Pentaclethra macrophylla popularly known as African oil bean is a member of the Leguminosae family. A decoction of fermented extract of the plant has been known to be effective in the management of malnutrition, gastrointestinal disorders and dental caries. This study evaluated the antiulcerogenic potentials of aqueous extract of fermented P. macrophylla seeds using acetic acid, aspirin, ethanol, indomethacin and pyloric ligation of ethanol induced ulcer models at the doses of 400 and 800mg/kg body weight. Omeprazole at 5mg/kg was used as a standard reference drug. The result of the acute toxicity test showed that up to 5,000mg/kg body weight of the extract did not cause any mortality of the animals. The different doses of the extract and the reference drug decreased significantly (p<0.05) the ulcer parameters in a dose-dependent manner in all the ulcer models. The degree of ulcer index for the negative control groups is in the order: Indomethacin (11.10±0.10) < Pyloric-ligation (11.57±0.06) < Aspirin (11.60±0.10)
Peptic ulcers, otherwise known as “ulcus pepticum”, are sores or open wounds that occur along the lining of the gastrointestinal tract due to loss of tissues. Although the etiopathology of ulcers is still questionable, Odenbreit 1 and Nartey et al. 2 opined that peptic ulcers are caused by an imbalance between aggressive factors (Helicobacter pylori, stomach acid and pepsin production, non-steroidal anti-inflammatory drugs, ethanol, bile salts, free radicals, chronic alcohol consumption, smoking) and protective factors (mucin secretion, cellular mucus, prostaglandins, bicarbonate secretion, increased mucosal blood flow, cell turn over and impermeability to hydrogen ions), thus leading to an interruption in the mucosal integrity. Several conventional drugs have been employed over the years to arrest this “red devil” called peptic ulcers. Such drugs include H2-blockers (Cimetidine, ranitidine), M1-blockers (porenzepine, telezepine), prostaglandin analogue (misoprostol), proton pump antagonists (omeprazole, lansoprazole), antacids (calcium tetraoxosulphate (iv) [CaSO4], sodium hydrogen trioxocarbonate (iv) [NaHCO3), triple drug therapy (to eradicate Helicobacter pylori). The successes of these drugs are limited by several adverse effects: darkening of the stool and/or tongue, metallic taste in the mouth, hypotension, loss of libido, impotence, relapse of the disease, drug resistance, constipation and nausea 3, 4. These shortcomings have led to the search for more effective therapeutic targets with better protection and decrease in incidence of relapse 5.
Mankind relies upon products from medicinal plants for the management of diseases including ulcers. The wide use of medicinal plants in the management of diseases is due to their bioavailability, higher safety margin, efficacy, quality, affordability 6, 7 and most importantly, the ability to target biochemical pathways. Several plants have been tested in the laboratory for antiulcerogenicity. Included in the pharmacopeia are extracts of the roots and barks of Cassia sieberiana in rats 2 extracts of the roots and leaves of Flabellaria paniculata Cav in rats 8, extracts of the stem of Synclisa scabrida in mice 9, extracts of Cochlospermum planchonii in both male and female wistar rats 10, extracts of Enicosanthelum pulchrum in Sprague Dowley rats 11 and extract of unripe Musa paradisiaca Linn. peel in wistar rats 6. Pentaclethra macrophylla (Benth) is a leguminous plant native to tropical Africa and belongs to the family Leguminosae (sub-family Mimosoideae) in the order Fabales. The trees of P. macrophylla thrive in the Eastern and Southern parts of Nigeria 12. The local names include “Congo acacia” in Congo, “Duala Kombola” in Cameroon and “Ugba”, Ukpkala” in South Eastern part of Nigeria 13. In the traditional setting, the plant is used as salt substitute, charcoal, carvings, seed craft, dye, mild poison, medicine (against convulsion, abortion, diarrhoea, infertility), wound treatment, lactogenicity, ornamental as well as fencing, timber and structural work 14. The participation of probiotics (products of fermentation) in the management of infectious diseases has not been given proper attention over the years. Probiotics are live microorganisms that, when administered in adequate amounts, confer health benefits on the host 15. It is on this backdrop that this present study was developed. Therefore, the study was aimed at investigating the antiulcerogenic potentials of aqueous extract of fermented P. macrophylla (Benth) seeds on different ulcer models (acetic acid, aspirin, ethanol, indomethacin and pyloric ligation-induced) in wistar rats.
Pentaclethra macrophylla seeds were purchased from Eke Okigwe, Okigwe Local Government Area of Imo State, Nigeria. Eke Okigwe lies between latitude 505010.9IIN and 5049155IIN and longitude 7021132.6IIE and 7023117IIE.The plants were identified in the Department of Plant Science and Biotechnology, Abia State University, Uturu.
2.2. Sample PreparationP. macrophylla seeds upon purchased were sorted to remove rotten seeds, dust and extraneous materials and washed with clean water. Exactly 100g of the fermented P. macrophylla (ugba) was weighed using G & G® Electronic Scale into a beaker containing 270ml of distilled water. The beaker was covered with foil and allowed to stand for 15 hours. The extract was filtered using cheese cloth and the membrane filter paper of 47.0mm diameter and the pore size approximately 0.45μm. The filtrate was stored in the refrigerator prior to use.
Lorke 16 method was adopted for the determination of median lethal dose of fermented aqueous extract of P. macrophylla seed. In the pilot study, twelve rats weighing between 150-200g were randomly divided into four groups (A, B, C and D) of three rats each and were administered aqueous extract of fermented P. macrophylla seeds at 500, 1000, 2000 and 5000mg/kg body weight respectively. The animals were then observed for behavioural changes and mortality for 24 hours. The LD50 is usually calculated as the geographic mean of the least lethal dose that killed a rat and the highest dose that did not kill a rat.
