Alpha-terpineol prevents myocardial damage against isoproterenol-MI induced in Wistar-Kyoto rats: new possible to promote cardiovascular integrity

Alpha-terpineol (TPN) is one of the major components of the resin obtained from Protium heptaphyllum. This plant has been utilized as medicine by Brazilian indigenous tribes to treat cardiovascular diseases. Scientific reports have shown that the TPN possesses vasorelaxant and antihypertensive effec...

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Veröffentlicht in:Life sciences (1973) 2022-02, Vol.290, p.120087-120087, Article 120087
Hauptverfasser: Paulino, Emanuel Tenório, Rodrigues, Amanda Karine Barros Ferreira, Machado, Maria Luiza Dal Pont, de Oliveira, Kelly Rayane Vital, Bernardino, Alessando César, Quintans-Júnior, Lucindo José, Oliveira, Aldeídia Pereira, Ribeiro, Êurica Adélia Nogueira
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container_title Life sciences (1973)
container_volume 290
creator Paulino, Emanuel Tenório
Rodrigues, Amanda Karine Barros Ferreira
Machado, Maria Luiza Dal Pont
de Oliveira, Kelly Rayane Vital
Bernardino, Alessando César
Quintans-Júnior, Lucindo José
Oliveira, Aldeídia Pereira
Ribeiro, Êurica Adélia Nogueira
description Alpha-terpineol (TPN) is one of the major components of the resin obtained from Protium heptaphyllum. This plant has been utilized as medicine by Brazilian indigenous tribes to treat cardiovascular diseases. Scientific reports have shown that the TPN possesses vasorelaxant and antihypertensive effects. This study was conducted to assess the cardioprotective action of TPN against isoproterenol (ISO)-induced cardiotoxicity. Wistar rats were randomly divided into six groups. Rats were orally administered with TPN (25, 50, and 75 mg/kg, respectively) for 15 days, and ISO was administered (85 mg/kg, subcutaneously) on the 14th and 15th days. At the end of the experiment, the hemodynamic, baroreflex test, ECG, biochemical, histological, and morphometric changes were monitored from control and experimental groups, i.e., on the 15th day. ISO-induced myocardial infarcted rats showed an increase in mortality rates, cardiac marker enzymes, tachycardia, hypertrophy, myocardium necrosis, edema, hemorrhagic areas, infiltration of inflammatory cells like lymphocytes, and increased myocardial infarct size. However, pretreatment with TPN significantly inhibited these effects of ISO. The histopathological findings obtained for the myocardium further confirmed the biochemical results. Thus, the present study provides evidence for the efficacy of TPN against ISO-induced myocardial infarction in rats. [Display omitted]
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This plant has been utilized as medicine by Brazilian indigenous tribes to treat cardiovascular diseases. Scientific reports have shown that the TPN possesses vasorelaxant and antihypertensive effects. This study was conducted to assess the cardioprotective action of TPN against isoproterenol (ISO)-induced cardiotoxicity. Wistar rats were randomly divided into six groups. Rats were orally administered with TPN (25, 50, and 75 mg/kg, respectively) for 15 days, and ISO was administered (85 mg/kg, subcutaneously) on the 14th and 15th days. At the end of the experiment, the hemodynamic, baroreflex test, ECG, biochemical, histological, and morphometric changes were monitored from control and experimental groups, i.e., on the 15th day. ISO-induced myocardial infarcted rats showed an increase in mortality rates, cardiac marker enzymes, tachycardia, hypertrophy, myocardium necrosis, edema, hemorrhagic areas, infiltration of inflammatory cells like lymphocytes, and increased myocardial infarct size. However, pretreatment with TPN significantly inhibited these effects of ISO. The histopathological findings obtained for the myocardium further confirmed the biochemical results. Thus, the present study provides evidence for the efficacy of TPN against ISO-induced myocardial infarction in rats. 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This plant has been utilized as medicine by Brazilian indigenous tribes to treat cardiovascular diseases. Scientific reports have shown that the TPN possesses vasorelaxant and antihypertensive effects. This study was conducted to assess the cardioprotective action of TPN against isoproterenol (ISO)-induced cardiotoxicity. Wistar rats were randomly divided into six groups. Rats were orally administered with TPN (25, 50, and 75 mg/kg, respectively) for 15 days, and ISO was administered (85 mg/kg, subcutaneously) on the 14th and 15th days. At the end of the experiment, the hemodynamic, baroreflex test, ECG, biochemical, histological, and morphometric changes were monitored from control and experimental groups, i.e., on the 15th day. ISO-induced myocardial infarcted rats showed an increase in mortality rates, cardiac marker enzymes, tachycardia, hypertrophy, myocardium necrosis, edema, hemorrhagic areas, infiltration of inflammatory cells like lymphocytes, and increased myocardial infarct size. However, pretreatment with TPN significantly inhibited these effects of ISO. The histopathological findings obtained for the myocardium further confirmed the biochemical results. Thus, the present study provides evidence for the efficacy of TPN against ISO-induced myocardial infarction in rats. 