Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo

To determine the efficacy of potential cystic fibrosis (CF) therapies we have developed a novel mucociliary transit (MCT) measurement that uses synchrotron phase contrast X-ray imaging (PCXI) to non-invasively measure the transit rate of individual micron-sized particles deposited into the airways o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Scientific reports 2014-01, Vol.4 (1), p.3689-3689, Article 3689
Hauptverfasser: Donnelley, Martin, Morgan, Kaye S., Siu, Karen K. W., Farrow, Nigel R., Stahr, Charlene S., Boucher, Richard C., Fouras, Andreas, Parsons, David W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3689
container_issue 1
container_start_page 3689
container_title Scientific reports
container_volume 4
creator Donnelley, Martin
Morgan, Kaye S.
Siu, Karen K. W.
Farrow, Nigel R.
Stahr, Charlene S.
Boucher, Richard C.
Fouras, Andreas
Parsons, David W.
description To determine the efficacy of potential cystic fibrosis (CF) therapies we have developed a novel mucociliary transit (MCT) measurement that uses synchrotron phase contrast X-ray imaging (PCXI) to non-invasively measure the transit rate of individual micron-sized particles deposited into the airways of live mice. The aim of this study was to image changes in MCT produced by a rehydrating treatment based on hypertonic saline (HS), a current CF clinical treatment. Live mice received HS containing a long acting epithelial sodium channel blocker (P308); isotonic saline; or no treatment, using a nebuliser integrated within a small-animal ventilator circuit. Marker particle motion was tracked for 20 minutes using PCXI. There were statistically significant increases in MCT in the isotonic and HS-P308 groups. The ability to quantify in vivo changes in MCT may have utility in pre-clinical research studies designed to bring new genetic and pharmaceutical treatments for respiratory diseases into clinical trials.
doi_str_mv 10.1038/srep03689
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3891397</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1897783501</sourcerecordid><originalsourceid>FETCH-LOGICAL-c438t-d5fa4153691cc15496270ba3d679beea18d2f7d7be2c779949e037c9afe843433</originalsourceid><addsrcrecordid>eNplkU-L1TAUxYMozjDOwi8gATc6UM2_No0LQQZHhUEX6jrkpbevGdrkmaSVrv3i5vHGx1OzScj55dx7cxB6SskrSnj7OkXYEd606gE6Z0TUFeOMPTw5n6HLlO5IWTVTgqrH6IwJQVvF63P063PwlfOLSW4BbFz8aVY8gBnzgE1KkNIEPr_BX1dvhxhyDB67yWyd3-IISwEThr4HmxMOfbka1i6avJdzBJP3r4vi8TTbYN3oTFyLYnxyGTtfLW4JT9CjvvjA5f1-gb7fvP92_bG6_fLh0_W728oK3uaqq3sjaM0bRa2ltVANk2RjeNdItQEwtO1YLzu5AWalVEooIFxaZXpoBRecX6C3B9_dvJmgs6W1aEa9i2WguOpgnP5b8W7Q27Bo3irKlSwGL-4NYvgxQ8p6csnCOBoPYU6aCkWkbCjbo8__Qe_CHH0ZT5efl7LlNaGFenmgbAypBNkfm6FE79PVx3QL--y0-yP5J8sCXB2AVCS_hXhS8j-33z7Bslc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1897783501</pqid></control><display><type>article</type><title>Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo</title><source>MEDLINE</source><source>Nature Free</source><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature OA Free Journals</source><creator>Donnelley, Martin ; Morgan, Kaye S. ; Siu, Karen K. W. ; Farrow, Nigel R. ; Stahr, Charlene S. ; Boucher, Richard C. ; Fouras, Andreas ; Parsons, David W.</creator><creatorcontrib>Donnelley, Martin ; Morgan, Kaye S. ; Siu, Karen K. W. ; Farrow, Nigel R. ; Stahr, Charlene S. ; Boucher, Richard C. ; Fouras, Andreas ; Parsons, David W.</creatorcontrib><description>To determine the efficacy of potential cystic fibrosis (CF) therapies we have developed a novel mucociliary transit (MCT) measurement that uses synchrotron phase contrast X-ray imaging (PCXI) to non-invasively measure the transit rate of individual micron-sized particles deposited into the airways of live mice. The aim of this study was to image changes in MCT produced by a rehydrating treatment based on hypertonic saline (HS), a current CF clinical treatment. Live mice received HS containing a long acting epithelial sodium channel blocker (P308); isotonic saline; or no treatment, using a nebuliser integrated within a small-animal ventilator circuit. Marker particle motion was tracked for 20 minutes using PCXI. There were statistically significant increases in MCT in the isotonic and HS-P308 groups. The ability to quantify in vivo changes in MCT may have utility in pre-clinical research studies designed to bring new genetic and pharmaceutical treatments for respiratory diseases into clinical trials.