Indoleamine 2,3-dioxygenase is upregulated in the brain of rats with acute pancreatitis

Abstract Background Acute pancreatitis (AP) has an effect on both inflammatory/autoimmune processes and psychological states, but the pathophysiological causes of pancreatic encephalopathy in the brain are unclear. We hypothesized that the peripheral immune/inflammatory response during AP can affect...

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Veröffentlicht in:Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2015-05, Vol.15 (3), p.281-285
Hauptverfasser: Jiang, Hua, Li, Fei, Liu, Shuang, Sun, Haichen, Cui, Yeqing, Wu, Yanchuan, Gao, Chongchong
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container_issue 3
container_start_page 281
container_title Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]
container_volume 15
creator Jiang, Hua
Li, Fei
Liu, Shuang
Sun, Haichen
Cui, Yeqing
Wu, Yanchuan
Gao, Chongchong
description Abstract Background Acute pancreatitis (AP) has an effect on both inflammatory/autoimmune processes and psychological states, but the pathophysiological causes of pancreatic encephalopathy in the brain are unclear. We hypothesized that the peripheral immune/inflammatory response during AP can affect indolamine 2,3-dioxygenase (IDO) expression and serotonin content in the brain. Methods About 210 male Sprague Dawley rats were randomly divided into five groups: control (0 h) and 6 h, 24 h, 48 h and 72 h experimental groups. Acute pancreatitis was induced by an injection of a sodium taurocholate solution via a cannulated bile-pancreatic duct. We measured the plasma TNF-α and IL-6 levels; serotonin, 5-HIAA and the protein concentration levels of IDO and monoamine oxidase A (MAO-A) were evaluated in the striatum, hippocampus and left prefrontal cortex. Results The IL-6 and the TNF-α levels increased in the 24 h, 48 h and 72 h groups. The IDO concentrations of both the 72 h group in the hippocampus and 48 h, 72 h groups in the prefrontal cortex increased; in the corpus striatum, the IDO concentrations fluctuated without statistical significance. The MAO-A protein concentration of the 6 h and 24 h groups decreased in the striatum, hippocampus and prefrontal cortex. There were no statistically significant differences found in the serotonin and 5-HIAA concentrations. Conclusions During the process of AP, cytokines, such as IL-6 and TNF-α, may play a role in activation of neuronal pathways utilizing the metabolic enzyme IDO, which may play an important role in determining the mental symptomatology accompanying AP.
doi_str_mv 10.1016/j.pan.2015.03.002
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We hypothesized that the peripheral immune/inflammatory response during AP can affect indolamine 2,3-dioxygenase (IDO) expression and serotonin content in the brain. Methods About 210 male Sprague Dawley rats were randomly divided into five groups: control (0 h) and 6 h, 24 h, 48 h and 72 h experimental groups. Acute pancreatitis was induced by an injection of a sodium taurocholate solution via a cannulated bile-pancreatic duct. We measured the plasma TNF-α and IL-6 levels; serotonin, 5-HIAA and the protein concentration levels of IDO and monoamine oxidase A (MAO-A) were evaluated in the striatum, hippocampus and left prefrontal cortex. Results The IL-6 and the TNF-α levels increased in the 24 h, 48 h and 72 h groups. The IDO concentrations of both the 72 h group in the hippocampus and 48 h, 72 h groups in the prefrontal cortex increased; in the corpus striatum, the IDO concentrations fluctuated without statistical significance. The MAO-A protein concentration of the 6 h and 24 h groups decreased in the striatum, hippocampus and prefrontal cortex. There were no statistically significant differences found in the serotonin and 5-HIAA concentrations. Conclusions During the process of AP, cytokines, such as IL-6 and TNF-α, may play a role in activation of neuronal pathways utilizing the metabolic enzyme IDO, which may play an important role in determining the mental symptomatology accompanying AP.</description><identifier>ISSN: 1424-3903</identifier><identifier>EISSN: 1424-3911</identifier><identifier>DOI: 10.1016/j.pan.2015.03.002</identifier><identifier>PMID: 25829217</identifier><language>eng</language><publisher>Switzerland: Elsevier B.V</publisher><subject>Acute Disease ; Acute pancreatitis ; Animals ; Biomarkers - metabolism ; Brain - enzymology ; Brain - immunology ; Cytokines ; Cytokines - metabolism ; Endocrinology &amp; Metabolism ; Gastroenterology and Hepatology ; Indolamine 2,3-dioxygenase ; Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism ; Male ; Mental depression ; Monoamine oxidase ; Pancreas ; Pancreatic encephalopathy ; Pancreatitis - enzymology ; Pancreatitis - immunology ; Random Allocation ; Rats ; Rats, Sprague-Dawley ; Rodents ; Serotonin ; Studies ; Up-Regulation</subject><ispartof>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2015-05, Vol.15 (3), p.281-285</ispartof><rights>IAP and EPC</rights><rights>2015 IAP and EPC</rights><rights>Copyright © 2015 IAP and EPC. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Limited May/Jun 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-3921ae18af3a02217779958833665563e5b1e1a11d6d979fe9f4bc61b26c9f23</citedby><cites>FETCH-LOGICAL-c539t-3921ae18af3a02217779958833665563e5b1e1a11d6d979fe9f4bc61b26c9f23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25829217$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Hua</creatorcontrib><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Liu, Shuang</creatorcontrib><creatorcontrib>Sun, Haichen</creatorcontrib><creatorcontrib>Cui, Yeqing</creatorcontrib><creatorcontrib>Wu, Yanchuan</creatorcontrib><creatorcontrib>Gao, Chongchong</creatorcontrib><title>Indoleamine 2,3-dioxygenase is upregulated in the brain of rats with acute pancreatitis</title><title>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</title><addtitle>Pancreatology</addtitle><description>Abstract Background Acute pancreatitis (AP) has an effect on both inflammatory/autoimmune processes and psychological states, but the pathophysiological causes of pancreatic encephalopathy in the brain are unclear. We hypothesized that the peripheral immune/inflammatory response during AP can affect indolamine 2,3-dioxygenase (IDO) expression and serotonin content in the brain. Methods About 210 male Sprague Dawley rats were randomly divided into five groups: control (0 h) and 6 h, 24 h, 48 h and 72 h experimental groups. Acute pancreatitis was induced by an injection of a sodium taurocholate solution via a cannulated bile-pancreatic duct. We measured the plasma TNF-α and IL-6 levels; serotonin, 5-HIAA and the protein concentration levels of IDO and monoamine oxidase A (MAO-A) were evaluated in the striatum, hippocampus and left prefrontal cortex. Results The IL-6 and the TNF-α levels increased in the 24 h, 48 h and 72 h groups. The IDO concentrations of both the 72 h group in the hippocampus and 48 h, 72 h groups in the prefrontal cortex increased; in the corpus striatum, the IDO concentrations fluctuated without statistical significance. The MAO-A protein concentration of the 6 h and 24 h groups decreased in the striatum, hippocampus and prefrontal cortex. There were no statistically significant differences found in the serotonin and 5-HIAA concentrations. Conclusions During the process of AP, cytokines, such as IL-6 and TNF-α, may play a role in activation of neuronal pathways utilizing the metabolic enzyme IDO, which may play an important role in determining the mental symptomatology accompanying AP.</description><subject>Acute Disease</subject><subject>Acute pancreatitis</subject><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Brain - enzymology</subject><subject>Brain - immunology</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Gastroenterology and Hepatology</subject><subject>Indolamine 2,3-dioxygenase</subject><subject>Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism</subject><subject>Male</subject><subject>Mental depression</subject><subject>Monoamine oxidase</subject><subject>Pancreas</subject><subject>Pancreatic encephalopathy</subject><subject>Pancreatitis - enzymology</subject><subject>Pancreatitis - immunology</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Serotonin</subject><subject>Studies</subject><subject>Up-Regulation</subject><issn>1424-3903</issn><issn>1424-3911</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksFrFTEQxoNYbK3-AV4k4MWDb5tJNtkNQkFK1UKhBwseQzY72-a5L_tMstr335vl1Qo92NPM4fd9zHwzhLwBVgEDdbKutjZUnIGsmKgY48_IEdS8XgkN8PyhZ-KQvExpXQAOoF-QQy5brjk0R-T7ReinEe3GB6T8g1j1frrb3WCwCalPdN5GvJlHm7GnPtB8i7SLtnTTQKPNif72-ZZaN2ekZRgX0WaffXpFDgY7Jnx9X4_J9efz67Ovq8urLxdnny5XTgqdy3AcLEJrB2GX6Zqm0Vq2rRBKSakEyg4QLECvet3oAfVQd05Bx5XTAxfH5P3edhunnzOmbDY-ORxHG3Cak4GmlZxrreFpVLVCNqKu24K-e4SupzmGsseeamumZKFgT7k4pRRxMNvoNzbuDDCz3MesTYnELPcxTJgSf9G8vXeeuw32D4q_BynAxz2AJbRfHqNJzmNw2PuILpt-8v-1P32kdqMP3tnxB-4w_dvCJG6Y-bY8yPIfIBljNYD4AypfspA</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Jiang, Hua</creator><creator>Li, Fei</creator><creator>Liu, Shuang</creator><creator>Sun, Haichen</creator><creator>Cui, Yeqing</creator><creator>Wu, Yanchuan</creator><creator>Gao, Chongchong</creator><general>Elsevier B.V</general><general>Elsevier