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International Journal of Phytomedicine and Phytotherapy

Current findings and future prospective of high-value trans Himalayan medicinal plant Lycium ruthenicum Murr: a systematic review



The genus Lycium is commercially known for its nutrient dense goji-berries, among these berries, black goji-berries obtained from Lycium ruthenicum Murr are highly valued and widely used as traditional medicine in trans-himalayan cold desert Ladakh and as functional food in several countries.


The current collection of data and literature was done by exploring different scientific portals like SciFinder, Google scholar, PubMed, Dictonary of Natural Products, Institute for Scientific Information, Web of Science and Scopus by searching keywords like black goji berry, crystal pearl, and trans-Himalayan plant.


Fruits of L. ruthenicum Murr, are overwhelmingly enriched in anthocyanins, proanthocyanidins, polysaccharides, spermine and spermidine alkaloids. The presence of these bioactive phyto-chemicals has been linked with reported anti-diabetic, anti-inflammatory, anti-fatigue, anti-atherosclerosis and neuro-protective properties of black goji berries. A unique color of these berries makes them exceptional as compared to other berries.


In this article, we have reviewed the variety of high value phytochemicals of Lycium ruthenicum Murr, with a special focus on health promoting anthocyanins which will provide an insight to the readers for exploring novel applications of L. ruthenicum Murr in field of medicine and food industries.


For thousands of years in Southeast Asia, more precisely in China, the Lycium genus has been a valued source of medicines and nutrients. This genus carries perennial flowering plants in the family Solanaceae and has 97 species and 6 varieties predominantly distributed across South America, South Africa, China and a few species in temperate Europe and Asia [1]. Among them, only twelve species have been studied to date, out of which three species, viz. L. chinese, L. barbarum and L. ruthenicum Murr are highly valued for their medicinal properties. Due to presence of plethora of biological active compounds, this genus has gained attention in recent years. The berries of L. barbarum and L. chinese are red colored while those of L. ruthenicum Murr are of purple-black color, all these are commonly known as Goji-berry or wolfberry. L. barbarum and L. Chinese are well- studied plants and have been found to possess various therapeutic properties like anti-glaucoma, immune-regulatory, anti-tumor, anti-oxidant, anti-aging, neuroprotective and blood sugar level reducing activities to name a few while L. ruthenicum Murr remains a relatively under-studied plant of the genus [2]. Its unique violet-black appearance make it more promising in respect of nutritional food as well as a potent candidate for health promoting effects in world.

The present review compiles available information concerning phyto-fingerprinting, geographical distribution in the Indian Himalayan region, and traditional medicinal uses of L. ruthenicum Murr with a special focus on its natural habitat in Jammu, Kashmir and Ladakh regions in India till date, earlier Wang et al [3] studies were mainly focused on Chinese medicinal uses and restricted to China only thus it create our necessity to compile this review aimed at providing comprehensive and current information regarding the pharmacological potentials of Lycium ruthenicum Murr based on its geographical location too. The present review critically analyzes the findings of scientific studies conducted on L. ruthenicum Murr to date and presents detailed phytochemistry of its bioactive compounds along with their respective pharmacology. For this purpose, a total of 106 scientific references have been studied and compared to compile the present review.

Habitat and botanical characteristics

The population of L. ruthenicum Murr is localized to the areas of central Asia, Turan and generally dispersed in SW Asia, Europe and America. In Asia, it is distributed from China (Gansu, Nei Mongol, Ningxia, Qinghai, N Shaanxi, Xinjiang, Xizang) to Afghanistan, Pakistan, Russia, Tajikistan, Turkmenistan, Uzbekistan and Indian Himalayas [4]. In India only two species, viz. L. ruthenicum Murr and L. barbarum have been reported date. L. ruthenicum Murr is widely distributed in the Trans-Himalayan Ladakh region at an altitude of 3063–3196 m (34ﹾ35.28′ N, 077ﹾ27.48′E) above mean sea level, chiefly growing on roadsides of Hunder and Udmaru areas of Nubra valley where it is locally known as ‘Khizer’ [5]. The earliest floristic record of L. barbarum mentioned that it is an endemic plant of Kashmir, India, and supposed to be the “Wozej Beri” ( Lycium ruthenicum Murr is a long-lived, deciduous, perennial and thorny shrub that belongs to the nightshade plant family, i.e. Solanaceae (Fig. 1). It can grow up to 2 m and has small sessile leaves; zig- zagged bending of stems, internodes with short thorns and extensive roots [6,7,8].

Fig. 1

a. Lycium ruthenicum Plant b & c. Plant with ripen Fruits d. Developmental stages of Fruit e Close up view of leaves

The hermaphrodite funnel- shaped flowers are pale-purple in color and are pollinated by bees (PFAF Plant Database One to two flowers are found on short shoots with 5–10 mm pedicel with the campanulated calyx of the size of 4.5 mm that are irregularly lobed and are ciliated. The seeds of L. ruthenicum Murr germinate during the late spring or early summer season, while the bushes flower during months of June–July and fruits are borne during August–September [5]. The fruits are 6–9 mm long, black-purple ellipsoid berries, commonly called black goji berry (Fig. 1). Being a native of an arid environment, this plant prefers well-drained soil and can grow in nutritionally poor soil which makes it an extremely draught and salt-resistant [9, 10].

Local and traditional uses

These dark violet purple color berries have been recorded in the classic Tibetan pharmacological book “Crystal Pearl of Materia Medica” and in Chinese medical monographs as Jing Zhu Ben Cao” and “Si Bu Yao Dian” [11]. In India, these berries have been used by Amchi in various herbal formulations as medicine or as a coloring agent [12]. It has been reported that traditionally the fruits have been used as remedies for the treatment of many diseases such as heart diseases, abnormal menstruation, urethral stones, tinea, furuncle, hypertension, menopause, treatment of blindness in camels in mountain communities especially in the Chinese and Tibet medicine systems [11,12,13,14,15,16]. while leaves are used as diuretic agent to remove blocked urine [17]. The berries have been endorsed as one of the richest known sources of anthocyanins, essential oils, organic acids, trace minerals and polysaccharides have long been used as traditional functional food and used as a herbal tea too (Organic-Natural-Wolfberry-Ruthenicum-Berries/dp/B07P3VGK25). Even in modern pharmacological research, it’s utility as an anti-atherosclerotic, anti-oxidant, cell-mediated immune-enhancer, anti-tumorogenic, hepatic-function protector, anti-fatigue, anti-aging, hypolipidemic and hypoglycemic agent [18]. Although, scientific validation of such medicinal use is missing till date. Most of these traditional uses are based on folk experiences passed over generations without a scientific understanding of the underlying biological mechanism and detailed structure-activity relationship (SAR) of its key bioactive phyto-compounds warranting in-depth scientific studies on biological mechanisms and activities of specific phytoconstituents. Only recently some of the biological activities of berries have been studied in pre-clinical experimental settings discussed below.

Phytochemical composition and their pharmacological activities

Though limited in number, few research reports are available that describe the phytochemical profile of the Lycium ruthenicum Murr, the same has been compiled in Table 1. The reported chemical constituents majorly include anthocyanins, proanthocyaninidins, carotenoids, fatty acids and essential oils, coumarins and cinnamate derivates, polysaccharides, alkaloids and phenolic acids. Among all these, the anthocyanins, which fall under the flavonoids class of compounds, are the most bioactive chemical constituents responsible for most of the reported medicinal properties of L. ruthenicum Murr [3]. A comparison of anthocyanin content in L. ruthenicum Murr concerning other known sources of anthocyanins is given in Table 2. Their unique color makes them more valuable, due to scarcity of these berries in China; their price is 10 times of red goji berries [30].

Table 1 Class of Compounds and their percentage of Black Goji Berry
Table 2 Anthocyanins content of different plant’s Berries

Nutritional enrichment

The fruit of L. ruthenicum Murr has been reported to contain γ- Vitamin E (VE, (0.0075 mg/g) and δ-Vitamin E (VE) (0.016 mg/g). Also, the oil from L. ruthenicum Murr is known to be rich in α-VE, γ-VE and δ-VE, the reported values of these are 0.1906,1.8939 and 0.045 mg/100 g, respectively. Among these leucine, methionine, isoleucine and phenylalanine are present at a significantly higher level compared to other amino acids Overall, these tiny berries are nutritionally dense and offer a holistic package of health promoting phytonutrients [31, 32].

