Ziziphus nummularia: A Comprehensive Review of Its Phytochemical Constituents and Pharmacological Properties
Abstract
:1. Introduction
2. Scientific Classification (Index Kewensis)
3. Methods
4. Phytoconstituents of Zizyphus nummularia
Plant Part | Solvent Used | Main Results | Major Compounds | References |
---|---|---|---|---|
Root bark | Benzene | Isolation of new peptide alkaloids containing the 14-membered ring system | Amphibin-H | [29,30,31,32] |
Nummularine-A | ||||
Nummularine-B | ||||
Nummularine-C | ||||
Nummularine-D | ||||
Nummularine-E | ||||
Nummularine-F | ||||
Nummularine-G | ||||
Nummularine-K | ||||
Nummularine-H | ||||
Mucronin-D | ||||
Methanol | Identification of new cyclopeptide alkaloids and peptide alkaloids | Jubanine-A | [30] | |
Jubanine-B | ||||
Mauritine-C | ||||
Stem bark | Methanol | Identification of new cyclopeptide alkaloids and peptide alkaloids | Amphibinine-H | [19,21,22,30,33,34,35,36] |
Frangufoline | ||||
Fubanine-B | ||||
Jubanine-B | ||||
Nummularine-B | ||||
Nummularine-M | ||||
Nummularine-N | ||||
Nummularine-O | ||||
Nummularine-P | ||||
Nummularine-R | ||||
Nummularine-S | ||||
Nummularine-T | ||||
Nummularine-U | ||||
Mauritine-A | ||||
Mauritine-F | ||||
Mauritine-D | ||||
Scutianine-C | ||||
Leaves | Petroleum ether | Detection of glycosides, and saponins | [37] | |
Ethanol | Isolation of a pure saponin | Zizynummin | [38] | |
Ethanol | Detection of alkaloids, glycosides, and saponins | [37] | ||
Presence of carbohydrates, protein, alkaloids, phenol, flavonoids, tannins, and saponins | [39] | |||
Identification of 56 phytoconstituents. Ethyl alpha-d-glucopyranoside polysaccharide was the main constituent. Some phytosterols and fatty acids were also extracted. | 2 methoxy-4-vinylphenol | [25] | ||
Ethyl alpha-d- glucopyranoside Behenyl behenate | ||||
Linoleic acid | ||||
Gamma sitosterol | ||||
Stigmasterol | ||||
Phytol | ||||
Squalene | ||||
Pleic acid | ||||
Tricosane | ||||
Tetradecane | ||||
n-hexane | Presence of carbohydrates, protein, alkaloids, phenol, flavonoids, tannins, saponins, and glycoside, in addition to fixed oils, fats, and volatile oils | [39] | ||
Identification of 105 phytoconstituents, mainly terpenoids. A few fatty acids and some phytosterols have also been extracted | 1-eicosanol | [25] | ||
Betulin | ||||
Campesterol | ||||
Gamma sitosterol | ||||
Geranyl linalool isomer | ||||
Linoleic acid | ||||
Lupeol | ||||
Palmitic acid | ||||
Phytol | ||||
Stearic acid | ||||
Squalene | ||||
Stigmasterol | ||||
Vitamin E | ||||
Trans-geranylgeran oil | ||||
Hydro-alcoholic | Detection of saponins, flavonoids, glycosides, tannins, and phenolic compound. Protein and amino acid were absent | Quercetin | [40] | |
Methanol | Presence of saponins, triterpenes and flavonoids Sequential fractionation of the crude methanolic extract was carried out with n-hexane, chloroform, ethyl acetate, and water. | [41] | ||
Roots | Methanol | Presence of alkaloids, tannins, terpenoids, reducing sugars, saponins, flavonoids, steroids, cardiac glycosides, coumarins, emodines, and anthocyanins and betacyanins in the crude extract. Anthraquinones, glycosides, and phlobatanins were absent. Solvent fractionation of the crude methanolic extract was carried out with n-hexane, chloroform, ethyl acetate, and ethanol | [42] | |
Fruits | Hydro-alcoholic | Detection of flavonoids, glycosides, tannins, and phenolic compound Proteins and amino acid were absent | Quercetin | [40] |
Acetone | High phenolic content and presence of flavonoids and flavonols | [26] | ||
Dichloromethane | Very high flavonoid content and presence of phenolics | [26] | ||
Hydro-alcoholic | Detection of flavonoids, glycosides, tannins, and phenolic compound Proteins and amino acid were absent | Quercetin | [40] | |
