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SHORT COMMUNICATION
Year : 2011  |  Volume : 73  |  Issue : 3  |  Page : 328-332
Evaluation of the Antibacterial and Antidiarrhoeal activities of Heeria Insignis O. Ktze


1 Department of Pharmacognosy and Drug Development, Ahmadu Bello University, Zaria-810006, Nigeria
2 Department of Pharmaceutical and Medical Chemistry, Niger-Delta University, Yenegoa-560001, Nigeria
3 Department of Pharmacology, Bayero University, Kano-700006, Nigeria
4 Department of Pharmaceutics and Pharmaceutical Microbiology, Ahmadu Bello University, Zaria-810006, Nigeria

Date of Submission10-Apr-2010
Date of Decision17-Jun-2011
Date of Acceptance20-Jun-2011
Date of Web Publication3-Mar-2012

Correspondence Address:
A Agunu
Department of Pharmacognosy and Drug Development, Ahmadu Bello University, Zaria-810006
Nigeria
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DOI: 10.4103/0250-474X.93513

PMID: 22457562

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   Abstract 

Heeria insignis O. Ktze (Anacardiaceae) is an indigenous African shrub used in treatment of diarrhea, venereal diseases, tapeworm, hookworm, schistosomiasis, kidney trouble and for increasing lactation in women after childbirth. The methanol and dichloromethane extracts of the leaves were evaluated for antibacterial activity (using agar-diffusion method) and antidairrheal activity (using isolated rabbit jejunum and castor-oil induced diarrhea in mice). The methanol extract gave higher antibacterial activity than dichloromethane. The order of susceptibility of test microorganisms to methanol extract were Salmonella typhi>Pseudomous aeruginosa> Staphylococcus aureus>Bacillus subtilis>Escherichia coli which were comparable to standard. The minimum inhibitory concentration of the methanol extract for these microorganisms was also determined. The minimum inhibitory concentration (mg/ml) of methanol extract against microorganisms is; B. subtilis (3.9), S. aureus (1.95), E. coli (62.5), Ps. aeruginosa (3.9) and S. typhi (1.95). On the isolated rabbit jejunum evaluation, both extracts produced concentration-dependent relation of isolated rabbit jejunum that was not blocked by phentolamine, suggesting that extracts act via mechanisms other than alpha-adrenergic receptor. In the castor oil-induced diarrheoeal test, each extract gave 80% protection at 200 mg/kg, which is comparable to loperamide 2 mg/kg with 80% protection. This finding may explain the use of the plant in diarrhea and bacterial diseases.


Keywords: Antibacterial, antidairrhoea, dichloromethane extract, Heeria insignis, methanol extract


How to cite this article:
Agunu A, Ahmadu A A, Afolabi S O, Yaro A U, Ehinmidu J O, Mohammed Z. Evaluation of the Antibacterial and Antidiarrhoeal activities of Heeria Insignis O. Ktze. Indian J Pharm Sci 2011;73:328-32

How to cite this URL:
Agunu A, Ahmadu A A, Afolabi S O, Yaro A U, Ehinmidu J O, Mohammed Z. Evaluation of the Antibacterial and Antidiarrhoeal activities of Heeria Insignis O. Ktze. Indian J Pharm Sci [serial online] 2011 [cited 2014 Aug 22];73:328-32. Available from: http://www.ijpsonline.com/text.asp?2011/73/3/328/93513


Diarrhea is a major health worry and sources of malnutrition in developing countries [1] . It is an impaired absorption and hypersecretion syndrome of the gastrointestinal tract [2] . Diarrhea may be brought about by viruses, bacteria, fungi, protozoa, drugs and bacteria endotoxins [3] . In Nigeria, diarrhea remains the major killer disease among children under 5 years, while 7-12 months-old-babies remain the most susceptible [4] . It is estimated that diarrhea causes 4-5 million deaths annually throughout the world. Eighty percent of these deaths are reported in developing countries including Nigeria. To combat the problem of diarrhea in developing countries, the World health organization (WHO) has constituted a diarrhea disease control program aimed at the holistic approach to include all aspects of traditional medical practices, evaluation of health education and preventive approaches [5],[6] .