Limited</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20150501</creationdate><title>Indoleamine 2,3-dioxygenase is upregulated in the brain of rats with acute pancreatitis</title><author>Jiang, Hua ; Li, Fei ; Liu, Shuang ; Sun, Haichen ; Cui, Yeqing ; Wu, Yanchuan ; Gao, Chongchong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-3921ae18af3a02217779958833665563e5b1e1a11d6d979fe9f4bc61b26c9f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acute Disease</topic><topic>Acute pancreatitis</topic><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Brain - enzymology</topic><topic>Brain - immunology</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Gastroenterology and Hepatology</topic><topic>Indolamine 2,3-dioxygenase</topic><topic>Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism</topic><topic>Male</topic><topic>Mental depression</topic><topic>Monoamine oxidase</topic><topic>Pancreas</topic><topic>Pancreatic encephalopathy</topic><topic>Pancreatitis - enzymology</topic><topic>Pancreatitis - immunology</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Serotonin</topic><topic>Studies</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Hua</creatorcontrib><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Liu, Shuang</creatorcontrib><creatorcontrib>Sun, Haichen</creatorcontrib><creatorcontrib>Cui, Yeqing</creatorcontrib><creatorcontrib>Wu, Yanchuan</creatorcontrib><creatorcontrib>Gao, Chongchong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Hua</au><au>Li, Fei</au><au>Liu, Shuang</au><au>Sun, Haichen</au><au>Cui, Yeqing</au><au>Wu, Yanchuan</au><au>Gao, Chongchong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Indoleamine 2,3-dioxygenase is upregulated in the brain of rats with acute pancreatitis</atitle><jtitle>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</jtitle><addtitle>Pancreatology</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>15</volume><issue>3</issue><spage>281</spage><epage>285</epage><pages>281-285</pages><issn>1424-3903</issn><eissn>1424-3911</eissn><abstract>Abstract Background Acute pancreatitis (AP) has an effect on both inflammatory/autoimmune processes and psychological states, but the pathophysiological causes of pancreatic encephalopathy in the brain are unclear. We hypothesized that the peripheral immune/inflammatory response during AP can affect indolamine 2,3-dioxygenase (IDO) expression and serotonin content in the brain. Methods About 210 male Sprague Dawley rats were randomly divided into five groups: control (0 h) and 6 h, 24 h, 48 h and 72 h experimental groups. Acute pancreatitis was induced by an injection of a sodium taurocholate solution via a cannulated bile-pancreatic duct. We measured the plasma TNF-α and IL-6 levels; serotonin, 5-HIAA and the protein concentration levels of IDO and monoamine oxidase A (MAO-A) were evaluated in the striatum, hippocampus and left prefrontal cortex. Results The IL-6 and the TNF-α levels increased in the 24 h, 48 h and 72 h groups. The IDO concentrations of both the 72 h group in the hippocampus and 48 h, 72 h groups in the prefrontal cortex increased; in the corpus striatum, the IDO concentrations fluctuated without statistical significance. The MAO-A protein concentration of the 6 h and 24 h groups decreased in the striatum, hippocampus and prefrontal cortex. There were no statistically significant differences found in the serotonin and 5-HIAA concentrations. Conclusions During the process of AP, cytokines, such as IL-6 and TNF-α, may play a role in activation of neuronal pathways utilizing the metabolic enzyme IDO, which may play an important role in determining the mental symptomatology accompanying AP.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>25829217</pmid><doi>10.1016/j.pan.2015.03.002</doi><tpages>5</tpages></addata></record>
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ispartof Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2015-05, Vol.15 (3), p.281-285
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subjects Acute Disease
Acute pancreatitis
Animals
Biomarkers - metabolism
Brain - enzymology
Brain - immunology
Cytokines
Cytokines - metabolism
Endocrinology & Metabolism
Gastroenterology and Hepatology
Indolamine 2,3-dioxygenase
Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism
Male
Mental depression
Monoamine oxidase
Pancreas
Pancreatic encephalopathy
Pancreatitis - enzymology
Pancreatitis - immunology
Random Allocation
Rats
Rats, Sprague-Dawley
Rodents
Serotonin
Studies
Up-Regulation
title Indoleamine 2,3-dioxygenase is upregulated in the brain of rats with acute pancreatitis
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