Effect of in vitro simulated digestion on the anti- Helicobacter Pylori activity of different Propolis extracts.
Paolo GovernaGiulia RomagnoliPaola AlbaneseFederico RossiFabrizio ManettiMarco BiagiPublished in: Journal of enzyme inhibition and medicinal chemistry (2023)
Helicobacter pylori (HP) is among the most common pathogens causing infection in humans worldwide. Oxidative stress and gastric inflammation are involved in the progression of HP-related gastric diseases, and they can be targeted by integrating conventional antibiotic treatment with polyphenol-enriched natural products. In this work, we characterised three different propolis extracts and evaluated their stability under in vitro simulated gastric digestion, compared to their main constituents alone. The extract with the highest stability to digestion (namely, the dark propolis extract, DPE) showed a minimum bactericidal concentration (MBC) lower than 1 mg/mL on HP strains with different virulence factors. Finally, since urease is one of the virulence factors contributing to the establishment of a microenvironment that promotes HP infection, we evaluated the possible inhibition of this enzyme by using molecular docking simulations and in vitro colorimetric assay, showing that galangin and pinocembrin may be involved in this activity.
Keyphrases
- helicobacter pylori
- oxidative stress
- molecular docking
- escherichia coli
- antimicrobial resistance
- helicobacter pylori infection
- pseudomonas aeruginosa
- staphylococcus aureus
- anaerobic digestion
- biofilm formation
- molecular dynamics simulations
- dna damage
- diabetic rats
- induced apoptosis
- gold nanoparticles
- ischemia reperfusion injury
- stem cells
- high throughput
- gram negative
- hydrogen peroxide
- cancer therapy
- sensitive detection
- multidrug resistant
- combination therapy
- monte carlo
- fluorescent probe
- signaling pathway
- candida albicans
- replacement therapy