Polysaccharides (1–7)

Polysaccharides are the functional components found in the fruits of the Lycium genus and have been extensively studied for their therapeutic merits. The polysaccharides in L. ruthenicum Murr berries constitute nearly 10 to 17% of the total dry weight [19, 32, 33]. Several polysaccharides from L. ruthenicum Murr (LRPs) have been isolated and purified from aqueous extracts of fruits using various methods such as anion-exchange chromatography, gel filtration chromatography, high-performance gel permeation chromatography and high-performance liquid chromatography (HPLC) [3]. Their structural composition has been studied by analytical and chemical methods, including methylation analysis, partial acid hydrolysis, IR (infrared spectroscopy), 1D and 2D NMR (nucleic magnetic resonance) and ESI-MS (electrospray ionization mass spectrometry), gas chromatography. These polysaccharides are complex glycopeptides consisting of hetero-polysaccharides and proteins. Various LRPs isolated and characterized from crude L. ruthenicum Murr have been described earlier by Wang et al [3] with their molecular mass, yield and structural composition which includes water-soluble glycoconjugate polysaccharide LRGP1 with molar mass 56.2 kDa, an arabinogalactan-protein LRGP3 with a molecular mass of 75.6 Kd LRP4-A with a molecular mass of 1.05 × 105 Da, LRP4-A and LRGP5 from fruit extract [34,35,36,37]. Researchers had isolated another immunological active polysaccharides named LRLP4-A with a molecular mass of 135 kDa from leaves of L. ruthenicum Murr [38]. In our section we have described two more polysaccharides isolated from the fruit extract i.e LRP-S2A with a relative molecular weight of 2.65 × 106 Da and an uronic acid content of 41.8%, contained Rha, Ara, Gal, Glc and GlcA in a molar ratio of 1.00: 2.07: 0.57: 2.59: 4.33 was composed of a backbone consisting of 6-O-Me-α-(1 → 4)-D-GlcpA, 2-O-acetyl-α-(1 → 4)-D-Glcp, α-(1 → 2,4)-L-Rhap, β-(1 → 3)-D-Galp andα-(1 → 3,5)-L-Araf, and some branches consisting of 6-O-Me-α-(1 → 4)-D-GlcpA and terminal α-L-Araf [39]. Another homogeneous polysaccharide, LRP3-S1 with a relative molecular weight of 114.8 kDa was purified by anion-exchange chromatography on DEAE Sepharose™ fast flow and sephacryl S− 300 HR column by Zhang et al. [33]. All LRPs isolated and characterized from L. ruthenicum have been compiled in Table 3. Given well- established safety and therapeutic merits of plant-based polysaccharides, L. ruthenicum Murr holds promise as an enriched source of bioactive polysaccharides and thus calls for a more intense analytical investigation.

Table 3 Isolated Polysaccharides in fruit and Leaves of Black Goji berries

Alkaloids (8–42)

They are one of the large groups of organic compounds that usually contain at least one nitrogen atom in a heterocyclic ring occurring chiefly in the flowering plants. The presence of nitrogen makes them alkaline. Based upon their respective structures, they can be divided into various types like indoles, quinolines, isoquinolines, pyrrolidines, pyridines, pyrrolizidines, tropanes etc [40]. There have been concerns regarding the presence of certain alkaloids, viz. atropine and hyoscyamine, in other members of the Lycium genus, i.e. L. halimifolium and L. europaeum, although these compounds are found in concentrations far below their reported toxic doses. However, the presence of such toxic tropane alkaloids has not been reported in L. ruthenicum Murr to date. Naturally occurring polyamines are one of the classes of alkaloids that are involved in cell multiplication and its regulation in plants. L. ruthenicum Murr is the rich source of spermidine or spermine alkaloids, a pharmacologically important class of alkaloids reported to protect heart from aging, lowering of blood pressure and helpful in fruit ripening. Earlier 24 alkaloids have been reported by Wang et al [3], herein, we have reported some more spermidine or spermine alkaloids from black goji berry. A total of 36 spermine and spermidine has been compiled in Table 4 and Figs. 2 and 3 [43, 44].

Table 4 Identified Alkaloids in Black goji berry
Fig. 2

Representative Structure of Alkaloids

Fatty acids and essential oil (43–78)

Plant-based fatty acids and essential oils are always been valued for their pharmacological utilities such as improving immunity, brain health, mood, cell signaling regulation and reducing inflammation etc. Chi et al [22] studied the lipophilic compound composition of L. ruthenicum Murr seed and fruit essential oil in the samples collected from the Qinghai-Tibetan Plateau in China. Both the essential oils were shown to contain saturated, monounsaturated (MUFA), and polyunsaturated fatty acids (PUFA) with a predominance of linoleic, oleic and palmitic acids. It is worth mentioning here that linoleic acid is an essential fatty acid with a key role in the eicosanoid synthesis pathway as a precursor of arachidonic acid [47]. Earlier review had compiled 25 fatty acids and essentials oils, we have reported total of 36 fatty acids and essentials oils where the key fatty acids from L. ruthenicum Murr oil included linoleic, oleic, palmitic, linolenic and stearic acids which together comprised 95.59% of the total fatty acids. According to literature the comparative ratio of PUFAs, MUFAs and SFs in berries and seed oil are (59.10%: 63.99%), (21.47%: 21.76%),(19.43%: 14.26%) [45, 46] (Fig. 3 and Table 5).

Fig. 3

Representative Structure of fatty acid and essential oils

Table 5 Identified fatty acid and Essential Oil content of Black Goji berries

Phytosterols (79–87)

Phytosterols are cholesterol-like molecules found in all plant foods, with the highest concentrations occurring in vegetable oils. They are absorbed only in trace amounts but inhibit the absorption of intestinal cholesterol including recirculating endogenous biliary cholesterol, a key step in cholesterol elimination. The sterol composition has been used as an important marker to mark the geographical locations of various goji berry samples (including L. chinense and L. barbarum) using linear discriminant analysis (LDA) and principal component analysis (PCA) [48]. In our study, we have compiled total nine phytosterols isolated from seed oil of L.ruthenicum Murr (Table 6 and Fig. 4), which were not analyzed in previous studies [46]. The total content of phytosterol was approx 489.2 mg/100 g samples of black gojiberries which majorly consisted of stigmasterol, campesterol and β-sitosterol. Additionally, the Vitamin A and E contents were 0.3 mg/100 g and 46.3 mg/100 g in tested samples, proposing the blackberry vegetable oil worth exploration for further development.

Table 6 Identified phytosterols of Black Goji berries
Fig. 4

Representative Structure of Phytosterols

Carotenoids (88–93)

Carotenoids are a class of phytonutrients (“plant chemicals”) belonging to the terpenoid family, called tetraterpenoids. They are yellow, orange and red- colored pigments that are produced by plants, algae, several bacteria and fungi. Zeaxanthin, β-cryptoxanthin, β-carotene are some of the common carotenoids which have been reported from L. ruthenicum Murr and play a crucial antioxidant function of deactivating free radicals such as single oxygen atoms that can damage cells by reacting with other bio-molecules. As expected owing to its black-purple color, the black goji berry from Qinghai Province in China showed a much lower carotenoid content (1.51–3.19 μg/g) compared to red goji berry (212.24–233.08 μg/g) [23, 24]. In a very interesting study by Liu Y et al. [49], it was shown that undetectable carotenoid content in black goji berry is due to lack of chromoplast biosynthesis and not due to inactivation of carotenoid biosynthesis pathway during fruit ripening. Since, chromoplasts are the reservoirs for colored pigments, in absence of these in L. ruthenicum Murr fruits and overexpression of carotenoid cleavage dioxygenase 4 enzyme leads to continuous degradation of carotenoids. The carotenoids reported from gojiberries have been compiled in Table 7 and Fig. 5.

Table 7 Carotenoids content of Red and Black Goji berries
Fig. 5 

Representative structure of carotenoids

Phenolic acid and flavonoids (94–133)

As discussed in detail in forthcoming sections, the black goji berries have been repeatedly shown to possess significantly higher anti-oxidant properties than other closely related gojiberries, i.e. L. barbarum and L. chinense despite their much lower carotenoid contents. Research studies have established the supremacy of phenolic compounds, such as condensed tannins, phenolic acids and flavonoids as contributors to plant’s antioxidant capacities [50]. Different extraction methods have been followed for the detection of different phenolic acids in L. ruthenicum Murr samples such as ultrasonic-assisted extraction using the surface methodology, UPLC-Q-Orbitrap MS etc. Observations of significantly higher total phenolic content (8.33 mg GAE/g), total flavonoid content (11.09 mg CAE/g) and condensed tannins (20.87 mg CAE/g) in black goji berry samples than in red goji berry (3.16 mg GAE/g, 2.83 mg CAE/g and 1.08 mg CAE/g) respectively is a highly convincing [24, 51]. Since retention of these superior anti-oxidant properties in dried black goji berries is a highly desired feature for its commercialization as a functional food, the effect of different drying methods on the content of polyphenols has been extensively studied by several researchers [52, 53]. It has been concluded that the contents of total polyphenols remain highest by the air-drying method as compare to other methods viz. low- temperature oven drying and vacuum freeze- drying. Table 8 gives details of the forty phenolic acid and flavonoids detected in black goji berry to date and their respective structures have been shown in Fig. 6.

