alexa Phytochemical Screening and Anthelmintic Evaluations of the Stem Bark of Afzelia Africana ‘ SM ’ (Keay, 1989) against Nippostrongylus Barziliensis in Wistar Rats | Open Access Journals
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Phytochemical Screening and Anthelmintic Evaluations of the Stem Bark of Afzelia Africana ‘ SM ’ (Keay, 1989) against Nippostrongylus Barziliensis in Wistar Rats

Simon MK* and Jegede CO
Department of Veterinary Parasitology and Entomology, Faculty of Veterinary Medicine, University of Abuja, Nigeria
*Corresponding Author : Simon MK
Department of Veterinary Parasitology and Entomology
University of Abuja, Nigeria
Received April 27, 2013; Accepted April 29, 2013; Published July 15, 2013
Citation: Simon MK, Jegede CO (2013) Phytochemical Screening and Anthelmintic Evaluations of the Stem Bark of Afzelia Africana ‘SM’ (Keay, 1989) against Nippostrongylus Barziliensis in Wistar Rats. Agrotechnol 2:111. doi:10.41272/2168-9881.1000111

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In-vivo; Phytochemistry; Anthelmintic; Afzelia africana; Nippostrongylus braziliensis
Parasitic nematodes are among the most common and economically important agents of infectious disease of grazing livestock, especially in small ruminants; in the tropics, subtropics and other parts of the world [1,2]. Livestock production in tropical climates suffers heavy economic losses due to gastrointestinal parasites [3,4]. The greatest losses associated with nematode parasite infections are sub-clinical, and economic assessment shows that the financial costs of internal parasitism are enormous [5,6]. The loss is characterized by lower output of animal products (meat, milk, hides and skins), low manure, poor traction power, poor carcass quality/organ condemnation, death and medication costs, which all impact negatively on the livelihood of small holder farmers [7,8].
Livestock producers have generally derived substantial benefit from the use of conventional anthelmintic drugs in controlling livestock parasitosis. In Africa, however, declining funding for veterinary services and the rising costs (occasioned by depreciating value of local currencies) of these services has made it difficult for resource-poor farmers to have access to such services. This has led to the increasing demand for effective and low cost anthelmintic drug by African smallholder livestock producers and pastoralist in order to reduce having to pay for the high cost of the services [9-12]. There is equally the need to produce animal products free from industrial chemical input [13,14] and avoid possible tendencies of environmental pollution [15]; also the need to discover new therapeutic substances of natural origin with low toxicity to man and animals [16], as well as overcoming the rapid escalation in anthelmintic resistance worldwide [17]. Afzelia africana SM is a tree species commonly found in savanna fringing forest and drier parts of forest regions. It is commonly referred to as; mahogany, kawo, apa and akpalata in English, Hausa, Yoruba and Igbo respectively [18]. The seed is widely used for medicinal purposes, for industrial production of soap, margarine, and candle making and as diets such as condiments and seasoning in soup [19]. Atawodi [20] identified the use of herbal preparations including Afzelia africana in the treatment of helminthiasis. This study therefore asseed the in vivo anthelmintic effects of the crude methanolic extract and partitioned portions of the crude methanolic extract of the bark of Afzelia africana against adult Nippostrongylus braziliensis in experimentally infected rats and also identified the active fractions from the crude methanolic extracts of the plant via a separation process, with the view of providing scientific basis for their use in ethno-veterinary practices.
