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Communication

Antifungal Activity of Euclea divinorum Root and Study of its Ethnobotany and Phytopharmacology

by
Mohamed Al-Fatimi
Department of Pharmacognosy, Faculty of Pharmacy, Aden University, P.O. Box 5411 (Maalla), Aden, Yemen
Processes 2019, 7(10), 680; https://doi.org/10.3390/pr7100680
Submission received: 9 August 2019 / Revised: 25 September 2019 / Accepted: 25 September 2019 / Published: 1 October 2019
(This article belongs to the Special Issue Green Separation and Extraction Processes)
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Abstract

:
The ethnobotanical survey of Euclea divinorum Hiern (Ebenaceae) was conducted on Soqotra Island, Yemen. The root bark is used to treat mouth, dental, dermal and blood diseases in the traditional medicine of the island. The study is the first report about the effect of the plant root barks against six human pathogenic fungi. The non-polar dichloromethane extract of Euclea divinorum root bark showed stronger antifungal activities compared to polar direct and sequential methanolic extracts. These extracts showed significant broad antifungal activity against Absidia corymbifera, Aspergillus fumigatus, Candida krusei, Microsporum gypseum, Mucor sp. and Trichophyton mentagrophytes compared to the standard antibiotic drug nystatin. Thin-layer chromatography (TLC) revealed the presence of the naphthoquinones in the extracts. The results showed an extraction process to separate most antifungal naphthoquinones from the root bark by using non-polar solvent dichloromethane, while flavonoids remained in the polar methanolic extracts; therefore, the polar sequential and direct methanolic extracts recorded higher antioxidant activity than the non-polar extracts with less toxicity. The biological and chemical results identified the presence of antifungal and antioxidant constituents in the root bark and confirm its traditional use in Soqotra Island as crude powder to treat dental and dermal diseases and to clean teeth. Moreover, our results are compared with literature review on ethnobotany and phytopharmacology of E. divinorum to present a medicinal monograph about the plant.

1. Introduction

Fungal infections of the mouth and skin are common diseases in tropical developing countries, including Yemen. Medicinal plants are a potential and natural source for treatment of fungal infections. For treatment of these tropical fungal diseases, many traditional plant species have been reported in different traditional medicine systems in the world, such as Dracaena cinnabari [1], Piper guineense [2]. Toothbrush and/or chewing pieces (miswak) are the most frequently traditional modes prepared from the plant parts and used for teeth and mouth problems. These used parts can be classified into: (a) plant toothbrush with colouring properties such as such as Euclea divinorum [3], Euclea natalensis [4] and Diospyros lyciodes [5]; (b) plant toothbrush without colouring agents such as Salvadora persica [6].
Euclea divinorum Hiern (Ebenaceae) is a famous plant in the ethnomedicine of Soqotra Island, the root bark is used mostly as a toothbrush or as powder for cleaning of the teeth by rubbing on the teeth and chewing or rubbing to dye the lips and mouth red. Similar traditional uses of Euclea divinorum root were found in the ethnobotany of Namibia and Kenya [5,7,8]. However, in the ethnomedicine systems of some African countries, the roots of different Euclea species were reported in use as medicines, such as Euclea undulata roots that are used to relieve toothache in Botswana [9], and E. natalensis to clean teeth in Zanzibar [10], while Euclea pseudebenus roots are used to clean teeth on the southwest coast of Africa [11]. In addition, in other tropical African countries the most traditional uses of E. divinorum were reported for internal applications [8]. The root decoction of E. divinorum is used in ethnomedicine in Zambia to treat different genital and oral diseases in the case of HIV/AIDS-related diseases [12] and the root bark to treat diarrhoea, cancer and dermal ailments in Zimbabwe [13]. In Kenya, the decoction or infusion of E. divinorum root are used to induce or augment labor [14]. Fruits are chewed to treat abdominal upsets, skin, kidney and respiratory disorders [15]. In Ethiopia, urine retention is treated by root decoction of E. divinorum [16] while the leaves are used to treat malaria, leprosy, gonorrhea, syphilis and tapeworm [17].
Preliminary phytochemical investigations identified previously secondary bioactive metabolites in different parts of E. divinorum. Methanol and aqueous extracts of the E. divinorum root have been reported to contain polyphenols, saponins, tannins, flavonoids, steroids, terpenoids, glycosides and alkaloids [5,16]. Polyphenols and glycosides have been identified in the methanol extracts of leaves, stems and fruits [5,17]. Some triterpenoids including lupeol, botulin and lupene [13,18] and naphthoquinones including methyljuglone, mamegakinone, diospyrin and isodiospyrin [13,18,19] have been previously identified and isolated as main constituents of the non-polar chloroform extract of the E. divinorum root [13,18,19]. In contrast, the leaves, stems and fruits contain no naphthoquinones [13,19]. However, from the ethyl acetate extract of the plant leaf, two naphthalene derivatives, Eucleanal A and B, were isolated [8]. From the methanol extract of the aerial parts, some flavonoids including myricitrin, quercetin and kaempferol were isolated [20].
The cytotoxic, antibacterial, oxytocic, and diuretic activity of the root of E. divinorum have been demonstrated [3,5,14,16] (Table 1). Moreover, different biological and pharmacological investigations of the other parts of E. divinorum including leaves, fruits and barks of the plant were previously studied and reported, which are presented in Table 1.
This is the first report about the antifungal activity of E. divinorum root bark against six human pathogenic fungal strains to validate the ethnomedicinal uses of the plant on Soqotra Island, Yemen.

