Black Chinese Wolfberry Market size was valued at USD 145.8 Million in and is projected to reach USD 423.2 Million by , growing at a CAGR of 14.8% during the forecast period -.
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To Learn More:The expansion and progress of the Black Chinese Wolfberry Industry can be ascribed to specific driving forces within the market. Possible market catalysts for a product such as black Chinese Wolfberry (Lycium ruthenicum), alternatively referred to as black goji berry. A number of significant market factors include the following:
The Black Chinese Wolfberry Market has a lot of room to grow, but there are several industry limitations that could make it harder for it to do so. It&#;s imperative that industry stakeholders comprehend these difficulties. Among the significant market limitations are:
The Global Black Chinese Wolfberry Market is Segmented on the basis of Type, End-Use Application, and Geography.
The major players in the Black Chinese Wolfberry Market are:
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Lycium barbarum L. is a species widely used in dietary supplements and natural healthcare products. The berries, also known as goji or wolfberries, mostly grow in China, but recent reports on their outstanding bioactive properties have increased their popularity and cultivation around the world. Goji berries are a remarkable source of phenolic compounds (such as phenolic acids and flavonoids), carotenoids, organic acids, carbohydrates (fructose and glucose), and vitamins (ascorbic acid). Several biological activities, such as antioxidant, antimicrobial, anti-inflammatory, prebiotic, and anticancer activities, have been associated with its consumption. Hence, goji berries were highlighted as an excellent source of functional ingredients with promising applications in food and nutraceutical fields. This review aims to summarize the phytochemical composition and biological activities, along with various industrial applications, of L. barbarum berries. Simultaneously, the valorization of goji berries by-products, with its associated economic advantages, will be emphasized and explored.
Recently, several reports highlighted the impressive bioactive capacities of goji berries [ 2 , 4 , 10 , 12 , 13 , 14 , 15 , 16 ], not only in cell assays [ 17 , 18 , 19 ] but also in animal studies [ 3 , 14 , 20 ] and human trials [ 21 ]. Despite the growing numbers of published papers regarding the bioactive composition of goji berries, few of them give particular emphasis to in vivo studies as well as to the by-products generated during berry production. Therefore, the aim of this work is to provide a comprehensive review of the bioactive compounds of goji berries, along with their biological activity, giving a particular focus to in vivo studies and clinical trials. The various industrial applications of L. barbarum berries will also be highlighted, as well as the valorization of goji berries by-products.
Plants have been used for thousands of years as a source of compounds for traditional medicine, aiming to prevent and treat health problems [ 1 ]. Due to a broad number of studies that describe the influence of natural products on the human endogenous defense system [ 2 , 3 ] as well as &#;curative&#; effects against a wide spectrum of disorders, including cardiovascular and neurodegenerative diseases, obesity, and certain types of cancer [ 4 ], multiple natural products have been used for healthcare proposes. Nowadays, the interest in exotic berry-type fruits has expanded worldwide [ 5 , 6 , 7 , 8 ]. Society has become more concerned with eating habits, mostly due to the reinforcement of a positive relationship between good eating habits and the prevention of disease development, particularly diabetes and cardiovascular and neurological pathologies [ 9 ]. Simultaneously, the emergent awareness of the planet and the impact that various types of industries have on it has boosted the population&#;s concerns and demands for greener formulations with bioactive ingredients recovered from natural sources [ 5 , 10 ]. Therefore, the consumption of natural matrices has increased in recent years, not only as supplements for imbalanced diets but also as an integral part of a normal healthy diet [ 7 , 11 ].
All these pro-healthy properties have attracted the attention of consumers to goji juices and fruits, transforming goji berries into one of the most popular functional food ingredients/supplements worldwide [ 13 ]. Nevertheless, the consumption of natural supplements needs to be balanced to avoid negative effects related to overuse or interaction with other medical treatments [ 7 ]. Therefore, risk/benefit evaluations are urgently needed when used in foods or health-promoting formulations in order to avoid negative impacts [ 4 ].
For thousands of years, goji berries have been used as herbal medicine in Asian countries [ 24 ]. Based on their rich nutritional value and medical properties, such as their antioxidant, antimicrobial, immunomodulatory, and anti-inflammatory effects [ 15 , 23 , 31 ], the fruit has been employed as an anti-aging treatment, tranquilizer, and thirst-quenching treatment [ 2 , 13 ]. As a folk medicine, L. barbarum fruits have been employed by the local population for blood nourishing, in the treatment of early onset diabetes, tuberculosis, dizziness, and chronic cough, and for the protection of eye health [ 15 ].
