Literature DB >> 21924598

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

Liz Girardi Müller1, Camila Simonetti Pase, Patrícia Reckziegel, Raquel C S Barcelos, Nardeli Boufleur, Ana Cristina P Prado, Roseane Fett, Jane Mara Block, Maria Amália Pavanato, Liliane F Bauermann, João Batista Teixeira da Rocha, Marilise Escobar Burger.   

Abstract

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 Fe(2+)-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.
Copyright © 2011 Elsevier GmbH. All rights reserved.

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Year:  2011        PMID: 21924598     DOI: 10.1016/j.etp.2011.08.002

Source DB:  PubMed          Journal:  Exp Toxicol Pathol        ISSN: 0940-2993


  13 in total

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