Protective effects of 3, 4‐dihydroxybenzoic acid on myocardial infarction induced by isoproterenol in rats

Despite considerable advances in interventions and treatment, there is a high mortality rate in patients with myocardial infarction (MI). This is the first study to investigate the protective effects of 3, 4‐dihydroxybenzoic acid against isoproterenol induced MI in rats. MI was induced by isoprotere...

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Veröffentlicht in:Journal of biochemical and molecular toxicology 2024-08, Vol.38 (8), p.e23773-n/a
Hauptverfasser: Vincent, Sikha, Stanely, Shervin Prince, Ponnian, Stanely Mainzen Prince
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Stanely, Shervin Prince
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description Despite considerable advances in interventions and treatment, there is a high mortality rate in patients with myocardial infarction (MI). This is the first study to investigate the protective effects of 3, 4‐dihydroxybenzoic acid against isoproterenol induced MI in rats. MI was induced by isoproterenol (100‐mg/kg body weight) in rats. Then, rats were treated with 3, 4‐dihydroxybenzoic acid (16‐mg/kg body weight) for 2 weeks. Serum creatine kinase‐MB, cardiac troponin‐T, cardiac troponin‐I, and heart thiobarbituric acid reactive substances were significantly (p 
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This is the first study to investigate the protective effects of 3, 4‐dihydroxybenzoic acid against isoproterenol induced MI in rats. MI was induced by isoproterenol (100‐mg/kg body weight) in rats. Then, rats were treated with 3, 4‐dihydroxybenzoic acid (16‐mg/kg body weight) for 2 weeks. Serum creatine kinase‐MB, cardiac troponin‐T, cardiac troponin‐I, and heart thiobarbituric acid reactive substances were significantly (p < 0.05) increased and heart superoxide dismutase and catalase activities were significantly (p < 0.05) reduced in isoproterenol‐induced myocardial infarcted rats. Isoproterenol induction significantly (p < 0.05) elevated the plasma homocysteine and serum high sensitivity‐C‐reactive protein levels. Furthermore, an enzyme‐linked immunosorbent assay, reverse transcription polymerase chain study, and immunohistochemical (IHC) staining revealed significantly (p < 0.05) elevated levels and expression of serum/myocardial nuclear factor‐κB, tumor necrosis factor‐alpha, interleukin‐1 beta, and Interleukin‐6 and significantly (p < 0.05) reduced levels/expression of serum/myocardial interleukin‐10 in myocardial infarcted rats. Nevertheless, isoproterenol‐induced rats treated with 3, 4‐dihydroxybenzoic acid considerably (p < 0.05) attenuated all the biochemical, molecular, and IHC parameters investigated and inhibited oxidative stress and inflammation and protected the heart, through its antioxidant and anti‐inflammatory mechanisms. 3, 4‐dihydroxy benzoic acid's effects on myocardial infarction were appraised. It reduced lipid peroxidation in rats. 3, 4‐dihydroxy benzoic acid improved antioxidants in rats. 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This is the first study to investigate the protective effects of 3, 4‐dihydroxybenzoic acid against isoproterenol induced MI in rats. MI was induced by isoproterenol (100‐mg/kg body weight) in rats. Then, rats were treated with 3, 4‐dihydroxybenzoic acid (16‐mg/kg body weight) for 2 weeks. Serum creatine kinase‐MB, cardiac troponin‐T, cardiac troponin‐I, and heart thiobarbituric acid reactive substances were significantly (p < 0.05) increased and heart superoxide dismutase and catalase activities were significantly (p < 0.05) reduced in isoproterenol‐induced myocardial infarcted rats. Isoproterenol induction significantly (p < 0.05) elevated the plasma homocysteine and serum high sensitivity‐C‐reactive protein levels. Furthermore, an enzyme‐linked immunosorbent assay, reverse transcription polymerase chain study, and immunohistochemical (IHC) staining revealed significantly (p < 0.05) elevated levels and expression of serum/myocardial nuclear factor‐κB, tumor necrosis factor‐alpha, interleukin‐1 beta, and Interleukin‐6 and significantly (p < 0.05) reduced levels/expression of serum/myocardial interleukin‐10 in myocardial infarcted rats. Nevertheless, isoproterenol‐induced rats treated with 3, 4‐dihydroxybenzoic acid considerably (p < 0.05) attenuated all the biochemical, molecular, and IHC parameters investigated and inhibited oxidative stress and inflammation and protected the heart, through its antioxidant and anti‐inflammatory mechanisms. 3, 4‐dihydroxy benzoic acid's effects on myocardial infarction were appraised. It reduced lipid peroxidation in rats. 3, 4‐dihydroxy benzoic acid improved antioxidants in rats. 