The berries have a sweet taste [ 16 ] and are widely used as a dietary supplement and natural health product [ 4 , 23 , 25 ]. Although mostly consumed fresh in the regions of cultivation [ 9 ], around the world, goji berries are essentially consumed dried [ 9 , 12 ] or transformed into alimentary products, such as juices, herbal teas, yogurt products, granola, powders, and tablets, among others [ 9 , 12 , 30 ]. The most commonly sold goji berry-based products are beverages, wine, juice, tea, and concentrates [ 4 , 14 , 23 ]. A popular goji berry juice brand, &#;GoChi&#;, has shown increasing effectiveness as an antioxidant, giving rise to subjective feelings of general well-being as well as improvements in neurologic/psychologic performance and human gastrointestinal functions [ 23 ], which has led to huge popularity among consumers.
The goji berries can be divided into different classes according to their ripening stage, dimension, weight, color, firmness, solid soluble content, pH, and titratable acidity [ 22 ]. The mature fruit ( ) is between 1 and 2 cm long, presenting an ellipsoid shape and a bright orange-red color, similar to a mature mini-tomato, and contains between 20 and 40 tiny seeds per fruit [ 6 , 13 , 22 ].
Lycium barbarum L. is one of the most common species of the Solanaceae family [ 13 , 22 ]. The berries traditionally grow in China, Tibet, and other parts of Asia [ 6 , 13 , 23 ]. China is the primary worldwide supplier [ 24 , 25 ], with about 25,000&#;30,000 tons of dried fruit annually produced in Ningxia, Xinjiang, Gansu, Qinghai, and Mongolia [ 26 ]. Asia is the region with the highest production (71.2%), followed by Africa (15.8%), America (8.3%), Oceania (3.4%) and Europe (1.3%) [ 27 ]. Due to the rising reports of the positive correlation between the consumption of natural matrices and health improvement [ 9 ], the production of fruit has been increasing in the last 20 years all over the world. This is the case of goji berries, whose production has been increasing in the last decades [ 28 ], particularly in Europe (Italy, Romania, Bulgaria, Portugal, Greece, Serbia), Northern America, and Australia. Currently, Romania has the largest cultivated area of L. barbarum in the European Union [ 4 , 10 ]
The variations observed between the different studies may be explained by several reasons. As mentioned earlier, a broad number of biological variables interfere with the bioactive composition of fruits, such as ripeness, geographic origin, or climatic conditions [ 26 , 31 , 32 , 36 ]. On the other hand, the extraction techniques employed, the extractor solvents used, and the quantification techniques employed, may lead to different results [ 9 , 43 ]. Generally, mature fruits are associated with huge amounts of bioactive compounds with pro-healthy effects.
In what concerns vitamins, ascorbic acid (48.94 mg/100 g fw) and tocopherols (0.33 mg/100 g dw) have been described in goji berries [ 13 , 14 , 30 , 33 , 41 ]. Vitamin E, also known as α-tocopherol, is the major liposoluble antioxidant present in the cells&#; antioxidant defense system, being able to inhibit membrane lipidic peroxidation [ 5 , 42 ], while vitamin C, also known as ascorbic acid, is an important antioxidant compound of goji berries [ 10 ].
Concerning the mineral content, numerous studies showed that the principal minerals present in goji berries are potassium, sodium, and calcium. Bora et al. [ 23 ] reported that 100 g of goji berries contain 434 mg of potassium, 60 mg of calcium, 5.4 mg of iron, and 1.5 mg of zinc. Llorent-Martínez et al. [ 6 ] reported a higher amount of potassium ( mg/100 g), sodium (550 mg/100 g), and calcium (50 mg/100 g), while Ilić et al. [ 33 ] quantified potassium (445.12 mg/100 g dw), phosphor (231.52 mg/100 g dw), sodium (74.57 mg/100 g dw), and calcium (29.02 mg/100 g dw).
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Regarding organic acids, Pires et al. [ 30 ] stated that citric, succinic, and oxalic acids (respectively, 1.29 g/100 g dw, 0.77 g/100 g dw, and 0.010 g/100 g dw) were detected, as well as tocopherols, namely α-tocopherol and δ-tocopherol (0.23 mg/100 g dw and 0.09 mg/100 g dw, respectively). The authors also determined the fatty acids content (4.1 g/100 g dw), more specifically detecting sixteen fatty acids, with polyunsaturated fatty acids being the predominant group, namely linoleic acid (53.4%), oleic acid (16.5%) and palmitic acid (12.77%). In parallel, Ilić et al. [ 33 ] reported that the most abundant fatty acids were linoleic (52.1%), oleic (23.6%) and palmitic (17.6%) acids, accounting for 95% of the total fatty acids, which is in concordance with Skenderidis et al. [ 32 ], who reported concentrations of 37.89&#;43.96%, 16.71&#;20.07%, and 15.08&#;21.79%, respectively.
