| Literature DB >> 35807485 |
Joelle Mesmar1, Rola Abdallah1, Adnan Badran2, Marc Maresca3, Abdullah Shaito4, Elias Baydoun1.
Abstract
Ziziphus nummularia, a small bush of the Rhamnaceae family, has been widely used in traditional folk medicine, is rich in bioactive molecules, and has many reported pharmacological and therapeutic properties. Objective: To gather the current knowledge related to the medicinal characteristics of Z. nummularia. Specifically, its phytochemical contents and pharmacological activities in the treatment of various diseases such as cancer, diabetes, and cardiovascular diseases, are discussed.Entities:
Keywords: Ziziphus nummularia; anti-inflammatory; antioxidant; cyclopeptide alkaloids; nummularine-M; phytochemicals
Mesh:
Substances:
Year: 2022 PMID: 35807485 PMCID: PMC9268283 DOI: 10.3390/molecules27134240
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.927
Figure 1(A) Ziziphus nummularia plant, (B) Ziziphus nummularia fruit, and (C) Ziziphus nummularia leaves. Images were obtained from https://www.floraofqatar.com/ziziphus_nummularia.htm (accessed on 20 June 2022).
Summary of the phytochemical composition of extracts from different parts of the Zizyphus nummularia, using different solvents.
| Plant Part | Solvent Used | Main Results | Major Compounds | References |
|---|---|---|---|---|
|
| Benzene | Isolation of new peptide alkaloids containing the 14-membered ring system | Amphibin-H | [ |
| 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 | [ | |
| Jubanine-B | ||||
| Mauritine-C | ||||
|
| Methanol | Identification of new cyclopeptide alkaloids and peptide alkaloids | Amphibinine-H | [ |
| 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 | ||||
|
| Petroleum ether | Detection of glycosides, and saponins | [ | |
| Ethanol | Isolation of a pure saponin | Zizynummin | [ | |
| Ethanol | Detection of alkaloids, glycosides, and saponins | [ | ||
| Presence of carbohydrates, protein, alkaloids, phenol, flavonoids, tannins, and saponins | [ | |||
| 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 | [ | ||
| 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 | [ | ||
| Identification of 105 phytoconstituents, mainly terpenoids. A few fatty acids and some phytosterols have also been extracted | 1-eicosanol | [ | ||
| 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. | Quercetin | [ | |
| Methanol | Presence of saponins, triterpenes and flavonoids | [ | ||
|
| 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. | [ | |
|
| Hydro-alcoholic | Detection of flavonoids, glycosides, tannins, and phenolic compound | Quercetin | [ |
| Acetone | High phenolic content and presence of flavonoids and flavonols | [ | ||
| Dichloromethane | Very high flavonoid content and presence of phenolics | [ | ||
| Hydro-alcoholic | Detection of flavonoids, glycosides, tannins, and phenolic compound | Quercetin | [ | |
| Methanol | Presence of phenolics and flavonoids in equal amounts | [ | ||
| Identification of different phenolic compounds from different plant genotypes | Chlorogenic acid | [ | ||
| Hydroxy benzoic acid | ||||
| Quercetin | ||||
| Mandelic acid | ||||
| Morin | ||||
| Pyrogallol | ||||
| Rutin | ||||
|
| Benzene | Isolation of a new (25 S)-spirostane: nummularogenin | Nummularogenin | [ |
| Methanol | Identification of 45 compounds with high-resolution mass spectra in positive and negative ionization modes | Guanidinosuccinic acid | [ | |
| 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 | [ | |
| Hexadecane | ||||
| dl-limonene | ||||
| Cyclohexan-1-ol | ||||
| 3 meth | ||||
| Trans-caryophyllene | ||||
| Beta-myrcene |
Chemical structures of the main phytoconstituents in the stem bark, root bark, leaves, and fruits of Ziziphus nummularia.
