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The Protective Effects of Caffeic Acid Phenethyl Ester on Acetylsalicylic Acid-induced Lung Injury in Rats.
Taylan, Mahsuk; Kaya, Halide; Demir, Melike; Evliyaoglu, Osman; Sen, Hadice Selimoglu; Firat, Ugur; Keles, Aysenur; Yilmaz, Sureyya; Sezgi, Cengizhan.
Afiliação
  • Taylan M; a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Kaya H; a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Demir M; a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Evliyaoglu O; b Department of Biochemistry , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Sen HS; a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Firat U; c Department of Pathology , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Keles A; c Department of Pathology , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Yilmaz S; a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.
  • Sezgi C; a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.
J Invest Surg ; 29(6): 328-334, 2016 Dec.
Article em En | MEDLINE | ID: mdl-26980558
ABSTRACT

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 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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Base de dados: MEDLINE Assunto principal: Álcool Feniletílico / Ácidos Cafeicos / Lesão Pulmonar Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Álcool Feniletílico / Ácidos Cafeicos / Lesão Pulmonar Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article