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Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats

OBJECTIVE: (−) Epicatechin (EP) is a naturally occurring antioxidant flavonoid found in some green plants. The current study was designed to evaluate the potential role of antioxidant mechanisms in the hepatoprotective properties of EP using the carbon tetrachloride (CCl(4))-induced acute liver inju...

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Autores principales: Alkinani, Khadijah B., Ali, Ehab M. M., Al-Shaikh, Turki M., Awlia Khan, Jalaluddin A., Al-naomasi, Tahani M., Ali, Soad S., Abduljawad, Asaad A., Mosa, Osama F., Zafar, Tariq A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716200/
https://www.ncbi.nlm.nih.gov/pubmed/34976093
http://dx.doi.org/10.1155/2021/4655150
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author Alkinani, Khadijah B.
Ali, Ehab M. M.
Al-Shaikh, Turki M.
Awlia Khan, Jalaluddin A.
Al-naomasi, Tahani M.
Ali, Soad S.
Abduljawad, Asaad A.
Mosa, Osama F.
Zafar, Tariq A.
author_facet Alkinani, Khadijah B.
Ali, Ehab M. M.
Al-Shaikh, Turki M.
Awlia Khan, Jalaluddin A.
Al-naomasi, Tahani M.
Ali, Soad S.
Abduljawad, Asaad A.
Mosa, Osama F.
Zafar, Tariq A.
author_sort Alkinani, Khadijah B.
collection PubMed
description OBJECTIVE: (−) Epicatechin (EP) is a naturally occurring antioxidant flavonoid found in some green plants. The current study was designed to evaluate the potential role of antioxidant mechanisms in the hepatoprotective properties of EP using the carbon tetrachloride (CCl(4))-induced acute liver injury model. MATERIALS AND METHODS: Rats (n = 7 per group) were divided into five groups including control group, (−) epicatechin group (20 mg·kg(−1) body weight), CCl(4) group (1 mL(−1) body weight), CCl(4)-EP treatment group, and CCl(4)-silymarin (SILY) group. The levels of enzymes including hepatic malondialdehyde (MDA), glutathione (GSH), catalase (CAT), glutathione S-transferase (GST), nitric oxide synthase (NOS), glutathione peroxidase (GPx), and cytochrome P450 (CYP450) were analyzed via enzyme-linked immunosorbent assay (ELISA). Histological studies were performed on all groups to assess the regenerative effects of test sample and compare it with the control group. RESULTS: Test compound EP and standard drug silymarin (SILY) considerably reduced liver function enzyme levels in the blood, which were raised by CCl(4) administration, and increased serum albumin and total protein (TP) concentrations. The hepatic malondialdehyde (MDA) level was considerably declined, whereas glutathione (GSH), catalase (CAT), glutathione S-transferase (GST), nitric oxide synthase (NOS), glutathione peroxidase (GPx), and cytochrome P450 (CYP450) levels were upregulated in the EC-treated groups. The hepatoprotective results of the study were further confirmed via the histological assessments, which indicated a regeneration of the damaged hepatic tissue in treated rats. CONCLUSIONS: The results of this study revealed a significant protective efficacy of EP against CCl(4)-induced liver injury, which was potentially mediated via upregulation of antioxidant enzymes and direct scavenging effects of the compound against free radicals.
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spelling pubmed-87162002021-12-30 Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats Alkinani, Khadijah B. Ali, Ehab M. M. Al-Shaikh, Turki M. Awlia Khan, Jalaluddin A. Al-naomasi, Tahani M. Ali, Soad S. Abduljawad, Asaad A. Mosa, Osama F. Zafar, Tariq A. Evid Based Complement Alternat Med Research Article OBJECTIVE: (−) Epicatechin (EP) is a naturally occurring antioxidant flavonoid found in some green plants. The current study was designed to evaluate the potential role of antioxidant mechanisms in the hepatoprotective properties of EP using the carbon tetrachloride (CCl(4))-induced acute liver injury model. MATERIALS AND METHODS: Rats (n = 7 per group) were divided into five groups including control group, (−) epicatechin group (20 mg·kg(−1) body weight), CCl(4) group (1 mL(−1) body weight), CCl(4)-EP treatment group, and CCl(4)-silymarin (SILY) group. The levels of enzymes including hepatic malondialdehyde (MDA), glutathione (GSH), catalase (CAT), glutathione S-transferase (GST), nitric oxide synthase (NOS), glutathione peroxidase (GPx), and cytochrome P450 (CYP450) were analyzed via enzyme-linked immunosorbent assay (ELISA). Histological studies were performed on all groups to assess the regenerative effects of test sample and compare it with the control group. RESULTS: Test compound EP and standard drug silymarin (SILY) considerably reduced liver function enzyme levels in the blood, which were raised by CCl(4) administration, and increased serum albumin and total protein (TP) concentrations. The hepatic malondialdehyde (MDA) level was considerably declined, whereas glutathione (GSH), catalase (CAT), glutathione S-transferase (GST), nitric oxide synthase (NOS), glutathione peroxidase (GPx), and cytochrome P450 (CYP450) levels were upregulated in the EC-treated groups. The hepatoprotective results of the study were further confirmed via the histological assessments, which indicated a regeneration of the damaged hepatic tissue in treated rats. CONCLUSIONS: The results of this study revealed a significant protective efficacy of EP against CCl(4)-induced liver injury, which was potentially mediated via upregulation of antioxidant enzymes and direct scavenging effects of the compound against free radicals. Hindawi 2021-12-22 /pmc/articles/PMC8716200/ /pubmed/34976093 http://dx.doi.org/10.1155/2021/4655150 Text en Copyright © 2021 Khadijah B. Alkinani et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Alkinani, Khadijah B.
Ali, Ehab M. M.
Al-Shaikh, Turki M.
Awlia Khan, Jalaluddin A.
Al-naomasi, Tahani M.
Ali, Soad S.
Abduljawad, Asaad A.
Mosa, Osama F.
Zafar, Tariq A.
Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats
title Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats
title_full Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats
title_fullStr Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats
title_full_unstemmed Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats
title_short Hepatoprotective Effects of (−) Epicatechin in CCl(4)-Induced Toxicity Model Are Mediated via Modulation of Oxidative Stress Markers in Rats
title_sort hepatoprotective effects of (−) epicatechin in ccl(4)-induced toxicity model are mediated via modulation of oxidative stress markers in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716200/
https://www.ncbi.nlm.nih.gov/pubmed/34976093
http://dx.doi.org/10.1155/2021/4655150
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