The fatty acid (FA) composition of human milk (HM) from N = 9 Italian healthy donors following a free diet exhibited FA-dependent ranges of variability, as assessed by GC-FID. The possible short-term changes in the FA profile were monitored in the milk of lactating mothers (three) collected at five time points over a 6 h period, following an oral load (200 mL) of bovine milk. An array of techniques was exploited, including UHPLC-ESI-MS/MS of intact lipids and MALDI-TOF MS before and after chemical hydrogenation or bromination, in addition to MALDI-TOF MS analysis of FA after saponification, to monitor short-chain and odd-chain FA in HM as markers of bovine milk fat. A single administration of bovine milk did not appreciably modify the lipid pattern, suggesting that the maternal diet could induce not detectable short-term changes on the lipid composition of HM. Diet-induced increase of butyric acid was also excluded by 13C-NMR. The functions that HM FA exert in infant physiology appear finely regulated through maternal metabolism.
Short-term effects of dietary bovine milk on fatty acid composition of human milk: a preliminary multi-analytical study / Cutignano, Adele; Siano, Francesco; Romano, Raffaele; Aiello, Alessandra; Pizzolongo, Fabiana; Berni Canani, Roberto; Paparo, Lorella; Nocerino, Rita; Di Scala, Carmen; Addeo, Francesco; Picariello, Gianluca. - In: JOURNAL OF CHROMATOGRAPHY. B. - ISSN 1570-0232. - (2020). [10.1016/j.jchromb.2020.122189]
Short-term effects of dietary bovine milk on fatty acid composition of human milk: a preliminary multi-analytical study
Romano, Raffaele;Pizzolongo, Fabiana;Berni Canani, Roberto;Paparo, Lorella;Nocerino, Rita;Addeo, Francesco;
2020
Abstract
The fatty acid (FA) composition of human milk (HM) from N = 9 Italian healthy donors following a free diet exhibited FA-dependent ranges of variability, as assessed by GC-FID. The possible short-term changes in the FA profile were monitored in the milk of lactating mothers (three) collected at five time points over a 6 h period, following an oral load (200 mL) of bovine milk. An array of techniques was exploited, including UHPLC-ESI-MS/MS of intact lipids and MALDI-TOF MS before and after chemical hydrogenation or bromination, in addition to MALDI-TOF MS analysis of FA after saponification, to monitor short-chain and odd-chain FA in HM as markers of bovine milk fat. A single administration of bovine milk did not appreciably modify the lipid pattern, suggesting that the maternal diet could induce not detectable short-term changes on the lipid composition of HM. Diet-induced increase of butyric acid was also excluded by 13C-NMR. The functions that HM FA exert in infant physiology appear finely regulated through maternal metabolism.File | Dimensione | Formato | |
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