Permeability of Intestinal and Blood—Tissue Barriers in Rats for Evans Blue Dye under Conditions of Acute Intoxication with Cyclophosphamide

Myeloablative therapy was modeled by administration of cyclophosphamide to rats in a dose of 2.1 LD50 for 14 days. Under these conditions, increased accumulation of Evans blue dye given by gavage was observed in the blood, brain, lung, liver, kidney, and ileum (by 34, 1.6, 149, 46, 30, and 6.2 times...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bulletin of experimental biology and medicine 2019-11, Vol.168 (1), p.38-40
Hauptverfasser: Schäfer, T. V., Ivnitsky, Ju. Ju, Rejniuk, V. L.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 40
container_issue 1
container_start_page 38
container_title Bulletin of experimental biology and medicine
container_volume 168
creator Schäfer, T. V.
Ivnitsky, Ju. Ju
Rejniuk, V. L.
description Myeloablative therapy was modeled by administration of cyclophosphamide to rats in a dose of 2.1 LD50 for 14 days. Under these conditions, increased accumulation of Evans blue dye given by gavage was observed in the blood, brain, lung, liver, kidney, and ileum (by 34, 1.6, 149, 46, 30, and 6.2 times, respectively). After intravenous injection of the dye, its accumulation was increased only in the lung and ileum. Thus, simulation of myeloablation cytostatic therapy by cyclophosphamide injection to rats is associated with impairment of the intestinal and lung—blood barriers. These alterations predispose to penetration of biologically active substances from the small intestine, gastrointestinal chyme, and lungs to the blood, thus contributing to the development of the early toxic effects of cyclophosphamide.
doi_str_mv 10.1007/s10517-019-04640-8
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2380538878</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A613923310</galeid><sourcerecordid>A613923310</sourcerecordid><originalsourceid>FETCH-LOGICAL-c571t-55b780645211e65e0ab9b7ec2fcf6c279d80a71ac9d48f636a71d8de4680a6a3</originalsourceid><addsrcrecordid>eNqNksFu1DAQhiMEokvhBTggS0jcUuw4sZ3jdilQqVIrtHfLsSeNq8Re7ATYG0_AiSfkSXC6hW4ltEI-WDPzzW_N-M-ylwSfEIz520hwRXiOSZ3jkpU4F4-yBak4zUVRkMfZAicqL4UQR9mzGG_mEDPyNDuihKc0qxfZjysIA6jG9nbcIt-iczdCHK1TPVLOoNPee_Pr-8-1jXECdKpCsBAisg59UmNErQ_o7ItyMZGp_m4LaHIGAlp5Z-xofaok1aWeRpi1_Ter1ZxGX-3YodVW937T-bjp1GANPM-etKqP8OLuPs7W78_Wq4_5xeWH89XyItcVJ2NeVQ0XmJVVQQiwCrBq6oaDLlrdMl3w2gisOFG6NqVoGWUpMMJAyVKeKXqcvd7JboL_PKV55Y2fQpo5yoIKXFEhuLinrlUP0rrWj0HpwUYtl0wUmLOqZIcpQuuCUoITdfIPKh0Dg9XeQWtT_oHs_zXsvfBmr6ED1Y9d9P10-wcPlQ-De4rFDtTBxxiglZtgBxW2kmA5O1DuHCiTA-WtA-W8tFd3q52aAczflj-WSwDdATGV3DWE-90fkP0NYq_kMA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2380538878</pqid></control><display><type>article</type><title>Permeability of Intestinal and Blood—Tissue Barriers in Rats for Evans Blue Dye under Conditions of Acute Intoxication with Cyclophosphamide</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Schäfer, T. V. ; Ivnitsky, Ju. Ju ; Rejniuk, V. L.</creator><creatorcontrib>Schäfer, T. V. ; Ivnitsky, Ju. Ju ; Rejniuk, V. L.</creatorcontrib><description>Myeloablative therapy was modeled by administration of cyclophosphamide to rats in a dose of 2.1 LD50 for 14 days. Under these conditions, increased accumulation of Evans blue dye given by gavage was observed in the blood, brain, lung, liver, kidney, and ileum (by 34, 1.6, 149, 46, 30, and 6.2 times, respectively). After intravenous injection of the dye, its accumulation was increased only in the lung and ileum. Thus, simulation of myeloablation cytostatic therapy by cyclophosphamide injection to rats is associated with impairment of the intestinal and lung—blood barriers. These alterations predispose to penetration of biologically active substances from the small intestine, gastrointestinal chyme, and lungs to the blood, thus contributing to the development of the early toxic effects of cyclophosphamide.</description><identifier>ISSN: 0007-4888</identifier><identifier>EISSN: 1573-8221</identifier><identifier>DOI: 10.1007/s10517-019-04640-8</identifier><identifier>PMID: 31748869</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Acute intoxication ; Animals ; Biological activity ; Biomedical and Life Sciences ; Biomedicine ; Blood ; Blood-Brain Barrier - drug effects ; Brain - drug effects ; Brain - metabolism ; Cell Biology ; Cyclophosphamide ; Cyclophosphamide - pharmacology ; Dyes ; Evans Blue - metabolism ; Ileum ; Injection ; Internal Medicine ; Intestines - drug effects ; Intoxication ; Intravenous administration ; Kidney - drug effects ; Kidney - metabolism ; Kidneys ; Laboratory Medicine ; Liver ; Liver - drug