Table 2.
Study (First Author, Year) |
Species | Sample Size | Oxylipin Pool | Oxylipin Classes Quantified | Sample Type | Study Oxylipin Outcomes |
---|---|---|---|---|---|---|
Weiss, 2013 [21] | Human | n = 30 |
|
|
|
17-HDoHE decreases across first 4 weeks of lactation in mothers of pre-term infants; Other pro-resolving mediator and precursor concentrations remain stable. |
Gouveia-Figueira, 2015 [59] | Human | n = 3 |
|
|
|
Many oxylipins were detectable in human milk, but extraction efficiency was lower in human milk than many other biological sample types. |
Arnardottir, 2016 [22] | Human | n = 13 |
|
|
|
Lipid mediator concentrations were recorded for donor milk from commercial supplier; Concentrations differed between donors with and without mastitis by principal components analysis. |
Wu, 2016 [57] | Human | n = 1 |
|
|
|
Some oxylipin concentrations increase significantly with extended storage, especially when held for any period of time at -20oC or above. |
Robinson, 2017 [23] | Human | n = 30 |
|
|
|
Oxylipin concentrations stayed stable across 4 weeks of lactation in mothers delivering full-term. |
Alexandre-Gouabau, 2017 [60] | Human | n = 22 |
|
|
|
10,11-dihydro-20-trihydroxy-LTB4 and PGs were associated with faster infant growth trajectories; 11-dihydro-2,3-dinor-TXB2 was associated with slower infant growth trajectories. |
Pitino, 2019 [55] | Human | n = 17 (pooled) |
|
|
|
Oxylipin profiles were altered significantly with different pasteurization techniques. |
Gan, 2020 [52] | Human | n = 5 (pooled) |
|
|
|
Non-esterified oxylipins were most abundant in skim milk, while esterified oxylipins were most abundant in cream layer and cell pellet; Over 90% of milk oxylipins were derived from linoleic acid. |
Mavangira, 2015 [61] | Bovine | n = 24 |
|
|
|
Many oxylipin classes had increased concentrations in dairy cows with mastitis. |
Ryman, 2015 [62] | Bovine | n = 8 |
|
|
|
Milk from cows with S. uberis infection was higher in HODEs and 11-HETE. |
Kuhn, 2017 [63] | Bovine | n = 36 |
|
|
|
Most oxylipin concentrations increased with time across lactation. |
Teixeira, 2021 [53] | Bovine | Pooled milk from storage tanks |
|
|
|
Over 95% of oxylipins in milk were bound; Approximately 90% of milk oxylipins were linoleic acid-derived oxylipins; Lipid extraction followed by base hydrolysis in methanol was the best method for measuring total oxylipins. |
Llaurado-Calero, 2021 [64] | Porcine | n = 36 |
|
|
|
Fish oil feeding improved piglet growth and survival; Fish oil feeding increased concentrations of most milk oxylipins. |
DiHDPEs—Dihydroxy docosapentaenoic acids; DiHETEs—Dihydroxy eicosatetraenoic acids; DiHETrEs—Dihydroxy eicosatrienoic acids; DiHOMEs—Dihydroxy octadecamonoenoic acids; EpDPEs—Epoxy docosapentaenoic acids; EpETEs—Epoxy eicosatetraenoic acids; EpETrEs—Epoxy eicosatrienoic acids; EpOMEs—Epoxy octadecamonoenoic acids; HDoHEs—Hydroxy docosahexaenoic acids; HEPEs—Hydroxy eicosapentaenoic acids; HETEs—Hydroxy eicosatetraenoic acids; HODEs—Hydroxy octadecadienoic acids; HOTrEs—Hydroxy octadecatrienoic acids; LTs—Leukotrienes; oxo-ETEs—Oxo eicosatetraenoic acids; oxo-ODEs—Oxo octadecadienoic acid; PGs—Prostaglandins; SPMs—Specialized pro-resolving lipid mediators; TriHOMEs—Trihydroxy octadecamonoenoic acids; TXs—Thromboxanes.