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Rectal Administration of Lactobacillus casei DG Modifies Flora Composition and Toll-Like Receptor Expression in Colonic Mucosa of Patients with Mild Ulcerative Colitis
Background An imbalance in gut microbiota seems to contribute to the development of chronic inflammatory disorders of the gastrointestinal tract, such as ulcerative colitis (UC). Although it has been suggested that probiotic supplementation is an effective approach to colitis, its effects on intesti...
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Published in: | Digestive diseases and sciences 2011-04, Vol.56 (4), p.1178-1187 |
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container_title | Digestive diseases and sciences |
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creator | D’Incà, Renata Barollo, Michela Scarpa, Marco Grillo, Alessia Rosaria Brun, Paola Vettorato, Maria Grazia Castagliuolo, Ignazio Sturniolo, Giacomo Carlo |
description | Background
An imbalance in gut microbiota seems to contribute to the development of chronic inflammatory disorders of the gastrointestinal tract, such as ulcerative colitis (UC). Although it has been suggested that probiotic supplementation is an effective approach to colitis, its effects on intestinal flora and on mucosal cytokine balance have never been explored.
Aim
To evaluate the effect of
Lactobacillus casei
(
L. casei
) DG, a probiotic strain, on colonic-associated microbiota, mucosal cytokine balance, and toll-like receptor (TLR) expression.
Methods
Twenty-six patients with mild left-sided UC were randomly allocated to one of three groups for an 8-week treatment period: the first group of 7 patients received oral 5-aminosalicylic acid (5-ASA) alone, the second group of 8 patients received oral 5-ASA plus oral
L. casei
DG, and the third group of 11 patients received oral 5-ASA and rectal
L. casei
DG. Biopsies were collected from the sigmoid region to culture mucosal-associated microbes and to assess cytokine and TLR messenger RNA (mRNA) levels by quantitative real-time polymerase chain reaction (RT-PCR).
Results
5-ASA alone or together with oral
L. casei
DG failed to affect colonic flora and TLR expression in a significant manner, but when coupled with rectally administered
L. casei
DG, it modified colonic microbiota by increasing
Lactobacillus
spp. and reducing
Enterobacteriaceae
. It also significantly reduced TLR-4 and interleukin (IL)-1β mRNA levels and significantly increased mucosal IL-10.
Conclusions
Manipulation of mucosal microbiota by
L. casei
DG and its effects on the mucosal immune system seem to be required to mediate the beneficial activities of probiotics in UC patients. |
doi_str_mv | 10.1007/s10620-010-1384-1 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_907158681</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A712948978</galeid><sourcerecordid>A712948978</sourcerecordid><originalsourceid>FETCH-LOGICAL-c499t-1994b33a4ed24793bdfe817641148d1786e3eb554606a42e18b328363f2865a83</originalsourceid><addsrcrecordid>eNqFks1u1DAUhSMEokPhAdggC4RYpfjaju0sR0NbkGYEQu06cpyb4uLEUzvDzxPxmjjMQAUCIS_8951zfOVbFI-BngCl6mUCKhktKdASuBYl3CkWUCleskrqu8WCgsxrAHlUPEjpmlJaK5D3iyNGFVcM6KL49h7tZDxZdoMbXZqimVwYSejJ2tgptMY673eJWJPQkVfnZBM61ztM5MyHaMgqDNuQ3A-RGTtyEbwv1-4jkmyM2ylEcvplGzGlmXBjFvgwOks2OxuSmYPe5Ugcp0Q-u-kD2TjfkUtvcX7JJ5z57J4eFvd64xM-OszHxeXZ6cXqdbl-e_5mtVyXVtT1VEJdi5ZzI7BjQtW87XrUoKQAELoDpSVybKtKSCqNYAi65UxzyXumZWU0Py5e7H23MdzsME3N4JJF782IYZeamiqotNTwX1JXSoOoeZXJp3-Q12EXx1zGDHFW1WIOfraHrozHxo19yH9hZ8tmqYBlpFYzdfIXKo8OB2fDiL3L578JYC-wMaQUsW-20Q0mfm2ANnMTNfsmaui8z03UzJU9Obx31w7Y_VL87JoMPD8AJlnj-2hG69ItJ2hdUWCZY3su5avxCuNt4f9O_w6TQN0W</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>857325948</pqid></control><display><type>article</type><title>Rectal Administration of Lactobacillus casei DG Modifies Flora Composition and Toll-Like Receptor Expression in Colonic Mucosa of Patients with Mild Ulcerative Colitis</title><source>Springer Nature</source><creator>D’Incà, Renata ; Barollo, Michela ; Scarpa, Marco ; Grillo, Alessia Rosaria ; Brun, Paola ; Vettorato, Maria Grazia ; Castagliuolo, Ignazio ; Sturniolo, Giacomo Carlo</creator><creatorcontrib>D’Incà, Renata ; Barollo, Michela ; Scarpa, Marco ; Grillo, Alessia Rosaria ; Brun, Paola ; Vettorato, Maria Grazia ; Castagliuolo, Ignazio ; Sturniolo, Giacomo Carlo</creatorcontrib><description>Background
An imbalance in gut microbiota seems to contribute to the development of chronic inflammatory disorders of the gastrointestinal tract, such as ulcerative colitis (UC). Although it has been suggested that probiotic supplementation is an effective approach to colitis, its effects on intestinal flora and on mucosal cytokine balance have never been explored.
Aim
To evaluate the effect of
Lactobacillus casei
(
L. casei
) DG, a probiotic strain, on colonic-associated microbiota, mucosal cytokine balance, and toll-like receptor (TLR) expression.
Methods
Twenty-six patients with mild left-sided UC were randomly allocated to one of three groups for an 8-week treatment period: the first group of 7 patients received oral 5-aminosalicylic acid (5-ASA) alone, the second group of 8 patients received oral 5-ASA plus oral
L. casei
DG, and the third group of 11 patients received oral 5-ASA and rectal
L. casei
DG. Biopsies were collected from the sigmoid region to culture mucosal-associated microbes and to assess cytokine and TLR messenger RNA (mRNA) levels by quantitative real-time polymerase chain reaction (RT-PCR).
Results
5-ASA alone or together with oral
L. casei
DG failed to affect colonic flora and TLR expression in a significant manner, but when coupled with rectally administered
L. casei
DG, it modified colonic microbiota by increasing
Lactobacillus
spp. and reducing
Enterobacteriaceae
. It also significantly reduced TLR-4 and interleukin (IL)-1β mRNA levels and significantly increased mucosal IL-10.
Conclusions
Manipulation of mucosal microbiota by
L. casei
DG and its effects on the mucosal immune system seem to be required to mediate the beneficial activities of probiotics in UC patients.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/s10620-010-1384-1</identifier><identifier>PMID: 20737210</identifier><identifier>CODEN: DDSCDJ</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Administration, Rectal ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Biochemistry ; Biological and medical sciences ; Colitis, Ulcerative - drug therapy ; Colitis, Ulcerative - therapy ; Colon - microbiology ; Cytokines ; Enterobacteriaceae ; Feeding. Feeding behavior ; Fundamental and applied biological sciences. Psychology ; Gastroenterology ; Gastroenterology. Liver. Pancreas. Abdomen ; Gastrointestinal system ; Hepatology ; Humans ; Interleukin-10 - biosynthesis ; Interleukin-1beta - biosynthesis ; Intestinal Mucosa - chemistry ; Intestinal Mucosa - microbiology ; Lactobacillus casei ; Medical sciences ; Medicine ; Medicine & Public Health ; Mesalamine ; Mesalamine - therapeutic use ; Microbiota (Symbiotic organisms) ; Oncology ; Original Article ; Other diseases. Semiology ; Probiotics ; Probiotics - administration & dosage ; RNA ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Toll-Like Receptor 4 - biosynthesis ; Transplant Surgery ; Treatment Outcome ; Ulcerative colitis ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>Digestive diseases and sciences, 2011-04, Vol.56 (4), p.1178-1187</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Springer</rights><rights>Springer Science+Business Media, LLC 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-1994b33a4ed24793bdfe817641148d1786e3eb554606a42e18b328363f2865a83</citedby><cites>FETCH-LOGICAL-c499t-1994b33a4ed24793bdfe817641148d1786e3eb554606a42e18b328363f2865a83</cites></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&idt=24095012$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20737210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>D’Incà, Renata</creatorcontrib><creatorcontrib>Barollo, Michela</creatorcontrib><creatorcontrib>Scarpa, Marco</creatorcontrib><creatorcontrib>Grillo, Alessia Rosaria</creatorcontrib><creatorcontrib>Brun, Paola</creatorcontrib><creatorcontrib>Vettorato, Maria Grazia</creatorcontrib><creatorcontrib>Castagliuolo, Ignazio</creatorcontrib><creatorcontrib>Sturniolo, Giacomo Carlo</creatorcontrib><title>Rectal Administration of Lactobacillus casei DG Modifies Flora Composition and Toll-Like Receptor Expression in Colonic Mucosa of Patients with Mild Ulcerative Colitis</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><addtitle>Dig Dis Sci</addtitle><description>Background
An imbalance in gut microbiota seems to contribute to the development of chronic inflammatory disorders of the gastrointestinal tract, such as ulcerative colitis (UC). Although it has been suggested that probiotic supplementation is an effective approach to colitis, its effects on intestinal flora and on mucosal cytokine balance have never been explored.
Aim
To evaluate the effect of
Lactobacillus casei
(
L. casei
) DG, a probiotic strain, on colonic-associated microbiota, mucosal cytokine balance, and toll-like receptor (TLR) expression.
Methods
Twenty-six patients with mild left-sided UC were randomly allocated to one of three groups for an 8-week treatment period: the first group of 7 patients received oral 5-aminosalicylic acid (5-ASA) alone, the second group of 8 patients received oral 5-ASA plus oral
L. casei
DG, and the third group of 11 patients received oral 5-ASA and rectal
L. casei
DG. Biopsies were collected from the sigmoid region to culture mucosal-associated microbes and to assess cytokine and TLR messenger RNA (mRNA) levels by quantitative real-time polymerase chain reaction (RT-PCR).
Results
5-ASA alone or together with oral
L. casei
DG failed to affect colonic flora and TLR expression in a significant manner, but when coupled with rectally administered
L. casei
DG, it modified colonic microbiota by increasing
Lactobacillus
spp. and reducing
Enterobacteriaceae
. It also significantly reduced TLR-4 and interleukin (IL)-1β mRNA levels and significantly increased mucosal IL-10.
