Terminalia avicennioides is a plant widely used in the Central African Republic for the treatment of numerous pathologies with anti-inflammatory components. The main objective of this study was to identify the chemical constituents and evaluate the antioxidant and antibacterial activities of Terminalia avicennioides root bark extracts. The phytochemical study showed that the methanolic extract was the best extraction solvent with a yield of 21.78%. Qualitative analysis revealed the presence of flavonoids, tannins, saponins, sterols and triterpenes. Quantitative analysis showed that the methanolic extract had a high total phenolic content, i.e. 2149 ± 1391,10 mg EqAG/g Ms. Evaluation of the free radical scavenging capacity of methanolic extracts of Terminala. avicennioides using the DPPH method gave a moderate IC50 value with an R2 = 0,75. The antimicrobial activity against Staphylococcus aureus and Escherichia coli was studied using the diffusion method. The zone of inhibition, inhibitory concentration and minimum bactericidal concentration of the extracts on the organisms were evaluated. The methanolic extract inhibited the growth of E. coli and S. aureus with MICs between 0,45-4,00 µg/mL and MBCs between 4,50-22,2 µg/mL. The root bark of T. avicennioides showed significant antibacterial activity due to its high content of polyphenolic compounds.
According to the World Health Organization, approximately 81% of the population relies on traditional herbal preparations for primary health care 1.
Currently, more than 120 plant compounds are used in modern medicine, and almost 75% of these are used according to their traditional use 2. From the 25 best-selling pharmaceutical compounds in the world, 12 are derived from natural products 3, demonstrating that the number of drugs derived from combinatorial chemistry, where more than 10,000 molecules must be synthesized and then tested, has led to the development of one drug.
Compounds derived from natural substances have the advantage of having a very large diversity of chemical structures and a very wide range of biological activities 4.
Antibiotic resistance among pathogenic microorganisms has become an increasingly important public health problem worldwide. Plant-derived antimicrobial compounds are capable of inhibiting bacterial growth by acting on cellular targets different from those targeted by currently used antibiotics such as penicillins, macrolides or tetracyclines. They could also be of significant clinical value in the treatment of infections with resistant microbial strains 5. With antibacterial treatments, we are seeing more and more strains that are resistant to common antibiotics 6.
In Africa, medicinal plants generally play a very important role in therapy due to their relatively low cost and availability. For this reason, the World Health Organization encourages the inclusion of controlled and effective medicinal plants in primary health care in developing countries 7.
In Central African Republic, recent political crises have destroyed the entire health system. In remote areas, poor people are forced to use medicinal plants for primary treatment, not to mention the fact that these medicinal plants have secondary metabolites that have not yet been evaluated.
One such plant is Terminalia avicennioides, a savannah plant known by different ethnic groups in Central Africa under different popular names. Why Terminalia avicennioides?
Terminalia. avicennoiides has been selected for its uses in traditional medicine both in Africa and in Asia for the treatment of microbial infection. Terminalia avicennioides is indicated in the treatment of certain diseases such as gastrointestinal disorders, urinary tract infections, ulcers moebic dysentery, hemorrhoids, cavities and malaria 8. Many of the species from combretaceae family are reputed to contain antimicrobial constituents 9 in the treatment of a range of conditions, including syphilis, wounds gastric ulcer 10
Pharmacological sutides have shown that the stem barks of Terminalia avicennioides are used in traditional medicine in Nigeria in the treatment of painful menstruation, menorrhagia, trypanosomiasis, diarrhea, tuberculosis, cough, wounds especially for a better healing of skin infections, dental caries 11, 12.
The frequent use of this species in the treatment of these various pathologies in the Central African Republic has shown interesting antioxidant, antibacterial and even antifungal activities. Terminalia avicennioides has shown remarkable antioxidant activity and significant antibacterial activity against certain bacteria and micro-organisms. The aim of this study is to evaluate the antioxidant and antibacterial activities of the methanolic extract of Terminalia avicennioides on microbial strains.
Origin of the plant: The study was carried out on the root bark of Terminalia avicennioides, collected in September 2023 in the village of Yassara, about 15 km north of Bangui (Central African Republic) (figure 1).
Roots were harvested at 8 am on 18 September 2024 in the village of Yassara, 15 km from Bangui in the Begoua region, and taken to the laboratory the following day. One week later, the stem bark was removed from the root and dried in a dark, dry place for 24 days before being ground into a powder and stored in a jar in the laboratory for extraction.
To evaluate the antibacterial activity of the plant studied, two important pathogenic bacterial species were selected for the study, namely Staphylococus aureus and Escherichia coli. These bacterial strains were isolated at the National Laboratory of Clinical Biology and Public Health (LNBCSP) in Bangui (Central African Republic).
2.4. Chemical CharacterizationThe cold maceration method was used to extract the plant under study. 100 g of Terminalia avicennioides powder was extracted successively with four solvents of increasing polarity (dichloromethane, acetone, cyclohexane and methanol). 400 mL of cyclohexane was added to the plant powder and stirred for 4 hours at room temperature. After filtration, the extract was evaporated with a Rotavapor at 25°C and the residue was taken up with the next solvent.