Methanol | Presence of phenolics and flavonoids in equal amounts | [26] | ||
Identification of different phenolic compounds from different plant genotypes | Chlorogenic acid | [43] | ||
Hydroxy benzoic acid | ||||
Quercetin | ||||
Mandelic acid | ||||
Morin | ||||
Pyrogallol | ||||
Rutin | ||||
Whole plant | Benzene | Isolation of a new (25 S)-spirostane: nummularogenin | Nummularogenin | [20] |
Methanol | Identification of 45 compounds with high-resolution mass spectra in positive and negative ionization modes | Guanidinosuccinic acid | [44] | |
Daidzin | ||||
N-isovaleroylglycine | ||||
Guaiphenesin | ||||
Sucrose | ||||
Quinic acid | ||||
Coumaroylquinic acid | ||||
Myricetin-3-O-galactoside | ||||
Essential oils | 39 chemical compounds were isolated form the plant, mainly: monoterpenes, aliphatic hydrocarbons, alkane hydrocarbons, primary terpene compounds, and decarbonated alcohol | Tetradecane | [28] | |
Hexadecane | ||||
dl-limonene | ||||
Cyclohexan-1-ol | ||||
3 meth | ||||
Trans-caryophyllene | ||||
Beta-myrcene |
Class | Name | Structure | Description | References |
---|---|---|---|---|
Alkaloids | Nummularine D | Cyclopeptide alkaloid isolated from the root bark | [29] | |
Nummularine N | Cyclopeptide alkaloid isolated from the stem bark | [19] | ||
Nummularine P | Cyclopeptide alkaloid isolated from the stem bark | [21] | ||
Nummularine R | Peptide alkaloid isolated from the stem bark | [34] | ||
Jubanine B | Peptide alkaloid isolated from the root bark and stem bark | [30,33] | ||
Terpenoids | Geranyl linalool | Diterpenoid isolated from the leaves | [25] | |
Squalene | Triterpene isolated from the leaves | [25] | ||
Lupeol | Triterpene isolated from the leaves | [25] | ||
Phytol | Diterpene alcohol isolated from the leaves | [25] | ||
IC | A triterpene derivative (octadecahydro-picene-2,3-14-15-tetranone) isolated from the root bark with in vitro activity against human breast cancer, leukaemia, ovarian cancer, colon adenocarcinoma, and human kidney carcinoma. It also showed in vivo anticancer activity in mice againt Ehrlich ascites carcinoma | [45] | ||
Flavonoids | Chlorogenic acid | Polyphenol isolated from the fruits, suggested to play an important role in the management of Alzheimer’s disease by potentially inhibiting acetylcholinesterase | [43] | |
Quercetin | Polyphenol isolated from the fruits and leaves, suggested to play an important role in the management of Alzheimer’s disease by potentially inhibiting acetylcholinesterase | [40,43] | ||
Morin | Phenolic compound isolated from the fruits in high concentrations, suggested to play an important role in the management of Alzheimer’s disease by potentially inhibiting acetylcholinesterase | [43] | ||
Pyrogallol | Polyphenol isolated from the fruits | [43] | ||
Rutin | Glycoside isolated from the fruits, suggested to play an important role in the management of Alzheimer’s disease by potentially inhibiting acetylcholinesterase | [43] | ||
Glycosides | Ethyl alpha-d-glucopyranoside | Glycoside isolated from the leaves | [25] | |
Benzenoids | Mandelic acid | Alpha hydroxy acid isolated from the fruits | [43] | |
Quinones | Lapachol | Naphtoquinone isolated from the plant and was shown to have strong anticancer activity | [46] |
5. Properties of Ziziphus nummularia
5.1. Anti-Drought and Anti-Thermal Characteristics of Ziziphus nummularia
5.2. Pharmacological Properties of Ziziphus nummularia
5.2.1. Antimicrobial Activity
5.2.2. Anthelmintic Activity
5.2.3. Antioxidant Activity
5.2.4. Anti-Inflammatory Effect
5.2.5. Anticancer Activity
5.2.6. Antidiabetic Effect
5.2.7. Anticholinesterase Activity
5.2.8. Analgesic and Sedative Activities
5.2.9. Gastrointestinal Properties
5.2.10. Other Activities
