Documente Academic
Documente Profesional
Documente Cultură
ABSTRACT
Aginanthus brunneus is a specie of Africa mistletoe and is hemiparasitic in nature growing on
many trees. Phytochemical screening showed the presence of carbohydrates, Alkaloids,
Tannins and flavonoids. The ethanolic and aqueous extracts inhibited growth of Klesiella
aerogenes, Proteus spp Escherichia coli, Pseudomonas aeruginosa. Gentamycin and
Cloxacillin did not exhibit any activity against Pseudomonas aeruginosa.
INTRODUCTION
The plant Aginanthus brunneus is a specie of Africa mistletoe and belongs to the Loranthaceae family. It is a partial
parasite found growing on the branches of other trees. This particular species was found and chosen from the
Botanical garden of Ahmadu Bello University parasitizing on Albizza lebbeck (see Fig. 1).
There is increasing evidence that it threatens the establishment of trees on which this parasitic plant parasitizes
(Richardson, 1978) and is known to grow on various trees in Nigeria. In the Northern part of the country, it is found
1
V.O Aina et al.,: Continental J. Pharmacology and Toxicology Research 3: 1 - 4, 2010.
growing on the fruit trees and various woody trees common in the northern vegetation which are not annuals such as
the eucalyptus family, thus this parasitic plant is ubiquitous in distribution.
The extracts from the leaves of this plant stimulate insulin secretion from pancreas cells and help in the treatment of
arthritis (Blumenthal et al, 1998). Earlier research has also shown that the leaf contains choline, acetylcholine,
lectins, polypeptides and polysaccharides. Studies have also shown that Aginanthus brunneus alkaloids can help to
kill cancer cells both in vivo and in vitro (Khwaja et al, 1986). The decoction of the leaves is one of the most
effective extracts used in treating high blood pressure in man, epilepsy and other nervous conditions (Gill, 1992).
Preparation of Extracts
Fresh leaves were sun dried for about 2 weeks and macerated into a powder form.
A 100g each was extracted separately using 500ml distilled water and 90% ethanol as solvent. The solvent
extraction lasted 72h at room temperature (25oC). The crude extracts were concentrated to give 40g of ethanolic and
65g of aqueous extracts.
Test Microorganisms
Five bacteria species were employed as test microorganisms. These include; Staphylococcus aureus, Klebsiella
aerogenes, Proteus spp, Escherichia coil and Pseudomonas aeruginosa. These were sourced from the
Microbiological unit of the Department of Applied Sciences, Kaduna Polytechnic, Kaduna and maintained on
Muller Hinton slants at 40C before testing.
Antibacterial Screening/Assay
Each test organism was cultured and incubated for 4h. These were used to inoculate plates of Muller Hinton agar.
The disks containing the different crude extracts were transferred using sterilized forceps to the agar plates. Sterile
water and 95% ethanol were used as control. Standard antibiotic disks were used for comparison. The plates were
incubated at 35oC for 36h before the examination for zones of inhibition of growth.
Phytochemical Analysis
The extracts were subjected to analysis for the presence of saponins, steroids, alkaloids, flavonoids, tannins,
carbohydrates, lipids and terpenoids using the standard method of (Harborne, Trease and Evans 1978).
Class of Product
Extract Saponins Steroids Flavonoids Tannins Alkaloid Terpenoids Liqids
Aqueous - + +++ +++ - +++ -
Ethanolic - + +++ +++ - +++ -
Key +++ = Present, + = Weakly present, = Absent
2
V.O Aina et al.,: Continental J. Pharmacology and Toxicology Research 3: 1 - 4, 2010.
Table 2: Antibacterial activity and zone of inhibition (mm) of the leaf of Aginanthus brunneus extracts zone of
inhibition (mm).
Table 1 shows the result of preliminary phytochemical analysis. The results obtained indicated the presence of
tannins, alkaloids, flavonoids, carbohydrates. Terpenoids, lipids and saponins were absent.
The crude extracts (ethanolic and aqueous) of the leaf were heated with concentrated hydrochloric acid and
magnesium turnings giving a red colouration indicating the presence of flavonoids.
From the results of Table 2: None of the extracts inhibited Staphylococcus aureus, Pseudomonas aeruginosa was
resistant to both Cloxacillin and Gentamycin.
Other tests such as susceptibility test showed that the cold aqueous and ethanolic extracts had similar activities on
the test organisms, although cold aqueous extract had a slightly high inhibition zone than the ethanolic extract. The
antibacterial activity of Aginanthus brunneus extracts correlated well with its traditional use (Pamplona-Roger,
1999).
Furthermore, the antibacterial activity of the extract compared favourably well with standard antibiotic used in this
work namely (Gentamycin and Cloxacillin).
This work has shown that this specie of Africa mistletoe (Aginanthus brunneus) contained many classes of natural
products namely: Flavonoids, carbohydrates, tannins and alkaloids. Both aqueous and ethanolic extracts were shown
to be active against Pseudomonas aeruginosa, Escherichia coli, Proteus spp, and Klebsiella aerogenes.
REFERENCES
Blumenthal, M., Busse W.R, and Goldberg, A., (1998); Therapeutic guide to herbal medicine. The complete
German Commission. E. Monogr., 171:2-3.
Gill, L. S., (1992): Globimetulla browni. Ethnomedical uses of plants in Nigeria. University of Benin Press, Benin
Pp: 244 – 245.
Khwaja, T.A, Dias, C.B., Pentecost, S. (1986): Recent studies on the anticancer activities of some species of
mistletoe and its alkaloid. Aucology, 3:1 – 10.
Neilson, M. S (1965): Introduction to the flowering plants of West Africa. University of London Press. Pp 28 – 31,
101 – 106.
Pamplona – Roger, G. H; (1999): Medicinal plants; Encyclopedia of Medicinal plants. Safeliz Publication. Spain,
Pp: 245 – 247.
Richardson I. B K (1978): Lorantheceae (Mistletoe) in flowering plants world (Heymond V. H et al Edn.) Oxford
3
V.O Aina et al.,: Continental J. Pharmacology and Toxicology Research 3: 1 - 4, 2010.
Harborne, Trease, G. E and Evans, W. C. (1978): Pharmacognosy. 11th Edn. Bailner Tindall Ltd, London, Pp: 784.
Corresponding Author:
V.O Aina
Department of Biochemistry, Ahmadu Bello University, Zaria - Nigeria.
E-mail: vocwummi2006@yahoo.com