In this investigation, Heeria insignis O. Ktze (Anacardiaceae) is evaluated for its traditional usage in bacterial and diarrhea infections. It is an indigenous African shrub found extensively in the southern savanna from .Senegal to Niger and Nigeria [7] . This specie has a wide range of healing properties namely: in the treatment of diarrhea and veneral diseases, tapeworm and hookworm, schistosomiasis, kidney diseases and for increasing lactation in women after childbirth [8] . It is known among the Hausas (majority tribe in northern Nigeria) as Kykenleshi daji.

The leaves of Heeria insignis were collected in Zaria, in December, 2006. This was identified by taxonomical means and authenticated at the herbarium unit of the Department of Biological Science, Ahmadu Bello University Zaria, Nigeria where a voucher specimen number 0015 is available for reference. The air-dried and grounded leaves of the plant were successively extracted first with dichloromethane and latter with 70% methanol at room temperature. The filtrate from the maceration was concentrated and evaporated under normal conditions [9] , to give the dichloromethane (yield of 4.6% w/w) and methanol (yield of 7.8% w/w) extract, respectively.

New Zealand rabbits weighing 2.0 kg and Swiss albino mice weighing 18-25 g maintained in the Animal House of the Department of Pharmacology and Clinical Pharmacy, Ahmadu Bello University, Zaria, Nigeria were used for the experiments. The animals were kept in a well-ventilated area, fed with standard feed (feed masters Ilorin, Nigeria) and water ad libitum. This research was carried out in Ahmadu Bello University, Zaria, Nigeria according to the rules governing the use of laboratory animals as acceptable internationally.

A preliminary phytochemical study was carried out on the leaf using standard methods [9],[10] . Antibacterial activity was carried out using agar-diffusion method. MIC was conducted using serial dilution method while antidiairrhoeal property was evaluated using rabbit jejunum and castor oil models.

Antibacterial susceptibility test of standardized log phase cells (10 6 cells/ml) of Bacillus subtilis NCTC 8326 B76, Staphylococcus aureus ATCC 25923,  Escherichia More Details coli ATCC 25722, Pseudomonas aeruginosa ATCC 27853 and  Salmonella More Details typhi (clinical isolate in Zaria, Nigeria) against selected antibacterial agents namely amoxicillin (25 μg), amoxicillin-clavulanic acid (20/10 μg), tetracycline (30 μg), ofloxacin (30 μg), nalidixic acid (30 μg), co-trimoxazole (25 μg), nitrofurantoin (30 μg), and Heeria insignis methanol extract (100 mg/hole) was determined using the official microbiological protocol of agar diffusion method [11],[12] .

Standardized overnight cultures of test bacterial cells was used to seed melted Murller Hinton Agar (MHA) at 45 0 and poured into sterilized plate in triplicates aseptically. These were allowed to solidify. Antibiotic discs were then aseptically placed at reasonable equidistant on the seeded MHA plates and allowed to stand for one hour. For the methanol extract of Heeria insignis, each seeded plate of test bacteria was bored with 6.0 mm diameter sterile cork borer. The base of the hole sealed with 1.0 ml of the plant extract and allowed to stand for one hour, for proper diffusion. These plates were then incubated at 37 0 for 18 h. The diameter of zone of inhibition produced by each antibiotic disc or plant extract was measured (using metric rule) and the result interpreted [13] .

In determining the MIC, graded concentration of the extract were prepared and mixed with melted (45 o ) Mueller Hinton Agar in triplicates using doubling dilution method aseptically. The plates were then inoculated with 0.1 ml of 10 6 cells/ml of log-phase washed cells of test bacteria. Negative and positive controls were also set up. The plates were incubated at 37 o for 18 h. The lowest concentration that showed no visible growth was considered as the MIC of the plant extract against the test bacteria [14] .