2.4. Experimental AnimalsThe albino wistar rats were obtained from University of Nigeria, Nsukka, and were allowed to acclimatize for two (2) weeks in the Animal House of the Department of Biochemistry, Abia State University, Uturu. These animals were fed on grower mash. All the animals used had free access to clean water. They were kept in well ventilated rooms with 12/12 h light/dark condition and ambient room temperature. The experimental procedures used in this study conformed to the United States National Institutes of Health Guidelines for Care and Use of Laboratory Animals in Biomedical Research 17.
2.5. Experimental DesignThe anti-ulcerogenic potentials of fermented aqueous extract of P. macrophylla seed on acetic acid-induced ulcer model in wistar rats was investigated using modified method 18. A total of fifteen wistar rats (150-200g body weight) was starved for 24 hours and grouped into five groups (Group 1 to V) of three rats each based on their body weights. Each administration in the various groups was done according to the specification below:
Group I: Normal Control (n=3) given orally distilled water (0.25ml/kg) body weight.
Group II: Negative control (n=3) given orally acetic acid (0.4ml/kg) body weight
Group III: Reference drug (n=3) given orally omeprazole (5mg/kg) body weight.
Group IV: Plant extract (n=3) given orally plantain extract (400mg/kg) body weight.
Group V: Plant extract (n=3) given orally plantain extract (800mg/kg) body weight.
After 30 minutes of treatment, each animal in Groups II- V received 0.5ml of 80% acetic acid orally. After 1 hour, all the animals were anaesthetized with chloroform and dissected. The stomachs were excised and carefully opened along the line of greater curvature to expose the walls. The stomachs’ contents were then washed off and the stomach walls viewed with the aid of hand lens (x10) to determine the ulcer scores using the method 19. The ulcerative lesions were counted and scored as follows:
The anti-ulcerogenic potentials of fermented aqueous extract of P. macrophylla seeds on aspirin induced ulcer model in wistar rats was investigated using modified method 19. A total of fifteen wistar rats (150-200g body weight) was starved for 24 hours and grouped into five groups (Group 1 to V) of three rats each based on their body weights. Each administration in the various groups was done according to the specification below:
Group I: Normal Control (n=3) given orally distilled water (0.25ml/kg) body weight.
Group II: Negative control (n=3) given orally aspirin (1000mg/kg) body weight.
Group III: Reference drug (n=3) given orally omeprazole (5mg/kg) body weight.
Group IV: Plant extract (n=3) given orally plantain extract (400mg/kg) body weight.
Group V: Plant extract (n=3) given orally plantain extract (800mg/kg) body weight.
After 30 minutes of treatment, each animal in Groups II-V received 1000mg/kg of aspirin orally. After 1 hour, all the animals were anaesthetized with chloroform and dissected. The stomachs were excised and carefully opened along the line of greater curvature to expose the walls. Their stomachs were removed and treated as mentioned and the ulcers scored.
The anti-ulcerogenic potentials of fermented aqueous extract of P. macrophylla seed on ethanol-induced ulcer model in wistar rats was investigated using the method 20. A total of fifteen wistar rats (150-200g body weight) was starved for 24 hours and grouped into five groups (Group 1 to V) of three rats each based on their body weights. Each administration in the various groups was done according to the specification below:
Group I: Normal Control (n=3) given orally distilled water (0.25ml/kg) body weight.
Group II: Negative control (n=3) given orally ethanol (absolute) (1.2ml/kg) body weight
Group III: Reference drug (n=3) given orally omeprazole (5mg/kg) body weight.
Group IV: Plant extract (n=3) given orally plantain extract (400mg/kg) body weight.
Group V: Plant extract (n=3) given orally plantain extract (800mg/kg) body weight.
After 30 minutes of treatment, each animal in Groups II- V received 1.2ml/kg of absolute ethanol orally. After 1 hour, all the animals were anaesthetized with chloroform and dissected. Their stomachs were removed and treated as previously mentioned and the ulcer scores determined.
2.5.4. Indomethacin-induced Ulcer StudyThe anti-ulcerogenic potentials of fermented aqueous extract of P. macrophylla seeds on indomethacin-induced ulcer model in wistar rats was investigated using the method 21. A total of fifteen wistar rats (150-200g body weight) was starved for 24 hours and grouped into five groups (Group 1 to V) of three rats each based on their body weights. Each administration in the various groups was done according to the specification below:
Group I: Normal Control (n=3) given orally distilled water (0.25ml/kg) body weight.
Group II: Negative control (n=3) given orally indomethacin (100mg/kg) body weight
Group III: Reference drug (n=3) given orally omeprazole (5mg/kg) body weight.
Group IV: Plant extract (n=3) given orally plantain extract (400mg/kg) body weight.
Group V: Plant extract (n=3) given orally plantain extract (800mg/kg) body weight.
After 30 minutes of treatment, each animal in Groups II- V received 100mg/kg indomethacin orally. After 1 hour, all the animals were anaesthetized with chloroform and dissected. Their stomachs were removed and treated as previously mentioned and the ulcer scores determined.
The anti-ulcerogenic potentials of fermented aqueous extract of P. macrophylla seeds was studied using the pyloric ligation method 19. A total of fifteen wistar rats (150-200g body weight) was starved for 24 hours and grouped into five groups (Groups I-V) of three rats each based on their body weights. The abdomen was slightly opened under mild chloroform anesthesia, and their pylorous carefully lifted and ligated. The stomachs were quickly replaced and the abdomen sutured. Each administration in the various groups was done according to the specification below:
Group I: Normal Control (n=3) given orally distilled water (0.25ml/kg) body weight.
