Milk cholesterol concentration in mice is not affected by high cholesterol diet- or genetically-induced hypercholesterolaemia

• Published in: Scientific reports 2018-06, Vol.8 (1), p.8824-9, Article 8824
• Main Authors: Dimova, Lidiya G., Lohuis, Mirjam A. M., Bloks, Vincent W., Tietge, Uwe J. F., Verkade, Henkjan J.
• Format: Article
• Language: English
• Subjects: 631/1647/767; 631/1647/767/722; 631/443/319; 631/45/287/1197; 64/110; 64/60; Animal models; Breast milk; Cholesterol; Diet; High cholesterol diet; Homeostasis; Humanities and Social Sciences; Lipids; Liver; Low density lipoprotein; Low density lipoprotein receptors; Mammary gland; multidisciplinary; Offspring; Postpartum; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-27115-8

Breast milk cholesterol content may imply to affect short- and long-term cholesterol homeostasis in the offspring. However, mechanisms of regulating milk cholesterol concentration are only partly understood. We used different mouse models to assess the impact of high cholesterol diet (HC)- or genetically-induced hypercholesterolaemia on milk cholesterol content. At day 14 postpartum we determined milk, plasma and tissue lipids in wild type (WT), LDL receptor knockout ( Ldlr −/−), and ATP-binding cassette transporter G8 knockout ( Abcg8 −/−) mice fed either low- or 0.5% HC diet. In chow-fed mice, plasma cholesterol was higher in Ldlr −/− dams compared to WT. HC-feeding increased plasma cholesterol in all three models compared to chow diet. Despite the up to 5-fold change in plasma cholesterol concentration, the genetic and dietary conditions did not affect milk cholesterol levels. To detect possible compensatory changes, we quantified de novo cholesterol synthesis in mammary gland and liver, which was strongly reduced in the various hypercholesterolaemic conditions. Together, these data suggest that milk cholesterol concentration in mice is not affected by conditions of maternal hypercholesterolaemia and is maintained at stable levels via ABCG8- and LDLR-independent mechanisms. The robustness of milk cholesterol levels might indicate an important physiological function of cholesterol supply to the offspring.