Human gallbladder mucosal function : Effects on intraluminal fluid and lipid composition in health and disease

Gallbladder mucosal absorption of fluid during fasting is a well-known process. Indirect in vivo and recent in vitro evidence for physiologically relevant gallbladder absorption of cholesterol and phospholipids from bile has been observed in humans. The present study explored and compared by indirec...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Digestive diseases and sciences 1998-02, Vol.43 (2), p.335-343
Hauptverfasser: CORRADINI, S. G, YAMASHITA, G, CAPOCACCIA, L, HOLZBACH, R. T, NUUTINEN, H, CHERNOSKY, A, WILLIAMS, C, HAYS, L, SHIFFMAN, M. L, WILLIAMS, R. M, SVANVIK, J, DELLA GUARDIA, P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 343
container_issue 2
container_start_page 335
container_title Digestive diseases and sciences
container_volume 43
creator CORRADINI, S. G
YAMASHITA, G
CAPOCACCIA, L
HOLZBACH, R. T
NUUTINEN, H
CHERNOSKY, A
WILLIAMS, C
HAYS, L
SHIFFMAN, M. L
WILLIAMS, R. M
SVANVIK, J
DELLA GUARDIA, P
description Gallbladder mucosal absorption of fluid during fasting is a well-known process. Indirect in vivo and recent in vitro evidence for physiologically relevant gallbladder absorption of cholesterol and phospholipids from bile has been observed in humans. The present study explored and compared by indirect means the relative efficiences of human gallbladder mucosal absorption of fluid and lipids in health and disease. Biliary lipids and pigment content were measured in fasting gallbladder bile samples obtained from gallstone-free controls and from four study groups: multiple and solitary cholesterol gallstone patients, and morbidly obese subjects with and without gallstones. Bile salts and pigment content were significantly greater in gallstone-free controls than in all other disease study groups. This was interpreted as evidence of more effective gallbladder mucosal fluid absorption in nonobese gallstone-free controls compared to that in all other groups. Correlation plot analyses of biliary lipids showed lower concentrations of phospholipids than expected from the index bile salt concentrations. The same was found for cholesterol concentrations but only in supersaturated samples. These findings were much more pronounced in gallstone free-controls and were accordingly interpreted as evidence of more efficient gallbladder absorption of both phospholipids and cholesterol in controls compared with that found in each of the disease study groups. Moreover, impaired gallbladder mucosal function, while invariably associated with cholesterol gallstone disease, was not found to be a necessary consequence of the physical presence of stones. It is concluded that efficient gallbladder mucosal absorption of both fluid and apolar lipids from bile is a normal physiological process that is often seriously impaired in the presence of either cholesterol gallstone disease or at least one of its precursor forms.
doi_str_mv 10.1023/A:1018858406560
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_79737681</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>404184281</sourcerecordid><originalsourceid>FETCH-LOGICAL-c310t-998247477de5795a4a2ee69f17d38c6d2b8f74e43007d24a114f8d493af2b6d43</originalsourceid><addsrcrecordid>eNpdkL1PHDEQxS0EIhegThXJQlG6A4_t9QcdQgSQkGigXs35Ixh5vcd6XfDfs5ATRap5o_eb0Zsh5AewM2BcnF9eAANjOiOZ6hTbIyvotFjzTpl9smKgFg2gvpHvtb4wxqwGdUgObQccuF6RctsGLPQv5rzJ6H2Y6NDcWDHT2Iqb01joBb2OMbi50qVJZZ4wtyGVDyS35CkWT3PaLsqNw3as6XMqFfocMM_Pn75PNWANx-QgYq7hZFePyNOf68er2_X9w83d1eX92glg89paw6WWWvvQaduhRB6CshG0F8YpzzcmahmkYEx7LhFARuOlFRj5Rnkpjsjvf3u30_jaQp37IVUXcsYSxlZ7bbXQysACnv4HvoxtWm6rPQcpljTyA_q5g9pmCL7fTmnA6a3ffXHxf-18rA5znLC4VL8wDpbpToh3_IyALQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>214331041</pqid></control><display><type>article</type><title>Human gallbladder mucosal function : Effects on intraluminal fluid and lipid composition in health and disease</title><source>MEDLINE</source><source>SpringerNature Complete Journals</source><creator>CORRADINI, S. G ; YAMASHITA, G ; CAPOCACCIA, L ; HOLZBACH, R. T ; NUUTINEN, H ; CHERNOSKY, A ; WILLIAMS, C ; HAYS, L ; SHIFFMAN, M. L ; WILLIAMS, R. M ; SVANVIK, J ; DELLA GUARDIA, P</creator><creatorcontrib>CORRADINI, S. G ; YAMASHITA, G ; CAPOCACCIA, L ; HOLZBACH, R. T ; NUUTINEN, H ; CHERNOSKY, A ; WILLIAMS, C ; HAYS, L ; SHIFFMAN, M. L ; WILLIAMS, R. M ; SVANVIK, J ; DELLA GUARDIA, P</creatorcontrib><description>Gallbladder mucosal absorption of fluid during fasting is a well-known process. Indirect in vivo and recent in vitro evidence for physiologically relevant gallbladder absorption of