Loading…
Whole‐body recruitment of glycocalyx volume during intravenous adenosine infusion
Adenosine‐mediated recruitment of microvascular volume in heart and muscle has been suggested to include, in addition to vasodilation of resistance vessels, an increased accessibility of the endothelial glycocalyx for flowing plasma as a result of an impairment of its barrier properties. The aim of...
Saved in:
Published in: | Physiological reports 2013-10, Vol.1 (5), p.e00102-n/a |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613 |
---|---|
cites | cdi_FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613 |
container_end_page | n/a |
container_issue | 5 |
container_start_page | e00102 |
container_title | Physiological reports |
container_volume | 1 |
creator | Brands, Judith Haare, Judith Vink, Hans VanTeeffelen, Jurgen W. G. E. |
description | Adenosine‐mediated recruitment of microvascular volume in heart and muscle has been suggested to include, in addition to vasodilation of resistance vessels, an increased accessibility of the endothelial glycocalyx for flowing plasma as a result of an impairment of its barrier properties. The aim of the current study was to investigate the effect of systemic intravenous administration of adenosine on the glycocalyx‐dependent exclusion of circulating blood at a whole‐body level. In anesthetized goats (N = 6), systemic blood‐excluded glycocalyx volume was measured by comparing the intravascular distribution volume of the suggested glycocalyx accessible tracer dextrans with a molecular weight of 40 kDa (Dex‐40) to that of circulating plasma, derived from the dilution of labeled red blood cells and large vessel hematocrit. Systemic glycocalyx volume was determined at baseline and during intravenous infusion of adenosine (157 ± 11.6 μg/kg min−1). Blood‐inaccessible glycocalyx volume decreased from 458.1 ± 95.5 to 18.1 ± 62.2 mL (P |
doi_str_mv | 10.1002/phy2.102 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3841038</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1891867736</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613</originalsourceid><addsrcrecordid>eNqFkc1qFTEUx4MottSCT1AGunEzbU6SOx-bghRtCwUFC-oqZJIz96ZkktvkztXZ9RH6jD6JGVprFUSyOIfkl__5-BPyGugRUMqO16uJ5Yw9I7uMLqBsoP7y_Em-Q_ZTuqaUAuW8peIl2WGCUw612CWfPq-Cwx-3d10wUxFRx9FuBvSbIvTF0k06aOWm78U2uHHAwozR-mVh_SaqLfowpkKZHJP1mG_7MdngX5EXvXIJ9x_iHrl6_-7q9Ly8_HB2cfr2stS8qVhZMwQjTG0qKpThqCoErboGjc5nARxa1FoAF7RbqF5zUzddZ1TNqw4q4Hvk5F52PXZD_oRzU06uox1UnGRQVv754u1KLsNW8kbkVTRZ4M2DQAw3I6aNHGzS6JzymCeT0LTQVHWu939UVC2jLQWe0cO_0OswRp8XIRlrW2BsUbPfgjqGlCL2j30DlbOtcrY1ZzN68HTOR_CXiRko74Fv1uH0TyH58fwrmwV_AkcbrxU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2299122572</pqid></control><display><type>article</type><title>Whole‐body recruitment of glycocalyx volume during intravenous adenosine infusion</title><source>Publicly Available Content Database</source><source>Wiley Open Access</source><source>PubMed Central</source><creator>Brands, Judith ; Haare, Judith ; Vink, Hans ; VanTeeffelen, Jurgen W. G. E.</creator><creatorcontrib>Brands, Judith ; Haare, Judith ; Vink, Hans ; VanTeeffelen, Jurgen W. G. E.</creatorcontrib><description>Adenosine‐mediated recruitment of microvascular volume in heart and muscle has been suggested to include, in addition to vasodilation of resistance vessels, an increased accessibility of the endothelial glycocalyx for flowing plasma as a result of an impairment of its barrier properties. The aim of the current study was to investigate the effect of systemic intravenous administration of adenosine on the glycocalyx‐dependent exclusion of circulating blood at a whole‐body level. In anesthetized goats (N = 6), systemic blood‐excluded glycocalyx volume was measured by comparing the intravascular distribution volume of the suggested glycocalyx accessible tracer dextrans with a molecular weight of 40 kDa (Dex‐40) to that of circulating plasma, derived from the dilution of labeled red blood cells and large vessel hematocrit. Systemic glycocalyx volume was determined at baseline and during intravenous infusion of adenosine (157 ± 11.6 μg/kg min−1). Blood‐inaccessible glycocalyx volume decreased from 458.1 ± 95.5 to 18.1 ± 62.2 mL (P < 0.01) during adenosine administration. While circulating plasma volume did not change significantly (617.1 ± 48.5 vs. 759.2 ± 47.9 mL, NS), the decrease in blood‐excluded glycocalyx volume was associated with a decrease in Dex‐40 distribution volume (from 1075.2 ± 71.0 to 777.3 ± 60.0 mL, P < 0.01). Intravenous administration of adenosine is associated with a robust impairment of whole‐body glycocalyx barrier properties, reflected by a greatly reduced exclusion of circulating blood compared to small dextrans. The observed decrease in Dex‐40 distribution volume suggests that the reduction in glycocalyx volume coincides with a reduction in tracer‐accessible vascular volume.