Group II: Negative control (n=3) given orally ethanol absolute (1.2ml/kg) body weight.
Group III: Reference drug (n=3) given orally omeprazole (5mg/kg) body weight.
Group IV: Plant extract (n=3) given orally plantain extract (400mg/kg) body weight.
Group V: Plant extract (n=3) given orally plantain extract (800mg/kg) body weight.
After 30 minutes of treatment, each animal in Groups II- V received 1.2ml of absolute ethanol orally. After 1 hour, all the animals were anaesthetized with chloroform and dissected. Their stomachs were removed and treated as previously mentioned and the ulcer scores determined.
2.6. Calculation of Ulcer Index and Percentage InhibitionUlcer Index (UI) = Mean of ulcer scores per rats
Percentage Ulcer inhibition:
The percentage ulcer protection was determined using the formula from reference 22.
 |
Results were expressed as mean ± SD (standard deviation). Statistical analysis was performed by One-way analysis of variance (ANOVA) with the Graph Pad Prism® Statistic software package, version 7.01. One-way ANOVA with a Tukey’s multiple comparisons test was used to identify statistical differences among groups. A p-value of <0.05 was considered statistically significant.
The result of acute oral toxicity (LD50) in experimental rats (Table 1) showed that doses of fermented aqueous extract of P. macrophylla seed as high as 5,000mg/kg body weight did not cause any behavioural change or mortality in the animals.
The gastro-protective effect of omeprazole and treatments at different doses of aqueous extract of fermented P. macrophylla seed on acetic acid induced ulcer in wistar rats after one hour is presented in Table 2 below. The result showed that fermented aqueous extract of P. macrophylla seeds prevented ulcerogenesis. Group II (negative control) has the highest ulcer score of 39.17±0.76 while Group V (800mg/kg) has the lowest ulcer score of 37.00 ±0.00. There was significant difference (p<0.05) in ulcer score and ulcer index between the negative control and pretreated groups. The highest percentage inhibition was observed in Group V. The reference drug (omeprazole) offered more percentage gastro-protection of 1.47% when compared with fermented aqueous extract of P. macrophylla seeds at 400 and 800mg/kg body weight, which offered percentage gastro-protective activities of 0.95 and 0.21% respectively.
The gastro-protective effect of omeprazole and treatments at different doses of aqueous extract of fermented P. macrophylla seeds on aspirin induced ulcer in wistar rats after one hour is presented in Table 3 below. The injection of Aspirin (1000mg/kg body weight) to the experimental rats in Groups II to V produced mucosal erosions with ulcer index of 11.60±0.10, 11.35±0.09, 11.50±0.10 and 11.00±0.10 respectively. The result revealed that ulcer indices among the test groups were not statistically significant at p<0.05 level of significance. The mean percentage ulcer inhibition (gastro-protection) obtained for different groups revealed that Group V (800mg/kg) of aqueous extract of fermented P. macrophylla seeds extract offered the highest percentage gastro-protection activity of 5.17% whereas Group III (5mg/kg body weight of omeprazole) offered percentage gastro-protection of 2.14%. The result revealed that the mean percentage gastro-protective activity between the test groups was statistically significant (p<0.05).
The gastro-protective effect of omeprazole and treatments at different doses of fermented aqueous extract of P. macrophylla seeds on ethanol induced ulcer in wistar rats after one hour is presented in Table 4 below. The injection of ethanol (1.2ml/kg body weight) to the experimental rats in Groups II to V produced haemorrhagic streaks and mucosal erosions with ulcer index of 16.30±0.18, 14.50±0.05, 11.62±0.08 and 11.43±0.06 respectively. The result revealed that ulcer indices among the test groups were not statistically significant at p<0.05 level of significance. The mean percentage ulcer inhibition (gastro-protection) obtained for different groups revealed that Group V (800mg/kg) body weight of aqueous extract of fermented P. macrophylla seeds extract offered the highest percentage gastro-protection activity of 29.85% whereas Group III (5mg/kg body weight of omeprazole) offered percentage gastro-protection of 11.04%. The result further revealed that the mean percentage gastro-protective activity between the groups pretreated with omeprazole (5mg/kg) and those with 400 and 800mg/kg body weight of fermented aqueous extract of P. macrophylla seeds was statistically significant (p<0.05).
The gastro-protective effect of omeprazole and treatments at different doses of fermented aqueous extract of P. macrophylla seeds on indomethacin induced ulcer in wistar rats after one hour is presented in Table 5 below. The administration of indomethacin (100mg/kg body weight) to the experimental rats in Groups II to V produced mucosal erosions with ulcer index of 11.10±0.10, 10.87±0.06, 10.67±0.12 and 10.67±0.12 respectively. The result revealed that ulcer indices among the test groups were not statistically significant at p<0.05 level of significance. The result showed that fermented aqueous extract of P. macrophylla seeds produced a dose dependent protection post one hour administration when compared with the reference drug (omeprazole). The mean percentage ulcer inhibition (gastro-protection) obtained for different groups revealed that Group V (800mg/kg) of aqueous extract of fermented P. macrophylla seeds extract offered the highest percentage gastro-protection activity of 3.89% whereas Group III (5mg/kg body weight of omeprazole) offered percentage gastro-protection of 2.09%. This suggests that if the dose of fermented aqueous extract of P. macrophylla seeds is increased above 800mg/kg, it will have a higher antiulcer effect than omeprazole and the gastro-protective activity will be statistically significant at (p< 0.05).
The result of gastro-protective effect of different doses of fermented aqueous extract of P. macrophylla seeds on pylorous ligation of ethanol induced ulcer in wistar rats after one hour is presented in Table 6 below. The results showed that the different doses of fermented aqueous extract of P. macrophylla seeds were effective in protecting the gastro-mucosa and decreasing the severity of the ulcer and the ulcer index when compared to those pretreated with omeprazole. The negative control has the highest ulcer index of 11.57±0.06, because it was not pretreated and the severity of the ulcer increases thereby promoting ulcer formation, which includes, among other, haemorrhagic streak and mucosal erosion. The ulcer indexes for groups pretreated with omeprazole, 400 and 800mg/kg were 11.15±0.00, 10.73±0.06 and 10.57±0.12 respectively. There was no significant difference (p<0.05) in ulcer index between the negative control and the pretreated groups. The mean percentage ulcer inhibition (gastro-protection) obtained for different groups revealed that Group V (800mg/kg) of aqueous extract of fermented P. macrophylla seeds extract offered the highest percentage gastro-protection activity of 8.64% whereas Group III (5mg/kg body weight of omeprazole) offered percentage gastro-protection of 3.60%. The result further revealed that there was a significant increase (p<0.05) in gastro-protective activity between the different doses of the extract and omeprazole group.
Peptic ulcer is caused by distortion of the equilibrium that exists between the aggressive factors such as gastric acid, pepsin, NSAIDs, Helicobacter pyloric, ethanol; and the defensive factors (mucin, mucus, bicarbonate, prostaglandins) which are responsible for the maintenance of the integrity of gastrointestinal membrane 6, 19. Acetic acid, aspirin, ethanol, stress, indomethacin are possible risk factor responsible for the pathogenesis of peptic ulcer 18, 19, 20, 21. Omeprazole is a proton pump inhibitor used to treat peptic ulcer. It is effective in suppressing gastric secretion by blocking enzyme; hydrogen-potassium ATPase responsible for acid secretion 23. The present study was aimed at investigating the antiulcerogenic potentials of aqueous extract of fermented P. macrophylla (Benth) seeds on acetic acid, aspirin, ethanol, indomethacin and pyloric ligation of ethanol induced ulcer models in wistar rats. The result of our studies revealed that the oral administration of acetic acid, aspirin, ethanol and indomethacin led to the manifestation of ulceration, and these were epitomized by severe gastric lesions or erosions and haemorrhagic streaks on the experimental animals. The etio-pathology of peptic ulcers by acetic acid, aspirin, ethanol, indomethacin and pylorous ligation of ethanol could be due to the following reasons: blockage of the enzyme cyclooxygenase 24, which converts arachidonic acid to prostaglandins, expression of histamine, gastrin and acetycholine receptors 23, which are responsible for gastric acid secretion and generation of reactive oxygen species 25, which are implicated in the inflammation of the mucosal cells of the gastrointestinal tract. The result of the acute toxicity study showed no mortality with a higher dose of up to 5,000 mg/kg body weight of fermented aqueous extract of P. macrophylla seeds, indicating that the LD50 of the extracts are above 5,000 mg/kg (Table 1). This result shows that the extract is safe for oral usage and can be characterized as non-toxic 26.
Acetic acid is a weak acid, which is able to induce ulcerogenesis by increasing the stomach acid. The administration of fermented aqueous extract of P. macrophylla seeds prevented ulceration of the wall of gastrointestinal tract. The result showed that the reference drug (omeprazole) offered better gastro-protection when compared to that offered by the different doses of the extract of the plant (Table 2). The findings are in agreement with the works of 27, who evaluated the antiulcerogenic and antiulcer properties of Ocimum sativum (Linn.). Acetylsalicyclic acid (aspirin) is a non-steroidal inflammatory drug (NSAID), which produced ulcer lesions in the glandular part of the rat’s stomach. Aspirin is able to cause ulcerogenesis by direct injuries to the stomach walls 28 and suppression of prostaglandin synthesis 29. In this study, fermented aqueous extract of P. macrophylla seeds at different doses interfered with ulcerogenesis by aspirin (Table 3). This suggests that the extract of the plant might have the capability of activating cyclooxygenase, thus cancelling the effect due to aspirin. This observation is not unconnected with the work of 10, who reported the antiulcerogenic activities of methanol root-bark extract of Cochlospermum planchonii on both male and female wistar rats. Ethanol is highly implicated in the etiopathology of peptic ulcer. The oral administration of ethanol produces severe gastric lesions and haemorrhagic streaks. The first pass metabolism of ethanol in the stomach is responsible for the