cholesterol and phospholipids from bile has been observed in humans. The present study explored and compared by indirect means the relative efficiences of human gallbladder mucosal absorption of fluid and lipids in health and disease. Biliary lipids and pigment content were measured in fasting gallbladder bile samples obtained from gallstone-free controls and from four study groups: multiple and solitary cholesterol gallstone patients, and morbidly obese subjects with and without gallstones. Bile salts and pigment content were significantly greater in gallstone-free controls than in all other disease study groups. This was interpreted as evidence of more effective gallbladder mucosal fluid absorption in nonobese gallstone-free controls compared to that in all other groups. Correlation plot analyses of biliary lipids showed lower concentrations of phospholipids than expected from the index bile salt concentrations. The same was found for cholesterol concentrations but only in supersaturated samples. These findings were much more pronounced in gallstone free-controls and were accordingly interpreted as evidence of more efficient gallbladder absorption of both phospholipids and cholesterol in controls compared with that found in each of the disease study groups. Moreover, impaired gallbladder mucosal function, while invariably associated with cholesterol gallstone disease, was not found to be a necessary consequence of the physical presence of stones. It is concluded that efficient gallbladder mucosal absorption of both fluid and apolar lipids from bile is a normal physiological process that is often seriously impaired in the presence of either cholesterol gallstone disease or at least one of its precursor forms.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1023/A:1018858406560</identifier><identifier>PMID: 9512127</identifier><identifier>CODEN: DDSCDJ</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Absorption ; Adult ; Bile - chemistry ; Bile - metabolism ; Bile Acids and Salts - metabolism ; Biological and medical sciences ; Cholelithiasis - complications ; Cholelithiasis - metabolism ; Fasting - metabolism ; Female ; Fundamental and applied biological sciences. Psychology ; Gallbladder - metabolism ; Humans ; Lipid Metabolism ; Liver. Bile. Biliary tracts ; Male ; Middle Aged ; Mucous Membrane - metabolism ; Obesity, Morbid - complications ; Obesity, Morbid - metabolism ; Phospholipids - metabolism ; Regression Analysis ; Vertebrates: digestive system</subject><ispartof>Digestive diseases and sciences, 1998-02, Vol.43 (2), p.335-343</ispartof><rights>1998 INIST-CNRS</rights><rights>Copyright Kluwer Academic Publishers Feb 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c310t-998247477de5795a4a2ee69f17d38c6d2b8f74e43007d24a114f8d493af2b6d43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2190753$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9512127$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CORRADINI, S. G</creatorcontrib><creatorcontrib>YAMASHITA, G</creatorcontrib><creatorcontrib>CAPOCACCIA, L</creatorcontrib><creatorcontrib>HOLZBACH, R. T</creatorcontrib><creatorcontrib>NUUTINEN, H</creatorcontrib><creatorcontrib>CHERNOSKY, A</creatorcontrib><creatorcontrib>WILLIAMS, C</creatorcontrib><creatorcontrib>HAYS, L</creatorcontrib><creatorcontrib>SHIFFMAN, M. L</creatorcontrib><creatorcontrib>WILLIAMS, R. M</creatorcontrib><creatorcontrib>SVANVIK, J</creatorcontrib><creatorcontrib>DELLA GUARDIA, P</creatorcontrib><title>Human gallbladder mucosal function : Effects on intraluminal fluid and lipid composition in health and disease</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><description>Gallbladder mucosal absorption of fluid during fasting is a well-known process. Indirect in vivo and recent in vitro evidence for physiologically relevant gallbladder absorption of cholesterol and phospholipids from bile has been observed in humans. The present study explored and compared by indirect means the relative efficiences of human gallbladder mucosal absorption of fluid and lipids in health and disease. Biliary lipids and pigment content were measured in fasting gallbladder bile samples obtained from gallstone-free controls and from four study groups: multiple and solitary cholesterol gallstone patients, and morbidly obese subjects with and without gallstones. Bile salts and pigment content were significantly greater in gallstone-free controls than in all other disease study groups. This was interpreted as evidence of more effective gallbladder mucosal fluid absorption in nonobese gallstone-free controls compared to that in all other groups. Correlation