Kappa opioid receptor agonists improve postoperative cognitive dysfunction in rats via the JAK2/STAT3 signaling pathway

Postoperative cognitive dysfunction (POCD) is a common and well-known complication following surgery, particularly cardiopulmonary bypass (CPB) surgery. There are currently no suitable treatments for POCD, which is associated with increased illness and mortality rates. The present study aimed to ide...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of molecular medicine 2019-11, Vol.44 (5), p.1866-1876
Hauptverfasser: Li, Xi, Sun, Yingjie, Jin, Qiang, Song, Dandan, Diao, Yugang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1876
container_issue 5
container_start_page 1866
container_title International journal of molecular medicine
container_volume 44
creator Li, Xi
Sun, Yingjie
Jin, Qiang
Song, Dandan
Diao, Yugang
description Postoperative cognitive dysfunction (POCD) is a common and well-known complication following surgery, particularly cardiopulmonary bypass (CPB) surgery. There are currently no suitable treatments for POCD, which is associated with increased illness and mortality rates. The present study aimed to identify a novel treatment for POCD. The protective effect of kappa opioid receptor (KOR) agonists on POCD in rats following CPB was determined and the regulatory mechanism of the Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway was examined. The rats were randomly divided into five groups: Sham operation (Sham group), CPB operation (CPB group), KOR agonist + CPB (K group), KOR agonist + norbinaltorphimine (nor-BNI) + CPB (NK group), and KOR agonist + JAK2-STAT3 specific pathway inhibitor + CPB (AG group). A water maze test and neurological function scores were used to evaluate POCD. Hematoxylin and eosin staining was used to observe hippocampal neurons. ELISA was used to detect the levels of inflammatory factors, oxidative stress factors and brain injury markers. Immunofluorescence was used to visualize the neurons. TUNEL staining and western blotting were used to detect neuronal apoptosis, and western blotting was also used to detect JAK2/STAT3 pathway-related proteins. The KOR agonists significantly improved POCD. S-100[beta] and NSE detection revealed that KOR agonists alleviated brain damage in CPB rats, and this result was reversed by KOR antagonists. The KOR agonists led to a significantly reduced inflammatory response and oxidative stress, as determined by ELISA detection, and attenuated hippocampal neuronal apoptosis, as revealed by TUNEL staining and western blotting, compared with the results in the CPB group. Finally, the KOR agonists inhibited the expression levels of phosphorylated (p-)JAK2 and p-STAT3, rather than total JAK2 and STAT3, compared with levels in the CPB group. Taken together, KOR agonists improved POCD in rats with CPB by inhibiting the JAK2/STAT3 signaling pathway.
doi_str_mv 10.3892/ijmm.2019.4339
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6777679</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A603761514</galeid><sourcerecordid>A603761514</sourcerecordid><originalsourceid>FETCH-LOGICAL-c462t-6c8002e2dfd57ace489b9bb44e603468af3542d64b4a228a3c8a2e379d8f98d93</originalsourceid><addsrcrecordid>eNptUU1r3DAQFaWhSdNeexb07I0tyZZ0KSyh6UcCOWQDvQlZlr2zrCVV0m7Yf1-5DS2FMIf5evN4w0PoQ1OvqJDkCnbzvCJ1I1eMUvkKXTRcNhVh7MfrUjc1ryhvu3P0NqVdXZOWSfEGndOmZS0T7QV6utUhaOwDeBhwtMaG7CPWk3eQcsIwh-iPFgefsg826gylM35y8LsaTmk8OJPBOwwOl33CR9A4by3-vr4lVw-b9YbiBJPTe3ATDjpvn_TpHTob9T7Z98_5Ej3efN5cf63u7r98u17fVYZ1JFedEUW1JcM4tFwby4TsZd8zZruask7okbaMDB3rmSZEaGqEJpZyOYhRikHSS_TpD2849LMdjHU56r0KEWYdT8prUP9vHGzV5I-q45x3fCH4-EwQ_c-DTVnt_CGWZ5IitCaUkqLgH2rSe6vAjb6QmRmSUeuilHdN2yyo1QuoEoOdwXhnRyjzlw5M9ClFO_4V3tRq8V8t_qvFf7X4T38B0kWjzA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2302332354</pqid></control><display><type>article</type><title>Kappa opioid receptor agonists improve postoperative cognitive dysfunction in rats via the JAK2/STAT3 signaling pathway</title><source>Spandidos Publications Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Li, Xi ; Sun, Yingjie ; Jin, Qiang ; Song, Dandan ; Diao, Yugang</creator><creatorcontrib>Li, Xi ; Sun, Yingjie ; Jin, Qiang ; Song, Dandan ; Diao, Yugang</creatorcontrib><description>Postoperative cognitive dysfunction (POCD) is a common and well-known complication following