Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats

Cardiovascular disease represents a vital global disease burden. This study aims to assess the possible cardioprotective effect of thymol against adrenaline-induced myocardial injury (MI) in rats. Furthermore the effect of thymol on cardiac function biomarkers, electrocardiogram (ECG) alterations, o...

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Main Authors: Salma A. El-Marasy, Sally A. El Awdan, Azza Hassan, Heba M.I. Abdallah
Format: Article
Language:English
Published: Elsevier 2020-07-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844020312755
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author Salma A. El-Marasy
Sally A. El Awdan
Azza Hassan
Heba M.I. Abdallah
author_facet Salma A. El-Marasy
Sally A. El Awdan
Azza Hassan
Heba M.I. Abdallah
author_sort Salma A. El-Marasy
collection DOAJ
description Cardiovascular disease represents a vital global disease burden. This study aims to assess the possible cardioprotective effect of thymol against adrenaline-induced myocardial injury (MI) in rats. Furthermore the effect of thymol on cardiac function biomarkers, electrocardiogram (ECG) alterations, oxidative stress, inflammation, apoptosis and histopathological changes was assessed. MI was induced by adrenaline (2 mg/kg, s.c.) injected as a single dose for 2 consecutive days (24 h apart). Normal and control groups received the vehicle for 21 consecutive days. The other 3 groups were orally administered thymol (15, 30, 60 mg/kg) for 21 consecutive days and on day 22, adrenaline was injected as a single dose for 2 consecutive days. Then ECG examination, biochemical, histopathological, immunohistochemical analyses were carried out. Thymol reversed adrenaline-induced reduction of heart rate, prolongation of RR interval and elevation of ST interval. Thymol pretreatment significantly reduced serum aspartate dehydrogenase (AST), lactate dehydrogenase (LDH), and creatine kinase (CK) levels in MI rats. Oral pretreatment with thymol increased reduced glutathione (GSH), reduced malondialdehyde (MDA), nuclear factor-kappa B (NF-κB), and interleukin-1β (IL-1β) cardiac contents in MI rats. Additionally, thymol administration significantly decreased protein expression of caspase-3, increased Bcl-2 protein expression in cardiac tissue and ameliorated histopathological changes. This study reveals that thymol exerted cardioprotective effect against adrenaline-induced MI in rats evidenced by improving cardiac function, attenuating ECG and histopathological changes which may be partly mediated through its anti-oxidant, anti-inflammatory and anti-apoptotic effect.
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spelling doaj.art-8c51d417fd454e8c9e8b57053c7b59e62022-12-22T01:17:11ZengElsevierHeliyon2405-84402020-07-0167e04431Cardioprotective effect of thymol against adrenaline-induced myocardial injury in ratsSalma A. El-Marasy0Sally A. El Awdan1Azza Hassan2Heba M.I. Abdallah3Department of Pharmacology, National Research Centre, Giza, Egypt; Corresponding author.Department of Pharmacology, National Research Centre, Giza, EgyptDepartment of Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, EgyptDepartment of Pharmacology, National Research Centre, Giza, EgyptCardiovascular disease represents a vital global disease burden. This study aims to assess the possible cardioprotective effect of thymol against adrenaline-induced myocardial injury (MI) in rats. Furthermore the effect of thymol on cardiac function biomarkers, electrocardiogram (ECG) alterations, oxidative stress, inflammation, apoptosis and histopathological changes was assessed. MI was induced by adrenaline (2 mg/kg, s.c.) injected as a single dose for 2 consecutive days (24 h apart). Normal and control groups received the vehicle for 21 consecutive days. The other 3 groups were orally administered thymol (15, 30, 60 mg/kg) for 21 consecutive days and on day 22, adrenaline was injected as a single dose for 2 consecutive days. Then ECG examination, biochemical, histopathological, immunohistochemical analyses were carried out. Thymol reversed adrenaline-induced reduction of heart rate, prolongation of RR interval and elevation of ST interval. Thymol pretreatment significantly reduced serum aspartate dehydrogenase (AST), lactate dehydrogenase (LDH), and creatine kinase (CK) levels in MI rats. Oral pretreatment with thymol increased reduced glutathione (GSH), reduced malondialdehyde (MDA), nuclear factor-kappa B (NF-κB), and interleukin-1β (IL-1β) cardiac contents in MI rats. Additionally, thymol administration significantly decreased protein expression of caspase-3, increased Bcl-2 protein expression in cardiac tissue and ameliorated histopathological changes. This study reveals that thymol exerted cardioprotective effect against adrenaline-induced MI in rats evidenced by improving cardiac function, attenuating ECG and histopathological changes which may be partly mediated through its anti-oxidant, anti-inflammatory and anti-apoptotic effect.http://www.sciencedirect.com/science/article/pii/S2405844020312755ThymolAdrenalineMyocardial injuryECG examinationOxidative stressInflammation
spellingShingle Salma A. El-Marasy
Sally A. El Awdan
Azza Hassan
Heba M.I. Abdallah
Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats
Heliyon
Thymol
Adrenaline
Myocardial injury
ECG examination
Oxidative stress
Inflammation
title Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats
title_full Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats
title_fullStr Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats
title_full_unstemmed Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats
title_short Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats
title_sort cardioprotective effect of thymol against adrenaline induced myocardial injury in rats
topic Thymol
Adrenaline
Myocardial injury
ECG examination
Oxidative stress
Inflammation
url http://www.sciencedirect.com/science/article/pii/S2405844020312755
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