| Literature DB >> 35050040 |
Adriana Ramona Memete1, Adrian Vasile Timar2, Adrian Nicolae Vuscan2, Florina Miere Groza3, Alina Cristiana Venter3, Simona Ioana Vicas2.
Abstract
In recent years, mulberry has acquired a special importance due to its phytochemical composition and its beneficial effects on human health, including antioxidant, anticancer, antidiabetic and immunomodulatory effects. Botanical parts of Morus sp. (fruits, leaves, twigs, roots) are considered a rich source of secondary metabolites. The aim of our study was to highlight the phytochemical profile of each of the botanical parts of Morus tree, their health benefits and applications in food industry with an updated review of literature. Black and white mulberries are characterized in terms of predominant phenolic compounds in correlation with their medical applications. In addition to anthocyanins (mainly cyanidin-3-O-glucoside), black mulberry fruits also contain flavonols and phenolic acids. The leaves are a rich source of flavonols, including quercetin and kaempferol in the glycosylated forms and chlorogenic acid as predominant phenolic acids. Mulberry bark roots and twigs are a source of prenylated flavonoids, predominantly morusin. In this context, the exploitation of mulberry in food industry is reviewed in this paper, in terms of developing novel, functional food with multiple health-promoting effects.Entities:
Keywords: Morus sp.; anthocyanins; chlorogenic acid; flavonols; functional food; health benefits; morusin
Year: 2022 PMID: 35050040 PMCID: PMC8777750 DOI: 10.3390/plants11020152
Source DB: PubMed Journal: Plants (Basel) ISSN: 2223-7747
Figure 1PRISMA 2020 flow diagram for the present review.
Figure 2The nutrients components of mulberry fruits.
The content of phytochemicals (polyphenols, anthocyanins and flavonoids) from mulberry fruits and leaves from data of literature of the last years (2016–2021).
| Species | Organs | Total Polyphenols | Anthocyanins | Flavonoids | References |
|---|---|---|---|---|---|
|
| fruits | 6.93 ± 0.58 mg GAE/g dw | 233.77 ± 24.02 µg/g dw | Not recorded | [ |
| 485.5 ± 7.1 mg GAE/100 g fw | 206.1 ± 1.8 mg C3GE/100 g fw | Not recorded | [ | ||
| Not recorded | Not recorded | 20.8703 ± 0.9091 mg RE/g dw | [ | ||
| 502.43 ± 5.10 mg GAE/100 g fw | 81.36 ± 2.05 mg C3GE/100 g fw | 219.12 ± 4.45 mg QE/100 g fw | [ | ||
| 1422 mg GAE/100 g dw | Not recorded | 276 mg QE/100 g dw | [ | ||
| 3.7 mg GAE/g fw | 11.3–20.3 mg C3GE/g fw | Not recorded | [ | ||
| 6585 ± 146 mg GAE/kg fw | Not recorded | 1292 ± 52.7 mg QE/kg fw | [ | ||
| leaf | Not recorded | Not recorded | 68.32 mg RE/g dw | [ | |
| 24.37 ± 2.14 GAE/100 g dw | Not recorded | Not recorded | [ | ||
|
| fruits | 11.33 ± 0.7 mg GAE/g fw | 1177.36 ± 136.14 mg C3GE/100 g fw | 15.1 ± 1.22 mg RE/g fw | [ |
|
| fruits | 60.4 ± 3.1 mg GAE/100 g fw | 289.2 ± 0.9 mg C3GE/100 g fw | Not recorded | [ |
| 181 mg GAE/100 g dw | Not recorded | 0.0816 mg QE/g dw | [ | ||
| 663 ± 28.5 mg GAE/kg fw | Not recorded | 217 ± 18.2 mg QE/kg fw | [ | ||
| 5.68 to 40.46 mg GAE/g dw | 0.51 to 28.61 mg/g dw | 0.65 to 3.70 mg QE/g dw | [ | ||
| 534.2 ± 12.46 mg GAE/g dw | 15.5 ± 2.27 mg C3GE/g dw | 427.6 ± 15.94 mg CE/g dw | [ | ||
| leaf | 2.468 ± 0.05 mg GAE/g | Not recorded | Not recorded | [ | |
| 51.43 ± 1.11 mg GAE/g dw | Not recorded | 43.75 ± 0.78 mg QE/g dw | [ | ||
| 16.21 ± 1.34 mg GAE/g dw | Not recorded | 26.41 ± 1.14 mg RE/g | [ | ||
|
| fruits | 1035 mg GAE/100 g dw | Not recorded | 219 QE/100 g dw | [ |
| leaf | Not recorded | Not recorded | 31.28 ± 2.12 mg RE/g | [ |
GAE—gallic acid equivalent, C3GE—cyanidin-3-glucoside equivalent, RE—rutin equivalents, QE—quercetin equivalent, CE—catechin equivalents, fw—fresh weight, dw—dry weight.
