Dietary Supplements - toxicity ; ERYTHROCYTES ; GLUTATHIONE ; HEMATOXYLIN ; High altitudes ; INFLAMMATION ; INJURIES ; IRON ; Iron - toxicity ; Iron supplementation ; Lipid Peroxidation - drug effects ; Lipid Peroxidation - physiology ; Lung tissue injury ; LUNGS ; LYMPHOKINES ; Male ; Medical sciences ; Metals and various inorganic compounds ; OXIDATION ; Oxidative stress ; Oxidative Stress - drug effects ; Oxidative Stress - physiology ; Pneumonia - chemically induced ; Pneumonia - metabolism ; Pneumonia - pathology ; Pneumonia - prevention &amp; control ; POLYCYTHEMIA ; Proinflammatory cytokines ; RATS ; Rats, Wistar ; Reactive Oxygen Species - metabolism ; Toxicology ; Trolox</subject><ispartof>Toxicology and applied pharmacology, 2014-01, Vol.274 (1), p.1-6</ispartof><rights>2013 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-454526f0f4f03544826016631a7c89f6a48b461e7181157a965d5129649b22033</citedby><cites>FETCH-LOGICAL-c414t-454526f0f4f03544826016631a7c89f6a48b461e7181157a965d5129649b22033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.taap.2013.10.034$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28302018$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24215938$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/22285550$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Salama, Samir A.</creatorcontrib><creatorcontrib>Omar, Hany A.</creatorcontrib><creatorcontrib>Maghrabi, Ibrahim A.</creatorcontrib><creatorcontrib>AlSaeed, Mohammed S.</creatorcontrib><creatorcontrib>EL-Tarras, Adel E.</creatorcontrib><title>Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats</title><title>Toxicology and applied pharmacology</title><addtitle>Toxicol Appl Pharmacol</addtitle><description>Exposure to high altitudes is associated with hypoxia and increased vulnerability to oxidative stress. Polycythemia (increased number of circulating erythrocytes) develops to compensate the high altitude associated hypoxia. Iron supplementation is, thus, recommended to meet the demand for the physiological polycythemia. Iron is a major player in redox reactions and may exacerbate the high altitudes-associated oxidative stress. The aim of this study was to explore the potential iron-induced oxidative lung tissue injury in rats at high altitudes (6000ft above the sea level). Iron supplementation (2mg elemental iron/kg, once daily for 15days) induced histopathological changes to lung tissues that include severe congestion, dilatation of the blood vessels, emphysema in the air alveoli, and peribronchial inflammatory cell infiltration. The levels of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), lipid peroxidation product and protein carbonyl content in lung tissues were significantly elevated. Moreover, the levels of reduced glutathione and total antioxidant capacity were significantly reduced. Co-administration of trolox, a water soluble vitamin E analog (25mg/kg, once daily for the last 7days of iron supplementation), alleviated the lung histological impairments, significantly decreased the pro-inflammatory cytokines, and restored the oxidative stress markers. Together, our findings indicate that iron supplementation at high altitudes induces lung tissue injury in rats. This injury could be mediated through excessive production of reactive oxygen species and induction of inflammatory responses. The study highlights the tissue injury induced by iron supplementation at high altitudes and suggests the co-administration of antioxidants such as trolox as protective measures. [Display omitted] •Iron supplementation at high altitudes induced lung histological changes in rats.•Iron induced oxidative stress in lung tissues of rats at high altitudes.•Iron increased the levels of IL-1β, IL-6 &amp; TNF-α in lung tissues at high altitudes.•Trolox alleviated the iron-induced histological and biochemical changes to the lungs.