Loading…
Role of high-mobility group box 1 in patients with acute obstructive suppurative cholangitis-induced sepsis
High-mobility group box 1 (HMGB1) is a proinflammatory cytokine that plays an active role during the pathogenesis of inflammatory processes. The primary aim of this study was to detect whether HMGB1 is involved in the pathogenesis of acute obstructive suppurative cholangitis (AOSC). We collected per...
Saved in:
Published in: | Journal of inflammation research 2015-01, Vol.8 (default), p.71-77 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c611t-7ce68806b0588f186a3df1b0ed010f3b1044667088cff097cdb209cbc1daaec13 |
---|---|
cites | |
container_end_page | 77 |
container_issue | default |
container_start_page | 71 |
container_title | Journal of inflammation research |
container_volume | 8 |
creator | Singh, Akanand Feng, Yi Mahato, Nisha Li, Jinzheng Wu, Chuanxin Gong, Jianping |
description | High-mobility group box 1 (HMGB1) is a proinflammatory cytokine that plays an active role during the pathogenesis of inflammatory processes. The primary aim of this study was to detect whether HMGB1 is involved in the pathogenesis of acute obstructive suppurative cholangitis (AOSC).
We collected peripheral blood samples from 23 patients with AOSC and 23 healthy volunteers who served as normal controls. All participants were tested for HMGB1 mRNA level, HMGB1 protein, tumor necrosis factor alpha (TNF-alpha), and interleukin 10 (IL-10). HMGB1 mRNA levels were tested using real-time polymerase chain reaction. HMGB1 protein expression was measured using Western blot. TNF-alpha and IL-10 were tested using enzyme-linked immunosorbent assay.
The expression of HMGB1 mRNA and HMGB1 protein was higher in the AOSC group than in the normal controls (P |
doi_str_mv | 10.2147/JIR.S77539 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_788b895bc0f0479b947f60eafe2ee5e6</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A446735640</galeid><doaj_id>oai_doaj_org_article_788b895bc0f0479b947f60eafe2ee5e6</doaj_id><sourcerecordid>A446735640</sourcerecordid><originalsourceid>FETCH-LOGICAL-c611t-7ce68806b0588f186a3df1b0ed010f3b1044667088cff097cdb209cbc1daaec13</originalsourceid><addsrcrecordid>eNptkl1rFDEUhgdRbKm98QfIgCBFmDWZjyRzI5Tix0pBqHodkszJTNbZyZiP1f57s91u3S0mFzmcPOfNycvJspcYLUpc03dfljeLb5Q2VfskO8WYsoKiCj89iE-yc-9XaLsoqsv6eXZSNrQtWd2eZj9v7Ai51flg-qFYW2lGE27z3tk459L-yXFupnwWwcAUfP7bhCEXKoZUI31wUQWzgdzHeY5O3MVqsKOYehOML8zURQVd7mH2xr_Inmkxeji_P8-yHx8_fL_6XFx__bS8urwuFME4FFQBYQwRiRrGNGZEVJ3GEkGHMNKVxKiuCaGIMaU1aqnqZIlaJRXuhACFq7NsudPtrFjx2Zm1cLfcCsPvEtb1XLhg1AicMiZZ20iFNKppK9uaaoJAaCgBGiBJ6_1Oa45yDZ1KLjgxHoke30xm4L3d8LoiJWvbJID2zWxgduD9o472WWXXvESsqlLJxf2bzv6K4ANfG69gTLaCjZ5jQhqcUIQS-voRurLRTcldXpZViRvKUPOP6kX6s5m0Ta2qrSi_TF7SqiH1VmvxHyrtDtZG2Qm0SfmjgjcHBQOIMQzejjEYO_lj8O0OVM5670A_WIAR304xT1PMd1Oc4FeHjj-g-5mt_gIyle1c</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2232157805</pqid></control><display><type>article</type><title>Role of high-mobility group box 1 in patients with acute obstructive suppurative cholangitis-induced sepsis</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>Taylor & Francis Open Access</source><source>PubMed Central Free</source><source>IngentaConnect Journals</source><creator>Singh, Akanand ; Feng, Yi ; Mahato, Nisha ; Li, Jinzheng ; Wu, Chuanxin ; Gong, Jianping</creator><creatorcontrib>Singh, Akanand ; Feng, Yi ; Mahato, Nisha ; Li, Jinzheng ; Wu, Chuanxin ; Gong, Jianping</creatorcontrib><description>High-mobility group box 1 (HMGB1) is a proinflammatory cytokine that plays an active role during the pathogenesis of inflammatory processes. The primary aim of this study was to detect whether HMGB1 is involved in the pathogenesis of acute obstructive suppurative cholangitis (AOSC).