activation of tumor necrosis factor-alpha (TNF-α), mitogen activated protein kinase (MAPK) and release of reactive oxygen species 25. These cause lipid peroxidation, inflammation of mucosal cells of the stomach, lowering of the concentration of non-protein sulphydryl especially glutathione, lowering of bicarbonate secretion, activation of endothelin-1 30 and finally apoptosis. Ulcerogenesis by ethanol was prevented significantly (p<0.05) by the oral injection of fermented aqueous extract of P. macrophylla seeds (Table 4). This suggests that the fermented aqueous extract of P. macrophylla was able to regain the balance between the aggressive and defensive factors, by scavenging reactive oxygen species. Ngbolua et al. 31 earlier reported that the extract of the plant, P. macrophylla is rich in antioxidants, which are responsible for preventing the generation of reactive oxygen species. The findings of this study is also in line with the work of 20, who reported the antiulcer activity of ethanolic leaf extract of Musa paradisiaca in rats. Indomethacin is also an example of non-steroidal anti-inflammatory drugs which are used to relieve pain, fever, and to manage rheumatoid arthritis 32. The administration of indomethacin resulted in the manifestation of severe gastric lesions (Table 5). There was no significant difference (p<0.05) in the percentage gastro-protective activity between the reference drug and the doses of fermented aqueous extract of P. macrophylla. The mechanism of action of indomethacin and aspirin are quite similar. They cause peptic ulcer by inhibiting the enzyme cyclooxygenase. This blockage will therefore result in the release of endothelin-1 (ET-1), generation of reactive oxygen species (ROS) 33), marked reduction in mucosal blood flow, mucus-bicarbonate secretion, impaired platelet aggregation, reduced epithelial cell renewal and increased leukocyte adherence 32. Pylorous ligation of ethanol induced ulcer model is also another parameter to study the antiulcer activities of conventional and alternative drugs. The increased gastric acid of the stomach due to pylorous ligation interferes with gastric blood circulation, thus inducing ulcerogenesis 34. The administration of the extract of P. macrophylla interferes with the activation of gastric acid secretion (Table 6). The observation is in agreement with the work of 18, who investigated the antiulcer of Qualae grandiflora. The antiulcerogenic potentials could be due to the preponderance of probiotics and phytochemicals resident in fermented aqueous extract of P. macrophylla seeds. Probiotics have been known over the years to enhance gut health 15 and treatment of gastrointestinal infections and diseases 35. Phytochemicals are compounds such as flavonoid, saponins, tannins and flavonoids 6 found in medicinal plants, which confer health benefits on the host. The synergistic roles of phytochemicals and probiotics are responsible for the enhanced cessation of gastric erosions as observed in the present study.
The present study was undertaken to ascertain whether the fermented aqueous extract of P.macrophylla seeds could offer antiulcerogenic activity on acetic acid, aspirin, ethanol, indomethacin and pyloric ligation of ethanol-induced ulcer models in wistar rats. The results showed that the doses of the extract of the plant effectively inhibited ulceration of the wall of the gastrointestinal tract comparable to that of omeprazole. However, the decoction of the plant could be employed in ethnomedicine for the treatment of peptic ulcer.
The authors have not declared any conflict of interests.
The authors would like to thank the Vice Chancellor of Abia State University, Professor E.U. Ikonne and his management team for providing favourable environment to carry out this research.
This work was supported by Tertiary Education Trust Fund Institutional Base Research Grant (TETFUND/ABSU/RP/2016/011) from Abia State University, Uturu, Nigeria.
| [1] | Odenbreit S. Adherence properties of Helicobacter pylori: impact on pathogenesis and adaptation to the host. Inter J Med Microbio, 2005; 295(5): 317-324. | ||
| In article | View Article PubMed | ||
| [2] | Nartey ET, Ofosuhene M, Agbale C. Anti-ulcerogenic activity of the root bark extract of the African laburnum “Cassia sieberiana” and its effects on the antioxidant defense system in rats. BMC Compl Alter Med, 2012; 12(247):1-9. | ||
| In article | View Article | ||
| [3] | Srikanta BM, Siddaraju MN, Dharmesh, SM. A novel phenol-bound pectic polysaccharide from Decalepis hamiltonii with multi-step ulcer preventive activity. World J Gastroenterol, 2007; 13(39): 5196-207. | ||
| In article | View Article PubMed | ||
| [4] | Muralidharan P, Srikanth J. Antiulcer activity of Morinda citrifolia (Linn) fruit extract. J Sci Res, 2009; 1(2):345-352. | ||
| In article | View Article | ||
| [5] | Schhmeda HG, Yesilada E. Traditional medicine and gastroprotective crude drugs. J Ethnopharmacol 2005; 100:61-68. | ||
| In article | View Article PubMed | ||