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep03689</identifier><identifier>PMID: 24418935</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14/63 ; 59 ; 639/166/985 ; 64/60 ; 692/308/2778 ; 692/698 ; Animals ; Clinical trials ; Cystic fibrosis ; Cystic Fibrosis - diagnosis ; Cystic Fibrosis - diagnostic imaging ; Diagnostic Imaging - methods ; Humanities and Social Sciences ; Mice ; Mice, Inbred C57BL ; multidisciplinary ; Particle Size ; Radionuclide Imaging ; Respiratory diseases ; Respiratory System - diagnostic imaging ; Respiratory tract ; Rodents ; Saline Solution, Hypertonic - administration &amp; dosage ; Science ; Sodium ; Statistical analysis ; Synchrotrons ; X-Rays</subject><ispartof>Scientific reports, 2014-01, Vol.4 (1), p.3689-3689, Article 3689</ispartof><rights>The Author(s) 2014</rights><rights>Copyright Nature Publishing Group Jan 2014</rights><rights>Copyright © 2014, Macmillan Publishers Limited. All rights reserved 2014 Macmillan Publishers Limited. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-d5fa4153691cc15496270ba3d679beea18d2f7d7be2c779949e037c9afe843433</citedby><cites>FETCH-LOGICAL-c438t-d5fa4153691cc15496270ba3d679beea18d2f7d7be2c779949e037c9afe843433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891397/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891397/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,41099,42168,51554,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24418935$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Donnelley, Martin</creatorcontrib><creatorcontrib>Morgan, Kaye S.</creatorcontrib><creatorcontrib>Siu, Karen K. W.</creatorcontrib><creatorcontrib>Farrow, Nigel R.</creatorcontrib><creatorcontrib>Stahr, Charlene S.</creatorcontrib><creatorcontrib>Boucher, Richard C.</creatorcontrib><creatorcontrib>Fouras, Andreas</creatorcontrib><creatorcontrib>Parsons, David W.</creatorcontrib><title>Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>To determine the efficacy of potential cystic fibrosis (CF) therapies we have developed a novel mucociliary transit (MCT) measurement that uses synchrotron phase contrast X-ray imaging (PCXI) to non-invasively measure the transit rate of individual micron-sized particles deposited into the airways of live mice. The aim of this study was to image changes in MCT produced by a rehydrating treatment based on hypertonic saline (HS), a current CF clinical treatment. Live mice received HS containing a long acting epithelial sodium channel blocker (P308); isotonic saline; or no treatment, using a nebuliser integrated within a small-animal ventilator circuit. Marker particle motion was tracked for 20 minutes using PCXI. There were statistically significant increases in MCT in the isotonic and HS-P308 groups. The ability to quantify in vivo changes in MCT may have utility in pre-clinical research studies designed to bring new genetic and pharmaceutical treatments for respiratory diseases into clinical trials.</description><subject>14/63</subject><subject>59</subject><subject>639/166/985</subject><subject>64/60</subject><subject>692/308/2778</subject><subject>692/698</subject><subject>Animals</subject><subject>Clinical trials</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - diagnosis</subject><subject>Cystic Fibrosis - diagnostic imaging</subject><subject>Diagnostic Imaging - methods</subject><subject>Humanities and Social Sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>multidisciplinary</subject><subject>Particle Size</subject><subject>Radionuclide Imaging</subject><subject>Respiratory diseases</subject><subject>Respiratory System - diagnostic imaging</subject><subject>Respiratory tract</subject><subject>Rodents</subject><subject>Saline Solution, Hypertonic - administration &amp; dosage</subject><subject>Science</subject><subject>Sodium</subject><subject>Statistical analysis</subject><subject>Synchrotrons</subject><subject>X-Rays</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNplkU-L1TAUxYMozjDOwi8gATc6UM2_No0LQQZHhUEX6jrkpbevGdrkmaSVrv3i5vHGx1OzScj55dx7cxB6SskrSnj7OkXYEd606gE6Z0TUFeOMPTw5n6HLlO5IWTVTgqrH6IwJQVvF63P063PwlfOLSW4BbFz8aVY8gBnzgE1KkNIEPr_BX1dvhxhyDB67yWyd3-IISwEThr4HmxMOfbka1i6avJdzBJP3r4vi8TTbYN3oTFyLYnxyGTtfLW4JT9CjvvjA5f1-gb7fvP92_bG6_fLh0_W728oK3uaqq3sjaM0bRa2ltVANk2RjeNdItQEwtO1YLzu5AWalVEooIFxaZXpoBRecX6C3B9_dvJmgs6W1aEa9i2WguOpgnP5b8W7Q27Bo3irKlSwGL-4NYvgxQ8p6csnCOBoPYU6aCkWkbCjbo8__Qe_CHH0ZT5efl7LlNaGFenmgbAypBNkfm6FE79PVx3QL--y0-yP5J8sCXB2AVCS_hXhS8j-33z7Bslc</recordid><startdate>20140114</startdate><enddate>20140114</enddate><creator>Donnelley, Martin</creator><creator>Morgan, Kaye S.</creator><creator>Siu, Karen K. W.</creator><creator>Farrow, Nigel R.</creator><creator>Stahr, Charlene S.</creator><creator>Boucher, Richard C.</creator><creator>Fouras, Andreas</creator><creator>Parsons, David W.