Risk factors for postpartum uterine infections in dairy herds

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Background: Hypoadiponectinaemia is a risk factor for endocrinopathic laminitis, but the directionality and nature of its association with insulin dysregulation is unclear.Objectives: To investigate the effects of short-term induced hyperinsulinaemia and dexamethasone challenge on circulating [total adiponectin] and whole blood expression of adiponectin (AdipoR1 and AdipoR2), insulin, and insulin-like growth factor 1 (IGF-1) receptors in insulin-sensitive ponies.Study design: In vivo experiment.Methods: Six never-laminitic, insulin-sensitive, native-breed UK ponies first underwent a dexamethasone challenge (0.08 mg/kg i.v.) with blood samples collected every 15 min over 3 h.After a 14-day washout period, hyperinsulinaemia was induced for 9 h via a euglycaemic-hyperinsulinaemic clamp (EHC), with blood samples collected every 30 min.Serum [insulin], plasma [total adiponectin], and plasma [IGF-1] were measured using validated assays and receptor gene expression was assessed via quantitative polymerase chain reaction (qPCR).Finally, whole blood was incubated with 10-1000 ng/mL dexamethasone for 3 h at 37 C to investigate its direct effects on gene expression.Results: There were no adverse effects observed during either protocol.Dexamethasone challenge did not alter circulating [insulin] or [total adiponectin] at any timepoint, but significantly upregulated AdipoR1 and IGF-1R expression at 150 and 180 min.Ex vivo incubation of whole blood with dexamethasone did not alter expression of the genes examined.There was no change in [total adiponectin] or expression of the genes examined associated with EHC-induced hyperinsulinemia.Main limitations: This was a small sample size that included only native-breed ponies; total adiponectin was measured rather than high-molecular-weight adiponectin.Conclusions: Short-term induced hyperinsulinaemia and dexamethasone challenge did not affect circulating [total adiponectin] in insulin-sensitive ponies.However, dexamethasone administration was associated with upregulation of two receptors linked to adiponectin signalling, suggesting that a physiological response occurred

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