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Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat

This study was aimed at evaluating the protective effect of coenzyme Q10 on L-arginine-induced acute pancreatitis in rats regarding biomarkers and morphologic changes. Thirty-two male Sprague-Dawley rats were divided into 4 equal groups. Control group received intraperitoneal normal saline, while in...

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Autores principales: Mirmalek, Seyed Abbas, Gholamrezaei Boushehrinejad, Ala, Yavari, Hassan, Kardeh, Bahareh, Parsa, Yekta, Salimi-Tabatabaee, Seyed Alireza, Yadollah-Damavandi, Soheila, Parsa, Tina, Shahverdi, Ehsan, Jangholi, Ehsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844882/
https://www.ncbi.nlm.nih.gov/pubmed/27190575
http://dx.doi.org/10.1155/2016/5818479
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author Mirmalek, Seyed Abbas
Gholamrezaei Boushehrinejad, Ala
Yavari, Hassan
Kardeh, Bahareh
Parsa, Yekta
Salimi-Tabatabaee, Seyed Alireza
Yadollah-Damavandi, Soheila
Parsa, Tina
Shahverdi, Ehsan
Jangholi, Ehsan
author_facet Mirmalek, Seyed Abbas
Gholamrezaei Boushehrinejad, Ala
Yavari, Hassan
Kardeh, Bahareh
Parsa, Yekta
Salimi-Tabatabaee, Seyed Alireza
Yadollah-Damavandi, Soheila
Parsa, Tina
Shahverdi, Ehsan
Jangholi, Ehsan
author_sort Mirmalek, Seyed Abbas
collection PubMed
description This study was aimed at evaluating the protective effect of coenzyme Q10 on L-arginine-induced acute pancreatitis in rats regarding biomarkers and morphologic changes. Thirty-two male Sprague-Dawley rats were divided into 4 equal groups. Control group received intraperitoneal normal saline, while in sham and experimental groups 1 and 2 pancreatitis was induced with L-arginine. E1 and E2 groups were treated with a single dose of 100 and 200 mg/kg Q10, respectively. Serum lipase and amylase, along with pancreas IL-10, IL-1β, and TNF-α, were measured. For evaluation of oxidative stress, pancreatic superoxide dismutase (SOD), glutathione (GSH), malondialdehyde (MDA), and myeloperoxidase (MPO) were assessed. Histopathological examination for morphologic investigation was conducted. Serum amylase and lipase, as well as TNF-α and IL-1β cytokines, reverted with administration of Q10 in consistence with dosage. In contrast, Q10 assisted in boosting of IL-10 with higher dosage (200 mg/kg). A similar pattern for oxidative stress markers was noticed. Both MDA and MPO levels declined with increased dosage, contrary to elevation of SOD and GSH. Histopathology was in favor of protective effects of Q10. Our findings proved the amelioration of pancreatic injury by Q10, which suggest the anti-inflammatory and antioxidant property of Q10 and its potential therapeutic role.
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spelling pubmed-48448822016-05-17 Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat Mirmalek, Seyed Abbas Gholamrezaei Boushehrinejad, Ala Yavari, Hassan Kardeh, Bahareh Parsa, Yekta Salimi-Tabatabaee, Seyed Alireza Yadollah-Damavandi, Soheila Parsa, Tina Shahverdi, Ehsan Jangholi, Ehsan Oxid Med Cell Longev Research Article This study was aimed at evaluating the protective effect of coenzyme Q10 on L-arginine-induced acute pancreatitis in rats regarding biomarkers and morphologic changes. Thirty-two male Sprague-Dawley rats were divided into 4 equal groups. Control group received intraperitoneal normal saline, while in sham and experimental groups 1 and 2 pancreatitis was induced with L-arginine. E1 and E2 groups were treated with a single dose of 100 and 200 mg/kg Q10, respectively. Serum lipase and amylase, along with pancreas IL-10, IL-1β, and TNF-α, were measured. For evaluation of oxidative stress, pancreatic superoxide dismutase (SOD), glutathione (GSH), malondialdehyde (MDA), and myeloperoxidase (MPO) were assessed. Histopathological examination for morphologic investigation was conducted. Serum amylase and lipase, as well as TNF-α and IL-1β cytokines, reverted with administration of Q10 in consistence with dosage. In contrast, Q10 assisted in boosting of IL-10 with higher dosage (200 mg/kg). A similar pattern for oxidative stress markers was noticed. Both MDA and MPO levels declined with increased dosage, contrary to elevation of SOD and GSH. Histopathology was in favor of protective effects of Q10. Our findings proved the amelioration of pancreatic injury by Q10, which suggest the anti-inflammatory and antioxidant property of Q10 and its potential therapeutic role. Hindawi Publishing Corporation 2016 2016-04-12 /pmc/articles/PMC4844882/ /pubmed/27190575 http://dx.doi.org/10.1155/2016/5818479 Text en Copyright © 2016 Seyed Abbas Mirmalek 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
Mirmalek, Seyed Abbas
Gholamrezaei Boushehrinejad, Ala
Yavari, Hassan
Kardeh, Bahareh
Parsa, Yekta
Salimi-Tabatabaee, Seyed Alireza
Yadollah-Damavandi, Soheila
Parsa, Tina
Shahverdi, Ehsan
Jangholi, Ehsan
Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
title Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
title_full Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
title_fullStr Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
title_full_unstemmed Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
title_short Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
title_sort antioxidant and anti-inflammatory effects of coenzyme q10 on l-arginine-induced acute pancreatitis in rat
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844882/
https://www.ncbi.nlm.nih.gov/pubmed/27190575
http://dx.doi.org/10.1155/2016/5818479
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