The effect of endotoxin on gastrointestinal transit time and intestinal permeability
Acute changes in gastrointestinal transit time, creatinine clearance and dual sugar (lactulose/mannitol) intestinal permeability have been assessed following endotoxin administration ( E. coli 0111:134, phenol extract) to 6 week old rats. Monitoring the progress of orally administered 51Cr-EDTA thro...
Gespeichert in:
Veröffentlicht in: | Clinical nutrition (Edinburgh, Scotland) Scotland), 1995, Vol.14 (1), p.35-41 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 41 |
---|---|
container_issue | 1 |
container_start_page | 35 |
container_title | Clinical nutrition (Edinburgh, Scotland) |
container_volume | 14 |
creator | Jennings, G. Lunn, P.G. Elia, M. |
description | Acute changes in gastrointestinal transit time, creatinine clearance and dual sugar (lactulose/mannitol) intestinal permeability have been assessed following endotoxin administration (
E. coli 0111:134, phenol extract) to 6 week old rats. Monitoring the progress of orally administered
51Cr-EDTA through the digestive tract showed that, compared to saline injected controls, stomach emptying was considerably delayed in endotoxin treated animals (t 1/2 = 26 ± 2 vs 162 ± 20 min (p < 0.01), but transit time through the small intestine was not significantly altered (81 ± 17 v 93 ± 29 min).
Intestinal permeability assessed by the ratio of lactulose to mannitol excretion in urine was higher in endotoxin compared to saline injected rats, 1.01 ± 0.08 vs 0.60 ± 0.04 (p < 0.01). After correcting the individual sugar excretion to take into account the amount of marker available to the small intestine for absorption during the test period, it was concluded that endotoxin treatment was associated with increased lactulose uptake but no change in mannitol absorption. The study also shows that endotoxaemia, uncomplicated by drug administration or other therapeutic manoeuvres, can markedly delay gastric emptying, which is associated with intolerance to oral or nasogastric feeding. |
doi_str_mv | 10.1016/S0261-5614(06)80008-7 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_15632970</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0261561406800087</els_id><sourcerecordid>15632970</sourcerecordid><originalsourceid>FETCH-LOGICAL-c367t-eb8464809e454af01cc0cb00febea543ec9bd1ac01c9cac6cae84ddfc6c534053</originalsourceid><addsrcrecordid>eNqFkE1LAzEQhoMoWKs_QchBRA-rSfOxuycR8QsED9ZzyGYnGtlNahLF_nvTVsSbpwnMMzN5H4QOKTmjhMrzJzKTtBKS8hMiTxtCSFPVW2hCBZtVtG3YNpr8IrtoL6W3wghWNxM0n78CBmvBZBwsBt-HHL6cx8HjF51yDM5nSNl5PeActU8u4-xGwNr3-E9vAXEE3bnB5eU-2rF6SHDwU6fo-eZ6fnVXPTze3l9dPlSGyTpX0DVc8oa0wAXXllBjiOkIsdCBFpyBabuealMardFGGg0N73tbXoLxEmCKjjd7FzG8f5SfqNElA8OgPYSPpKiQbNbWpIBiA5oYUopg1SK6UcelokStHKq1Q7USpIhUa4eqLnNHPwd0MnqwJb9x6XeYccFo0xbsYoNBCfvpIKpkHHgDvYtFrOqD--fQN48uiA8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15632970</pqid></control><display><type>article</type><title>The effect of endotoxin on gastrointestinal transit time and intestinal permeability</title><source>Access via ScienceDirect (Elsevier)</source><creator>Jennings, G. ; Lunn, P.G. ; Elia, M.</creator><creatorcontrib>Jennings, G. ; Lunn, P.G. ; Elia, M.</creatorcontrib><description>Acute changes in gastrointestinal transit time, creatinine clearance and dual sugar (lactulose/mannitol) intestinal permeability have been assessed following endotoxin administration (
E. coli 0111:134, phenol extract) to 6 week old rats. Monitoring the progress of orally administered
51Cr-EDTA through the digestive tract showed that, compared to saline injected controls, stomach emptying was considerably delayed in endotoxin treated animals (t 1/2 = 26 ± 2 vs 162 ± 20 min (p < 0.01), but transit time through the small intestine was not significantly altered (81 ± 17 v 93 ± 29 min).
