Molecules · 2012 · 674 citations · 20 references
MedicineMicrobiologyPharmacologyAntimicrobial PharmacologyAntimicrobial ResistancePharmacodynamicsAntibacterial AgentsAntifungal AgentsAntimicrobial Susceptibility TestingAntimicrobial ToxicityBactericidal AgentsCandida Albicans InfectionConcentration-dependent ActivityMicrobicidal MechanismsNatural Antifungal CompoundsTime-kill KineticsToxicity Of Antifungal Drugs
The study evaluated antimicrobial activity of pinene isomers and enantiomers against bacteria and fungi, and assessed inhibition of phospholipase and esterase activities, particularly with (+)-a‑ and (+)-β‑pinene. Positive (+)-a‑ and (+)-β‑pinene enantiomers exhibited broad antimicrobial activity with MICs 117–4,150 µg/mL, rapidly killing Candida albicans within 60 min and MRSA after 6 h, synergized with ciprofloxacin against MRSA, inhibited fungal biofilm formation, and reduced murine macrophage viability to 66.8 % and 57.7 % at 250 µg/mL, whereas negative enantiomers showed no activity up to 20 mg/mL.
The antimicrobial activities of the isomers and enantiomers of pinene were evaluated against bacterial and fungal cells. The agar diffusion test showed that only the positive enantiomers of the a- and β-isomers of pinene were active. The minimal inhibitory concentration (MIC) and minimal microbicidal concentration (MMC) of these monoterpenes were also determined, confirming that the positive enantiomers exhibited microbicidal activity against all fungi and bacteria tested with MICs ranging from 117 to 4,150 µg/mL. However, no antimicrobial activity was detected with the negative enantiomers up to 20 mg/mL. Time-kill curves showed that (+)-a-pinene and (+)-β-pinene were highly toxic to Candida albicans, killing 100% of inoculum within 60 min. By contrast, the bactericidal effect occurred after 6 h in methicillin-resistant Staphylococcus aureus (MRSA). In combination with commercial antimicrobials, ciprofloxacin plus (+)-a-pinene or (+)-β-pinene presented synergistic activity against MRSA whereas an indifferent effect against all fungi was detected when amphotericin B was combined with the positive enantiomers of pinene. The potential of (+)-a-pinene and (+)-β-pinene to inhibit phospholipase and esterase activities was also evaluated, and the best inhibition results were obtained with Cryptococcus neoformans. C. albicans biofilm formation was prevented with the MIC concentration of (+)-a-pinene and twice the MIC value of (+)-β-pinene. Finally, the cytotoxicity of the positive enantiomers of pinene to murine macrophages was evaluated, and 250 µg/mL of (+)-a-pinene and (+)-β-pinene reduced the cell viability to 66.8% and 57.7%, respectively.
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Aristides Medeiros Leite, Edeltrudes de Oliveira Lima, Evandro Leite de Souza et al. · Revista Brasileira de Ciências Farmacêuticas · 2007 · 238 citations · Full text