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Peer-reviewed veterinary case report

Propolis as an alternative remedy for the treatment of subclinical mastitis in dairy cows.

Journal:
Frontiers in veterinary science
Year:
2025
Authors:
Mikniene, Zoja et al.
Affiliation:
Lithuanian University of Health Sciences

Abstract

BACKGROUND: Subclinical mastitis is a widespread condition in dairy cows, often treated with antibiotics. Due to rising antimicrobial resistance, natural alternatives like propolis are gaining interest. OBJECTIVES: To evaluate the antibacterial efficacy of 5 and 10% propolis alginate emulsions in cows with subclinical mastitis and assess their effects on milk quality and systemic biomarkers. METHODS: Ten dairy cows diagnosed with subclinical mastitis were divided into two treatment groups (5 and 10% propolis emulsions). Emulsions were administered intramammarily and orally for 5&#x202f;days. Bacterial load in milk, milk composition, blood biochemical and immunological parameters, phenolic compound profiles, and antioxidant activity were analysed using standard microbiological and biochemical methods. RESULTS: The 5% emulsion reduced bacterial load by 2.27 log CFU/ml, outperforming the 10% emulsion (0.89 log CFU/ml;&#x202f;<&#x202f;0.05). Significant changes were observed in hepatic enzymes (ALT, AST), electrolytes (Ca, Mg, P), and renal markers (creatinine, urea). Immunological shifts included an increase in lymphocytes (+21%) and a decrease in neutrophils (-30%) in the 5% group. Antioxidant capacity was confirmed, with the highest activity observed in CUPRAC and ABTS assays. Phenolic compounds, including p-coumaric acid and flavonoids, contributed to the bioactivity. CONCLUSION: A 5% propolis alginate emulsion was more effective than the 10% formulation in reducing bacterial counts and improving immunological and biochemical profiles. These findings support propolis as a promising natural alternative for treating subclinical mastitis, warranting further investigation into optimal formulations and long-term safety.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/41705118/