Resistant starch alters gut microbiome and metabolomic profiles concurrent with amelioration of chronic kidney disease in rats
Patients and animals with chronic kidney disease (CKD) exhibit profound alterations in the gut environment including shifts in microbial composition, increased fecal pH, and increased blood levels of gut microbe-derived metabolites (xenometabolites). The fermentable dietary fiber high amylose maize-...
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creator | Kieffer, Dorothy A Piccolo, Brian D Vaziri, Nosratola D Liu, Shuman Lau, Wei L Khazaeli, Mahyar Nazertehrani, Sohrab Moore, Mary E Marco, Maria L Martin, Roy J Adams, Sean H |
description | Patients and animals with chronic kidney disease (CKD) exhibit profound alterations in the gut environment including shifts in microbial composition, increased fecal pH, and increased blood levels of gut microbe-derived metabolites (xenometabolites). The fermentable dietary fiber high amylose maize-resistant starch type 2 (HAMRS2) has been shown to alter the gut milieu and in CKD rat models leads to markedly improved kidney function. The aim of the present study was to identify specific cecal bacteria and cecal, blood, and urinary metabolites that associate with changes in kidney function to identify potential mechanisms involved with CKD amelioration in response to dietary resistant starch. Male Sprague-Dawley rats with adenine-induced CKD were fed a semipurified low-fiber diet or a high-fiber diet [59% (wt/wt) HAMRS2] for 3 wk (n = 9 rats/group). The cecal microbiome was characterized, and cecal contents, serum, and urine metabolites were analyzed. HAMRS2-fed rats displayed decreased cecal pH, decreased microbial diversity, and an increased Bacteroidetes-to-Firmicutes ratio. Several uremic retention solutes were altered in the cecal contents, serum, and urine, many of which had strong correlations with specific gut bacteria abundances, i.e., serum and urine indoxyl sulfate were reduced by 36% and 66%, respectively, in HAMRS2-fed rats and urine p-cresol was reduced by 47% in HAMRS2-fed rats. Outcomes from this study were coincident with improvements in kidney function indexes and amelioration of CKD outcomes previously reported for these rats, suggesting an important role for microbial-derived factors and gut microbe metabolism in regulating host kidney function. |
doi_str_mv | 10.1152/ajprenal.00513.2015 |
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The fermentable dietary fiber high amylose maize-resistant starch type 2 (HAMRS2) has been shown to alter the gut milieu and in CKD rat models leads to markedly improved kidney function. The aim of the present study was to identify specific cecal bacteria and cecal, blood, and urinary metabolites that associate with changes in kidney function to identify potential mechanisms involved with CKD amelioration in response to dietary resistant starch. Male Sprague-Dawley rats with adenine-induced CKD were fed a semipurified low-fiber diet or a high-fiber diet [59% (wt/wt) HAMRS2] for 3 wk (n = 9 rats/group). The cecal microbiome was characterized, and cecal contents, serum, and urine metabolites were analyzed. HAMRS2-fed rats displayed decreased cecal pH, decreased microbial diversity, and an increased Bacteroidetes-to-Firmicutes ratio. Several uremic retention solutes were altered in the cecal contents, serum, and urine, many of which had strong correlations with specific gut bacteria abundances, i.e., serum and urine indoxyl sulfate were reduced by 36% and 66%, respectively, in HAMRS2-fed rats and urine p-cresol was reduced by 47% in HAMRS2-fed rats. Outcomes from this study were coincident with improvements in kidney function indexes and amelioration of CKD outcomes previously reported for these rats, suggesting an important role for microbial-derived factors and gut microbe metabolism in regulating host kidney function.</description><identifier>ISSN: 1931-857X</identifier><identifier>EISSN: 1522-1466</identifier><identifier>DOI: 10.1152/ajprenal.00513.2015</identifier><identifier>PMID: 26841824</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Bacteria ; Carbohydrates ; Cecum - microbiology ; Cresols - urine ; Diet ; Dietary fiber ; Dietary Fiber - pharmacology ; Gastrointestinal Microbiome - drug effects ; Hydrogen-Ion Concentration ; Kidney diseases ; Kidney Function Tests ; Male ; Metabolites ; Metabolomics ; Rats ; Rats, Sprague-Dawley ; Renal Insufficiency, Chronic - microbiology ; Renal Insufficiency, Chronic - physiopathology ; Rodents ; Starch - pharmacology ; Uremia - metabolism</subject><ispartof>American journal of physiology. Renal physiology, 2016-05, Vol.310 (9), p.F857-F871</ispartof><rights>Copyright © 2016 the American Physiological Society.