Modulation of oxidative stress response by flaxseed oil: Role of lipid peroxidation and underlying mechanisms
[Display omitted] •Flaxseed oil is a good source of ω-3 and ω-6 fatty acids.•ALA (ω-3:18-3) and LA (ω-6:18-2) showed numerous pharmacological activities.•Lipid peroxidation plays a critical role in the formation of metabolites of ω-3 and ω-6 fatty acids. Polyunsaturated fatty acids (PUFA’s) are majo...
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Veröffentlicht in: | Prostaglandins & other lipid mediators 2018-03, Vol.135, p.21-26 |
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Sprache: | eng |
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Zusammenfassung: | [Display omitted]
•Flaxseed oil is a good source of ω-3 and ω-6 fatty acids.•ALA (ω-3:18-3) and LA (ω-6:18-2) showed numerous pharmacological activities.•Lipid peroxidation plays a critical role in the formation of metabolites of ω-3 and ω-6 fatty acids.
Polyunsaturated fatty acids (PUFA’s) are majorly classified as ω-3 and ω-6 fatty acids. The eicosapentaenoic acid (EPA, ω-3:20-5), docosahexaenoic acid (DHA, ω-3:22-6) and alpha-linolenic acid (ALA, ω-3:18-3) are known ω-3 fatty acids, extracted from animal (e.g fish oil) and plant sources (e.g flaxseed oil). Furthermore, linoleic acid (LA, ω-6:18-2) is recognized as ω-6 fatty acid and the most prominent biological fatty acid with a pro-inflammatory response. Flaxseed oil has variety of biological roles, due to the significant amount of ω-3/ω-6 fatty acids. Numerous studies have reported that ALA (ω-3:18-3) and LA (ω-6:18-2) has diverse pharmacological activities. The ALA (ω-3:18-3) and LA (ω-6:18-2) are recognised to be the pharmacological antagonist. For example, ALA (ω-3:18-3) is recognised as anti-inflammatory, whereas LA (ω-6:18-2) is considered to be pro-inflammatory. PUFA’s get oxidized in three ways; firstly, free radical-mediated pathway, secondly non-free radical non-enzymatic metabolism, and lastly enzymatic degradation. The present report is an attempt to summarize various modes of PUFA’s metabolism and elaborate biological effects of the associated metabolites concerning flaxseed oil. |
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ISSN: | 1098-8823 |
DOI: | 10.1016/j.prostaglandins.2018.02.003 |