Summary of phenolic components isolated from different parts of mulberry tree across-studies (2017–2021).
| Species | Organs | Type of Sample | Technique | Identified Components in | References |
|---|---|---|---|---|---|
|
| fruits | Lyophilized samples | HPLC-DAD-ESI HRMS | Anthocyanins: cyanidin-hexoside, cyanidin-pentosyl-hexoside, cyanidin-rhamnosyl-hexoside, cyanidin-sambubiosyl-rhamnoside, cyanidin-sambubiosyl-glucoside; delphinidin-pentoside, delphinidin-dirhamnosyl-hexoside, petunidin-pentoside, peonidin-hexoside | [ |
| Freeze-dried samples | LC-MS | Anthocyanins: cyanidin hexoside, cyanidin hexose-deoxyhexose; pelargonidin hexoside, pelargonidin hexose-deoxyhexose | [ | ||
| Mulberry dry powder | UPLC-TUV/QDa | Anthocyanins: cyanidin-3-O-glucoside, cyanidin-3-O-rutinoside, pelargonidin-3-O-glucoside | [ | ||
| leaves | Ethanolic extract | HPLC-DAD | Anthocyanins: cyanidin; | [ | |
| Aqueous extract | HPLC-PDA | Flavonols: quercetin, rutin | [ | ||
| twigs | Powder | HPLC; LC-MS-MS; UV-spectra; IR-spectra | Prenylated flavonoids: morunigrols A, B, C, D; cudraflavone B; morusin; moracin C and P. | [ | |
| roots bark | Air-dried roots bark. | RP-MPLC; MS | Prenylated flavonoids: kuwanon L, G and H; cudraflavanonă A; morusin; chalcomoracin, norartocarpetin. | [ | |
|
| fruits | Powder samples | HPLC-DAD | Flavonols: rutin; isoquercitrin; | [ |
| Freeze-dried sample | LC-MS | Flavonols: quercetin-3-O-rutinoside, quercetin-3-O-rutinoside-7-O-glucoside, quercetin-malonylhexoside, quercetin-hexoside, quercetin hexoside malonyl hexoside, quercetin hexose hexose, quercetin-hexose-hexose-deoxyhexose, kaempferol-3-O-rutinoside, kaempferol-3-O-rutinoside-7-O-glucoside, kaempferol-hexoside, kaempferol hexoside malonyl hexoside, kaempferol hexose-hexose deoxyhexose, kaempferol malonyl hexoside | [ | ||
| Dry powder | UPLC-TUV/QDa | Flavonols: rutoside, morin, isoquercetin, quercetin, kaempferol | [ | ||
| leaves | Powder sample | HPLC-DAD | Flavonols: isoquercitrin; rutin; quercitrin, astragalin (kaempferol-3-O-glucoside). | [ | |
| twigs | Powder samples | HPLC-DAD | Prenylated flavonoids: kuwanon G; morusin; | [ | |
| root bark | Powder bark samples | HPLC-DAD | Flavanonol: taxifolin | [ | |
| Dried root bark | MPLC | Prenylated flavonoid: kuwanon G | [ |
UPLC-TUV/QDa—high-performance liquid chromatography with tunable ultraviolet and quadrupole dalton detectors; HPLC-DAD-ESI-HRMS—ultra-high-performance liquid chromatography diode array detector electrospray ionisation high-resolution mass spectrometry; HPLC—high-performance liquid chromatography; LC-MS-MS —liquid chromatography with tandem mass spectrometry (LC-MS-MS); LC-MS—reversed-phase coupled to high-resolution mass spectrometry; RP-MPLC—reversed-phase medium-pressure liquid chromatography; MS—mass spectrometry; HPLC-MS—high-performance liquid chromatography-mass spectrometry; HPLC-DAD—high-performance liquid chromatography with diode array detection; MPLC—medium-pressure preparative liquid chromatography.