</rights><rights>Copyright American Physiological Society May 1, 2016</rights><rights>Copyright © 2016 the American Physiological Society 2016 American Physiological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-762cc59469ca974493abcd020d8ac55cabf273ca7fda434c3a78d48f62c442933</citedby><cites>FETCH-LOGICAL-c433t-762cc59469ca974493abcd020d8ac55cabf273ca7fda434c3a78d48f62c442933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26841824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kieffer, Dorothy A</creatorcontrib><creatorcontrib>Piccolo, Brian D</creatorcontrib><creatorcontrib>Vaziri, Nosratola D</creatorcontrib><creatorcontrib>Liu, Shuman</creatorcontrib><creatorcontrib>Lau, Wei L</creatorcontrib><creatorcontrib>Khazaeli, Mahyar</creatorcontrib><creatorcontrib>Nazertehrani, Sohrab</creatorcontrib><creatorcontrib>Moore, Mary E</creatorcontrib><creatorcontrib>Marco, Maria L</creatorcontrib><creatorcontrib>Martin, Roy J</creatorcontrib><creatorcontrib>Adams, Sean H</creatorcontrib><title>Resistant starch alters gut microbiome and metabolomic profiles concurrent with amelioration of chronic kidney disease in rats</title><title>American journal of physiology. Renal physiology</title><addtitle>Am J Physiol Renal Physiol</addtitle><description>Patients and animals with chronic kidney disease (CKD) exhibit profound alterations in the gut environment including shifts in microbial composition, increased fecal pH, and increased blood levels of gut microbe-derived metabolites (xenometabolites). The fermentable dietary fiber high amylose maize-resistant starch type 2 (HAMRS2) has been shown to alter the gut milieu and in CKD rat models leads to markedly improved kidney function. The aim of the present study was to identify specific cecal bacteria and cecal, blood, and urinary metabolites that associate with changes in kidney function to identify potential mechanisms involved with CKD amelioration in response to dietary resistant starch. Male Sprague-Dawley rats with adenine-induced CKD were fed a semipurified low-fiber diet or a high-fiber diet [59% (wt/wt) HAMRS2] for 3 wk (n = 9 rats/group). The cecal microbiome was characterized, and cecal contents, serum, and urine metabolites were analyzed. HAMRS2-fed rats displayed decreased cecal pH, decreased microbial diversity, and an increased Bacteroidetes-to-Firmicutes ratio. Several uremic retention solutes were altered in the cecal contents, serum, and urine, many of which had strong correlations with specific gut bacteria abundances, i.e., serum and urine indoxyl sulfate were reduced by 36% and 66%, respectively, in HAMRS2-fed rats and urine p-cresol was reduced by 47% in HAMRS2-fed rats. Outcomes from this study were coincident with improvements in kidney function indexes and amelioration of CKD outcomes previously reported for these rats, suggesting an important role for microbial-derived factors and gut microbe metabolism in regulating host kidney function.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Carbohydrates</subject><subject>Cecum - microbiology</subject><subject>Cresols - urine</subject><subject>Diet</subject><subject>Dietary fiber</subject><subject>Dietary Fiber - pharmacology</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kidney diseases</subject><subject>Kidney Function Tests</subject><subject>Male</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Renal Insufficiency, Chronic - microbiology</subject><subject>Renal Insufficiency, Chronic - physiopathology</subject><subject>Rodents</subject><subject>Starch - pharmacology</subject><subject>Uremia - metabolism</subject><issn>1931-857X</issn><issn>1522-1466</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUuLFTEQhYMozkN_gSABN276mmcnvRFkUEcYEETBXahOp-fmmk6uSXpkNv52c-eFuklC1TmHSn0IvaBkQ6lkb2C3zy5C2BAiKd8wQuUjdNw6rKOi7x-398Bpp6X6foROStkRQihl9Ck6Yr0WVDNxjH5_ccWXCrHidma7xRCqywVfrhUv3uY0-rQ4DHHCi6swppBaGe9zmn1wBdsU7ZrbIBX_8rXZFxd8ylB9ijjN2G5zis3ww0_RXePJFwfFYR9x05Rn6MkMobjnd_cp-vbh_dez8-7i88dPZ-8uOis4r53qmbVyEP1gYVBCDBxGOxFGJg1WSgvjzBS3oOYJBBeWg9KT0HOzCcEGzk_R29vc_ToubrJt3AzB7LNfIF-bBN7824l-ay7TlRG6V5weAl7fBeT0c3WlmsUX60KA6NJaDFVakbZuopv01X_SXVpzA3WjGiSTQhxU_FbVVlxKdvPDMJSYA19zz9fc8DUHvs318u9_PHjugfI_W2enUw</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Kieffer, Dorothy A</creator><creator>Piccolo, Brian D</creator><creator>Vaziri, Nosratola D</creator><creator>Liu, Shuman</creator><creator>Lau, Wei L</creator><creator>Khazaeli, Mahyar</creator><creator>Nazertehrani, Sohrab</creator><creator>Moore, Mary E</creator><creator>Marco, Maria L</creator><creator>Martin, Roy J</creator><creator>Adams, Sean