Intestinal permeability assessed by the ratio of lactulose to mannitol excretion in urine was higher in endotoxin compared to saline injected rats, 1.01 ± 0.08 vs 0.60 ± 0.04 (p < 0.01). After correcting the individual sugar excretion to take into account the amount of marker available to the small intestine for absorption during the test period, it was concluded that endotoxin treatment was associated with increased lactulose uptake but no change in mannitol absorption. The study also shows that endotoxaemia, uncomplicated by drug administration or other therapeutic manoeuvres, can markedly delay gastric emptying, which is associated with intolerance to oral or nasogastric feeding.</description><identifier>ISSN: 0261-5614</identifier><identifier>EISSN: 1532-1983</identifier><identifier>DOI: 10.1016/S0261-5614(06)80008-7</identifier><identifier>CODEN: CLNUDP</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Bacterial diseases ; Bacterial diseases of the digestive system and abdomen ; Biological and medical sciences ; Escherichia coli ; Human bacterial diseases ; Infectious diseases ; Medical sciences</subject><ispartof>Clinical nutrition (Edinburgh, Scotland), 1995, Vol.14 (1), p.35-41</ispartof><rights>1995 Pearson Professional Ltd</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-eb8464809e454af01cc0cb00febea543ec9bd1ac01c9cac6cae84ddfc6c534053</citedby><cites>FETCH-LOGICAL-c367t-eb8464809e454af01cc0cb00febea543ec9bd1ac01c9cac6cae84ddfc6c534053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0261-5614(06)80008-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,4025,27928,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3453189$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jennings, G.</creatorcontrib><creatorcontrib>Lunn, P.G.</creatorcontrib><creatorcontrib>Elia, M.</creatorcontrib><title>The effect of endotoxin on gastrointestinal transit time and intestinal permeability</title><title>Clinical nutrition (Edinburgh, Scotland)</title><description>Acute changes in gastrointestinal transit time, creatinine clearance and dual sugar (lactulose/mannitol) intestinal permeability have been assessed following endotoxin administration (
E. coli 0111:134, phenol extract) to 6 week old rats. Monitoring the progress of orally administered
51Cr-EDTA through the digestive tract showed that, compared to saline injected controls, stomach emptying was considerably delayed in endotoxin treated animals (t 1/2 = 26 ± 2 vs 162 ± 20 min (p < 0.01), but transit time through the small intestine was not significantly altered (81 ± 17 v 93 ± 29 min).
Intestinal permeability assessed by the ratio of lactulose to mannitol excretion in urine was higher in endotoxin compared to saline injected rats, 1.01 ± 0.08 vs 0.60 ± 0.04 (p < 0.01). After correcting the individual sugar excretion to take into account the amount of marker available to the small intestine for absorption during the test period, it was concluded that endotoxin treatment was associated with increased lactulose uptake but no change in mannitol absorption. The study also shows that endotoxaemia, uncomplicated by drug administration or other therapeutic manoeuvres, can markedly delay gastric emptying, which is associated with intolerance to oral or nasogastric feeding.</description><subject>Bacterial diseases</subject><subject>Bacterial diseases of the digestive system and abdomen</subject><subject>Biological and medical sciences</subject><subject>Escherichia coli</subject><subject>Human bacterial diseases</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><issn>0261-5614</issn><issn>1532-1983</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LAzEQhoMoWKs_QchBRA-rSfOxuycR8QsED9ZzyGYnGtlNahLF_nvTVsSbpwnMMzN5H4QOKTmjhMrzJzKTtBKS8hMiTxtCSFPVW2hCBZtVtG3YNpr8IrtoL6W3wghWNxM0n78CBmvBZBwsBt-HHL6cx8HjF51yDM5nSNl5PeActU8u4-xGwNr3-E9vAXEE3bnB5eU-2rF6SHDwU6fo-eZ6fnVXPTze3l9dPlSGyTpX0DVc8oa0wAXXllBjiOkIsdCBFpyBabuealMardFGGg0N73tbXoLxEmCKjjd7FzG8f5SfqNElA8OgPYSPpKiQbNbWpIBiA5oYUopg1SK6UcelokStHKq1Q7USpIhUa4eqLnNHPwd0MnqwJb9x6XeYccFo0xbsYoNBCfvpIKpkHHgDvYtFrOqD--fQN48uiA8</recordid><startdate>1995</startdate><enddate>1995</enddate><creator>Jennings, G.