| [6] | Ezekwesili CN, Ghasi S, Adindu CS, Mefoh NC. Evaluation of the anti-ulcer property of aqueous extract of unripe Musa paradisiaca Linn. Peel in wistar rats.” African J Pharm Pharmacol, (2014); 89(39): 1006-1011. | ||
| In article | View Article | ||
| [7] | Jini J, Sindhu TJ, Girly V, David P, Kumar BD, Bhat AR, Krishakumar K. (2014). Review on in vivo and in vitro studies on the pharmacological activities of Musa species. World J Pharm Pharm Sci, 2014; 3(2): 1133-1142. | ||
| In article | |||
| [8] | Sofidiya MO, Agufobi L, Akindele AJ, Olowe, JA, Familoni OB. Effect of Flabellaria paniculata Cav. extract on gastric ulcer in rats. BMC Compl Alternative Med, 2012; 12(168):1-6. | ||
| In article | View Article | ||
| [9] | Onwudiwe TC, Ughachukwu PO, Unekwe PC, Ogamba JO. Evaluation of anti-ulcer properties of ethanolic and hot aqueous stem extracts of Synclisia scabrida on experimentally induced ulcer models in albino mice. Ann Med Health Sci Res, 2012; 2(2): 134-139. | ||
| In article | View Article PubMed | ||
| [10] | Ezeja MI, Anaga AO (2013). Anti-ulcerogenic activity of the methanol root bark extract of Cochlospermum planchonii (hook f). Afr J Trad Compl Alter Med, 2013; 10(5):394-400. | ||
| In article | View Article | ||
| [11] | Nordin N, Salama SM, Golbabapour S, Hajrezaie M, Hassandarvish P, Kamalidehghan B, Majid NA, Hashim NM, Omar H, Fadaienasab M, Karimian H, Taha H, Ali HM, Abdulla MA. Anti-Ulcerogenic effects of methanolic extracts from Enicosanthelum pulchrum (King) Heusden against ethanol-induced acute gastric lesion in animal models. PLOS ONE, 2014; 9(11): 1-12. | ||
| In article | View Article PubMed | ||
| [12] | Enujiugha VN, Agbede JO. Nutritional and anti-nutritional characteristics of African oil bean seeds (Pentaclethra macrophylla Benth). Appl Trop Agric, 2005; 5: 11-14. | ||
| In article | |||
| [13] | Nwanjo H, Iroagba I, Nnatuanya I, Eze N. Is fermented Pentactethra macrophylla nutritional or antinutritional? Response from hamatological studies in protein malnourished guinea pigs. Internet J Nutr Wellness, 2006; 4(2):1-5. | ||
| In article | |||
| [14] | Asoegwu SN, Ohanyere SO, Kanu OP, Iwueke CN. Physical properties of African oil bean seed (Pentaclethra macrophylla). Agric Eng Inter: the CIGR Ejournal, 2006; 8: 1-16. | ||
| In article | View Article | ||
| [15] | Saarela M, Mogensen G, Fonden R, Matto J, Mattila-Sandholm T. Probiotic bacteria: safety, functional and technological properties. J Biotechnol 2000; 84: 197-215. | ||
| In article | View Article | ||
| [16] | Lorke DA. A new approach to practical acute toxicity testing. Arch Toxicol 1983; 54: 275-287. | ||
| In article | View Article PubMed | ||
| [17] | National Research Council (1985). A guide for the care and use of laboratory animals. A report of the Institute of Laboratory Animal Research Committee on Care and Use of Laboratory Animals. Washington DC: National Academy Press. National Institute of Health Publication No. 85-23; 2000. | ||
| In article | View Article | ||
| [18] | Hiruma-Lima CA, Santos LC, Kushima H, Pellizzon CH, Silveira GG, Vasconcelos PCP, Vilegas W, Souza-Brito ARM. Qualae grandiflora, a Brazilian “Cerrado” medicinal plant presents an important antiulcer activity. J Ethnopharmacol, 2006; 104 (2006): 207-214. | ||
| In article | View Article PubMed | ||
| [19] | Raju D, Ilango K, Chitra V, Ashish K. Evaluation of anti-ulcer activity of methanolic extract of Terminalia chebula fruits in experimental rats. J Pharmacol Sci Res, 2009; 1(3):101-107. | ||
| In article | |||
| [20] | Mbagwu H, Jackson C, Ekpo M, Okopedi E, Anah V, Ugwu C. Gastroprotective effects of ethanolic leaf extract of Musa paradisiaca L. (Musaceae) in rats. J Chem Pharmacol Res, 2011; 3(3): 322-327. | ||
| In article | |||
| [21] | Ubaka MC, Ukwe VC, Okoye CT, Adibe OM. Investigation into the anti-ulcer activity of the aqueous leaf extract of Aspilia africana. Asian J Med Sci, 2010; 2(2):40-43. | ||
| In article | View Article | ||
| [22] | Suziki YM, Hayachi MI, Yamagani T. Antiulcer effect of cetrexate on various experimental gastric ulcers in rats. Japan J Pharmacol, 1976; 26:471. | ||
| In article | |||
| [23] | Pahwa R, Neeta Kumar V, Kohli K. Clinical manifestations, causes and management strategies of peptic ulcer disease. Inter J Pharm Sci Drug Res, 2010; 2(2): 99-106. | ||
| In article | |||
| [24] | Burke A, Smyth E, Fitzgerald GA. Analgesic-antipyretic agents, pharmacotherapy of gout. In: Brunton, LL, Lazo JS, Parker KL. (Eds.), Goodman and Gilman. Pharmacological Bases of Therapeutics. 11th Ed, McGraw Hill Company Incorporation, New York, 2006; pp. 671-715. | ||
| In article | PubMed | ||
| [25] | Bairy KL, Roopa K, Malini S, Reo CM. Protective effect of Tinospora cardifolia on experimentally induced gastric ulcers in rats. J Nat Remedies, 2000; 24:49-53. | ||
| In article | View Article | ||
| [26] | Zbinden G, Flury-Roversi, M. Significance of the LD50-test for the toxicological evaluation of chemical substances. Arch Toxicol, 1981; 47: 77-99. | ||
