The Protective Effects of Caffeic Acid Phenethyl Ester on Acetylsalicylic Acid-induced Lung Injury in Rats

被引:10
|
作者
Taylan, Mahsuk [1 ]
Kaya, Halide [1 ]
Demir, Melike [1 ]
Evliyaoglu, Osman [2 ]
Sen, Hadice Selimoglu [1 ]
Firat, Ugur [3 ]
Keles, Aysenur [3 ]
Yilmaz, Sureyya [1 ]
Sezgi, Cengizhan [1 ]
机构
[1] Dicle Univ, Dept Pulm Dis, Sch Med, TR-21280 Diyarbakir, Turkey
[2] Dicle Univ, Dept Biochem, Sch Med, Diyarbakir, Turkey
[3] Dicle Univ, Dept Pathol, Sch Med, Diyarbakir, Turkey
关键词
caffeic acid phenethyl ester; cape; acetylsalicylic acid; asa; lung injury; NF-KAPPA-B; NITRIC-OXIDE; LIPID-PEROXIDATION; REPERFUSION INJURY; PULMONARY-EDEMA; CAPE; ACTIVATION; EXPRESSION; MODEL; MANAGEMENT;
D O I
10.3109/08941939.2016.1149641
中图分类号
R61 [外科手术学];
学科分类号
摘要
Aim: We aimed to investigate the protective effect of caffeic acid phenethyl ester (CAPE) on acetylsalicylic acid (ASA)-induced lung damage in rats in the present study. Methods: A total of 40 rats were randomly divided into five groups, with eight rats in each groupgroup 1: control, not receiving any medication; group 2: ASA (50mg/kg/day); group 3: ASA (50mg/kg/day) plus CAPE (20g/kg/day); group 4: ASA (100mg/kg/day); and group 5: ASA (100mg/kg/day) plus CAPE (20g/kg/day). ASA and CAPE were given via orogastric gavage for 5days. 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.
引用
收藏
页码:328 / 334
页数:7
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