Bioactive Essential Oils from the Cameroonian Rain Forest: a Review - Part II

Eighty-nine essential oil analyses carried out on Cameroonian plant material by gas chromatography are reviewed, and structures of sixty one main oil compounds are presented. Plant samples had been collected all over the rainforest area and further northwards, covering forty plant species belonging to ten families. For these plants, common names, traditional use as well as bioactivity and toxicity of their essential oils in vitro and in vivo are compiled. Data show that oils from leaves, bark, roots, fruit, rhizome or seeds display their own one to four main essential oil components. Each of them contributing more than 10% to over 90% of the oil ́s volume, which sums up to species-unique essential oil fingerprints and decreasing similarity of these fingerprints with increasing phylogenetic distance between species. This review article shows that the environmental factor include, temperature, rainfall (Littoral region), humidity (Center, South, East and West regions) and solar radiation (Adamaoua, North and Far-north regions) as well as the soil nutrients influence the secondary metabolite composition of the plants. Bioassays valorized traditional use of a good number of oils, for example against the dermatophytic fungus Trichophyton rubrum being twice as effective as amphothericin B®; against the chloroquine resistant Plasmodium falciparum; against cancer cell lines; and against a variety of human pathogen bacteria, being up to ten times as effective as ciproxin®, lidaprim®, tetracycline hydrochloride® and lidaprim®. Importantly, in an experiment employing the stored product beetle Callosobruchus maculatus, the leaf oil of Lippia adoensis (Verbenaceae) indicated neurotoxicity, so that preparations should be applied with care. Follow up work may focus on bioassays with commercial pure compounds, with the goal to improve effectivity and doses calculation for traditional essential oil medicines and agricultural products

Cytotoxic Properties of the Stem Bark of Citrus Reticulata Blanco (Rutaceae)

The bioassay-guided fractionation of the n-hexane extract of Citrus reticulata Blanco (Rutaceae) stem bark yielded scoparone (1), xanthyletin (2), lupeol (3), β-amyrin (4), stigmasterol (5), β-sitosterol (6) and palmitic acid. The structures of these compounds were determined by comprehensive spectroscopic analyses, i.e., 1D and 2D NMR and EI-MS, and by comparison with the reported data. Extracts, fractions and isolated compounds 1–6 were assessed for cytotoxicity by the 3-(4,5-dimethylthiazol-2-yl)-2,5-dphenyltetrazolium bromide (MTT) assay against three human cancer cell lines, i.e., human lung adenocarcinoma cell line A549, human breast adenocarcinoma cell line MCF7 and human Caucasian prostate adenocarcinoma cell line PC3. Significant activity of the n-hexane and the dichloromethane extracts was observed against the breast cancer cell line MCF7 with IC50s of 45.6 and 54.7 μg/mL, respectively. Moreover, the 70% ethyl acetate in n-hexane chromatographic fraction showed significant activity displaying IC50 values of 53.0, 52.4 and 49.1 μg/mL against the cancer cell lines A549, MCF7 and PC3, respectively. Encouragingly, an IC50 of 510.0 μg/mL against the human normal prostate cell line PNT2 indicated very low toxicity and hence favourable selectivity indices for the 70% ethyl acetate in n-hexane fraction in the range of 9.6–10.4 towards cell lines A549, MCF7 and PC3. Because compounds isolated from the above fraction only delivered IC50 values in the range of 18.2–96.3, 9.2–34.1 and 7.5–97.2 μg/mL against A549, MCF7 and PC3 cell lines, respectively, synergistic action between compounds is suggested. Bioassay results valorize the anticancer effectivity of the stem bark of this plant in Cameroonian pharmacopoeia. Copyright © 2017 John Wiley & Sons, Ltd

Terpenoids from Cameroonian Oxystigma mannii (Baill.) Harms

We describe two new terpenoids, 3″,5″-dihydroxycinnamoyl-3β,28,30-dihydroxylup-20(29)-ene (1) and 6S,9S-dihydroxycasbe-3E,7E,11E-trien-5,10‑dione (2) and ten known asperglaucide, aridanin, isoscopoletin, maslinic acid, ursolic acid, oleanolic acid, lupeol, sitosterol, stigmasterol and stigmasterol-glucoside from a West African, GuineoCongolian mangrove and strand forest tree, Oxystigma mannii (Baill.) Harms. The structures of the new compounds were determined based on their 1D and 2D NMR, HRMS and FTIR. DP4+ probabilities were used to assign the configurations for compound 2. The two compounds were tested for their antimicrobial effects against Saccharomyces cerevisiae (BY4743), Escherichia coli (BW25113) and Bacillus subtilis (BY4743), but no inhibition was observed at the maximum concentrations tested (800 µM)