2. Materials and Methods

2.1. Ethnobotanical Survey

The ethnobotanical survey of E. divinorum was conducted in one city (Hadibou) and in nine villages on Soqotra Island (Reyged, Qalansieh, Haggeher, Noged, Mori, Qubah, Qadheb, Dihamidh and Shuub) during February–March 1990. Fifty indigenous peoples were interviewed (male 45; female 5) in the Arabic language. 80% of the informants were above 35 years old. Ten informants were in primary schools between 12–16 years. All interviewees were local people and spoke Soqotri and Arabic language. Informants asked to identify the Soqotri local name of the plant tree in the nature and the specimen (root) collected during the survey.

2.2. Plant Material

The plant parts samples of Euclea divinorum (Ebenaceae) were collected from Reyged, Soqotra Island, Yemen, in February 1990 for taxonomic identification. The plant species was identified by the Pharmacognosy Department, Aden University, Yemen and at the personal Herbarium of the author.

2.3. Extraction

Roots of E. divinorum were collected for the extraction in March 2006. The dried root barks were powdered in a grinder.
  • Direct extract: 2 g powdered root barks were extracted direct with 100 ml methanol (DM)
  • Sequential extracts: a sequential extraction way was demonstrated to produce different subextracts from the dried root bark; 30 g powdered root bark was extracted with different solvents of increasing polarity, 300 mL for each: dichloromethane, ethyl acetate and methanol successively at room temperature for 8 hours.
The crude and sequential extracts (direct methanolic extract (DM), sequential dichloromethane extract (SD), sequential ethyl acetate extract (SE), sequential methanolic extract (SM) were concentrated under reduced pressure at 40 °C. They were dried by lyophilization-freezing and stored in exsiccator (Figure 1).

2.4. Antifungal Test—Agar Diffusion Test

The antifungal activities of the direct and sequential extracts of E. divinorum (2 mg dried extract per disc) were identified using the agar diffusion assay [6,26]. Inhibition zone diameters include diameter of the disc (6 mm). The tested human pathogenic fungi strains: Absidia corymbifera (100798), Aspergillus fumigatus (13550/99), Candida krusei (ATCC 90878), Microsporum gypseum, Mucor spp. and Trichophyton mentagrophytes (05/2004). Nystatin was used as positive control (100 µg/disc).

2.5. Determination of Antioxidant Activity

1,1-Diphenyl-2-picryl-hydrazyl (DPPH) assay were used to determine the quantitative of radical scavenging activity of the extracts. Quantitative estimation was performed according to the method described by Brand et al. [27]. Ascorbic acid was used as positive control. The DPPH radical concentration (antioxidant activity) was calculated using this equation:
Scavenging activity (%) = [(Absorbance control – Absorbance sample)/Absorbance control] × 100.
Antioxidant activity was also expressed as inhibitory concentration (IC50), defined as the concentration of phenolic compounds in the extract required to cause a 50% decrease in initial DPPH radical absorbance at 517 nm.

2.6. Determination of Cytotoxicity Activity

The cytotoxicity of the extracts was estimated by the neutral red uptake assay, using FL-cells, a human amniotic epithel cell line [28]. Quantitative determination was carried out as described in our previous study [1].

2.7. Identification of Naphthoquinones on Thin-Layer Chromatography (TLC)

Extracts were analyzed by silica gel thin layer chromatography (TLC) according to Wagner and Bladt [29] to identify the presence of naphthoquinones in the extracts. The following mobile phases of TLC were used: A: toluene-formic acid (9:1); B: ethyl acetate-glacial acetic acid-formic acid-water (100:1:11:26). The following indicators were used to detect the spots on TLC: a) Physical method: visual and ultraviolet (UV) light (254 and 365 nm), b) Chemical reagents used as spray: 10% methanolic potassium hydroxide KOH and vanillin–sulphuric acid reagent [29].

3. Results

3.1. Ethnobotany of Euclea divinorum

Table 2 shows the collected data of ethnobotanical survey for Euclea divinorum Hiern (Ebenaceae) and its traditional uses in Soqotra Island compared with the literature [3,30]. In the present study, we interviewed 50 informants (female: 5; male: 45) in different locations of Soqotra Island, Yemen. The root bark is the most frequently used part of the plant. All respondents (100%) knew and/or used E. divinorum for medicinal purposes in all different selected 10 localities in the Island. According to our results (Table 2), the plant is recognized to treat dental and dermal ailments. Furthermore, the root bark is used as cosmetic red colouring agent for the lips and mouth cited by (90%) of informants (Table 2). The plant is the second famous and most important medicinal plant from Soqotra Island after Dracaena cinnabari that used in Soqotra Island; whereas both are transported as medicines into inland Yemen [1].

3.2. Antifungal Activity

The antifungal activity results are reported in Table 3 and Figure 2. This study demonstrated the antifungal activity of E. divinorum root bark by measuring the inhibition zone of the fungi growth in a paper disc diffusion assay. The tested extracts showed a clear inhibition on all tested fungi. The best specific strong antifungal activity was demonstrated by the dichloromethane extract of E. divinorum against Trichophyton mentagrophytes (30 mm, minimal inhibition concentration (MIC): 200 µg) and Microsporum gypseum (25 mm) followed by the direct methanolic extract (20 and 25 mm) (MIC: 500 µg), compared with nystatin.

3.3. Antioxidant Activity

The antioxidant activity results are shown in Table 4 comparable with ascorbic acid. The direct sequential and direct methanolic extracts showed significant antioxidant activities (IC50 = 225.0, 550.0 µg/mL) respectively. Non-polar extracts: dichloromethane and ethyl acetate extract showed moderate antioxidant activity (IC50 > 600 µg/mL).

3.4. Cytotoxic Activity

The concentration of each extract that is required for 50% growth inhibition of FL-cells, was measured using neutral red uptake assay. The sequential and direct methanolic extract showed less cytotoxicity. (IC50 > 800 µg/mL) than dichloromethane and ethyl acetate extracts (IC50 < 240.0 µg/mL) (Table 4).