plot analyses of biliary lipids showed lower concentrations of phospholipids than expected from the index bile salt concentrations. The same was found for cholesterol concentrations but only in supersaturated samples. These findings were much more pronounced in gallstone free-controls and were accordingly interpreted as evidence of more efficient gallbladder absorption of both phospholipids and cholesterol in controls compared with that found in each of the disease study groups. Moreover, impaired gallbladder mucosal function, while invariably associated with cholesterol gallstone disease, was not found to be a necessary consequence of the physical presence of stones. It is concluded that efficient gallbladder mucosal absorption of both fluid and apolar lipids from bile is a normal physiological process that is often seriously impaired in the presence of either cholesterol gallstone disease or at least one of its precursor forms.</description><subject>Absorption</subject><subject>Adult</subject><subject>Bile - chemistry</subject><subject>Bile - metabolism</subject><subject>Bile Acids and Salts - metabolism</subject><subject>Biological and medical sciences</subject><subject>Cholelithiasis - complications</subject><subject>Cholelithiasis - metabolism</subject><subject>Fasting - metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gallbladder - metabolism</subject><subject>Humans</subject><subject>Lipid Metabolism</subject><subject>Liver. Bile. Biliary tracts</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mucous Membrane - metabolism</subject><subject>Obesity, Morbid - complications</subject><subject>Obesity, Morbid - metabolism</subject><subject>Phospholipids - metabolism</subject><subject>Regression Analysis</subject><subject>Vertebrates: digestive system</subject><issn>0163-2116</issn><issn>1573-2568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkL1PHDEQxS0EIhegThXJQlG6A4_t9QcdQgSQkGigXs35Ixh5vcd6XfDfs5ATRap5o_eb0Zsh5AewM2BcnF9eAANjOiOZ6hTbIyvotFjzTpl9smKgFg2gvpHvtb4wxqwGdUgObQccuF6RctsGLPQv5rzJ6H2Y6NDcWDHT2Iqb01joBb2OMbi50qVJZZ4wtyGVDyS35CkWT3PaLsqNw3as6XMqFfocMM_Pn75PNWANx-QgYq7hZFePyNOf68er2_X9w83d1eX92glg89paw6WWWvvQaduhRB6CshG0F8YpzzcmahmkYEx7LhFARuOlFRj5Rnkpjsjvf3u30_jaQp37IVUXcsYSxlZ7bbXQysACnv4HvoxtWm6rPQcpljTyA_q5g9pmCL7fTmnA6a3ffXHxf-18rA5znLC4VL8wDpbpToh3_IyALQ</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>CORRADINI, S. G</creator><creator>YAMASHITA, G</creator><creator>CAPOCACCIA, L</creator><creator>HOLZBACH, R. T</creator><creator>NUUTINEN, H</creator><creator>CHERNOSKY, A</creator><creator>WILLIAMS, C</creator><creator>HAYS, L</creator><creator>SHIFFMAN, M. L</creator><creator>WILLIAMS, R. M</creator><creator>SVANVIK, J</creator><creator>DELLA GUARDIA, P</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>19980201</creationdate><title>Human gallbladder mucosal function : Effects on intraluminal fluid and lipid composition in health and disease</title><author>CORRADINI, S. G ; YAMASHITA, G ; CAPOCACCIA, L ; HOLZBACH, R. T ; NUUTINEN, H ; CHERNOSKY, A ; WILLIAMS, C ; HAYS, L ; SHIFFMAN, M. L ; WILLIAMS, R. M ; SVANVIK, J ; DELLA GUARDIA, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-998247477de5795a4a2ee69f17d38c6d2b8f74e43007d24a114f8d493af2b6d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Absorption</topic><topic>Adult</topic><topic>Bile - chemistry</topic><topic>Bile - metabolism</topic><topic>Bile Acids and Salts - metabolism</topic><topic>Biological and medical sciences</topic><topic>Cholelithiasis - complications</topic><topic>Cholelithiasis - metabolism</topic><topic>Fasting - metabolism</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gallbladder - metabolism</topic><topic>Humans</topic><topic>Lipid Metabolism</topic><topic>Liver. Bile. Biliary tracts</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mucous Membrane - metabolism</topic><topic>Obesity, Morbid - complications</topic><topic>Obesity, Morbid - metabolism</topic><topic>Phospholipids - metabolism</topic><topic>Regression Analysis</topic><topic>Vertebrates: digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CORRADINI, S. G</creatorcontrib><creatorcontrib>YAMASHITA, G</creatorcontrib><creatorcontrib>CAPOCACCIA, L</creatorcontrib><creatorcontrib>HOLZBACH, R. T</creatorcontrib><creatorcontrib>NUUTINEN, H</creatorcontrib><creatorcontrib>CHERNOSKY, A</creatorcontrib><creatorcontrib>WILLIAMS, C</creatorcontrib><creatorcontrib>HAYS, L</creatorcontrib><creatorcontrib>SHIFFMAN, M. L</creatorcontrib><creatorcontrib>WILLIAMS, R. M</creatorcontrib><creatorcontrib>SVANVIK, J</creatorcontrib><creatorcontrib>DELLA GUARDIA, P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing &amp; Allied Health Source</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma 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>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</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><jtitle>Digestive diseases and sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CORRADINI, S. G</au><au>YAMASHITA, G</au><au>CAPOCACCIA, L</au><au>HOLZBACH, R. T</au><au>NUUTINEN, H</au><au>CHERNOSKY, A</au><au>WILLIAMS, C</au><au>HAYS, L</au><au>SHIFFMAN, M. L</au><au>WILLIAMS, R. M</au><au>SVANVIK, J</au><au>DELLA GUARDIA, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human gallbladder mucosal function : Effects on intraluminal fluid and lipid composition in health and disease</atitle><jtitle>Digestive diseases and sciences</jtitle><addtitle>Dig Dis Sci</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>43</volume><issue>2</issue><spage>335</spage><epage>343</epage><pages>335-343</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><coden>DDSCDJ</coden><abstract>Gallbladder mucosal absorption of fluid during fasting is a well-known process. Indirect in vivo and recent in vitro evidence for physiologically relevant gallbladder absorption of cholesterol and phospholipids from bile has been observed in humans. The present study explored and compared by indirect means the relative efficiences of human gallbladder mucosal absorption of fluid and lipids in health and disease. Biliary lipids and pigment content were measured in fasting gallbladder bile samples obtained from gallstone-free controls and from four study groups: multiple and solitary cholesterol gallstone patients, and morbidly obese subjects with and without gallstones. Bile salts and pigment content were significantly greater in gallstone-free controls than in all other disease study groups. This was interpreted as evidence of more effective gallbladder mucosal fluid absorption in nonobese gallstone-free controls compared to that in all other groups. Correlation plot analyses of biliary lipids showed lower concentrations of phospholipids than expected from the index bile salt concentrations. The same was found for cholesterol concentrations but only in supersaturated samples. These findings were much more pronounced in gallstone free-controls and were accordingly interpreted as evidence of more efficient gallbladder absorption of both phospholipids and cholesterol in controls compared with that found in each of the disease study groups. Moreover, impaired gallbladder mucosal function, while invariably associated with cholesterol gallstone disease, was not found to be a necessary consequence of the physical presence of stones. It is concluded that efficient gallbladder mucosal absorption of both fluid and apolar lipids from bile is a normal physiological process that is often seriously impaired in the presence of either cholesterol gallstone disease or at least one of its precursor forms.</abstract><cop>Heidelberg</cop><pub>Springer</pub><pmid>9512127</pmid><doi>10.1023/A:1018858406560</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0163-2116
ispartof Digestive diseases and sciences, 1998-02, Vol.43 (2), p.335-343
issn 0163-2116
1573-2568
language eng
recordid cdi_proquest_miscellaneous_79737681
source MEDLINE; SpringerNature Complete Journals
subjects Absorption
Adult
Bile - chemistry
Bile - metabolism
Bile Acids and Salts - metabolism
Biological and medical sciences
Cholelithiasis - complications
Cholelithiasis - metabolism
Fasting - metabolism
Female
Fundamental and applied biological sciences. Psychology
Gallbladder - metabolism
Humans
Lipid Metabolism
Liver. Bile. Biliary tracts
Male
Middle Aged
Mucous Membrane - metabolism
Obesity, Morbid - complications
Obesity, Morbid - metabolism
Phospholipids - metabolism
Regression Analysis
Vertebrates: digestive system
title Human gallbladder mucosal function : Effects on intraluminal fluid and lipid composition in health and disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T14%3A06%3A06IST&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=Human%20gallbladder%20mucosal%20function%20:%20Effects%20on%20intraluminal%20fluid%20and%20lipid%20composition%20in%20health%20and%20disease&rft.jtitle=Digestive%20diseases%20and%20sciences&rft.au=CORRADINI,%20S.%20G&rft.date=1998-02-01&rft.volume=43&rft.issue=2&rft.spage=335&rft.epage=343&rft.pages=335-343&rft.issn=0163-2116&rft.eissn=1573-2568&rft.coden=DDSCDJ&rft_id=info:doi/10.1023/A:1018858406560&rft_dat=%3Cproquest_pubme%3E404184281%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=214331041&rft_id=info:pmid/9512127&rfr_iscdi=true