Materials and Methods
Plant collection, identification and preparations
The stem barks of Afzelia africana was collected in April, 2005 from New Bussa in Niger State, Nigeria. The plant was identified by a botanist from the department of biological sciences Ahmadu Bello University, Zaria and a specimen voucher number 2276 was deposited. The samples (5 kg) of the plant bark were sun dried, pulverized into powdered form using mortar and pestle and sieved as described by Onyeyili et al. [21]. The methanolic extract was obtained using 500 g the powdered plant material in a soxhlet apparatus (Quick fit corning Ltd, Stafford England) after which the solution was evaporated to dryness in vacuum using a rotary evaporator coupled to a thermo-regulator (RII-35). Twenty grammes (20 g) of the dried crude methanolic extract were partitioned with petroleum ether, chloroform and N-butanol (150 ml each) using separating funnel as described by Suleiman et al. [22]. The portions were then referred to as petroleum ether, chloroform, N-butanol and aqueous methanol portion respectively. After evaporating the solvents, the portions were tested for anthelmintic activity on albino rat experimentally infected with L3 stage of Nippostrongylus braziliensis.
Phytochemical screening
Before the experimental treatment, the crude methanolic extract, petroleum ether, chloroform, N-butanol and the aqueous methanol portions of the extracts were subjected to phytochemical screening using standard techniques of Ciulei [23]; Sofowora [24] and Brain and Turner [25]. The three solvents used have different polarity, thus, it is expected that they extract the various active principles in the plant base on their polarity.
Experimental animal
Sixty three (63), six to seven weeks old albino Wistar rats of both sexes and weighing between 100 to 160 g were used. The rats were acclimatized for two weeks in the laboratory and fed commercially prepared feed; water was given ad lib. Rats for the anthelmintic study were dewormed using albendazole at 200 mgkg-1 two weeks before infection [22].
Toxicity test
Due to dearth of information on the precise dosage of the plant preparation, a maximum tolerated dose experiment described by Lorke [26] was determined using fifteen (15) rats. The established maximum tolerated dose was then used as the basis for the administration of the crude methanolic extract and the various portions of the plant extract in the anthelmintic activity studies.
Experimental infection/design
Forty two worm-free rats were infected subcutaneously in the cervical region with 200 viable L3 stage of N. braziliensis in 0.2 ml of distil water using an 18-gauge needle attached to an insulin syringe [22]. Five days post infection, fresh faecal sample from each infected rat was collected by squeezing it out from the rectum. Faecal samples were examined quantitatively for N. braziliensis egg using the simple floatation method [27]. Rats not shedding ova of N. braziliensis were excluded from the experiment. The infected rats were randomly allocated to three (3) experimental groups (A-C). Group A (positive control group) having six rats, were treated with albendazole at 200 mgkg-1 body weight [22], Group B (experimental group) having twenty four rats; were divided into four sub-groups of six rats each and treated with the crude methanolic, chloroform, N-butanol and aqueous methanol portions of the extract based on the maximum tolerated dose [28]; whereas group C (negative control) having twelve rats; were subdivided into two groups of six rats each and given distil water and propylene glycol as placebo based on the maximum convenient volume (MCV) of 5 mlkg-1 [22].
Treatment with crude methanolic extract and the various portions
Oral treatment with the crude methanolic extract and the various portions of the plant extract was administered on day seven (7) post infection. Before the treatment all rats were weighed to determine the appropriate dose and the maximum convenient volume (MCV) for individual rats. Observation was made daily for two days for abnormal behavioral signs.
Worm counts
Two days post treatment; the treated rats were fasted for 24 hours, salvaged for adult worm count using the WAAVP guides [29]. The first 15 cm of the small intestine was removed, cut longitudinally and placed between two clean 20 cm glass slides. The section was examined at 40X magnification of a dissecting microscope. Visible worms were counted and recorded. The fraction that caused the highest reduction in worm count and does not produce any behavioral changes in the rats was considered to be the most active portion.
Percentage deparasitization
Percentage efficacy (deparasitization) of the crude methanolic extract and the various portions of was calculated according to the method used by Cavier [30].
Statistical analysis
Means of data obtained were analyzed statistically using the software package for GraphPad prism (version 4.0-----2003). Statistical significance for the anthelmintic effect of crude methanol extract, chloroform, butanol portion and aqueous portion was assessed by ANOVA; subsequently Borferroni’s multiple comparison tests. P value <0.05 was considered significant.