The presence of major chemical groups in the extracts was investigated using the tests described by 13, 14: flavonoids (cyanidine reaction), alkaloids (Dragendorff and Mayer test), triterpenes and sterols (Libermann-Burchard test), saponosides (foam index), tannins (ferric chloride test and Stiasny reaction).
2.5. Quantitative AnalysisTotal polyphenols were determined using the method described by 15, 16 with slight modifications.
A solution of gallic acid (So solution) with a concentration of 2,3 mg/mL was prepared and diluted 20 times in water. This solution was used to prepare a series of gallic acid solutions at different concentrations. We then prepared a 3 mg/mL solution of each extract in DMSO.
We added 20 mL of the extract solution to the cells of a 96-well microplate and then added 100 mL of Folin-Ciocalteu reagent. For the extract blank, Folin was replaced by water. The mixture was shaken for 30 seconds and then incubated in the dark for 5 minutes, to which 80 mL of Na2CO3 solution (75 g/l) was added, shaken again for 30 seconds and then incubated for 15 minutes. The absorbance was read at a wavelength of 620nm. Three tests were performed for each product concentration tested.
Total flavonoid content was determined according to the method described by 15, 16 with some modifications.
Briefly, 100 mL of the extracts at 3 mg/mL were added to 96-well microplates, followed by 100 mL of AlCl3 solution prepared at 0,02 g in 50 mL methanol. The blank was prepared by replacing the AlCl3 solution with MeOH. For the control blank, DMSO was used instead of the extracts. The mixture was vortexed for 30 seconds and incubated for 15 minutes. Absorbance was measured at a wavelength of 415 nm against the blank. Quercetin was used as a reference standard to establish the calibration curve and to quantify the total flavonoid content, expressed as milligrams of quercetin equivalent per gram of extract (mg Eq Quer/g extract). Assays were performed in triplicate for each sample.
The condensed tannin content was determined according to the method described by 15, 16
A 1% vanillin solution was prepared in H2SO4 (7M). 50 mL of the extracts (3 mg/mL) were added to 96-well microplates. 150 mL vanillin solution was then added. The mixture was vortexed for 30 seconds and incubated for 15 minutes at room temperature. The absorbance was measured at a wavelength of 500 nm. Tests were performed in triplicate for each sample. A stock solution of catechin was used as a reference standard to establish the calibration curve and to quantify the condensed tannin content, expressed as milligrams of catechin equivalent per gram of dry matter (mg Cat Eq/g dry matter).
The determination of anthocyanins was carried out according to the method described by 15 with a slight modification.
Two solutions were prepared. A solution at pH = 1 containing KCl (0,2M) and HCl (0,2M). The mixture of CH3COOH, CH3COONa with concentrations (0,2M) and water (H2O). For anthocyanin quantification, 100 μL of extract is added to 100 mL of pH = 1 solution in four wells, then the other four wells contain the mixture of 100 µL of extract + 100 µL of pH = 4,5 solution. The absorbance of the extract is measured at 450 and 620 nm after incubation for 15 minutes at room temperature. The change in absorbance is calculated using the following expression:
The total anthocyanins in the samples are expressed as milligram equivalents of cyanidin-3-glucoside per gram of dry matter (mg Eq C3GE/g Ms).
2.6. Biological ActivityThis method is based on the use of a free radical: DPPH, as described by 15, 17 with a slight modification. The reduction of DPPH is accompanied by a change in the colour of the solution from purple to yellow, which can be measured spectrophotometrically at 750 nm. This indicates antioxidant activity. The intensity of the colour change, measured with a spectrophotometer, is inversely proportional to the antioxidant activity of the extracts whose activity is being determined.
For our extract, we prepared a solution of DPPH at 0.35 mg/ml in methanol. This solution was diluted 10 times and stored in a refrigerator at 4°C, protected from light. Four dilutions were prepared from the stock solution of each extract (MeOH, acetone, dichloromethane and cyclohexane) at different concentrations (60, 150, 240 and 300 mg/L).
A pasteurized pipette was used to add 20 µL of each extract and 180 µL of DPPH to each microplate well. The blank was 20 µL DMSO and 180 µL MeOH. Readings were taken at 750 nm after 25 minutes incubation in the dark. Ascorbic acid was used as a standard, prepared under the same conditions as the extracts. All extracts were reproduced at least 4 times to minimize error. The results were expressed as percentage inhibition (%I).
Microorganisms were provided by the National Laboratory of Clinical Biology and Public Health. Two strains of bacteria were isolated and provided for the test.
For the evaluation of antibacterial activity, the methanolic extract of Terminalia avicennioides was used.
The microdilution method was used to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC).
We prepared a series of antibiotics of decreasing concentration by successive dilutions (0,5; 0,1 and 0,01 mg/mL) from a solution of 0,5 mg/mL of antibiotic. We prepared a series with the same volume of liquid culture, and then the same amount of bacteria was added to each tube (inoculum). The prepared tubes were incubated at 37ºC for 24 hours and examined. The MIC is determined from the cloudiness of the tubes: a cloudy medium means that the culture has grown and the concentration is not high enough to block bacterial growth. Conversely, a clear medium indicates that the culture has not grown.
A slightly modified serial micro-dilution test 18, 19 was used to determine the value of the minimum inhibitory concentration of the methanolic extract of Terùinalia avicennioides.
