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Cytokine Effects on Mechano-Induced Electrical Activity in Atrial Myocardium
The role of cytokines as regulators of stretch-related mechanisms is of special importance since mechano-sensitivity plays an important role in a wide variety of biological processes. Here, we elucidate the influence of cytokine application on mechano-sensitivity and mechano-transduction. The atrial...
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Published in: | Immunological investigations 2017-01, Vol.46 (1), p.22-37 |
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description | The role of cytokines as regulators of stretch-related mechanisms is of special importance since mechano-sensitivity plays an important role in a wide variety of biological processes. Here, we elucidate the influence of cytokine application on mechano-sensitivity and mechano-transduction. The atrial myocardial stretch induces production of interleukin (IL)-2, IL-6, IL-13, IL-17A, and IL-18 with exception of tumor necrosis factor α (TNF-α), IL-1β, and vascular endothelial growth factor B (VEGF-B). Positive ionotropic effect was specific for VEGF-B, negative ionotropic effects were specific for TNF-α, IL-1β, IL-2, IL-6, IL-13, IL-17A and IL-18, while IL-1α doesn't show direct ionotropic effect. The IL-2, IL-6, IL-17A, IL-18, and VEGF-B cause elongation of the APD, in comparison with the reduced APD caused by the IL-13. The TNF-α, IL-1β, and IL-18 influences L-type Ca
2+
channels, IL-2 has an inhibitory effect on the fast Na
+
channels while IL-17A and VEGF-B were specific for Kir channels. With exception of the IL-1α, IL-2, and VEGF-B, all analyzed cytokines include nitric oxide dependent signaling with resultant combined effects on mechano-gated and Ca
2+
channels. The relationships between these pathways and the time-dependence of their activation are of important considerations in the evaluation of cytokine-induced electrical abnormality, specific for cardiac dysfunctions.
In general, the discussion presented in this review covers research devoted to counterbalance between different cytokines in the regulation of stretch-induced effects in rat atrial myocardium.
Abbreviations: APs: action potentials; APD25: action potential durations to 25% of re-polarization; APD50: action potential durations to 50% of repolarization; APD90: action potential durations to 90% of repolarization; MGCs: mechanically gated channels |
doi_str_mv | 10.1080/08820139.2016.1208220 |
format | article |
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2+
channels, IL-2 has an inhibitory effect on the fast Na
+
channels while IL-17A and VEGF-B were specific for Kir channels. With exception of the IL-1α, IL-2, and VEGF-B, all analyzed cytokines include nitric oxide dependent signaling with resultant combined effects on mechano-gated and Ca
2+
channels. The relationships between these pathways and the time-dependence of their activation are of important considerations in the evaluation of cytokine-induced electrical abnormality, specific for cardiac dysfunctions.
In general, the discussion presented in this review covers research devoted to counterbalance between different cytokines in the regulation of stretch-induced effects in rat atrial myocardium.
Abbreviations: APs: action potentials; APD25: action potential durations to 25% of re-polarization; APD50: action potential durations to 50% of repolarization; APD90: action potential durations to 90% of repolarization; MGCs: mechanically gated channels</description><identifier>ISSN: 0882-0139</identifier><identifier>EISSN: 1532-4311</identifier><identifier>DOI: 10.1080/08820139.2016.1208220</identifier><identifier>PMID: 27617892</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Action Potentials - immunology ; Animals ; Atrial Function - immunology ; Atrial myocardium ; cytokines ; Cytokines - immunology ; Cytokines - metabolism ; Electric Conductivity ; Electricity ; Heart Atria - pathology ; Humans ; mechanical stretch ; Mechanotransduction, Cellular - immunology ; Myocardial Contraction ; Myocardium - immunology ; Myocardium - metabolism ; Rats ; Signal Transduction ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>Immunological investigations, 2017-01, Vol.46 (1), p.22-37</ispartof><rights>2016 Taylor & Francis 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-8ea119a1db2b4a1c477f680262b7f9dd1e0e73652f388a62b87297712422553f3</citedby><cites>FETCH-LOGICAL-c432t-8ea119a1db2b4a1c477f680262b7f9dd1e0e73652f388a62b87297712422553f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27617892$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kazanski, V.