We collected peripheral blood samples from 23 patients with AOSC and 23 healthy volunteers who served as normal controls. All participants were tested for HMGB1 mRNA level, HMGB1 protein, tumor necrosis factor alpha (TNF-alpha), and interleukin 10 (IL-10). HMGB1 mRNA levels were tested using real-time polymerase chain reaction. HMGB1 protein expression was measured using Western blot. TNF-alpha and IL-10 were tested using enzyme-linked immunosorbent assay.
The expression of HMGB1 mRNA and HMGB1 protein was higher in the AOSC group than in the normal controls (P<0.01), and the levels gradually decreased to normal after treatment of the disease (P<0.01). The content of TNF-alpha and IL-10 in peripheral blood of patients with AOSC was significantly higher than that of normal controls (P<0.01) but decreased to normal levels after the necessary treatment (P<0.01).
The levels of HMGB1 mRNA and HMGB1 protein were elevated in patients with AOSC, which may play an important role in the inflammation of the bile duct and appears to be associated with the development of sepsis. This suggests the importance of monitoring HMGB1 levels in the management of AOSC-induced sepsis.</description><identifier>ISSN: 1178-7031</identifier><identifier>EISSN: 1178-7031</identifier><identifier>DOI: 10.2147/JIR.S77539</identifier><identifier>PMID: 25792849</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>AOSC ; Appendicitis ; Cholangitis ; Chromosomal proteins ; Cytokines ; Deoxyribonucleic acid ; DNA ; Endoscopy ; Gallbladder diseases ; HMGB1 ; Hospitals ; Infections ; Inflammation ; interleukin 10 ; Interleukins ; Original Research ; Pathogenesis ; Patients ; Polymerase chain reaction ; Proteins ; Sepsis ; Signal transduction ; Surgery ; TNF-alpha ; Tumor necrosis factor ; Tumor necrosis factor-TNF</subject><ispartof>Journal of inflammation research, 2015-01, Vol.8 (default), p.71-77</ispartof><rights>COPYRIGHT 2015 Dove Medical Press Limited</rights><rights>2015. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Singh et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c611t-7ce68806b0588f186a3df1b0ed010f3b1044667088cff097cdb209cbc1daaec13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2232157805/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2232157805?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25792849$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh, Akanand</creatorcontrib><creatorcontrib>Feng, Yi</creatorcontrib><creatorcontrib>Mahato, Nisha</creatorcontrib><creatorcontrib>Li, Jinzheng</creatorcontrib><creatorcontrib>Wu, Chuanxin</creatorcontrib><creatorcontrib>Gong, Jianping</creatorcontrib><title>Role of high-mobility group box 1 in patients with acute obstructive suppurative cholangitis-induced sepsis</title><title>Journal of inflammation research</title><addtitle>J Inflamm Res</addtitle><description>High-mobility group box 1 (HMGB1) is a proinflammatory cytokine that plays an active role during the pathogenesis of inflammatory processes. The primary aim of this study was to detect whether HMGB1 is involved in the pathogenesis of acute obstructive suppurative cholangitis (AOSC).
We collected peripheral blood samples from 23 patients with AOSC and 23 healthy volunteers who served as normal controls. All participants were tested for HMGB1 mRNA level, HMGB1 protein, tumor necrosis factor alpha (TNF-alpha), and interleukin 10 (IL-10). HMGB1 mRNA levels were tested using real-time polymerase chain reaction. HMGB1 protein expression was measured using Western blot. TNF-alpha and IL-10 were tested using enzyme-linked immunosorbent assay.