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control</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - pathology</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reverse transcription</subject><subject>Superoxide dismutase</subject><subject>Thiobarbituric acid</subject><subject>Troponin</subject><subject>Troponin I - blood</subject><subject>Troponin I - metabolism</subject><issn>1095-6670</issn><issn>1099-0461</issn><issn>1099-0461</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctKxDAUhoMo3he-gATcKFgnTdI0WergFUEXui5pLpih02jSqnXlI_iMPomZGXUhuMohfHzn8gOwk6OjHCE8mtTdESZlSZbAeo6EyBBl-fK8LjLGSrQGNmKcIIQKURarYI0IRBBnfB00t8F3RnXu2UBjbaoi9BaSQ0g_3z-0exh08K9Dbdo37xSUymnoWzgdvJJBO9lA11oZkiD9ulb3ymhYD9BF_zgzB9P6GQOD7OIWWLGyiWb7-90E92end-OL7Prm_HJ8fJ0pTAnJKNcE14yWWnHLNBZ5LUlBEKY6bSsop4RzJDhXxAqbWyysLAtjtCmZkLIkm2B_4U0jPPUmdtXURWWaRrbG97FKu2NRCEZZQvf-oBPfhzZNlyiBC5yaiUQdLCgVfIzB2OoxuKkMQ5WjahZBlSKo5hEkdvfb2NdTo3_Jn5snYLQAXlxjhv9N1dXJ3UL5BbBHkM4</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Vincent, Sikha</creator><creator>Stanely, Shervin Prince</creator><creator>Ponnian, Stanely Mainzen Prince</creator><general>Wiley Subscription Services, Inc</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6840-4074</orcidid></search><sort><creationdate>202408</creationdate><title>Protective effects of 3, 4‐dihydroxybenzoic acid on myocardial infarction induced by isoproterenol in rats</title><author>Vincent, Sikha ; 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control</topic><topic>Myocardium - metabolism</topic><topic>Myocardium - pathology</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reverse transcription</topic><topic>Superoxide dismutase</topic><topic>Thiobarbituric acid</topic><topic>Troponin</topic><topic>Troponin I - blood</topic><topic>Troponin I - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vincent, Sikha</creatorcontrib><creatorcontrib>Stanely, Shervin Prince</creatorcontrib><creatorcontrib>Ponnian, Stanely Mainzen Prince</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; 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This is the first study to investigate the protective effects of 3, 4‐dihydroxybenzoic acid against isoproterenol induced MI in rats. MI was induced by isoproterenol (100‐mg/kg body weight) in rats. Then, rats were treated with 3, 4‐dihydroxybenzoic acid (16‐mg/kg body weight) for 2 weeks. Serum creatine kinase‐MB, cardiac troponin‐T, cardiac troponin‐I, and heart thiobarbituric acid reactive substances were significantly (p < 0.05) increased and heart superoxide dismutase and catalase activities were significantly (p < 0.05) reduced in isoproterenol‐induced myocardial infarcted rats. Isoproterenol induction significantly (p < 0.05) elevated the plasma homocysteine and serum high sensitivity‐C‐reactive protein levels. Furthermore, an enzyme‐linked immunosorbent assay, reverse transcription polymerase chain study, and immunohistochemical (IHC) staining revealed significantly (p < 0.05) elevated levels and expression of serum/myocardial nuclear factor‐κB, tumor necrosis factor‐alpha, interleukin‐1 beta, and Interleukin‐6 and significantly (p < 0.05) reduced levels/expression of serum/myocardial interleukin‐10 in myocardial infarcted rats. Nevertheless, isoproterenol‐induced rats treated with 3, 4‐dihydroxybenzoic acid considerably (p < 0.05) attenuated all the biochemical, molecular, and IHC parameters investigated and inhibited oxidative stress and inflammation and protected the heart, through its antioxidant and anti‐inflammatory mechanisms. 3, 4‐dihydroxy benzoic acid's effects on myocardial infarction were appraised. It reduced lipid peroxidation in rats. 3, 4‐dihydroxy benzoic acid improved antioxidants in rats. It also reduced nuclear factor‐κB, tumor necrosis factor‐alpha, interleukin‐1 beta, and Interleukin‐6, and raised interleukin‐10. 3, 4‐dihydroxy benzoic acid's antioxidant and anti‐inflammatory mechanisms.]]></abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39030868</pmid><doi>10.1002/jbt.23773</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-6840-4074</orcidid></addata></record>
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subjects 3, 4‐dihydroxybenzoic acid
Acids
Animals
antioxidant
Body weight
Catalase
Creatine
Creatine kinase
Cytokines
Dihydroxybenzoic acid
Gentisates - metabolism
Gentisates - pharmacology
Heart
Heart attacks
Homocysteine
Hydroxybenzoates - pharmacology
Interleukin 6
Interleukins
Isoproterenol
Isoproterenol - toxicity
Kinases
Male
Myocardial infarction
Myocardial Infarction - chemically induced
Myocardial Infarction - metabolism
Myocardial Infarction - prevention & control
Myocardium - metabolism
Myocardium - pathology
Oxidative stress
Oxidative Stress - drug effects
Rats
Rats, Sprague-Dawley
Reverse transcription
Superoxide dismutase
Thiobarbituric acid
Troponin
Troponin I - blood
Troponin I - metabolism
title Protective effects of 3, 4‐dihydroxybenzoic acid on myocardial infarction induced by isoproterenol in rats
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