Serum plant sterols and biliary cholesterol secretion in humans: studies with ursodeoxycholic acid
Ratios of cholestanol, campesterol, and sitosterol to cholesterol in serum are known to reflect cholesterol absorption efficiency. Here, a possible link between these ratios and biliary secretion rates of cholesterol was investigated. Biliary lipid secretion rates and serum sterols were determined i...
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Veröffentlicht in: | Journal of lipid research 2002-07, Vol.43 (7), p.1072-1077 |
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creator | Lindenthal, Bernhard Sudhop, Thomas Schiedermaier, Peter Agnan, Mohamed Sauerbruch, Tilman von Bergmann, Klaus |
description | Ratios of cholestanol, campesterol, and sitosterol to cholesterol in serum are known to reflect cholesterol absorption efficiency. Here, a possible link between these ratios and biliary secretion rates of cholesterol was investigated. Biliary lipid secretion rates and serum sterols were determined in 13 patients with gallstones. Seven were treated with ursodeoxycholic acid (UDCA) (1,000 mg/d). Serum cholesterol and non-cholesterol sterols were also measured in a cross over study in 20 healthy volunteers, who received either placebo or UDCA (750 mg/d). Biliary cholesterol secretion was significantly lower, whereas the non-cholesterol sterols and their ratio to cholesterol were higher in patients with gallstones treated with UDCA. A highly significant negative linear correlation between the ratios of non-cholesterol sterols to cholesterol and biliary cholesterol secretion was observed. In volunteers, administration of UDCA for 4 weeks was followed by a significant increase in non-cholesterol sterols and their ratios. Even 4 weeks after discontinuing UDCA administration, campesterol and sitosterol were still significantly higher than pretreatment levels, which was also true for the campesterol-cholesterol ratio after 8 weeks. The results suggest that the ratios of cholestanol, campesterol, and sitosterol to cholesterol can be used as indicators of changes in biliary cholesterol secretion rates. |
doi_str_mv | 10.1194/jlr.M100438-JLR200 |
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Here, a possible link between these ratios and biliary secretion rates of cholesterol was investigated. Biliary lipid secretion rates and serum sterols were determined in 13 patients with gallstones. Seven were treated with ursodeoxycholic acid (UDCA) (1,000 mg/d). Serum cholesterol and non-cholesterol sterols were also measured in a cross over study in 20 healthy volunteers, who received either placebo or UDCA (750 mg/d). Biliary cholesterol secretion was significantly lower, whereas the non-cholesterol sterols and their ratio to cholesterol were higher in patients with gallstones treated with UDCA. A highly significant negative linear correlation between the ratios of non-cholesterol sterols to cholesterol and biliary cholesterol secretion was observed. In volunteers, administration of UDCA for 4 weeks was followed by a significant increase in non-cholesterol sterols and their ratios. Even 4 weeks after discontinuing UDCA administration, campesterol and sitosterol were still significantly higher than pretreatment levels, which was also true for the campesterol-cholesterol ratio after 8 weeks. The results suggest that the ratios of cholestanol, campesterol, and sitosterol to cholesterol can be used as indicators of changes in biliary cholesterol secretion rates.</description><identifier>ISSN: 0022-2275</identifier><identifier>DOI: 10.1194/jlr.M100438-JLR200</identifier><identifier>PMID: 12091491</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Bile - chemistry ; Bile - drug effects ; Bile - metabolism ; Cholagogues and Choleretics - pharmacology ; Cholesterol - analogs & derivatives ; Cholesterol - blood ; Cholesterol - metabolism ; Female ; Humans ; Male ; Middle Aged ; Phytosterols - blood ; Sitosterols - blood ; Ursodeoxycholic Acid - pharmacology</subject><ispartof>Journal of lipid research, 2002-07, Vol.43 (7), p.1072-1077</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12091491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lindenthal, Bernhard</creatorcontrib><creatorcontrib>Sudhop, Thomas</creatorcontrib><creatorcontrib>Schiedermaier, Peter</creatorcontrib><creatorcontrib>Agnan, Mohamed</creatorcontrib><creatorcontrib>Sauerbruch, Tilman</creatorcontrib><creatorcontrib>von Bergmann, Klaus</creatorcontrib><title>Serum plant sterols and biliary cholesterol secretion in humans: studies with ursodeoxycholic acid</title><title>Journal of lipid research</title><addtitle>J Lipid Res</addtitle><description>Ratios of cholestanol, campesterol, and sitosterol to cholesterol in serum are known to reflect cholesterol absorption efficiency. Here, a possible link between these ratios and biliary secretion rates of cholesterol was investigated. Biliary lipid secretion rates and serum sterols were determined in 13 patients with gallstones. Seven were treated with ursodeoxycholic acid (UDCA) (1,000 mg/d). Serum cholesterol and non-cholesterol sterols were also measured in a cross over study in 20 healthy volunteers, who received either placebo or UDCA (750 mg/d). Biliary cholesterol secretion was significantly lower, whereas the non-cholesterol sterols and their ratio to cholesterol were higher in patients with gallstones treated with UDCA. A highly significant negative linear correlation between the ratios of non-cholesterol sterols to cholesterol and biliary cholesterol secretion was observed. In volunteers, administration of UDCA for 4 weeks was followed by a significant increase in non-cholesterol sterols and their ratios. Even 4 weeks after discontinuing UDCA administration, campesterol and sitosterol were still significantly higher than pretreatment levels, which was also true for the campesterol-cholesterol ratio after 8 weeks. The results suggest that the ratios of cholestanol, campesterol, and sitosterol to cholesterol can be used as indicators of changes in biliary cholesterol secretion rates.