A modified method as described by Agunu [15] was used. A 24 h fasted rabbit was scarified by a blow on the head and exsanguinated. Segments of the jejunum (2-3 cm) were removed and dissected free of adhering mesentery. The intestinal contents were removed by flushing with tyrode solution of composition (in mM): NaCl 136.8, KCl 2.7, CaCl 2 1.3, NaHCO 3 12.0, MgCl 2 0.5, NaPO 4 0.14 and glucose 5.5. The tissues were mounted in a 25 ml organ bath containing tyrode solution maintained at 37±1.0 o and aerated with air. An equilibrium period of 60 min was allowed during which physiological solution was changed every 15 min. Effects of acetylcholine (2.0×10 -3 -3.2×10 -8 g/ml), methanol extract (1.6×10 -4 -3.2×10 -3 ), and dichloromethane extract (8.0×10 -6 -1.6×10 -3 ) were investigated non-cumulatively. The contact time for each concentration was 1 min, which was followed by washing the tissue three times. The tissue was allowed to rest for 15 min before the next edition. At 2.0 and 4.0 mg/ml dose of extract, the effect of phentolamine (PTA) on tissue responses was also determined. Responses were recorded isometrically using Ugo Basile microdynamometer 7050 and maintained at sensitivity of 2 and paper speed of 24 mm/min.

The mice were fasted for 12 h prior to the commencement of the experiment and were randomly divided into six groups of five mice each. The mice in the first group received normal saline i.p while mice in the second and third groups received 100 and 200 mg/kg orally of methanol extract while the fourth and fifth groups received 100 and 200 mg/kg orally of dichloromethane extract. The sixth group received loperamide 2 mg/kg orally. After 30 min of administration of the extract, castor oil (0.2 ml/mouse) was given intragastrically. The animals were placed in individual cages over clean filter paper. Three hours after caster oil challenge, the cages were inspected (by an observer unaware of the particular treatment) for the presence of the characteristic diarrhea [16] and the percentage protection calculated [17] . The result was analyzed using chi-square.

Preliminary phytochemical study on the leaves reveals the presence of tannins, flavoniods, saponins, cardiac glycosides and steroids. Alkaloids and anthraquinones are absent. The methanol extract gave higher antibacterial activity than dichloromethane extract. The order of susceptibility of test microorganisms to methanol extract were Salmonella typhi>Pseudomonas aeruginosa>Staphylococcus aureus>Bacillus subtilis>Escherichia coli which were comparable to standard [Table 1]. The methanol extract at 100 mg/hole had greater zone of inhibition compared to standard drugs used except ofloxacin on S. typhi. Similarly, only ofloxacin and nitrofurantion gave higher activity on E. coli compared to the methanol extract.
Table 1: Susceptibility Profile of Test Bacteria Against Antibiotics and Heeria insignis

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The MIC of the methanol extract for the microorganisms were also determined [Table 2]. The MIC (mg/ml) of methanol extract against microorganisms is; B. subtilis (3.9), S. aureus (1.95), E. coli (62.5), Ps. aeruginosa (3.9) and S. typhi (1.95). The extract is particularly very effective against S. aureus and S. typhi both with MIC of 1.95.
Table 2: MIC of Heeria insignis Methanol Extract Against Test Bacteria

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On the isolated rabbit jejunum evaluation, both extracts produced concentration-dependent relaxation of isolated rabbit jejunum up to a point. At doses of 0.5 to 4.0 mg/ml, extracts exhibit increased relaxation of rabbit jejunum. However at 8.0 mg/ml, there was no increase in tissue relaxation compared to 4.0 mg/ml [Table 3]. Similarly activity of both extracts was not blocked by pentolamine, suggesting that extracts act via mechanisms other than alpha-adrenergic receptors.
Table 3: Inhibitory Effects of Plant Extracts Compared to Acetylcholine on Rabbit Jejunum

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In the castor oil-induced diarrhoeal test, the methanol extract gave 60% protection at 100 mg/kg, which increased to 80% at 200 mg/kg. However, dichloromethane gave 80% protection at 100 mg/kg, which did not increase with increase in dosage (200 mg/kg) and is comparable to loperamide (2 mg/kg) with 80% protection [Table 4]. Extracts significantly (P<0.05) protected mice from diarrhea compared to control.
Table 4: Plant Extract Protection Compared to Standard Andcontrol

