Bile acid profiles within the enterohepatic circulation in a diabetic rat model after bariatric surgeries
Bile acids (BAs), which are synthesized in the liver and cycled in the enterohepatic circulation, have been recognized as signaling molecules by activating their receptors in the intestine and liver. Serum taurine-conjugated BAs have been shown to be elevated after bariatric surgeries although the p...
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Veröffentlicht in: | American journal of physiology: Gastrointestinal and liver physiology 2018-05, Vol.314 (5), p.G537-G546 |
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description | Bile acids (BAs), which are synthesized in the liver and cycled in the enterohepatic circulation, have been recognized as signaling molecules by activating their receptors in the intestine and liver. Serum taurine-conjugated BAs have been shown to be elevated after bariatric surgeries although the postoperative BA profiles within the enterohepatic circulation have not been investigated. Clarification of these profiles could help explain the mechanisms by which bariatric surgery leads to BA profile alterations and subsequent metabolic effects. We performed duodenal-jejunal bypass (DJB), sleeve gastrectomy (SG), and sham procedures in an obese diabetic rat model induced by high-fat diet and streptozotocin. The weight loss and antidiabetic effects were evaluated postsurgery. BA profiles in the systemic serum and within the enterohepatic circulation were analyzed, together with the expression of related BA transporters and enzymes at week 12 after surgery. Compared with sham, SG induced sustained weight loss, and both DJB and SG significantly improved glucose tolerance and insulin sensitivity with enhanced glucagon-like peptide 1 secretion. Similar to changes in the serum, BAs, especially taurine-conjugated species, were also elevated in the enterohepatic circulation (bile and portal vein) after DJB and SG. In addition, the expression of key BA transporters and conjugational enzymes was elevated postoperatively, whereas the enzymes responsible for BA synthesis were decreased. In conclusion, DJB and SG elevated BA levels in the systemic serum and enterohepatic circulation, especially taurine-conjugated species, which likely indicates increased ileal reabsorption and hepatic conjugation rather than synthesis. NEW & NOTEWORTHY Bile acids (BAs) have been implicated as potential mediators of the weight-independent effects of bariatric surgery. For the first time, we discovered that duodenal-jejunal bypass and sleeve gastrectomy elevated BAs, particularly the taurine-conjugated species in the enterohepatic circulation, likely through the promotion of ileal reabsorption and hepatic conjugation rather than BA synthesis. These findings will improve our understanding of BA metabolism after bariatric surgery and their subsequent metabolic effects. |
doi_str_mv | 10.1152/ajpgi.00311.2017 |
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Serum taurine-conjugated BAs have been shown to be elevated after bariatric surgeries although the postoperative BA profiles within the enterohepatic circulation have not been investigated. Clarification of these profiles could help explain the mechanisms by which bariatric surgery leads to BA profile alterations and subsequent metabolic effects. We performed duodenal-jejunal bypass (DJB), sleeve gastrectomy (SG), and sham procedures in an obese diabetic rat model induced by high-fat diet and streptozotocin. The weight loss and antidiabetic effects were evaluated postsurgery. BA profiles in the systemic serum and within the enterohepatic circulation were analyzed, together with the expression of related BA transporters and enzymes at week 12 after surgery. Compared with sham, SG induced sustained weight loss, and both DJB and SG significantly improved glucose tolerance and insulin sensitivity with enhanced glucagon-like peptide 1 secretion. Similar to changes in the serum, BAs, especially taurine-conjugated species, were also elevated in the enterohepatic circulation (bile and portal vein) after DJB and SG. In addition, the expression of key BA transporters and conjugational enzymes was elevated postoperatively, whereas the enzymes responsible for BA synthesis were decreased. In conclusion, DJB and SG elevated BA levels in the systemic serum and enterohepatic circulation, especially taurine-conjugated species, which likely indicates increased ileal reabsorption and hepatic conjugation rather than synthesis. NEW & NOTEWORTHY Bile acids (BAs) have been implicated as potential mediators of the weight-independent effects of bariatric surgery. For the first time, we discovered that duodenal-jejunal bypass and sleeve gastrectomy elevated BAs, particularly the taurine-conjugated species in the enterohepatic circulation, likely through the promotion of ileal reabsorption and hepatic conjugation rather than BA synthesis. These findings will improve our understanding of BA metabolism after bariatric surgery and their subsequent metabolic effects.