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An investigation of the medicinal properties of Siphonochilus aethiopicus.Light, Marnie Elizabeth. 09 December 2013 (has links)
Siphonochilus aethiopicus (Schweinf.) B.L. Burtt (Zingiberaceae), commonly known as wild ginger, is a highly sought after plant for use in traditional medicine in South Africa. Over-exploitation of this medicinal plant has resulted in regional extinction in the wild. As a result, there is great interest in the medicinal properties of S. aethiopicus, and as a plant for small scale cultivation to increase the supply for use in traditional medicine. Water, ethanol and ethyl acetate extracts were prepared from the leaves, rhizomes and roots of S. aethiopicus. These extracts were tested for in vitro anti-inflammatory activity
in the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) assays, and in the microdilution antibacterial assay.
The aqueous extracts showed no significant prostaglandin synthesis inhibition in the COX-1 and COX-2 assays. The ethanol and ethyl acetate extracts of the leaves showed the highest levels of activity at a concentration of 250 µg ml¯¹ per test solution, in both the COX-1 and COX-2 assays. The ethanol and ethyl acetate extracts of the
rhizomes and roots also had moderate levels of activity in the COX-1 assay. These results provide some evidence for the rational use of S. aethiopicus in traditional medicine for anti-inflammatory purposes. In the microdilution antibacterial assay, no inhibitory activity against the test bacteria was detected with the aqueous extracts. The ethanol and ethyl acetate extracts tested showed greater antibacterial activity at minimal inhibitory concentrations ranging from 0.78 to 3.13 mg ml¯¹ against the gram-positive bacteria (Bacillus subtilis, Staphylococcus aureus) than the Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae). No distinct differences were observed between the ethanol and ethyl acetate extracts, or between the different plant parts. A serial extraction of S. aethiopicus rhizome material was conducted and the extracts were tested in the COX-1 assay and the microdilution assay as a preliminary investigation for a bulk extraction. The hexane and ethyl acetate extracts gave slightly higher COX-1 inhibition than the ethanol extract. No distinct differences were observed in the microdilution assay. A bulk ethyl acetate extract of S. aethiopicus rhizome material was prepared, yielding 6.3 g of a thin orange oil. Vacuum liquid chromatography (VLC) was used to fractionate ≈4 g of the extract. The VLC fractions were evaluated using thin layer chromatography (TLC) and a bioautographic assay, using S. aureus as a test organism. The fractions were also tested in the COX-1 assay. The bioautography revealed a number of compounds which exhibited antibacterial activity. Fraction C was purified further using preparative TLC, and 24.9 mg of a pure compound from R,0.54 (toluene:ethyl acetate 93:7) was isolated. The structure of the compound was elucidated from nuclear magnetic resonance (NMR) spectra, and mass
spectroscopy of the compound was also recorded. The compound was identified as the sesquiterpenoid furanoeremophil-2-en-1-one, which is structurally identical to the recently reported compound 4aαH-3,5α,8aβ-trimethyl-4,4a,9-tetrahydro-naphtho[2,3-b]-furan-8-one. The compound showed only a very minimal bacteriostatic effect in the microdilution assay.
S. aethiopicus plants were harvested before and after seasonal senescence. Ethanol extracts were prepared from fresh or dried material of the leaves, rhizomes and roots,
and tested in the COX-1 assay and the microdilution assay TLC fingerprints of the various extracts were also prepared.
No noteworthy changes in COX-1 inhibition, due to senescence, were observed with extracts prepared from fresh material, although there did appear to be a slight decrease in activity in the α-roots and an increase in the β-roots after senescence (fresh and dry). A decrease in the antibacterial activity of the leaves and an increase in the antibacterial activity of the α-roots was observed after senescence. These results suggest that the time of harvest may only have a minimal influence on the degree of anti-inflammatory and antibacterial activity. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 2002.
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Bioprospecting the flora of southern Africa : optimising plant selections.Douwes, Errol. January 2005 (has links)
Focused procedures which streamline and optimise plant prioritisation and selection in
bioprospecting have the potential to save both time and resources. A variety of semiquantitative
techniques were assessed for their ability to prioritise ethnomedicinal taxa in
the Flora of Southern Africa (FSA) region. These techniques were subsequently
expanded upon for application in plant selection for the Novel Drug Development
Platform bioprospecting programme.
Least squares regression analyses were used to test the hypothesis that ethnomedicinal
plant use in southern Africa is strictly random, i.e. no order or family contains
significantly more medicinal plants, than any other order or family. This hypothesis was
falsified revealing several 'hot' plant orders. The distribution of southern African
ethnomedicinal taxa was investigated, and revealed low ethnomedicinal plant usage in
the Western Cape and Northern Cape. The historical settlement of Bantu tribes in the
eastern regions of southern Africa was one explanation for this discrepancy. Growth
forms of ethnomedicinal taxa in 'hot' orders (identified in the regression analysis) were
analysed. The results indicated no clear preferences across orders, but rather a
preference for particular growth forms in certain orders. With respect to distribution,
endemism and Red Data List status of ethnomedicinal taxa, the Western Cape had the
greatest proportion of endemics and Namibia had the highest proportion of Red Data
Listed ethnomedicinal taxa. With respect to chemotaxonomy, the Asteraceae contained
the highest proportion of terpenoids, the Rubiaceae the highest proportion of alkaloids
and the Fabaceae the highest proportion of flavonoids.
The predictive value of regression analyses was tested against an existing analysis of
anti-malarials and the subsequent in vitro bioassays on Plasmodium falciparum. In
particular, the ability of these analyses to identify plants with anti plasmodial IC50 values
of [less than or equal to] 10 [micro]g/ml was assessed. Most species in 'hot' genera showed comparatively good
antiplasmodial activities (IC50 [less than or equal to] 10 [micro]g/ml).
Plant candidates were prioritised for screening anti-tuberculosis, anti-diabetes and
immune-modulatory compounds, using a weighting system based on;
their ethnomedicinal application, chemotaxonomic potential, frequency in ethnomedicinal
trade, association with the relative disease, toxicity, Red Data status, indigenous or
endemic status, and family selection in ethnomedicine (identified through regression
analyses). Other taxa were short-listed due to their presence in biodiversity hotspots
where few ethnomedicinal plant use records are documented, and still others were
incorporated due to their taxonomic association with efficacious exotic allies. Statistical
analyses of the weighting processes employed were not possible in the absence of
screening results which are due only in December 2006.
The legislation governing bioprospecting in South Africa is discussed and several
recommendations are presented to minimise negative impacts on the industry. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2005.
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