Table 8 Identified Phenolic acid and Flavonoids of Black goji berry
Fig. 6

Representative Structure of Phenolic acid and Flavonoids

Coumarins and Cinamate derivatives (134–136)

Coumarins act as an antioxidants, enzyme inhibitors, and precursors of toxic substances. In addition to biological activities, they are used as additives in food, cosmetics and optical brightening agents [55]. The phytochemical investigation of ethyl acetate extract of black goji berry has lead to the isolation of two coumarins (Scopoletin and Esculetin) and Methyl-2-hydroxy-4-undecanoxy-trans- cinamate which was characterized by 1H-NMR, 13C-NMR and FT- IR spectroscopic data, MS spectrometry, elemental analysis and by comparison with the literature values [56]. Table 9 gives the details of these derivatives and structures are described in Fig. 7.

Table 9 Coumarins and Cinamate derivatives
Fig. 7

Representative Structure of Coumarins and Cinamate derivatives

Anthocyanins and Proanthocyanidins (137–185)

The most important bioactive constituents of L. ruthenicum Murr are anthocyanins which are a large family of naturally occurring water-soluble plant pigments including glycoside or acyl glycoside anthocyanidins. They belong to the flavonoids class of compounds. They are found in the vacuolar sap of the epidermal tissues of fruits and flowers. These pigments belong to the most common class of phenolic compounds that share the same basic flavonoid structure with a positively charged oxygen atom at the c-ring of the structure connected with sugar moieties [57]. These sugar moieties are primarily monosaccharides and disaccharides like glucose, rhamnose, galactose, arabinose, sambubiose, rutinose, and sophorose, which are further acylated by organic acids like acetic acid, oxalic acid, phenolic acids such as p-coumaric acid, p-cinnamic acid and ferulic acid etc. The core structure of all anthocyanins remains a phenolated benzopyran referred to as flavylium cation (2-phenylchromenylium) which is described as a C6-C3-C6 skeleton. These pigments are responsible for the blue, purple, red and intermediate colours based on the pH of the microenvironment. They are widely used as nutraceuticals and found in our daily diets especially in berries, thus are extensively consumed by humans among all the flavonoids [58, 59].

These berries are also an affluent source of health-promoting proanthocyanidins and claimed to be richer than malts and hops. A recent study revealed that on addition L.ruthenicum Murr berries in beer improved the content of proanthocyanidin from 10 to 68 mg/L in finished beer, and the total polyphenol content in beer was increased from 246 to 457 mg/L [21].

Although the total flavonoid content in L. ruthenicum Murr is lower as compared to L. chinense and L. barbarum but its anthocyanin content is higher. In fact, in case of L. barbarum, anthocyanins have not been detected at any stage of the fruit development [60]. Among the chemical constituents of L. ruthenicum Murr fruit, the most well- researched component is the group of water-soluble anthocyanins, which are estimated to comprise approx 2.3% of the dried fruits [61]. It has been claimed that black gojiberries are one of the highest anthocyanin- containing natural sources with a maximum reported content of 24.04 ± 0.07 mg/g [43]. Several anthocyanins have been isolated and purified from L. ruthenicum Murr berry extracts by various extraction methods such as ultrasound-assisted aqueous two-phase extraction (UA-ATPE) and other analytical techniques such as D-101 resin- based column chromatography and high-performance liquid chromatography (HPLC) [25, 42, 62,63,64]. Ealier total 38 anthocyanins have been discussed by Wang et al [3], in our study we compiled total 49 anthocyanins included anthocyanidin with their respected structures [65, 66] (Table 10 and Fig. 8). These anthocyanins are responsible for the organoleptic flavour of the black-purple colored L. ruthenicum Murr fruits. The predominant anthocyanin is petunidin 3-O-[6-O-(4-O-(trans-p-coumaroyl) -α-L-rhamnopyranosyl) -β-D-glucopyranoside] 5-O-[b-glucopyranoside, accounting for the largest proportion of anthocyanins in wolfberry fruits, although the contents varies in samples obtained from different geographical locations [25, 42, 64]. The total anthocyanins content determined by the pH differential method ranged from 9.28 ± 1.19 to 82.58 ± 0.95 mg C3GE/ g DW. Five anthocyanidins and five anthocyanins were qualitatively and quantitatively analyzed by Zhang et al [65] among these, 10 constituents (delphinidin-3-glu, cyanidin-3-glu, petunidin-3-glu, peonidin-3-glu, malvidin-3-glu, delphinidin, cyanidin, petunidin, pelargonidin and malvidin) were detected. Anthocyanins are well recognized to promote health benefits owing to their potent anti-oxidative, anti-inflammatory, anti-carcinogenic, cardio-protective and neuroprotective effects [70, 71].

Table 10 Identified Anthocyanins of Black Goji Berry
Fig. 8

Representative Structure of Anthocyanins

Reported biological activities of L. ruthenicum Murr fruits

As it has already been discussed that L.ruthenicum Murr is rich in many biological active natural compounds which leads its potential towards many pharmacological activity like antioxidant activity due to presence of abundant of polyphenols, anti-fatigue effect due to existence of polysaccharides etc. So, herein we have categorized and described different biological activity reported from L.ruthenicum Murr in depth.

Anti-oxidant effect

The anti-oxidant properties of L. ruthenicum Murr berries have been most extensively worked out by various researchers in in-vitro and in-vivo study models, especially of the berry extracts, which are known to be rich in anthocyanins content [41, 63, 68, 72,73,74]. These pigments exhibit a noticeable inhibition of lipid oxidation induced by free radicals owing to their strong free radical scavenging activities. L. ruthenicum Murr has higher antioxidant potential as compared to L. barbarum, most obviously owing to a higher anthocyanin content of L. ruthenicum Murr in comparison with L. barbarum [24, 51, 75]. Major constituents that were found to be responsible for anti-oxidant properties in several studies are rutin, chlorogenic acid, p-coumaric acid, caffeic acid, syringic acid, dhc-caffeoyl spermidine isomer, quercetin-o-rut, kaempferol-o- rut, isorhamnetin-o-rut, ascorbic acid, lycium spermidine A, tocopherols, carotenoids, anthocyanins, polysaccharides [54, 61, 68]. In general, plants with higher TPC and TFC show stronger antioxidant activity since there is a positive correlation between total polyphenols and positive findings in DPPH (2,2-diphenyl-1-picrylhydrazyl) and ABTS (2,2′-azino-bis-3- ethylbenzothiazoline-6-sulphonic acid) assays [76]. In Lycium plant, the TPC was found to range from 698.14 ± 27.15 to 1311.10 ± 80.05 mg GAE per 100 g FW, which was significantly higher than those of bayberry fruit extracts (360.3–446.1 mg/100 g FW) and black berry extracts (261.9–929.6 mg per 100 g FW) [68]. The DPPH free radical- scavenging activity, ABTS, FRAP values of fruit extracts were 49.65 ± 3.1, 47.8 ± 6.6, 56.3 ± 6.9 uM TE/g FW respectively. The chlorogenic acid (112.5 ± 8.4 μg/g FW) was the most abundant phenolic acid found in Lycium [77]. Recently, Fatty acids and mineral contents of L. ruthenicum Murr have showed antioxidant activity against isoproterenol-induced acute myocardial ischemia in mice reported by Nzeuwa et al [45]. The most bioactive constituent, anthocyanin, has been reported to possess an inhibitory effect on tyrosinase monophenolase with IC50 = 1.483 ± 0.058 mg/mL by Shen et al. [78]. Petunidin3-O-[6-O-(4-O-(trans-p-coumaroyl)-a-L-rhamnopyranosyl)-b-D-glucopyranoside]-5-O-[b-Dglucopyranoside] which belongs to class of anthocyanins isolated from L. ruthenicum Murr exhibited higher scavenging activities against ABTS, DPPH and superoxide radicals than the crude extract of anthocyanins. Moreover, this compound has a significant effect on inhibition of the reactive oxygen damage induced by H2O2 in PC12 cells, reflecting in the recovery of plasma membrane integrity, decreased production of MDA, and increased secretion of antioxidant enzymes (glutathione peroxidase: 146.24 ± 7.25 mg/protein, superoxide dismutase: 91.83 ± 5.81 mg/protein and catalase: 23.45 ± 3.01 mg/protein) vitamin E as a positive control [62]. Chinese researchers have patented black goji berry as a natural composite PCT Int. Appl. (2017). Liu et al [79] had studied the antioxidant scavenging activity of L. ruthenicum Murr seed oil by using assays based on three kinds of radicals (DPPH·, ·OH and O2·) and lipid peroxidation and found that oil had the potential to be a novel antioxidant agent for use in the field of food, pharmaceuticals and cosmetics. Wang et al. [80] has proposed that in vitro gastrointestinal digestion may enhance the biological activities of anthocyanins especially for antioxidant activity and α-glucosidase inhibition.

Anti-inflammatory effect

Inflammation is a well-established cause as well as the effect of the plethora of human diseases, thus the need for dietary as well as pharmaceutical anti-inflammatory entities remains unmet to date. Since L. ruthenicum Murr is naturally packed with potent anti-inflammatory phyto-compounds (esp polysaccharides and polyphenols), the in-vitro and in-vivo efficacy of crude extracts of black goji berry fruits has been evaluated in several animal models of inflammatory diseases. Polysaccharides from natural sources are known to be very potent anti-inflammatory bio-molecules [81, 82]. In-vitro anti inflammatory action of isolated water-soluble arabinogalactan polysaccharide from L. ruthenicum Murr, LRGP3 has been investigated by Peng et al. [37]. The authors reported that LRGP3 could inhibit the expression of iNOS, production of NO and inflammatory cytokines in RAW264 cells and proposed the anti-inflammatory activity to be mediated by the NF-β-iNOS-NO signaling pathway. A metabolite of LRGP3, i.e. LRGP3-AF, has immune effectors properties viz. significant complement-fixing and macrophage stimulation activities. The galactan backbone of this polysaccharide is shown to be essential for its immunomodulatory activity [83].

The enrichment of anthocyanins in black gojiberry makes it a promising subject for anti-inflammatory activity exploration. In a hyperlipidemia atherosclerosis animal model, L. ruthenicum Murr anthocyanins (doses of 100, 200, 400 mg/kg fed for 6w) have shown significant improvement in lipid profile, percent aortic plaque area and severity of inflammatory damage in aorta, heart and liver tissue which were promising in comparison to simvastatin drug group [84]. Further, Shu and Hou [85] also endorsed the anti-inflammatory potential of anthocyanin extract of L. ruthenicum Murr in a rat model of carbon tetra-chloride induced hepatic injury. Oral administration of 30 mg L. ruthenicum Murr extract for 7 days, led to significant decrease in the levels of ROS, SGOT and SGPT and pro- inflammatory markers including NO, ROS, IL-1 and IL-6. The Plausible mechanism of action of anthocyanins via RAGE/NF-κB/JNK pathway has been explained by Chen S et al [69] in their rat model of d-galactose induced memory impairment. In the same study, it has been shown that these black gojiberry anthocyanins could significantly downregulate inflammatory markers, tumor necrosis factor-α (TNF-α), cyclooxygenase-2 (COX-2), nuclear factor kappa B (NF-κB) and interleuin-1-β (IL-1β) which are hallmarks of inflammatory diseases. Further, in a separate study, L. ruthenicum Murr ethanol extract inhibited colonic inflammation by regulating mitogen-activated protein kinase (MAPK) pathways and downregulating NF-κB levels, proposing these black gojiberry as a promising functional food for the management of inflammatory bowel disease (IBD). This in-vivo study was conducted in rat model of dextran sulfate sodium- induced colitis wherein supplementation with berry extracts could suppress activation of (NOD)-like receptor family pyrin domain containing 3 (NLRP3) inflammasome and regulate inflammation-inducing immune cell infiltration [86].

Supplementation with L. ruthenicum Murr has shown promise in a pre-clinical animal model of western diet-induced fatty liver disease. The extract-treated animal group showed reduced triglyceride accumulation and reduced hepatic inflammation [87]. Although in this study, supplementation could not influence the body weight, in a separate study by Yin et al. consumption of anthocyanin-rich extract of L. ruthenicum Murr was shown to be cause significant reduction in body weight and decrease in the Lee’s index along with elevation of serum HDLC, fecal fatty acid content, SOD activities besides reduction in MDA and hepatic lipids. Anti-inflammatory efficacy was shown with marked down-regulation of established pro-inflammatory markers; TNF-α, IL-6, NF-κB, IFN-γ and iNOS. The authors claimed that black wolfberry anthocyanins potentially alleviate diet-induced obesity by regulating accelerating fat decomposition, inflammation, oxidative stress [88].

Neuroprotective effects

Neurodegenerative diseases like Alzheimer’s are associated with progressive cognitive dysfunction and neuronal damage and have become a clinical challenge with modern- daylifestyle. Neuro-protective phyto-compound rich functional foods are in vogue in consideration with the rampant emergence of progressive neurodegenerative diseases worldwide. Several pre-clinical studies have unfolded the promising neuroprotective efficacy of L. ruthenicum Murr fruits and offered compelling evidences for biological activity. Lycium ruthenicum Murr anthocyanin extract has shown promise in an animal model of amyloid beta-protein 1–42 induced Alzheimer’s disease. The extract at a dose of 80 mg/kg, could improve the animal’s memory capacity in a passive-avoidance test in a shuttle box and significantly reduce markers of neuronal oxidative stress and inflammation in the hippocampus tissue of the rat brain [70, 89]. In the following years, Chen et al [69] re-validated and suggested an underlying biological mechanism for the protective benefits of L. ruthenicum Murr anthocyanins in an animal model of d-galactose induced memory impairment. In their study, anthocyanins were shown to lower the Bax/Bcl-2 ratio, caspase-3, C-jun N-terminal kinase (p-JNK) levels with evident alleviation of memory dysfunction and neuroinflammation in an animal model.

Hypoxia is the hallmark of most neurodegenerative diseases. Preclinical evidence has been generated to show that black gojiberry extracts could protect the cortical neurons against conditions of oxygen-glucose deprivation/reperfusion. In a recent study, the specific activity of polysaccharide 3 (LRP3) of L. ruthenicum Murr was evaluated in an animal model of hypoxic-ischemic encephalopathy. LRP3 pre-treatment could induce expression of protective nuclear factor erythroid 2-related factor (Nrf2) and heme oxygenase-1 (HO-1). The specificity of protection was shown by reversal of protection by s-RNA based inhibition Nrf2/HO-1 pathway [90]. Based on existing knowledge, very recently a network of L.ruthenicum Murr chemicals, putative biological targets and major pathways of Alzheimer’s disease has been produced. Interestingly, in this path-breaking study, 12 core genes have been identified which are potentially modulated by Lycium ruthenicum Murr extract and could be responsible for its potent activities [91]. Such studies are set to give most sought after answer to biological mechanisms behind the plethora of observed biological efficacies of black goji berries.

Gastrointestinal (GI) activity

In an in-vitro digestion stimulation study, anthocyanins from L. ruthenicum Murr have been reported to positively impact intestinal health both by encouraging the growth of health- promoting human gut microbiota as well as biosynthesis of short-chain fatty acids (SCFAs) during in-vitro fermentation [92]. It is reported earlier that gut microbiota participates in anthocyanin metabolism and absorption; in turn anthocyanin metabolites have pro-biotic activities for maintenance of healthy gut microbiota [93]. Anthocyanins significantly increased the relative abundances of Bifidobacterium and Allisonella, and reduced the relative abundances of Prevotella, Dialister, Megamonas and Clostridium. In proof of concept in-vivo study by Peng et al [94], prolonged treatment of mice with crude extract of anthocyanins from L. ruthenicum Murr fruits, showed its positive effect of strengthening intestinal barrier (via. Upregulation of barrier proteins Zo-1, Occludin, Claudin-1 and Muc1) and proliferation of gut microbiota (Coprobacter, Barnesiella, Eisenbergiella, Alistipes, and Odoribacter). This was a recapitulation and validation of findings by Luo et al [91] wherein C57BL/6 mice fed with L. ruthenicum Murr showed significant enrichment of fecal microbiota and SCFAs along with improved intestinal immune barrier functions, reduced permeability, free ammonia etc in comparison to the antibiotic treatment group.

Hypoglycemic effect

Very limited evidence of the hypoglycemic effect of L. ruthenicum Murr fruits is available in the scientific literature. In a study by Wang et al., the anti-hyperglycemic efficacy of polysaccharide extracts of L. ruthenicum Murr fruits was evaluated in alloxan- induced diabetes model in mice. In this study, 21 days of polysaccharide extract supplementation could downregulate hyperglycemia and restored conversion of blood glucose into liver glycogen reserves along with lowering of oxidative damage markers [95].

Antifatigue effect

The polysaccharides from medicinal plants have been reported as natural anti-fatigue substances by several researchers [54, 96,97,98,99]. Different doses of water-soluble polysaccharides from L. ruthenicum Murr (50, 100 and 200 mg/kg) have been tested for anti-fatigue activity in a rodent model of forced swim test (FST) [96]. The highest dose showed promising anti-fatigue activity based on standard fatigue markers such as lactic dehydrogenase, blood urea nitrogen, triglycerides, creatine phosphokinases etc. Plausible underlying mechanisms are proposed to be triglyceride mobilization for energy generation and upregulation of anti-oxidant activity markers such as GSH, GPx and SOD [19]. In a study of anti-fatigue and myocardial protection by L. ruthenicum extract (extracts 0.10, 0.1, 0.15 g/mL, drug dose 0.1 ml/10 g), American Ginseng powder (0.05 g/mL) was used as a positive control. L. ruthenicum Murr extract could extend the weight loaded swimming time, decreased blood lactic acid and urea nitrogen levels along with enhanced muscle and liver glycogen reservoirs [67]. Improved anti-fatigue effect of microcapsules loading of L. ruthenicum Murr anthocyanidins by modified b-glucan from highland barley has also been shown [100]. Some experimental results demonstrate that L. ruthenicum Murr can increase blood sugar, reduce lactic acid content and increase glycogen reserve in mice, which has good alleviating resistance to exercise-induced fatigue [32].

Radioprotective effects

In a mice model of radiation- induced injury, L. ruthenicum Murr extract (dose 2 g/kg and 4 g/kg) shows a reduction in caspase-3 and caspase-6 expression following 5Gy irradiation. This was also associated with a significant increase in total red blood cells, DNA and hemoglobin content in comparison with the standard drug control group amifostine (WR-27212015) [101].

Immuno-modulatory effects

The pectin content of L. ruthenicum Murr has been proposed to be responsible for its observed immunomodulatory efficacy. In an in-vitro study, Peng et al. [37] have shown immunomodulatory functions of isolated pectin from L. ruthenicum Murr in mouse macrophage RAW264.7 cell line. The results indicated that treatment with pectin stimulated the macrophages to produce a higher level of NO which is the mediator in the regulation of immunological functions. In an in-vivo evaluation, the efficacy of its polysaccharide preparation (LRGP3) has been tested in a mouse model of cyclophosphamide-induced immunosuppression [102]. Administration of all the doses (25, 50 and 100 mg/kg) for 10 days boosted recovery of indices in thymus and spleen, B and T cell proliferation, phagocytic activities of peritoneal macrophages, restoration of cytokine profile.

Hepatoprotective effects

Treatment of high-fat-diet fed C57/BL mice with L. ruthenicum Murr fruit extract (2 g/kg and 5 g/kg doses) has been shown to have hepatoprotective effects by regulation of AMPK signaling pathway. L. ruthenicum Murr extract supplementation could downregulate fatty acid synthase and sterol regulatory element-binding protein 1c along with upregulation of peroxisome proliferator -activated receptor α and peroxisome proliferator activated receptor γ coactivator 1α. This also co-existed with significantly reduced triglycerides, total cholesterol, aspartate aminotransferase and alanine aminotransferase in the serum, improved glucose metabolism and insulin sensitivity in NAFLD mice [103].

Toxicology and adverse reactions

Like most other commonly consumed wild fruits, L. ruthenicum Murr is also proposed to be non-toxic and has been used traditionally as food as well as herbal medicine without any observed or reported toxicity. A Chinese study, about the toxicological investigations on this plant has concluded L. ruthenicum Murr fruit as non-toxic. In this study, acute toxicity test, Ames test, bone marrow cell micronucleus, sperm shape abnormality test, thirty days feeding test were conducted. The MTD of L. ruthenicum Murr pigment growth in mice and rats was found greater than 30,000 mg/( and thus claimed safe for consumption. Also, the mutagenic test was found negative and no abnormal phenomenon was observed in rats after being fed for 90 days. Interestingly, anthocyanin enriched herbal extracts of black gojiberries showed activity for the treatment of chronic myeloid leukemia (CML) [104]. Biological activity tests showed that LRP3-S1 could inhibit the growth of pancreatic cancer cells. Also, LRP3-S1 could attenuate the invasion ability of BxPC-3 cells and down-regulate protein expression of p-FAK, p-AKT, p-GSK-3β and p-p38 MAP kinase [33].

Natural colorant

In recent years, the use of natural pigments has remarkably increased in the food color industry due to growing awareness of the environmental hazards and the potential side effects of the synthetic chemicals being used as food colorants. Thus, many researchers are exploring the potentials of black goji berries to be used as a natural food grade blue color across wide range of pH conditions. Petunidin-3-trans-p-coumaroyl-rutinoside-5-glucoside is proposed to be the biggest contributor in color of black gojiberry [105, 106].

Future perspective

Phytochemical studies of L. ruthenicum Murr have revealed the presence of more than a hundred compounds. The crude extracts and some of the purified constituents of the black goji berry are reported to possess plethora of biological activities as well. Chiefly, the significantly higher content of anthocyanins, polysaccharides, spermine and spermidine alkaloids are accounted for most of these biological activities. Black goji berry has been used in the traditional medicinal system without any reported toxicity. The altitudes at which this plant is known to grow wildly, acute mountain sickness (AMS) is a predominant health concern to the sojourners that can further lead to potentially life threatening altitude illnesses such as High Altitude Cerebral Oedema (HACE) and High Altitude Pulmonary Oedema (HAPE). Oxidative stress, inflammatory stress and nitrosative stress are the main underlying causes behind high altitude sickness. Since black goji berry possess strong anti inflammatory, anti-fatigue and antioxidant activities, it deserves to be explored for its utility for development of a range of pharmaceuticals, cosmetics, food additives and nutraceutical products for curing diseases and general maintenance of well being at high altitude. Additionally, owing to its enriched content of photo-stable and thermo-stable anthocyanins, the plant has tremendous applications as natural food colorant. There are ample research opportunities to explore the phyto-chemistry, biological activities and safety for development of quality products from Lycium ruthenicum Murr with wide applications (Fig. 9). Hence, from the above mentioned reports it can be concluded that L. ruthenicum Murr has immense potential to cure various diseases and this less explored but high value medicinal plant of Indian Trans-Himalaya, particularly Ladakh has enormous importance in traditional system of medicine (Amchi System of Medicine). Although a lot of exploration has been done, still there is a need of in-depth scientific validation of its biological activities and underlying biological mechanisms for bio-active components of this plant for development of herbal preparations/products.

Fig. 9

Phytochemical and Pharmacological evidence of Lycium ruthenicum 


We have critically reviewed the bioactive components and their biological activities from L.ruthenicum Murr with their respective structures. A unique color of anthocyanins reported from black goji berries possesses most of the pharmacological activities which makes L.ruthenicum Murr, a good candidate for exploration of therapeutic properties.

Availability of data and materials

Not applicable.



2,2′-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid


Dry weight






Fresh weight


Ferric reducing/antioxidant power


Gallic Acid Equivalent


inducible nitric oxide synthase




Nuclear factor κB


Reactive oxygen species


Superoxide dismutase


Total phenolic content


Total flavonoid content


Tanin equivalent

TNF- α:

Tumor necrosis factor-α


Vitamin E


  1. 1.

    Hong DY, Pan KY, Nicholas JT. Flora of China. 6th ed. Beijing: Science Press; 2001. p. 127–32.

    Google Scholar 

  2. 2.

    Qian D, Zhao Y, Yang G, Huang L. Systematic review of chemical constituents in the genus Lycium (Solanaceae). Molecule. 2017;22(6):911.

    CAS  Article  Google Scholar 

  3. 3.

    Wang H, Li J, Tao W, Zhang X, Gao X, Yong J, et al. Lycium ruthenicum studies: Molecular biology, Phytochemistry and pharmacology. Food Chem. 2018;240:759–66.

    CAS  Article  Google Scholar 

  4. 4.

    Dhar P, Tayade A, Ballabh B, Chaurasia OP, Bhatt RP, Srivastava RB. Lycium ruthenicum murray: a less-explored but high value medicinal plant from trans-himalayan cold deserts of Ladakh, India. Plant Archives. 2011;11:583–6.

    Google Scholar 

  5. 5.

    Chaurasia OP, Ahmed Z, Ballabh B. Ethnobotany and plants of trans-Himalaya. New Delhi: SSPL; 2007.

    Google Scholar 

  6. 6.

    Kuang KZ, Lu AM, Wu CY, Huang SC. Solanaceae. Flora Reipublicae Popularis Sinicae. 1978;67:1–175.

    Google Scholar 

  7. 7.

    Tutin TG, Heywood VH, Burges NA, Moore DM, Valentine DH, Walters SM, et al. Flora Europaea, vol. 3. Cambridge: Cambridge University Press; 1972. p. 89–94.

    Google Scholar 

  8. 8.

    Gregor RL. Barkley TM. Kansas: Flora of the great plains University Press of Kansas; 1986.

    Google Scholar 

  9. 9.

    Zhang HF, Li X, Wang JG, Yang YJ. The structure characteristic of the plant community in the lower reaches of Tarim River. Ecol Environ. 2007;16:1219–24.

    Google Scholar 

  10. 10.

    Zhang X, Zhang F, Gao XJ, Yong JJ, Zhang WH, Zhao JJ, et al. Effects of different drying methods on content of bioactive component and antioxidant activity in Lycium ruthenicum. Zhongguo Zhong yao za zhi. China J Chin Mat Med. 2017;42(20):3926–31.

    Article  Google Scholar 

  11. 11.

    Dierma D, Mao J. Crystal pearl of materia medica. Shanghai: Shanghai Scientific and Technical Publishers; 2012. p. 66.

    Google Scholar 

  12. 12.

    Chaurasia, OP, Singh B. Cold desert plants Field Research Laboratory, Leh-Ladakh, 1996–2001: Vol-I-V.

  13. 13.

    Yutuo Y. Medical canon in four sections, vol. 321. Shanghai: Shanghai Scientific and Technical Publishers; 1987.

    Google Scholar 

  14. 14.

    Liu YM. Pharmacography of Uighur part one Xinjiang Science & Technology & hygiene publishing house, Urumqi,1999.

    Google Scholar 

  15. 15.

    Ballabh B, Chaurasia OP, Ahmed Z, Singh SB. Traditional medicinal plants of cold desert Ladakh--used against kidney and urinary disorders. J Ethnopharmacol. 2008;118(2):331–9.

    Article  PubMed  Google Scholar 

  16. 16.

    Chopra RN, Nayar SL, Chopra IC. Glossary of Indian medicinal plants (including the supplement). New Delhi: Council of Scientific and Industrial Research; 1986.

    Google Scholar 

  17. 17.

    Gairola S, Sharma J, Bedi YS. A cross-cultural analysis of Jammu, Kashmir and Ladakh (India) medicinal plant use. J Ethnopharmacol. 2014;155(2):925–86.

    Article  PubMed  Google Scholar 

  18. 18.

    Nzeuwa IB, Xia Y, Qiao Z, Feng F, Bian J, Liu W, et al. Comparison of the origin and phenolic contents of Lycium ruthenicum murr. By high-performance liquid chromatography fingerprinting combined with quadrupole time-of-flight mass spectrometry and Chemometrics. J Sep Sci. 2017;40(6):1234–43.

    CAS  Article  Google Scholar 

  19. 19.

    Ni W, Gao T, Wang H, Du Y, Li J, Li C, et al. Anti-fatigue activity of polysaccharides from the fruits of four Tibetan platea indigenous medicinal plants. J Ethnopharmacol. 2013;150(2):529–35.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Quan SH, Hai-xia ZH, Yu L, Yan L. The research on chemical component and antioxidant activity of wild Lycium ruthenicum. Sci Technol Food Ind. 2017;4:10.

    Google Scholar 

  21. 21.

    Zhao W, Song Y, Zhou G. Study on Proanthocyanidin-rich beer. J Am Soc Brew. 2017;75(2):109–15.

    CAS  Article  Google Scholar 

  22. 22.

    Chi X, Xiao Y, Dong Q, Yang YQ, Hu F. Fatty acid composition of Lycium ruthenicum collected from the Qinghai- tibetan plateau. Chem Nat Compd. 2016;54(4):674–5.

    CAS  Article  Google Scholar 

  23. 23.

    Peng Y, Ma C, Li Y, Leung KS, Jiang ZH, Zhao ZZ. Quantification of zeaxanthin dipalmitate and total carotenoids in Lycium fruits (Fructus Lycii). Plant Foods Hum Nutr. 2005;60(4):161–4.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Islam T, Yu X, Badwal TS, Xu B. Comparative studies on phenolic profiles, antioxidant capacities and carotenoid contents of red goji berry (Lycium barbarum) and black goji berry (Lycium ruthenicum). Chem Cent J. 2017;11(1):59.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Tian Z, Aierken A, Pang H, Du S, Feng M, Ma K, et al. Constituent analysis and quality control of anthocyanin constituents of dried Lycium ruthenicum Murray fruits by HPLC–MS and HPLC–DAD. J Liq Chromatogr Relat Technol. 2016;39(9):453–8.

    CAS  Article  Google Scholar 

  26. 26.

    Pantelidis GE, Vasilakakis M, Manganaris GA, Diamantidis G. Antioxidant capacity, phenol, anthocyanin and ascorbic acid contents in raspberries, blackberries, red currants, gooseberries and cornelian cherries. Food Chem. 2007;102(3):777–83.

    CAS  Article  Google Scholar 

  27. 27.

    Bajpai KP, Warghat AR, Sharma KR, Yadav A, Thakur KA, Srivastava RB, et al. Structure and genetic diversity of natural populations of Morus alba in the trans-Himalayan Ladakh region. Biochem Genet. 2014;52(3-4):137–52.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    López OP, Cervantes ML, Pérez MV, Pérez TH. Berries: improving human health and healthy aging, and promoting quality life -a review. Plant Foods Hum Nutr. 2010;65(3):299–308.

    CAS  Article  Google Scholar 

  29. 29.

    Stanciu G, Lupsor S, Sava C, Zagan S. Spectrophotometric study on stability of anthocyanins extracts from black grapes skins. Ovidius Univ Ann Ser Chem. 2010;21(1):101–4.

    CAS  Google Scholar 

  30. 30.

    Liu B, Xu Q, Sun Y. Black goji berry (Lycium ruthenicum) tea has higher phytochemical contents and in vitro antioxidant properties than red goji berry (Lycium barbarum) tea. Food Qual Saf. 2020;4(4):193–201.

    CAS  Article  Google Scholar 

  31. 31.

    Jiao XL, Chi XF, Dong Q, Xiao YC, Fengzu HU. Analysis of the nutritional components of Lycium ruthenicum. Amino Acids Biotic Resour. 2011;03:60–2.

    Google Scholar 

  32. 32.

    Xing X, Ke Y. Nutritional value of Lycium ruthenicum Murr. And its relieving resistance to exercise-induced fatigue. Prog Nutr. 2019;21:876–81.

    CAS  Google Scholar 

  33. 33.

    Zhang S, He F, Chen X, Ding K. Isolation and structural characterization of a pectin from Lycium ruthenicum Murr and its anti-pancreatic ductal adenocarcinoma cell activity. Carbohydr Polym. 2019;223:115104.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Peng Q, Lv X, Xu Q, Li Y, Huang L, Du Y. Isolation and structural characterization of the polysaccharide LRGP1 from Lycium ruthenicum. Carbohydr Polym. 2012;90(1):95–101.

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Peng Q, Song J, Lv X, Wang Z, Huang L, Du Y. Structural characterization of an arabinogalactan-protein from the fruits of Lycium ruthenicum. J Agric Food Chem. 2012;60(37):9424–9.

    CAS  Article  PubMed  Google Scholar 

  36. 36.

    Lv X, Wang C, Cheng Y, Huang L, Wang Z. Isolation and structural characterization of a polysaccharide LRP4-a from Lycium ruthenicum Murr. Carbohydr Res. 2013;365:20–5.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Peng Q, Xu Q, Yin H, Huang L, Du Y. Characterization of an immunologically active pectin from the fruits of Lycium ruthenicum. Int J Biol Macromol. 2014;64:69–75.

    CAS  Article  PubMed  Google Scholar 

  38. 38.

    Liu Y, Gong G, Sun Y, Gu X, Huang L, Wang Z. Isolation, structural characterization, and immunological activity of a polysaccharide LRLP4-A from the leaves of Lycium ruthenicum. J Carbohyd Chem. 2006;35:40–56.

    Article  Google Scholar 

  39. 39.

    Wang SQ, Liu B, Liu S, Xie SZ, Pan LH, Zha XQ, et al. Structural features of an acidic polysaccharide with the potential of promoting osteoblast differentiation from Lycium ruthenicum Murr. Nat Prod Res. 2018;34(16):2249–54.

    CAS  Article  PubMed  Google Scholar 

  40. 40.

    Debnath B, Singh W, Das M, Goswami S, Singh KM, Maitic D, et al. Role of plant alkaloids on human health: a review of biological activities. Mater Today Chem. 2018;9:56–72.

    CAS  Article  Google Scholar 

  41. 41.

    Wu T, Lv H, Wang F. Wang Y characterization of polyphenols from Lycium ruthenicum fruit by UPLC-Q-TOF/MSE and their antioxidant activity in Caco-2 cells. J Agri Food Chem. 2016;64(11):2280–8.

    CAS  Article  Google Scholar 

  42. 42.

    Jin H, Zhao J, Zhou W, Shen A, Yang F, Liu Y, et al. Preparative separation of a challenging anthocyanin from Lycium ruthenicum Murr by two dimensional reversed-phase liquid chromatography/ hydrophilic interaction chromatography. RSC Adv. 2015;5(76):62134–41.

    CAS  Article  Google Scholar 

  43. 43.

    Yang X, Lin S, Jia Y, Rehman F, Zeng S, Wang Y. Anthocyanin and spermidine derivative hexoses coordinately increase in the ripening fruit of Lycium ruthenicum. Food Chem. 2019;311:125874.

    CAS  Article  PubMed  Google Scholar 

  44. 44.

    Qi JJ, Yan YM, Cheng LZ, Liu BH, Qin FY, Cheng YX. A novel flavonoid glucoside from the fruits of Lycium ruthenicum. Molecules. 2018;23(2):325.

    CAS  Article  PubMed Central  Google Scholar 

  45. 45.

    Nzeuwa IB, Xia H, Shi Y, Yang C, Shah SM, Guo B, et al. Fatty acid and mineral contents of Lycium ruthenicum Murr and antioxidant activity against isoproterenol-induced acute myocardial ischemia in mice. Food Sci Nutr. 2020;8(2):1075–81.

    CAS  Article  Google Scholar 

  46. 46.

    Zhao X, Dong B, Li P, Wei W, Dang J, Liu Z, et al. Fatty acid and phytosterol composition, and biological activities of Lycium ruthenicum Murr. Seed oil. J Food Sci. 2018;83:2448–56.

    CAS  Article  Google Scholar 

  47. 47.

    Keys A, Anderson JT, Grande F. Prediction of serum cholesterol response of man to change in fats in the diet. Lancet. 1957;2(7003):959–66.

    Article  Google Scholar 

  48. 48.

    Jarouche M, Suresh H, Hennell J, Sullivan S, Lee S, Singh S, et al. The quality assessment of commercial Lycium berries using LC-ESI-MS/MS and Chemometrics. Plants (Basel). 2019;8(12):604.

    CAS  Article  Google Scholar 

  49. 49.

    Liu Y, Zeng S, Sun W, Wu M, Hu W, Shen X, et al. Comparative analysis of carotenoid accumulation in two goji (Lycium barbarum L. and L. ruthenicum Murr.) fruits. BMC Plant Biol. 2014;14(1):269.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  50. 50.

    Cai YZ, Luo Q, Sun M, Corke H. Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer. J Life Sci. 2004;74(17):2157–84.

    CAS  Article  Google Scholar 

  51. 51.

    Xin G, Zhu F, Du B, Xu B. Antioxidants distribution in pulp and seeds of black and red goji berries as affected by boiling processing. J Food Qual. 2017 Article ID 3145946.

  52. 52.

    Zhang G, Chen S, Zhou W, Meng J, Deng K, Zhou H, et al. Rapid qualitative and quantitative analyses of eighteen phenolic compounds from Lycium ruthenicum Murray by UPLC-Q-Orbitrap MS and their antioxidant activity. Food Chem. 2018;269:150–6.

    CAS  Article  PubMed  Google Scholar 

  53. 53.

    Jia Q, Zhang S, Zhang H, Yang X, Cui X, Su Z, et al. A comparative study on polyphenolic composition of berries from the Tibetan plateau by UPLC-Q-Orbitrap MS system. Chem Biodivers. 2020;17(4):1612–872.

    CAS  Article  Google Scholar 

  54. 54.

    Chen X, Zhang G. Scavenging and anti-fatigue activity of Wu-Wei-Zi aqueous extracts. African J Microbiol Res. 2011;5:5933–40.

    Google Scholar 

  55. 55.

    Zahradnik M. The production and application of fluorescent brightening agents. New York: John Wiley & Sons; 1992. p. 164.

    Google Scholar 

  56. 56.

    Valizadeh H, Kordi FM, Kouhkan R, Bahadori MB, Farimani MM. Isolation and structure elucidation of coumarin and cinamate derivatives from Lycium ruthenicum Iran. Chem Commun. 2014;2:277–82.

    Google Scholar 

  57. 57.

    Khoo HE, Azlan A, Tang TS, Lim MS. Anthocyanidins and anthocyanins: colored pigment as food, pharmaceutical ingredients, and the potential health benefits. Food Nutr Res. 2017;61(1):1361779.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  58. 58.

    Mazza G, Miniati E. Types of anthocyanins. In: Anthocyanins in fruits, vegetables, and grains. FL, USA: CRC Press; 1993. p. 1–28.

    Google Scholar 

  59. 59.

    Castañeda A, Pacheco HL, Páez E, Rodriguez J, Galán-Vidal CA. Chemical studies of anthocyanins: a review. Food Chem. 2009;113(4):859–71.

    CAS  Article  Google Scholar 

  60. 60.

    Zeng S, Wu M, Zou C, Liu X, Shen X, Hayward A, et al. Comparative analysis of anthocyanin biosynthesis during fruit development in two Lycium species. Physiol Plant. 2014;150(4):505–16.

    CAS  Article  PubMed  Google Scholar 

  61. 61.

    Shuang Q, Zhang HX, Lu Y. The research on chemical component and antioxidant activity of wild Lycium ruthenicum. Sci Technol Food Ind. 2017;04:94–100.

    Google Scholar 

  62. 62.

    Tang J, Yan Y, Ran L, Mi J, Sun Y, Lu L, et al. Isolation, antioxidant property and protective effect on PC12 cell of the main anthocyanin in fruit of Lycium ruthenicum Murray. J Funct Foods. 2017;30:97–107.

    CAS  Article  Google Scholar 

  63. 63.

    Chen C, Shao Y, Tao Y, Mei L, Shu Q, Wang L. Main anthocyanins compositions and corresponding H-ORAC assay for wild Lycium ruthenicum Murr. Fruits from the Qaidam Basin. J Pharm Techol Drug Res. 2013;2(1):1–10.

    CAS  Article  Google Scholar 

  64. 64.

    Jin H, Liu Y, Yang F, Wang J, Fu D, Zhang X. Characterization of anthocyanins in wild Lycium ruthenicum Murray by HPLC-DAD/QTOF-MS/MS. Anal Methods. 2015;7(12):4947–56.

    CAS  Article  Google Scholar 

  65. 65.

    Zhang G, Chen S, Zhou W, Meng J, Deng K, Zhou H, et al. Anthocyanin composition of fruit extracts from Lycium ruthenicum and their protective effect for gouty arthritis. Ind Crop Prod. 2019;129:414–23.

    CAS  Article  Google Scholar 

  66. 66.

    Liu P, Li W, Hu Z, Qin X, Liu G. Isolation, purification, identification, and stability of anthocyanins from Lycium ruthenicum Murr from LWT. Food Sci Technol. 2020;126:109334.

    CAS  Article  Google Scholar 

  67. 67.

    Yang J-F, Wang Q, Sun J, Feng D-Z. Anti-fatigue and improvement effect of exhausting exercise-induced myocardial damage of aqueous extract from Lycium Ruthenicum murr. In mice. Sci Technol Food Ind. 2018;39(16):296–9.312.

    Google Scholar 

  68. 68.

    Zheng J, Ding C, Wang L, Li G, Shi J, Li H, et al. Anthocyanins composition and antioxidant activity of wild Lycium ruthenicum Murr. From Qinghai-Tibet plateau. Food Chem. 2011;126:859–65.

    CAS  Article  Google Scholar 

  69. 69.

    Chen S, Zhou H, Zhang G, Meng J, Deng K, Zhou W, et al. Anthocyanins from Lycium ruthenicum Murr. Ameliorated d-galactose-induced memory impairment, oxidative stress, and Neuroinflammation in adult rats. J Agric Food Chem. 2019;20(11):3140–9.

    CAS  Article  Google Scholar 

  70. 70.

    Kelsey N, Hulick W, Winter A, Ross E, Linseman D. Neuroprotective effects of anthocyanins on apoptosis induced by mitochondrial oxidative stress. Nutr Neurosci. 2011;14(6):249–59.

    CAS  Article  PubMed  Google Scholar 

  71. 71.

    Prior RL, Wu X. Anthocyanins: structural characteristics that result in unique metabolic patterns and biological activities. Free Radic Res. 2006;40(10):1014–28.

    CAS  Article  PubMed  Google Scholar 

  72. 72.

    Liu Z, Dang J, Wang Q, Yu M, Jiang L, Mei L, et al. Optimization of polysaccharides from Lycium ruthenicum fruit using RSM and its anti-oxidant activity, Int J Biol Macromol. 2013;61:127–34.

  73. 73.

    Song JL, Gao Y, Xu J. Protective effects of methanolic extract form fruits of Lycium ruthenicum Murr on 2, 2’-azobis (2-amidinopropane) dihydrochloride-induced oxidative stress in LLC-PK1 cells. Pharmacogn Mag. 2014;10(40):522.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  74. 74.

    Li J, Zhao HY, Yuan H, Zhu CQ, Shi DH. Study on the pigment of Lycium ruthenicum Murr. Food Sci. 2006;27:146–51.

    CAS  Google Scholar 

  75. 75.

    Castro V, Aierken A, Zhang X, Dias A. Comparative study of antioxidant potential and cytotoxic effects of methanolic extracts from Lycium barbarum and Lycium ruthenicum berries. Plant Med Int Open. 2017;S 01:Tu-PO.

    Google Scholar 

  76. 76.

    Kosar M, Altintas A, Kirimer N, Baser KHC. Determination of the free radical scavenging activity of Lycium extracts. Chem Nat Compd. 2003;39(6):531–5.

    CAS  Article  Google Scholar 

  77. 77.

    Fang Z, Zhang M, Wang L. HPLC-DAD-ESIMS analysis of phenolic compounds in bayberries (Myrica rubra Sieb. Et Zucc.). Food Chem. 2007;100(2):845–52.

    CAS  Article  Google Scholar 

  78. 78.

    Shen M, Liu K, Liang Y, Liu G, Sang J, Li C. Extraction optimization and purification of anthocyanins from Lycium ruthenicum Murr. And evaluation of tyrosinase inhibitory activity of the anthocyanins. J Food Sci. 2020;85(3):696–706.