effects ; Liver - metabolism ; Lung - drug effects ; Lung - metabolism ; Male ; Methylene blue ; Pathology ; Permeability ; Rats ; Small intestine</subject><ispartof>Bulletin of experimental biology and medicine, 2019-11, Vol.168 (1), p.38-40</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>COPYRIGHT 2019 Springer</rights><rights>COPYRIGHT 2020 Springer</rights><rights>Bulletin of Experimental Biology and Medicine is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-55b780645211e65e0ab9b7ec2fcf6c279d80a71ac9d48f636a71d8de4680a6a3</citedby><cites>FETCH-LOGICAL-c571t-55b780645211e65e0ab9b7ec2fcf6c279d80a71ac9d48f636a71d8de4680a6a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10517-019-04640-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10517-019-04640-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31748869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schäfer, T. V.</creatorcontrib><creatorcontrib>Ivnitsky, Ju. Ju</creatorcontrib><creatorcontrib>Rejniuk, V. L.</creatorcontrib><title>Permeability of Intestinal and Blood—Tissue Barriers in Rats for Evans Blue Dye under Conditions of Acute Intoxication with Cyclophosphamide</title><title>Bulletin of experimental biology and medicine</title><addtitle>Bull Exp Biol Med</addtitle><addtitle>Bull Exp Biol Med</addtitle><description>Myeloablative therapy was modeled by administration of cyclophosphamide to rats in a dose of 2.1 LD50 for 14 days. Under these conditions, increased accumulation of Evans blue dye given by gavage was observed in the blood, brain, lung, liver, kidney, and ileum (by 34, 1.6, 149, 46, 30, and 6.2 times, respectively). After intravenous injection of the dye, its accumulation was increased only in the lung and ileum. Thus, simulation of myeloablation cytostatic therapy by cyclophosphamide injection to rats is associated with impairment of the intestinal and lung—blood barriers. These alterations predispose to penetration of biologically active substances from the small intestine, gastrointestinal chyme, and lungs to the blood, thus contributing to the development of the early toxic effects of cyclophosphamide.</description><subject>Acute intoxication</subject><subject>Animals</subject><subject>Biological activity</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood</subject><subject>Blood-Brain Barrier - drug effects</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Cell Biology</subject><subject>Cyclophosphamide</subject><subject>Cyclophosphamide - pharmacology</subject><subject>Dyes</subject><subject>Evans Blue - metabolism</subject><subject>Ileum</subject><subject>Injection</subject><subject>Internal Medicine</subject><subject>Intestines - drug effects</subject><subject>Intoxication</subject><subject>Intravenous administration</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kidneys</subject><subject>Laboratory Medicine</subject><subject>Liver</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Lung - drug effects</subject><subject>Lung - metabolism</subject><subject>Male</subject><subject>Methylene blue</subject><subject>Pathology</subject><subject>Permeability</subject><subject>Rats</subject><subject>Small intestine</subject><issn>0007-4888</issn><issn>1573-8221</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</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>eNqNksFu1DAQhiMEokvhBTggS0jcUuw4sZ3jdilQqVIrtHfLsSeNq8Re7ATYG0_AiSfkSXC6hW4ltEI-WDPzzW_N-M-ylwSfEIz520hwRXiOSZ3jkpU4F4-yBak4zUVRkMfZAicqL4UQR9mzGG_mEDPyNDuihKc0qxfZjysIA6jG9nbcIt-iczdCHK1TPVLOoNPee_Pr-8-1jXECdKpCsBAisg59UmNErQ_o7ItyMZGp_m4LaHIGAlp5Z-xofaok1aWeRpi1_Ter1ZxGX-3YodVW937T-bjp1GANPM-etKqP8OLuPs7W78_Wq4_5xeWH89XyItcVJ2NeVQ0XmJVVQQiwCrBq6oaDLlrdMl3w2gisOFG6NqVoGWUpMMJAyVKeKXqcvd7JboL_PKV55Y2fQpo5yoIKXFEhuLinrlUP0rrWj0HpwUYtl0wUmLOqZIcpQuuCUoITdfIPKh0Dg9XeQWtT_oHs_zXsvfBmr6ED1Y9d9P10-wcPlQ-De4rFDtTBxxiglZtgBxW2kmA5O1DuHCiTA-WtA-W8tFd3q52aAczflj-WSwDdATGV3DWE-90fkP0NYq_kMA</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Schäfer, T. V.</creator><creator>Ivnitsky, Ju. Ju</creator><creator>Rejniuk, V. L.