Final test concentration ranges of 0,5; 0,1 and 0,01 mg/mL were used from an aqueous solution of Terùinalia avicennioides from a 0,5 mg/mL solution of the antibiotic. Each tube was covered and incubated at 37°C for 24 hours. Clear staining of the well was interpreted as absence of growth and wells with a turbid appearance were considered positive due to bacterial growth. Each experiment was replicated twice.
The minimum bactericidal concentration is the concentration of antibiotic required to achieve 0.01% viable bacteria after 24 hours incubation at 37°C 20. It was determined according to the method of 18.
It can be determined using a broth dilution minimum inhibitory concentration (MIC) test by subculturing bacteria that do not contain the antibacterial agent being tested. The susceptibility of the bacterial strains was assessed on the basis of macroscopic and microscopic aspects. The concentration of the tube containing less than 0.01% viable bacteria with respect to the initial inoculum constitutes the MBC 21. The results are interpreted using the ratio (MBC/MIC).
The yields of the cyclohexane extract and the different fractions are shown in Figure 3, which shows that the yield of the cyclohexane extract of Terminalia avicennioides root bark was 0,22%. The yields of the fractions varied from 1,17% for the dichloromethane fraction, 7,.42% for the acetone fraction and 21,78% for the methanol fraction. The best yield was obtained with the methanol fraction, with a value of 21,78%.
The yield obtained with the methanol fraction, with a value of 21.78%, indicates the greater presence of moderately polar secondary metabolites in the methanol extract of the root bark of Terùinalia vicennioides. Our yields are significantly lower than those obtained by 22, with a value of 0,8% for the cyclohexane extract and 2,10% for the dichloromethane extract, and higher than those obtained by 23.
The qualitative analysis by tube reactions carried out on extracts of the root bark of Terminalia. avicennioides is presented in Table 1.
The results of the chemical screening showed the presence of secondary metabolites: flavonoids, tannins, saponosides, triterpenes and sterols. Alkaloids and anthocyanins were not found in the plant organ studied.
Phytochemical analysis of the extract showed that it was rich in flavonoids, tannins, saponins, triterpenes and sterols. The results obtained are identical to those obtained by 24 on the same species. The presence of flavonoids, tannins and saponosides would demonstrate the potential of the extract for antibacterial activities 25.
The contents of total polyphenols, total flavonoids, condensed tannins and anthocyanins in Terminalia avicennioides extracts were determined separately by colorimetric methods (Folin-Ciocalteu, aluminium chloride, sulphuric vanillin and the change in anthocyanin colour as a function of pH (differential pH method)). The quantitative analyses of total phenolics, total flavonoids, condensed tannins and anthocyanins were determined from the linear regression equations of the calibration curves, expressed as mg gallic acid equivalent, mg quercetin equivalent, mg catechin equivalent and mg cyanidin-3-glucoside equivalent per gram of dry matter, respectively.
The results of the quantitative analyses are given in Table 2.
The results of quantitative analyses by UV-visible spectrophotometry of the various Terminalia avicennioides root bark extracts studied are shown in Table 2 above.
We note that the methanolic extract of the root bark of this species is quantitatively richer in phenolic compounds with a content of 2149,90 ± 13 mg Eq AG/g Ms, followed by the acetone extract with a content of 1980,4 ± 145,6 mg Eq AG/g Ms. The dichloromethane and cyclohexane extracts have low contents ranging from 830,20 ± 119,8 to 100,7 ± 0,90 mg Eq AG/g Ms. Flavonoids were present but at very low levels in the different extracts. Anthocyanins were also present in the dichloromethane and cyclohexane extracts. We found that this plant has high levels of total polyphenols compared to flavonoids in the different extracts.
These results confirm the high level of phenolic substances present in Terminalia. avicennioides, as shown by the tube reactions.
3.3. DPPH radical Reduction Test on a 96-Well MicroplateThe four (04) Terminalia avicennioides extracts studied showed high inhibition percentages in the root bark (Table 3).
The results of the antioxidant activity of the four extracts carried out on 96-well microplates gave inhibition percentages of around 90,76 ± 02,81, 92,94 ± 00,42, 82,44 ± 00,53, 52,70 ± 05,66 for the methanol, acetone, dichloromethane and cyclohexane extracts respectively. Polar extracts had a higher inhibition percentage than apolar extracts. However, the four (04) extracts studied had a relatively high free radical scavenging capacity compared to the reference molecule, ascorbic acid, which had an inhibition percentage of 94,43 ± 00,42.
These results show that all the extracts have a better antioxidant activity, which is consistent with the total polyphenol content, which is high in the polar extracts and moderately low in the apolar extracts (Table 2). Our results are close to those obtained by 25
3.4. Correlation between Total Phenolics and Antioxidant Activity (DPPH)The results obtained show a good linear correlation (R2 = 0.75) between the total phenolic content and the antiradical power of Terminalia avicennioides extracts (Figure 4).
Looking at the results in Figure 4 above, a positive correlation was observed due to the fact that plants richer in phenolic compounds have the highest oxidative activity. These results are in line with what has been stated in the literature by some authors that the antioxidant activity potential of an extract depends on its phenolic compound content 26, 27. It is clear that the high antioxidant activity recorded in our different extracts (Table 2) is due to their richness in phenolic compounds.