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Plants have long being in use by man in maintaining health and wellbeing, Worldwide, there is increase in the use of medicinal plants both in developed and developing countries. Heeria insignis is a medical plant used in Nigeria for various purposes including skin diseases and diarrhea. The antibacterial investigation shows that the methanol extract produced significant zone of inhibition against test bacteria in the order Salmonella typhi>Pseudomonas aeruginosa>Staphylococcus aureus>Bacillius subtilis>Escherichia coli [Table 1]. The extract had highest antibacterial activity (zone of inhibition) against Salmonella typhi. At the concentrations used, the methanol leaves extract appears significantly better than standard antibiotics such as amoxicillin, gentamicin, tetracycline, nalidixic acid, co-trimoxazole on E. coli. The MICs (in mg/ml) of methanol extract against microorganisms [Table 2] are; B. subtilis (3.9), S. aureus (1.95), E. coli (62.5), Ps. aeruginosa (3.9) and S. typhi (1.95). The MICs, especially for S. aureus and S. typhi at 1.90 mg/ml, shows the strong antibacterial activity of the plant, as these bacteria are implicated in diarrhoea [3] . On the isolated rabbit jejunum evaluation, both extracts produced concentration-dependent relaxation of isolated rabbit jejunum up to a point. At doses of 0.5 to 4.0 mg/ml, extracts exhibit increased relaxation of rabbit jejunum. However at 8.0 mg/ml, there was no increase in tissue relaxation compared to 4.0 mg/ml. Similarly activity of both extracts was not blocked by pentolamine, suggesting that extracts act via mechanisms other than alpha-adrenergic receptors.

Flavonoids have been found in vitro to be effective antimicrobial substances against a wide array of microorganisms. Their activity is probably due to their ability to complex with extracellular and soluble proteins, and to complex with bacterial cell walls. They can also disrupt microbial membranes [18] . Tannins on the other hand have many human physiological activities such as stimulation of phygocytic cells, host-cell mediated activity, and a wide range of antiinfective actions [19] . Tannins form complex with proteins through so-called nonspecific forces such as hydrogen bonding and hydrophobic effects as well as by covalent bond formation [19],[20] . Saponins acts by complexing with the small amount of sterol in the cell membrane, thus interfering with bacteria cell membrane permeability [18] .

In the pathophysiology of diarrhea and cholera toxin, prostaglandins are implicated. Extracts of plants that contain flavonoids [18] are known to modify the production of cyclooxygenase 1 and 2 and lipooxygenase [19] thereby inhibiting prostaglandins production. Some plants show antidairrhoea properties by their antimicrobial activities [21],[22] or by blocking the eicosanoids (prostaglandins and congeners) [20] . Though, several constituents are present in the leave extract, it's, possible that flavonoids, tannins or steroids are singly or in combination are responsible for the observed effects. The pharmacological effect of loperamide is due to its antimotility and antisecretary properties [23] .

WHO [1] recommends that for diarrhea treatment, oral rehydration salt (ORS) is preferable over antibiotics. However, the traditional treatment of diarrhea is less cumbersome, inexpensive and naturally tolerate by the body system. The observed antibacterial activity coupled with the effects on smooth muscle and castor oil-induced diarrhea may justify the usage of the plant leaves in the treatment of diarrhea.


   Acknowledgements Top


The authors are grateful to Mr. M. D. Musa, the Herbarium keeper at the Department of Biological Science, Ahmadu Bello University Zaria, Nigeria for authenticating the plant sample.