| In article | View Article PubMed | ||
| [27] | Dharmani P, Kuchibhotla VK, Maurya R, Srivastava S, Sharma S, Palit G. Evaluation of anti-ulcerogenic and ulcer-healing properties of Ocimum santum Linn. J Ethnopharmacol, 2004; 93: 197-206. | ||
| In article | View Article PubMed | ||
| [28] | Susan EA, Mays A. Pharmacology. In: The Merck Veterinary Manual, 9th edition, Merck and Co. Inc. New Jersey, U. S. A. 2006; pp 301-302, 1672-1907. | ||
| In article | |||
| [29] | Wallace JL (2001). Mechanisms of protection and healing: current knowledge and future research. Amer J Med, 2001, 110: 195-225. | ||
| In article | View Article | ||
| [30] | Mahmood AA, Al-Bayaty FH, Salmah I, Nor-Syuhada AB, Harita H, Mughrabi FF. Enhancement of gastric ulcer by areca catechu nut in ethanol induced gastric mucosal injuries in rats. J Med Plant Res, 2011 (5): 2562-2569. | ||
| In article | View Article | ||
| [31] | Ngbolua KN, Bishola TT, Mpiana TP, Mudogo V, Tshibangu SD, Ngombe KN, Tshilanda DD, Baholy R. In vitro antisickling and free radical scavenging activities of Pentaclethra macrophylla Benth (Fabaceae). J Adv Med Life Sci, 2014; 1(2):1-6. | ||
| In article | View Article | ||
| [32] | Kumar S, Kaur A, Singh R, Sharma R. Peptic ulcer: a review on etiology and pathogenesis. Inter Res J Pharmacy, 2012; 3(6):34-38. | ||
| In article | |||
| [33] | Valkhoff VE, Sturkenboom MC, Kurpers EJ. Risk factors for gastrointestinal bleeding associated with low-dose aspirin. Best Prac Res Clinical Gastroenterol, 2012; 26:125-140. | ||
| In article | View Article PubMed | ||
| [34] | Brodie DA. Effects of various secretagogues on ulceration. Am J Digest Dis, 1996; 11:231-241. | ||
| In article | View Article | ||
| [35] | Haukioja, A. (2010). Probiotics and oral health. Euro J Den, 4: 348-355. | ||
| In article | PubMed PubMed | ||
Published with license by Science and Education Publishing, Copyright © 2017 Ugbogu A.E., Arunsi U.O., Uche-Ikonne O. O, Ude V.C and Okezie E
This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit
https://creativecommons.org/licenses/by/4.0/
| [1] | Odenbreit S. Adherence properties of Helicobacter pylori: impact on pathogenesis and adaptation to the host. Inter J Med Microbio, 2005; 295(5): 317-324. | ||
| In article | View Article PubMed | ||
| [2] | Nartey ET, Ofosuhene M, Agbale C. Anti-ulcerogenic activity of the root bark extract of the African laburnum “Cassia sieberiana” and its effects on the antioxidant defense system in rats. BMC Compl Alter Med, 2012; 12(247):1-9. | ||
| In article | View Article | ||
| [3] | Srikanta BM, Siddaraju MN, Dharmesh, SM. A novel phenol-bound pectic polysaccharide from Decalepis hamiltonii with multi-step ulcer preventive activity. World J Gastroenterol, 2007; 13(39): 5196-207. | ||
| In article | View Article PubMed | ||
| [4] | Muralidharan P, Srikanth J. Antiulcer activity of Morinda citrifolia (Linn) fruit extract. J Sci Res, 2009; 1(2):345-352. | ||
| In article | View Article | ||
| [5] | Schhmeda HG, Yesilada E. Traditional medicine and gastroprotective crude drugs. J Ethnopharmacol 2005; 100:61-68. | ||
| In article | View Article PubMed | ||
| [6] | Ezekwesili CN, Ghasi S, Adindu CS, Mefoh NC. Evaluation of the anti-ulcer property of aqueous extract of unripe Musa paradisiaca Linn. Peel in wistar rats.” African J Pharm Pharmacol, (2014); 89(39): 1006-1011. | ||
| In article | View Article | ||
| [7] | Jini J, Sindhu TJ, Girly V, David P, Kumar BD, Bhat AR, Krishakumar K. (2014). Review on in vivo and in vitro studies on the pharmacological activities of Musa species. World J Pharm Pharm Sci, 2014; 3(2): 1133-1142. | ||
| In article | |||
| [8] | Sofidiya MO, Agufobi L, Akindele AJ, Olowe, JA, Familoni OB. Effect of Flabellaria paniculata Cav. extract on gastric ulcer in rats. BMC Compl Alternative Med, 2012; 12(168):1-6. | ||
| In article | View Article | ||
| [9] | Onwudiwe TC, Ughachukwu PO, Unekwe PC, Ogamba JO. Evaluation of anti-ulcer properties of ethanolic and hot aqueous stem extracts of Synclisia scabrida on experimentally induced ulcer models in albino mice. Ann Med Health Sci Res, 2012; 2(2): 134-139. | ||
| In article | View Article PubMed | ||
| [10] | Ezeja MI, Anaga AO (2013). Anti-ulcerogenic activity of the methanol root bark extract of Cochlospermum planchonii (hook f). Afr J Trad Compl Alter Med, 2013; 10(5):394-400. | ||
| In article | View Article | ||
| [11] | Nordin N, Salama SM, Golbabapour S, Hajrezaie M, Hassandarvish P, Kamalidehghan B, Majid NA, Hashim NM, Omar H, Fadaienasab M, Karimian H, Taha H, Ali HM, Abdulla MA. Anti-Ulcerogenic effects of methanolic extracts from Enicosanthelum pulchrum (King) Heusden against ethanol-induced acute gastric lesion in animal models. PLOS ONE, 2014; 9(11): 1-12. | ||
| In article | View Article PubMed | ||
| [12] | Enujiugha VN, Agbede JO. Nutritional and anti-nutritional characteristics of African oil bean seeds (Pentaclethra macrophylla Benth). Appl Trop Agric, 2005; 5: 11-14. | ||
| In article | |||
