Creatine Supplementation Exacerbates Allergic Lung Inflammation and Airway Remodeling in Mice
Creatine supplement is the most popular nutritional supplement, and has various metabolic functions and sports medicine applications. Creatine supplementation increases muscle mass and can decrease muscular inflammation. Some studies have also suggested a beneficial role of creatine supplementation...
Gespeichert in:
Veröffentlicht in: | American journal of respiratory cell and molecular biology 2007-12, Vol.37 (6), p.660-667 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 667 |
---|---|
container_issue | 6 |
container_start_page | 660 |
container_title | American journal of respiratory cell and molecular biology |
container_volume | 37 |
creator | Vieira, Rodolfo P Duarte, Anna Cecilia S Claudino, Renata C Perini, Adenir Santos, Angela B. G Moriya, Henrique T Arantes-Costa, Fernanda M Martins, Milton A Carvalho, Celso R. F Dolhnikoff, Marisa |
description | Creatine supplement is the most popular nutritional supplement, and has various metabolic functions and sports medicine applications. Creatine supplementation increases muscle mass and can decrease muscular inflammation. Some studies have also suggested a beneficial role of creatine supplementation on chronic pulmonary diseases such as chronic obstructive pulmonary disease and cystic fibrosis. Among athletes, the prevalence of asthma is high, and many of these individuals may be taking creatine. However, the effects of creatine supplementation on chronic pulmonary diseases of allergic origin have not been investigated. In the present study, we analyzed the effects of creatine supplementation on a model of chronic allergic lung inflammation. Thirty-one Balb/c mice were divided into four groups: control, creatine (Cr), ovalbumin (OVA), and OVA+Cr. OVA and OVA+Cr groups were sensitized with intraperitoneal injections of OVA on Days 0, 14, 28, and 42. OVA challenge (OVA 1%) and Cr treatment (0.5 g/kg/d) were initiated on Day 21 and lasted until Day 53. We determined the index of hyperresponsiveness, the serum levels of OVA-specific immunoglobulin (Ig)E and IgG(1), and the total and differential cell counts in bronchoalveolar lavage fluid. We also quantified airway inflammation, and the airway density of IL-4+, IL-5+, IL-2+, IFN-gamma+, and insulin-like growth factor (IGF)-1+ cells, collagen and elastic fibers, and airway smooth muscle thickness. Our results showed that creatine in OVA-sensitized mice increased hyperresponsiveness; eosinophilic inflammation; airway density of IL-4+, IL-5+, and IGF-1 inflammatory cells; airway collagen and elastin content; and smooth muscle thickness. The results show that creatine supplementation exacerbates the lung allergic response to OVA through a T helper cell type 2 pathway and increased IGF-1 expression. |
doi_str_mv | 10.1165/rcmb.2007-0108OC |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_207577608</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1388431111</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-aa32d69b56cdfb3d3db125d8acce6320d7415ce258cb53a40c2d21cfa163aedb3</originalsourceid><addsrcrecordid>eNpFkE1Lw0AQhhdRrFbvniR48pK6s5vdJMdSqhYqBT-Osmx2J-2WfNRNQu2_NyUFTzMDz_sOPITcAZ0ASPHkTZlNGKVxSIEmq9kZuQLBRRilSXre7zSKQhBROiLXTbOlFFgCcElGEMsIWCquyPfMo25dhcFHt9sVWGLV9nddBfNfbdBnusUmmBYF-rUzwbKr1sGiygtdlgOmKxtMnd_rQ_COZW2xcD3iquDNGbwhF7kuGrw9zTH5ep5_zl7D5eplMZsuQ8NF3IZac2ZlmglpbJ5xy20GTNhEG4OSM2rjCIRBJhKTCa4japhlYHINkmu0GR-Th6F35-ufDptWbevOV_1LxWgs4ljSpIfoABlfN43HXO28K7U_KKDqqFMddaqjTjXo7CP3p94uK9H-B07-euBxADZuvdk7j6opdVH0OCi9PfbxWEklJeV_yu6A3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>207577608</pqid></control><display><type>article</type><title>Creatine Supplementation Exacerbates