3.5. Evaluation of Antibacterial ActivityThe results of the in vitro antibacterial activity of the methanolic extracts of Terminalia avicennioides with the different concentrations on the bacterial strains, viz: Staphylococus aureus and Escherichia coli are presented in Table 4 below.
This table shows the macroscopic and microscopic aspects of Terminalia. avicennioides methanolic extract in liquid medium at different concentrations on S. aureus and E. coli strains.
In view of the results obtained (Table 4), the antibacterial activity was carried out up to a concentration of 0,25 mg/mL on S. aureus and 0,05 mg/mL on E. coli. The disturbances observed in the tubes between 0,05 mg/mL and 0,005 mg/mL for S. aureus and then at 0,005 mg/mL for E. coli explain the resistance of the bacteria at these concentrations.
The MIC is the lowest concentration of the substance at which no growth is visible to the naked eye after 24 hours incubation. It is determined by the absence of cloudiness in the tube. On the other hand, the minimum bactericidal concentration (MBC) is the lowest concentration of a substance that leaves no more than 0.01% of germs behind.
The results giving MIC and BMC values in mg/ml and the ratio of BMC to MIC for the methanolic extract of Terminalia. avicennioides are given in Table 5 below.
In view of the results in Table 5, we note that the methanolic extract of Terminalia avicennioides root bark inhibits the growth of S. aureus and E. coli with a minimum inhibitory concentration of 0,25 mg/L for S. aureus and 0,05 mg/L for E. coli respectively.
These results suggest that this plant could be a potential source of compounds with significant antibacterial activity. The antibacterial activity in the methanolic extract would therefore be linked to a synergistic effect between the different phytochemical groups present, such as tannins, flavonoids, saponins, triterpenes and sterols, all of which have antibacterial activity according to the literature 28, 29.
This antibacterial activity is due to its high tannin and flavonoid content according to 19. Similarly, 30 found a MIC between 0,06 and 0,512 mg/mL, while 31 found an MIC between 0,1 and 10 mg/mL in the methanolic extract of different organs of the same species (leaves, stems and roots) against Pseudomonas aeruginosa, Salmonella typhi, Bacillus subtilis and Escherichia coli. These differences have been explained by the parts of the plant used, the germs of the bacteria tested and the solvents used for the extractions.
The ratio of MBC to MIC has made it possible to specify the mode of action of the substance 32. According to 33, the extract is bactericidal if its MBC is equal to its MIC or if the ratio of MBC to MIC is less than or equal to 4. It is bacteriostatic if its MBC is greater than or equal to its MIC or if the ratio of MBC to MIC is greater than 4.
With regard to the MBC to MIC activity ratio, S. aureus gives a value of 5, which is more than 4 times the MIC 19, so S. aureus is considered to be an antibacterial agent. The MBC to MIC ratio for Escherichia coli gives a value of 10, which is more than 4 times the MIC, so E. coli is considered to be a bactericidal agent. This result shows and confirms that the plant Terminalia avicennioides is highly active in the treatment of digestive disorders, abdominal pain and diarrhea. The effect of the methanolic extract on S. aureus is also confirmed by the work carried out by 34 with ethanol and acetone extracts on the same strains.
The evaluation of antibacterial activity of Terminali avicennioides on the strains responsible of dysentery disorder is realized from the methanolic extract. The results show that the extract is confirmed by the results obtained by 30 that shows that the methanolic extract of Terminalia avicennioides inhibited the Growth of diverse bacteria. The methanolic extract is then more active and concentrate better antibacterial components. The fact that the methanolic extract is more active shows that the bioactive molecules solubilize better in methanol and concentrate better the active components. The antibacterial activity of the Terminalia avicennioides would be attributed to secondary metabolites such polyphenols and flavonoids 35 which would justify the significant activity of the metabolic extract.
This study identified several major chemical families in the root bark of Terminalia avicennioides. Phenolic assays showed that the different extracts of Terminalia avicennioides were rich in total phenolics. DPPH methods on 96-well microplates revealed the antioxidant activity of the different extracts of this plant. The results showed a good linear correlation between total phenolic content and antioxidant activity. The methanolic extract of Terminalia avicennioides also showed antibacterial activity against S. aureus and E. coli. Terminalia avicennioides could be used in the treatment of infectious diseases of bacterial origin. Supplementary in vivo studies could be envisaged to confirm the antibacterial activity, as well as acute toxicity tests using the methanolic extract of Terminalia. avicennioides, and the highlighted compounds could be isolated and identified.
The authors would like to think the National Laboratory of Clinical Biology and Public Health (LNBCSP) in Bangui (Central African Republic) for isolating and providing the bacterial strains.