6. Toxicology Studies
7. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Antibacterial | ||||
Aqueous and ethanolic extracts | 0.4 parts per million (ppm), 0.8 ppm, 1.6 ppm, and 3.2 ppm) | Strains: Staphylococcus aureus, Streptococcus pyogenes, Bacillus subtilis, and Pseudomonas aeruginosa Methods: Agar disk diffusion method and dry weight method | Showed potential antibacterial activity. Most susceptible was Staphylococcus aureus Ethanolic extract was more active than the aqueous one. | [60] |
Acetone, benzene, chloroform, petroleum ether, and water extracts from the leaves | Acetone: 3.7 mg Benzene: 4 mg Chlorofom: 3.45 Petroleum ether: 2.5 Water: 4.8 | Strains: Staphylococcus aureus and Escherichia coli Method: Agar disk diffusion method | No antibacterial activity against Escherichia coli. All extracts showed activity against Staphylococcus aureus. | [61] |
Crude methanolic from the fruits and fractions | Strains: 13 g-positive bacterial strains and 15 g-negative bacterial strains Method: Agar disk diffusion method | Higher activity observed against gram-positive strains, with no activity against gram-negative strains with certain fractions | [59] | |
Methanolic, aqueous, chloroform and hexane extracts from the fruits, leaves and bark | 100 mg/mL | Strains: Staphylococcus aureus and Escherichia coli Method: Agar disk diffusion method | The methanolic and hexane extracts from the fruit showed significant antibacterial activity. The chloroform extract from the fruit showed moderate activity. The aqueous extract from all plant parts showed no activity. | [58] |
Methanolic extract from the leaves and fractions | 1 and 2 mg/mL | Strains: Staphylococcus aureus, Bacillus subtillus, Listeria monocytogenes, Klebsiella pneumoniae, Escherichia coli, and Pseudomonas aureginosa Method: Agar disk diffusion method | The chloroform and ethyl acetate fractions showed strongest effect against both gram-negative and positive bacteria. The methanolic and aqueous fraction did show any activity against tested microorganism | [41] |
Methanolic extract from the leaves and fractions | 1 and 2 mg/mL | Strain: Pseudomonas aureginosa Methods: Biofilm activity assay | Dose-dependent inhibition observed with all fractions.The n-hexane fraction showed the highest inhibition (88%), followed by ethyl acetate (69%), and chloroform (65%) fraction at concentration of 2 mg/mL | [41] |
Methanolic crude extract from the leaves and fractions | Strains: Staphylococcus aureus, Bacillus subtilis and Klebsiella pneumoniaMethod: Agar disk diffusion method | All the tested solvent fractions showed moderate activity | [42] | |
Antifungal | ||||
Aqueous and ethanolic extracts | 0.4 parts per million (ppm), 0.8 ppm, 1.6 ppm, and 3.2 ppm) | Strains: Aspergillus niger, Aspergillus flavus, Candida albicans, and Trichophyton rubrum Method: Agar well diffusion method and dry weight method | Showed potential antifungal activity. Most susceptible was Trichophyton rubrum. | [60] |
Methanolic crude extract from the leaves and fractions | Strains: Aspergills flavus, Aspergills niger and Alternaria solani Method: Tube dilution method | The extract and all fractions showed strong anti-fungal activity, with the n-hexane fraction showing maximum activity. | [42] | |
Methanolic extract from the leaves and fractions | 10 mg/mL | Strains: Aspergills flavus, Aspergills niger and Alternaria solani Method: Antifungal assay | None of the fractions, including crude extract inhibited fungal growth | [41] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Crude methanolic extract (CME) from the bark | 500–8000 μg/mL of CME | Adult motility assay on mature live Haemonchus contortus of sheep | Caused mortality of worms in dose and time-dependent manner | [64] |