 
   References Top

1.WHO. Diarrhoea disease control programme. WHO export committee, technical report series. Geneva, 27 Switzerland: WHO; 1986. p. 722, 1211.  Back to cited text no. 1
    
2.Alan B. Health Digest. J Am Chem Soc 1982;2930:10-2.  Back to cited text no. 2
    
3.Jawetz E, Melnick JL, Aldelberg EA. Review of Medical microbiology. 16th ed. Los Altos, California: Lange Medical Publication; 1984.  Back to cited text no. 3
    
4.Audu R, Umilabug SA, Renner JK, Awodiji JA. Diarrhoea management. J Niger Infect Control Assoc 2000;3:15.  Back to cited text no. 4
    
5.Syder JH, Merson MH. The magnitude of the global problem of acute diarrhoea disease. A review of acute surveillance data. Bull WHO 1982;60:605.  Back to cited text no. 5
    
6.Abdullahi AI, Agbo MO, Amos S, Gammanial KS, Wembebe C. Antidiarrhoeal activity of the aqueous extract of Terminalia avicennoids root. Phytother Res 2001;15:431-4.  Back to cited text no. 6
    
7.Daziel JM. The useful plants of west tropical Africa. London: Crown agents for overseas government and Administration; 1955. p. 738.  Back to cited text no. 7
    
8.Burkill HM. The useful plants of West Africa, Vol. 1, 2nd ed. Kew: Royal Botanical gardens; 1985.  Back to cited text no. 8
    
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10.Sofowora A. Medicinal plants and Traditional medicine in Africa. In: Standardization of herbal medicine. Lagos, Nigeria: Spectrum Books Ltd; 1993. p. 56-61.  Back to cited text no. 10
    
11.Wolf PL. Practical clinical microbiology and mycology techniques and interpretation. New York: John Wiley and Sons Inc; 1975. p. 186.  Back to cited text no. 11
    
12.Baver AW, Kirby WM, Sherries JC, Turck M. Antibiotic susceptibility testing by a standardized single disc method. Am J Clin Pathol 1966;45:493-6.  Back to cited text no. 12
    
13.NCCLS. Performance standards for antimicrobial disc susceptibility test. Approved standard M2-45 National committee for clinical laboratory standards villanova pan USA, 1993.  Back to cited text no. 13
    
14.Ehinmidu JO, Ibrahim YK. Antibacterial activity of low concentration of antibiotic concentrations against resistant S. typhi isolate in Zaria, Nigeria. Nig J Exp Appl Biol 2004;2:133-9.  Back to cited text no. 14
    
15.Agunu A, Yusuf S, Andrew GO, Zezi AU, Abdurahman EM. Evaluation of five medicinal plants used in treatment of diarrhea in Nigeria. J Ethnopharmacol 2005;101:27-30.  Back to cited text no. 15
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16.Diurno MV, Izzo AA, Mazzoni B, Bologgnese A, Capasso F. Antidiarrhoeal activity of two new thiazolidinones related to loperamide. J Pharm Pharmacol 1996;48:760-2.  Back to cited text no. 16
    
17.Akah PA, Offiah VN. Gastrointestinal effects of Allamanda cathartica leaf extracts. Int J Pharmacogn 1996;30:213-7.  Back to cited text no. 17
    
18.Stern JL, Iiagerman AE, Steinberg PD, Masion PK. Phorotannin-protein interactions. J Chem Ecol 1996;22:1877-99.  Back to cited text no. 18
    
19.Ladeji O, Zebulon SC, Okoye EU. Effects of Vitex doniana stem-bark on blood pressure. Niger J Nat Prod Med 1997;1:19-20.  Back to cited text no. 19
    
20.Christopher S, Williams A, Dubios RN. Prostaglandin endoperoxide synthase. Why two isomer? Am J Physiol 1996;270:G392-400.  Back to cited text no. 20
    
21.Dicarlo G, Autore G, Izzo A. Inhibition of intestinal motility and the secretion by flavonoids in mice and rats: Structural activity relationship. J Pharm Pharmacol 1993;45:1054-9.  Back to cited text no. 21
    
22.Ilyas M, Haruna AK, Ilyas N. Plant constituents with antidiarrhoeal properties. Bull Sci Ass Nig 1995;10:5-12.  Back to cited text no. 22
    
23.Couper IM. Opiod action on intestinal. The importance of intestinal mucosa. Life Sci 1987;41:917-25.  Back to cited text no. 23
    



 
 
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  [Table 1], [Table 2], [Table 3], [Table 4]



 

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