The authors declare that they have no competing interests.
| [1] | World Health Organisation, 2000. A report of the consultation meeting on traditional and modern medicine: Harmonizing two approaches, Beijing, China: 22-26. | ||
| In article | |||
| [2] | Cordell G.A., Colvard M.D., 2005. Some thoughts on the futures of ethnopharmacology, Journal of Ethnopharmacology 100: 5-14. | ||
| In article | View Article PubMed | ||
| [3] | Gordon M., Cragg G.M., Newman D.J., Snader K.M., 1997. Natural products in drug discovery and development, Journal of Natural Products 60, pp 52-60. | ||
| In article | View Article PubMed | ||
| [4] | Rollinger J.M., Haupt S., Stuppner H., Langer T.J., 2004. Combining ethnopharmacology and virtual screening for lead structure discovery: COX-inhibitors as application example, Journal of Chemical Information and Computer Sciences 44: pp480-488. | ||
| In article | View Article PubMed | ||
| [5] | Eloff J.N., 1998. Which extractant should be used for the screening and isolation of antimicrobial components from plants? Journal of Ethnopharmacology 60, pp1-8. | ||
| In article | View Article PubMed | ||
| [6] | Cohen M.L., 2000. Changing patterns of infectious disease, Nature 17, pp762-767. | ||
| In article | View Article PubMed | ||
| [7] | Amos S., Kolawole E., Akah P., Wambele C., Gamaniel K., 2001. Behavioral effects of the aqueous extract of Guiera senegalensis in mice and rats. International Journal of Phytotherapy and Phytopharmacology, 8, pp 356-361. | ||
| In article | |||
| [8] | Mapi P. (1988). Contribution à l’étude ethnobotanique et analyses chimiques de quelques plantes utilisées en médecine traditionnelle dans la région de Nkongsamba (Mongo. (Thèse de Doctorat 3ème cycle). Université de Yaoundé, Cameroun, 236 P). | ||
| In article | |||
| [9] | Baba-Moussa F, Akpagana K, Bouchet P (1999). Antifungal activities of seven West African Combretaceae used in traditional medicine. J. Ethnopharmacol., 66: 335-338. | ||
| In article | View Article PubMed | ||
| [10] | Arbonier, M., 2005. Arbres, Arbustes et lianes des Zones Seches d’Afrique de l’Ouest. 1st Edn., CIRAD, National Museum of Natural History, France, pages: 541. | ||
| In article | |||
| [11] | Mann. A, K. Ibrahim, A. O. Oyewale, J. O. Amupitan, M. O. Fatope, J. I. Okogun. (2012). “Isolation and Elucidation of Three Triterpenoids and Its Antimycobacterial Activty of Terminalia aviccinniodes”. Am. J. Org. Chem. 2, 14-20. | ||
| In article | View Article | ||
| [12] | Mann. A, O.S. Ajiboso, Ajeigbe, S., Gbate, M., Isaiah, S, “Evaluation of the wound healing activity of ethanol extract of Terminalia aviccinniodes root bark on two wound models in rats”. Int. J. Med. Aromat. Plants, 95-100, 2011. | ||
| In article | |||
| [13] | Onuminya T.O., Shodiya O.E., Olubiyi O.O. (2017). Comparative proximate and phytochemical analysis of leafy vegetables in Lagos, Nigeria. NJPAS 30 (3): 3097–3103. | ||
| In article | |||
| [14] | Worowounga Xavier., 2016. Identification des molécules bioactives dans les plantes médicinales de la république centrafricaine. Thèse de doctorat université de Bangui (RCA). | ||
| In article | |||
| [15] | Namkona Armel Frédéric, Bolevane Ouantinam Serge Florent, Moustapha Fatia, Worowounga Xavier, Ngaissona Paul, Koane Jean Noël, Syssa-Magalé Jean-Laurent., 2017. Biological activities and phytochemical analysis of extracts Afrostyrax lepidophyllus Mildbr. | ||
| In article | View Article | ||
| [16] | Worowounga X., Rahmani, R., Namkona A.F., Cazaux S., Syssa-magalé J.L., Matondo H., And Bouajila J., 2022. Metabolites Profiling of Manilkara mabokeensis Aubrev Bark and Investigation of Biological Activities”. International Journal of Analytical Chemistry. | ||
| In article | View Article PubMed | ||
| [17] | Kouamé T., Siaka S., Kassi A.B., Soro Y., 2021. Determination of total polyphenols, total flavonoids and tannins in young unopened leaves of Piliostigma thonningii (Caesalpiniaceae). International Journal of Biological Chemical Sciences; 15 (1): 97-10. | ||
| In article | View Article | ||
| [18] | Rahul R., Arrivukkarasan S., Anhuradha S., 2022. In Vitro Antioxidant and Free Radical Scavenging Activity of Curcuma longa, Acorus calamus and Camellia sinensis. Food and Nutrition Sciences, 13: 750-760. | ||
| In article | View Article | ||
| [19] | Yimta F., Ramond R.S., Francois N., Guy N.S., Jean de Di T., 2014. Antibacterial Activity of Methanol Extracts and Hydroethanolic and Aqueous Extracts of Terminalia Avicennoides and Sarcocephalus latifolius. Pharmacologia 33: pp199-204. | ||