The in vitro SET assays that investigated antioxidant capacity of mulberry fruits and leaves from data from the literature (2016–2021).
| Species | Organs | ABTS | DPPH | FRAP | References |
|---|---|---|---|---|---|
|
| fruits | Not recorded | Not recorded | 21.33 ± 0.35 µmol TE/g dw | [ |
| 600.31 µmol TE/L | 131.27 µmol TE/L | Not recorded | [ | ||
| 5.842 ± 0.1155 mmol TE/L | 46.94 ± 1.68% | 0.4627 ± 0.0101 mmol TE/L | [ | ||
| 6.43 mg VCE/g fw | 2.51 mg VCE/g fw | Not recorded | [ | ||
| leaf | 21.85 mg TE/g dw | 146.04 mg TE/g dw | 52.71 mg TE/g dw | [ | |
| 9.89 ± 0.87 mM TE | Not recorded | Not recorded | [ | ||
|
| fruits | 4.11 ± 0.48 µg/mL (IC 50) | 10.08 ± 1.12 µg/mL (IC 50) | Not recorded | [ |
|
| fruits | 92.15 g TE/100 g dw | 10.70 g TE/100 g dw | Not recorded | [ |
| 0.52 mg VCE/g fw | 0.21 mg VCE/g fw | Not recorded | [ | ||
| Not recorded | 5.85 to 40.73 mg TE/g dw | 1.33 to 82.87 mg TE/g dw | [ | ||
| 19.37 ± 3.67 µg/mL (EC 50) | 38.31 ± 2.13 µg/mL (EC50) | 1.23 µM Fe2+ | [ | ||
| leaf | 23.63 ± 0.019 µM TE/g | 49.42 ± 0.005 µM TE/g | 0.0221 ± 0.042 µM Fe2+/mg | [ | |
| 4.47 ± 0.20 mg/mL (IC 50) | 2.95 ± 0.66 mg/mL (IC 50) | Not recorded | [ | ||
| 6.12 ± 0.53 mM TE | Not recorded | Not recorded | [ | ||
| twig | 92.15 g TE/100 g dw | 10.70 g TE/100 g dw | Not recorded | [ |
DPPH—2–2 diphenyl-1-picrylhydrazyl assay, FRAP—ferric reducing ability of plasma assay, ABTS—2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) assay, TE—Trolox Equivalent; VCE—vitamin C equivalent.
The health-promoting properties of different parts of mulberry fruits, as determined in various experimental designs (animal and cell models) (2017–2021).
| Health Effect | Part | Species | Sample Type | Experimental Model | Main Outcomes | References |
|---|---|---|---|---|---|---|
| Anti-inflammatory effect | fruits |
| Aqueous extract | Male Wistar rats, periodontal soft tissues | Decreased MMP-8 and MMP-13 levels in periodontal tissue. Inhibited alveolar bone resorption by suppressing the expression of RANKL and OPG. | [ |
| Anti-Parkinson effect |
| Mulberry juice (cyanidin-3-glucoside, 137 mg/100 g) | LID in MPTP MPTP)-induced PD in male BALB/c mice | Mulberry juice (10–15 mL/kg) for one week may be effective for controlling LID in MPTP-induced PD. | [ | |
|
| Lyophilized mulberry extract | MPTP/p model of early PD in | Improved PD-related, non-motor symptoms by inhibiting olfactory dysfunction and motor deficits. | [ | ||
| Cardiovascular effect/Antiatherosclerosis |
| Ethanolic extract | Rats, Sprague–Dawley | Significantly decreased the content of malondialdehyde and improved the anti-oxidative enzymatic activities, attenuated hepatic steatosis, reduced intima-media thickness and suppressed the development of arterial atherosclerosis by regulating lipid metabolism abnormalities, strengthening anti-oxidant activities and reducing atherosclerotic lesions. | [ | |
| Hepatoprotective effect |
| Aqueous extracts. | Human hepatocellular carcinoma (HepG2)-three concentrations (0.01, 0.1 and 1 mg/mL) and compared to silymarin | Black mulberries; phenolic compounds are beneficial for counteracting liver toxins. | [ | |
| Gastroprotective effect |
| Methanolic extract | Female Swiss mice | Effective defense of the gastric mucosa against the acidified methanol, only at 300 mg/kg (p.o.), reducing the ulcer area by 64.06%. | [ | |