</description><subject>Adult</subject><subject>Bile - chemistry</subject><subject>Bile - drug effects</subject><subject>Bile - metabolism</subject><subject>Cholagogues and Choleretics - pharmacology</subject><subject>Cholesterol - analogs & derivatives</subject><subject>Cholesterol - blood</subject><subject>Cholesterol - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Phytosterols - blood</subject><subject>Sitosterols - blood</subject><subject>Ursodeoxycholic Acid - pharmacology</subject><issn>0022-2275</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kEtPwzAQhH0A0VL4AxyQT9xSvLbjxNxQxVNFSDzOkWM7iisnKXYs6L8nqOW00ux8q51B6ALIEkDy640PyxcghLMye16_UUKO0JwQSjNKi3yGTmPcEAKcCzhBM6BEApcwR_W7DanDW6_6EcfRhsFHrHqDa-edCjus28Hb_QJHq4Md3dBj1-M2daqPNxOUjLMRf7uxxSnEwdjhZ_eHOY2VduYMHTfKR3t-mAv0eX_3sXrM1q8PT6vbddZSxsasEQWVTCuhbEMNq7XK67qBQhvOQJbCGA60AJlDozUxjE66LI2xKgcuaM4W6Gp_dxuGrzT9XHUuauunaHZIsSqgFEQwmIyXB2OqO2uqbXDdFLX6b4X9AlJ2ZaQ</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>Lindenthal, Bernhard</creator><creator>Sudhop, Thomas</creator><creator>Schiedermaier, Peter</creator><creator>Agnan, Mohamed</creator><creator>Sauerbruch, Tilman</creator><creator>von Bergmann, Klaus</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20020701</creationdate><title>Serum plant sterols and biliary cholesterol secretion in humans: studies with ursodeoxycholic acid</title><author>Lindenthal, Bernhard ; Sudhop, Thomas ; Schiedermaier, Peter ; Agnan, Mohamed ; Sauerbruch, Tilman ; von Bergmann, Klaus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h233t-f67293ca6aef2d3bca5bbf17cd431986dd41271951fcc0d32d4398ddea5146253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Bile - chemistry</topic><topic>Bile - drug effects</topic><topic>Bile - metabolism</topic><topic>Cholagogues and Choleretics - pharmacology</topic><topic>Cholesterol - analogs & derivatives</topic><topic>Cholesterol - blood</topic><topic>Cholesterol - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Phytosterols - blood</topic><topic>Sitosterols - blood</topic><topic>Ursodeoxycholic Acid - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lindenthal, Bernhard</creatorcontrib><creatorcontrib>Sudhop, Thomas</creatorcontrib><creatorcontrib>Schiedermaier, Peter</creatorcontrib><creatorcontrib>Agnan, Mohamed</creatorcontrib><creatorcontrib>Sauerbruch, Tilman</creatorcontrib><creatorcontrib>von Bergmann, Klaus</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of lipid research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lindenthal, Bernhard</au><au>Sudhop, Thomas</au><au>Schiedermaier, Peter</au><au>Agnan, Mohamed</au><au>Sauerbruch, Tilman</au><au>von Bergmann, Klaus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum plant sterols and biliary cholesterol secretion in humans: studies with ursodeoxycholic acid</atitle><jtitle>Journal of lipid research</jtitle><addtitle>J Lipid Res</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>43</volume><issue>7</issue><spage>1072</spage><epage>1077</epage><pages>1072-1077</pages><issn>0022-2275</issn><abstract>Ratios of cholestanol, campesterol, and sitosterol to cholesterol in serum are known to reflect cholesterol absorption efficiency. Here, a possible link between these ratios and biliary secretion rates of cholesterol was investigated. Biliary lipid secretion rates and serum sterols were determined in 13 patients with gallstones. Seven were treated with ursodeoxycholic acid (UDCA) (1,000 mg/d). Serum cholesterol and non-cholesterol sterols were also measured in a cross over study in 20 healthy volunteers, who received either placebo or UDCA (750 mg/d). Biliary cholesterol secretion was significantly lower, whereas the non-cholesterol sterols and their ratio to cholesterol were higher in patients with gallstones treated with UDCA. A highly significant negative linear correlation between the ratios of non-cholesterol sterols to cholesterol and biliary cholesterol secretion was observed. In volunteers, administration of UDCA for 4 weeks was followed by a significant increase in non-cholesterol sterols and their ratios. Even 4 weeks after discontinuing UDCA administration, campesterol and sitosterol were still significantly higher than pretreatment levels, which was also true for the campesterol-cholesterol ratio after 8 weeks. The results suggest that the ratios of cholestanol, campesterol, and sitosterol to cholesterol can be used as indicators of changes in biliary cholesterol secretion rates.</abstract><cop>United States</cop><pmid>12091491</pmid><doi>10.1194/jlr.M100438-JLR200</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Bile - chemistry Bile - drug effects Bile - metabolism Cholagogues and Choleretics - pharmacology Cholesterol - analogs & derivatives Cholesterol - blood Cholesterol - metabolism Female Humans Male Middle Aged Phytosterols - blood Sitosterols - blood Ursodeoxycholic Acid - pharmacology |
title | Serum plant sterols and biliary cholesterol secretion in humans: studies with ursodeoxycholic acid |
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