Pasture versus indoor feeding systems differentially affect the composition of polar lipids of Cheddar cheeses and their antiplatelet properties against platelet-activating factor
Highlights
- •UHPLC–HRAM-MS/MS revealed feeding-dependent cheese polar lipid profiles.
- •Pasture feeding increased bioactive polar lipid species in Cheddar cheese.
- •Clover-fed cheese exhibited the greatest antiplatelet activity in vitro.
- •Phosphatidylcholine, phosphatidylethanolamine, and sphingomyelin species may antagonise PAF.
- •Feeding strategy influences the functional properties of dairy products.
Abstract
Bovine feeding systems alter milk lipid composition, but their effects on cheese polar lipids (PL) and platelet-modulating activity remain incompletely characterised.
This study compared PL profiles and in vitro antiplatelet activity of full-fat Cheddar cheeses from cows fed indoor total mixed ration (TMR), perennial ryegrass pasture (GRS), or perennial ryegrass-white clover pasture (CLV).
Fifty-four Friesian cows were assigned to TMR, GRS, or CLV (n = 18/group) throughout lactation. Cheeses were manufactured in triplicate per treatment, ripened for 270 days, and PL were isolated. Lipid composition was analysed using C30 reversed-phase UHPLC-high-resolution accurate-mass tandem mass spectrometry.
Inhibition of platelet aggregation induced by platelet-activating factor (PAF), ADP, and thrombin was assessed. CLV cheese PL showed the greatest inhibition of PAF-induced aggregation, with an IC₅₀ of 85.9 ± 7.4 μg, compared with 126.9 ± 25.2 μg for GRS and 129.5 ± 28.9 μg for TMR (p = 0.04), representing 32–34% lower IC₅₀ values. GRS and TMR did not differ significantly. Neutral-lipid fractions were inactive, while effects against ADP- and thrombin-induced aggregation were weak.
Phosphatidylethanolamine (PE) was the predominant PL class (48–67%), followed by phosphatidylcholine (PC; 14–20%) and sphingomyelin (SM; 7–22%).
Statistical analysis distinguished TMR from pasture-derived cheeses and identified treatment-dependent differences in PE, PC, SM, phosphatidylserine, and phosphatidylinositol. Several molecular species were associated with lower PAF IC₅₀ values.
Overall, bovine feeding regimen influenced Cheddar PL composition and selective in vitro inhibition of PAF-induced platelet aggregation. White-clover pasture produced PL with greater anti-PAF potency, warranting further investigation.
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This is a study on the impact of different diets to the functional properties of cheese in relation to the aggregation of platelets. We can suggest that specific diet components affect the lipid composition and the anti-thrombotic bioactivities of cheeses.