| Antinociceptive effect | Mulberry dry powder | Male Kunming mice, three main flavonoids tested (C3G, Ru and IQ) | Neither C3G, Ru nor IQ individually reduced the duration of both phases, while the mix (C3G, Ru and IQ) significantly reduced the duration of the secondary phase (inflammatory pain phase). | [ | ||
| Antibacterial effect | Mulberry dry powder of | [ | ||||
| Antimicrobial effect | seed |
| Hydroethanolic extracts lyophilized | Six Gram-negative bacteria, three Gram-positive bacteria and one yeast | Efficacy of mulberry extract was shown against | [ |
| Cytotoxic effect |
| Hydroethanolic extracts lyophilized | Human tumor cell lines: MCF-7, HepG2 NCI-H460 and HeLa cells. | The mulberry extract at concentration of 400 µg/mL was not effective against tumor and normal cells. | [ | |
| Treating climacteric symptoms | leaves |
| Leaves powder | 62 climacteric women | Climacteric symptoms and quality of life analysis (functional capacity, vitality, mental health and social aspect) were improved after administration of 250 mg of | [ |
| Antidepressant and neuroprotective effects |
| Aqueous extract | Ex vivo and in vitro model in male Swiss mice, gavage administration | Treatment with | [ | |
| Anti-Melanogenesis effect |
| Dried leaves | B16-F10 mouse skin melanoma cells | [ | ||
| α-Glucosidase inhibition and tyrosinase inhibitory | twigs |
| Dried powder | Ethanol extract portioned in 6 fractions | Among13 compounds isolated from the twigs, Nigranol B and sanggenol H exhibited powerful α-glucosidase inhibitory activities with IC50 values at 1.63 and 1.43 µM, respectively. | [ |
| Anti-hyperuricemic effect |
| Mori ramulus refined extract (ZY1402-A) | Adult male SPF Kunming mice, intragastric administration | The extract significantly reduced the serum uric acid levels of SPF Kunming mice. | [ | |
| Antileukemic effect | bark |
| Bark meal | Parental Jurkat A3 leukemia cell line; FADD-deficient Jurkat Cells; caspase 9-deficient Jurkat cells; Caspase 8- and 10-doubly deficient Jurkat cells | Morniga-G activates T, B, and NK Lymphocytes and induces the cell death of Tn-positive leukemia lymphocytes. cells via concomitant O-glycosylation, caspase and TRAIL/DR5-dependent pathways. | [ |
| Vascular protective effect |
| Ethanolic extract | Male rats (Sprague–Dawley) | Potent endothelium-dependent vasodilator through endothelial-dependent NO-cGMP pathway, including the activation of TEA sensitive K+ channels. | [ | |
| Relaxant effect |
MM-8 = Matrix metalloproteinase-8; MM-13 = Matrix metalloproteinase-13; RANKL—receptor activation of nuclear factor κB (RANK) ligand; OPG—osteoprotegerin; MPTP—1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; LID—levodopa-induced dyskinesia; MBC—minimum bactericidal concentration; C3G—cyanidin 3-O-glucoside; TST—tail suspension test; Ru—rutinoside; IQ—isoquercetin; MCF-7—mammary adenocarcinoma; HepG2 cells—human hepatocellular carcinoma; NCI-H460—small cell carcinoma; HeLa—cervical carcinoma; QoL—quality of life analysis; MRSA—Staphylococcus aureus, resistant to methicillin; MIC—minimal inhibitory concentrations; SRB—sulforodamine B; PD—Parkinson’s disease; NO-cGMP—nitric oxide cyclic-guanosine monophosphate; TEA—tetraethylammonium; K+—potassium; PDGF—platelet-derived growth factors; VSMCs—vascular smooth muscle cells.
Product foodstuffs, their compositions and health benefits (2016–2021).
| Product Foodstuff | Major Findings | Reference |
|---|---|---|
| Black mulberry food colorants | Three formulations of solid natural colorants based on black mulberry anthocyanins (cyanidin-3-O-glucoside and cyanidin-O-rhamnoside), obtained through the spray-drying technique, were developed. These natural additives have a good stability in time and a variation of anthocyanin content and color parameters during the 12 weeks of storage, at room and refrigerated temperatures. | [ |
| Mulberry gummy candies | Gummy candies obtained from 5, 7.5 and 10 g of mulberry molasses/100 g gelatin illustrate the potential for using molasses in a healthier development of confectionery products. These candies contain natural sugars, thus replacing sugar syrup or artificial sweeteners. | [ |
| Mulberry leaf powder drink | The effect on adults of consuming of biscuits with a beverage of powdered mulberry leaves in the afternoon on postprandial glucose levels at dinner was a significant reduction in postprandial increases in glucose. | [ |
| Mulberry leaf tea | The quercetin 3-O-malonylglucoside and kaempferol 3-O-malonylglucoside found in white mulberry leaves can be used as ingredients for a functional food to improve the health benefits, such as controlling blood glucose, preventing aging-related diseases and regulating glycolipid metabolic abnormalities. | [ |
| Black mulberry dietary syrup | Administered in different concentrations in the diet of fish, the syrup, increased activities of serum lysozyme, myeloperoxidase, superoxide dismutase and catalase, and increased the expression levels of immune-related genes in the spleen and antioxidant-related genes in the liver of fish fed. | [ |
| Rapeseed honey with mulberry leaves and fruits | The addition of dried leaves and freeze-dried fruits (4%, w/v) to rapeseed honey added value to the product by increasing the content of flavonoids and phenolic acids and antioxidant capacity. | [ |
| Black mulberry-aged wines | The non-thermal processing applied at wine maturation point can be a potential method of improving the maturation process by modifying the chromatic properties of the wine. | [ |
| In the volatile composition of the non-thermal, accelerated, aged wines, many volatile compounds were found that are grouped into nine chemical families: alcohols (32), esters (53), acids (14), volatile phenols (11), aldehydes (16), ketones (15), terpenes (11), lactones (11) and furans (3). | [ | |
| Black mulberry jam | Black mulberries were processed into jam on an industrialized scale. The total phenols, flavonoids, anthocyanins and antioxidant capacity was significantly decreased but % recovery of bioaccessible the natural compounds increased after jam processing. | [ |
| Dark chocolate with black mulberry | Dark chocolate was fortified with dry black mulberry waste extract, encapsulated in chitosan-coated liposomes. This formula was shown to protect the anthocyanin content and increase the bioavailability of these pigments in vitro. | [ |
List of patents based on the therapeutic and functional applications of Morus (2017–2021).
| Application No. | Species/Part | Sample Type | Results/Mechanism | Ref. |
|---|---|---|---|---|
| US 11,090,349 B2 | Raw material, | Inhibits α-glucosidase. It has the ability to control blood glucose levels and reduce melanin production for the treatment of conditions caused by pigmentation, such as freckles, chloasma, striae gravidarum, sensitive plaque and melanoma. | [ | |
| AU 2019201188 B2 | Mixture extract | The compound mixture, demonstrated beneficial synergistic effects with improved anti-inflammatory and anti-nociceptive efficacy, but also the attenuation of joint stiffness. | [ | |
| US 10,588,927 B2 | Mulberry ( | Mixed extract | Used either as a food product or as a pharmaceutical composition with the aim of preventing or treating degenerative neurological diseases, having the ability to improve memory and protection on neurons. | [ |
| US 2020/0360457 A1 | Macerate extract | As an active ingredient, at least one extract from the root of the plant is used, according to the invention. It is rich in moracenine A, moracenin B, kuwanon C, wittiorumin F and mulberrofuran T, also used in cosmetic composition and a pharmaceutical or nutraceutical composition. | [ | |
| US 2020/0178585 A1 | Savory concentrate/seasoning, with vegetable fat. | Used as a cooking aid in the preparation of starch-rich food. | [ | |
| US 2020/0197429 A1 | Astragalus root; phlorizin; | Standardized extracts | Dietary supplement with the aim of controlling postprandial blood sugar. | [ |