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Thymol attenuates inflammation in isoproterenol induced myocardial infarcted rats by inhibiting the release of lysosomal enzymes and downregulating the expressions of proinflammatory cytokines
Inflammation plays an important role in the development of myocardial infarction (MI). The current study dealt with the protective effects of thymol on inflammation in isoproterenol (ISO) induced myocardial infarcted rats. Male albino Wistar rats were pre and co-treated with thymol (7.5mg/kg body we...
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Published in: | European journal of pharmacology 2015-05, Vol.754, p.153-161 |
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description | Inflammation plays an important role in the development of myocardial infarction (MI). The current study dealt with the protective effects of thymol on inflammation in isoproterenol (ISO) induced myocardial infarcted rats. Male albino Wistar rats were pre and co-treated with thymol (7.5mg/kg body weight) daily for 7 days. ISO (100mg/kg body weight) was injected subcutaneously into rats at an interval of 24h for two days (6th and 7th day) to induce MI. ISO induced myocardial infarcted rats showed increased levels of serum cardiac troponin-T, high sensitive C-reactive protein (hsCRP), lysosomal thiobarbituric acid reactive substances (TBARS) and elevated ST-segments. Also, the activities of lysosomal enzymes such as β-glucuronidase, β-galactosidase, cathepsin-B and D, the stimulators of inflammatory mediators were increased in the serum and heart of ISO induced myocardial infarcted rats. Furthermore, ISO up regulates the expressions of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and interleukin-1β (IL-1β) genes in the myocardium of rats analyzed by reverse transcription polymerase chain reaction (RT-PCR). Pre and co-treatment with thymol (7.5mg/kg body weight) near normalized the levels of lysosomal TBARS, activities of serum and heart lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines in the myocardium of ISO induced myocardial infarcted rats. Histopathological and transmission electron microscopic findings were also found in line with biochemical findings. Thus, the results of our study revealed that thymol attenuates inflammation by inhibiting the release of lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines by its potent anti-inflammatory effect. |
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The current study dealt with the protective effects of thymol on inflammation in isoproterenol (ISO) induced myocardial infarcted rats. Male albino Wistar rats were pre and co-treated with thymol (7.5mg/kg body weight) daily for 7 days. ISO (100mg/kg body weight) was injected subcutaneously into rats at an interval of 24h for two days (6th and 7th day) to induce MI. ISO induced myocardial infarcted rats showed increased levels of serum cardiac troponin-T, high sensitive C-reactive protein (hsCRP), lysosomal thiobarbituric acid reactive substances (TBARS) and elevated ST-segments. Also, the activities of lysosomal enzymes such as β-glucuronidase, β-galactosidase, cathepsin-B and D, the stimulators of inflammatory mediators were increased in the serum and heart of ISO induced myocardial infarcted rats. Furthermore, ISO up regulates the expressions of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and interleukin-1β (IL-1β) genes in the myocardium of rats analyzed by reverse transcription polymerase chain reaction (RT-PCR). Pre and co-treatment with thymol (7.5mg/kg body weight) near normalized the levels of lysosomal TBARS, activities of serum and heart lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines in the myocardium of ISO induced myocardial infarcted rats. Histopathological and transmission electron microscopic findings were also found in line with biochemical findings. Thus, the results of our study revealed that thymol attenuates inflammation by inhibiting the release of lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines by its potent anti-inflammatory effect.</description><identifier>ISSN: 0014-2999</identifier><identifier>EISSN: 1879-0712</identifier><identifier>DOI: 10.1016/j.ejphar.2015.02.028</identifier><identifier>PMID: 25724787</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-Inflammatory Agents - therapeutic use ; C-Reactive Protein - metabolism ; Cytokines - metabolism ; Down-Regulation - drug effects ; Electrocardiography ; Heart - drug effects ; Inflammation ; Inflammation - blood ; Inflammation - complications ; Inflammation - drug therapy ; Inflammation - pathology ; Inflammation Mediators - blood ; Inflammation Mediators - metabolism ; Isoproterenol ; Lipid Peroxidation - drug effects ; Lysosomal enzymes ; Lysosomes - drug effects ; Lysosomes - metabolism ; Lysosomes - ultrastructure ; Male ; Myocardial infarction ; Myocardial Infarction - blood ; Myocardial Infarction - chemically induced ; Myocardial Infarction - enzymology ; Myocardial Infarction - pathology ; Myocardium - enzymology ; Myocardium - immunology ; Myocardium - pathology ; Myocardium - ultrastructure ; Pro-inflammatory cytokines ; Rats ; Thiobarbituric Acid Reactive Substances ; Thymol ; Thymol - pharmacology ; Thymol - therapeutic use ; Troponin T - blood ; Up-Regulation - drug effects</subject><ispartof>European journal of