3.5. Identification of Naphthoquinones

The dichloromethane, ethyl acetate and methanolic extracts showed positive results to naphthoquinones as described by Wagner and Bladt [29]: A) four spots by Rf values 0.3 to 0.5 reacted positive with potassium hydroxide KOH and vanillin–sulphuric acid to give red, orange and violet in each extract. In the thin-layer chromatography (TLC) of dichloromethane extract, three spots showed orange red to yellow colors under ultraviolet–visible (UV–vis) light; quenching under 245 nm and red-brown to red fluorescence under 365 nm.

4. Discussion

Euclea divinorum Hiern (Ebenaceae) is the botanical name of a wild tree growing to 4 m [30] on Soqotra Island. The plant is abundantly grown in different localities in Soqotra Island, such as Reyged and Shauub. “kala” is the local name of the E. divinorum tree in Soqotra. “doreeb” is the Soqotri name of the used part, “root”, that is employed as a traditional crude drug. The plant is also tropically widespread in Africa and the Old World. The family, Ebenaceae has only two genera with 500 species; fourteen species belong to Euclea genus [30]. It is also native to South and East Africa [16]. In Yemen, there are two plant species which are most frequently used as toothbrushes “miswak” and found in the markets of the inland; the famous common plant Salvadora persica besides E. divinorum. Salvadora persica is called locally “erhik” in Soqotra Island and “rak” in the inland. We interviewed informants in ten different localities in the Island, where the medicinal use of the plant is known in all the Island parts, even in the Inland Yemen. This widespread traditional knowledge of the plant indicates its high importance as a famous medicinal plant. Tooth cleaning is the most cited ailment by all informants (100%), followed by wound and dermal infectious diseases (70%). The most frequent administration route of the root bark is topically, while fewer citations were documented for oral application to clean the blood (Table 2). In the inland, we documented the traditional use of the root bark as an infusion to treat jaundice besides its traditional uses as powder or toothbrush to clean teeth. We compared our present ethnobotanical survey with some traditional uses of the plant have been previously reported by Miller [30] and in our previous paper [3].
Generally, naphthoquinones were reported as antibacterial agents [5,17,21,22,23] and to inhibit viral infection [31]. Some naphthoquinone derivatives have been identified and isolated from the plant root [13,18,19]. The plant root contains a large amount of naphthalene, which is responsible for the red color on the lips and mouth by using the root pieces as “miswak”. Due to its popularity as a traditional medicinal herb in Soqotra Island and inland Yemen, the roots of E. divinorum are available in the markets in the inland. It may be used as substitutional adulterant for the red resin of Dracaena cinnabari that is used also in the traditional herbal medicine in Yemen for treat oral diseases including tooth ailments [1].
The low polar dichloromethane and ethyl acetate extracts showed considerable antifungal activity (10 to 30 mm) against all tested pathogenic fungi strains. Previous phytochemical investigation of the non-polar chloroform extract of E. divinorum root reported the isolation of four coloring naphthoquinones: 7-methyljuglone, diospyrin, isodiospyrin, shinanolone, [13,18] besides three triterpenoids lupeol, lupene, and botulin [13,18,19]. Moreover, nine naphthoquinones have been previously isolated from different Ebenaceae species [32,33,34,35].
However, these naphthoquinones were reported to have the ability of extraction by different polarity of solvents; they have been previously isolated from the roots of different species of Euclea, Diospyros, and Drosera. For instance, 8-hydroxyisodiospyrin, diospyrin from polar methanolic extract [36]; shinanolone, from the ethanolic extract [37]; 7-methyljuglone from the methanolic [38] and dichloromethane extracts [39]. These lead to the fact that the aforementioned naphthoquinones could be extracted, identified and isolated from different plant species using a different polarity of solvents: either non-polar (e.g., chloroform, dichloromethane) or polar (e.g., methanol, ethanol, acetone). By the partitioned extraction between polar solvents and non-polar solvents, these naphthoquinones showed a high ability to separate from polar solvent into non-polar solvents, example, partition from the methanol phase to dichloromethane or chloroform phase [36,37,39].
The spots of the E. divinorum obtained from the three extracts on TLC, showed positive reaction with the UV and chemical reagents that used to identify naphthoquinones in the extracts according to method used by Wagner and Bladt [29]. The study identified for the first time, the presence of the naphthoquinones in three polar and non-polar extracts of E. divinorum root bark collected from Soqotra Island. This result is consistent with the previous studies that reported the identification and isolation of seven pure naphthoquinones from the roots of E. divinorum samples collected from different African localities, in Ethiopia [19], Zimbabwe [13] and Mozambique [18]. Moreover, this study result confirms the chemotaxonomy of Ebenaceae.
The naphthoquinones are mostly stored in the roots of different Ebenaceae species and investigated for their antifungal activities. Previous biological examination of the naphthoquinones 7-methyljuglone, diospyrin and isodiospyrin isolated from the root acetone extract of Diospyros virginiana showed antifungal activities on some plant pathogenic fungi [40]. Against human pathogenic fungi, only three pure isolated naphthoquinones: 7-methyljuglone, plumbagin and shinanolone were reported to have antifungal activity, which were isolated from the methanolic extract of Diospyros maritima bark [38]. 