Propriétés antibactériennes d’extraits de propolis contre des souches de Staphylococcus aureus sensibles ou résistantes à la méthicilline

La résistance aux antibiotiques est devenue l\u27un des problèmes majeurs de santé publique du XXIème siècle. Il existe donc un réel intérêt thérapeutique dans la recherche de composés ou d\u27extraits naturels capables de limiter cette résistance. La propolis est un mélange complexe composé de substances résineuses collectées par les abeilles sur différentes parties des plantes et arbres, de cires et de sécrétions salivaires de l\u27abeille. Elle sert principalement à colmater les interstices des parois de la ruche et comme véritable arme chimique contre les microorganismes. La propolis est utilisée depuis longtemps en médecine traditionnelle puisqu\u27elle possède des propriétés pharmacologiques intéressantes notamment antioxydante, anti-inflammatoire mais aussi antimicrobienne. Un échantillon de propolis, composé de 24 lots collectés en France (majoritairement dans le sud-ouest) en 2010 et 2011, a été extrait par différents solvants : EtOH 70%, MeOH, DCM et DCM/MeOH/eau 31/19/4 (mixte). La composition chimique des extraits a préalablement été déterminée au moyen d’analyses HPLC/DAD/MS et RMN 1H et 13C. L\u27activité antibactérienne a été évaluée sur des bactéries responsables d\u27infections nosocomiales, et plus spécifiquement sur 13 souches de Staphylococcus aureus [ATCC25923, six isolats cliniques de souches résistantes à la méthiciline (SARM) et six isolats cliniques de souches sensibles à la méthiciline (SASM)] par détermination de la concentration minimum d\u27inhibition (CMI) en milieu gélosé [1]. Les résultats ont montré que, parmi les quatre extraits, le DCM et le "mixte" présentaient une bonne activité antibactérienne contre S. aureus (SA) avec des CMI respectives de 60±10 et 67±15 µg/mL mais également sur quasiment toutes les souches SARM et SASM testées (CMI entre 30 et 97 µg/mL). Ces bonnes activités des extraits DCM et mixte peuvent être reliées à des teneurs élevées en polyphénols totaux et en flavonoïdes [1]. Diverses études ont en effet montré que ce type de mélange complexe, riche en polyphénols, était plus actif que les composés isolés les constituant. Les polyphénols agiraient ainsi de façon synergique, potentialisant l\u27activité antibactérienne de ces extraits [2]. D\u27autres études, menées in vitro, ont par ailleurs mis en évidence un réel synergisme entre propolis et antibiotiques [3], [4]. Ainsi, ces extraits de propolis présentent-ils un réel potentiel dans une lutte alternative contre des infections à staphylocoques.   Références [1]          S. Boisard et al., "Antifungal and Antibacterial Metabolites from a French Poplar Type Propolis", Evid. Based Complement. Alternat. Med., vol. 2015, p. e319240, 2015. [2]          A. Kujumgiev, I. Tsvetkova, Y. Serkedjieva, V. Bankova, R. Christov, et S. Popov, "Antibacterial, antifungal and antiviral activity of propolis of different geographic origin", J. Ethnopharmacol., vol. 64, no 3, p. 235‑240, 1999. [3]          S. Stepanović, N. Antić, I. Dakić, et M. Švabić-Vlahović, "In vitro antimicrobial activity of propolis and synergism between propolis and antimicrobial drugs", Microbiol. Res., vol. 158, no 4, p. 353‑357, 2003. [4]          A. Fernandes Júnior, E. C. Balestrin, J. E. C. Betoni, R. de O. Orsi, M. de L. R. de S. da Cunha, et A. C. Montelli, "Propolis: anti-Staphylococcus aureus activity and synergism with antimicrobial drugs", Mem. Inst. Oswaldo Cruz, vol. 100, no 5, p. 563‑566, 2005

Voltage Sensor Probes (VSPs) as an Efficient Tool to Screen for Inhibitors of Voltage-Gated Sodium Channels