Crude methanolic extract (CME) from the bark | 62.5–4000 μg/mL | Egg hatch test | Inhibited egg hatching in dose and time-dependent manner (LC50 = 676.08 μg/mL). | [64] |
Crude methanolic extract (CME) from the bark | 62.5–4000 μg/mL | Larval development assay | Inhibited larval development in dose- and time-dependent manner (LC50 = 398.11 μg/mL). | [64] |
Crude powder and crude methanolic extract (CME) from the bark | 1.0–3.0 g/kg | In vivo study: sheep naturally infected with gastrointestinal nematodes | Maximum reduction in fecal egg count reduction (84.7%) recorded on day 13 post-treatment in sheep with CME at 3.0 g/kg | [64] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Acetone and methanolic extracts | DPPH free radical scavenging assay | Showed strong activity. | [70] | |
Acetone and methanolic extracts | Hydroxyl radical scavenging assay | Showed strong activity. | [70] | |
Acetone and methanolic extracts | Superoxide anion radical scavenging assay | Showed strong activity. | [70] | |
Acetone and methanolic extracts | 20–180 μg/mL | Reducing capacity assessment | Exhibited increased reducing power in dose-dependent manner | [70] |
Methanolic extract from the fruits | 50–250 μg/mL | DPPH free radical scavenging assay | Showed significant free radical scavenging activity in a dose-dependent manner (77.5% at 250 μg/mL). | [71] |
Methanolic extract from the fruits | 50–250 μg/mL | H2O2 free radical scavenging assay | Showed significant free radical scavenging activity in a dose-dependent manner (71% at 250 μg/mL). | [71] |
Methanolic extract from the fruits | 31.25, 62.5, 125, 250, 500, 1000 μg/mL | DPPH free radical scavenging assay | All genotypes showed potent scavenging activity against DPPH. Highest % DPPH inhibition value was 67.03 ± 1.04 mg/mL at 31.25 μg/mL. | [43] |
Methanolic extract from the fruits | 31.25, 62.5, 125, 250, 500, 1000 μg/mL | ABTS Radical Scavenging assay | All genotypes showed potent scavenging activity against ABTS. Highest % ABTS inhibition value was 65.31 ± 1.74 mg/mL at 31.25 μg/mL. | [43] |
Methanolic crude extract from the leaves and fractions (n-hexane, chloroform, ethyl acetate, ethanol) | 10–100 μg/mL | DPPH free radical scavenging assay | The ethyl acetate fraction exhibited maximum (97.77%) free radical scavenging activity at the 100 μg/mL. | [42] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Ethanolic extract (EE) from the leaves | 0.5 g of formulated gels containing 20% and 30% extract | Carrageenan-induced paw edema in Wister albino rats | Significantly reduced paw edema in dose-dependent manner. | [75] |
EE from the leaves | 0.5 g of formulated gels containing 20% and 30% extract | Excision wound model in wister albino rats | Showed an acceleration in the wound healing process and high wound contraction rate. | [75] |
EE from the leaves | 100, 200 and 300 mg/kg | Carrageenan-induced paw edema in rats | Dose-dependent increase in percentage inhibition of paw edema, with 38.37% inhibition at 300 mg/kg. | [79] |
EE from the leaves | 100, 200 and 300 mg/kg | Histamine-induced inflammation in rats | Dose-dependent increase in percentage inhibition of paw edema, with 42.1% inhibition at 300 mg/kg. | [79] |
EE from the root bark and isolated identified compound (IC) | EE: 100 and 200 mg/kg IC: 400 and 600 μg/kg | Carrageenan-induced paw edema in mice | Exhibited significant inhibition of paw edema, with strong activity observed with IC. | [76] |
EE from the root bark and isolated IC | EE: 100 and 200 mg/kg IC: 400 and 600 μg/kg | Arachidonic acid-induced ear edema in mice | Exhibited significant inhibition of ear edema, with stronger activity observed with IC. | [76] |
