fibrin and Mastitis--Bovine

fibrin has been researched along with Mastitis--Bovine* in 3 studies

Other Studies

3 other study(ies) available for fibrin and Mastitis--Bovine

ArticleYear
Effect of anemoside B4 on milk whey in clinical mastitis-affected cows elucidated using tandem mass tag (TMT)-based quantitative proteomics.
    Scientific reports, 2022, 11-05, Volume: 12, Issue:1

    Intramuscular injection of anemoside B4 (AB4) has a superior therapeutic effect on clinical mastitis in lactating cows. Here, we explored AB4's effect on milk whey in clinical mastitis-affected cows using proteomics. Among fifty clinical mastitis cows received AB4 administration (0.05 ml/kg/day, for 7 days), twelve healed cows were selected and marked as group T. Twelve clinically heathy cows received the same dose of saline for 7 days, marked as group C. Collected milk whey of group T before and after AB4 administration marked as T1 and T2, respectively. The milk whey of group C after saline injection marked as C1. Milk whey protein changes were detected using tandem mass tag-based quantitative proteomic. We identified 872 quantifiable proteins in the samples. Among them, 511 proteins between T1 and C1, and 361 proteins between T2 and T1 were significantly altered. T1 than C1 had significantly more proteins associated with inflammatory damage and trans-endothelial migration of leukocytes, whereas these proteins were reduced in T2 treated with AB4. Compared with C, proteins associated with fibrin clot degradation and complement system activation were downregulated in T1 but upregulated in T2. In summary, AB4 can exert its therapeutic effect on clinical mastitis in cows mainly by reducing inflammatory damage, activating the complement system, inhibiting trans-endothelial migration of leukocytes, and promoting degradation of milk fibrin clots.

    Topics: Animals; Cattle; Female; Fibrin; Lactation; Mastitis, Bovine; Milk; Milk Proteins; Proteomics; Whey; Whey Proteins

2022
Effect of mastitis on plasminogen activator activity of milk somatic cells.
    The Journal of dairy research, 1992, Volume: 59, Issue:4

    This study was conducted to examine the effects of mastitis and stage of lactation on plasminogen activator (PA) activity in milk somatic cells. An assay system, which measures the plasmin-mediated hydrolysis of the chromogenic substrate D-valyl-leucyl-lysine p-nitroanilide, was used to assess PA activity present within milk somatic cells. Milk cell associated PA activity was increased (P < 0.05) by 50% in the presence of fibrin fragments. This suggests that milk somatic cells contain tissue PA which, unlike urokinase PA, is preferentially activated in the presence of fibrin fragments. An increase of the milk somatic cell count from < 5 x 10(4) to > 10(6) cells/ml resulted in an 8-fold increase in PA activity per cell. Elevated levels of PA activity were associated with milk somatic cells isolated from mastitic quarters obtained from cows in early (< 4 months in lactation) or late lactation (> 8 months in lactation). We conclude that PA activity is increased during severe mastitic inflammation. Although the physiological function of this enzyme is as yet unclear, we propose that it may be involved in the conversion of plasminogen to plasmin, contributing to the higher levels of plasmin occurring in milk isolated from mastitic quarters.

    Topics: Animals; Cattle; Chromogenic Compounds; Female; Fibrin; Fibrinolysin; Hydrolysis; Lactation; Mastitis, Bovine; Milk; Oligopeptides; Plasminogen Activators; Tissue Plasminogen Activator

1992
Ultrastructural and associated observations on clinical cases of mastitis in cattle.
    Journal of comparative pathology, 1973, Volume: 83, Issue:2

    Topics: Animals; Basement Membrane; Cattle; Cell Membrane; Cell Nucleus; Collagen; Connective Tissue; Cytoplasm; Cytoplasmic Granules; Endoplasmic Reticulum; Epithelium; Extracellular Space; Female; Fibrin; Glycogen; Inflammation; Leukocytes; Lipids; Mammary Glands, Animal; Mastitis, Bovine; Microscopy, Electron; Milk Proteins; Organoids; Staphylococcal Infections; Streptococcal Infections

1973