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Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice
The present study delineates the effects of incorporation of 1% diallyl sulfide (DAS) into extra virgin olive oil (EVOO) on the physico‐chemical characteristics, in vitro antioxidant, and in vivo hepatoprotective properties in CCl(4)‐induced acute liver injury in mice. Results showed that the DAS‐ri...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645721/ https://www.ncbi.nlm.nih.gov/pubmed/34925810 http://dx.doi.org/10.1002/fsn3.2638 |
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author | Habibi, Emna Baâti, Tarek Njim, Leila M’Rabet, Yassine Hosni, Karim |
author_facet | Habibi, Emna Baâti, Tarek Njim, Leila M’Rabet, Yassine Hosni, Karim |
author_sort | Habibi, Emna |
collection | PubMed |
description | The present study delineates the effects of incorporation of 1% diallyl sulfide (DAS) into extra virgin olive oil (EVOO) on the physico‐chemical characteristics, in vitro antioxidant, and in vivo hepatoprotective properties in CCl(4)‐induced acute liver injury in mice. Results showed that the DAS‐rich EVOO exhibited good oxidative stability over one‐month storage and preserved its original quality‐related parameters including major components (oleic acid, linoleic acid, and palmitic acid), and minor components (tocopherols, chlorophylls and carotenoids, tyrosol, hydroxytyrosol, elenolic acid, oleuropein and its aglycone, pinoresinol, vanilic acid, cinnamic acid, ferulic acid, luteolin, apigenin, and sterols). Compared with EVOO or DAS, the DAS‐rich EVOO displayed the highest DPPH and ABTS‐radical scavenging activities and showed the strongest cellular antioxidant activity (CAA). In connection with its free radical scavenging activity and CAA, DAS‐rich EVOO significantly normalized the serum ALT and AST levels and prevented the increase in interleukin‐6 in CCl(4)‐intoxicated mice. The manifest anti‐inflammatory and hepatoprotective effects of DAS‐rich EVOO were further supported by liver histopathological examinations. Overall, the EVOO enrichment with DAS could open up opportunities for the development of novel functional food with improved antioxidant and hepatoprotective properties. |
format | Online Article Text |
id | pubmed-8645721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86457212021-12-17 Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice Habibi, Emna Baâti, Tarek Njim, Leila M’Rabet, Yassine Hosni, Karim Food Sci Nutr Original Research The present study delineates the effects of incorporation of 1% diallyl sulfide (DAS) into extra virgin olive oil (EVOO) on the physico‐chemical characteristics, in vitro antioxidant, and in vivo hepatoprotective properties in CCl(4)‐induced acute liver injury in mice. Results showed that the DAS‐rich EVOO exhibited good oxidative stability over one‐month storage and preserved its original quality‐related parameters including major components (oleic acid, linoleic acid, and palmitic acid), and minor components (tocopherols, chlorophylls and carotenoids, tyrosol, hydroxytyrosol, elenolic acid, oleuropein and its aglycone, pinoresinol, vanilic acid, cinnamic acid, ferulic acid, luteolin, apigenin, and sterols). Compared with EVOO or DAS, the DAS‐rich EVOO displayed the highest DPPH and ABTS‐radical scavenging activities and showed the strongest cellular antioxidant activity (CAA). In connection with its free radical scavenging activity and CAA, DAS‐rich EVOO significantly normalized the serum ALT and AST levels and prevented the increase in interleukin‐6 in CCl(4)‐intoxicated mice. The manifest anti‐inflammatory and hepatoprotective effects of DAS‐rich EVOO were further supported by liver histopathological examinations. Overall, the EVOO enrichment with DAS could open up opportunities for the development of novel functional food with improved antioxidant and hepatoprotective properties. John Wiley and Sons Inc. 2021-10-25 /pmc/articles/PMC8645721/ /pubmed/34925810 http://dx.doi.org/10.1002/fsn3.2638 Text en © 2021 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Habibi, Emna Baâti, Tarek Njim, Leila M’Rabet, Yassine Hosni, Karim Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice |
title | Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice |
title_full | Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice |
title_fullStr | Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice |
title_full_unstemmed | Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice |
title_short | Antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against CCl(4)‐induced acute liver injury in mice |
title_sort | antioxidant and protective effects of extra virgin olive oil incorporated with diallyl sulfide against ccl(4)‐induced acute liver injury in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645721/ https://www.ncbi.nlm.nih.gov/pubmed/34925810 http://dx.doi.org/10.1002/fsn3.2638 |
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