Please use this identifier to cite or link to this item: 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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