Abstract | AIM: METHODS: A total of 40 rats were randomly divided into five groups, with eight rats in each group-group 1: control, not receiving any medication; group 2: ASA (50 mg/kg/day); group 3: ASA (50 mg/kg/day) plus CAPE (20 μg/kg/day); group 4: ASA (100 mg/kg/day); and group 5: ASA (100 mg/kg/day) plus CAPE (20 μg/kg/day). ASA and CAPE were given via orogastric gavage for 5 days. The total oxidant status (TOS), total antioxidant capacity (TAC), oxidant stress index (OSI), and paraoxonase-1 (PON-1) activity of the blood samples and lung tissues were determined. Histopathological examinations of the lung tissues were performed by using light microscopic methods. RESULTS: CAPE treatment significantly increased antioxidant PON-1 level both in the lung tissue and plasma (p < .05). Plasma antioxidant marker (TAC, PON-1) levels significantly increased and oxidant marker (TOS, OSI) levels significantly decreased in CAPE-treated rats (groups 3,5) compared to ASA given no-CAPE groups (group 2,4) (p < .05). Treatment with CAPE improved pulmonary interstitial inflammation and eosinophil accumulation due to ASA histopathologically. CONCLUSION: Eosinophil-rich inflammation and oxidative stress play important roles in ASA-induced lung toxicity, and CAPE may protect against ASA-induced lung toxicity by reduction of oxidative damage and inflammation in rats.
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Authors | Mahşuk Taylan, Halide Kaya, Melike Demir, Osman Evliyaoğlu, Hadice Selimoglu Sen, Ugur Fırat, Aysenur Keles, Sureyya Yilmaz, Cengizhan Sezgi |
Journal | Journal of investigative surgery : the official journal of the Academy of Surgical Research
(J Invest Surg)
Vol. 29
Issue 6
Pg. 328-334
(Dec 2016)
ISSN: 1521-0553 [Electronic] United States |
PMID | 26980558
(Publication Type: Journal Article)
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Chemical References |
- Caffeic Acids
- caffeic acid phenethyl ester
- Phenylethyl Alcohol
- Aspirin
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Topics |
- Animals
- Aspirin
- Caffeic Acids
(pharmacology, therapeutic use)
- Drug Evaluation, Preclinical
- Female
- Lung
(pathology)
- Lung Injury
(chemically induced, pathology, prevention & control)
- Oxidative Stress
(drug effects)
- Phenylethyl Alcohol
(analogs & derivatives, pharmacology, therapeutic use)
- Random Allocation
- Rats, Wistar
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