e00102
We demonstrate that intravenous administration of a clinical dose of adenosine in goats greatly decreases blood‐excluded intravascular glycocalyx volume at whole‐body level. During adenosine infusion, the difference between the glycocalyx inaccessible and accessible tracer reduced to nearly zero, illustrating adenosine's potency to robustly increase glycocalyx accessibility for flowing blood. The decrease in blood‐inaccessible glycocalyx volume was associated with an almost equivalent decrease in perfused anatomic vascular volume, reflecting the body's compensation to limit the fall in peripheral resistance during adenosine.</description><identifier>ISSN: 2051-817X</identifier><identifier>EISSN: 2051-817X</identifier><identifier>DOI: 10.1002/phy2.102</identifier><identifier>PMID: 24303174</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Adenosine ; Blood pressure ; Cardiovascular disease ; Cardiovascular system ; Coronary vessels ; Erythrocytes ; glycocalyx ; Hematocrit ; indicator dilution ; Intravenous administration ; Laboratory animals ; Microvasculature ; Molecular weight ; Original Research ; Ostomy ; Physiology ; Recruitment ; Surgery ; systemic ; Vasodilation</subject><ispartof>Physiological reports, 2013-10, Vol.1 (5), p.e00102-n/a</ispartof><rights>2013 The Authors. published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.</rights><rights>2013. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613</citedby><cites>FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2299122572/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2299122572?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24303174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brands, Judith</creatorcontrib><creatorcontrib>Haare, Judith</creatorcontrib><creatorcontrib>Vink, Hans</creatorcontrib><creatorcontrib>VanTeeffelen, Jurgen W. G. E.</creatorcontrib><title>Whole‐body recruitment of glycocalyx volume during intravenous adenosine infusion</title><title>Physiological reports</title><addtitle>Physiol Rep</addtitle><description>Adenosine‐mediated recruitment of microvascular volume in heart and muscle has been suggested to include, in addition to vasodilation of resistance vessels, an increased accessibility of the endothelial glycocalyx for flowing plasma as a result of an impairment of its barrier properties. The aim of the current study was to investigate the effect of systemic intravenous administration of adenosine on the glycocalyx‐dependent exclusion of circulating blood at a whole‐body level. In anesthetized goats (N = 6), systemic blood‐excluded glycocalyx volume was measured by comparing the intravascular distribution volume of the suggested glycocalyx accessible tracer dextrans with a molecular weight of 40 kDa (Dex‐40) to that of circulating plasma, derived from the dilution of labeled red blood cells and large vessel hematocrit. Systemic glycocalyx volume was determined at baseline and during intravenous infusion of adenosine (157 ± 11.6 μg/kg min−1). Blood‐inaccessible glycocalyx volume decreased from 458.1 ± 95.5 to 18.1 ± 62.2 mL (P < 0.01) during adenosine administration. While circulating plasma volume did not change significantly (617.1 ± 48.5 vs. 759.2 ± 47.9 mL, NS), the decrease in blood‐excluded glycocalyx volume was associated with a decrease in Dex‐40 distribution volume (from 1075.2 ± 71.0 to 777.3 ± 60.0 mL, P < 0.01). Intravenous administration of adenosine is associated with a robust impairment of whole‐body glycocalyx barrier properties, reflected by a greatly reduced exclusion of circulating blood compared to small dextrans. The observed decrease in Dex‐40 distribution volume suggests that the reduction in glycocalyx volume coincides with a reduction in tracer‐accessible vascular volume.