7-Methyljuglone showed high activity against Aspergillus niger, Candida albicans, and Saccharomyces cerevisiae with growth inhibition of 99.9% at concentration 20, 1, 1, 300 µg/mL, respectively [38]. From the root bark of E. natalensis, shinanolone and octahydroeuclein were isolated and showed significant inhibition against Aspergillus niger and Cladosporium cladosporioides by 0.01 mg/mL [41]. Ten naphthoquinone derivatives of dehydroiso-ß-lapachone were isolated from a dichloromethane extract of Newbouldia laevis roots, and reported with antifungal activity against Cladosporium cucumerinum and Candida albicans [42]. Shikonin and deoxyshikonin were isolated from roots of Lithospermum erythrorhizon showed strong antifungal activities, against Candida krusei (MIC: 4 mg/mL) [43]. The antifungal activities of 30 different naphthoquinones against some Candida species such as C. albicans were demonstrated [44]. Thirteen synthetic naphthoquinones containing sulphur atoms showed higher antifungal activity than amphotericin B against Candida tropicalis, Aspergillus niger, Trychophyton tonsurans and Fusarum oxysporum [45]. In addition, previous biological examinations of the triterpenoids lupeol, Lupene and betulin isolated from the of E. natalensis root bark showed antifungal activity against Aspergillus flavus, A. niger and Cladosporium cladosporioides (0.01 mg/mL) [41]. These results suggest that the four naphthoquinones 7-methyljuglone, diospyrin, isodiospyrin and shinalone and the three triterpenes lupeol, lupene, and botulin that were previously isolated from the root chloroform extract of E. divinorum [13,18], must be responsible for the specific antifungal activity of the root dichloromethane extract of E. divinorum tested in the present study. Therefore, both groups of naphthoquinones and triterpenes showed synergistic effects on the antifungal activity of the dichloromethane extract. While the naphthoquinones were reported as the main constituents in the plant root [13], the plant leaves were reported to be naphthoquinones free [5]. Furthermore, two naphthalene derivatives, Eucleanal A and B have been previously isolated from the leaves’ ethyl acetate extract [8]; however, the leaves extracts were reported to give negative or weak antifungal effects on some fungi including Candida albicans and Tricophyton mentagrophytes (Table 1) [17,23]. This observation leads to suggest that the responsible chemical part for the strong antifungal activity is related to the ketone functional groups that are found in the general chemical structure of naphthoquinones, while lack in the naphthalene derivatives: Eucleanal A and B.
On the other hand, the direct methanolic extract showed higher antifungal activity (15–30 mm) than the sequential methanolic extract (15–18 mm). This led us to suggest that the differences in antifungal activity between the two extracts were essentially due to more naphthoquinones content in direct methanolic extract. The antifungal naphthoquinones of the root powder are separated in the first step of the sequential extraction process in the dichloromethane extract, and therefore they are lacking in the sequential methanolic extract. However, by the direct extraction of the root powder, most naphthoquinones are soluble also in methanol and can be separated in the methanol extract (Figure 2). The direct methanol extract contains naphthoquinones besides other phenolic compounds, and therefore it showed stronger antifungal activity than the sequential methanol and ethyl acetate extracts. In previous chemical investigation, many phenolic compounds have been investigated in the methanol extract of E. divinorum root with different functional groups, flavonoids and tannins [5,16]. From the leaves, pure flavonoids have been isolated (myricitin, quercetin, kaempferol and tannins including gallic acid and catechin [20]. These polyphenols as the main constituents of the polar extract might account for the moderate antifungal activity of sequential methanolic fraction and for the additive action on the antifungal activities of direct methanolic extracts presented in this study.
The present study shows for the first time the antifungal activity of E. divinorum on six selected human pathogenic fungi. The study indicated the suitable method to separate the antifungal extracts with no-polar solvents to obtain higher antifungal activity; these non-polar extracts were identified previously to contain antifungal naphthoquinones as their main constituents. On the other hand, the antibacterial activities of the plant extracts against some bacterial strains have been determined against the oral pathogens to tooth surface Streptococcus mutans, S. sanguinis [4,5] and Bacteroides gingivalis [22]. According to the previously antibacterial activities reports [4,5,22], the tested fungi strains demonstrated more sensibility to root extracts than to the bacteria. However, some naphthoquinones identified in Euclea natalensis root were reported with significant antimycobacterial activity against Mycobacterium tuberculosis including diospyrin (MIC values 8.0 μg/mL), 7-methyljuglone (0.5 μg/mL) [39] and shinanolone (0.1 mg/mL) [46].
Methanolic extracts of the root were previously investigated to contain many polyphenols such as tannins and flavonoids [5,16]. Some flavonoids (myricitrin, quercetin, kaempherol) and tannins (catechin and gallic acid) were isolated as major constituents from the plant leaves [20]. These polyphenols are known antioxidant compounds [35], which might be responsible for the significant antioxidant effect of polar methanolic fractions. Furthermore, methanolic extract of E. divinorum leaves was reported to have antioxidant activity at 2000 µg/mL; which acts as an antidote against the nephrotoxicity caused by gentamicin [25].
The low toxicity of both polar methanolic extracts against FL-cells confirms the safe traditional medicinal uses of the root bark as an entire crude powder. This indicates that the flavonoids in combination with naphthoquinones in a methanolic extract showed antagonist effect on the cytotoxic activity. Our previous study reported the cytotoxic activity of different of E. divinorum extracts on the human ECV-304 cells [3]. The methanol extract exhibited markedly low toxicity (IC50 value 36 µg/mL) against ECV-304 cells, while the lipophilic (Petrol ether/ethyl acetate) (1:1) extract of E. divinorum root displayed strong toxicity IC50 11.6 μg/mL [3]. These results suggest the antifungal activity of the direct methanolic extract of the root in a safer dose than the dichloromethane extract, due presence of the four identified naphthoquinones, some of them were reported with high cytotoxic activity such as 7-methyljuglone. The high cytotoxic activity of 7-methyljuglone was previously reported against five cell lines including murine lymphocyticleukemia 0.1 and human breast cancer 2.2 µg/mL [13].
The antifungal and antioxidant activities and the low toxicity of the direct methanolic extract support the traditional Soqotri use of the plant root to treat fungal infection in the mouth and to clean teeth. Furthermore, the results confirm the administration mode of the root as raw powder to rub on teeth, because the crude powder contains all the bioactive constituents of the entire root bark: the antifungal naphthoquinones and the antioxidant phenols and flavonoids.