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Altitude</subject><subject>Animals</subject><subject>ANOXIA</subject><subject>ANTIOXIDANTS</subject><subject>Antioxidants - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>BLOOD VESSELS</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Chromans - therapeutic use</subject><subject>Dietary Supplements - toxicity</subject><subject>ERYTHROCYTES</subject><subject>GLUTATHIONE</subject><subject>HEMATOXYLIN</subject><subject>High altitudes</subject><subject>INFLAMMATION</subject><subject>INJURIES</subject><subject>IRON</subject><subject>Iron - toxicity</subject><subject>Iron supplementation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipid Peroxidation - physiology</subject><subject>Lung tissue injury</subject><subject>LUNGS</subject><subject>LYMPHOKINES</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>OXIDATION</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - physiology</subject><subject>Pneumonia - chemically induced</subject><subject>Pneumonia - metabolism</subject><subject>Pneumonia - pathology</subject><subject>Pneumonia - prevention &amp; control</subject><subject>POLYCYTHEMIA</subject><subject>Proinflammatory cytokines</subject><subject>RATS</subject><subject>Rats, Wistar</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Toxicology</subject><subject>Trolox</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMouq7-AQ8SEI9dJ5_bghdZ_ALBi4K3kk1TN0ubliQV_femu6vePA0z87zDOy9CZwRmBIi8Ws-iUv2MAmFpMAPG99CEQCEzYIztowkAJxlA_naEjkNYA0DBOTlER5RTIgqWT9Dq0XcOh6HvG9MaF1W0qVcRr-z7Cqsm2jhUJmDrqkFvat2ott1hrsLdp61S92HSaj34Lxw73AzuHUcbwrBRYK9iOEEHtWqCOd3VKXq9u31ZPGRPz_ePi5unTHPCY8YFF1TWUPMamOA8pzK9KhlRc50XtVQ8X3JJzJzkhIi5KqSoBKGF5MWS0vT3FF1s73Yh2jJoG41e6c45o2NJKc2FEJAouqW070Lwpi57b1vlv0oC5RhuuS7HcMsx3HGWwk2i862oH5atqX4lP2km4HIHqKBVU3vltA1_XM4g3Ru56y1nUhAf1vjRp3HaVNaPNqvO_ufjG4nIlxs</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Salama, Samir A.</creator><creator>Omar, Hany A.</creator><creator>Maghrabi, Ibrahim A.</creator><creator>AlSaeed, Mohammed S.</creator><creator>EL-Tarras, Adel E.</creator><general>Elsevier Inc</general><general>Elsevier</general><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>OTOTI</scope></search><sort><creationdate>20140101</creationdate><title>Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats</title><author>Salama, Samir A. ; Omar, Hany A. ; Maghrabi, Ibrahim A. ; AlSaeed, Mohammed S. ; EL-Tarras, Adel E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-454526f0f4f03544826016631a7c89f6a48b461e7181157a965d5129649b22033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>Altitude</topic><topic>Animals</topic><topic>ANOXIA</topic><topic>ANTIOXIDANTS</topic><topic>Antioxidants - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>BLOOD VESSELS</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Chromans - therapeutic use</topic><topic>Dietary Supplements - toxicity</topic><topic>ERYTHROCYTES</topic><topic>GLUTATHIONE</topic><topic>HEMATOXYLIN</topic><topic>High altitudes</topic><topic>INFLAMMATION</topic><topic>INJURIES</topic><topic>IRON</topic><topic>Iron - toxicity</topic><topic>Iron supplementation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipid Peroxidation - physiology</topic><topic>Lung tissue injury</topic><topic>LUNGS</topic><topic>LYMPHOKINES</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>OXIDATION</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Oxidative Stress - physiology</topic><topic>Pneumonia - chemically induced</topic><topic>Pneumonia - metabolism</topic><topic>Pneumonia - pathology</topic><topic>Pneumonia - prevention &amp; control</topic><topic>POLYCYTHEMIA</topic><topic>Proinflammatory cytokines</topic><topic>RATS</topic><topic>Rats, Wistar</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Toxicology</topic><topic>Trolox</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salama, Samir A.</creatorcontrib><creatorcontrib>Omar, Hany A.</creatorcontrib><creatorcontrib>Maghrabi, Ibrahim A.</creatorcontrib><creatorcontrib>AlSaeed, Mohammed S.</creatorcontrib><creatorcontrib>EL-Tarras, Adel E.</creatorcontrib><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>OSTI.GOV</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salama, Samir A.</au><au>Omar, Hany A.</au><au>Maghrabi, Ibrahim A.</au><au>AlSaeed, Mohammed S.