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https://hdl.handle.net/11499/10691
Title: | Curcumin protects heart tissue against irinotecan-induced damage in terms of cytokine level alterations, oxidative stress, and histological damage in rats | Authors: | Çiftçi, Osman Turkmen, N.B. Taslıdere, A. |
Keywords: | Curcumin Cytokine Histological alterations Irinotecan Oxidative stress bovine serum albumin caspase 3 catalase curcumin glutathione glutathione disulfide glutathione peroxidase glutathione reductase interleukin 4 irinotecan nicotinamide adenine dinucleotide phosphate reduced nicotinamide adenine dinucleotide phosphate superoxide dismutase thiobarbituric acid reactive substance tumor necrosis factor antiinflammatory agent antineoplastic agent antioxidant camptothecin cardiotonic agent cytokine animal cell animal experiment animal model animal tissue antiinflammatory activity antioxidant activity Article blood sampling cardiotoxicity comparative study controlled study Curcuma longa drug effect heart injury heart protection heart tissue histopathology inflammatory cell male nonhuman oxidative stress protein blood level rat analogs and derivatives animal metabolism pathology Sprague Dawley rat Animals Anti-Inflammatory Agents Antineoplastic Agents, Phytogenic Antioxidants Camptothecin Cardiotonic Agents Cardiotoxicity Cytokines Male Oxidative Stress Rats Rats, Sprague-Dawley |
Publisher: | Springer Verlag | Abstract: | Irinotecan (CPT-11), commonly used in the treatment of many cancer types, may have several side effects that limit the use of CPT-11 in specific tissues such as the heart. In the current study, positive effects of curcumin (CRC) was determined in terms of antioxidant and anti-inflammatory properties against heart damage, caused by CPT-11, in rats. Rats were divided randomly into four equal groups (Control, CPT-11, CRC, and CPT-11 + CRC). CPT-11 10 mg/kg/day was administered intraperitoneally and CRC 100 mg/kg -1 was given orally. Blood and tissue samples were collected from all groups at day 30 for the detection of oxidative stress, histological changes, and cytokine levels. Results showed that CPT-11 caused dramatic changes in heart tissue for oxidative stress parameters (TBARS, SOD, CAT, GSH, and GPx levels), histological tissue damage, and cytokine levels (TNF and IL-4). CRC therapy reversed the elevated oxidative stress, histological tissue damages, and immunological changes and protected cardiac tissue against CPT-11 toxicity when given together with CPT-11. In conclusion, CPT-11 caused adverse effects on cytokine levels, histological alterations, and oxidative stress in rats. However, CRC treatment eliminated these toxic effects with its antioxidant and anti-inflammatory properties. Thus, these results suggest that CRC may play a protective role against CPT-11 toxicity in heart tissue of rats. © 2018, Springer-Verlag GmbH Germany, part of Springer Nature. | URI: | https://hdl.handle.net/11499/10691 https://doi.org/10.1007/s00210-018-1495-3 |
ISSN: | 0028-1298 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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