A study carried out by Bora et al. [ 23 ] attested to the presence of carbohydrates (46 g/100 g of fw), dietary fibers (16 g/100 g fw), proteins (13 g/100 g fw) and fat (1.5 g/100 g fw) in goji berries. In another study, Ilić et al. [ 33 ] reported the presence of moisture (75.32 g/100 g of fw), carbohydrates (16.93 g/100 g fw,), dietary fiber (3.63 g/100 g fw), protein (1.98 g/100 g fw), fat (1.15 g/100 g fw), and ash (0.84 g/100 g fw) in L. barbarum berries. Similarly, Pires et al. [ 30 ] evaluated the presence of carbohydrates (87 g/100 g dw), proteins (5.3 g/100 g dw), fat (4.1 g/100 g dw), and ash (3.21 g/100 g dw) in dried goji berry fruits and stems. The same authors also reported the presence of soluble sugars (27.9 g/100 g dw), such as fructose (12.7 g/100 g dw), glucose (14.4 g/100 g dw), and sucrose (0.8 g/100 g dw). However, different authors [ 10 , 16 , 20 , 21 , 38 , 39 , 40 , 41 ] attested that polysaccharides are the major carbohydrates present in goji berries, being the principal active ingredients isolated from the fruit. Among them, water-soluble polysaccharides, homogeneous polysaccharides, pectin polysaccharides, acidic heteropolysaccharides, and arabinogalactans (composed of arabinose, glucosamine, galactose, glucose, xylose, mannose, fructose, ribose, galacturonic acid, and glucuronic acid) are the most prevalent.
A study conducted by Donno et al. [ 13 ] using goji berries supplied by a farm located in Alzate di Momo, Northern Italy, reported the presence of organic acids (.02 mg/100 g fw) and polyphenolic compounds (12,697.90 mg/100 g fw). Meanwhile, in a study [ 31 ] using goji berries provided by a planting base in Gansu Province, China, the researchers identified nine phenolic compounds by UPLC-MS/MS, including quercetin, isoquercitrin, chlorogenic acid, ferulic acid, p-coumaric acid, caffeic acid, isorhamnetin, cinnamic acid, and rutin, being rutin, isoquercitrin, and chlorogenic acid. Similarly, Pires et al. [ 30 ] extracted goji berries supplied by a Portuguese company and reported the presence of nineteen phenolic compounds (71 mg/g dw): eight flavonols (27.6 mg/g dw), seven phenolic acid derivatives (32.7 mg/g dw), one flavan-3-ol (10.4 mg/g dw), and three chlorogenic acids (25.07 mg/g dw). According to the authors, the principal phenolic compounds quantified were quercetin-3-O-rutinoside (16.6 mg/g dw) and p-coumaric acid (12.3 mg/g dw). Nardi et al. [ 3 ] conducted a phytochemical analysis on a methanolic extract of goji berries, revealing the presence of phenolic compounds (142.2 mg/100 g of extract) and flavonoids (74.5 mg/100 g of extract), while the qualitative analysis identified rutin and quercetin as the principal compounds. Wojdyło et al. [ 36 ] highlighted the carotenoid content of goji berries from new cultivars in Poland (212.94 mg/100 g dw). The authors identified different types of carotenoids, namely zeaxanthin (84.54 mg/100 g dw), β-carotene (19.35 mg/100 g dw), neoxanthin (16.04 mg/100 g dw) and cryptoxanthin (72.29 mg/100 g dw).
As can be observed in , the values achieved for the different assays (TPC, TFC, and TCC) are slightly different between studies. For example, the TPC varied between 31.6 mg GAE/100 g dw [ 2 ] and mg GAE/100 g dw [ 12 ]. These variations are mostly due to the different postharvest techniques used that mainly affect the bioactive components present, as well as the extraction solvents employed and the samples&#; geographical origin. Islam et al. [ 2 ] studied the phenolic profile, antioxidant capacity, and carotenoid content of dried goji berries harvested in China and extracted with a mixture of acetone/water/acetic acid (70:29.5:0.5). According to the authors, the TPC achieved a value of 31.6 mg GAE/100 g dw, while the TFC was 28.3 mg CAE/100 g dw. These values were considerably lower than the ones reported by Magalhães et al. [ 12 ]. Despite the same geographical origin, the authors lyophilized the samples and extracted them for 5 days using methanol (80%), which could justify the huge differences observed.
Oxidative stress is implicated in the aging process as well as in several pathologies (e.g., cardiovascular dysfunction, various typologies of cancer, inflammation, rheumatism, diabetes, rheumatoid arthritis, pulmonary emphysema, dermatitis, cataract, neurodegenerative diseases, endothelial cell dysfunction, and several autoimmune diseases linked to degenerative processes of aging) that frequently lead to invalidity or death [ 3 , 9 , 13 ]. When the endogenous antioxidant mechanisms are not enough to stop and prevent oxidative stress, supplementation is needed to strengthen the antioxidant state and the cell defense mechanisms of organisms [ 25 ]. Fruit phenolic compounds are excellent candidates to perform this scavenging effect against ROS and other radical species [ 35 ].
Reactive oxygen species (ROS) naturally occur in living organisms, being involved in processes such as proliferation and apoptosis [ 25 ]. However, when the quantities of ROS, such as superoxide radicals (O 2 ·&#; ), hydrogen peroxide (H 2 O 2 ), and hydroxyl radicals (OH ·-&#; ), overcome the activity of endogenous antioxidant mechanisms, namely antioxidant enzymes (e.g., superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx)) and non-enzymatic molecules (e.g., glutathione (GSH), ascorbic acid, α-tocopherol), a state of oxidative stress is initiated [ 10 , 25 , 35 ].
Phenolic compounds act as a defense mechanism to provide adaptation and survival capacity in adverse environmental conditions to plants, such as protection against ultraviolet radiation (UV), pathogen aggression, parasites, and predators [ 5 , 35 ]. These compounds usually add nutritional and functional value, contributing to the fruit&#;s organoleptic characteristics, such as astringency, bitterness, and aroma. Simultaneously, they guarantee outstanding biological activities and pro-healthy properties against oxidative stress [ 5 , 13 , 31 ], being capable of delaying, preventing, and inhibiting oxidation by scavenging free radicals and, therefore, reducing oxidative stress [ 35 ].
The bioactive composition of plants is influenced by many factors, such as variety, ripeness, geographic location, and climatic conditions. Since during fruit growth, physiological, biochemical, and molecular changes occur, ripeness might be the most influential factor in the fruit&#;s bioactive composition [ 31 , 32 ]. Therefore, deep knowledge about the ripening stage of goji berries is needed to determine the best stage and obtain the most adequate bioactive compounds. Yet, in general, various researchers have reported that goji berries have a remarkable concentration of antioxidants, fat, dietary fibers, essential amino acids, valuable trace minerals, and vitamins [ 3 , 6 , 13 , 23 , 30 , 33 , 34 ]. In the next subsections, the different classes of bioactive compounds present in goji berries will be deeply analyzed.
Goji berries have been used for thousands of years as herbal medicines in Asian countries due to their rich nutritional value, medical properties, and biological activities [2,13,23,31]. Several studies highlighted the pro-healthy effects of goji berries, particularly in regarding their antioxidant [2,4,12,13], anti-tumor [4,10,15,40], antimicrobial [10,24], hypoglycemic [10], hypolipidemic [10,14], anti-mutagenic [40], immunomodulatory [16], prebiotic [10,23,24], anti-aging [10], anti-fatigue [10] and neuroprotective activities [12]. These biological activities have been closely related to the fruits&#; phenolic composition, particularly phenolic acids, flavonoids, carotenoids, and tannins, which are associated with different biological effects [2,5,23,31,42]. This correlation led to reports of health benefits associated with liver, kidney, eyesight, immune system, circulation, and longevity disorders [4,19,24,30,36]. The following sections will discuss each biological activity in detail.
Oxidative stress is a phenomenon that occurs due to an imbalance between pro-oxidants and antioxidants, being a consequence of the excessive production of reactive species [3]. In some situations, external antioxidant supplementation is required to reestablish the balance, and fruits&#; phenolic compounds are well-known for this capacity [35]. The main contributors to the antioxidant capacity of food, especially fruits and vegetables, are phenolic compounds, particularly phenolic acids and flavonoids, carotenoids, tocopherol, polysaccharides, ascorbic acid, and condensed tannins [2,5,10,36,42]. These molecules stimulate the antioxidant defenses by delaying, inhibiting, or preventing the free radicals from damaging proteins, DNA, and lipids, as well as by scavenging free radicals by hydrogen atom transfer or electron donation or enhancing endogenous antioxidant defenses, such as antioxidant enzymes (SOD, CAT, GPx, &#;) [3,10,13,35].