| Class | Name | Structure | Description | References |
|---|---|---|---|---|
|
| Nummularine D |
| Cyclopeptide alkaloid isolated from the root bark | [ |
| Nummularine N |
| Cyclopeptide alkaloid isolated from the stem bark | [ | |
| Nummularine P |
| Cyclopeptide alkaloid isolated from the stem bark | [ | |
| Nummularine R |
| Peptide alkaloid isolated from the stem bark | [ | |
| Jubanine B |
| Peptide alkaloid isolated from the root bark and stem bark | [ | |
|
| Geranyl linalool |
| Diterpenoid isolated from the leaves | [ |
| Squalene |
| Triterpene isolated from the leaves | [ | |
| Lupeol |
| Triterpene isolated from the leaves | [ | |
| Phytol |
| Diterpene alcohol isolated from the leaves | [ | |
| 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 | [ | |
|
| Chlorogenic acid |
| Polyphenol isolated from the fruits, suggested to play an important role in the management of Alzheimer’s disease by potentially inhibiting acetylcholinesterase | [ |
| 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 | [ | |
| 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 | [ | |
| Pyrogallol |
| Polyphenol isolated from the fruits | [ | |
| Rutin |
| Glycoside isolated from the fruits, suggested to play an important role in the management of Alzheimer’s disease by potentially inhibiting acetylcholinesterase | [ | |
|
| Ethyl alpha-d-glucopyranoside |
| Glycoside isolated from the leaves | [ |
|
| Mandelic acid |
| Alpha hydroxy acid isolated from the fruits | [ |
|
| Lapachol |
| Naphtoquinone isolated from the plant and was shown to have strong anticancer activity | [ |
Figure 2Reported therapeutic applications of Ziziphus nummularia.
The antimicrobial effects of Zizphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| ||||
|
| 0.4 parts per million (ppm), 0.8 ppm, 1.6 ppm, and 3.2 ppm) | Showed potential antibacterial activity. | [ | |
|
| Acetone: 3.7 mg | No antibacterial activity against | [ | |
|
| Higher activity observed against gram-positive strains, with no activity against gram-negative strains with certain fractions | [ | ||
|
| 100 mg/mL | The methanolic and hexane extracts from the fruit showed significant antibacterial activity. | [ | |
|
| 1 and 2 mg/mL | The chloroform and ethyl acetate fractions showed strongest effect against both gram-negative and positive bacteria. | [ | |
|
| 1 and 2 mg/mL | 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 | [ | |
|
| All the tested solvent fractions showed moderate activity | [ | ||
|
| ||||
|
| 0.4 parts per million (ppm), 0.8 ppm, 1.6 ppm, and 3.2 ppm) | Showed potential antifungal activity. | [ | |
|
| The extract and all fractions showed strong anti-fungal activity, with the n-hexane fraction showing maximum activity. | [ | ||
|
| 10 mg/mL | None of the fractions, including crude extract inhibited fungal growth | [ |
The anthelmintic effects of Ziziphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| 500–8000 μg/mL of CME | Adult motility assay on mature live | Caused mortality of worms in dose and time-dependent manner | [ |
|
| 62.5–4000 μg/mL | Egg hatch test | Inhibited egg hatching in dose and time-dependent manner (LC50 = 676.08 μg/mL). | [ |
|
| 62.5–4000 μg/mL | Larval development assay | Inhibited larval development in dose- and time-dependent manner (LC50 = 398.11 μg/mL). | [ |
|
| 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 | [ |
The antioxidant effects of Ziziphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| DPPH free radical scavenging assay | Showed strong activity. | [ | |
|
| Hydroxyl radical scavenging assay | Showed strong activity. | [ | |
|
| Superoxide anion radical scavenging assay | Showed strong activity. | [ | |
|
| 20–180 μg/mL | Reducing capacity assessment | Exhibited increased reducing power in dose-dependent manner | [ |
|
| 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). | [ |
|
| 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). | [ |
|
| 31.25, 62.5, 125, 250, 500, 1000 μg/mL | DPPH free radical scavenging assay | All genotypes showed potent scavenging activity against DPPH. | [ |
|
| 31.25, 62.5, 125, 250, 500, 1000 μg/mL | ABTS Radical Scavenging assay | All genotypes showed potent scavenging activity against ABTS. | [ |