Conclusions
Manipulation of mucosal microbiota by
L. casei
DG and its effects on the mucosal immune system seem to be required to mediate the beneficial activities of probiotics in UC patients.</description><subject>Administration, Rectal</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Colitis, Ulcerative - drug therapy</subject><subject>Colitis, Ulcerative - therapy</subject><subject>Colon - microbiology</subject><subject>Cytokines</subject><subject>Enterobacteriaceae</subject><subject>Feeding. Feeding behavior</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gastrointestinal system</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Interleukin-10 - biosynthesis</subject><subject>Interleukin-1beta - biosynthesis</subject><subject>Intestinal Mucosa - chemistry</subject><subject>Intestinal Mucosa - microbiology</subject><subject>Lactobacillus casei</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mesalamine</subject><subject>Mesalamine - therapeutic use</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Other diseases. Semiology</subject><subject>Probiotics</subject><subject>Probiotics - administration & dosage</subject><subject>RNA</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Toll-Like Receptor 4 - biosynthesis</subject><subject>Transplant Surgery</subject><subject>Treatment Outcome</subject><subject>Ulcerative colitis</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0163-2116</issn><issn>1573-2568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFks1u1DAUhSMEokPhAdggC4RYpfjaju0sR0NbkGYEQu06cpyb4uLEUzvDzxPxmjjMQAUCIS_8951zfOVbFI-BngCl6mUCKhktKdASuBYl3CkWUCleskrqu8WCgsxrAHlUPEjpmlJaK5D3iyNGFVcM6KL49h7tZDxZdoMbXZqimVwYSejJ2tgptMY673eJWJPQkVfnZBM61ztM5MyHaMgqDNuQ3A-RGTtyEbwv1-4jkmyM2ylEcvplGzGlmXBjFvgwOks2OxuSmYPe5Ugcp0Q-u-kD2TjfkUtvcX7JJ5z57J4eFvd64xM-OszHxeXZ6cXqdbl-e_5mtVyXVtT1VEJdi5ZzI7BjQtW87XrUoKQAELoDpSVybKtKSCqNYAi65UxzyXumZWU0Py5e7H23MdzsME3N4JJF782IYZeamiqotNTwX1JXSoOoeZXJp3-Q12EXx1zGDHFW1WIOfraHrozHxo19yH9hZ8tmqYBlpFYzdfIXKo8OB2fDiL3L578JYC-wMaQUsW-20Q0mfm2ANnMTNfsmaui8z03UzJU9Obx31w7Y_VL87JoMPD8AJlnj-2hG69ItJ2hdUWCZY3su5avxCuNt4f9O_w6TQN0W</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>D’Incà, Renata</creator><creator>Barollo, Michela</creator><creator>Scarpa, Marco</creator><creator>Grillo, Alessia Rosaria</creator><creator>Brun, Paola</creator><creator>Vettorato, Maria Grazia</creator><creator>Castagliuolo, Ignazio</creator><creator>Sturniolo, Giacomo Carlo</creator><general>Springer US</general><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>AAYXX</scope><scope>CITATION</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><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>20110401</creationdate><title>Rectal Administration of Lactobacillus casei DG Modifies Flora Composition and Toll-Like Receptor Expression in Colonic Mucosa of Patients with Mild Ulcerative Colitis</title><author>D’Incà, Renata ; Barollo, Michela ; Scarpa, Marco ; Grillo, Alessia Rosaria ; Brun, Paola ; Vettorato, Maria Grazia ; Castagliuolo, Ignazio ; Sturniolo, Giacomo Carlo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-1994b33a4ed24793bdfe817641148d1786e3eb554606a42e18b328363f2865a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Administration, Rectal</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Colitis, Ulcerative - drug therapy</topic><topic>Colitis, Ulcerative - therapy</topic><topic>Colon - microbiology</topic><topic>Cytokines</topic><topic>Enterobacteriaceae</topic><topic>Feeding. Feeding behavior</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gastrointestinal system</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Interleukin-10 - biosynthesis</topic><topic>Interleukin-1beta - biosynthesis</topic><topic>Intestinal Mucosa - chemistry</topic><topic>Intestinal Mucosa - microbiology</topic><topic>Lactobacillus casei</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mesalamine</topic><topic>Mesalamine - therapeutic use</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Other diseases. Semiology</topic><topic>Probiotics</topic><topic>Probiotics - administration & dosage</topic><topic>RNA</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Toll-Like Receptor 4 - biosynthesis</topic><topic>Transplant Surgery</topic><topic>Treatment Outcome</topic><topic>Ulcerative colitis</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>D’Incà, Renata</creatorcontrib><creatorcontrib>Barollo, Michela</creatorcontrib><creatorcontrib>Scarpa, Marco</creatorcontrib><creatorcontrib>Grillo, Alessia Rosaria</creatorcontrib><creatorcontrib>Brun, Paola</creatorcontrib><creatorcontrib>Vettorato, Maria