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Rodrigues, Amanda Karine Barros Ferreira ; Machado, Maria Luiza Dal Pont ; de Oliveira, Kelly Rayane Vital ; Bernardino, Alessando César ; Quintans-Júnior, Lucindo José ; Oliveira, Aldeídia Pereira ; Ribeiro, Êurica Adélia Nogueira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-a504edda85a6163404e7b5a856fe550290b2b1f3c3efd01f363f953c2a7a4a163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alpha-terpineol</topic><topic>Animals</topic><topic>Antihypertensives</topic><topic>Antioxidants - pharmacology</topic><topic>Baroreceptors</topic><topic>Biomarkers - metabolism</topic><topic>Cardioprotection</topic><topic>Cardiotonic Agents - pharmacology</topic><topic>Cardiotoxicity</topic><topic>Cardiotoxicity - drug therapy</topic><topic>Cardiotoxicity - metabolism</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - drug therapy</topic><topic>Cyclohexane Monoterpenes - metabolism</topic><topic>Cyclohexane Monoterpenes - pharmacology</topic><topic>Damage prevention</topic><topic>Edema</topic><topic>EKG</topic><topic>Heart - drug effects</topic><topic>Hemodynamics</topic><topic>Hemodynamics - drug effects</topic><topic>Hemorrhage</topic><topic>Hypertrophy</topic><topic>Inflammation</topic><topic>Isoproterenol</topic><topic>Isoproterenol - pharmacology</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lymphocytes</topic><topic>Male</topic><topic>Medicinal plants</topic><topic>Myocardial infarction</topic><topic>Myocardial Infarction - pathology</topic><topic>Myocardium</topic><topic>Myocardium - metabolism</topic><topic>Necrosis</topic><topic>Oral administration</topic><topic>Protium heptaphyllum</topic><topic>Rats</topic><topic>Rats, Inbred WKY</topic><topic>Reflexes</topic><topic>Rodents</topic><topic>Tachycardia</topic><topic>Terpineol</topic><topic>Wistar-Kyoto rats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paulino, Emanuel Tenório</creatorcontrib><creatorcontrib>Rodrigues, Amanda Karine Barros Ferreira</creatorcontrib><creatorcontrib>Machado, Maria Luiza Dal Pont</creatorcontrib><creatorcontrib>de Oliveira, Kelly Rayane Vital</creatorcontrib><creatorcontrib>Bernardino, Alessando César</creatorcontrib><creatorcontrib>Quintans-Júnior, Lucindo José</creatorcontrib><creatorcontrib>Oliveira, Aldeídia Pereira</creatorcontrib><creatorcontrib>Ribeiro, Êurica Adélia Nogueira</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; 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This plant has been utilized as medicine by Brazilian indigenous tribes to treat cardiovascular diseases. Scientific reports have shown that the TPN possesses vasorelaxant and antihypertensive effects. This study was conducted to assess the cardioprotective action of TPN against isoproterenol (ISO)-induced cardiotoxicity. Wistar rats were randomly divided into six groups. Rats were orally administered with TPN (25, 50, and 75 mg/kg, respectively) for 15 days, and ISO was administered (85 mg/kg, subcutaneously) on the 14th and 15th days. At the end of the experiment, the hemodynamic, baroreflex test, ECG, biochemical, histological, and morphometric changes were monitored from control and experimental groups, i.e., on the 15th day. ISO-induced myocardial infarcted rats showed an increase in mortality rates, cardiac marker enzymes, tachycardia, hypertrophy, myocardium necrosis, edema, hemorrhagic areas, infiltration of inflammatory cells like lymphocytes, and increased myocardial infarct size. However, pretreatment with TPN significantly inhibited these effects of ISO. The histopathological findings obtained for the myocardium further confirmed the biochemical results. Thus, the present study provides evidence for the efficacy of TPN against ISO-induced myocardial infarction in rats. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>34740575</pmid><doi>10.1016/j.lfs.2021.120087</doi><tpages>1</tpages></addata></record>
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subjects Alpha-terpineol
Animals
Antihypertensives
Antioxidants - pharmacology
Baroreceptors
Biomarkers - metabolism
Cardioprotection
Cardiotonic Agents - pharmacology
Cardiotoxicity
Cardiotoxicity - drug therapy
Cardiotoxicity - metabolism
Cardiovascular diseases
Cardiovascular Diseases - drug therapy
Cyclohexane Monoterpenes - metabolism
Cyclohexane Monoterpenes - pharmacology
Damage prevention
Edema
EKG
Heart - drug effects
Hemodynamics
Hemodynamics - drug effects
Hemorrhage
Hypertrophy
Inflammation
Isoproterenol
Isoproterenol - pharmacology
Lipid Peroxidation - drug effects
Lymphocytes
Male
Medicinal plants
Myocardial infarction
Myocardial Infarction - pathology
Myocardium
Myocardium - metabolism
Necrosis
Oral administration
Protium heptaphyllum
Rats
Rats, Inbred WKY
Reflexes
Rodents
Tachycardia
Terpineol
Wistar-Kyoto rats
title Alpha-terpineol prevents myocardial damage against isoproterenol-MI induced in Wistar-Kyoto rats: new possible to promote cardiovascular integrity
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