Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 on L-Arginine-Induced Acute Pancreatitis in Rat
Autor: | Hassan Yavari, Seyed Abbas Mirmalek, Yekta Parsa, Soheila Yadollah-Damavandi, Bahareh Kardeh, Ehsan Shahverdi, Tina Parsa, Ala Gholamrezaei Boushehrinejad, Ehsan Jangholi, Seyed Alireza Salimi-Tabatabaee |
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Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Male Aging Pathology medicine.medical_specialty Article Subject Ubiquinone Anti-Inflammatory Agents Pharmacology medicine.disease_cause Arginine Biochemistry Antioxidants Superoxide dismutase Rats Sprague-Dawley 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine medicine Animals lcsh:QH573-671 Pancreas Coenzyme Q10 biology business.industry lcsh:Cytology Cell Biology General Medicine Glutathione Lipase Malondialdehyde medicine.disease Oxidative Stress 030104 developmental biology chemistry Pancreatitis 030220 oncology & carcinogenesis Myeloperoxidase Amylases biology.protein Acute pancreatitis Cytokines business Oxidative stress Research Article |
Zdroj: | Oxidative Medicine and Cellular Longevity, Vol 2016 (2016) Oxidative Medicine and Cellular Longevity |
ISSN: | 1942-0994 1942-0900 |
Popis: | 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-αand IL-1βcytokines, 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. |
Databáze: | OpenAIRE |
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