Allergic Lung Inflammation and Airway Remodeling in Mice</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Vieira, Rodolfo P ; Duarte, Anna Cecilia S ; Claudino, Renata C ; Perini, Adenir ; Santos, Angela B. G ; Moriya, Henrique T ; Arantes-Costa, Fernanda M ; Martins, Milton A ; Carvalho, Celso R. F ; Dolhnikoff, Marisa</creator><creatorcontrib>Vieira, Rodolfo P ; Duarte, Anna Cecilia S ; Claudino, Renata C ; Perini, Adenir ; Santos, Angela B. G ; Moriya, Henrique T ; Arantes-Costa, Fernanda M ; Martins, Milton A ; Carvalho, Celso R. F ; Dolhnikoff, Marisa</creatorcontrib><description>Creatine supplement is the most popular nutritional supplement, and has various metabolic functions and sports medicine applications. Creatine supplementation increases muscle mass and can decrease muscular inflammation. Some studies have also suggested a beneficial role of creatine supplementation on chronic pulmonary diseases such as chronic obstructive pulmonary disease and cystic fibrosis. Among athletes, the prevalence of asthma is high, and many of these individuals may be taking creatine. However, the effects of creatine supplementation on chronic pulmonary diseases of allergic origin have not been investigated. In the present study, we analyzed the effects of creatine supplementation on a model of chronic allergic lung inflammation. Thirty-one Balb/c mice were divided into four groups: control, creatine (Cr), ovalbumin (OVA), and OVA+Cr. OVA and OVA+Cr groups were sensitized with intraperitoneal injections of OVA on Days 0, 14, 28, and 42. OVA challenge (OVA 1%) and Cr treatment (0.5 g/kg/d) were initiated on Day 21 and lasted until Day 53. We determined the index of hyperresponsiveness, the serum levels of OVA-specific immunoglobulin (Ig)E and IgG(1), and the total and differential cell counts in bronchoalveolar lavage fluid. We also quantified airway inflammation, and the airway density of IL-4+, IL-5+, IL-2+, IFN-gamma+, and insulin-like growth factor (IGF)-1+ cells, collagen and elastic fibers, and airway smooth muscle thickness. Our results showed that creatine in OVA-sensitized mice increased hyperresponsiveness; eosinophilic inflammation; airway density of IL-4+, IL-5+, and IGF-1 inflammatory cells; airway collagen and elastin content; and smooth muscle thickness. The results show that creatine supplementation exacerbates the lung allergic response to OVA through a T helper cell type 2 pathway and increased IGF-1 expression.</description><identifier>ISSN: 1044-1549</identifier><identifier>EISSN: 1535-4989</identifier><identifier>DOI: 10.1165/rcmb.2007-0108OC</identifier><identifier>PMID: 17641295</identifier><identifier>CODEN: AJRBEL</identifier><language>eng</language><publisher>United States: Am Thoracic Soc</publisher><subject>Animals ; Bronchoalveolar Lavage Fluid - cytology ; Bronchoconstriction ; Cell Count ; Creatine - pharmacology ; Dietary Supplements ; Eosinophils - cytology ; Hypersensitivity - physiopathology ; Immunoglobulin E - immunology ; Immunoglobulin G - immunology ; Interleukin-4 ; Male ; Mice ; Mice, Inbred BALB C ; Ovalbumin ; Passive Cutaneous Anaphylaxis - immunology ; Pneumonia - chemically induced ; Pneumonia - pathology ; Pneumonia - physiopathology ; Respiratory Hypersensitivity - physiopathology ; Respiratory System - drug effects ; Respiratory System - pathology ; Respiratory System - physiopathology</subject><ispartof>American journal of respiratory cell and molecular biology, 2007-12, Vol.37 (6), p.660-667</ispartof><rights>Copyright American Thoracic Society Dec 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-aa32d69b56cdfb3d3db125d8acce6320d7415ce258cb53a40c2d21cfa163aedb3</citedby><cites>FETCH-LOGICAL-c357t-aa32d69b56cdfb3d3db125d8acce6320d7415ce258cb53a40c2d21cfa163aedb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17641295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vieira, Rodolfo