Journal article
Marine drugs, 2019
APA
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Tsoupras, A., Lordan, R., Shiels, K., Saha, S., Nasopoulou, C., & Zabetakis, I. (2019). In Vitro Antithrombotic Properties of Salmon (Salmo salar) Phospholipids in a Novel Food-Grade Extract. Marine Drugs.
Chicago/Turabian
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Tsoupras, A., R. Lordan, Katie Shiels, S. Saha, Constantina Nasopoulou, and I. Zabetakis. “In Vitro Antithrombotic Properties of Salmon (Salmo Salar) Phospholipids in a Novel Food-Grade Extract.” Marine drugs (2019).
MLA
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Tsoupras, A., et al. “In Vitro Antithrombotic Properties of Salmon (Salmo Salar) Phospholipids in a Novel Food-Grade Extract.” Marine Drugs, 2019.
BibTeX Click to copy
@article{a2019a,
title = {In Vitro Antithrombotic Properties of Salmon (Salmo salar) Phospholipids in a Novel Food-Grade Extract},
year = {2019},
journal = {Marine drugs},
author = {Tsoupras, A. and Lordan, R. and Shiels, Katie and Saha, S. and Nasopoulou, Constantina and Zabetakis, I.}
}
Marine and salmon polar lipids (PLs) extracted by conventional extractions with non-food-grade solvents (CE-salmon-PLs) possess antithrombotic bioactivities against platelet-activating factor (PAF) and thrombin. Similar effects of food-grade-extracted (FGE) marine PLs have not yet been reported. In this study, food-grade solvents were used to extract PLs from Irish organic farmed salmon (Salmo salar) fillets (FGE-salmon-PLs), while their antithrombotic bioactivities were assessed in human platelets induced by platelet aggregation agonists (PAF/thrombin). FGE-salmon-PLs were further separated by thin layer chromatography (TLC) into lipid subclasses, and the antithrombotic bioactivities of each subclass were also assessed. LC-MS was utilized to elucidate the structure-activity relationships. FGE-salmon-PLs strongly inhibited PAF-induced platelet aggregation, while their relevant anti-thrombin effects were at least three times more potent than the previously reported activities of CE-salmon-PLs. TLC-derived lipid fractions corresponding to phosphatidylcholines (PC) and phosphatidylethanolamines (PE) were the most bioactive lipid subclasses obtained, especially against thrombin. Their LC-MS analysis elucidated that they are diacyl- or alkyl-acyl- PC and PE moieties baring ω3 polyunsaturated fatty acids (PUFA) at their sn-2 position, such as eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA). Our results concerning the potent antithrombotic effects of FGE-salmon-PLs against both PAF and thrombin pathways strongly suggest that such food-grade extracts are putative candidates for the development of novel cardioprotective supplements and nutraceuticals.