|
| 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. | [ |
The anti-inflammatory effects of Ziziphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| 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. | [ |
|
| 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. | [ |
|
| 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. | [ |
|
| 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. | [ |
|
| EE: 100 and 200 mg/kg | Carrageenan-induced paw edema in mice | Exhibited significant inhibition of paw edema, with strong activity observed with IC. | [ |
|
| EE: 100 and 200 mg/kg | Arachidonic acid-induced ear edema in mice | Exhibited significant inhibition of ear edema, with stronger activity observed with IC. | [ |
|
| EE: 100 and 200 mg/kg | Xylene-induced ear edema in mice | Exhibited significant inhibition of ear edema, with stronger activity observed with IC. | [ |
|
| EE: 100 and 200 mg/kg | Chronic cotton pellet granuloma models in mice | Showed significant inhibition in granuloma tissue formation, with significant inhibition observed with IC. | [ |
|
| 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. | [ |
|
| 50–200 μg/mL | Human aortic smooth muscle cells (HASMCs) | Decreased FBS-induced HASMC proliferation, migration, invasion, and adhesion to fibronectin. | [ |
The anticancer effects of Ziziphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| Swiss albino mice with sarcoma-180 (S-180) ascetic tumor cell | Showed strong antitumor activity. | [ | |
|
| 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. | [ |
|
| EE:100 and 200 mg/kg | Female Swiss albino mice with | Decreased tumor parameters: tumor volume, viable tumor cell count and increased body weight, haematological parameters and life span. | [ |
|
| 50–300 μg/mL | HeLa cells (cervical carcinoma cells) | Showed increased cytotoxicity and altered morphology of cancer cells. | [ |
|
| 100–300 μg/mL | Human pancreatic cancer | Inhibited cell proliferation, migration, invasion, adhesion, and angiogenesis, and it increased cell-cell aggregation. | [ |
The antidiabetic effects of Ziziphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| 250 and 500 mg/kg | Dexamethasone induced diabetic rat model | Maintenance of body weight throughout the experiment in treated group. | [ |
|
| 250 and 500 mg/kg | Alloxan-induced rat diabetic model | Maintenance of body weight throughout the experiment in treated group. | [ |
|
| 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. | [ |
|
| 80–160 μg/mL | α-amylase inhibition assay | All extracts showed strong inhibitory activity with maximum inhibition observed with the saponin extract. | [ |
The anticholinesterase effects of Ziziphus nummularia.
| Extract | Dose | Experimental Model | Observations | References |
|---|---|---|---|---|
|
| 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) | [ |
The analgesic and sedative effects of Ziziphus nummularia.
| 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. | [ |
| 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. | [ |
| 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. | [ |
| 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. | [ |
| 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. | [ |
| Crude methanolic from the roots and fractions | 50 and 100 mg/kg | Brewer’s-yeast-induced hyperthermia | Pronounced reduction in induced pyrexia. | [ |
| Crude methanolic from the roots and fractions | 50 and 100 mg/kg | Acetic acid-induced writhing test in mice | Significant reduction pain sensation. | [ |
The gastrointestinal effects of Ziziphus nummularia.
| 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. | [ |
| 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. | [ |
| 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. | [ |
| 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. | [ |
Figure 3Reported therapeutic applications of Ziziphus nummularia. Padalia and Chanda, 2017 [97]; Padalia, H. and Chanda, S., 2021 [98]; Padalia, H. and Chanda, S., 2021 [96], Khan et al., 2016 [94]; Parmar and Jangir, 2017 [95].