</description><identifier>ISSN: 0193-1857</identifier><identifier>EISSN: 1522-1547</identifier><identifier>DOI: 10.1152/ajpgi.00311.2017</identifier><identifier>PMID: 29351394</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Bariatric Surgery - adverse effects ; Bariatric Surgery - classification ; Bariatric Surgery - methods ; Bile ; Bile acids ; Bile Acids and Salts - blood ; Bile Acids and Salts - metabolism ; Blood Glucose - metabolism ; Body Weight - physiology ; Body weight loss ; Diabetes mellitus ; Diabetes Mellitus, Experimental - metabolism ; Diabetes Mellitus, Type 2 ; Enterohepatic Circulation - physiology ; Enzymes ; Gastrectomy ; Gastrointestinal surgery ; Glucagon ; Glucagon-like peptide 1 ; Glucose tolerance ; High fat diet ; Insulin ; Insulin Resistance ; Intestinal Reabsorption - physiology ; Intestine ; Liver ; Metabolism ; Molecules ; Obesity - metabolism ; Obesity - physiopathology ; Obesity - surgery ; Portal vein ; Postoperative Complications - metabolism ; Rats ; Reabsorption ; Streptozocin ; Surgery ; Taurine ; Taurine - metabolism</subject><ispartof>American journal of physiology: Gastrointestinal and liver physiology, 2018-05, Vol.314 (5), p.G537-G546</ispartof><rights>Copyright American Physiological Society May 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-6ed6748597c610c23dc43501638e5a6559917145f7de10ea43a73ad161d6e7e63</citedby><cites>FETCH-LOGICAL-c435t-6ed6748597c610c23dc43501638e5a6559917145f7de10ea43a73ad161d6e7e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29351394$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wei, Meng</creatorcontrib><creatorcontrib>Shao, Yi</creatorcontrib><creatorcontrib>Liu, Qiao-Ran</creatorcontrib><creatorcontrib>Wu, Qun-Zheng</creatorcontrib><creatorcontrib>Zhang, Xiang</creatorcontrib><creatorcontrib>Zhong, Ming-Wei</creatorcontrib><creatorcontrib>Liu, Shao-Zhuang</creatorcontrib><creatorcontrib>Zhang, Guang-Yong</creatorcontrib><creatorcontrib>Hu, San-Yuan</creatorcontrib><title>Bile acid profiles within the enterohepatic circulation in a diabetic rat model after bariatric surgeries</title><title>American journal of physiology: Gastrointestinal and liver physiology</title><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><description>Bile acids (BAs), which are synthesized in the liver and cycled in the enterohepatic circulation, have been recognized as signaling molecules by activating their receptors in the intestine and liver. Serum taurine-conjugated BAs have been shown to be elevated after bariatric surgeries although the postoperative BA profiles within the enterohepatic circulation have not been investigated. Clarification of these profiles could help explain the mechanisms by which bariatric surgery leads to BA profile alterations and subsequent metabolic effects. We performed duodenal-jejunal bypass (DJB), sleeve gastrectomy (SG), and sham procedures in an obese diabetic rat model induced by high-fat diet and streptozotocin. The weight loss and antidiabetic effects were evaluated postsurgery. BA profiles in the systemic serum and within the enterohepatic circulation were analyzed, together with the expression of related BA transporters and enzymes at week 12 after surgery. Compared with sham, SG induced sustained weight loss, and both DJB and SG significantly improved glucose tolerance and insulin sensitivity with enhanced glucagon-like peptide 1 secretion. Similar to changes in the serum, BAs, especially taurine-conjugated species, were also elevated in the enterohepatic circulation (bile and portal vein) after DJB and SG. In addition, the expression of key BA transporters and conjugational enzymes was elevated postoperatively, whereas the enzymes responsible for BA synthesis were decreased. In conclusion, DJB and SG elevated BA levels in the systemic serum and enterohepatic circulation, especially taurine-conjugated species, which likely indicates increased ileal reabsorption and hepatic conjugation rather than synthesis. NEW & NOTEWORTHY Bile acids (BAs) have been implicated as potential mediators of the weight-independent effects of bariatric surgery. For the first time, we discovered that duodenal-jejunal bypass and sleeve gastrectomy elevated BAs, particularly the taurine-conjugated species in the enterohepatic circulation, likely through the promotion of ileal reabsorption and hepatic conjugation rather than BA synthesis. These findings will improve our understanding of BA metabolism after bariatric surgery and their subsequent metabolic effects.