pharmacology, 2015-05, Vol.754, p.153-161</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-8c777bd2704620a35ff72f3af7bf99145a0402e38678af3598094c3ef223d13e3</citedby><cites>FETCH-LOGICAL-c362t-8c777bd2704620a35ff72f3af7bf99145a0402e38678af3598094c3ef223d13e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25724787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagoor Meeran, Mohamed Fizur</creatorcontrib><creatorcontrib>Jagadeesh, Govindan Sangaran</creatorcontrib><creatorcontrib>Selvaraj, Palanisamy</creatorcontrib><title>Thymol attenuates inflammation in isoproterenol induced myocardial infarcted rats by inhibiting the release of lysosomal enzymes and downregulating the expressions of proinflammatory cytokines</title><title>European journal of pharmacology</title><addtitle>Eur J Pharmacol</addtitle><description>Inflammation plays an important role in the development of myocardial infarction (MI). The current study dealt with the protective effects of thymol on inflammation in isoproterenol (ISO) induced myocardial infarcted rats. Male albino Wistar rats were pre and co-treated with thymol (7.5mg/kg body weight) daily for 7 days. ISO (100mg/kg body weight) was injected subcutaneously into rats at an interval of 24h for two days (6th and 7th day) to induce MI. ISO induced myocardial infarcted rats showed increased levels of serum cardiac troponin-T, high sensitive C-reactive protein (hsCRP), lysosomal thiobarbituric acid reactive substances (TBARS) and elevated ST-segments. Also, the activities of lysosomal enzymes such as β-glucuronidase, β-galactosidase, cathepsin-B and D, the stimulators of inflammatory mediators were increased in the serum and heart of ISO induced myocardial infarcted rats. Furthermore, ISO up regulates the expressions of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and interleukin-1β (IL-1β) genes in the myocardium of rats analyzed by reverse transcription polymerase chain reaction (RT-PCR). Pre and co-treatment with thymol (7.5mg/kg body weight) near normalized the levels of lysosomal TBARS, activities of serum and heart lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines in the myocardium of ISO induced myocardial infarcted rats. Histopathological and transmission electron microscopic findings were also found in line with biochemical findings. Thus, the results of our study revealed that thymol attenuates inflammation by inhibiting the release of lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines by its potent anti-inflammatory effect.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>C-Reactive Protein - metabolism</subject><subject>Cytokines - metabolism</subject><subject>Down-Regulation - drug effects</subject><subject>Electrocardiography</subject><subject>Heart - drug effects</subject><subject>Inflammation</subject><subject>Inflammation - blood</subject><subject>Inflammation - complications</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - pathology</subject><subject>Inflammation Mediators - blood</subject><subject>Inflammation Mediators - metabolism</subject><subject>Isoproterenol</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lysosomal enzymes</subject><subject>Lysosomes - drug effects</subject><subject>Lysosomes - metabolism</subject><subject>Lysosomes - ultrastructure</subject><subject>Male</subject><subject>Myocardial infarction</subject><subject>Myocardial Infarction - blood</subject><subject>Myocardial Infarction - chemically induced</subject><subject>Myocardial Infarction - enzymology</subject><subject>Myocardial Infarction - pathology</subject><subject>Myocardium - enzymology</subject><subject>Myocardium - immunology</subject><subject>Myocardium - pathology</subject><subject>Myocardium - ultrastructure</subject><subject>Pro-inflammatory cytokines</subject><subject>Rats</subject><subject>Thiobarbituric Acid Reactive Substances</subject><subject>Thymol</subject><subject>Thymol - pharmacology</subject><subject>Thymol - therapeutic use</subject><subject>Troponin T - blood</subject><subject>Up-Regulation - drug effects</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9UU2LFDEUDKK44-o_EMnRS4_56O50LoIsfsGCl_UcMumXnYzdyZiXVttf508zw6xzFB6EV1S9qlCEvORsyxnv3xy2cDjubd4KxrstE3WGR2TDB6Ubprh4TDaM8bYRWusr8gzxwBjrtOiekivRKdGqQW3In7v9OqeJ2lIgLrYA0hD9ZOfZlpBiXWjAdMypQIZYiSGOi4ORzmtyNo_BniBvsysVzLYg3a0V2YddKCHe07IHmmECi0CTp9OKCdNcVRB_r3O1s3GkY_oZM9wvk71o4NcxA2LNgCddTXDJlfJK3VrStxABn5Mn3k4ILx7ea_L1w_u7m0_N7ZePn2_e3TZO9qI0g1NK7UahWNsLZmXnvRJeWq92Xmvedpa1TIAcejVYLzs9MN06CV4IOXIJ8pq8Pt-tSb4vgMXMAR1Mk42QFjS87_UgW9bxSm3PVJcTYgZvjjnMNq-GM3PqzhzMuTtz6s4wUWeoslcPDstuhvEi-ldWJbw9E6D-80eAbNAFiLWNkMEVM6bwf4e_m7WzaQ</recordid><startdate>20150505</startdate><enddate>20150505</enddate><creator>Nagoor Meeran, Mohamed Fizur</creator><creator>Jagadeesh, Govindan Sangaran</creator><creator>Selvaraj, Palanisamy</creator><general>Elsevier B.V</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>20150505</creationdate><title>Thymol attenuates inflammation in isoproterenol induced myocardial infarcted rats by inhibiting the release of lysosomal enzymes and downregulating the expressions of proinflammatory cytokines</title><author>Nagoor Meeran, Mohamed Fizur ; Jagadeesh, Govindan Sangaran ; Selvaraj, Palanisamy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-8c777bd2704620a35ff72f3af7bf99145a0402e38678af3598094c3ef223d13e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-Inflammatory