Grazia</creatorcontrib><creatorcontrib>Castagliuolo, Ignazio</creatorcontrib><creatorcontrib>Sturniolo, Giacomo Carlo</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>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>ProQuest Health and Medical</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: 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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Database (Proquest)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & 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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Digestive diseases and sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>D’Incà, Renata</au><au>Barollo, Michela</au><au>Scarpa, Marco</au><au>Grillo, Alessia Rosaria</au><au>Brun, Paola</au><au>Vettorato, Maria Grazia</au><au>Castagliuolo, Ignazio</au><au>Sturniolo, Giacomo Carlo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rectal Administration of Lactobacillus casei DG Modifies Flora Composition and Toll-Like Receptor Expression in Colonic Mucosa of Patients with Mild Ulcerative Colitis</atitle><jtitle>Digestive diseases and sciences</jtitle><stitle>Dig Dis Sci</stitle><addtitle>Dig Dis Sci</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>56</volume><issue>4</issue><spage>1178</spage><epage>1187</epage><pages>1178-1187</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><coden>DDSCDJ</coden><abstract>Background
An imbalance in gut microbiota seems to contribute to the development of chronic inflammatory disorders of the gastrointestinal tract, such as ulcerative colitis (UC). Although it has been suggested that probiotic supplementation is an effective approach to colitis, its effects on intestinal flora and on mucosal cytokine balance have never been explored.
Aim
To evaluate the effect of
Lactobacillus casei
(
L. casei
) DG, a probiotic strain, on colonic-associated microbiota, mucosal cytokine balance, and toll-like receptor (TLR) expression.
Methods
Twenty-six patients with mild left-sided UC were randomly allocated to one of three groups for an 8-week treatment period: the first group of 7 patients received oral 5-aminosalicylic acid (5-ASA) alone, the second group of 8 patients received oral 5-ASA plus oral
L. casei
DG, and the third group of 11 patients received oral 5-ASA and rectal
L. casei
DG. Biopsies were collected from the sigmoid region to culture mucosal-associated microbes and to assess cytokine and TLR messenger RNA (mRNA) levels by quantitative real-time polymerase chain reaction (RT-PCR).
Results
5-ASA alone or together with oral
L. casei
DG failed to affect colonic flora and TLR expression in a significant manner, but when coupled with rectally administered
L. casei
DG, it modified colonic microbiota by increasing
Lactobacillus
spp. and reducing
Enterobacteriaceae
. It also significantly reduced TLR-4 and interleukin (IL)-1β mRNA levels and significantly increased mucosal IL-10.
Conclusions
Manipulation of mucosal microbiota by
L. casei
DG and its effects on the mucosal immune system seem to be required to mediate the beneficial activities of probiotics in UC patients.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>20737210</pmid><doi>10.1007/s10620-010-1384-1</doi><tpages>10</tpages></addata></record> |
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source | Springer Nature |
subjects | Administration, Rectal Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Biochemistry Biological and medical sciences Colitis, Ulcerative - drug therapy Colitis, Ulcerative - therapy Colon - microbiology Cytokines Enterobacteriaceae Feeding. Feeding behavior Fundamental and applied biological sciences. Psychology Gastroenterology Gastroenterology. Liver. Pancreas. Abdomen Gastrointestinal system Hepatology Humans Interleukin-10 - biosynthesis Interleukin-1beta - biosynthesis Intestinal Mucosa - chemistry Intestinal Mucosa - microbiology Lactobacillus casei Medical sciences Medicine Medicine & Public Health Mesalamine Mesalamine - therapeutic use Microbiota (Symbiotic organisms) Oncology Original Article Other diseases. Semiology Probiotics Probiotics - administration & dosage RNA Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Toll-Like Receptor 4 - biosynthesis Transplant Surgery Treatment Outcome Ulcerative colitis Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Rectal Administration of Lactobacillus casei DG Modifies Flora Composition and Toll-Like Receptor Expression in Colonic Mucosa of Patients with Mild Ulcerative Colitis |
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