期刊
JOURNAL OF DAIRY SCIENCE
卷 96, 期 2, 页码 889-896出版社
ELSEVIER SCIENCE INC
DOI: 10.3168/jds.2012-5410
关键词
blood-milk barrier; immunoglobulin G; lactate; beta-hydroxybutyrate
资金
- DSM Nutritional Products
- Swiss National Science Foundation (Bern, Switzerland) [320030-120317]
- Swiss National Science Foundation (SNF) [320030_120317] Funding Source: Swiss National Science Foundation (SNF)
During a mammary immune response, the integrity of the blood-milk barrier is negatively affected and becomes leaky. The aim of the present study was to demonstrate the blood origin, and to investigate changes in the concentration, of various constituents including immunoglobulins in blood and milk during the early phase of lipopolysaccharide (LPS)-induced mastitis. Five lactating dairy cows received continuous beta-hydroxybutyrate (BHBA) clamp infusions to maintain elevated BHBA blood concentrations (1.5 to 2.0 mmol/L) from 48 h before and 8 h after LPS administration. One udder quarter was infused with 200 mu g of Escherichia coli LPS. A second quarter served as control. Milk and blood samples were taken hourly for 8 h postchallenge (PC). The somatic cell count in LPS-challenged quarters was increased from 4 h PC to the end of the experiment compared with control quarters. In LPS-challenged quarters, L-lactate, BHBA, lactate dehydrogenase (LDH), IgG(1), and IgG(2) were increased at 3 h PC and remained elevated until the end of experiment (8 h PC) compared with control quarters. In addition, the optical density values in milk in a nonquantitative ELISA for antibodies directed against bluetongue virus (used as a measure of nonspecific antibody transfer; all animals were vaccinated) increased and, thus, indicates an increase in these antibodies in response to LPS treatment. L-Lactate concentration also increased in blood 2 h PC and in the milk of control quarters during the experiment from 3 h PC. A second experiment was conducted in vitro to investigate a possible contribution from destructed milk cells to L-lactate concentration and activity of LDH in milk. Aliquots of milk samples (n = 8) were frozen (-20 degrees C) or disrupted with ultrasound, respectively. Freeze thawing and ultrasound treatment increased LDH in milk samples, but had no effect on L-lactate concentrations. Results suggest that intramammary infusion of LPS induces a systemic response, as evidenced by an elevation of blood L-lactate concentration. The concomitant changes of all investigated components suggest that they were blood derived. However, the increase in blood components in the milk is not necessarily supportive of the mammary immune system, and likely a side effect of reduced blood-milk barrier integrity.
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