Agents - therapeutic use</topic><topic>C-Reactive Protein - metabolism</topic><topic>Cytokines - metabolism</topic><topic>Down-Regulation - drug effects</topic><topic>Electrocardiography</topic><topic>Heart - drug effects</topic><topic>Inflammation</topic><topic>Inflammation - blood</topic><topic>Inflammation - complications</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - pathology</topic><topic>Inflammation Mediators - blood</topic><topic>Inflammation Mediators - metabolism</topic><topic>Isoproterenol</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lysosomal enzymes</topic><topic>Lysosomes - drug effects</topic><topic>Lysosomes - metabolism</topic><topic>Lysosomes - ultrastructure</topic><topic>Male</topic><topic>Myocardial infarction</topic><topic>Myocardial Infarction - blood</topic><topic>Myocardial Infarction - chemically induced</topic><topic>Myocardial Infarction - enzymology</topic><topic>Myocardial Infarction - pathology</topic><topic>Myocardium - enzymology</topic><topic>Myocardium - immunology</topic><topic>Myocardium - pathology</topic><topic>Myocardium - ultrastructure</topic><topic>Pro-inflammatory cytokines</topic><topic>Rats</topic><topic>Thiobarbituric Acid Reactive Substances</topic><topic>Thymol</topic><topic>Thymol - pharmacology</topic><topic>Thymol - therapeutic use</topic><topic>Troponin T - blood</topic><topic>Up-Regulation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagoor Meeran, Mohamed Fizur</creatorcontrib><creatorcontrib>Jagadeesh, Govindan Sangaran</creatorcontrib><creatorcontrib>Selvaraj, Palanisamy</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>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagoor Meeran, Mohamed Fizur</au><au>Jagadeesh, Govindan Sangaran</au><au>Selvaraj, Palanisamy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thymol attenuates inflammation in isoproterenol induced myocardial infarcted rats by inhibiting the release of lysosomal enzymes and downregulating the expressions of proinflammatory cytokines</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>2015-05-05</date><risdate>2015</risdate><volume>754</volume><spage>153</spage><epage>161</epage><pages>153-161</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><abstract>Inflammation plays an important role in the development of myocardial infarction (MI). The current study dealt with the protective effects of thymol on inflammation in isoproterenol (ISO) induced myocardial infarcted rats. Male albino Wistar rats were pre and co-treated with thymol (7.5mg/kg body weight) daily for 7 days. ISO (100mg/kg body weight) was injected subcutaneously into rats at an interval of 24h for two days (6th and 7th day) to induce MI. ISO induced myocardial infarcted rats showed increased levels of serum cardiac troponin-T, high sensitive C-reactive protein (hsCRP), lysosomal thiobarbituric acid reactive substances (TBARS) and elevated ST-segments. Also, the activities of lysosomal enzymes such as β-glucuronidase, β-galactosidase, cathepsin-B and D, the stimulators of inflammatory mediators were increased in the serum and heart of ISO induced myocardial infarcted rats. Furthermore, ISO up regulates the expressions of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and interleukin-1β (IL-1β) genes in the myocardium of rats analyzed by reverse transcription polymerase chain reaction (RT-PCR). Pre and co-treatment with thymol (7.5mg/kg body weight) near normalized the levels of lysosomal TBARS, activities of serum and heart lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines in the myocardium of ISO induced myocardial infarcted rats. Histopathological and transmission electron microscopic findings were also found in line with biochemical findings. Thus, the results of our study revealed that thymol attenuates inflammation by inhibiting the release of lysosomal enzymes and downregulates the expressions of pro-inflammatory cytokines by its potent anti-inflammatory effect.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25724787</pmid><doi>10.1016/j.ejphar.2015.02.028</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - pharmacology Anti-Inflammatory Agents - therapeutic use C-Reactive Protein - metabolism Cytokines - metabolism Down-Regulation - drug effects Electrocardiography Heart - drug effects Inflammation Inflammation - blood Inflammation - complications Inflammation - drug therapy Inflammation - pathology Inflammation Mediators - blood Inflammation Mediators - metabolism Isoproterenol Lipid Peroxidation - drug effects Lysosomal enzymes Lysosomes - drug effects Lysosomes - metabolism Lysosomes - ultrastructure Male Myocardial infarction Myocardial Infarction - blood Myocardial Infarction - chemically induced Myocardial Infarction - enzymology Myocardial Infarction - pathology Myocardium - enzymology Myocardium - immunology Myocardium - pathology Myocardium - ultrastructure Pro-inflammatory cytokines Rats Thiobarbituric Acid Reactive Substances Thymol Thymol - pharmacology Thymol - therapeutic use Troponin T - blood Up-Regulation - drug effects |
title | Thymol attenuates inflammation in isoproterenol induced myocardial infarcted rats by inhibiting the release of lysosomal enzymes and downregulating the expressions of proinflammatory cytokines |
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