Milk Lipids and Neonatal Fat Digestion: Relationship between Fatty Acid Composition, Endogenous and Exogenous Digestive Enzymes and Digestion of Milk Fat

Author(s):  
Margit Hamosh ◽  
Sara J. Iverson ◽  
Charlotte L. Kirk ◽  
Paul Hamosh
1972 ◽  
Vol 39 (2) ◽  
pp. 211-218 ◽  
Author(s):  
L. J. Cook ◽  
T. W. Scott ◽  
Y. S. Pan

SummaryThis study reports the effect of feeding formaldehyde-treated or untreated spray-dried casein–safflower oil (1:1, w/w) particles on the fatty-acid composition of milk and plasma lipids of cows.When the formaldehyde-treated particles were given to Jersey, Sahiwal and Jersey × Sahiwal crossbred cows (1 kg per cow per day) the linoleic acid (18:2) present in the safflower oil was not hydrogenated by the rumen micro-organisms and was incorporated into milk fat.When the untreated supplement was fed, however, the 18:2 fatty acid was hydrogenated in the rumen and there was an increased proportion of octadecenoic acid (18:1) in the milk fat.The increased proportions of 18:2 (treated supplement) and 18:1 (untreated supplement) were associated with decreased proportions of palmitic (16:0) and myristic (14:0) acids in the milk fat. All 3 breeds showed similar responses.The fatty-acid composition of plasma triglycerides, which are an important source of long-chain fatty acids for mammary-gland lipogenesis, was similarly affected. Furthermore, there were significant changes in the fatty-acid composition of other plasma lipids (e.g. phospholipids and cholesteryl esters). The interrelationships between dietary, plasma and milk fatty-acid compositions are discussed.


2021 ◽  
Vol 53 (3) ◽  
Author(s):  
Akansha Singh ◽  
Amit Kumar ◽  
Cedric Gondro ◽  
Andrea Renata da Silva Romero ◽  
A. Karthikeyan ◽  
...  

1973 ◽  
Vol 40 (2) ◽  
pp. 207-214 ◽  
Author(s):  
I. K. Gray

SummaryThe fatty-acid composition of 17 samples of New Zealand milk fat obtained throughout one dairy season is reported.The weight percentage of butyric (C4:0) acid was significantly correlated with that of caproic (C6:0) acid and that of caprylic (C8:0) acid. Percentages of C6:0and C8:0showed a highly significant correlation with each other and with weight percentages of capric (C10:0) and lauric (C12:0) acids.There was a highly significant negative correlation between palmitic (C16:0) and stearic (C18:0) acids and between C4:0and C16:0acids. Oleic (C18:1) acid showed significant negative correlations with C8:0, C10:0, C12:0, myristic (C14:0) and C16:0acids.


1966 ◽  
Vol 47 (3) ◽  
pp. 542-542 ◽  
Author(s):  
J. W. Stull ◽  
W. H. Brown ◽  
G. L. Kooyman ◽  
W. H. Huibregtse

1980 ◽  
Vol 31 (4) ◽  
pp. 368-374 ◽  
Author(s):  
William Banks ◽  
John L. Clapperton ◽  
Morag E. Kelly ◽  
Agnes G. Wilson ◽  
Robert J. M. Crawford

Nutrients ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1972 ◽  
Author(s):  
Wesolowska ◽  
Brys ◽  
Barbarska ◽  
Strom ◽  
Szymanska-Majchrzak ◽  
...  

Human milk fat plays an essential role as the source of energy and cell function regulator; therefore, the preservation of unique human milk donors’ lipid composition is of fundamental importance. To compare the effects of high pressure processing (HPP) and holder pasteurization on lipidome, human milk was processed at 62.5 °C for 30 min and at five variants of HPP from 450 MPa to 600 MPa, respectively. Lipase activity was estimated with QuantiChrom™ assay. Fatty acid composition was determined with the gas chromatographic technique, and free fatty acids content by titration with 0.1 M KOH. The positional distribution of fatty acid in triacylglycerols was performed. The oxidative induction time was obtained from the pressure differential scanning calorimetry. Carotenoids in human milk were measured by liquid chromatography. Bile salt stimulated lipase was completely eliminated by holder pasteurization, decreased at 600 MPa, and remained intact at 200 + 400 MPa; 450 MPa. The fatty acid composition and structure of human milk fat triacylglycerols were unchanged. The lipids of human milk after holder pasteurization had the lowest content of free fatty acids and the shortest induction time compared with samples after HPP. HPP slightly changed the β-carotene and lycopene levels, whereas the lutein level was decreased by 40.0% up to 60.2%, compared with 15.8% after the holder pasteurization.


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