Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtrer
Plus de filtres










Base de données
Gamme d'année
1.
J Ethnopharmacol ; 271: 113884, 2021 May 10.
Article de Anglais | MEDLINE | ID: mdl-33529639

RÉSUMÉ

ETHNOPHARMACOLOGICAL RELEVANCE: Piper capense is a medicinal spice whose fruits are traditionally used as aqueous decoction to heal several ailments such as trypanosomiasis, helminthic infections, and cancer. AIM OF THE STUDY: (1) To perform phytochemical investigation of the methanol extract of Piper capense; (2) to evaluate the cytotoxicity of botanicals (PCF, fractions PCFa-e), isolated phytochemicals on a broad panel of animal and human cancer cell lines; (3) to evaluate the induction of apoptosis of the most active samples. MATERIAL AND METHODS: Resazurin reduction assay (RRA) was used to determine the cytotoxicity of the studied samples. Cell cycle distribution (PI staining), apoptosis (annexin V/PI staining), mitochondrial membrane potential (MMP; JC-1) and reactive oxygen species (ROS; H2DCFH-DA) were measured by flow cytometry. Column chromatography (CC) was used for the purification of PCF, whilst nuclear magnetic resonance (NMR) spectroscopic and mass spectrometric (MS) analyses were applied for structural elucidation. RESULTS: The phytochemical investigation of PCF led to the isolation of 11 compounds: licarin B (1), licarin A (2), 7-(1,3-benzodioxol-5-yl)-7,8-dihydro-8-methyl-5-(2-propenyl)-furo[3,2-e]-1,3-benzodioxole (3), nitidine isocyanate (4), 5-hydroxy-7,4'-dimethoxyflavone (5), cardamomin (6), sitosterol (7) and stigmasterol (8), ß-sitosterol 3-O-ß-D-glucopyranoside (9), oleanolic acid (10) and lupeol (11). Fraction PCFb, compound 2 and doxorubicin (as positive control drug) revealed cytotoxic effects towards the 18 tested cancer cell lines. The IC50 values ranged from 6.1 µg/mL (against CCRF-CEM cells) to 44.2 µg/mL (against BRAF-V600E homozygous mutant melanoma cells) for PSCb; from 4.3 µM (against CCRF-CEM cells) to 21.8 µM (against HCT116 p53-/-) for compound 2 and from 0.02 µM (against CCRF-CEM cells) to 123.0 µM (against CEM/ADR5000 cells) for doxorubicin. PCFb and compound 2 induced apoptosis in CCRF-CEM cells mediated by activation of caspase 3/7, 8 and 9, MMP alteration and increased ROS production. CONCLUSION: Piper capense is a source of potent cytotoxic botanicals and phytochemicals that could help to fight various types of cancer including multidrug resistance phenotypes. PCFb and compound 2 should further be explored to develop new drugs to fight malignancies.


Sujet(s)
Antinéoplasiques d'origine végétale/pharmacologie , Fruit/composition chimique , Composés phytochimiques/pharmacologie , Piper/composition chimique , Extraits de plantes/pharmacologie , Animaux , Antinéoplasiques d'origine végétale/composition chimique , Apoptose/effets des médicaments et des substances chimiques , Caspases/métabolisme , Cycle cellulaire/effets des médicaments et des substances chimiques , Lignée cellulaire tumorale , Doxorubicine/pharmacologie , Résistance aux médicaments antinéoplasiques/effets des médicaments et des substances chimiques , Humains , Peroxyde d'hydrogène/pharmacologie , Lignanes/pharmacologie , Potentiel de membrane mitochondriale/effets des médicaments et des substances chimiques , Composés phytochimiques/composition chimique , Extraits de plantes/composition chimique , Espèces réactives de l'oxygène/métabolisme , Valinomycine/pharmacologie
2.
BMC Complement Med Ther ; 20(1): 342, 2020 Nov 12.
Article de Anglais | MEDLINE | ID: mdl-33183278

RÉSUMÉ

BACKGROUND: Multidrug-resistant (MDR) bacteria remain a major cause of morbidity and mortality globally. The present study was designed to investigate the in vitro antibacterial activities of crude methanol extract and constituents isolated by Column Chromatography (CC) from Cassia sieberiana bark (CSB) against ten MDR Gram-negative bacteria, as well as the mechanisms of action of the most active sample. METHODS: The antibacterial activity of the tested samples (extract, the fractions and their compounds isolated by CC and the structures obtained by exploiting 1H and 13C Nuclear magnetic resonance (NMR) spectra) in the presence and absence of an efflux pumps inhibitor, phenylalanine-arginine ß-naphthylamide (PAßN), was evaluated using the micro-dilution method. The effects of the most active sample were evaluated on the cell growth kinetic and on the bacterial H+-ATPase proton pumps. RESULTS: Phytochemical composition of the crude extract showed a rather selective distribution of secondary metabolites (presence of polyphenols, tannins, steroids, triterpenes, flavonoids, alkaloids, saponins and absence of anthocyanins, anthraquinones). The tested samples displayed different antibacterial activities with minimal inhibitory concentrations (MICs) ranging from 64 to 512 µg/mL. Crude extract (CS) and fraction CSc showed the highest inhibitory spectra, both inhibiting all of the studied bacteria except Enterobacter aerogenes EA27 strain. Fraction CSc exerted bactericidal effects on most bacteria meanwhile, crude extract (CS) and sub-fraction CSc2 exerted bacteriostatic effects. Compounds 1 (spectaline) and 2 (iso-6-cassine) inhibited the growth of 70% (Escherichia coli ATCC8739 and AG102, Klebsiella pneumoniae ATCC11296, Enterobacter aerogenes ATCC13048 and EA27, Providencia stuartii ATCC29916, Pseudomonas aeruginosa PA01) and 60% (Escherichia coli ATCC8739, Klebsiella pneumoniae ATCC11296 and KP55, Providencia stuartii ATCC29916, Pseudomonas aeruginosa PA01 and PA124) of bacteria respectively with MICs ranging from 128 to 512 µg/mL. In the presence of PAßN, the activities of crude extract CS, fraction CAc and sub-fraction CSc2 strongly increased on most bacteria strains as their MICs significantly decreased. Sub-fraction CSc2 inhibited the H+-ATPase proton pumps and altered growth kinetic of Escherichia coli ATCC8739. CONCLUSION: The overall results justify the traditional use of C. sieberiana for the treatment of bacterial infections.


Sujet(s)
Antibactériens/pharmacologie , Cassia/composition chimique , Dipeptides/pharmacologie , Bactéries à Gram négatif/effets des médicaments et des substances chimiques , Extraits de plantes/pharmacologie , Antibactériens/composition chimique , Antibactériens/métabolisme , Protéines bactériennes/antagonistes et inhibiteurs , Protéines bactériennes/métabolisme , Multirésistance bactérienne aux médicaments , Bactéries à Gram négatif/croissance et développement , Tests de sensibilité microbienne , Écorce/composition chimique , Extraits de plantes/composition chimique , Proton-Translocating ATPases/antagonistes et inhibiteurs , Proton-Translocating ATPases/métabolisme
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE