Isorhamnetin Glycosides as Phytonutrients

Isorhamnetin Glycosides as Phytonutrients: Comparison

Please note this is a comparison between Version 2 by hong wang and Version 4 by Peter Tang.

Isorhamnetin glycosides (IGs) are a class of essential flavonoids derived from dietary and medicinal plants such as Opuntia ficus-indica, Hippophae rhamnoides, and Ginkgo biloba.

isorhamnetin glycosides
phytonutrients
health-promoting effects
sources

1. Introduction

Phytonutrients are chemical compounds that are only present in natural plants and are beneficial to the human body [1]. They are widely used in food and nutraceuticals due to their health-promoting benefits [2]. Flavonoids are a class of polyphenolic compound distributed in many fruits, vegetables, and plants [3]. The six major subclasses of flavonoids, which include flavones (e.g., luteolin), flavonols (quercetin), flavanones (hesperidin), catechins or flavanols (epicatechin), anthocyanidins (cyanidin), and isoflavones (daidzein), have been reported to represent various families of phytonutrients [4]. Accumulating evidence based on observational and clinical studies shows that a plant-based dietary pattern rich in fruits, vegetables, and whole grains has a clear effect on the prevention of various chronic diseases [5], and people also tend to consume dietary flavonoids from fruits and vegetables. Flavonoids are widely found in food, and most of them exist in their glycosidic forms ^[6][7][6,7].

Isorhamnetin glycosides (IGs), as natural flavonol compounds, are primarily extracted from various plant-based foods or medicinal plants such as Opuntia ficus-indica, Hippophae rhamnoides, and Ginkgo biloba ^[8][9][10][8,9,10]. IGs are biologically important flavonols with proven beneficial properties that give them medicinal value ^[11][12][11,12]. They possess diverse biological and pharmacological properties, such as antioxidant, anti-inflammatory, anti-cancer, antidiabetic, anti-obesity, and hepatoprotective properties ^{[13][14][15][16][17]}[13,14,15,16,17]. Due to their beneficial biological activities, IGs have been considered a significant potential class of phytonutrients, and an increasing number of products containing IGs are circulating on the market in many countries, including the United States, Canada, Mexico, China, India, and some European countries ^[18][19][18,19].

2. Structure of IGs

IGs are a type of glycosylated flavonol composed of an isorhamnetin skeleton and sugar groups. Their aglycone isorhamnetin, i.e., 3,4′,5,7-tetrahydroxy-3′-methoxyflavone, is an O-methylated flavonol (Figure 1). Generally, d-glucose, d-galactose, l-rhamnose, d-xylose, l-arabinose, sophorose, and rutinose are the most common sugar groups of IGs. They are linked to the aglycone by an O-glycosidic bond. According to the number of sugar groups, IGs are classified as mono-, di-, tri-, or tetra-glycosides. Position substitutions mostly happen at C-3 and C-7, for example, isorhamnentin-3-O-β-d-glucoside (4) and isorhamnetin-3-O-β-d-glucoside-7-O-α-l-rhamnoside (20) from Hippophae rhamnoids [20]; isorhamnetin-3-O-α-l-rhamnoside (3) from Laportea bulbifera Wedd. [21]; and isorhamnetin-7-O-β-d-glucoside (1) and isorhamnetin-7-O-α-l-rhamnoside (2) from Nitraria tangutorum Bolor [22]. Of course, sometimes, substitution occurs at C-4′, for instance, isorhamnetin-4′-O-β-d glucoside (9) from Allium cepa L. [23]; isorhamnetin-3,4′-O-β-d-diglucoside (17) from Allium ascalonicum [24]; isorhamnetin-3-O-β-d -glucoside-4′-O-β-d-xyloside (21) [25]; and isorhammetin-3-O-α-l-rhamnoside-(1→6)-β-d-glucoside-4′-O-β-d-glucoside (35) [26]. In addition, some sugar group derivatives, such as isorhamnetin-3-O-[2‴-O-acetyl−β-d-xyloside-(1→6)-β-d-glucoside] (10) [27] and isorhamnetin-3-O-β-d (6-acetyl-glucoside) (7) [28], have also been obtained.

Figure 1.

Basic parent nucleus of isorhamnetin glycosides (IGs).

Here, the researchers systematically summarize the 49 compounds of IGs reported thus far (Table 1 and Figure 2).

Figure 2. Chemical structures of IGs (compounds 1–49). Monoglycosides (1–9), diglycosides (10–34), triglycosides (35–48), and tetraglycosides (49). Abbreviations: Glc: D-glucose, Rha: L-rhamnose, Glccur: D-glucuronic, Gal: D-galactose, Xyl: D-xylose, Ara: L-arabinose. Abbreviations: Glc: d-glucose, Rha: l-rhamnose, Glccur: d-glucuronic, Gal: d-galactose, Xyl: d-xylose, Ara: l-arabinose.

Table 1. Isorhamnetin glycoside (IG) compounds (1–49). According to the number of sugar groups, IGs are divided into monoglycosides (1–9), diglycosides (10–34), triglycosides (35–48), and tetraglycosides (49).

No.	Name	Trivial Name	Source	Ref.
Monoglycosides
1	Isorhamnetin-7-O-β-d-glucoside	Brassicin	Centaurea cyanus Centaurea kotschyi var. kotschyi Cnicus wallichi Russowia Sogdiana Tagetes lucida (Asteraceae) Sedum sarmentosum Bunge Nitraria tangutorum Bolor	[29] [30] [31] [32] [33] [34] [22]
2	Isorhamnetin-7-O-α-l-rhamnoside		Carduncellus eriocephalus Nitraria tangutorum Bolor Atriplex centralasiatica Laportea bulbifera Wedd. V. galamensis ssp. galamensis var. petitiana (A. Rich) M. Gilbert Raphanus raphanistrum L. Caragana intermedia	[35] [22] [36] [21] [37] [38] [39]
3	Isorhamnetin-3-O-α-l-rhamnoside		Laportea bulbifera Wedd.	[21]
4	Isorhamnentin-3-O-β-d-glucoside		Astragalus centralpinus Solidago canadensis L. Hippophae rhamnoids Sambucus nigra L. Calendula officinalis	[40] [28] [20] [41] [42]
5	Isorhamnetin-3-O-β-d-glucuronide		Arnica montana Persicaria thunbergii Senecio giganteus Polygonum aviculare L. Senecio argunensis Turcz.	[43] [44] [45] [46] [47]
6	Isorhamnetin-3-O-β-d-(2-acetyl-glucuronide)		Polygonum aviculare L.	[46]
7	Isorhamnetin-3-O-β-d (6-acetyl-glucoside)		Solidago canadensis L.	[28]
8	Isorhamnetin-3-O-β-d-galactoside		Senecio argunensis Turcz.	[47]
9	Isorhamnetin-4′-O-β-d glucoside		Allium cepa L.	[23]
Diglycosides
10	Isorhamnetin-3-O-[2‴-O-acetyl−β-d-xyloside-(1→6)-β-d-glucoside]		Gymnocarpos decander	[27]
11	Isorhamnetin-3-O-[2‴,3‴-O-isopropylidene-α-l-rhamnoside]—(1→6)-β-d-glucoside		Tetraena aegyptia	[48]
12	Isorhamnetin-7-O-α-l-rhamnoside-(1→2)-β-d-glucoside	Isorhamnetin-7-O-β-neohesperidoside	Cleome droserifolia	[12]
13	Isorhamnetin-7-O-β-d-glucoside-(1→6)-β-d-glucoside	Astragaloside or Isorhamnetin-7-O-gentiobioside	Astragalus altaicus	[49]
14	Isorhamnetin-3-O-β-(4‴-p-coumaroyl-α-rhamnosy]—(1→6)-galactoside)		Aerva javanica	[50]
15	Isorhamnetin-3-O-α-l-rhamnoside-(1→2)-β-d-glucoside	Isorhamnetin-3-O-β-neohesperidoside	Hippophae rhamnoids Typha augustifolia L. Calendula officinalis	[20] [51] [42]
16	Isorhamnetin-3-O-β-d-xylosidel-(1→2)-β-d-galactoside		Prunus padus L.	[52]
17	Isorhamnetin-3,4′-O-β-d-diglucoside		Allium ascalonicum Lepidium apetalum willd	[24] [53]
18	Isorhamnetin-3,7-O-β-d-diglucoside		Sedum sarmentosum Bunge Carduncellus eriocephalus	[34] [35]
19	Isorhamnetin-3,7-O-α-l-dirhamnoside		Laportea bulbifera Wedd.	[21]
20	Isorhamnetin-3-O-β-d-glucoside-7-O-α-l-rhamnoside	Brassidine	Sinapis arvensis Atriplex centralasiatica Hippophae rhamnoids	[54] [36] [20]
21	Isorhamnetin-3-O-β-d-glucoside-4′-O-β-d-xyloside		Diplotaxis harra (Forssk.) Boiss	[26]
22	Isorhamnetin-3-O-α-l-rhamnoside-(1→6)-β-d-galactoside	Isorhamnetin-3-O-robinobioside	Nitraria retusa	[55]
23	Isorhamnetin-3-O-α-rhamnoside-(1→2)-rhamnoside		Laportea bulbifera Wedd.	[21]
24	Isorhamnetin-3-O-α-l-rhamnoside-(1→6)-β-d-glucoside	Narcissin Isorhamnetin-3-O-rutinoside	V. galamensis ssp. galamensis var. petitiana (A. Rich) M. Gilbert opuntia ficus-indica Hippophae rhamnoids Ginkgo biloba Sambucus nigra L. Calendula officinalis	[37] [18] [20] ^[9]^[56][9,56] [41] [42]
25	Isorhamnetin-3-O-β-d-apioide (1→2)-β-d-galactoside		V. galamensis ssp. galamensis var. petitiana (A. Rich) M. Gilbert	[37]
26	Isorhamnetin-3-O-α-l-arabinoside-7-O-β-d-glucoside		Callianthemum taipaicum Narcissus pseudonarcissus	[57] [58]
27	Isorhamnetin-3-O-β-d- (6‴-p-coumaroyl-α-glucoside-(1→2)-rhamnoside)		Ginkgo biloba	[56]
28	Isorhamnetin-3-O-β-d-glucoside-(1→2)-α-l-rhamnoside		Ginkgo biloba	[56]
29	Isorhamnetin-3-O-[2‴-O-acetyl−α-l-arabinoside-(1→6)-β-d-galactoside]		Trillium tschonoskii Maxim. Trillium apetalon Makino. and T. kamtschaticum Pallas.	[59] [60]
30	Isorhamnetin-3-O−α-l-arabinoside-(1→6)-β-d-galactoside		Trillium apetalon Makino. and T. kamtschaticum Pallas.	[60]
31	Isorhamnetin-3-O-α-(4″-acetyl-rhamnoside)-7-O-α-rhamnoside		Cleome droserifolia	[12]
32	Isorhamnetin-3-O-β-d-glucoside-7-O-α-l-arabinoside		Eschscholtzia mexicana Greene	[61]
33	Isorhamnetin-3-O-α-l-rhamnoside(1→2)]-β-d-galactoside		Glycine max (L.) Merr.	[62]
34	Isorhamnetin-3-O-β-glucoside-7-O-α-(3″′-isovaleryl)-rhamnoside		Lepidium apetalum	[53]
Triglycosides
35	Isorhamnetin-3-O-α-l-rhamnoside-(1→6)-β-d-glucoside-4′-O-β-d-glucoside	Isorhamnetin-3-rutinoside-4′-glucoside	Mercurialis annua	[26]
36	Isorhamnetin-3-O-(2^G-β-d-apiofuranosyl) [2‴-O-acetyl−β-d-xyloside-(1→6)-β-d-glucoside]		Gymnocarpos decander	[27]
37	Isorhamnetin-3-O-(2″,6″-O-α-l-dirhamnoside)-β-d-galactoside		Alangium premnifolium Lysimachia fortunei	[63] [64]
38	Isorhamnetin-3-O-(4^Rham-β-d-galactosyl)-α-l-rhamnoside-(1→6)-β-d-galactoside]	Isorhamnetin-3-O-4^Rham-galactosyl-robinobioside	Nitraria retusa	^[55]^[65][55,65]
39	Isorhamnetin-3-O-α-l-rhamnoside-(1→2)-β-d-galactoside-7-O-β-d-glucoside		Blackstonia perfoliata	[66]
40	Isorhamnetin-3-O-α-l-rhamnoside-(1→6)-β-d-glucoside-7-O-α-l-rhamnoside	Isorhamnetin-3-rutinoside-7-rhamnoside	Cassia italica Hippophae rhamnoides	[67] [68]
41	Isorhamnetin-3-O-β-glucoside-(1→2)-β-d-glucoside-7-β-d-glucoside	Brassicoside or Isorhamnetin-3-O-sophoroside-7-O-β-d-glucoside	Brassica napus	[54]
42	Isorhamnetin-3-O-β-d-xyloside-(1→3^Rham)-α-l-rhamnoside-(1→6)-β-d-galactoside	Isorhamnetin 3-xylosyl-robinobioside	Nitraria retusa	[55]
43	Isorhamnetin-3-O-β-glucoside-(1→2)-β-d-glucoside-7-O-α-l-rhamnoside	Isorhamnetin-3-O-sophoroside-7-O-rhamnoside	Hippophae rhamnoids	[20]
44	Isorhamnetin-3-O-[(6-O-E-sinapoyl)-β-d-glucoside-(1 → 2)]-β-d-glucoside-7-O-α-l-rhamnoside		Hippophae rhamnoids	[20]
45	Isorhamnetin-3-O-(2^G-α-l-rhamnoside)-α-l-rhamnoside-(1→6)-β-d-glucoside	Typhaneoside	Typha augustifolia L. Calendula officinalis	[51] [42]
46	Isorhamnetin-3-O-(2^G-β-d-glucoside)-α-l-rhamnoside-(1→6)-β-d-glucoside		Boldo Folium	[69]
47	Isorhammetin-3-O-α-l-rhamnoside-(1→6)-β-d-glucoside-7-O-β-d-glucoside	Isorhammetin-3-rutinoside-7-glucoside	Hippophae rhamnoids Mercurialis annua	[20] [26]
48	Isorhamnetin-3-O-β-d-glucoside-7-O-β-d-glucoside-(1→6)-β-d-glucoside	Isorhamnetin-3-O-glucoside-7-O-gentiobioside	Lepidium apetalum willd	[53]
Tetraglycosides
49	Isorhamnetin-3-O-[2^G-α-l-rhamnoside-(1→6)-β-d-glucoside]-α-l-rhamnoside-(1→6)-β-d-glucoside		Boldo Folium	[69]

3. Sources of IGs

IGs as nutritional supplements can be obtained from some foods and medicinal plants. Commonly consumed foods containing IGs include Hippophae rhamnoides, Opuntia ficus-indica, Vaccinium corymbosum, Vaccinium myrtillus, Brassica juncea, rice, and onions. The main medicinal sources of Igs are Ginkgo biloba, pollen Typhae, Microctis folium, Sambucus nigra, and Calendula officinalis (Figure 3).

Figure 3.

Plants with IG content.

4. IG Identification and Quantification Methods

Different techniques have been used for the characterization, identification, and quantification of IGs, including spectral techniques and chromatographic techniques. The following resviearchw addresses the applicability of the ultraviolet–visible spectrum (UV), infrared spectroscopy (IR), nuclear magnetic resonance (NMR), mass spectrometry (MS), thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), ultra-performance liquid chromatography (UPLC), and high-speed counter-current chromatography (HSCCC) methods developed for the determination of IGs.

4.1. Spectral Techniques and Mass Spectrometry

Various spectral methods have been employed for the identification and quantification of IGs. UV, IR, MS, and NMR have been used to determine the structure of IGs.

4.2. Chromatographic Techniques

IGs can be distinguished from each other on the basis of chromatographic techniques. Therefore, the analysis, characterization, and quantification of IGs are usually performed using the following chromatographic techniques: TLC, HPLC, UPLC, and HSCCC.

5. The Health-Promoting Effects of IGs

IGs possess a variety of biological properties, including antioxidant, anti-inflammatory, and anti-cancer properties. Research has recently been undertaken to investigate their pharmacological benefits for the treatment of various diseases, such as diabetes, obesity, hepatic diseases, and thrombosis.

5.1. Antioxidant Activity

Oxidative damage induced by free radicals results in detrimental outcomes, such as a loss of cellular function and the dysfunction of organic systems ^[70][121]. It is worth mentioning that numerous in vitro and in vivo studies have demonstrated the strong antioxidant and radical-scavenging properties of IGs. β-carotene-linoleic acid, 2,2-diphenyl-1-picrylhydrazil (DPPH) scavenging, 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS), oxygen radical absorbance capacity (ORAC), peroxyl radical-scavenging capacity (PSC), superoxide scavenging, peroxynitrite (ONOO(-)) assays, and CUPric reducing antioxidant capacity (CUPRAC) are commonly used indirect assays for identifying antioxidant activity. IGs isolated from the stamens of Nelumbo nucifera showed significant antioxidant activity, as determined via DPPH and ONOO(-) assays [11]. Brassicin (1) exhibited stronger free radical-scavenging ability than vitamin C [13] and exhibited DPPH radical- and ONOO(-)-scavenging activity ^[71][122]. Isorhamnetin 3-O-robinobioside (22), isorhamnetin 3-O-(2″,6″-O-α-dirhamnosyl)-β-galactoside (37) ^[72][123], typhaneoside (45), and isorhamnetin 3-O-neohesperidoside (15) ^[73][124] have been demonstrated to exhibit antioxidant activity using a DPPH radical-scavenging activity assay. Astragaloside (13) and narcissin (24) possessed antioxidant capacity, which was evaluated using ABST ^[74][118]. Narcissin (24) and isorhamnetin 3-O-rutinoside-7-O-glucoside (47) exhibited obvious antioxidant activity, which was detected using DPPH, β-carotene-linoleic acid, and ABST ^[65][75][65,125]. Isorhamnetin 3-O-neohesperidoside (15) was a potent inhibitor of xanthine oxidase and superoxide anion scavengers ^[76][126]. Furthermore, researchers have revealed the antioxidant properties of isorhamnetin 3-O-glucoside (4) and isorhamnetin 3-O-galactoside (8) in all the antioxidant activity tests employed ^{[77][78][79][80]}[127,128,129,130]. Evaluation of the antioxidant properties of IGs were also carried out using various cell type experiments and animal models. The oral administration of isorhamnetin-3,7-diglucoside (18) to streptozotocin-induced diabetic rats significantly reduced their levels of 5-(hydroxymethyl) furfural (5-HMF), which is an indicator of the glycosylation of hemoglobin, and of stress ^[81][95]. Similarly, isorhamnetin 3-O-robinobioside (22) exhibited significant antioxidant effects on the human chronic myelogenous leukemia cell line K562 ^[82][131]. IGs had the ability to inhibit the formation of H₂O₂-induced radicals in the surrounding environment of intestinal epithelial cells ^[83][132]. Moreover, the transcriptional genes of the antioxidant system and the DNA repair pathway were upregulated after incubation with isorhamnetin 3-O-neohesperidoside (15) in pKS plasmid DNA ^[84][133]. Narcissin (24) and isorhamnetin 3-O-glucoside (4) demonstrated strong inhibition of reactive oxygen species (ROS) production in the oxidative burst activity of whole blood, neutrophils, and mononuclear cells ^[85][134]. Plant extracts rich in IGs also exhibited antioxidant activity. IG-rich concentrate from Opuntia ficus-indica juice had the ability to inhibit the formation of H₂O₂-induced radicals in the surrounding environment of intestinal epithelial cells ^[86][135]. The total antioxidant activity of Hippophae rhamnoides berry extracts, evaluated via ORAC and PSC, was significantly associated with total phenolics, including isorhamnetin-3-rutinoside (24) and isorhamnetin-3-glucoside (4) ^[87][136].

5.2. Anti-Inflammatory Activity

IGs have anti-inflammatory properties due to different mechanisms. As an important inflammatory mediator, high-mobility-group protein 1 (HMGB1) contributes to organ damage and inflammation ^[88][138]. Isorhamnetin 3-O-galactoside (8) (5 μM) has been demonstrated to significantly inhibit the release of HMGB1 and reduce HMGB1-dependent inflammatory responses in human endothelial cells. It was found that 8 (4.8 mg/mouse) could also inhibit HMGB1 receptor expression, the HMGB1-mediated activation of NF-kB, and the production of tumor necrosis factor (TNF-α) in mice ^[89][139]. Mitogen-activated protein kinase (MAPK) signaling pathways, including p38, c-Jun N-terminal kinase (JNK), and extracellular regulated kinases (ERK), play crucial roles in inflammatory responses ^[90][140]. Isorhamnetin 3-O-galactoside (8) (50 μM) reduced cecal ligation and endothelin C receptor perforation-mediated shedding and down-regulated the phosphorylation of p38 MAPK, ERK 1/2, and JNK [14]. Similarly, isorhamnetin 3-O-glucuronide (5) exhibited anti-inflammatory activity by increasing heme oxygenase-1 (HO-1) expression and suppressing the JNK and p38 signaling pathways in LPS-induced RAW264.7 macrophage cells ^[91][141]. Moreover, isorhamnetin 3-O-glucuronide (5) inhibited the production of ROS (10 μM), as well as the release of elastase, in a human neutrophil model (1 μM) and suppressed the upregulation of inducible nitric oxide synthase (iNOS) expression (5 μM), and could be considered to display anti-inflammatory activity ^[46][92][46,142]. Many studies have shown the anti-inflammatory properties of IGs by inhibiting inflammatory cytokines. The inflammatory activity of narcissin (24) (100 μM) and isorhamnetin 3-O-glucoside (4) (100 μM) was mediated via the inhibition of nuclear factor kappa-B (NFκB) and inflammatory mediators such as TNF-α, interleukin-1β (IL-1β), and interleukin-6 (IL-6) in phytohaemagglutinin-stimulated human peripheral blood mononuclear cells (PBMC) ^[83][132]. Likewise, narcissin (24) (40 μM) achieved the inhibition of inflammatory cytokines (TNF-α, IL-1β, and IL-6) in advanced glycation end product (AGE)-induced RAW264.7 cells ^[93][143]. Isorhamnetin-3-O-[2,3-O-isopropylidene-α-l-rhamnopyranosyl]-(1→6)-O-β-d-glucopyranoside (11) (25 μM) showed a significant inhibitory effect on NO release and the secretion of the cytokines IL-6 and TNF-α [48]. Isorhamnetin-3,4′-diglucoside (17) (100 μg/mL) and isorhamnetin 3-O-glucoside (4) (100 μg/mL) have shown the inhibitory effect of IL-6 production on TNF-α-stimulated human osteosarcoma MG-63 cells ^[94][144]. Isorhamnetin 3-O-glucoside (4) (100 μg/mL) showed distinct anti-inflammatory activity with no toxicity on RAW 264.7 macrophage cells as compared to dexamethasone ^[95][145]. Seddik Ameur et al. studied the anti-inflammatory activity of IGs extracted from Opuntia ficus-indica flowers, and their results showed that isorhamnetin-3-O-robinobioside (22) is the product responsible for the anti-inflammatory activity ^[96][146]. Both Opuntia ficus-indica extract (OFI-E) and isorhamnetin-3-O-rhamnosylglucoside (24) (125 ng/mL) significantly inhibited cyclooxygenase-2 (COX-2), TNF-α, and IL-6 production, of which 24 compounds have been suggested to be suitable natural compounds for the development of a new anti-inflammatory ingredient ^[97][147]. The total flavonoid-rich IGs from sea buckthorn exhibited a protective effect against LPS/CS-induced airway inflammation by inhibiting the ERK, PI3K/Akt, and PKCα pathways and diminishing the expression of IL-1β, IL-6, and COX2 in mice ^[98][148].

5.3. Anti-Cancer Activity

Flavonoids have great potential for anticancer prevention ^[99][149]. IGs have also been proven to possess anticancer effects. Brassicin (1) (22.8 µg/mL) showed in vitro cytotoxicity against human colon cancer cells in the HCT116 cell line ^[100][150]. Isorhamnetin 3-O-neohesperidoside (15) (2.47 μg/mL) showed potent cytotoxicity against breast ductal carcinoma and colorectal adenocarcinoma (Caco-2) cells ^[101][151]. Narcissin (24) showed cytotoxic effects in Hela cells and the hormone dependent prostate carcinoma LNCaP cell line (IC₅₀ = 20.5 μg/mL) ^[102][103][152,153]. Mechanically, IGs have been involved in the induction of apoptosis and the inhibition of cancer cell proliferation (Figure 4A). Apoptosis, the most vital cell death mechanism, ultimately contributes to tumor progression ^[104][154]. Mitochondria play an essential role in cell death signaling and ROS generation ^[105][155]. The production of ROS above a threshold level can trigger apoptosis in cancer cells, thereby limiting further cancer progression ^[106][156]. After the excessive production of ROS, the expression of genes related to the mitochondrial apoptosis pathway (Bax, Caspase9, and Caspase3) was aggravated, and the expression of the anti-apoptotic gene Bcl-2 was reduced ^[107][157]. Emerging evidence suggests that IGs promote ROS generation and the activation of mitochondria-dependent apoptosis in cancer cells (Figure 4B).

Figure 4.

Anticancer activity (

) and mechanism of regulating the apoptotic pathway (

) of IGs.

5.4. Hepatoprotective Ability

The liver is the most essential and functional organ in the body, and it is where primary detox and metabolic events occur ^[108][167]. Liver injury can be caused by various factors, including alcohol, microbial infection, drugs, biological toxins, and chemical agents ^[109][168]. Flavonoids in many different foods and medicinal plants have therapeutic potential in liver disease ^[110][169]. Studies have confirmed that IGs play an important role in liver injury by modulating multiple pathways (Figure 5). The hepatoprotective effects of IGs are closely linked with their antioxidant and anti-inflammatory effects. Isorhamnetin 3-O-galactoside (8) (100 mg/kg) reduced serum TNF-α levels, aminotransferase activities, and the hepatic level of malondialdehyde (MDA); attenuated increases in iNOS and COX-2 protein and mRNA expression levels; attenuated increases in nuclear factor kappa-B (NF-κB) and c-Jun nuclear translocation; and augmented the levels of HO-1 and mRNA expression and the nuclear level of nuclear factor E2-related factor 2 (Nrf2) in a carbon tetrachloride (CCl₄)-induced hepatic damage model (Figure 5A). This suggests that IGs exhibit hepatoprotective effects by enhancing the antioxidative defense system and reducing the inflammatory signaling pathways [16]. A similar result was obtained for the hepatoprotective effects of isorhamnetin 3-O-glucoside (4) (20 μg/mL/mouse). It suppressed the increase in plasma alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities in CCl₄-induced liver injury mice ^[111][170]. Opuntia ficus-indica fruit juice (3 mL/rat) administration exerted protective and curative effects against the CCl₄-induced degenerative process in rat liver ^[112][171]. The oral administration of a phenolic-rich fraction of sea buckthorn leaves (25–75 mg/kg) significantly protected against CCl₄-induced elevation in AST, ALT, c-glutamyl transpeptidase, and bilirubin in the serum, and also protected against histopathological changes produced by CCl₄, such as hepatocytic necrosis, fatty changes, and vacuolation ^[113][172]. In another study, typhaneoside (45) exhibited hepatoprotective effects on D-GalN-induced cytotoxicity in primary cultured mouse hepatocytes ^[114][173]. The phytochemical constituents of cactus branch extract (92 mg/kg), which were found to possess excellent antioxidant properties, had protective effects against lithium-induced hepatotoxicity and oxidative stress in rats ^[115][174].

Figure 5. Hepatoprotective mechanism of IGs. Networks of molecular signaling underlying anti-oxidative stress and anti-inflammatory effects of IGs in CCl₄-induced hepatic damage(A). IGs inhibit TGF-β-induced activation of HSCs through the DNA damage pathway (B). Hepatic metabolic pathways through which IGs alleviate the adverse effects of ethanol (C).

IGs also had an improvement effect on hepatic lipid accumulation. In high-fat diet-fed mice, OFI-E (0.3%, 0.6%) reduced fatty acid synthesis and increased fatty acid oxidation and caused a decrease in hepatic fat accumulation, thereby preventing hepatic steatosis ^[116][70]. Isorhamnetin-3-O-glucoside (4), isorhamnetin, 3,4′-diglucoside (17), and isorhamnetin 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (47) (30 µM) had significant inhibitory effects on sodium oleate-induced triglyceride overloading in HepG2 cells [53]. Furthermore, biochemical and histopathological studies showed that sea buckthorn flavonoids (200 mg/kg, po) significantly improved biomarkers in the serum and liver of tetracycline-induced nonalcoholic fatty liver mice ^[117][175]. Zhang G et al. observed that isorhamnetin-3-O-β-d-glucopyranoside-7-O-α-l-rhamnoside (20) (40 μM) exhibited a profound inhibitory effect on the activation of hepatic stellate cells (HSCs) induced by transforming growth factor-β (TGF-β), and decreased the levels of inflammatory factors. It over-regulated the proteins of the DNA damage signaling pathway, including the ataxia telangiectasia mutated gene (ATM), Rad3-related gene (ATR), checkpoint kinase1 (Chk1), checkpoint kinase2 (Chk2), p53, and alpha-smooth muscle actin (α-SMA) (Figure 5B) ^[118][176]. In addition, the active components of sea buckthorn berry (20 and 40 mg/kg) had inhibitory effects on the development of fibrosis in rats after bile duct ligation, and they attenuated liver injury and inflammation by downregulating the expression of αSMA, while over-regulating the DNA damage signaling pathways and their related genes. Isorhamnetin 3-O-β-d-glucopyranoside (4) alleviated the adverse effect of ethanol ingestion by enhancing the activities of alcohol dehydrogenase (ADH), the microsomal ethanol oxidizing system (MEOS), and aldehyde dehydrogenase (ALDH) in a hepatic alcohol-metabolizing enzyme system in rats (Figure 5C) ^[119][177]. In addition, sea buckthorn fermentation liquid (1.75, 2.675, 5.35 g/kg) protected against alcoholic liver disease and modulated the composition of the gut microbiota. It lowered ALT, AST, TNF-α, MDA, and IL-6, while modulating the gut microbiota composition ^[120][178].

5.5. Antidiabetic Activity

The antidiabetic properties of IGs may appear through different functions. IGs inhibit various pathways associated with the progression of diabetes, including the regulation of glucose metabolism and enhancing insulin secretion ^[121][179]. IGs exert inhibitory activity on several enzymes involved in diabetes management. In the small intestine, IGs inhibit the activity of α-amylase and α-glucosidase, thereby reducing the conversion of dietary saccharides into easily absorbed monosaccharide, and thus, reducing the postprandial enhancement of blood glucose levels (Figure 6). Isorhamnetin-3-O-glucoside (4) showed a strong ability to bind to α-amylase and α-glucosidase (the IC₅₀ values were 0.16 ± 0.06 and 0.09 ± 0.01 µM) ^[122][180]. Narcissin (24) (IC₅₀ = 0.129 mM) could be useful in lowering postprandial blood glucose by inhibiting α-amylase activity ^[123][181]. Meanwhile, 24 was a good 15-lipoxygenase (IC₅₀ = 45 ± 2 µM) inhibitor ^[124][125][182,183]. Isorhamnetin glucosyl-rhamnosyl-pentoside (50 μg/mL) was reported to exhibit antihyperglycemic activity by inhibiting α-amylase activity ^[126][184]. Sea buckthorn aqueous extracts were correlated with lipase/α-amylase inhibitory activity in all phases of a digestion model in vitro, with gastric and intestinal fractions largely inhibiting enzyme activity ^[127][185].

Figure 6.

Mechanism of IGs inhibiting α-amylase and α-glucosidase.

5.6. Anti-Obesity Activity

Flavonoids could protect against obesity-related pathology by inhibiting adipogenesis and exerting anti-inflammatory activity ^[128][192]. Sea buckthorn leaf extract contains a high content of flavonoid glycosides, especially isorhamnine-3-glucoside (4) and quercetin-3-glucoside ^[129][78]. Flavonoid glycosides extracted from sea buckthorn leaves (SLGs) could suppress diet-induced obesity in C57BL/6J mice ^[130][98]. In this researchtudy, the researcheauthors mentioned that 12 weeks of oral administration with a high-fat diet (HFD, 60 kcal% fat) + 0.04% (w/w) SLGs significantly prevented adiposity and dyslipidemia by suppressing lipogenesis and the absorption of dietary fat. This anti-obesity effect was explained by the improvement of inflammation and a decrease in gluconeogenesis. Narcissin (24) and 4 (30 μM) showed moderate inhibitory effects on triglyceride and glycerol-3-phosphate dehydrogenase activity in a 3T3-L1 preadipocyte ^[131][193]. Furthermore, it was demonstrated by Chang-Suk Kong et al. that 4 (20 μM) potently suppressed adipogenic differentiation by downregulating peroxisome proliferator-activated receptor-γ, CCAAT/enhancer-binding proteins, sterol regulatory element-binding protein 1, and the adipocyte-specific proteins in 3T3-L1 preadipocytes. Furthermore, the specific mechanism mediating its action occurred through the activation of AMPK ^[132][194].

5.7. Antithrombotic Activity

Thrombosis is a critical event in diseases correlated with atherosclerosis, myocardial infarction, and stroke ^[133][198]. The aggregation of platelets at the site of injury, as well as thrombin generation and fibrin formation triggered by the activation of tissue factors, are involved in thrombosis formation ^[134][199]. Therefore, the therapeutic mechanism includes the inhibition of platelet activation, adhesion, and aggregation, the improvement of fibrinolytic system function, and the regulation of coagulation system function ^[135][200].

5.8. Toxic Effects

Flavonoids are natural components of fruits, vegetables, tea, wine, traditional medicines (such as ginkgo biloba), and a considerable number of herbal dietary supplements. With growing interest in alternative medicine, the general population is consuming more flavonoids ^[136][203]. Since flavonoids are common edible ingredients in our daily diets, research on their potential cytotoxicity is warranted. Currently, there are no systematic toxicological studies on 目前，还没有关于IGs, and further studies are needed. Bee bread (BB) is a fermented mixture of plant pollen, honey, and bee saliva, and is rich in flavonoid glycoside derivatives ^[137]. 的系统毒理学研究，需要进一步的研究。蜂面包（BB）是植物花粉、蜂蜜和蜂唾液的发酵混合物，富含类黄酮苷衍生物[204]。Filipa Sobral et al. collected a variety of 等收集了多种BB samples, and the most abundant compounds in BB1 (>400 µg/mL) were isrohamnetin样品，BB1（>400μg/mL）中丰度最高的化合物是异鼠李素-O-hexosyl己糖基-O-rutinoside and isorhamnetin芸香糖苷和异鼠李素-O-pentosyl-hexoside. They found that the 戊糖基己糖苷。他们发现BB1 sample showed no toxicity to non样本对非肿瘤猪肝原代细胞没有毒性[205]。从披针叶松花序分离的异鼠李素-tumor porcine liver primary cells ^[138]. Isorhamnetin-3-rutinoside芸香糖苷-4′-glucoside (葡萄糖苷（35), isolated from P. lanceolata inflorescences, showed significantly less cytotoxicity towards the nontumorigenic cell line ）在浓度为12μM时对非致瘤细胞系MCF-12A at a concentration of 400 µM ^[139]. IsorhamnetinA的细胞毒性显著降低[206]。异鼠李素-3-O-β-d-galactopyranoside (吡喃半乳糖苷（8) and isorhamnetin）和异鼠李素-3-O-β-d-glucopyranoside (吡喃葡萄糖苷（4) (）（100 µg/mL) isolated from Salsola imbricata μg/mL）从Forssk.分离。 exhibited no cytotoxicity in 在RAW 264.7 macrophage cells ^[140]. Furthermore, it was demonstrated that the viability of PBMCs was slightly decreased after 48 h of incubation with isoretin巨噬细胞细胞中无细胞毒性[158]。此外，结果表明，在与来自约翰斯托尼的异维视黄醇-348-O-O芦丁（3）（24-rutin (24) (0–μM）孵育180 µM) from Cyrtosperma johnstonii. However, the decrease in cell viability was no greater than 小时后，PBMC的活力略有降低。然而，细胞活力下降不超过30% ^[141]. A brine shrimp toxicity assay of extracts and isolated compounds from Terminalia macroptera leaves showed that narcissin ([207]。盐水虾毒性测定从大翅目终叶中提取物和分离的化合物显示，水仙素（24) was not toxic against brine shrimp larvae at the tested concentrations (）在测试浓度（200 µM) ^[124]. μM）下对盐水虾幼虫无毒[182]。

6. Bioaccessibility of IGs IG的生物可利用性

The bioaccessibility of bioactive compounds refers to the maximum fraction of the compound released from the food matrix into the lumen of the gastrointestinal tract to be absorbed ^[142]. Most flavonoids exist in nature as glycosides, in which sugar residues modify the absorption mechanism and their ability to enter cells or interact with transporters and cellular lipoproteins ^[143][144]. Flavonoid glycosides exhibit better bioavailability both in vitro and in vivo, which is probably due to their higher aqueous solubility and stability during digestion ^[8]. At the same time, the gut microbiota plays an important role in improving the bioavailability and enhancing the absorption of flavonoids ^[145]. The deglycosylation of flavonoid glycosides by the gut microbiota enhances the bioavailability of flavonoids ^[146].生物活性化合物的生物可利用性是指化合物从食物基质释放到胃肠道腔中被吸收的最大比例[208]。大多数类黄酮在自然界中以糖苷的形式存在，其中糖残基改变了吸收机制及其进入细胞或与转运蛋白和细胞脂蛋白相互作用的能力[209，210]。类黄酮苷在体外和体内均表现出更好的生物利用度，这可能是由于它们在消化过程中具有更高的水溶性和稳定性[8]。同时，肠道菌群在提高生物利用度和增强类黄酮吸收方面起着重要作用[211]。肠道微生物群对类黄酮苷的去糖基化可提高类黄酮的生物利用度[212]。 Compared with isorhamnetin aglycone, 与异鼠李素苷元相比，IGs have higher accessibility. 具有更高的可及性。Antunes-Ricardo et al. found that glycosylation protected isorhamnetin from degradation during simulated digestion, and IGs were better retained in the circulatory system than aglycone ^[8]. Isorhamnetin等人发现，糖基化可保护异鼠李素在模拟消化过程中不降解，IG比糖苷元更好地保留在循环系统中[8]。杏仁皮中的异鼠李素-3-O-rutinoside (24) (芸香糖苷（24）（93.2 ± 0.2%) and isorhamnetin 3-0.2%）和异鼠李素3-O-glucoside (葡萄糖苷（4) (66.8 ）（66.8± 1.7%) from almond skins showed higher bioaccessibility than isorhamnetin (25.1 ± 7.0%) after simulated digestion ^[147]. Isorhamnetin glucosyl）在模拟消化后表现出比异鼠李素（25.1±7.0%）更高的生物可利用性[213]。异鼠李素葡萄糖基-rhamnosyl鼠李糖基-rhamnoside, isorhamnetin glucosyl-rhamnosyl-pentoside, isorhamnetin hexosyl鼠李糖苷、异鼠李素葡萄糖基-鼠李糖基戊糖苷、异鼠李素己糖基-己糖基戊糖苷和异鼠李素葡萄糖基戊糖苷在体外模拟胃肠道消化过程中在214个仙人掌品种的果皮中显示出较高的生物可利用性[58]。异鼠李素葡萄糖基-hexosyl鼠李糖基-pentoside, and isorhamnetin glucosyl-pentoside showed high bioaccessibility in the peels of four prickly pear varieties during in vitro simulated gastrointestinal digestion ^[148]. Isorhamnetin glucosyl-rhamnosyl-rhamnoside and isorhamnetin glucosyl-pentoside in Opuntia ficus鼠李糖苷和异鼠李素葡萄糖基戊糖苷在仙人掌-indica cladodes showed bioaccessibility values of 5籼稻枝中的生物利用度值分别为38% and 38和215% ^[149].[<>]。 It was also reported that the antidiabetic, anti-inflammatory, and antiallergic activities of flavonoid glycosides were similar or even higher than those of aglycones when provided orally ^{[150][151][152][153]}. The effect of flavonoid glycosides is beneficial, probably due to the fact that flavonoid glycosides maintain higher plasma concentrations and have a longer mean residence time in the blood than aglycones ^[154]. Typhaneoside (另据报道，类黄酮苷类苷的抗糖尿病、抗炎和抗过敏活性与口服糖苷元相似甚至更高[216，217，218，219]。类黄酮苷的作用是有益的，可能是因为类黄酮苷比糖苷保持更高的血浆浓度，并且在血液中的平均停留时间更长[220]。大鼠口服花粉伤寒提取物后立即检测到鼠寒苷（45) and isorhamnetin）和异鼠李素-3-O-neohesperidoside (新橙皮苷（15) were detected immediately after the oral administrations of pollen typhae extract in rats, indicating that they were rapidly absorbed after oral administration ^[155][156]. ），表明口服后被迅速吸收[86，221]。沙棘浆果中的IGs in sea buckthorn berries were monoglucuronidated in humans and were readily bioavailable ^[157]. Following the ingestion of lightly fried onions, flavonols were absorbed into the plasma of humans as glycosides, with a higher accumulation of isorhamnetin在人类中是单葡萄糖醛酸化的，并且易于生物利用[222]。摄入轻炸洋葱后，黄酮醇以糖苷的形式被吸收到人血浆中，血浆和尿液中异鼠李素-4′-glucoside (葡萄糖苷（9) in the plasma and urine than quercetin conjugates, which indicated that ）的积累量高于槲皮素缀合物，这表明9 may be preferentially absorbed ^[158]. Similarly, the results of a randomized crossover supplementation trial in female volunteers showed that 可能优先被吸收[223]。同样，一项针对女性志愿者的随机交叉补充试验结果显示，9 underwent significant elevation in the plasma after the ingestion of onion powder ^[159]. 例在摄入洋葱粉后血浆显著升高[224]。Antunes-Ricardo et al. reported that 等报道，在榕树中天然发现的IGs found naturally in O. ficus-indica have a longer elimination half-life than isorhamnetin, suggesting that they can maintain constant plasma concentrations, and thus, prolong their biological effects ^[8].比异鼠李素具有更长的消除半衰期，这表明它们可以保持恒定的血浆浓度，从而延长其生物效应[8]。平面亲脂性多酚，如姜黄素、表没食子儿茶素没食子酸酯、槲皮素和染料木素，因其能够干扰膜偶极电位，被称为Planar lipophilic polyphenols, such as curcumin, epigallocatechin gallate, quercetin, and genistein, are known as Pan-Assay Interference Compounds (PAINS) or Invalid Metabolic Panaceas (IMPS) because of their ability to interfere with membrane dipole potential ^[160]. AINS或无效代谢灵丹妙药（IMPS）[225]。Ana Marta de Matos et al. demonstrated that compounds produced via 等人证明，通过C-glycosylation are no longer able to alter the membrane dipole potential ^[161]. However, 糖基化产生的化合物不再能够改变膜偶极电位[226]。然而，O-glycosylated compounds are easily hydrolyzed in the gut, so they are not suitable for this strategy. There are no more studies on the interference of isorhamnetin glycosides on membrane dipole potential, so further research in this field is warranted.糖基化的化合物很容易在肠道中水解，因此它们不适合这种策略。关于异鼠李素糖苷对膜偶极电位的干扰，目前还没有更多的研究，因此有必要在该领域进行进一步的研究。