Abstract
BackgroundLaminitis, an inflammation of the claw laminae, is one of the major causes of bovine lameness, which can lead to enormous economic losses and animal welfare problems in dairy farms. Angelica polysaccharide (AP) is proved to possess anti-inflammatory properties. But the role of AP on inflammatory response of the claw dermal cells has not been reported. The aim of this study was to investigate the anti-inflammatory effects of AP on lipopolysaccharide (LPS)-induced primary claw dermal cells of dairy cow and clarify the potential mechanisms. In the current research, the primary claw dermal cells were exposed to gradient concentrations of AP (10, 50, 100 µg/mL) in the presence of 10 µg/mL LPS. The levels of cytokines and nitric oxide (NO) were detected with ELISA and Griess colorimetric method. The mRNA expressions of TLR4, MyD88 and chemokines were measured with qPCR. The activation of NF-κB and MAPK signaling pathways was detected with western blotting.ResultsThe results indicated that AP reduced the production of inflammatory mediators (TNF-α, IL-1β, IL-6 and NO), downregulated the mRNA expression of TLR4, MyD88 and some pro-inflammatory chemokines (CCL2, CCL20, CXCL2, CXCL8, CXCL10), and suppressed the NF-κB and MAPK signaling pathways evidenced by inhibition of the phosphorylation of IκBα, p65 and ERK, JNK, p38.ConclusionsOur results demonstrated that AP may exert its anti-inflammatory effects on claw dermal cells of dairy cow by regulating the NF-κB and MAPK signaling pathways.
Highlights
Laminitis, an inflammation of the claw laminae, is one of the major causes of bovine lameness, which can lead to enormous economic losses and animal welfare problems in dairy farms
Effects of Angelica polysaccharide (AP) on the levels of inflammatory mediators LPS induced an increase in the levels of tumor necrosis factor-α (TNF-α), IL-1β, IL-6, nitric oxide (NO) compared with the control group (P < 0.01) (Fig. 2)
Administration of 1 μg/mL AP had no difference in TNF-α and IL-6 levels compared with those in the LPStreated group for 24 h (P > 0.05), but could significantly reduce the levels of TNF-α and IL-6 at 48 h
Summary
An inflammation of the claw laminae, is one of the major causes of bovine lameness, which can lead to enormous economic losses and animal welfare problems in dairy farms. The role of AP on inflammatory response of the claw dermal cells has not been reported. The aim of this study was to investigate the anti-inflammatory effects of AP on lipopolysaccharide (LPS)-induced primary claw dermal cells of dairy cow and clarify the potential mechanisms. The primary claw dermal cells were exposed to gradient concentrations of AP (10, 50, 100 μg/ mL) in the presence of 10 μg/mL LPS. Endotoxins activate the inflammatory response in claw lamellar tissue, increase the permeability of the capillary wall, lead to the microcirculation disorder of the claw, and contribute to the appearance of laminitis [11]
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