e00102
We demonstrate that intravenous administration of a clinical dose of adenosine in goats greatly decreases blood‐excluded intravascular glycocalyx volume at whole‐body level. During adenosine infusion, the difference between the glycocalyx inaccessible and accessible tracer reduced to nearly zero, illustrating adenosine's potency to robustly increase glycocalyx accessibility for flowing blood. The decrease in blood‐inaccessible glycocalyx volume was associated with an almost equivalent decrease in perfused anatomic vascular volume, reflecting the body's compensation to limit the fall in peripheral resistance during adenosine.</description><subject>Adenosine</subject><subject>Blood pressure</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular system</subject><subject>Coronary vessels</subject><subject>Erythrocytes</subject><subject>glycocalyx</subject><subject>Hematocrit</subject><subject>indicator dilution</subject><subject>Intravenous administration</subject><subject>Laboratory animals</subject><subject>Microvasculature</subject><subject>Molecular weight</subject><subject>Original Research</subject><subject>Ostomy</subject><subject>Physiology</subject><subject>Recruitment</subject><subject>Surgery</subject><subject>systemic</subject><subject>Vasodilation</subject><issn>2051-817X</issn><issn>2051-817X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNqFkc1qFTEUx4MottSCT1AGunEzbU6SOx-bghRtCwUFC-oqZJIz96ZkktvkztXZ9RH6jD6JGVprFUSyOIfkl__5-BPyGugRUMqO16uJ5Yw9I7uMLqBsoP7y_Em-Q_ZTuqaUAuW8peIl2WGCUw612CWfPq-Cwx-3d10wUxFRx9FuBvSbIvTF0k06aOWm78U2uHHAwozR-mVh_SaqLfowpkKZHJP1mG_7MdngX5EXvXIJ9x_iHrl6_-7q9Ly8_HB2cfr2stS8qVhZMwQjTG0qKpThqCoErboGjc5nARxa1FoAF7RbqF5zUzddZ1TNqw4q4Hvk5F52PXZD_oRzU06uox1UnGRQVv754u1KLsNW8kbkVTRZ4M2DQAw3I6aNHGzS6JzymCeT0LTQVHWu939UVC2jLQWe0cO_0OswRp8XIRlrW2BsUbPfgjqGlCL2j30DlbOtcrY1ZzN68HTOR_CXiRko74Fv1uH0TyH58fwrmwV_AkcbrxU</recordid><startdate>201310</startdate><enddate>201310</enddate><creator>Brands, Judith</creator><creator>Haare, Judith</creator><creator>Vink, Hans</creator><creator>VanTeeffelen, Jurgen W. G. E.</creator><general>John Wiley & Sons, Inc</general><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</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>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201310</creationdate><title>Whole‐body recruitment of glycocalyx volume during intravenous adenosine infusion</title><author>Brands, Judith ; Haare, Judith ; Vink, Hans ; VanTeeffelen, Jurgen W. G. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenosine</topic><topic>Blood pressure</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular system</topic><topic>Coronary vessels</topic><topic>Erythrocytes</topic><topic>glycocalyx</topic><topic>Hematocrit</topic><topic>indicator dilution</topic><topic>Intravenous administration</topic><topic>Laboratory animals</topic><topic>Microvasculature</topic><topic>Molecular weight</topic><topic>Original Research</topic><topic>Ostomy</topic><topic>Physiology</topic><topic>Recruitment</topic><topic>Surgery</topic><topic>systemic</topic><topic>Vasodilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brands, Judith</creatorcontrib><creatorcontrib>Haare, Judith</creatorcontrib><creatorcontrib>Vink, Hans</creatorcontrib><creatorcontrib>VanTeeffelen, Jurgen W. G. E.</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Biological Science Journals</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 China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Physiological reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brands, Judith</au><au>Haare, Judith</au><au>Vink, Hans</au><au>VanTeeffelen, Jurgen W. G. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Whole‐body recruitment of glycocalyx volume during intravenous adenosine infusion</atitle><jtitle>Physiological reports</jtitle><addtitle>Physiol Rep</addtitle><date>2013-10</date><risdate>2013</risdate><volume>1</volume><issue>5</issue><spage>e00102</spage><epage>n/a</epage><pages>e00102-n/a</pages><issn>2051-817X</issn><eissn>2051-817X</eissn><abstract>Adenosine‐mediated recruitment of microvascular volume in heart and muscle has been suggested to include, in addition to vasodilation of resistance vessels, an increased accessibility of the endothelial glycocalyx for flowing plasma as a result of an impairment of its barrier properties. The aim of the current study was to investigate the effect of systemic intravenous administration of adenosine on the glycocalyx‐dependent exclusion of circulating blood at a whole‐body level. In anesthetized goats (N = 6), systemic blood‐excluded glycocalyx volume was measured by comparing the intravascular distribution volume of the suggested glycocalyx accessible tracer dextrans with a molecular weight of 40 kDa (Dex‐40) to that of circulating plasma, derived from the dilution of labeled red blood cells and large vessel hematocrit. Systemic glycocalyx volume was determined at baseline and during intravenous infusion of adenosine (157 ± 11.6 μg/kg min−1). Blood‐inaccessible glycocalyx volume decreased from 458.1 ± 95.5 to 18.1 ± 62.2 mL (P < 0.01) during adenosine administration. While circulating plasma volume did not change significantly (617.1 ± 48.5 vs. 759.2 ± 47.9 mL, NS), the decrease in blood‐excluded glycocalyx volume was associated with a decrease in Dex‐40 distribution volume (from 1075.2 ± 71.0 to 777.3 ± 60.0 mL, P < 0.01). Intravenous administration of adenosine is associated with a robust impairment of whole‐body glycocalyx barrier properties, reflected by a greatly reduced exclusion of circulating blood compared to small dextrans. The observed decrease in Dex‐40 distribution volume suggests that the reduction in glycocalyx volume coincides with a reduction in tracer‐accessible vascular volume.
e00102
We demonstrate that intravenous administration of a clinical dose of adenosine in goats greatly decreases blood‐excluded intravascular glycocalyx volume at whole‐body level. During adenosine infusion, the difference between the glycocalyx inaccessible and accessible tracer reduced to nearly zero, illustrating adenosine's potency to robustly increase glycocalyx accessibility for flowing blood. The decrease in blood‐inaccessible glycocalyx volume was associated with an almost equivalent decrease in perfused anatomic vascular volume, reflecting the body's compensation to limit the fall in peripheral resistance during adenosine.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>24303174</pmid><doi>10.1002/phy2.102</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2051-817X |
ispartof | Physiological reports, 2013-10, Vol.1 (5), p.e00102-n/a |
issn | 2051-817X 2051-817X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3841038 |
source | Publicly Available Content Database; Wiley Open Access; PubMed Central |
subjects | Adenosine Blood pressure Cardiovascular disease Cardiovascular system Coronary vessels Erythrocytes glycocalyx Hematocrit indicator dilution Intravenous administration Laboratory animals Microvasculature Molecular weight Original Research Ostomy Physiology Recruitment Surgery systemic Vasodilation |
title | Whole‐body recruitment of glycocalyx volume during intravenous adenosine infusion |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T14%3A24%3A29IST&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=Whole%E2%80%90body%20recruitment%20of%20glycocalyx%20volume%20during%20intravenous%20adenosine%20infusion&rft.jtitle=Physiological%20reports&rft.au=Brands,%20Judith&rft.date=2013-10&rft.volume=1&rft.issue=5&rft.spage=e00102&rft.epage=n/a&rft.pages=e00102-n/a&rft.issn=2051-817X&rft.eissn=2051-817X&rft_id=info:doi/10.1002/phy2.102&rft_dat=%3Cproquest_pubme%3E1891867736%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3862-72e1d4d7d604ad3ea6e1cab8edcdcd51319ecc41340b5afc3d78bbda736b1613%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2299122572&rft_id=info:pmid/24303174&rfr_iscdi=true |