    CAS  Article  PubMed  Google Scholar 

  79. 79.

    Liu Z, Liu B, Kang H, Yue H, Chen C, Jiang L, et al. Subcritical fluid extraction of Lycium ruthenicum seeds oil and its antioxidant activity. Int J Food Sci Technol. 2019;54(1):161–9.

    CAS  Article  Google Scholar 

  80. 80.

    Wang ZC, Tanzeela N, Sun L, Fang Z, Yan Y, Li D, et al. Effect of in vitro gastrointestinal digestion on the composition and bioactivity of anthocyanins in the fruits of cultivated Lycium ruthenicum Murray. CyTA-J Food. 2019;17(1):552–62.

    CAS  Article  Google Scholar 

  81. 81.

    Wang Q, Kuang H, Su Y, Sun Y, Feng J, Guo R, et al. Naturally derived anti- inflammatory compounds from Chinese medicinal plants. J Ethnopharmacol. 2013;146(1):9–39.

    CAS  Article  PubMed  Google Scholar 

  82. 82.

    Du Z, Liu H, Zhang Z, Li P. Angtioxidant and anti- inflammatory activities of Radix Isatidis polysaccharide in murine alveolar macrophages. Int J Biol Macromol. 2013;58:329–35.

    CAS  Article  PubMed  Google Scholar 

  83. 83.

    Peng Q, Liu H, Lei H, Wang X. Relationship between structure and immunological activity of an arabinogalactan from Lycium ruthenicum. Food Chem. 2016;194:595–600.

    CAS  Article  PubMed  Google Scholar 

  84. 84.

    Lin L, Li J, Lv H, Ma Y, Qian Y. Effect of Lycium ruthenicum anthocyanins on atherosclerosis in mice. Zhongguo Zhong yao Za Zhi. J Chin Mat Med. 2012;37:1460–6.

  85. 85.

    Hou CW, Chen IC, Shu FR, Feng CH, Hung CT. Protective effect of supplementation with Lycium ruthenicum Murray extract from exhaustive exercise-induced cardiac injury in rats. Chin Med J (Engl). 2019;132(8):1005–6. PMID: 30958451; PMCID: PMC6595767.

  86. 86.

    Zong S, Yang L, Park HJ, Li J. Dietary intake of Lycium ruthenicum Murray ethanol extract inhibits colonic inflammation in dextran sulfate sodium-induced murine experimental colitis. Food Funct. 2020;11(4):2924–37.

    CAS  Article  PubMed  Google Scholar 

  87. 87.

    Lu K, Wang J, Yu Y, Wu Y, He Z. Lycium ruthenicum Murr. Alleviates nonalcoholic fatty liver in mice. Food Sci Nutr. 2020;8(6):2588–97.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  88. 88.

    Yin J, Wu T. Anthocyanins from black wolfberry (Lycium Ruthenicum Murr.) prevent inflammation and increase fecal fatty acid in diet-induced obese rats. RSC Adv. 2017;7:47848–53.

    CAS  Article  Google Scholar 

  89. 89.

    Wu X, Li X, Liang S, Liu Y, Dai X, Zheng Q, et al. Neuroprotective Effect of Anthocyanin Extract from Lycium ruthenicum Murray in Aβ1–42-induced Rat Model of AD; 2017.

    Book  Google Scholar 

  90. 90.

    Deng K, Li Y, Xiao M, Wang F, Zhou P, Zhang W, et al. Lycium ruthenicum Murr polysaccharide protects cortical neurons against oxygen-glucose deprivation/reperfusion in neonatal hypoxic-ischemic encephalopathy. Int J Biol Macromol. 2020;158:562–8.

    CAS  Article  PubMed  Google Scholar 

  91. 91.

    Luo Z, Yu G, Chen X, Liu Y, Zhou Y, Wang G, et al. Integrated phytochemical analysis based on UHPLC-LTQ-Orbitrap and network pharmacology approaches to explore the potential mechanism of Lycium ruthenicum Murr. For ameliorating Alzheimer’s disease. Food Funct. 2020;14(2):1362–72.

    Article  Google Scholar 

  92. 92.

    Yan Y, Peng Y, Tang J, Mi J, Lu L, Li X, et al. Effects of anthocyanins from the fruit of Lycium ruthenicum Murray on intestinal microbiota. J Funct Foods. 2018;48:533–41.

    CAS  Article  Google Scholar 

  93. 93.

    Faria A, Fernandes I, Norberto S, Mateus N, Calhau C. Interplay between anthocyanins and gut microbiota. J Agric Food Chem. 2014;62(29):6898–902.

    CAS  Article  PubMed  Google Scholar 

  94. 94.

    Peng Y, Yan Y, Wan P, Dong W, Huang K, Ran L, et al. Effects of long-term intake of anthocyanins from Lycium ruthenicum Murray on the organism health and gut microbiota in vivo. Food Res Int. 2020;130:108952.

    CAS  Article  PubMed  Google Scholar 

  95. 95.

    Wang JH, Chen XQ, Zhang WJ. Study on hypoglycemic function of polysaccharides from Lycium ruthenicum Murr. Fruit and its mechanism. Food Sci. 2009;30:244–8.

    Google Scholar 

  96. 96.

    Wang J, Li S, Fan Y, Chen Y, Liu D, Cheng H, et al. Anti-fatigue activity of the water-soluble polysaccharides isolated from Panax ginseng. J Ethnopharmacol. 2010;130(2):421–3.

    CAS  Article  PubMed  Google Scholar 

  97. 97.

    Sheng R, Xu X, Tang Q, Bian D, Li Y, Qian C, et al. Polysaccharide of radix pseudo stellariae improves chronic fatigue syndrome induced by poly I:C in mice. Evid Based Complement Alternat Med. 2011;840516:1–9.

    Article  Google Scholar 

  98. 98.

    Hu JH, Yan F, Zhang ZY, Lin JY. Evaluation of antioxidant and anti-fatigue activities of Ganoderma lucidum polysaccharides. J Anim Vet Adv. 2012;11:4040–4.

    Google Scholar 

  99. 99.

    Tan W, Yu KQ, Liu YY, Ouyang MZ, Yan MH, Luo R, et al. Anti- fatigue activity of polysaccharides extract from Radix Rehmanniae Preparata. Inte J Biol Macromol. 2012;50(1):59–62.

    CAS  Article  Google Scholar 

  100. 100.

    Gao Q, Shu T, Chang Y, Hu C, Cao X, Wang S. Evaluation of anti-fatigue function of solution of microcapsules loading anthocyanidins of Lycium ruthenicum murr by modified b-glucan from highland barley. Shipin Keji. 2019;44:316–20.

    Google Scholar 

  101. 101.

    Duan Y, Chen F, Yao X, Zhu J, Wang C, Zhang J, et al. Protective effect of Lycium ruthenicum Murr. Against radiation injury in mice. Int J Environ Res Public Health. 2015;12:8332–47.

    CAS  Article  Google Scholar 

  102. 102.

    Gong Y, Wu J, Li ST. Immuno-enhancement effects of Lycium ruthenicum Mur. Polysaccharide on cyclophosphamide- induced immunosuppression in mice. Int J Clin Exp Med. 2015;8(11):20631–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  103. 103.

    Lin J, Zhang Y, Wang X, Wang W. Lycium ruthenicum extract alleviates high-fat diet-induced nonalcoholic fatty liver disease via enhancing the AMPK signaling pathway. Mol Med Rep. 2015;12(3):3835–40.

    CAS  Article  PubMed  Google Scholar 

  104. 104.

    Li J, Yuan H, Zeng XC, Han B, Shi DH. Toxicological assessment of pigment of Lycium ruthenicum Murr. Food Sci. 2007;28:470–5.

    CAS  Google Scholar 

  105. 105.

    Tang P, Giusti MM. Black goji as a potential source of natural color in a wide pH range. Food Chem. 2018;269:419–26.

    CAS  Article  PubMed  Google Scholar 

  106. 106.

    Giusti MM, Peipei T. Uses of acylated anthocyanins extracted from black goji (lycium ruthenicum murr.) as a source of natural Color. 2017; PCT/US20 17/033290. W02017205173A1.

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We would like to dedicate this article to the ethnic communities who perfected and preserved the traditional knowledge about health promoting properties of the genus lycium.


This work was supported by the Defence Institute of High Altitude Research- Defence Research Development Organization.

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All authors contributed equally to literature research, writing manuscript etc. The author(s) read and approved the final manuscript.

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Correspondence to Shweta Saxena.

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Sharma, R., Raghuvanshi, R., Kumar, R. et al. Current findings and future prospective of high-value trans Himalayan medicinal plant Lycium ruthenicum Murr: a systematic review. Clin Phytosci 8, 3 (2022).

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  • Trans Himalayan
  • Lycium ruthenicum Murr
  • Anthocyanin
  • Anti-oxidant
  • Anti-inflammatory
  • Neuroprotective
  • Black gojiberry