Hepatoprotective effects of pecan nut shells on ethanol-induced liver damage

被引:42
|
作者
Mueller, Liz Girardi [1 ]
Pase, Camila Simonetti [1 ]
Reckziegel, Patricia
Barcelos, Raquel C. S.
Boufleur, Nardeli [1 ]
Prado, Ana Cristina P. [4 ]
Fett, Roseane [4 ]
Block, Jane Mara [4 ]
Pavanato, Maria Amalia
Bauermann, Liliane F. [1 ]
Teixeira da Rocha, Joao Batista [3 ]
Burger, Marilise Escobar [2 ,3 ]
机构
[1] Univ Fed Santa Maria, Dept Fisiol & Farmacol, BR-97105900 Santa Maria, RS, Brazil
[2] Univ Fed Santa Maria, Programa Posgrad Farmacol, Ctr Ciencias Saude, BR-97105900 Santa Maria, RS, Brazil
[3] Univ Fed Santa Maria, Programa Posgrad Bioquim Toxicol, BR-97105900 Santa Maria, RS, Brazil
[4] Univ Fed Santa Catarina, Ctr Ciencias Agr, Dept Tecnol Alimentos, Florianopolis, SC, Brazil
关键词
Hepatoprotective effect; Pecan shells; Liver injury; Chronic ethanol; Oxidative stress; ANTIOXIDANT CAPACITY; OXIDATIVE STRESS; VITAMIN-C; IRON; DISMUTASE; TISSUES; RATS;
D O I
10.1016/j.etp.2011.08.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The hepatoprotective activity of the aqueous extract of the shells of pecan nut was investigated against ethanol-induced liver damage. This by-product of the food industry is popularly used to treat toxicological diseases. We evaluated the phytochemical properties of pecan shell aqueous extract (AE) and its in vitro and ex vivo antioxidant activity. The AE was found to have a high content of total polyphenols (192.4 +/- 1.9 mg GAE/g), condensed tannins (58.4 +/- 2.2 mg CE/g), and antioxidant capacity, and it inhibited Fe2+-induced lipid peroxidation (LP) in vitro. Rats chronically treated with ethanol (Et) had increased plasmatic transaminases (ALT, AST) and gamma glutamyl transpeptidase (GGT) levels (96%, 59.13% and 465.9%, respectively), which were effectively prevented (87; 41 and 383%) by the extract (1:40, w/v). In liver, ethanol consumption increased the LP (121%) and decreased such antioxidant defenses as glutathione (GSH) (33%) and superoxide dismutase (SOD) (47%) levels, causing genotoxicity in erythrocytes. Treatment with pecan shell AE prevented the development of LP (43%), GSH and SOD depletion (33% and 109%, respectively) and ethanol-induced erythrocyte genotoxicity. Catalase activity in the liver was unchanged by ethanol but was increased by the extract (47% and 73% in AE and AE + Et, respectively). Therefore, pecan shells may be an economic agent to treat liver diseases related to ethanol consumption. (C) 2011 Elsevier GmbH. All rights reserved.
引用
收藏
页码:165 / 171
页数:7
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