</au><au>EL-Tarras, Adel E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>274</volume><issue>1</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Exposure to high altitudes is associated with hypoxia and increased vulnerability to oxidative stress. Polycythemia (increased number of circulating erythrocytes) develops to compensate the high altitude associated hypoxia. Iron supplementation is, thus, recommended to meet the demand for the physiological polycythemia. Iron is a major player in redox reactions and may exacerbate the high altitudes-associated oxidative stress. The aim of this study was to explore the potential iron-induced oxidative lung tissue injury in rats at high altitudes (6000ft above the sea level). Iron supplementation (2mg elemental iron/kg, once daily for 15days) induced histopathological changes to lung tissues that include severe congestion, dilatation of the blood vessels, emphysema in the air alveoli, and peribronchial inflammatory cell infiltration. The levels of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), lipid peroxidation product and protein carbonyl content in lung tissues were significantly elevated. Moreover, the levels of reduced glutathione and total antioxidant capacity were significantly reduced. Co-administration of trolox, a water soluble vitamin E analog (25mg/kg, once daily for the last 7days of iron supplementation), alleviated the lung histological impairments, significantly decreased the pro-inflammatory cytokines, and restored the oxidative stress markers. Together, our findings indicate that iron supplementation at high altitudes induces lung tissue injury in rats. This injury could be mediated through excessive production of reactive oxygen species and induction of inflammatory responses. The study highlights the tissue injury induced by iron supplementation at high altitudes and suggests the co-administration of antioxidants such as trolox as protective measures. [Display omitted] •Iron supplementation at high altitudes induced lung histological changes in rats.•Iron induced oxidative stress in lung tissues of rats at high altitudes.•Iron increased the levels of IL-1β, IL-6 &amp; TNF-α in lung tissues at high altitudes.•Trolox alleviated the iron-induced histological and biochemical changes to the lungs.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>24215938</pmid><doi>10.1016/j.taap.2013.10.034</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0041-008X
ispartof Toxicology and applied pharmacology, 2014-01, Vol.274 (1), p.1-6
issn 0041-008X
1096-0333
language eng
recordid cdi_osti_scitechconnect_22285550
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects 60 APPLIED LIFE SCIENCES
Altitude
Animals
ANOXIA
ANTIOXIDANTS
Antioxidants - therapeutic use
Biological and medical sciences
BLOOD VESSELS
Chemical and industrial products toxicology. Toxic occupational diseases
Chromans - therapeutic use
Dietary Supplements - toxicity
ERYTHROCYTES
GLUTATHIONE
HEMATOXYLIN
High altitudes
INFLAMMATION
INJURIES
IRON
Iron - toxicity
Iron supplementation
Lipid Peroxidation - drug effects
Lipid Peroxidation - physiology
Lung tissue injury
LUNGS
LYMPHOKINES
Male
Medical sciences
Metals and various inorganic compounds
OXIDATION
Oxidative stress
Oxidative Stress - drug effects
Oxidative Stress - physiology
Pneumonia - chemically induced
Pneumonia - metabolism
Pneumonia - pathology
Pneumonia - prevention & control
POLYCYTHEMIA
Proinflammatory cytokines
RATS
Rats, Wistar
Reactive Oxygen Species - metabolism
Toxicology
Trolox
title Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T22%3A51%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Iron%20supplementation%20at%20high%20altitudes%20induces%20inflammation%20and%20oxidative%20injury%20to%20lung%20tissues%20in%20rats&rft.jtitle=Toxicology%20and%20applied%20pharmacology&rft.au=Salama,%20Samir%20A.&rft.date=2014-01-01&rft.volume=274&rft.issue=1&rft.spage=1&rft.epage=6&rft.pages=1-6&rft.issn=0041-008X&rft.eissn=1096-0333&rft.coden=TXAPA9&rft_id=info:doi/10.1016/j.taap.2013.10.034&rft_dat=%3Celsevier_osti_%3ES0041008X13004821%3C/elsevier_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/24215938&rft_els_id=S0041008X13004821&rfr_iscdi=true