</description><subject>Animals</subject><subject>Bariatric Surgery - adverse effects</subject><subject>Bariatric Surgery - classification</subject><subject>Bariatric Surgery - methods</subject><subject>Bile</subject><subject>Bile acids</subject><subject>Bile Acids and Salts - blood</subject><subject>Bile Acids and Salts - metabolism</subject><subject>Blood Glucose - metabolism</subject><subject>Body Weight - physiology</subject><subject>Body weight loss</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Enterohepatic Circulation - physiology</subject><subject>Enzymes</subject><subject>Gastrectomy</subject><subject>Gastrointestinal surgery</subject><subject>Glucagon</subject><subject>Glucagon-like peptide 1</subject><subject>Glucose tolerance</subject><subject>High fat diet</subject><subject>Insulin</subject><subject>Insulin Resistance</subject><subject>Intestinal Reabsorption - physiology</subject><subject>Intestine</subject><subject>Liver</subject><subject>Metabolism</subject><subject>Molecules</subject><subject>Obesity - metabolism</subject><subject>Obesity - physiopathology</subject><subject>Obesity - surgery</subject><subject>Portal vein</subject><subject>Postoperative Complications - metabolism</subject><subject>Rats</subject><subject>Reabsorption</subject><subject>Streptozocin</subject><subject>Surgery</subject><subject>Taurine</subject><subject>Taurine - metabolism</subject><issn>0193-1857</issn><issn>1522-1547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkctPwzAMxiMEgvG4c0KRuHDpiJsmaY4w8ZKQuMA5yhJ3y9S1I2mF-O_JxuPAybH9-yzHHyHnwKYAory2q80iTBnjANOSgdojk1wuCxCV2icTBpoXUAt1RI5TWjHGRAlwSI5KzQVwXU1IuA0tUuuCp5vYNzlJ9CMMy9DRYYkUuwFjv8SNHYKjLkQ3tvnZdzQDlvpg57jtRDvQde-xpbbJCjq3Mdgh5k4a4wJjwHRKDhrbJjz7iSfk7f7udfZYPL88PM1ungtXcTEUEr1UVS20chKYK7nf1hlIXqOwUgitQUElGuURGNqKW8WtBwleokLJT8jV99z8n_cR02DWITlsW9thPyYDutairvOdMnr5D131Y-zydqZkSkhZ6brOFPumXOxTitiYTQxrGz8NMLO1wexsMDsbzNaGLLn4GTzO1-j_BL935188xYOK</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Wei, Meng</creator><creator>Shao, Yi</creator><creator>Liu, Qiao-Ran</creator><creator>Wu, Qun-Zheng</creator><creator>Zhang, Xiang</creator><creator>Zhong, Ming-Wei</creator><creator>Liu, Shao-Zhuang</creator><creator>Zhang, Guang-Yong</creator><creator>Hu, San-Yuan</creator><general>American Physiological Society</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>7X8</scope></search><sort><creationdate>20180501</creationdate><title>Bile acid profiles within the enterohepatic circulation in a diabetic rat model after bariatric surgeries</title><author>Wei, Meng ; Shao, Yi ; Liu, Qiao-Ran ; Wu, Qun-Zheng ; Zhang, Xiang ; Zhong, Ming-Wei ; Liu, Shao-Zhuang ; Zhang, Guang-Yong ; Hu, San-Yuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-6ed6748597c610c23dc43501638e5a6559917145f7de10ea43a73ad161d6e7e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Bariatric Surgery - adverse effects</topic><topic>Bariatric Surgery - classification</topic><topic>Bariatric Surgery - methods</topic><topic>Bile</topic><topic>Bile acids</topic><topic>Bile Acids and Salts - blood</topic><topic>Bile Acids and Salts - metabolism</topic><topic>Blood Glucose - metabolism</topic><topic>Body Weight - physiology</topic><topic>Body weight loss</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Enterohepatic Circulation - physiology</topic><topic>Enzymes</topic><topic>Gastrectomy</topic><topic>Gastrointestinal surgery</topic><topic>Glucagon</topic><topic>Glucagon-like peptide 1</topic><topic>Glucose tolerance</topic><topic>High fat diet</topic><topic>Insulin</topic><topic>Insulin Resistance</topic><topic>Intestinal Reabsorption - physiology</topic><topic>Intestine</topic><topic>Liver</topic><topic>Metabolism</topic><topic>Molecules</topic><topic>Obesity - metabolism</topic><topic>Obesity - physiopathology</topic><topic>Obesity - surgery</topic><topic>Portal vein</topic><topic>Postoperative Complications - metabolism</topic><topic>Rats</topic><topic>Reabsorption</topic><topic>Streptozocin</topic><topic>Surgery</topic><topic>Taurine</topic><topic>Taurine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei, Meng</creatorcontrib><creatorcontrib>Shao, Yi</creatorcontrib><creatorcontrib>Liu, Qiao-Ran</creatorcontrib><creatorcontrib>Wu, Qun-Zheng</creatorcontrib><creatorcontrib>Zhang, Xiang</creatorcontrib><creatorcontrib>Zhong, Ming-Wei</creatorcontrib><creatorcontrib>Liu, Shao-Zhuang</creatorcontrib><creatorcontrib>Zhang, Guang-Yong</creatorcontrib><creatorcontrib>Hu, San-Yuan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology: Gastrointestinal and liver physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Meng</au><au>Shao, Yi</au><au>Liu, Qiao-Ran</au><au>Wu, Qun-Zheng</au><au>Zhang, Xiang</au><au>Zhong, Ming-Wei</au><au>Liu, Shao-Zhuang</au><au>Zhang, Guang-Yong</au><au>Hu, San-Yuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bile acid profiles within the enterohepatic circulation in a diabetic rat model after bariatric surgeries</atitle><jtitle>American journal of physiology: Gastrointestinal and liver physiology</jtitle><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><date>2018-05-01</date><risdate>2018</risdate><volume>314</volume><issue>5</issue><spage>G537</spage><epage>G546</epage><pages>G537-G546</pages><issn>0193-1857</issn><eissn>1522-1547</eissn><abstract>Bile acids (BAs), which are synthesized in the liver and cycled in the enterohepatic circulation, have been recognized as signaling molecules by activating their receptors in the intestine and liver. Serum taurine-conjugated BAs have been shown to be elevated after bariatric surgeries although the postoperative BA profiles within the enterohepatic circulation have not been investigated. Clarification of these profiles could help explain the mechanisms by which bariatric surgery leads to BA profile alterations and subsequent metabolic effects. We performed duodenal-jejunal bypass (DJB), sleeve gastrectomy (SG), and sham procedures in an obese diabetic rat model induced by high-fat diet and streptozotocin. The weight loss and antidiabetic effects were evaluated postsurgery. BA profiles in the systemic serum and within the enterohepatic circulation were analyzed, together with the expression of related BA transporters and enzymes at week 12 after surgery. Compared with sham, SG induced sustained weight loss, and both DJB and SG significantly improved glucose tolerance and insulin sensitivity with enhanced glucagon-like peptide 1 secretion. Similar to changes in the serum, BAs, especially taurine-conjugated species, were also elevated in the enterohepatic circulation (bile and portal vein) after DJB and SG. In addition, the expression of key BA transporters and conjugational enzymes was elevated postoperatively, whereas the enzymes responsible for BA synthesis were decreased. In conclusion, DJB and SG elevated BA levels in the systemic serum and enterohepatic circulation, especially taurine-conjugated species, which likely indicates increased ileal reabsorption and hepatic conjugation rather than synthesis. NEW & NOTEWORTHY Bile acids (BAs) have been implicated as potential mediators of the weight-independent effects of bariatric surgery. For the first time, we discovered that duodenal-jejunal bypass and sleeve gastrectomy elevated BAs, particularly the taurine-conjugated species in the enterohepatic circulation, likely through the promotion of ileal reabsorption and hepatic conjugation rather than BA synthesis. These findings will improve our understanding of BA metabolism after bariatric surgery and their subsequent metabolic effects.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>29351394</pmid><doi>10.1152/ajpgi.00311.2017</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bariatric Surgery - adverse effects Bariatric Surgery - classification Bariatric Surgery - methods Bile Bile acids Bile Acids and Salts - blood Bile Acids and Salts - metabolism Blood Glucose - metabolism Body Weight - physiology Body weight loss Diabetes mellitus Diabetes Mellitus, Experimental - metabolism Diabetes Mellitus, Type 2 Enterohepatic Circulation - physiology Enzymes Gastrectomy Gastrointestinal surgery Glucagon Glucagon-like peptide 1 Glucose tolerance High fat diet Insulin Insulin Resistance Intestinal Reabsorption - physiology Intestine Liver Metabolism Molecules Obesity - metabolism Obesity - physiopathology Obesity - surgery Portal vein Postoperative Complications - metabolism Rats Reabsorption Streptozocin Surgery Taurine Taurine - metabolism |
title | Bile acid profiles within the enterohepatic circulation in a diabetic rat model after bariatric surgeries |
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