</creatorcontrib><creatorcontrib>Mitrokhin, V. M.</creatorcontrib><creatorcontrib>Mladenov, M. I.</creatorcontrib><creatorcontrib>Kamkin, A. G.</creatorcontrib><title>Cytokine Effects on Mechano-Induced Electrical Activity in Atrial Myocardium</title><title>Immunological investigations</title><addtitle>Immunol Invest</addtitle><description>The role of cytokines as regulators of stretch-related mechanisms is of special importance since mechano-sensitivity plays an important role in a wide variety of biological processes. Here, we elucidate the influence of cytokine application on mechano-sensitivity and mechano-transduction. The atrial myocardial stretch induces production of interleukin (IL)-2, IL-6, IL-13, IL-17A, and IL-18 with exception of tumor necrosis factor α (TNF-α), IL-1β, and vascular endothelial growth factor B (VEGF-B). Positive ionotropic effect was specific for VEGF-B, negative ionotropic effects were specific for TNF-α, IL-1β, IL-2, IL-6, IL-13, IL-17A and IL-18, while IL-1α doesn't show direct ionotropic effect. The IL-2, IL-6, IL-17A, IL-18, and VEGF-B cause elongation of the APD, in comparison with the reduced APD caused by the IL-13. The TNF-α, IL-1β, and IL-18 influences L-type Ca
2+
channels, IL-2 has an inhibitory effect on the fast Na
+
channels while IL-17A and VEGF-B were specific for Kir channels. With exception of the IL-1α, IL-2, and VEGF-B, all analyzed cytokines include nitric oxide dependent signaling with resultant combined effects on mechano-gated and Ca
2+
channels. The relationships between these pathways and the time-dependence of their activation are of important considerations in the evaluation of cytokine-induced electrical abnormality, specific for cardiac dysfunctions.
In general, the discussion presented in this review covers research devoted to counterbalance between different cytokines in the regulation of stretch-induced effects in rat atrial myocardium.
Abbreviations: APs: action potentials; APD25: action potential durations to 25% of re-polarization; APD50: action potential durations to 50% of repolarization; APD90: action potential durations to 90% of repolarization; MGCs: mechanically gated channels</description><subject>Action Potentials - immunology</subject><subject>Animals</subject><subject>Atrial Function - immunology</subject><subject>Atrial myocardium</subject><subject>cytokines</subject><subject>Cytokines - immunology</subject><subject>Cytokines - metabolism</subject><subject>Electric Conductivity</subject><subject>Electricity</subject><subject>Heart Atria - pathology</subject><subject>Humans</subject><subject>mechanical stretch</subject><subject>Mechanotransduction, Cellular - immunology</subject><subject>Myocardial Contraction</subject><subject>Myocardium - immunology</subject><subject>Myocardium - metabolism</subject><subject>Rats</subject><subject>Signal Transduction</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>0882-0139</issn><issn>1532-4311</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kE1PwzAMhiMEYuPjJ4B65NIRO22T3pim8SENcYFzlKWJCLTNSFpQ_z2dtnHkYkuvH9vSQ8gV0BlQQW-pEEiBlbOxFjNAKhDpEZlCzjDNGMAxmW6ZdAtNyFmMH5RSlhflKZkgL4CLEqdktRg6_-lakyytNbqLiW-TZ6PfVevTp7bqtamSZT1OgtOqTua6c9-uGxLXJvMxG6PnwWsVKtc3F-TEqjqay30_J2_3y9fFY7p6eXhazFepzhh2qTAKoFRQrXGdKdAZ57YQFAtcc1tWFRhqOCtytEwINaaCY8k5YIaY58yyc3Kzu7sJ_qs3sZONi9rUtWqN76MEkSMXDHg2ovkO1cHHGIyVm-AaFQYJVG5FyoNIuRUp9yLHvev9i37dmOpv62BuBO52gGutD4368aGuZKeG2gcbVKtdlOz_H7_o1oBk</recordid><startdate>20170102</startdate><enddate>20170102</enddate><creator>Kazanski, V.</creator><creator>Mitrokhin, V. M.</creator><creator>Mladenov, M. I.</creator><creator>Kamkin, A. G.