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</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>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>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20191101</creationdate><title>Permeability of Intestinal and Blood—Tissue Barriers in Rats for Evans Blue Dye under Conditions of Acute Intoxication with Cyclophosphamide</title><author>Schäfer, T. V. ; Ivnitsky, Ju. Ju ; Rejniuk, V. L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c571t-55b780645211e65e0ab9b7ec2fcf6c279d80a71ac9d48f636a71d8de4680a6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acute intoxication</topic><topic>Animals</topic><topic>Biological activity</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood</topic><topic>Blood-Brain Barrier - drug effects</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Cell Biology</topic><topic>Cyclophosphamide</topic><topic>Cyclophosphamide - pharmacology</topic><topic>Dyes</topic><topic>Evans Blue - metabolism</topic><topic>Ileum</topic><topic>Injection</topic><topic>Internal Medicine</topic><topic>Intestines - drug effects</topic><topic>Intoxication</topic><topic>Intravenous administration</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kidneys</topic><topic>Laboratory Medicine</topic><topic>Liver</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Lung - drug effects</topic><topic>Lung - metabolism</topic><topic>Male</topic><topic>Methylene blue</topic><topic>Pathology</topic><topic>Permeability</topic><topic>Rats</topic><topic>Small intestine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schäfer, T. V.</creatorcontrib><creatorcontrib>Ivnitsky, Ju. Ju</creatorcontrib><creatorcontrib>Rejniuk, V. L.</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 &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>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 &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>Bulletin of experimental biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schäfer, T. V.</au><au>Ivnitsky, Ju. Ju</au><au>Rejniuk, V. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Permeability of Intestinal and Blood—Tissue Barriers in Rats for Evans Blue Dye under Conditions of Acute Intoxication with Cyclophosphamide</atitle><jtitle>Bulletin of experimental biology and medicine</jtitle><stitle>Bull Exp Biol Med</stitle><addtitle>Bull Exp Biol Med</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>168</volume><issue>1</issue><spage>38</spage><epage>40</epage><pages>38-40</pages><issn>0007-4888</issn><eissn>1573-8221</eissn><abstract>Myeloablative therapy was modeled by administration of cyclophosphamide to rats in a dose of 2.1 LD50 for 14 days. Under these conditions, increased accumulation of Evans blue dye given by gavage was observed in the blood, brain, lung, liver, kidney, and ileum (by 34, 1.6, 149, 46, 30, and 6.2 times, respectively). After intravenous injection of the dye, its accumulation was increased only in the lung and ileum. Thus, simulation of myeloablation cytostatic therapy by cyclophosphamide injection to rats is associated with impairment of the intestinal and lung—blood barriers. These alterations predispose to penetration of biologically active substances from the small intestine, gastrointestinal chyme, and lungs to the blood, thus contributing to the development of the early toxic effects of cyclophosphamide.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31748869</pmid><doi>10.1007/s10517-019-04640-8</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0007-4888
ispartof Bulletin of experimental biology and medicine, 2019-11, Vol.168 (1), p.38-40
issn 0007-4888
1573-8221
language eng
recordid cdi_proquest_journals_2380538878
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Acute intoxication
Animals
Biological activity
Biomedical and Life Sciences
Biomedicine
Blood
Blood-Brain Barrier - drug effects
Brain - drug effects
Brain - metabolism
Cell Biology
Cyclophosphamide
Cyclophosphamide - pharmacology
Dyes
Evans Blue - metabolism
Ileum
Injection
Internal Medicine
Intestines - drug effects
Intoxication
Intravenous administration
Kidney - drug effects
Kidney - metabolism
Kidneys
Laboratory Medicine
Liver
Liver - drug effects
Liver - metabolism
Lung - drug effects
Lung - metabolism
Male
Methylene blue
Pathology
Permeability
Rats
Small intestine
title Permeability of Intestinal and Blood—Tissue Barriers in Rats for Evans Blue Dye under Conditions of Acute Intoxication with Cyclophosphamide
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T23%3A12%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Permeability%20of%20Intestinal%20and%20Blood%E2%80%94Tissue%20Barriers%20in%20Rats%20for%20Evans%20Blue%20Dye%20under%20Conditions%20of%20Acute%20Intoxication%20with%20Cyclophosphamide&rft.jtitle=Bulletin%20of%20experimental%20biology%20and%20medicine&rft.au=Sch%C3%A4fer,%20T.%20V.&rft.date=2019-11-01&rft.volume=168&rft.issue=1&rft.spage=38&rft.epage=40&rft.pages=38-40&rft.issn=0007-4888&rft.eissn=1573-8221&rft_id=info:doi/10.1007/s10517-019-04640-8&rft_dat=%3Cgale_proqu%3EA613923310%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2380538878&rft_id=info:pmid/31748869&rft_galeid=A613923310&rfr_iscdi=true