| In article | View Article | ||
| [20] | Masoko P., Eloff J.N., 2005. The diversity of antifungal compounds of six South African Terminalia species (Combretaceae) determined by bio-autography. African Journal of Biotechnology 4, 1425–1431. | ||
| In article | |||
| [21] | Moroh J.L.A., Bahi C., Dje K., Loukou Y.G. Guede-Guina F., 2008. Etude de l’activité antibactérienne de l’extrait acétatique (EAC) de Morinda morindoides (Baker) milne red heat (rubiaceae) sur la croissance in vitro des souches d’Escherichia coli. B. Soc. Royale des Sc. de Liège, Liège (Belgique), 77 (4) 44 -61. | ||
| In article | |||
| [22] | Marmonier A.A., 1990. Introduction aux techniques d’étude des antibiotiques. In Bactériologie Médicale, techniques usuelles, 227-236. | ||
| In article | |||
| [23] | Mathurin Issa-Madongo, Xavier Worowounga, Paul Ngaïssona, Armel Frédéric Namkona, Eugene Gbayonnon, Olivia Semboli, Fatia Moustapha, Jean-Laurent Syssa-Magalé., 2022. Qualitative, Quantitative Phytochemical Screening and Antioxidant Study of Root Bark Extracts of Terminalia aviccinniodes from Central African Republic. Research in Plant Sciences, 2022, Vol. 10, (1), 7-11. | ||
| In article | View Article | ||
| [24] | Musa, F.M., Ameh, J.B., Ado, S.A. and Olonitola, O.S., 2016. Evaluation of phytochemical and antibacterial properties of Terminalia aviccinniodes crude extract against selected bacteria from diarrhoeic patients”. Bayero Journal of Pure and Applied Sciences, 9(1): 129–137. | ||
| In article | View Article | ||
| [25] | Ndel Famen L.C., Talom. T.B., Tagne R.S., Kamsu T.G., Kodjio N., Lacmata T.S., Gatsing D., 2020. Journal international de recherché en microbiologie. 30(1) pp 1-14, 2020. | ||
| In article | View Article | ||
| [26] | Amri O., Elguiche R., Tahrouch S., Zekhnini A., Hatimi A., 2015. Antifungal and antioxidant activities of some aromatic and medicinal plants from the southwest of Morocco. Journal of Chemical and Pharmaceutical Research 7(7): 672-678. | ||
| In article | |||
| [27] | Guettaf S., Abidli N., Kariche S., Bellebcir L. et Bouriche H., 2016. Phytochemical screening and antioxidant activity of aqueous extract of Genista Saharae (Coss. & Dur). Der Pharmacia Lettre 8 (1):50-60. | ||
| In article | |||
| [28] | Sonogo Y., Guessennd N.K., Trabi H.F., Kouandio N.J., Konan F.K, Bamba M, Danho N., Bakayako A., Yao K., Dosso M., 2016. Evaluation in vitro de l’activité des écorces de tige de Anogeissus leiocarpus (DC) Guill. Et Perr. (Combretaceae) sur des bactéries responsables de maladies courantes en Afriques et criblage phytochimique. | ||
| In article | View Article | ||
| [29] | Kouadio N’guessan J., Kone M.W., Guessennd NK, Konan K.F., Moussa B., Yao K, Allagba-Atsain M.R., Tra-Bi F.H., Bakayoko A., Dosso M., 2017. Evaluation de l’activité antibactérienne des feuilles de Spondias mombin L. (Anacardiaceae) sur la croissance in-vitro de souches d’entérobactéries productrices de bêta-lactamases à spectre élargi (EBLSE) et tri phytochimique. International Journal of Innovation and Applied Studies, 20(2): 431-440. | ||
| In article | |||
| [30] | Famen LCN, Talom TB, Tagne RC, Kamsu GT, Kodjo N, et al. (2020). In vitro Antioxidant Actvities annd Effect of Hydroethanolic and Aqueous Extracts of Terminalia avicenniodes (Combretaceae) on Salmonella. MR JI 30: 1-14. | ||
| In article | View Article | ||
| [31] | Mann A., Adamu Ku Y., 2014. Antibacterial activity of methanolic extracts of Terminalia avicennioides against fish pathogenic Bacteria 2: 1 pp33-46. | ||
| In article | View Article | ||
| [32] | Fauchere l-L, Avril J-L., 2002. Bactériologie Générale et Médicale. Editions Ellipses: paris | ||
| In article | |||
| [33] | Kamanzi Atindehou, K., Koné, M., Terreaux, C., Traore, D., Hostettmann, K. and Dosso, M., (2002) Evaluation of the Antimicrobial Potential of Medicinal Plants from the Ivory Coast. Phytotherapy Research, 16, 497-502. | ||
| In article | View Article PubMed | ||
| [34] | Akpomie O.O., Olorungbon S., 2011. Antimicrobial screening of Terminalia avicennoides and Acalypha wilkesiana. African Journal of Biotechnology Vol. 10 (2), pp 180-182. | ||
| In article | |||
| [35] | ZAREEN S., (2006), Phytochemical studies on Terminalia glaucescens, Pteleopsis hylodendron and related medicinal plants, PhD thesis, H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences, University of Karachi, Karachi-75270, Pakistan, 204 p. | ||
| In article | |||
Published with license by Science and Education Publishing, Copyright © 2025 Issa-Madongo Mathurin, Ngaïssona Paul., Worowounga Xavier, Namkona Frederic Armel, Ouefio Mboïssio Angelique, Saravolia Marinette, Gbayonnon Eugene, Koane Jean Noel and Syssa-Magalé Jean Laurent