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</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>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140114</creationdate><title>Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo</title><author>Donnelley, Martin ; Morgan, Kaye S. ; Siu, Karen K. W. ; Farrow, Nigel R. ; Stahr, Charlene S. ; Boucher, Richard C. ; Fouras, Andreas ; Parsons, David W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-d5fa4153691cc15496270ba3d679beea18d2f7d7be2c779949e037c9afe843433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>14/63</topic><topic>59</topic><topic>639/166/985</topic><topic>64/60</topic><topic>692/308/2778</topic><topic>692/698</topic><topic>Animals</topic><topic>Clinical trials</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - diagnosis</topic><topic>Cystic Fibrosis - diagnostic imaging</topic><topic>Diagnostic Imaging - methods</topic><topic>Humanities and Social Sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>multidisciplinary</topic><topic>Particle Size</topic><topic>Radionuclide Imaging</topic><topic>Respiratory diseases</topic><topic>Respiratory System - diagnostic imaging</topic><topic>Respiratory tract</topic><topic>Rodents</topic><topic>Saline Solution, Hypertonic - administration &amp; dosage</topic><topic>Science</topic><topic>Sodium</topic><topic>Statistical analysis</topic><topic>Synchrotrons</topic><topic>X-Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Donnelley, Martin</creatorcontrib><creatorcontrib>Morgan, Kaye S.</creatorcontrib><creatorcontrib>Siu, Karen K. W.</creatorcontrib><creatorcontrib>Farrow, Nigel R.</creatorcontrib><creatorcontrib>Stahr, Charlene S.</creatorcontrib><creatorcontrib>Boucher, Richard C.</creatorcontrib><creatorcontrib>Fouras, Andreas</creatorcontrib><creatorcontrib>Parsons, David W.</creatorcontrib><collection>Springer Nature OA Free Journals</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>Health &amp; 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>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 One Sustainability</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 &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content 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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Donnelley, Martin</au><au>Morgan, Kaye S.</au><au>Siu, Karen K. W.</au><au>Farrow, Nigel R.</au><au>Stahr, Charlene S.</au><au>Boucher, Richard C.</au><au>Fouras, Andreas</au><au>Parsons, David W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2014-01-14</date><risdate>2014</risdate><volume>4</volume><issue>1</issue><spage>3689</spage><epage>3689</epage><pages>3689-3689</pages><artnum>3689</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>To determine the efficacy of potential cystic fibrosis (CF) therapies we have developed a novel mucociliary transit (MCT) measurement that uses synchrotron phase contrast X-ray imaging (PCXI) to non-invasively measure the transit rate of individual micron-sized particles deposited into the airways of live mice. The aim of this study was to image changes in MCT produced by a rehydrating treatment based on hypertonic saline (HS), a current CF clinical treatment. Live mice received HS containing a long acting epithelial sodium channel blocker (P308); isotonic saline; or no treatment, using a nebuliser integrated within a small-animal ventilator circuit. Marker particle motion was tracked for 20 minutes using PCXI. There were statistically significant increases in MCT in the isotonic and HS-P308 groups. The ability to quantify in vivo changes in MCT may have utility in pre-clinical research studies designed to bring new genetic and pharmaceutical treatments for respiratory diseases into clinical trials.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24418935</pmid><doi>10.1038/srep03689</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2045-2322
ispartof Scientific reports, 2014-01, Vol.4 (1), p.3689-3689, Article 3689
issn 2045-2322
2045-2322
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3891397
source MEDLINE; Nature Free; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature OA Free Journals
subjects 14/63
59
639/166/985
64/60
692/308/2778
692/698
Animals
Clinical trials
Cystic fibrosis
Cystic Fibrosis - diagnosis
Cystic Fibrosis - diagnostic imaging
Diagnostic Imaging - methods
Humanities and Social Sciences
Mice
Mice, Inbred C57BL
multidisciplinary
Particle Size
Radionuclide Imaging
Respiratory diseases
Respiratory System - diagnostic imaging
Respiratory tract
Rodents
Saline Solution, Hypertonic - administration & dosage
Science
Sodium
Statistical analysis
Synchrotrons
X-Rays
title Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T15%3A19%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Non-invasive%20airway%20health%20assessment:%20Synchrotron%20imaging%20reveals%20effects%20of%20rehydrating%20treatments%20on%20mucociliary%20transit%20in-vivo&rft.jtitle=Scientific%20reports&rft.au=Donnelley,%20Martin&rft.date=2014-01-14&rft.volume=4&rft.issue=1&rft.spage=3689&rft.epage=3689&rft.pages=3689-3689&rft.artnum=3689&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/srep03689&rft_dat=%3Cproquest_pubme%3E1897783501%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1897783501&rft_id=info:pmid/24418935&rfr_iscdi=true