Dr Ronan Lordan

Available to discuss new collaborations, science outreach or speaking opportunities. Feel free to make contact via email or twitter.


Curriculum vitae



Institute for Translational Medicine and Therapeutics

Perelman School of Medicine, University of Pennsylvania



Structural Elucidation of Irish Ale Bioactive Polar Lipids with Antithrombotic Properties


Journal article


A. Tsoupras, R. Lordan, E. O'Keefe, Katie Shiels, S. Saha, I. Zabetakis
Biomolecules, 2020

Semantic Scholar DOI PubMedCentral PubMed
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APA   Click to copy
Tsoupras, A., Lordan, R., O'Keefe, E., Shiels, K., Saha, S., & Zabetakis, I. (2020). Structural Elucidation of Irish Ale Bioactive Polar Lipids with Antithrombotic Properties. Biomolecules.


Chicago/Turabian   Click to copy
Tsoupras, A., R. Lordan, E. O'Keefe, Katie Shiels, S. Saha, and I. Zabetakis. “Structural Elucidation of Irish Ale Bioactive Polar Lipids with Antithrombotic Properties.” Biomolecules (2020).


MLA   Click to copy
Tsoupras, A., et al. “Structural Elucidation of Irish Ale Bioactive Polar Lipids with Antithrombotic Properties.” Biomolecules, 2020.


BibTeX   Click to copy

@article{a2020a,
  title = {Structural Elucidation of Irish Ale Bioactive Polar Lipids with Antithrombotic Properties},
  year = {2020},
  journal = {Biomolecules},
  author = {Tsoupras, A. and Lordan, R. and O'Keefe, E. and Shiels, Katie and Saha, S. and Zabetakis, I.}
}

Abstract

The structures of bioactive polar lipids (PLs) of Irish ale with potent antithrombotic and cardioprotective properties were elucidated. Ale PL was fractionated by preparative thin layer chromatography (TLC) into subclasses, and their antithrombotic effect was assessed against human platelet aggregation induced by the pro-inflammatory mediator, platelet-activating factor (PAF). The fatty acid content and the overall structures of ale PL were elucidated by liquid chromatography mass spectrometry (LC-MS). Phosphatidylcholines (PC) and molecules of the sphingomyelin (SM) family exhibited the strongest anti-PAF effects, followed by phosphatidylethanolamines (PE). PC contained higher amounts of omega-3 polyunsaturated fatty acids (n-3 PUFA) and thus the lowest n-6/n-3 ratio. Bioactive diacyl and alkyl-acyl PC and PE molecules bearing n-3 PUFA at their sn-2 position, especially docosahexaenoic acid (DHA) and α-linolenic acid (ALA) but mostly oleic acid (OA), were identified in both PC and PE subclasses. Eicosapentaenoic acid (EPA) was present only in bioactive PC molecules and not in PE, explaining the lower anti-PAF effects of PE. Bioactive sphingolipid and glycolipid molecules with reported anti-inflammatory and anti-tumour properties, such as specific ceramides and glucosylcerebrosides with sphingosine, phytosphingosine and dihydrosphingosine bases but also specific monogalactodiglycerides and SM species bearing ALA at their sn-2 position, were identified in the SM subclass, providing a rational for its strong bioactivities against the PAF pathway. Further studies are required on the health benefits of bioactive PL from beer and brewery by-products.


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