5. Conclusions

The ethnobotanical documentation of a medicinal plant is an important guide for the biological examinations and phytochemical isolation of bioactive compounds that lead to the discovery of new natural drugs. Therefore, the identification of new plant species regarding ethnomedicinal uses is also an essential process to isolate new antifungal compounds. The extraction type is a practical process to separate the bioactive fractions from a traditional medicinal plant. The root bark of E. divinorum is rich with naphthalene derivatives, naphthoquinones, tannins, flavonoids and other polyphenols, which have antimicrobial activities especially against dental microbes. Naphthoquinones are the main constituents of the E. divinorum root bark, which could be identified in the Soqotri sample using the TLC method. They can be separated with either the non-polar or the polar solvents. The low polar or non-polar dichloromethane extract was identified with high content of naphthoquinones; it showed significant and broad antifungal activity. The polar ethyl acetate and methanolic extracts contain fewer naphthoquinones but more flavonoids and tannins; therefore, they showed weak antifungal but more antioxidant activity with safe toxicity. The combination of different polyphenols (flavonoids and naphthoquinones) in the plant root can insert strong synergist effect on antifungal activity against the human pathogenic fungi. These findings validate the use of the traditional preparations of the root bark as a crude powder and/or as toothbrush, which contain both antifungal naphthoquinones and antioxidant flavonoids, to treat dental and mouth diseases in the tropical Soqotra Island. We suggest further research to investigate the natural naphthoquinones, especially 7-methyljugloneas semisynthetic derivatives on other broad human pathogenic fungi. These survey and experimental results are an additional part of the ethnobotany and phytopharmacology of E. divinorum, that were also reviewed based on literature to form an essential monograph for this important medicinal plant.

Author Contributions

M.A.-F. designed the research aim, performed data analysis, and wrote the manuscript.

Funding

This research received no external funding.

