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Anti-Inflammatory Mechanisms of Novel Synthetic Ruthenium Compounds
Inflammation is the primary biological reaction to induce severe infection or injury in the immune system. Control of different inflammatory cytokines, such as nitric oxide (NO), interleukins (IL), tumor necrosis factor alpha-(TNF-α), noncytokine mediator, prostaglandin E2 (PGE2), mitogen activated...
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Published in: | Applied sciences 2021-11, Vol.11 (21), p.10092 |
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description | Inflammation is the primary biological reaction to induce severe infection or injury in the immune system. Control of different inflammatory cytokines, such as nitric oxide (NO), interleukins (IL), tumor necrosis factor alpha-(TNF-α), noncytokine mediator, prostaglandin E2 (PGE2), mitogen activated protein kinases (MAPKs) and nuclear factor kappa B (NF-κB), facilitates anti-inflammatory effect of different substances. Coordination metal complexes have been applied as metallo-drugs. Several metal complexes have found to possess potent biological activities, especially anticancer, cardioprotective, chondroprotective and anti-parasitosis activities. Among the metallo drugs, ruthenium-based (Ru) complexes have paid much attention in clinical applications. Despite the kinetic nature of Ru complexes is similar to platinum in terms of cell division events, their toxic effect is lower than that of cisplatin. This paper reviews the anti-inflammatory effect of novel synthetic Ru complexes with potential molecular mechanisms that are actively involved. |
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Control of different inflammatory cytokines, such as nitric oxide (NO), interleukins (IL), tumor necrosis factor alpha-(TNF-α), noncytokine mediator, prostaglandin E2 (PGE2), mitogen activated protein kinases (MAPKs) and nuclear factor kappa B (NF-κB), facilitates anti-inflammatory effect of different substances. Coordination metal complexes have been applied as metallo-drugs. Several metal complexes have found to possess potent biological activities, especially anticancer, cardioprotective, chondroprotective and anti-parasitosis activities. Among the metallo drugs, ruthenium-based (Ru) complexes have paid much attention in clinical applications. Despite the kinetic nature of Ru complexes is similar to platinum in terms of cell division events, their toxic effect is lower than that of cisplatin. 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Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Control of different inflammatory cytokines, such as nitric oxide (NO), interleukins (IL), tumor necrosis factor alpha-(TNF-α), noncytokine mediator, prostaglandin E2 (PGE2), mitogen activated protein kinases (MAPKs) and nuclear factor kappa B (NF-κB), facilitates anti-inflammatory effect of different substances. Coordination metal complexes have been applied as metallo-drugs. Several metal complexes have found to possess potent biological activities, especially anticancer, cardioprotective, chondroprotective and anti-parasitosis activities. Among the metallo drugs, ruthenium-based (Ru) complexes have paid much attention in clinical applications. Despite the kinetic nature of Ru complexes is similar to platinum in terms of cell division events, their toxic effect is lower than that of cisplatin. This paper reviews the anti-inflammatory effect of novel synthetic Ru complexes with potential molecular mechanisms that are actively involved.</description><subject>anti-inflammatory effects</subject><subject>Cancer therapies</subject><subject>Cell division</subject><subject>Cisplatin</subject><subject>Cytokines</subject><subject>Drugs</subject><subject>Enzymes</subject><subject>Immune system</subject><subject>Immunosuppressive agents</subject><subject>Inflammation</subject><subject>inflammatory cytokines</subject><subject>Inflammatory diseases</subject><subject>Interleukins</subject><subject>Investigations</subject><subject>Kinases</subject><subject>Liver</subject><subject>MAPKs</subject><subject>Metal complexes</subject><subject>Metallography</subject><subject>Molecular modelling</subject><subject>NF-κB</subject><subject>NF-κB protein</subject><subject>Nitric oxide</subject><subject>Oxidative stress</subject><subject>Phosphorylation</subject><subject>Platinum</subject><subject>Prostaglandin E2</subject><subject>Protein kinase</subject><subject>ROS</subject><subject>Ruthenium</subject><subject>Ruthenium compounds</subject><subject>Transcription factors</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><issn>2076-3417</issn><issn>2076-3417</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNkFtLxDAQhYMouOi--QMKvlrNJE2aPC6Ll4VVwctzmKap26VtatIK---trsjOyxyGw5mPQ8gF0GvONb3BvgdgAJRqdkRmjOYy5Rnkxwf6lMxj3NJpNHAFdEaWi26o01VXNdi2OPiwSx6d3WBXxzYmvkqe_JdrktddN2zcUNvkZZxEV49tsvRt78eujOfkpMImuvnfPiPvd7dvy4d0_Xy_Wi7WqeUyH1LFizLjAnIhrHWSUwBVSCuUYJIB51C4HKgQyF1W0sK6QmAFAMKyUpau4Gdktc8tPW5NH-oWw854rM3vwYcPg2FibJwpHTKFFF2FOtOVQKcApVbCam0z66asy31WH_zn6OJgtn4M3YRvJpqMZUJJMbmu9i4bfIzBVf9fgZqf1s1h6_wbV9h0Ng</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Jayakumar, Thanasekaran</creator><creator>Sheu, Joen-Rong</creator><creator>Hsia, Chih-Wei</creator><creator>Bhavan, Periyakali Saravana</creator><creator>Chang, Chao-Chien</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4508-6181</orcidid><orcidid>https://orcid.org/0000-0003-2056-4607</orcidid><orcidid>https://orcid.org/0000-0001-8265-3678</orcidid></search><sort><creationdate>20211101</creationdate><title>Anti-Inflammatory Mechanisms of Novel Synthetic Ruthenium Compounds</title><author>Jayakumar, Thanasekaran ; 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subjects | anti-inflammatory effects Cancer therapies Cell division Cisplatin Cytokines Drugs Enzymes Immune system Immunosuppressive agents Inflammation inflammatory cytokines Inflammatory diseases Interleukins Investigations Kinases Liver MAPKs Metal complexes Metallography Molecular modelling NF-κB NF-κB protein Nitric oxide Oxidative stress Phosphorylation Platinum Prostaglandin E2 Protein kinase ROS Ruthenium Ruthenium compounds Transcription factors Tumor necrosis factor-TNF Tumor necrosis factor-α |
title | Anti-Inflammatory Mechanisms of Novel Synthetic Ruthenium Compounds |
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