EE from the root bark and isolated IC | EE: 100 and 200 mg/kg IC: 400 and 600 μg/kg | Xylene-induced ear edema in mice | Exhibited significant inhibition of ear edema, with stronger activity observed with IC. | [76] |
EE from the root bark and isolated IC | EE: 100 and 200 mg/kg IC: 400 and 600 μg/kg | Chronic cotton pellet granuloma models in mice | Showed significant inhibition in granuloma tissue formation, with significant inhibition observed with IC. | [76] |
IC from the root bark | 1–50 μM | Lipopolysaccharide-stimulated RAW 264.7 cells | Increased production of the pro-inflammatory cytokines and inflammatory mediators: NO, PGE-2 and TNF-α. | [76] |
EE from the leaves | 50–200 μg/mL | Human aortic smooth muscle cells (HASMCs) | Decreased FBS-induced HASMC proliferation, migration, invasion, and adhesion to fibronectin. Reduced TNF-α-induced expression of matrix metalloproteases (MMP-2 and MMP-9), NF-κB, and cell adhesion molecules (ICAM-1 and VCAM-1) in dose-dependent manner Decreased the adhesion of THP-1 monocytes in dose-dependent manner. | [78] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Lapachol | Swiss albino mice with sarcoma-180 (S-180) ascetic tumor cell | Showed strong antitumor activity. Enhanced the response of the engrafted tumors to radiation therapy. | [37] | |
Identified compound (IC) | 1–1000 μM | Human breast cancer, leukaemia, ovarian cancer, colon adenocarcinoma and human kidney carcinoma cell lines | Showed high cytotoxicity against all cell lines, with IC having stronger activity compared to EE. | [45] |
Ethanolic extract (EE) from the root bark and isolated identified compound (IC) | EE:100 and 200 mg/kg IC: 50 and 100 mg/kg | Female Swiss albino mice with Ehrlich ascites carcinoma | Decreased tumor parameters: tumor volume, viable tumor cell count and increased body weight, haematological parameters and life span. Decreased the viable cancer cell count and increased the total cell count of the cancer-bearing mice. Significantly elevated the levels of serum biochemical parameters. | [45] |
Methanolic extract from the fruit | 50–300 μg/mL | HeLa cells (cervical carcinoma cells) | Showed increased cytotoxicity and altered morphology of cancer cells. | [58] |
EE from the leaves | 100–300 μg/mL | Human pancreatic cancer | Inhibited cell proliferation, migration, invasion, adhesion, and angiogenesis, and it increased cell-cell aggregation. Inhibited ERK1/2(MAPK) and NFκB signaling pathways. | [81] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Ethanolic and aqueous extracts from the leaves | 250 and 500 mg/kg | Dexamethasone induced diabetic rat model | Maintenance of body weight throughout the experiment in treated group. Showed significant decrease in blood glucose level, particularly with the ethanolic extract at 500 mg/kg. Showed significant reduction in diabetes-induced hyperlipidemia. | [84,86] |
Ethanolic extract from the leaves | 250 and 500 mg/kg | Alloxan-induced rat diabetic model | Maintenance of body weight throughout the experiment in treated group. Showed significant reduction in blood glucose levels, observed on day 3 and day 7 with the 500 mg/kg and 250 mg/kg doses, respectively. | [85] |
Ethanolic extract from the leaves and fruits | Not determined | Glucose diffusion inhibitory test out of a hen’s egg dialysis membrane | Leaf and fruit extract showed significant inhibitory activity, maximum inhibition observed with with leaf extract of the soxhlet process. | [88] |