Acknowledgments

I thank Ulrike Lindequist, Institute for Pharmacy, Ernst-Moritz-Arndt University Greifswald, Germany, for the support in the cytotoxicity test, Gudrun Schröder, Institute of Microbiology, Greifswald University, Germany, for the support in the antifungal test.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Al-Fatimi, M. Ethnobotanical Survey of Dracaena cinnabari and investigation of the pharmacognostical properties, antifungal and antioxidant activity of its resin. Plants 2018, 7, 91. [Google Scholar] [CrossRef] [PubMed]
  2. Mgbeahuruike, E.E.; Holm, Y.; Vuorela, H.; Amandikwa, C.; Fyhrquist, P. An ethnobotanical survey and antifungal activity of Piper guineense used for the treatment of fungal infections in West-African traditional medicine. J. Ethnopharmacol. 2019, 229, 157–166. [Google Scholar] [CrossRef] [PubMed]
  3. Al-Fatimi, M.; Friedrich, U.; Jenett-Siems, K. Cytotoxicity of plants used for traditional medicine in Yemen. Fitoterapia 2005, 76, 355–358. [Google Scholar] [CrossRef] [PubMed]
  4. Lall, N.; Meyer, J.J. Antibacterial activity of water and acetone extracts of the roots of Euclea natalensis. J. Ethnopharmacol. 2000, 72, 313–316. [Google Scholar] [CrossRef]
  5. Nyambe, M.M.; Hans, R.; Beukes, M.; Morris, J.; Kandawa-Schulz, M. Phytochemical and antibacterial analysis of indigenous chewing sticks, Diospyros lyciodes and Euclea divinorum of Namibia. Biofarmasi J. Nat. Prod. Biochem. 2018, 16, 29–43. [Google Scholar] [CrossRef]
  6. Al-Fatimi, M.; Wurster, M.; Schröder, G.; Lindequist, U. Antioxidant, antimicrobial and cytotoxic activities of selected medicinal plants from Yemen. J. Ethnopharmacol. 2007, 111, 657–666. [Google Scholar] [CrossRef]
  7. Bussmann, R.W.; Gilbreath, G.G.; Solio, J.; Lutura, M.; Lutuluo, R.; Kunguru, K.; Wood, N.; Mathenge, S.G. Plant use of the Maasai of Sekenani Valley, Maasai Mara, Kenya. J. Ethnobiol. Ethnomed. 2006, 2, 22. [Google Scholar] [CrossRef]
  8. Ng’ang’a, M.M.; Hussain, H.; Chhabra, S.; Langat-Thoruwa, C.; Al-Harrasi, A.; Krohn, K.; Green, I.R. Eucleanal A and B: Two new napthalene derivatives from Euclea divinorum. Chin. Chem. Lett. 2012, 23, 576–578. [Google Scholar] [CrossRef]
  9. Maroyi, A. Euclea undulata Thunb.: Review of its botany, ethnomedicinal uses, phytochemistry and biological activities. Asian Pac. J. Trop. Med. 2017, 10, 1030–1036. [Google Scholar] [CrossRef]
  10. Stander, I.; Van Wyk, C.W. Toothbrushing with the root of Euclea natalensis. J. Biol. Buccale 1991, 19, 167–172. [Google Scholar]
  11. Van Damme, P.; Van Den Eynden, V.; Vernemmen, P. Plant uses by the Topnaar of the Sesfontein area (Namib Desert). Afr. Focus 1992, 8, 223–252. [Google Scholar] [CrossRef]
  12. Chinsembu, K.C. Ethnobotanical study of plants used in the management of HIV/AIDS-Related diseases in Livingstone, Southern Province, Zambia. Evid. Based Complement. Altern. Med. 2016, 2016, 4238625. [Google Scholar] [CrossRef] [PubMed]
  13. Mebe, P.P.; Cordell, G.A.; Pezzuto, J.M. Pentacyclic triterpenes and naphthoquinones from Euclea divinorum. Phytochemistry 1998, 47, 311–313. [Google Scholar] [CrossRef]
  14. Kaluwa Kaingu, C.; Oduma, J.A.; OduKanuima, T. Preliminary investigation of contractile activity of Ricinus communis and Euclea divinorum extracts on isolated rabbit uterine strips. J. Ethnopharmacol. 2012, 142, 496–502. [Google Scholar] [CrossRef] [PubMed]
  15. Kigen, G.; Kipkore, W.; Wanjohi, B.; Haruki, B.; Kemboi, J. Medicinal plants used by traditional healers in Sangurur, Elgeyo Marakwet County, Kenya. Pharmacogn. Res. 2017, 9, 333–347. [Google Scholar] [CrossRef] [PubMed]
  16. Woldemedhin, B.; Nedi, T.; Shibeshi, W.; Sisay, M. Evaluation of the diuretic activity of the aqueous and 80% methanol extracts of the root of Euclea divinorum Hiern (Ebenaceae) in Sprague Dawley rats. J. Ethnopharmacol. 2017, 202, 114–121. [Google Scholar] [CrossRef] [PubMed]
  17. Geyid, A.; Abebe, D.; Debella, A.; Makonnen, Z.; Aberra, F.; Teka, F.; Kebede, T.; Urga, K.; Yersaw, K.; Biza, T.; et al. Screening of some medicinal plants of Ethiopia for their anti-microbial properties and chemical profiles. J. Ethnopharmacol. 2005, 97, 421–427. [Google Scholar] [CrossRef] [PubMed]
  18. Cruz-Costa, M.A.; Lopes, M.H.; Paul, M.I.; Ferreira, M.A.; Correia-Alves, A. Naphthaquinones and triterpenoids of Euclea divinorum. Phytochemistry 1976, 15, 829. [Google Scholar] [CrossRef]
  19. Van der Vijver, L.M.; Gerritsma, K.W. Napthoquinones of Euclea and Diospyros species. Phytochemistry 1974, 13, 2322–2323. [Google Scholar] [CrossRef]
  20. Hattas, D.; Hjältén, J.; Julkunen-Tiitto, R.; Scogings, P.F.; Rooke, T. Differential phenolic profiles in six African savanna woody species in relation to antiherbivore defense. Phytochemistry 2011, 72, 1796–1803. [Google Scholar] [CrossRef]
  21. Homer, K.A.; Manji, F.; Beighton, D. Inhibition of peptidase and glycosidase activities of Porphyromonas gingivalis, Bacteroides intermedius and Treponema denticola by plant extracts. J. Clin. Periodontol. 1992, 19, 305–310. [Google Scholar] [CrossRef] [PubMed]
  22. Homer, K.A.; Manji, F.; Beighton, D. Inhibition of protease activities of periodontopathic bacteria by extracts of plants used in Kenya as chewing sticks (mswaki). Arch. Oral Biol. 1990, 35, 421–424. [Google Scholar] [CrossRef]
  23. More, G.; Tshikalange, T.E.; Lall, N.; Botha, F.; Meyer, J.J. Antimicrobial activity of medicinal plants against oral microorganisms. J. Ethnopharmacol. 2008, 119, 473–477. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Samie, A.; Tambani, T.; Harshfield, E.; Green, E.; Ramalivhana, J.N.; Bessong, P.O. Antifungal activities of selected Venda medicinal plants against Candida albicans, Candida krusei and Cryptococcus neoformans isolated from South African AIDS patients. Afr. J. Biotechnol. 2010, 9, 2965–2976. [Google Scholar] [CrossRef]