The expression of HMGB1 mRNA and HMGB1 protein was higher in the AOSC group than in the normal controls (P<0.01), and the levels gradually decreased to normal after treatment of the disease (P<0.01). The content of TNF-alpha and IL-10 in peripheral blood of patients with AOSC was significantly higher than that of normal controls (P<0.01) but decreased to normal levels after the necessary treatment (P<0.01).
The levels of HMGB1 mRNA and HMGB1 protein were elevated in patients with AOSC, which may play an important role in the inflammation of the bile duct and appears to be associated with the development of sepsis. This suggests the importance of monitoring HMGB1 levels in the management of AOSC-induced sepsis.</description><subject>AOSC</subject><subject>Appendicitis</subject><subject>Cholangitis</subject><subject>Chromosomal proteins</subject><subject>Cytokines</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Endoscopy</subject><subject>Gallbladder diseases</subject><subject>HMGB1</subject><subject>Hospitals</subject><subject>Infections</subject><subject>Inflammation</subject><subject>interleukin 10</subject><subject>Interleukins</subject><subject>Original Research</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Polymerase chain reaction</subject><subject>Proteins</subject><subject>Sepsis</subject><subject>Signal transduction</subject><subject>Surgery</subject><subject>TNF-alpha</subject><subject>Tumor necrosis factor</subject><subject>Tumor necrosis factor-TNF</subject><issn>1178-7031</issn><issn>1178-7031</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1rFDEUhgdRbKm98QfIgCBFmDWZjyRzI5Tix0pBqHodkszJTNbZyZiP1f57s91u3S0mFzmcPOfNycvJspcYLUpc03dfljeLb5Q2VfskO8WYsoKiCj89iE-yc-9XaLsoqsv6eXZSNrQtWd2eZj9v7Ai51flg-qFYW2lGE27z3tk459L-yXFupnwWwcAUfP7bhCEXKoZUI31wUQWzgdzHeY5O3MVqsKOYehOML8zURQVd7mH2xr_Inmkxeji_P8-yHx8_fL_6XFx__bS8urwuFME4FFQBYQwRiRrGNGZEVJ3GEkGHMNKVxKiuCaGIMaU1aqnqZIlaJRXuhACFq7NsudPtrFjx2Zm1cLfcCsPvEtb1XLhg1AicMiZZ20iFNKppK9uaaoJAaCgBGiBJ6_1Oa45yDZ1KLjgxHoke30xm4L3d8LoiJWvbJID2zWxgduD9o472WWXXvESsqlLJxf2bzv6K4ANfG69gTLaCjZ5jQhqcUIQS-voRurLRTcldXpZViRvKUPOP6kX6s5m0Ta2qrSi_TF7SqiH1VmvxHyrtDtZG2Qm0SfmjgjcHBQOIMQzejjEYO_lj8O0OVM5670A_WIAR304xT1PMd1Oc4FeHjj-g-5mt_gIyle1c</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Singh, Akanand</creator><creator>Feng, Yi</creator><creator>Mahato, Nisha</creator><creator>Li, Jinzheng</creator><creator>Wu, Chuanxin</creator><creator>Gong, Jianping</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove Press</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>KB0</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150101</creationdate><title>Role of high-mobility group box 1 in patients with acute obstructive suppurative cholangitis-induced sepsis</title><author>Singh, Akanand ; Feng, Yi ; Mahato, Nisha ; Li, Jinzheng ; Wu, Chuanxin ; Gong, Jianping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c611t-7ce68806b0588f186a3df1b0ed010f3b1044667088cff097cdb209cbc1daaec13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>AOSC</topic><topic>Appendicitis</topic><topic>Cholangitis</topic><topic>Chromosomal proteins</topic><topic>Cytokines</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Endoscopy</topic><topic>Gallbladder diseases</topic><topic>HMGB1</topic><topic>Hospitals</topic><topic>Infections</topic><topic>Inflammation</topic><topic>interleukin 10</topic><topic>Interleukins</topic><topic>Original Research</topic><topic>Pathogenesis</topic><topic>Patients</topic><topic>Polymerase chain reaction</topic><topic>Proteins</topic><topic>Sepsis</topic><topic>Signal transduction</topic><topic>Surgery</topic><topic>TNF-alpha</topic><topic>Tumor necrosis factor</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Akanand</creatorcontrib><creatorcontrib>Feng, Yi</creatorcontrib><creatorcontrib>Mahato, Nisha</creatorcontrib><creatorcontrib>Li, Jinzheng</creatorcontrib><creatorcontrib>Wu, Chuanxin</creatorcontrib><creatorcontrib>Gong, Jianping</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest research library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of inflammation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh, Akanand</au><au>Feng, Yi</au><au>Mahato, Nisha</au><au>Li, Jinzheng</au><au>Wu, Chuanxin</au><au>Gong, Jianping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of high-mobility group box 1 in patients with acute obstructive suppurative cholangitis-induced sepsis</atitle><jtitle>Journal of inflammation research</jtitle><addtitle>J Inflamm Res</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>8</volume><issue>default</issue><spage>71</spage><epage>77</epage><pages>71-77</pages><issn>1178-7031</issn><eissn>1178-7031</eissn><abstract>High-mobility group box 1 (HMGB1) is a proinflammatory cytokine that plays an active role during the pathogenesis of inflammatory processes. The primary aim of this study was to detect whether HMGB1 is involved in the pathogenesis of acute obstructive suppurative cholangitis (AOSC).
We collected peripheral blood samples from 23 patients with AOSC and 23 healthy volunteers who served as normal controls. All participants were tested for HMGB1 mRNA level, HMGB1 protein, tumor necrosis factor alpha (TNF-alpha), and interleukin 10 (IL-10). HMGB1 mRNA levels were tested using real-time polymerase chain reaction. HMGB1 protein expression was measured using Western blot. TNF-alpha and IL-10 were tested using enzyme-linked immunosorbent assay.
The expression of HMGB1 mRNA and HMGB1 protein was higher in the AOSC group than in the normal controls (P<0.01), and the levels gradually decreased to normal after treatment of the disease (P<0.01). The content of TNF-alpha and IL-10 in peripheral blood of patients with AOSC was significantly higher than that of normal controls (P<0.01) but decreased to normal levels after the necessary treatment (P<0.01).
The levels of HMGB1 mRNA and HMGB1 protein were elevated in patients with AOSC, which may play an important role in the inflammation of the bile duct and appears to be associated with the development of sepsis. This suggests the importance of monitoring HMGB1 levels in the management of AOSC-induced sepsis.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>25792849</pmid><doi>10.2147/JIR.S77539</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1178-7031 |
ispartof | Journal of inflammation research, 2015-01, Vol.8 (default), p.71-77 |
issn | 1178-7031 1178-7031 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_788b895bc0f0479b947f60eafe2ee5e6 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); Taylor & Francis Open Access; PubMed Central Free; IngentaConnect Journals |
subjects | AOSC Appendicitis Cholangitis Chromosomal proteins Cytokines Deoxyribonucleic acid DNA Endoscopy Gallbladder diseases HMGB1 Hospitals Infections Inflammation interleukin 10 Interleukins Original Research Pathogenesis Patients Polymerase chain reaction Proteins Sepsis Signal transduction Surgery TNF-alpha Tumor necrosis factor Tumor necrosis factor-TNF |
title | Role of high-mobility group box 1 in patients with acute obstructive suppurative cholangitis-induced sepsis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T13%3A47%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20high-mobility%20group%20box%201%20in%20patients%20with%20acute%20obstructive%20suppurative%20cholangitis-induced%20sepsis&rft.jtitle=Journal%20of%20inflammation%20research&rft.au=Singh,%20Akanand&rft.date=2015-01-01&rft.volume=8&rft.issue=default&rft.spage=71&rft.epage=77&rft.pages=71-77&rft.issn=1178-7031&rft.eissn=1178-7031&rft_id=info:doi/10.2147/JIR.S77539&rft_dat=%3Cgale_doaj_%3EA446735640%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c611t-7ce68806b0588f186a3df1b0ed010f3b1044667088cff097cdb209cbc1daaec13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2232157805&rft_id=info:pmid/25792849&rft_galeid=A446735640&rfr_iscdi=true |