| [13] | Nwanjo H, Iroagba I, Nnatuanya I, Eze N. Is fermented Pentactethra macrophylla nutritional or antinutritional? Response from hamatological studies in protein malnourished guinea pigs. Internet J Nutr Wellness, 2006; 4(2):1-5. | ||
| In article | |||
| [14] | Asoegwu SN, Ohanyere SO, Kanu OP, Iwueke CN. Physical properties of African oil bean seed (Pentaclethra macrophylla). Agric Eng Inter: the CIGR Ejournal, 2006; 8: 1-16. | ||
| In article | View Article | ||
| [15] | Saarela M, Mogensen G, Fonden R, Matto J, Mattila-Sandholm T. Probiotic bacteria: safety, functional and technological properties. J Biotechnol 2000; 84: 197-215. | ||
| In article | View Article | ||
| [16] | Lorke DA. A new approach to practical acute toxicity testing. Arch Toxicol 1983; 54: 275-287. | ||
| In article | View Article PubMed | ||
| [17] | National Research Council (1985). A guide for the care and use of laboratory animals. A report of the Institute of Laboratory Animal Research Committee on Care and Use of Laboratory Animals. Washington DC: National Academy Press. National Institute of Health Publication No. 85-23; 2000. | ||
| In article | View Article | ||
| [18] | Hiruma-Lima CA, Santos LC, Kushima H, Pellizzon CH, Silveira GG, Vasconcelos PCP, Vilegas W, Souza-Brito ARM. Qualae grandiflora, a Brazilian “Cerrado” medicinal plant presents an important antiulcer activity. J Ethnopharmacol, 2006; 104 (2006): 207-214. | ||
| In article | View Article PubMed | ||
| [19] | Raju D, Ilango K, Chitra V, Ashish K. Evaluation of anti-ulcer activity of methanolic extract of Terminalia chebula fruits in experimental rats. J Pharmacol Sci Res, 2009; 1(3):101-107. | ||
| In article | |||
| [20] | Mbagwu H, Jackson C, Ekpo M, Okopedi E, Anah V, Ugwu C. Gastroprotective effects of ethanolic leaf extract of Musa paradisiaca L. (Musaceae) in rats. J Chem Pharmacol Res, 2011; 3(3): 322-327. | ||
| In article | |||
| [21] | Ubaka MC, Ukwe VC, Okoye CT, Adibe OM. Investigation into the anti-ulcer activity of the aqueous leaf extract of Aspilia africana. Asian J Med Sci, 2010; 2(2):40-43. | ||
| In article | View Article | ||
| [22] | Suziki YM, Hayachi MI, Yamagani T. Antiulcer effect of cetrexate on various experimental gastric ulcers in rats. Japan J Pharmacol, 1976; 26:471. | ||
| In article | |||
| [23] | Pahwa R, Neeta Kumar V, Kohli K. Clinical manifestations, causes and management strategies of peptic ulcer disease. Inter J Pharm Sci Drug Res, 2010; 2(2): 99-106. | ||
| In article | |||
| [24] | Burke A, Smyth E, Fitzgerald GA. Analgesic-antipyretic agents, pharmacotherapy of gout. In: Brunton, LL, Lazo JS, Parker KL. (Eds.), Goodman and Gilman. Pharmacological Bases of Therapeutics. 11th Ed, McGraw Hill Company Incorporation, New York, 2006; pp. 671-715. | ||
| In article | PubMed | ||
| [25] | Bairy KL, Roopa K, Malini S, Reo CM. Protective effect of Tinospora cardifolia on experimentally induced gastric ulcers in rats. J Nat Remedies, 2000; 24:49-53. | ||
| In article | View Article | ||
| [26] | Zbinden G, Flury-Roversi, M. Significance of the LD50-test for the toxicological evaluation of chemical substances. Arch Toxicol, 1981; 47: 77-99. | ||
| In article | View Article PubMed | ||
| [27] | Dharmani P, Kuchibhotla VK, Maurya R, Srivastava S, Sharma S, Palit G. Evaluation of anti-ulcerogenic and ulcer-healing properties of Ocimum santum Linn. J Ethnopharmacol, 2004; 93: 197-206. | ||
| In article | View Article PubMed | ||
| [28] | Susan EA, Mays A. Pharmacology. In: The Merck Veterinary Manual, 9th edition, Merck and Co. Inc. New Jersey, U. S. A. 2006; pp 301-302, 1672-1907. | ||
| In article | |||
| [29] | Wallace JL (2001). Mechanisms of protection and healing: current knowledge and future research. Amer J Med, 2001, 110: 195-225. | ||
| In article | View Article | ||
| [30] | Mahmood AA, Al-Bayaty FH, Salmah I, Nor-Syuhada AB, Harita H, Mughrabi FF. Enhancement of gastric ulcer by areca catechu nut in ethanol induced gastric mucosal injuries in rats. J Med Plant Res, 2011 (5): 2562-2569. | ||
| In article | View Article | ||
| [31] | Ngbolua KN, Bishola TT, Mpiana TP, Mudogo V, Tshibangu SD, Ngombe KN, Tshilanda DD, Baholy R. In vitro antisickling and free radical scavenging activities of Pentaclethra macrophylla Benth (Fabaceae). J Adv Med Life Sci, 2014; 1(2):1-6. | ||
| In article | View Article | ||
| [32] | Kumar S, Kaur A, Singh R, Sharma R. Peptic ulcer: a review on etiology and pathogenesis. Inter Res J Pharmacy, 2012; 3(6):34-38. | ||
| In article | |||
| [33] | Valkhoff VE, Sturkenboom MC, Kurpers EJ. Risk factors for gastrointestinal bleeding associated with low-dose aspirin. Best Prac Res Clinical Gastroenterol, 2012; 26:125-140. | ||
| In article | View Article PubMed | ||
| [34] | Brodie DA. Effects of various secretagogues on ulceration. Am J Digest Dis, 1996; 11:231-241. | ||
| In article | View Article | ||
| [35] | Haukioja, A. (2010). Probiotics and oral health. Euro J Den, 4: 348-355. | ||
| In article | PubMed PubMed | ||
 value of fermented aqueous extract of unripe P. macrophylla seeds){kind=link}