This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit
http://creativecommons.org/licenses/by/4.0/
| [1] | World Health Organisation, 2000. A report of the consultation meeting on traditional and modern medicine: Harmonizing two approaches, Beijing, China: 22-26. | ||
| In article | |||
| [2] | Cordell G.A., Colvard M.D., 2005. Some thoughts on the futures of ethnopharmacology, Journal of Ethnopharmacology 100: 5-14. | ||
| In article | View Article PubMed | ||
| [3] | Gordon M., Cragg G.M., Newman D.J., Snader K.M., 1997. Natural products in drug discovery and development, Journal of Natural Products 60, pp 52-60. | ||
| In article | View Article PubMed | ||
| [4] | Rollinger J.M., Haupt S., Stuppner H., Langer T.J., 2004. Combining ethnopharmacology and virtual screening for lead structure discovery: COX-inhibitors as application example, Journal of Chemical Information and Computer Sciences 44: pp480-488. | ||
| In article | View Article PubMed | ||
| [5] | Eloff J.N., 1998. Which extractant should be used for the screening and isolation of antimicrobial components from plants? Journal of Ethnopharmacology 60, pp1-8. | ||
| In article | View Article PubMed | ||
| [6] | Cohen M.L., 2000. Changing patterns of infectious disease, Nature 17, pp762-767. | ||
| In article | View Article PubMed | ||
| [7] | Amos S., Kolawole E., Akah P., Wambele C., Gamaniel K., 2001. Behavioral effects of the aqueous extract of Guiera senegalensis in mice and rats. International Journal of Phytotherapy and Phytopharmacology, 8, pp 356-361. | ||
| In article | |||
| [8] | Mapi P. (1988). Contribution à l’étude ethnobotanique et analyses chimiques de quelques plantes utilisées en médecine traditionnelle dans la région de Nkongsamba (Mongo. (Thèse de Doctorat 3ème cycle). Université de Yaoundé, Cameroun, 236 P). | ||
| In article | |||
| [9] | Baba-Moussa F, Akpagana K, Bouchet P (1999). Antifungal activities of seven West African Combretaceae used in traditional medicine. J. Ethnopharmacol., 66: 335-338. | ||
| In article | View Article PubMed | ||
| [10] | Arbonier, M., 2005. Arbres, Arbustes et lianes des Zones Seches d’Afrique de l’Ouest. 1st Edn., CIRAD, National Museum of Natural History, France, pages: 541. | ||
| In article | |||
| [11] | Mann. A, K. Ibrahim, A. O. Oyewale, J. O. Amupitan, M. O. Fatope, J. I. Okogun. (2012). “Isolation and Elucidation of Three Triterpenoids and Its Antimycobacterial Activty of Terminalia aviccinniodes”. Am. J. Org. Chem. 2, 14-20. | ||
| In article | View Article | ||
| [12] | Mann. A, O.S. Ajiboso, Ajeigbe, S., Gbate, M., Isaiah, S, “Evaluation of the wound healing activity of ethanol extract of Terminalia aviccinniodes root bark on two wound models in rats”. Int. J. Med. Aromat. Plants, 95-100, 2011. | ||
| In article | |||
| [13] | Onuminya T.O., Shodiya O.E., Olubiyi O.O. (2017). Comparative proximate and phytochemical analysis of leafy vegetables in Lagos, Nigeria. NJPAS 30 (3): 3097–3103. | ||
| In article | |||
| [14] | Worowounga Xavier., 2016. Identification des molécules bioactives dans les plantes médicinales de la république centrafricaine. Thèse de doctorat université de Bangui (RCA). | ||
| In article | |||
| [15] | Namkona Armel Frédéric, Bolevane Ouantinam Serge Florent, Moustapha Fatia, Worowounga Xavier, Ngaissona Paul, Koane Jean Noël, Syssa-Magalé Jean-Laurent., 2017. Biological activities and phytochemical analysis of extracts Afrostyrax lepidophyllus Mildbr. | ||
| In article | View Article | ||
| [16] | Worowounga X., Rahmani, R., Namkona A.F., Cazaux S., Syssa-magalé J.L., Matondo H., And Bouajila J., 2022. Metabolites Profiling of Manilkara mabokeensis Aubrev Bark and Investigation of Biological Activities”. International Journal of Analytical Chemistry. | ||
| In article | View Article PubMed | ||
| [17] | Kouamé T., Siaka S., Kassi A.B., Soro Y., 2021. Determination of total polyphenols, total flavonoids and tannins in young unopened leaves of Piliostigma thonningii (Caesalpiniaceae). International Journal of Biological Chemical Sciences; 15 (1): 97-10. | ||
| In article | View Article | ||
| [18] | Rahul R., Arrivukkarasan S., Anhuradha S., 2022. In Vitro Antioxidant and Free Radical Scavenging Activity of Curcuma longa, Acorus calamus and Camellia sinensis. Food and Nutrition Sciences, 13: 750-760. | ||
| In article | View Article | ||