</creator><general>Taylor & Francis</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></search><sort><creationdate>20170102</creationdate><title>Cytokine Effects on Mechano-Induced Electrical Activity in Atrial Myocardium</title><author>Kazanski, V. ; Mitrokhin, V. M. ; Mladenov, M. I. ; Kamkin, A. G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-8ea119a1db2b4a1c477f680262b7f9dd1e0e73652f388a62b87297712422553f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Action Potentials - immunology</topic><topic>Animals</topic><topic>Atrial Function - immunology</topic><topic>Atrial myocardium</topic><topic>cytokines</topic><topic>Cytokines - immunology</topic><topic>Cytokines - metabolism</topic><topic>Electric Conductivity</topic><topic>Electricity</topic><topic>Heart Atria - pathology</topic><topic>Humans</topic><topic>mechanical stretch</topic><topic>Mechanotransduction, Cellular - immunology</topic><topic>Myocardial Contraction</topic><topic>Myocardium - immunology</topic><topic>Myocardium - metabolism</topic><topic>Rats</topic><topic>Signal Transduction</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kazanski, V.</creatorcontrib><creatorcontrib>Mitrokhin, V. M.</creatorcontrib><creatorcontrib>Mladenov, M. I.</creatorcontrib><creatorcontrib>Kamkin, A. G.</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><jtitle>Immunological investigations</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazanski, V.</au><au>Mitrokhin, V. M.</au><au>Mladenov, M. I.</au><au>Kamkin, A. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokine Effects on Mechano-Induced Electrical Activity in Atrial Myocardium</atitle><jtitle>Immunological investigations</jtitle><addtitle>Immunol Invest</addtitle><date>2017-01-02</date><risdate>2017</risdate><volume>46</volume><issue>1</issue><spage>22</spage><epage>37</epage><pages>22-37</pages><issn>0882-0139</issn><eissn>1532-4311</eissn><abstract>The role of cytokines as regulators of stretch-related mechanisms is of special importance since mechano-sensitivity plays an important role in a wide variety of biological processes. Here, we elucidate the influence of cytokine application on mechano-sensitivity and mechano-transduction. The atrial myocardial stretch induces production of interleukin (IL)-2, IL-6, IL-13, IL-17A, and IL-18 with exception of tumor necrosis factor α (TNF-α), IL-1β, and vascular endothelial growth factor B (VEGF-B). Positive ionotropic effect was specific for VEGF-B, negative ionotropic effects were specific for TNF-α, IL-1β, IL-2, IL-6, IL-13, IL-17A and IL-18, while IL-1α doesn't show direct ionotropic effect. The IL-2, IL-6, IL-17A, IL-18, and VEGF-B cause elongation of the APD, in comparison with the reduced APD caused by the IL-13. The TNF-α, IL-1β, and IL-18 influences L-type Ca
2+
channels, IL-2 has an inhibitory effect on the fast Na
+
channels while IL-17A and VEGF-B were specific for Kir channels. With exception of the IL-1α, IL-2, and VEGF-B, all analyzed cytokines include nitric oxide dependent signaling with resultant combined effects on mechano-gated and Ca
2+
channels. The relationships between these pathways and the time-dependence of their activation are of important considerations in the evaluation of cytokine-induced electrical abnormality, specific for cardiac dysfunctions.
In general, the discussion presented in this review covers research devoted to counterbalance between different cytokines in the regulation of stretch-induced effects in rat atrial myocardium.
Abbreviations: APs: action potentials; APD25: action potential durations to 25% of re-polarization; APD50: action potential durations to 50% of repolarization; APD90: action potential durations to 90% of repolarization; MGCs: mechanically gated channels</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>27617892</pmid><doi>10.1080/08820139.2016.1208220</doi><tpages>16</tpages></addata></record> |
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subjects | Action Potentials - immunology Animals Atrial Function - immunology Atrial myocardium cytokines Cytokines - immunology Cytokines - metabolism Electric Conductivity Electricity Heart Atria - pathology Humans mechanical stretch Mechanotransduction, Cellular - immunology Myocardial Contraction Myocardium - immunology Myocardium - metabolism Rats Signal Transduction Vascular Endothelial Growth Factor A - metabolism |
title | Cytokine Effects on Mechano-Induced Electrical Activity in Atrial Myocardium |
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