H</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><scope>5PM</scope></search><sort><creationdate>20160501</creationdate><title>Resistant starch alters gut microbiome and metabolomic profiles concurrent with amelioration of chronic kidney disease in rats</title><author>Kieffer, Dorothy A ; Piccolo, Brian D ; Vaziri, Nosratola D ; Liu, Shuman ; Lau, Wei L ; Khazaeli, Mahyar ; Nazertehrani, Sohrab ; Moore, Mary E ; Marco, Maria L ; Martin, Roy J ; Adams, Sean H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-762cc59469ca974493abcd020d8ac55cabf273ca7fda434c3a78d48f62c442933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Bacteria</topic><topic>Carbohydrates</topic><topic>Cecum - microbiology</topic><topic>Cresols - urine</topic><topic>Diet</topic><topic>Dietary fiber</topic><topic>Dietary Fiber - pharmacology</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kidney diseases</topic><topic>Kidney Function Tests</topic><topic>Male</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Renal Insufficiency, Chronic - microbiology</topic><topic>Renal Insufficiency, Chronic - physiopathology</topic><topic>Rodents</topic><topic>Starch - pharmacology</topic><topic>Uremia - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kieffer, Dorothy A</creatorcontrib><creatorcontrib>Piccolo, Brian D</creatorcontrib><creatorcontrib>Vaziri, Nosratola D</creatorcontrib><creatorcontrib>Liu, Shuman</creatorcontrib><creatorcontrib>Lau, Wei L</creatorcontrib><creatorcontrib>Khazaeli, Mahyar</creatorcontrib><creatorcontrib>Nazertehrani, Sohrab</creatorcontrib><creatorcontrib>Moore, Mary E</creatorcontrib><creatorcontrib>Marco, Maria L</creatorcontrib><creatorcontrib>Martin, Roy J</creatorcontrib><creatorcontrib>Adams, Sean H</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Renal physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kieffer, Dorothy A</au><au>Piccolo, Brian D</au><au>Vaziri, Nosratola D</au><au>Liu, Shuman</au><au>Lau, Wei L</au><au>Khazaeli, Mahyar</au><au>Nazertehrani, Sohrab</au><au>Moore, Mary E</au><au>Marco, Maria L</au><au>Martin, Roy J</au><au>Adams, Sean H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Resistant starch alters gut microbiome and metabolomic profiles concurrent with amelioration of chronic kidney disease in rats</atitle><jtitle>American journal of physiology. Renal physiology</jtitle><addtitle>Am J Physiol Renal Physiol</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>310</volume><issue>9</issue><spage>F857</spage><epage>F871</epage><pages>F857-F871</pages><issn>1931-857X</issn><eissn>1522-1466</eissn><abstract>Patients and animals with chronic kidney disease (CKD) exhibit profound alterations in the gut environment including shifts in microbial composition, increased fecal pH, and increased blood levels of gut microbe-derived metabolites (xenometabolites). The fermentable dietary fiber high amylose maize-resistant starch type 2 (HAMRS2) has been shown to alter the gut milieu and in CKD rat models leads to markedly improved kidney function. The aim of the present study was to identify specific cecal bacteria and cecal, blood, and urinary metabolites that associate with changes in kidney function to identify potential mechanisms involved with CKD amelioration in response to dietary resistant starch. Male Sprague-Dawley rats with adenine-induced CKD were fed a semipurified low-fiber diet or a high-fiber diet [59% (wt/wt) HAMRS2] for 3 wk (n = 9 rats/group). The cecal microbiome was characterized, and cecal contents, serum, and urine metabolites were analyzed. HAMRS2-fed rats displayed decreased cecal pH, decreased microbial diversity, and an increased Bacteroidetes-to-Firmicutes ratio. Several uremic retention solutes were altered in the cecal contents, serum, and urine, many of which had strong correlations with specific gut bacteria abundances, i.e., serum and urine indoxyl sulfate were reduced by 36% and 66%, respectively, in HAMRS2-fed rats and urine p-cresol was reduced by 47% in HAMRS2-fed rats. 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subjects | Animals Bacteria Carbohydrates Cecum - microbiology Cresols - urine Diet Dietary fiber Dietary Fiber - pharmacology Gastrointestinal Microbiome - drug effects Hydrogen-Ion Concentration Kidney diseases Kidney Function Tests Male Metabolites Metabolomics Rats Rats, Sprague-Dawley Renal Insufficiency, Chronic - microbiology Renal Insufficiency, Chronic - physiopathology Rodents Starch - pharmacology Uremia - metabolism |
title | Resistant starch alters gut microbiome and metabolomic profiles concurrent with amelioration of chronic kidney disease in rats |
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