Hepatoprotective Effect of Pretreatment with Thymus vulgaris Essential Oil in Experimental Model of Acetaminophen-Induced Injury

被引:30
|
作者
Grespan, Renata [1 ]
Aguiar, Rafael Pazinatto [1 ]
Giubilei, Frederico Nunes [1 ]
Fuso, Rafael Rocco [1 ]
Damiao, Marcio Jose [1 ]
Silva, Expedito Leite [2 ]
Mikcha, Jane Graton [3 ]
Hernandes, Luzmarina [4 ]
Amado, Ciomar Bersani [1 ]
Nakamura Cuman, Roberto Kenji [1 ]
机构
[1] Univ Estadual Maringa, Dept Pharmacol & Therapeut, BR-87020900 Maringa, Parana, Brazil
[2] Univ Estadual Maringa, Dept Chem, BR-87020900 Maringa, Parana, Brazil
[3] Univ Estadual Maringa, Dept Clin Anal, BR-87020900 Maringa, Parana, Brazil
[4] Univ Estadual Maringa, Dept Morphophysiol Sci, BR-87020900 Maringa, Parana, Brazil
关键词
MITOCHONDRIAL PERMEABILITY TRANSITION; OXIDATIVE STRESS; CELL-DEATH; KB CELLS; APOPTOSIS; LIVER; TOXICITY; HEPATOTOXICITY; PEROXYNITRITE; INHIBITION;
D O I
10.1155/2014/954136
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Acute liver damage caused by acetaminophen overdose is a significant clinical problem and could benefit from new therapeutic strategies. Objective. This study investigated the hepatoprotective effect of Thymus vulgaris essential oil (TEO), which is used popularly for various beneficial effects, such as its antiseptic, carminative, and antimicrobial effects. The hepatoprotective activity of TEO was determined by assessing serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) in mice. Their livers were then used to determine myeloperoxidase (MPO) enzyme activity and subjected to histological analysis. In vitro antioxidant activity was evaluated by assessing the free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH center dot)-scavenging effects of TEO and TEO-induced lipid peroxidation. TEO reduced the levels of the serum marker enzymes AST, ALT, and ALP and MPO activity. The histopathological analysis indicated that TEO prevented acetaminophen-induced necrosis. The essential oil also exhibited antioxidant activity, reflected by its DPPH radical-scavenging effects and in the lipid peroxidation assay. These results suggest that TEO has hepatoprotective effects on acetaminophen-induced hepatic damage in mice.
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页数:8
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