  25. Feyissa, T.; Asres, K.; Engidawork, E. Renoprotective effects of the crude extract and solvent fractions of the leaves of Euclea divinorum Hierns against gentamicin-induced nephrotoxicity in rats. J. Ethnopharmacol. 2013, 145, 758–766. [Google Scholar] [CrossRef]
  26. Bauer, A.W.; Kirby, W.M.M.; Sherris, J.C.; Turck, M.D. Antibiotic susceptibility testing by a standardized single disk method. Am. J. Clin. Pathol. 1966, 45, 493–496. [Google Scholar] [CrossRef] [PubMed]
  27. Brand-Williams, W.; Cuvelier, M.E.; Berset, C. Use of a free radical method to evaluate antioxidant activity. LWT-Food Sci. Technol. 1995, 28, 25–30. [Google Scholar] [CrossRef]
  28. Lindl, T.; Bauer, J. Zell- und Gewebekultur, Einführung in die Grundlagen Sowie Ausgewählte Methoden und Anwendungen; Gustav-Fischer-Verlag Jena: Stuttgart, Germany, 1989; p. 181. [Google Scholar]
  29. Wagner, H.; Bladt, S. Plant Drug Analysis. A Thin Layer Chromatography Atlas; Springer: Heidelberg, Germany, 2009; pp. 275–279. [Google Scholar]
  30. Miller, A.G.; Morris, M. Ethnoflora of the Soqotra Archipelago; Charlesworth Group: Huddersfield, UK, 2004; pp. 540–541. [Google Scholar]
  31. Evans, W.C. Trease and Evans Pharmacognosy, 15th ed.; Saunders Ltd.: London, UK, 2002; pp. 432–434. [Google Scholar]
  32. Bapela, M.J.; Lall, N.; Meyer, J.J.M. Seasonal variation of naphthoquinones in Euclea natalensis subspecies natalensis. S. Afr. J. Bot. 2008, 74, 218–224. [Google Scholar] [CrossRef]
  33. Babula, P.; Adam, V.; Havel, L.; Kizek, R. Noteworthy secondary metabolites naphthoquinones-their occurrence, pharmacological properties and analysis. Curr. Pharm. Anal. 2009, 5, 47–68. [Google Scholar] [CrossRef]
  34. Krenn, L.; Blaeser, U.; Hausknost-Chenicek, N. Determination of Naphthoquinones in Droserae herba by Reversed-Phase High Performance Liquid Chromatography. J. Liq. Chromatogr. Relat. Technol. 1998, 20, 3149–3160. [Google Scholar] [CrossRef]
  35. Joubert, A.; van der Kooy, F.; Meyer, J.J.M.; Lall, N. HPLC in the comparative study of the content of naphthoquinones (quinonoid constituents) in Euclea species of South Africa. Chroma 2006, 64, 399–403. [Google Scholar] [CrossRef]
  36. Uddin, G.; Rauf, A.; Arfan, M.; Rehman, T.U.; Khan, A.Z.; Ali, G.; Rehman, B.; Zia-ul-Haq, M. Molecular docking of Diospyrin as a LOX inhibitory compound. J. Saudi Chem. Soc. 2016, 20, S448–S450. [Google Scholar] [CrossRef]
  37. Weigenand, O.; Hussein, A.A.; Lall, N.; Meyer, J.J. Antibacterial activity of naphthoquinones and triterpenoids from Euclea natalensis root bark. J. Nat. Prod. 2004, 67, 1936–1938. [Google Scholar] [CrossRef] [PubMed]
  38. Gu, J.Q.; Graf, T.N.; Lee, D.; Chai, H.B.; Mi, Q.; Kardono, L.B.; Setyowati, F.M.; Ismail, R.; Riswan, S.; Farnsworth, N.R.; et al. Cytotoxic and antimicrobial constituents of the bark of Diospyros maritima collected in two geographical locations in Indonesia. J. Nat. Prod. 2004, 67, 1156–1161. [Google Scholar] [CrossRef] [PubMed]
  39. Ziaratnia, S.M.; Kunert, K.J.; Lall, N. Elicitation of 7-methyljuglone in Drosera capensis. S. Afr. J. Bot. 2009, 75, 97–103. [Google Scholar] [CrossRef]
  40. Wang, X.; Habib, E.; León, F.; Radwan, M.M.; Tabanca, N.; Gao, J.; Wedge, D.E.; Cutler, S.J. Antifungal metabolites from the roots of Diospyros virginiana by overpressure layer chromatography. Chem. Biodivers. 2011, 8, 2331–2340. [Google Scholar] [CrossRef] [PubMed]
  41. Lall, N.; Weiganand, O.; Hussein, A.A.; Meyer, J.J.M. Antifungal activity of naphthoquinones and triterpenes isolated from the root bark of Euclea natalensis. S. Afr. J. Bot. 2006, 72, 579–583. [Google Scholar] [CrossRef]
  42. Gafner, S.; Wolfender, J.L.; Nianga, M.; Stoeckli-Evans, H.; Hostettmann, K. Antifungal and antibacterial naphthoquinones from Newbouldia laevis roots. Phytochemistry 1996, 42, 1315–1320. [Google Scholar] [CrossRef]
  43. Sasaki, K.; Abe, H.; Yoshizaki, F. In vitro antifungal activity of naphthoquinone derivatives. Biol. Pharm. Bull. 2002, 25, 669–670. [Google Scholar] [CrossRef]
  44. Futuro, D.O.; Ferreira, P.G.; Nicoletti, C.D.; Borba-Santos, L.P.; Silva, F.C.D.; Rozental, S.; Ferreira, V.F. The antifungal activity of naphthoquinones: An integrative review. An. Acad. Bras. Cienc. 2018, 90, 1187–1214. [Google Scholar] [CrossRef]
  45. Errante, G.; La Motta, G.; Lagana, C.; Wittebolle, V.; Sarciron, M.E.; Barret, R. Synthesis and evaluation of antifungal activity of naphthoquinone derivatives. Eur. J. Med. Chem. 2006, 41, 773–778. [Google Scholar] [CrossRef] [PubMed]
  46. Van der Kooy, F.; Meyer, J.J.M.; Lall, N. Antimycobacterial activity and possible mode of action of newly isolated neodiospyrin and other naphthoquinones from Euclea natalensis. S. Afr. J. Bot. 2006, 72, 349–352. [Google Scholar] [CrossRef]
Processes 07 00680 g001 550
Figure 1. The extraction process of Euclea divinorum root bark.
Figure 1. The extraction process of Euclea divinorum root bark.
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Processes 07 00680 g002 550
Figure 2. Antifungal activity of the extracts (sequential dichloromethane (SD) sequential ethyl acetate (SE), sequential methanolic (SM), direct methanolic (DM)) against Trichophyton mentagrophytes as the inhibition zone in agar diffusion (mm).
Figure 2. Antifungal activity of the extracts (sequential dichloromethane (SD) sequential ethyl acetate (SE), sequential methanolic (SM), direct methanolic (DM)) against Trichophyton mentagrophytes as the inhibition zone in agar diffusion (mm).
Processes 07 00680 g002
Table
Table 1. Summary of previous biological and pharmacological studies of Euclea divinorum Hiern.
Table 1. Summary of previous biological and pharmacological studies of Euclea divinorum Hiern.