Phytochemical screening
The crude methanolic extract of the plant had alkaloids, steroids, saponins, carbohydrate, flavonoids, tannins and cardiac glycosides as constituents; the petroleum ether portion of the plant revealed the presence of only alkaloids and steroids; while the chloroform portion, when screened, showed the presence of alkaloids, steroids, flavonoids, tannins and cardiac glycosides. The screening of the N-butanol portion revealed the presence of carbohydrate, in addition to the constituent seen in the chloroform portion. The screening of the aqueous methanol portion revealed the presence of steroids, flavonoids, tannins, carbohydrate and cardiac glycosides (Table 1).
Toxicity test
At a dose range of 10 to 1000 mgkg-1, the crude methanol did not cause any visible toxic effect on the rats. On the other hand, from 1600 to 5000 mgkg-1, the rats demonstrated varying degrees of signs of toxicity which manifested as visible body weakness, inability to move and reduced appetite from 24 hrs to 7 days post administration. Therefore the doses of 1600 to 5000 mgkg-1 were considered unsafe for the rats; and the dose of 1000 mgkg-1 body weight was chosen as the experimental treatment dose for both the crude methanol extracts and the various portions (Table 2).
The anthelmintic effect of the crude methanolic extract and the various portions
Rats that had oral infection of 200 L3 followed by treatment with crude methanolic extract at 1000 mg/kg-1 had a mean worm count of 4.5; while those infected and treated with chloroform, N-butanol and aqueous methanol portion at 1000 mg/kg-1 and albendazole at 200 mg/ kg-1 had respective mean worm count of 2.5, 3.5, 6.0 and 0; compared to the mean worm count 12.83 and 12.0 from the negative controls (water and p. glycol) treated rats (Figure 1). The crude methanol extract and the respective portion produced percentage deparasitization of 62.50% (crude methanol extract), 79.20% (chloroform), 72.72% (N-butanol) and 71.40% (aqueous methanol). Albendazole-treated rats (positive control), gave a 100% deparasitization, while water and p. glycol (negative controls) gave 0% deparasitization (Table 3). The deparasitization produced by the crude methanol extract and the chloroform, N-butanol and aqueous methanol fractions were significant (p<0.05) when compared to that produced by the placebotreated negative control rats, while the deparasitization produced by the albendazole extract was highly-significant (p<0.001) (Table 3).
Recent harmonizations on anthelmintic efficacy guidelines in ruminants have indicated that for a drug to be considered efficacious, a 90% reduction in total worm count (TWC) should be achieved [28]. However, it was considered ‘a priori’ that the efficacy of the plant extracts would be biologically significant if a reduction in total worm count (TWC) above 70% occurred [31]. Rats treated with chloroform and N-butanol portions of the plant showed anthelmintic activity. The chloroform had the highest reduction in TWC of 79.20%; this was followed by N-butanol portion with reduction in TWC by 72.20%. The crude methanolic extract and aqueous portion did not produce the required biological significant reduction in TWC (62.50% and 53.24% respectively). However, the crude methanolic extract was statistically significant in comparison with the untreated control groups. The results of this study equally demonstrated that the parasite N. braziliensis crude methanolic extract and aqueous portion did not produce the required biological significant reduction in TWC (62.50% and 53.24% respectively). However, the crude methanolic extract was statistically significant in comparison with the untreated control groups. The results of this study equally demonstrated that the parasite was highly sensitive to albendazole with complete deparasitzation (100%) at a dose rate of 200 mg/kg-1 body weight; this is similar to the findings reported by Suleiman et al. [22]. The N-butanol and aqueous portions were soluble in water and other polar solvents like alcohol, suggesting that the constituents of these portions are mainly polar compounds. However, the crude methanol extract and chloroform fractions were only soluble in propylene glycol (a non polar solvent). The outcome of the phytochemical screening revealed that the plant had constituents including tannins, alkaloids, flavovoids, cardiac glycosides and sterols which may have helminthic activities [14,21,32-37]. Tannins have been shown to have anthelmintic activities [32]. However, the