surgery, particularly cardiopulmonary bypass (CPB) surgery. There are currently no suitable treatments for POCD, which is associated with increased illness and mortality rates. The present study aimed to identify a novel treatment for POCD. The protective effect of kappa opioid receptor (KOR) agonists on POCD in rats following CPB was determined and the regulatory mechanism of the Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway was examined. The rats were randomly divided into five groups: Sham operation (Sham group), CPB operation (CPB group), KOR agonist + CPB (K group), KOR agonist + norbinaltorphimine (nor-BNI) + CPB (NK group), and KOR agonist + JAK2-STAT3 specific pathway inhibitor + CPB (AG group). A water maze test and neurological function scores were used to evaluate POCD. Hematoxylin and eosin staining was used to observe hippocampal neurons. ELISA was used to detect the levels of inflammatory factors, oxidative stress factors and brain injury markers. Immunofluorescence was used to visualize the neurons. TUNEL staining and western blotting were used to detect neuronal apoptosis, and western blotting was also used to detect JAK2/STAT3 pathway-related proteins. The KOR agonists significantly improved POCD. S-100[beta] and NSE detection revealed that KOR agonists alleviated brain damage in CPB rats, and this result was reversed by KOR antagonists. The KOR agonists led to a significantly reduced inflammatory response and oxidative stress, as determined by ELISA detection, and attenuated hippocampal neuronal apoptosis, as revealed by TUNEL staining and western blotting, compared with the results in the CPB group. Finally, the KOR agonists inhibited the expression levels of phosphorylated (p-)JAK2 and p-STAT3, rather than total JAK2 and STAT3, compared with levels in the CPB group. Taken together, KOR agonists improved POCD in rats with CPB by inhibiting the JAK2/STAT3 signaling pathway.</description><identifier>ISSN: 1107-3756</identifier><identifier>EISSN: 1791-244X</identifier><identifier>DOI: 10.3892/ijmm.2019.4339</identifier><identifier>PMID: 31545485</identifier><language>eng</language><publisher>Athens: Spandidos Publications</publisher><subject>Agricultural associations ; Animal cognition ; Apoptosis ; Brain damage ; Brain injuries ; Cognitive disorders ; Coronary artery bypass ; Enzyme-linked immunosorbent assay ; Fluorescent antibody technique ; Health aspects ; Heart surgery ; Intubation ; Ischemia ; Kinases ; Laboratory animals ; Narcotics ; Nervous system ; Neurons ; Novels ; Oxidative stress ; Pharmaceuticals ; Phosphorylation ; Proteins ; Rodents ; Studies ; Veins &amp; arteries ; Water</subject><ispartof>International journal of molecular medicine, 2019-11, Vol.44 (5), p.1866-1876</ispartof><rights>COPYRIGHT 2019 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2019</rights><rights>Copyright: © Li et al. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-6c8002e2dfd57ace489b9bb44e603468af3542d64b4a228a3c8a2e379d8f98d93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids></links><search><creatorcontrib>Li, Xi</creatorcontrib><creatorcontrib>Sun, Yingjie</creatorcontrib><creatorcontrib>Jin, Qiang</creatorcontrib><creatorcontrib>Song, Dandan</creatorcontrib><creatorcontrib>Diao, Yugang</creatorcontrib><title>Kappa opioid receptor agonists improve postoperative cognitive dysfunction in rats via the JAK2/STAT3 signaling pathway</title><title>International journal of molecular medicine</title><description>Postoperative cognitive dysfunction (POCD) is a common and well-known complication following surgery, particularly cardiopulmonary bypass (CPB) surgery. There are currently no suitable treatments for POCD, which is associated with increased illness and mortality rates. The present study aimed to identify a novel treatment for POCD. The protective effect of kappa opioid receptor (KOR) agonists on POCD in rats following CPB was determined and the regulatory mechanism of the Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway was examined. The rats were randomly divided into five groups: Sham operation (Sham group), CPB operation (CPB group), KOR agonist + CPB (K group), KOR agonist + norbinaltorphimine (nor-BNI) + CPB (NK group), and KOR agonist + JAK2-STAT3 specific pathway inhibitor + CPB (AG group). A water maze test and neurological function scores