Aqueous, methanolic and saponin extracts from the leaves | 80–160 μg/mL | α-amylase inhibition assay | All extracts showed strong inhibitory activity with maximum inhibition observed with the saponin extract. | [87] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Methanolic from the fruits | 31.25, 62.5, 125, 250, 500, 1000 μg/mL | In-practice method for assessing the ability to inhibit AChE and BChE | All tested genotypes displayed significant inhibitory effects (highest AChE and BChE inhibition observed with IC50 = 20.52 μg/mL 22.76 μg/mL, respectively) | [43] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Ethanolic from the leaves | 100, 200 and 300 mg/kg | Mouse carrageenan peritonitis in mice | Dose-dependent inhibition of peritoneal leukocyte migration. | [79] |
Ethanolic from the leaves | 100, 200 and 300 mg/kg | Acetic acid-induced writhing response in mice | Dose-dependent decrease in the number of writhes, with 59.29% inhibition at 300 mg/kg. | [79] |
Ethanolic from the leaves | 100, 200 and 300 mg/kg | Tail-flick reaction in mice | Significantly increased tail flick latency, with 90% antinocieptive activity observed at 300 mg/kg. | [79] |
Crude methanolic from the roots and fractions | 50 and 100 mg/kg | Sedative activity using the open field method in mice | Marked sedative effect with decreased movement in dose-dependent manner. Strongest effect observed with the chloroform fraction. | [14] |
Crude methanolic from the roots and fractions | 50 and 100 mg/kg | Phenobarbitone-induced sleeping time in mice | Dose-dependent significant reduction in the sleep latency time (time taken for the onset of sleep) and increase in the sleep. Strongest effect observed with the chloroform fraction. | [14] |
Crude methanolic from the roots and fractions | 50 and 100 mg/kg | Brewer’s-yeast-induced hyperthermia | Pronounced reduction in induced pyrexia. Strongest effect observed with the chloroform fraction. | [14] |
Crude methanolic from the roots and fractions | 50 and 100 mg/kg | Acetic acid-induced writhing test in mice | Significant reduction pain sensation. Strongest effect observed with the chloroform fraction. | [14] |
Extract | Dose | Experimental Model | Observations | References |
---|---|---|---|---|
Crude extract from the leaves | 50, 100 and 300 mg/kg | Castor oil-induced diarrhea in mice | Exhibited a protective effect against castor oil-induced diarrhea. | [10] |
Crude extract from the leaves | 300 and 1000 mg/kg | Enteropooling assay for intestinal fluid accumulation in mice | Showed a protective effect on intestinal fluid accumulation. | [10] |
Crude extract from the leaves | 0.01–3 mg/mL | KCl (80 mM)-induced contractions in isolated rabbit jejunum tissues | Caused a concentration-dependent relaxation of spontaneous and KCl-induced contractions. | [10] |
Crude extract from the leaves | 300 and 1000 mg/kg | Ethanol-induced gastrointestinal ulcer model | Caused 52.5 and 93.6% inhibition of gastric lesions, respectively. | [10] |
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Mesmar, J.; Abdallah, R.; Badran, A.; Maresca, M.; Shaito, A.; Baydoun, E. Ziziphus nummularia: A Comprehensive Review of Its Phytochemical Constituents and Pharmacological Properties. Molecules 2022, 27, 4240. https://doi.org/10.3390/molecules27134240
Mesmar J, Abdallah R, Badran A, Maresca M, Shaito A, Baydoun E. Ziziphus nummularia: A Comprehensive Review of Its Phytochemical Constituents and Pharmacological Properties. Molecules. 2022; 27(13):4240. https://doi.org/10.3390/molecules27134240
Chicago/Turabian StyleMesmar, Joelle, Rola Abdallah, Adnan Badran, Marc Maresca, Abdullah Shaito, and Elias Baydoun. 2022. "Ziziphus nummularia: A Comprehensive Review of Its Phytochemical Constituents and Pharmacological Properties" Molecules 27, no. 13: 4240. https://doi.org/10.3390/molecules27134240
APA StyleMesmar, J., Abdallah, R., Badran, A., Maresca, M., Shaito, A., & Baydoun, E. (2022). Ziziphus nummularia: A Comprehensive Review of Its Phytochemical Constituents and Pharmacological Properties. Molecules, 27(13), 4240. https://doi.org/10.3390/molecules27134240