Voltage-gated sodium channels (Nav) represent a therapeutically validated group of targets for the development of antiepileptic drugs, analgesics and antiarrhythmics [1]. However most of the existing drugs acting as Nav blockers suffer from multiple side effects, but the existence of a multigene family of Nav [2] suggests that the identification of new compounds that selectively block Nav isoforms might have better therapeutic efficiency and reduced side effects. Due to their molecular interference with numerous ion channels, alkaloids represent a group of natural products of particular interest. This is the reason why we have evaluated the efficiency of an in-house method to screen a library of isoquinoline alkaloids formerly isolated in our laboratory. Mammalian GH3 cells constitutively expressing Nav where used in conjunction with Voltage Sensor Probes (VSPs), the signals being read on a fluorescence plate reader. Thanks to this technique, we were able to precisely detect Nav channels activators or blockers. Among 62 compounds tested, 5 isoquinolines appeared as potent Nav channels inhibitors. References: 1. Salat, K. et al. (2014) EOID 23:1093-1104 2. Yu, F.H. et al (2003) Genome Biol. 4

Screening an in house alkaloids library using Voltage-Sensor Probes for new modulators of voltage-gated sodium channels

Voltage-gated sodium channels (Nav) are molecular targets of clinically used drugs for treatments of various diseases (epilepsy, chronic pain, cardiac arrhythmia…) and also of numerous animal and plant neurotoxins. The development of easy-to-use screening assays for searching new ligands from chemicals libraries, animal venoms or plant extracts represents a challenge of a great interest to generate therapeutic hits. Here, we used the mammalian GH3B6 pituitary cell line, which constitutively expresses three different neuronal Nav channel isoforms (Nav1.2, Nav1.3 and Nav1.6), to identify novel compounds of pharmacological interest from a library of in-house vegetal alkaloids. The screening is based on a method using Voltage-Sensor Probes (VSPs) that we adapted to detect both activators and blockers of Nav channels. Over the 84 pure alkaloids or plant extracts that were screened, 17 increased the VSP signal. They operated as gating modifier, showing an action mechanism similar to that of batrachotoxin (BTX), known to strongly inhibit Nav channel inactivation. The remaining 67 plant products were assessed for their potency to inhibit BTX-induced VSP signal. We further selected 11 alkaloids as efficient Nav channels inhibitors. We focused our attention on two structural analogs belonging to the aporphine family, liriodenine and oxostephanine, which differ only by a methoxy group. Whereas liriodenine has been already described as a Nav channels blocker, oxostephanine has not been yet documented as an ion channel modulator. In conclusion, the novel VSPs-based screening assay we developed is a suitable method to challenge the discovery and to assess the activity of novel ligands on Nav channels

Effets anti-inflammatoire et immunomodulateur de composés polyphénoliques isolés de Clusiaceae et de Calophyllaceae

L’endothélium vasculaire joue un rôle central dans le développement des réponses inflammatoires et immunitaires conduisant notamment au phénomène de rejet de greffe1. Les Clusiaceae et Calophyllaceae, plantes des régions pantropicales, biosynthétisent des dérivés polyphénoliques originaux présentant des activités anti-inflammatoires intéressantes2-3. Divers polyphénols isolés de ces plantes ont été sélectionnés, afin d’évaluer in vitro leur potentiel anti-inflammatoire et immunomodulateur sur des cellules endothéliales humaines. Plusieurs coumarines et une benzophénone se sont alors révélées inhibitrices de l’expression de marqueurs de l’inflammation et de l’immunité. Parallèlement à cette étude, les extraits dichlorométhaniques (DCM) et méthanoliques d’un panel de plantes issues des genres Garcinia (Clusiaceae), Calophyllum et Mesua (Calophyllaceae), originaires de Malaisie, ont été analysés par déréplication (HPLC-PDA-MSn). Deux extraits contenant des pharmacophores d’intérêt ont ainsi été sélectionnés pour une étude phytochimique approfondie : l’extrait DCM de fruits de Mesua lepidota, duquel ont été identifiés sept phénylcoumarines originales, que nous avons baptisées lépidotols et lépidotines, et l’extrait DCM de feuille de Calophyllum tetrapterum, ce dernier riche en benzophénones polyprénylées. Références : 1.         Brick C, Atouf O, Benseffaj N, et al. Rejet de la greffe rénale : mécanisme et prévention. Nephrol Ther 2011;7:18-26. 2.         Ali M, Arfan M, Ahmad M, et al. Anti-inflammatory xanthones from the twigs of Hypericum oblongifolium Wall. Planta Med 2011;77:2013-2018. 3.         Santa-Cecilia FV, Freitas LAS, Vilela FC, et al. Antinociceptive and anti-inflammatory properties of 7-epiclusianone, a prenylated benzophenone from Garcinia brasiliensis. Eur J Pharmacol 2011;670:280-285