P</creatorcontrib><creatorcontrib>Duarte, Anna Cecilia S</creatorcontrib><creatorcontrib>Claudino, Renata C</creatorcontrib><creatorcontrib>Perini, Adenir</creatorcontrib><creatorcontrib>Santos, Angela B. G</creatorcontrib><creatorcontrib>Moriya, Henrique T</creatorcontrib><creatorcontrib>Arantes-Costa, Fernanda M</creatorcontrib><creatorcontrib>Martins, Milton A</creatorcontrib><creatorcontrib>Carvalho, Celso R. F</creatorcontrib><creatorcontrib>Dolhnikoff, Marisa</creatorcontrib><title>Creatine Supplementation Exacerbates Allergic Lung Inflammation and Airway Remodeling in Mice</title><title>American journal of respiratory cell and molecular biology</title><addtitle>Am J Respir Cell Mol Biol</addtitle><description>Creatine supplement is the most popular nutritional supplement, and has various metabolic functions and sports medicine applications. Creatine supplementation increases muscle mass and can decrease muscular inflammation. Some studies have also suggested a beneficial role of creatine supplementation on chronic pulmonary diseases such as chronic obstructive pulmonary disease and cystic fibrosis. Among athletes, the prevalence of asthma is high, and many of these individuals may be taking creatine. However, the effects of creatine supplementation on chronic pulmonary diseases of allergic origin have not been investigated. In the present study, we analyzed the effects of creatine supplementation on a model of chronic allergic lung inflammation. Thirty-one Balb/c mice were divided into four groups: control, creatine (Cr), ovalbumin (OVA), and OVA+Cr. OVA and OVA+Cr groups were sensitized with intraperitoneal injections of OVA on Days 0, 14, 28, and 42. OVA challenge (OVA 1%) and Cr treatment (0.5 g/kg/d) were initiated on Day 21 and lasted until Day 53. We determined the index of hyperresponsiveness, the serum levels of OVA-specific immunoglobulin (Ig)E and IgG(1), and the total and differential cell counts in bronchoalveolar lavage fluid. We also quantified airway inflammation, and the airway density of IL-4+, IL-5+, IL-2+, IFN-gamma+, and insulin-like growth factor (IGF)-1+ cells, collagen and elastic fibers, and airway smooth muscle thickness. Our results showed that creatine in OVA-sensitized mice increased hyperresponsiveness; eosinophilic inflammation; airway density of IL-4+, IL-5+, and IGF-1 inflammatory cells; airway collagen and elastin content; and smooth muscle thickness. The results show that creatine supplementation exacerbates the lung allergic response to OVA through a T helper cell type 2 pathway and increased IGF-1 expression.</description><subject>Animals</subject><subject>Bronchoalveolar Lavage Fluid - cytology</subject><subject>Bronchoconstriction</subject><subject>Cell Count</subject><subject>Creatine - pharmacology</subject><subject>Dietary Supplements</subject><subject>Eosinophils - cytology</subject><subject>Hypersensitivity - physiopathology</subject><subject>Immunoglobulin E - immunology</subject><subject>Immunoglobulin G - immunology</subject><subject>Interleukin-4</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Ovalbumin</subject><subject>Passive Cutaneous Anaphylaxis - immunology</subject><subject>Pneumonia - chemically induced</subject><subject>Pneumonia - pathology</subject><subject>Pneumonia - physiopathology</subject><subject>Respiratory Hypersensitivity - physiopathology</subject><subject>Respiratory System - drug effects</subject><subject>Respiratory System - pathology</subject><subject>Respiratory System - physiopathology</subject><issn>1044-1549</issn><issn>1535-4989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpFkE1Lw0AQhhdRrFbvniR48pK6s5vdJMdSqhYqBT-Osmx2J-2WfNRNQu2_NyUFTzMDz_sOPITcAZ0ASPHkTZlNGKVxSIEmq9kZuQLBRRilSXre7zSKQhBROiLXTbOlFFgCcElGEMsIWCquyPfMo25dhcFHt9sVWGLV9nddBfNfbdBnusUmmBYF-rUzwbKr1sGiygtdlgOmKxtMnd_rQ_COZW2xcD3iquDNGbwhF7kuGrw9zTH5ep5_zl7D5eplMZsuQ8NF3IZac2ZlmglpbJ5xy20GTNhEG4OSM2rjCIRBJhKTCa4japhlYHINkmu0GR-Th6F35-ufDptWbevOV_1LxWgs4ljSpIfoABlfN43HXO28K7U_KKDqqFMddaqjTjXo7CP3p94uK9H-B07-euBxADZuvdk7j6opdVH0OCi9PfbxWEklJeV_yu6A3w</recordid><startdate>20071201</startdate><enddate>20071201</enddate><creator>Vieira, Rodolfo P</creator><creator>Duarte, Anna Cecilia S</creator><creator>Claudino, Renata C</creator><creator>Perini, Adenir</creator><creator>Santos, Angela B. G</creator><creator>Moriya, Henrique T</creator><creator>Arantes-Costa, Fernanda M</creator><creator>Martins, Milton A</creator><creator>Carvalho, Celso R. F</creator><creator>Dolhnikoff, Marisa</creator><general>Am Thoracic Soc</general><general>American Thoracic 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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20071201</creationdate><title>Creatine Supplementation Exacerbates Allergic Lung Inflammation and Airway Remodeling in Mice</title><author>Vieira, Rodolfo P ; Duarte, Anna Cecilia S ; Claudino, Renata C ; Perini, Adenir ; Santos, Angela B. G ; Moriya, Henrique T ; Arantes-Costa, Fernanda M ; Martins, Milton A ; Carvalho, Celso R. F ; Dolhnikoff, Marisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-aa32d69b56cdfb3d3db125d8acce6320d7415ce258cb53a40c2d21cfa163aedb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Bronchoalveolar Lavage Fluid - cytology</topic><topic>Bronchoconstriction</topic><topic>Cell Count</topic><topic>Creatine - pharmacology</topic><topic>Dietary Supplements</topic><topic>Eosinophils - cytology</topic><topic>Hypersensitivity - physiopathology</topic><topic>Immunoglobulin E - immunology</topic><topic>Immunoglobulin G - immunology</topic><topic>Interleukin-4</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Ovalbumin</topic><topic>Passive Cutaneous Anaphylaxis - immunology</topic><topic>Pneumonia - chemically induced</topic><topic>Pneumonia - pathology</topic><topic>Pneumonia - physiopathology</topic><topic>Respiratory Hypersensitivity - physiopathology</topic><topic>Respiratory System - drug effects</topic><topic>Respiratory System - pathology</topic><topic>Respiratory System - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vieira, Rodolfo P</creatorcontrib><creatorcontrib>Duarte, Anna Cecilia S</creatorcontrib><creatorcontrib>Claudino, Renata C</creatorcontrib><creatorcontrib>Perini, Adenir</creatorcontrib><creatorcontrib>Santos, Angela B. G</creatorcontrib><creatorcontrib>Moriya, Henrique T</creatorcontrib><creatorcontrib>Arantes-Costa, Fernanda M</creatorcontrib><creatorcontrib>Martins, Milton A</creatorcontrib><creatorcontrib>Carvalho, Celso R. F</creatorcontrib><creatorcontrib>Dolhnikoff, Marisa</creatorcontrib><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>American journal of respiratory cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vieira, Rodolfo P</au><au>Duarte, Anna Cecilia S</au><au>Claudino, Renata C</au><au>Perini, Adenir</au><au>Santos, Angela B. G</au><au>Moriya, Henrique T</au><au>Arantes-Costa, Fernanda M</au><au>Martins, Milton A</au><au>Carvalho, Celso R. F</au><au>Dolhnikoff, Marisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Creatine Supplementation Exacerbates Allergic Lung Inflammation and Airway Remodeling in Mice</atitle><jtitle>American journal of respiratory cell and molecular biology</jtitle><addtitle>Am J Respir Cell Mol Biol</addtitle><date>2007-12-01</date><risdate>2007</risdate><volume>37</volume><issue>6</issue><spage>660</spage><epage>667</epage><pages>660-667</pages><issn>1044-1549</issn><eissn>1535-4989</eissn><coden>AJRBEL</coden><abstract>Creatine