</creator><creator>Lunn, P.G.</creator><creator>Elia, M.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>1995</creationdate><title>The effect of endotoxin on gastrointestinal transit time and intestinal permeability</title><author>Jennings, G. ; Lunn, P.G. ; Elia, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-eb8464809e454af01cc0cb00febea543ec9bd1ac01c9cac6cae84ddfc6c534053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Bacterial diseases</topic><topic>Bacterial diseases of the digestive system and abdomen</topic><topic>Biological and medical sciences</topic><topic>Escherichia coli</topic><topic>Human bacterial diseases</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jennings, G.</creatorcontrib><creatorcontrib>Lunn, P.G.</creatorcontrib><creatorcontrib>Elia, M.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Clinical nutrition (Edinburgh, Scotland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jennings, G.</au><au>Lunn, P.G.</au><au>Elia, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of endotoxin on gastrointestinal transit time and intestinal permeability</atitle><jtitle>Clinical nutrition (Edinburgh, Scotland)</jtitle><date>1995</date><risdate>1995</risdate><volume>14</volume><issue>1</issue><spage>35</spage><epage>41</epage><pages>35-41</pages><issn>0261-5614</issn><eissn>1532-1983</eissn><coden>CLNUDP</coden><abstract>Acute changes in gastrointestinal transit time, creatinine clearance and dual sugar (lactulose/mannitol) intestinal permeability have been assessed following endotoxin administration (
E. coli 0111:134, phenol extract) to 6 week old rats. Monitoring the progress of orally administered
51Cr-EDTA through the digestive tract showed that, compared to saline injected controls, stomach emptying was considerably delayed in endotoxin treated animals (t 1/2 = 26 ± 2 vs 162 ± 20 min (p < 0.01), but transit time through the small intestine was not significantly altered (81 ± 17 v 93 ± 29 min).
Intestinal permeability assessed by the ratio of lactulose to mannitol excretion in urine was higher in endotoxin compared to saline injected rats, 1.01 ± 0.08 vs 0.60 ± 0.04 (p < 0.01). After correcting the individual sugar excretion to take into account the amount of marker available to the small intestine for absorption during the test period, it was concluded that endotoxin treatment was associated with increased lactulose uptake but no change in mannitol absorption. The study also shows that endotoxaemia, uncomplicated by drug administration or other therapeutic manoeuvres, can markedly delay gastric emptying, which is associated with intolerance to oral or nasogastric feeding.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/S0261-5614(06)80008-7</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0261-5614 |
ispartof | Clinical nutrition (Edinburgh, Scotland), 1995, Vol.14 (1), p.35-41 |
issn | 0261-5614 1532-1983 |
language | eng |
recordid | cdi_proquest_miscellaneous_15632970 |
source | Access via ScienceDirect (Elsevier) |
subjects | Bacterial diseases Bacterial diseases of the digestive system and abdomen Biological and medical sciences Escherichia coli Human bacterial diseases Infectious diseases Medical sciences |
title | The effect of endotoxin on gastrointestinal transit time and intestinal permeability |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T09%3A29%3A34IST&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=The%20effect%20of%20endotoxin%20on%20gastrointestinal%20transit%20time%20and%20intestinal%20permeability&rft.jtitle=Clinical%20nutrition%20(Edinburgh,%20Scotland)&rft.au=Jennings,%20G.&rft.date=1995&rft.volume=14&rft.issue=1&rft.spage=35&rft.epage=41&rft.pages=35-41&rft.issn=0261-5614&rft.eissn=1532-1983&rft.coden=CLNUDP&rft_id=info:doi/10.1016/S0261-5614(06)80008-7&rft_dat=%3Cproquest_cross%3E15632970%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=15632970&rft_id=info:pmid/&rft_els_id=S0261561406800087&rfr_iscdi=true |