| [19] | Yimta F., Ramond R.S., Francois N., Guy N.S., Jean de Di T., 2014. Antibacterial Activity of Methanol Extracts and Hydroethanolic and Aqueous Extracts of Terminalia Avicennoides and Sarcocephalus latifolius. Pharmacologia 33: pp199-204. | ||
| In article | View Article | ||
| [20] | Masoko P., Eloff J.N., 2005. The diversity of antifungal compounds of six South African Terminalia species (Combretaceae) determined by bio-autography. African Journal of Biotechnology 4, 1425–1431. | ||
| In article | |||
| [21] | Moroh J.L.A., Bahi C., Dje K., Loukou Y.G. Guede-Guina F., 2008. Etude de l’activité antibactérienne de l’extrait acétatique (EAC) de Morinda morindoides (Baker) milne red heat (rubiaceae) sur la croissance in vitro des souches d’Escherichia coli. B. Soc. Royale des Sc. de Liège, Liège (Belgique), 77 (4) 44 -61. | ||
| In article | |||
| [22] | Marmonier A.A., 1990. Introduction aux techniques d’étude des antibiotiques. In Bactériologie Médicale, techniques usuelles, 227-236. | ||
| In article | |||
| [23] | Mathurin Issa-Madongo, Xavier Worowounga, Paul Ngaïssona, Armel Frédéric Namkona, Eugene Gbayonnon, Olivia Semboli, Fatia Moustapha, Jean-Laurent Syssa-Magalé., 2022. Qualitative, Quantitative Phytochemical Screening and Antioxidant Study of Root Bark Extracts of Terminalia aviccinniodes from Central African Republic. Research in Plant Sciences, 2022, Vol. 10, (1), 7-11. | ||
| In article | View Article | ||
| [24] | Musa, F.M., Ameh, J.B., Ado, S.A. and Olonitola, O.S., 2016. Evaluation of phytochemical and antibacterial properties of Terminalia aviccinniodes crude extract against selected bacteria from diarrhoeic patients”. Bayero Journal of Pure and Applied Sciences, 9(1): 129–137. | ||
| In article | View Article | ||
| [25] | Ndel Famen L.C., Talom. T.B., Tagne R.S., Kamsu T.G., Kodjio N., Lacmata T.S., Gatsing D., 2020. Journal international de recherché en microbiologie. 30(1) pp 1-14, 2020. | ||
| In article | View Article | ||
| [26] | Amri O., Elguiche R., Tahrouch S., Zekhnini A., Hatimi A., 2015. Antifungal and antioxidant activities of some aromatic and medicinal plants from the southwest of Morocco. Journal of Chemical and Pharmaceutical Research 7(7): 672-678. | ||
| In article | |||
| [27] | Guettaf S., Abidli N., Kariche S., Bellebcir L. et Bouriche H., 2016. Phytochemical screening and antioxidant activity of aqueous extract of Genista Saharae (Coss. & Dur). Der Pharmacia Lettre 8 (1):50-60. | ||
| In article | |||
| [28] | Sonogo Y., Guessennd N.K., Trabi H.F., Kouandio N.J., Konan F.K, Bamba M, Danho N., Bakayako A., Yao K., Dosso M., 2016. Evaluation in vitro de l’activité des écorces de tige de Anogeissus leiocarpus (DC) Guill. Et Perr. (Combretaceae) sur des bactéries responsables de maladies courantes en Afriques et criblage phytochimique. | ||
| In article | View Article | ||
| [29] | Kouadio N’guessan J., Kone M.W., Guessennd NK, Konan K.F., Moussa B., Yao K, Allagba-Atsain M.R., Tra-Bi F.H., Bakayoko A., Dosso M., 2017. Evaluation de l’activité antibactérienne des feuilles de Spondias mombin L. (Anacardiaceae) sur la croissance in-vitro de souches d’entérobactéries productrices de bêta-lactamases à spectre élargi (EBLSE) et tri phytochimique. International Journal of Innovation and Applied Studies, 20(2): 431-440. | ||
| In article | |||
| [30] | Famen LCN, Talom TB, Tagne RC, Kamsu GT, Kodjo N, et al. (2020). In vitro Antioxidant Actvities annd Effect of Hydroethanolic and Aqueous Extracts of Terminalia avicenniodes (Combretaceae) on Salmonella. MR JI 30: 1-14. | ||
| In article | View Article | ||
| [31] | Mann A., Adamu Ku Y., 2014. Antibacterial activity of methanolic extracts of Terminalia avicennioides against fish pathogenic Bacteria 2: 1 pp33-46. | ||
| In article | View Article | ||
| [32] | Fauchere l-L, Avril J-L., 2002. Bactériologie Générale et Médicale. Editions Ellipses: paris | ||
| In article | |||
| [33] | Kamanzi Atindehou, K., Koné, M., Terreaux, C., Traore, D., Hostettmann, K. and Dosso, M., (2002) Evaluation of the Antimicrobial Potential of Medicinal Plants from the Ivory Coast. Phytotherapy Research, 16, 497-502. | ||
| In article | View Article PubMed | ||
| [34] | Akpomie O.O., Olorungbon S., 2011. Antimicrobial screening of Terminalia avicennoides and Acalypha wilkesiana. African Journal of Biotechnology Vol. 10 (2), pp 180-182. | ||
| In article | |||
| [35] | ZAREEN S., (2006), Phytochemical studies on Terminalia glaucescens, Pteleopsis hylodendron and related medicinal plants, PhD thesis, H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences, University of Karachi, Karachi-75270, Pakistan, 204 p. | ||
| In article | |||