supplement is the most popular nutritional supplement, and has various metabolic functions and sports medicine applications. Creatine supplementation increases muscle mass and can decrease muscular inflammation. Some studies have also suggested a beneficial role of creatine supplementation on chronic pulmonary diseases such as chronic obstructive pulmonary disease and cystic fibrosis. Among athletes, the prevalence of asthma is high, and many of these individuals may be taking creatine. However, the effects of creatine supplementation on chronic pulmonary diseases of allergic origin have not been investigated. In the present study, we analyzed the effects of creatine supplementation on a model of chronic allergic lung inflammation. Thirty-one Balb/c mice were divided into four groups: control, creatine (Cr), ovalbumin (OVA), and OVA+Cr. OVA and OVA+Cr groups were sensitized with intraperitoneal injections of OVA on Days 0, 14, 28, and 42. OVA challenge (OVA 1%) and Cr treatment (0.5 g/kg/d) were initiated on Day 21 and lasted until Day 53. We determined the index of hyperresponsiveness, the serum levels of OVA-specific immunoglobulin (Ig)E and IgG(1), and the total and differential cell counts in bronchoalveolar lavage fluid. We also quantified airway inflammation, and the airway density of IL-4+, IL-5+, IL-2+, IFN-gamma+, and insulin-like growth factor (IGF)-1+ cells, collagen and elastic fibers, and airway smooth muscle thickness. Our results showed that creatine in OVA-sensitized mice increased hyperresponsiveness; eosinophilic inflammation; airway density of IL-4+, IL-5+, and IGF-1 inflammatory cells; airway collagen and elastin content; and smooth muscle thickness. The results show that creatine supplementation exacerbates the lung allergic response to OVA through a T helper cell type 2 pathway and increased IGF-1 expression.</abstract><cop>United States</cop><pub>Am Thoracic Soc</pub><pmid>17641295</pmid><doi>10.1165/rcmb.2007-0108OC</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1044-1549 |
ispartof | American journal of respiratory cell and molecular biology, 2007-12, Vol.37 (6), p.660-667 |
issn | 1044-1549 1535-4989 |
language | eng |
recordid | cdi_proquest_journals_207577608 |
source | MEDLINE; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Bronchoalveolar Lavage Fluid - cytology Bronchoconstriction Cell Count Creatine - pharmacology Dietary Supplements Eosinophils - cytology Hypersensitivity - physiopathology Immunoglobulin E - immunology Immunoglobulin G - immunology Interleukin-4 Male Mice Mice, Inbred BALB C Ovalbumin Passive Cutaneous Anaphylaxis - immunology Pneumonia - chemically induced Pneumonia - pathology Pneumonia - physiopathology Respiratory Hypersensitivity - physiopathology Respiratory System - drug effects Respiratory System - pathology Respiratory System - physiopathology |
title | Creatine Supplementation Exacerbates Allergic Lung Inflammation and Airway Remodeling in Mice |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T00%3A28%3A57IST&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=Creatine%20Supplementation%20Exacerbates%20Allergic%20Lung%20Inflammation%20and%20Airway%20Remodeling%20in%20Mice&rft.jtitle=American%20journal%20of%20respiratory%20cell%20and%20molecular%20biology&rft.au=Vieira,%20Rodolfo%20P&rft.date=2007-12-01&rft.volume=37&rft.issue=6&rft.spage=660&rft.epage=667&rft.pages=660-667&rft.issn=1044-1549&rft.eissn=1535-4989&rft.coden=AJRBEL&rft_id=info:doi/10.1165/rcmb.2007-0108OC&rft_dat=%3Cproquest_cross%3E1388431111%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=207577608&rft_id=info:pmid/17641295&rfr_iscdi=true |