anthelmintic effect of plants containing tannins depends on the type and content of tannins in the plant [32,38]. For instance, Kahiya et al. [39] in vitro studies reported that condensed tannins from the leave extract of Acarcia nitotica inhibited the development of H. contortus larvae in goat. In another study, tannins polyphenols from bryophytes were shown to have anthelmintic activity against N. braziliensis [34]. Tannins could binds to the free proteins available in the GIT of the host reducing nutrients available to the parasites resulting into starvation and death [40,41]. Also tannins are capable of binding with the glycoproteins on the cuticle of the parasites leading to their death of the parasite [42]. It is therefore probable to assume that the tannins contained in this plant could have had similar anthelmintic effect with the ones earlier described. Flavonoids are also believed to stimulate intestinal motility similar to that produced by acetylcholine [43], thereby causing rapid worm expulsion from the GIT. Lahlou [36] reported that flavonoid is one of the phytochemicals that have anthelmintic effect. Having identified flavonoids in almost all the portions used in this study, it is possible that it has had a significant anthelmintic effect on the N. braziliensis resulting in the observed deparasitization.The present study has shown that alkaloids are present in all the portions. It is possible that the presence of alkaloids has contributed to the significant deparasitization observed. Previous findings by Al-Qarawi et al. [44] reported that alkaloids extracted from both the latex and leaves of Calotropis procera, was effective in inhibiting the exsheatment of L3 of H. contortus to L4 in sheep, while Lateef et al. [37] also reported that alkaloids and their glycosides extracted from the root of Adhatoda vestica was effective against mixed gastrointestinal infections in sheep. Cardiac glycoside was identified and prominent in all the portions used in this study and therefore may have contributed to the observed anthelmintic effect of the plant. Cardiac glycoside has been shown to induce tonic contraction that resulted in the expulsion of the worms from rat GIT [37,45-47]. The dose determination studies (maximum tolerated dose) [28] was carried out on the premise that the plant extracts under investigation had nmgkg-1) o alternative data to support any intended dosage. In this work, the injurious dose (1600 to 5000 and the MTD (1000 mgkg-1) were determined. However, the plant extracts could not produce death even when the highest dose (5000 mgkg-1) was given; thus suggesting the safety of the extract. The investigation of chemical compounds from natural products is fundamentally important for the development of new anthelmintic drugs, especially in view of the vast worldwide flora. Thus a quality controlled extraction of A. africana and the isolation of their bioactive compounds could be a promising alternative to conventional anthelmintic for the treatment of gastrointestinal helminthes of ruminant in the future. One problem associated with the use of these plants in traditional medicine is lack of consistency of the dose. However, this was overcome by evaluating a maximum tolerated dose in order to reveal an appropriately non-toxic dose that was used in this study.
Result from this study demonstrated that the chloroform and N-butanol (partition portions of CME) of the plant are effective against experimental N. braziliensis infection in rats at a non-toxic dose of 1000 mgkg-1. The chemicals believed to constitute the active principles in A. africana have significant anthelmintic efficacy whereas albendazole was found to be highly efficacious. However, the efficacies of these portions have no statistical significant difference to those of albendazole at a dose rate of 200 mgkg-1. This demonstrates that the rat model was a reliable system for assessing in-vivo anthelmintic efficacy [48]. The result obtained in this study justifies further investigation into anthelmintic effects of the two portions of the plant extract in other animal species. More detailed studies are needed to isolate, characterized and evaluate the active components and the mechanism of action.
The authors thank the University of Abuja, Nigeria for granting the main author a staff development leave. The authors also like to thank all the technical staff of the Department of Veterinary Parasitology and Entomology for their assistance.

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