Used Part/
Extract Solvent		Pharmacological Activities/Details [References]Model
of Test
1. Antibacterial activity against oral pathogens
Root/MethanolActivity against Streptococcus mutans and S. sanguinis by
MIC < 2.5 mg/mL [5] 		in vitro
Stick (Stem)/
Dichloromethane 		Weak activity against Staphyloccocus aureus, Escherichia coli, Bacillus subtilis [21]in vitro
Stem/Aqueous Inhibition of enzymes activity of Porphyromonas gingivalis, Treponema denticola; Bacteroides gingivalis, B. intermedius up to 200 μg/mL [22]in vivo
Bark, Leaves/Ethanol Activity against Actinomyces naeslundii, Streptococcus mutans and Actinobacillus actinomycetemcomitans (MIC: 6.2–25.0 mg/mL) [23]in vitro
Fruit/Methanol Moderate activity against Neisseria gonorrhoea (250–2000 µg/mL) [17]in vitro
2. Antifungal activity
Leaves/HexaneNo activity against Candida albicans, and C. krusei [24]in vitro
Leaves/MethanolWeak activity against C. albicans; Cryptococcus neoformans (4000 µg/mL). No activity against Aspergillus flavus; A. niger; Tricophyton mentagrophytes and T. violacium [17]in vitro
Bark, Leaves/Ethanol No effect on C. albicans [23]in vitro
3. Cytotoxicity activity
Bark, Leaves/EthanolModerate cytotoxicity (inhibitory concentration (IC50): 142.3 μg/mL) on vero cell line [23]in vitro
Root/Petrol ether/
Ethyl acetate 1:1;
Methanol		The lipophilic extract displayed marked toxicity (IC50 value 11.6 µg/mL) [3];
The polar extract showed less toxicity (IC50 36.0 µg/mL) against ECV-304 cells [3]		in vitro
4. Oxytocic activity
Root, Bark/Aqueous, Ethanol Direct stimulation of the uterus contraction [14]in vivo
5. Diuretic activity
Root/80% Methanol Diuretic effect at 200–400 mg/kg [16]in vivo
6. Antioxidant activity
Root/Aqueous; MethanolAntioxidant activity at 2000 µg/mL with 74.5–82.5% DPPH inhibition [25]in vitro
7. Toxicity effect
Root/80% Methanol Safe extract at 2000 mg/kg [16]in vivo
8. Antidote effect
Leaves/Methanol Antidote for nephrotoxicity caused by gentamicin at (100 mg/kg) [25]in vivo
MIC, minimal inhibition concentration.
Table
Table 2. Data of ethnobotanical survey of Euclea divinorum on Soqotra Island.
Table 2. Data of ethnobotanical survey of Euclea divinorum on Soqotra Island.
Used Part/
Preparation Form/Administration Route 		Ethnobotanical
Uses		Ct %Ref
1. Medicinal uses
1.1. Dental diseases100
Root/dried, raw, cut pieces are used
as toothbrush (misawk)/topically 		dental diseases: mouth and dental fungal infection [3]
Root/dried powder of root barks/
rubbing on the teeth		tooth cleaning [3,30],
Root/root bark is powdered with little water and salt and inserted into the tooth cavitytoothache, tooth cavity [or], [30]
1.2. Dermal diseases70
Roots/dried powder of the root bark in little water as paste/topicallyfresh wound, abscesses and kin diseases [3,30]
Root/a piece is chewed and salvia used or
Root barks powdered and mixed in little water ass paste/ topically		skin complaints, sores, fungal skin complaints,
(ringworm)		 [or], [30]
1.3. Blood diseases20
Root/a piece of root is chewed and the produced salvia is swallowed/internalto purify blood [30]
2. Cosmetic90
Root pieces/fresh or dried root pieces used as chewing/ topicallyred colouring of lip and mouth [or], [30]
3. Economic uses50
Leaves, fruit/
dried or fresh parts		fodder for livestock
and for firewood		 [or], [30]
Dried stemsfirewood [or]
Dried stemshouse ceiling [or]
Ct, citations percentage: number of informants that cited traditional use(s) for the plant from the total informants number; [or], oral interview with local people on Soqotra Island; Ref, References; [3]: Al-Fatimi, et al., 2005; [30]: Miller and Morris, 2004.
Table
Table 3. Antifungal activity of the root bark extracts of Euclea divinorum in an agar diffusion test.
Table 3. Antifungal activity of the root bark extracts of Euclea divinorum in an agar diffusion test.
Fungi Strains IZ Diameter (mm)
SDSESMDMNys
Absidia corymbifera1710171825
Aspergillus fumigatus1615161524
Candida krusei1615161824
Microsporum gypseum2516152022
Mucor sp.1010101521
Trichophyton mentagrophytes3020182525
IZ: inhibition zone; SD: sequential dichloromethane extract; SE: sequential ethyl acetate extract; SM: sequential methanolic extract; DM: direct methanolic extract of E. divinorum; Nys, Nystatin (100 µg/disc).
Table
Table 4. Cytotoxic and antioxidant activity of root barks extracts of Euclea divinorum.
Table 4. Cytotoxic and antioxidant activity of root barks extracts of Euclea divinorum.
Extracts SolventsIC50 (μg/mL)
Antioxidant activityCytotoxicity
Dichloromethane690.5240.0
Sequential ethyl acetate680.8387.7
Sequential methanol225.0800.6
Direct methanol550.0900.5
Ascorbic acid a15.5-
a Positive control; IC50: a concentration required for 50% reduction in absorbance compared with control values.

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Al-Fatimi, M. Antifungal Activity of Euclea divinorum Root and Study of its Ethnobotany and Phytopharmacology. Processes 2019, 7, 680. https://doi.org/10.3390/pr7100680

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Al-Fatimi M. Antifungal Activity of Euclea divinorum Root and Study of its Ethnobotany and Phytopharmacology. Processes. 2019; 7(10):680. https://doi.org/10.3390/pr7100680

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Al-Fatimi, Mohamed. 2019. "Antifungal Activity of Euclea divinorum Root and Study of its Ethnobotany and Phytopharmacology" Processes 7, no. 10: 680. https://doi.org/10.3390/pr7100680

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Al-Fatimi, M. (2019). Antifungal Activity of Euclea divinorum Root and Study of its Ethnobotany and Phytopharmacology. Processes, 7(10), 680. https://doi.org/10.3390/pr7100680

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