Chemical composition and antiglycoxidant activities of French organic propolis extracts

International audienc

Polyphenolic content and pharmacological potential of french BFA propolis extracts

Propolis, or bee glue, is a natural resinous hive product collected by honeybees from buds and exudates of various trees and plants. Mixed with beewax and salivary enzymes, it is employed to fill cracks and embalm dead invaders in the hive. Propolis has been used in folk medecine since ancien times due to its pharmacological potential associated with antioxidant, antifungal, antibacterial as well as antitumoral properties. A batch of various French propolis extracts, supplied by “Ballot-Flurin Apiculteurs” (BFA), a company located in the South-West of France and specialized in apitherapy products, was fractionated and analysed by HPLC/MS. Its qualitative chemical composition highlights the presence of polyphenols such as hydroxycinnamic acid derivatives and flavonoids. Total polyphenol content and antioxidant activities were evaluated on six BFA propolis extracts, using respectively Folin-Ciocalteu, DPPH and ORAC assays. Preliminary antifungal (Candida albicans) and antibacterial (Staphylococcus aureus) evaluations will also be given

Chemical composition, antioxidant and anti-AGEs activities of a French propolis

Accumulation in tissues and serum of advanced glycation end-products (AGEs) plays an important role in pathologies such as Alzheimer\u27s disease or, in the event of complications of diabetes, atherosclerosis or renal failure. Therefore there is a potential therapeutic interest in natural antioxidants with true anti-AGEs capabilities for the prevention of this kind of pathologies. The aim of this study was to evaluate the antioxidant and anti-AGEs potential of a French propolis batch (natural resinous substance collected by honeybees from differents plants and trees), then to identify the main compounds responsible for this anti-AGEs effect. For this purpose, the phytochemical composition of a 70% ethanolic extract of propolis (EEP70) was determined, using HPLC/DAD/MS and/or 1H and 13C NMR (1D and 2D) analysis. This study showed the presence of phenolic acids and their esters as well as flavonoids. Then, the evaluation of the antioxidant, using DPPH and ORAC assays, and the anti-AGEs potential, using an automated test recently developed in our laboratory, showed that EEP70 exhibited both high antioxidant (1650 ± 149 µmol TE/g) and anti-AGEs (IC50=0.03 mg/ml) activities. A bio-guided fractionation allowed us to identify the most active anti-AGEs compounds: pinobanksin-3-acetate (IC50=0.06 mM) which is the major compound of EEP70. Thus, EEP70 represents a good candidate as food additive to prevent glycoxidation. Boisard S, Le Ray A-M, Gatto J, Aumond M-C, Blanchard P, Derbré S, Flurin C, Richomme P: Chemical Composition, Antioxidant and Anti-AGEs Activities of a French Poplar Type Propolis. J Agric Food Chem 2014, 62:1344–1351

Momentum Spectra of Electrons Rescattered from Rare-Gas Targets Following Their Extraction by One- and Two-Color Femtosecond Laser Pulses

We have used velocity-map imaging to measure the three-dimensional momenta of electrons rescattered from Xe and Ar following the liberation of the electrons from these atoms by 45 fs, 800 nm intense laser pulses. Strong structure in the rescattering region is observed in both angle and energy, and is interpreted in terms of quantitative rescattering (QRS) theory. Momentum images have also been taken with two-color (800 nm + 400 nm) pulses on Xe targets. A strong dependence of the spectra on the relative phase of the two colors is observed in the rescattering region. Interpretation of the phase dependence using both QRS theory and a full solution to the time-dependent Schrödinger equation shows that the rescattered electrons provide a much more robust method for determining the relative phase of the two colors than do the direct electrons

Monitoring the Bragg peak location of 73 MeV/u carbon ions by means of prompt γ\gamma-ray measurements

By means of a time-of-flight technique, we measured the longitudinal profile of prompt $\gamma$-rays emitted by 73 MeV/u $^{13}$C ions irradiating a PMMA target. This technique allowed us to minimize the shielding against neutrons and scattered $\gamma$-rays, and to correlate prompt gamma emission to the ion path. This correlation, together with a high counting rate, paves the way toward real-time monitoring of the longitudinal dose profile during ion therapy treatments. Moreover, the time correlation between the prompt gamma detection and the transverse position of the incident ions measured by a beam monitor can provide real-time 3D control of the irradiation.Comment: to be published in Applied Physics Letter