Chemical Composition and Pharmacological Effects of Geopropolis Produced by Melipona quadrifasciata anthidioides.
Cintia Miranda Dos SantosJaqueline Ferreira CamposHelder Freitas Dos SantosJosé Benedito Perrella BalestieriDenise Brentan SilvaKely de Picoli SouzaCarlos Alexandre CarolloLeticia M EstevinhoEdson Lucas Dos SantosPublished in: Oxidative medicine and cellular longevity (2017)
Stingless bees produce geopropolis, which is popularly described for its medicinal properties, but for which few scientific studies have demonstrated pharmacological effects. The objective of this study was to investigate the chemical composition of the geopropolis of Melipona quadrifasciata anthidioides and to evaluate its antioxidant, antimutagenic, anti-inflammatory, and antimicrobial activities. The composition of the hydroethanolic extract of geopropolis (HEG) included di- and trigalloyl and phenylpropanyl heteroside derivatives, flavanones, diterpenes, and triterpenes. HEG showed antioxidant action via the direct capture of free radicals and by inhibiting the levels of oxidative hemolysis and malondialdehyde in human erythrocytes under oxidative stress. HEG also reduced the frequency of gene conversion and the number of mutant colonies of S. cerevisiae. The anti-inflammatory action of HEG was demonstrated by the inhibition of hyaluronidase enzyme activity. In addition, HEG induced cell death in all evaluated gram-positive bacteria, gram-negative bacteria, and yeasts, including clinical isolates with antimicrobial drug resistance. Collectively, these results demonstrate the potential of M. q. anthidioides geopropolis for the prevention and treatment of various diseases related to oxidative stress, mutagenesis, inflammatory processes, and microbial infections.
Keyphrases
- oxidative stress
- anti inflammatory
- diabetic rats
- cell death
- staphylococcus aureus
- dna damage
- ischemia reperfusion injury
- endothelial cells
- induced apoptosis
- high glucose
- microbial community
- copy number
- genome wide
- gene expression
- gram negative
- escherichia coli
- cell cycle arrest
- drug induced
- biofilm formation
- cell proliferation
- risk assessment
- induced pluripotent stem cells
- heat shock
- combination therapy
- endoplasmic reticulum stress
- heat shock protein
- heat stress