were used to evaluate POCD. Hematoxylin and eosin staining was used to observe hippocampal neurons. ELISA was used to detect the levels of inflammatory factors, oxidative stress factors and brain injury markers. Immunofluorescence was used to visualize the neurons. TUNEL staining and western blotting were used to detect neuronal apoptosis, and western blotting was also used to detect JAK2/STAT3 pathway-related proteins. The KOR agonists significantly improved POCD. S-100[beta] and NSE detection revealed that KOR agonists alleviated brain damage in CPB rats, and this result was reversed by KOR antagonists. The KOR agonists led to a significantly reduced inflammatory response and oxidative stress, as determined by ELISA detection, and attenuated hippocampal neuronal apoptosis, as revealed by TUNEL staining and western blotting, compared with the results in the CPB group. Finally, the KOR agonists inhibited the expression levels of phosphorylated (p-)JAK2 and p-STAT3, rather than total JAK2 and STAT3, compared with levels in the CPB group. Taken together, KOR agonists improved POCD in rats with CPB by inhibiting the JAK2/STAT3 signaling pathway.</description><subject>Agricultural associations</subject><subject>Animal cognition</subject><subject>Apoptosis</subject><subject>Brain damage</subject><subject>Brain injuries</subject><subject>Cognitive disorders</subject><subject>Coronary artery bypass</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Fluorescent antibody technique</subject><subject>Health aspects</subject><subject>Heart surgery</subject><subject>Intubation</subject><subject>Ischemia</subject><subject>Kinases</subject><subject>Laboratory animals</subject><subject>Narcotics</subject><subject>Nervous system</subject><subject>Neurons</subject><subject>Novels</subject><subject>Oxidative stress</subject><subject>Pharmaceuticals</subject><subject>Phosphorylation</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Studies</subject><subject>Veins &amp; arteries</subject><subject>Water</subject><issn>1107-3756</issn><issn>1791-244X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptUU1r3DAQFaWhSdNeexb07I0tyZZ0KSyh6UcCOWQDvQlZlr2zrCVV0m7Yf1-5DS2FMIf5evN4w0PoQ1OvqJDkCnbzvCJ1I1eMUvkKXTRcNhVh7MfrUjc1ryhvu3P0NqVdXZOWSfEGndOmZS0T7QV6utUhaOwDeBhwtMaG7CPWk3eQcsIwh-iPFgefsg826gylM35y8LsaTmk8OJPBOwwOl33CR9A4by3-vr4lVw-b9YbiBJPTe3ATDjpvn_TpHTob9T7Z98_5Ej3efN5cf63u7r98u17fVYZ1JFedEUW1JcM4tFwby4TsZd8zZruask7okbaMDB3rmSZEaGqEJpZyOYhRikHSS_TpD2849LMdjHU56r0KEWYdT8prUP9vHGzV5I-q45x3fCH4-EwQ_c-DTVnt_CGWZ5IitCaUkqLgH2rSe6vAjb6QmRmSUeuilHdN2yyo1QuoEoOdwXhnRyjzlw5M9ClFO_4V3tRq8V8t_qvFf7X4T38B0kWjzA</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Li, Xi</creator><creator>Sun, Yingjie</creator><creator>Jin, Qiang</creator><creator>Song, Dandan</creator><creator>Diao, Yugang</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</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>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20191101</creationdate><title>Kappa opioid receptor agonists improve postoperative cognitive dysfunction in rats via the JAK2/STAT3 signaling pathway</title><author>Li, Xi ; Sun, Yingjie ; Jin, Qiang ; Song, Dandan ; Diao, Yugang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-6c8002e2dfd57ace489b9bb44e603468af3542d64b4a228a3c8a2e379d8f98d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Agricultural associations</topic><topic>Animal cognition</topic><topic>Apoptosis</topic><topic>Brain damage</topic><topic>Brain injuries</topic><topic>Cognitive disorders</topic><topic>Coronary artery bypass</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Fluorescent antibody technique</topic><topic>Health aspects</topic><topic>Heart surgery</topic><topic>Intubation</topic><topic>Ischemia</topic><topic>Kinases</topic><topic>Laboratory animals</topic><topic>Narcotics</topic><topic>Nervous system</topic><topic>Neurons</topic><topic>Novels</topic><topic>Oxidative stress</topic><topic>Pharmaceuticals</topic><topic>Phosphorylation</topic><topic>Proteins</topic><topic>Rodents</topic><topic>Studies</topic><topic>Veins &amp; arteries</topic><topic>Water</topic><toplevel>online_resources</toplevel><creatorcontrib>Li, Xi</creatorcontrib><creatorcontrib>Sun, Yingjie</creatorcontrib><creatorcontrib>Jin, Qiang</creatorcontrib><creatorcontrib>Song, Dandan</creatorcontrib><creatorcontrib>Diao, Yugang</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</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>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xi</au><au>Sun, Yingjie</au><au>Jin, Qiang</au><au>Song, Dandan</au><au>Diao, Yugang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kappa opioid receptor agonists improve postoperative cognitive dysfunction in rats via the JAK2/STAT3 signaling pathway</atitle><jtitle>International journal of molecular medicine</jtitle><date>2019-11-01</date><risdate>2019</risdate><volume>44</volume><issue>5</issue><spage>1866</spage><epage>1876</epage><pages>1866-1876</pages><issn>1107-3756</issn><eissn>1791-244X</eissn><abstract>Postoperative cognitive dysfunction (POCD) is a common and well-known complication following surgery, particularly cardiopulmonary bypass (CPB) surgery. There are currently no suitable treatments for POCD, which is associated with increased illness and mortality rates. The present study aimed to identify a novel treatment for POCD. The protective effect of kappa opioid receptor (KOR) agonists on POCD in rats following CPB was determined and the regulatory mechanism of the Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway was examined. The rats were randomly divided into five groups: Sham operation (Sham group), CPB operation (CPB group), KOR agonist + CPB (K group), KOR agonist + norbinaltorphimine (nor-BNI) + CPB (NK group), and KOR agonist + JAK2-STAT3 specific pathway inhibitor + CPB (AG group). A water maze test and neurological function scores were used to evaluate POCD. Hematoxylin and eosin staining was used to observe hippocampal neurons. ELISA was used to detect the levels of inflammatory factors, oxidative stress factors and brain injury markers. Immunofluorescence was used to visualize the neurons. TUNEL staining and western blotting were used to detect neuronal apoptosis, and western blotting was also used to detect JAK2/STAT3 pathway-related proteins. The KOR agonists significantly improved POCD. S-100[beta] and NSE detection revealed that KOR agonists alleviated brain damage in CPB rats, and this result was reversed by KOR antagonists. The KOR agonists led to a significantly reduced inflammatory response and oxidative stress, as determined by ELISA detection, and attenuated hippocampal neuronal apoptosis, as revealed by TUNEL staining and western blotting, compared with the results in the CPB group. Finally, the KOR agonists inhibited the expression levels of phosphorylated (p-)JAK2 and p-STAT3, rather than total JAK2 and STAT3, compared with levels in the CPB group. Taken together, KOR agonists improved POCD in rats with CPB by inhibiting the JAK2/STAT3 signaling pathway.</abstract><cop>Athens</cop><pub>Spandidos Publications</pub><pmid>31545485</pmid><doi>10.3892/ijmm.2019.4339</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1107-3756
ispartof International journal of molecular medicine, 2019-11, Vol.44 (5), p.1866-1876
issn 1107-3756
1791-244X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6777679
source Spandidos Publications Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Agricultural associations
Animal cognition
Apoptosis
Brain damage
Brain injuries
Cognitive disorders
Coronary artery bypass
Enzyme-linked immunosorbent assay
Fluorescent antibody technique
Health aspects
Heart surgery
Intubation
Ischemia
Kinases
Laboratory animals
Narcotics
Nervous system
Neurons
Novels
Oxidative stress
Pharmaceuticals
Phosphorylation
Proteins
Rodents
Studies
Veins & arteries
Water
title Kappa opioid receptor agonists improve postoperative cognitive dysfunction in rats via the JAK2/STAT3 signaling pathway
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T18%3A15%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Kappa%20opioid%20receptor%20agonists%20improve%20postoperative%20cognitive%20dysfunction%20in%20rats%20via%20the%20JAK2/STAT3%20signaling%20pathway&rft.jtitle=International%20journal%20of%20molecular%20medicine&rft.au=Li,%20Xi&rft.date=2019-11-01&rft.volume=44&rft.issue=5&rft.spage=1866&rft.epage=1876&rft.pages=1866-1876&rft.issn=1107-3756&rft.eissn=1791-244X&rft_id=info:doi/10.3892/ijmm.2019.4339&rft_dat=%3Cgale_pubme%3EA603761514%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2302332354&rft_id=info:pmid/31545485&rft_galeid=A603761514&rfr_iscdi=true