Different assays are usually employed to evaluate the radical and antioxidant scavenging capacity. The most frequently applied include the 2,2-diphenyl-1-picrylhydrazyl radical (DPPH&#;), the 2,20-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) radical cation (ABTS&#;+), scavenging activity, and ferric reducing antioxidant power (FRAP) [10,43]. summarizes the reported data on the antioxidant and antiradical activities of goji berries.
A study conducted by Islam et al. [2] assessed the TPC (3.16 mg GAE/g dw), TFC (2.83 mg CAE/g dw), condensed tannin content (CTC; 1.08 mg CAE/g dw), and monomeric anthocyanin content (MAC; 0.24 mg MAC/g dw) of goji berries, along with DPPH (16.65 µmol TE/g dw), ABTS (59.14 µmol TE/g dw), and FRAP (.75 mmol Fe2+E/g dw) capacity. The results showed a positive linear correlation between DPPH, ABTS, FRAP, and phenolic compounds (0.786, 0.643 and 0.856, respectively), flavonoids (0.857, 0.714 and 0.786, respectively), condensed tannin (0.429, 0.714 and 0.643, respectively) and anthocyanin content (0.643, 0.786 and 0.857, respectively), supporting the idea that phenolic compounds are the main contributors to the antioxidant/antiradical activities of goji berries, which is in line with previous studies [35]. Another study [13] evaluated the TPC (268.5 mg GAE/100 g fw), FRAP (19.36 µmol Fe2+E/g fw), and total bioactive compound content (TBCC; .80 mg/100 g fw) of a methanolic extract of goji berries and identified and quantified the principal bioactive compounds present, namely polyphenols (12,697.90 mg/100 g fw) and organic acids (.01 mg/100 g fw). Afterwards, the authors verified the correlation between the antioxidant activity and the variables evaluated, reporting a strong positive correlation between the antioxidant capacity and phenols (0.), organic acids (0.), TPC (0.) and TBCC (0.), which attests to the antioxidant capacity of goji berries.
Similarly, after identifying and quantifying the polyphenols (97.23 mg/100 g dw), carotenoids (212.94 mg/100 g dw), organic acids (24.7%), and flavonols (75.3%), Wojdyło et al. [36] determined the antioxidant/antiradical activities of goji berries by FRAP (1.44&#;6.30 mmol TE/100 g fw) and ABTS assays (1.60&#;6.83 mmol TE/100 g fw). The Pearson correlation allowed the verification of a linear correlation between ABTS or FRAP and the total polyphenolic compounds (0.523 and 0.038, respectively), phenolic acids (0.277 and 0.328, respectively), and flavonols (0.531 and 0.409, respectively). However, goji berries have a high content of carotenoids; therefore, the Pearson correlation between the ABTS or FRAP and the total carotenoids (0.462 and 0.409, respectively), zeaxanthin (0.381 and 0.315, respectively), β-carotene (0.316 and 0.277, respectively), neoxanthin (0.546 and 0.527, respectively) and cryptoxanthin (0.411 and 0.379, respectively) proved the importance of these compounds for the antioxidant power of this fruit.
Meanwhile, Pehlİvan Karakaçs et al. [20] evaluated the levels of antioxidant enzymes (namely SOD, CAT, and GPx) and malondialdehyde (MDA), a characteristic molecule of the oxidative state, when a L. barbarum polysaccharide (LBP) extract was orally administrated to rats for 4 weeks. The LBP extract was prepared by crushing 200 g of dried fruits and performing 2 extractions with 600 mL of a chloroform:methanol (2:1) solution at 80 °C. The results showed that the SOD, CAT, and GPx levels increased, while the MDA levels decreased in the blood serum of rats treated with LBP extract, supporting the in vivo antioxidant power of goji berries.
Skenderidis et al. [25] also demonstrated the antioxidant activity of an aqueous extract of L. barbarum berries cultivated in Greece and extracted by ultrasound-assisted extraction (UAE). The results of the XTT assay performed in C2C12 muscle cells showed cytotoxicity in concentrations higher than 125 µg/mL. The levels of GSH were also evaluated by flow cytometry after exposing C2C12 muscle cells to the extract (25 µg/mL and 100 µg/mL), and the results revealed an increase of 127.5% and 189.5%, respectively, when compared to the control. As for the thiobarbituric acid reactive substance (TBARS) levels, a marker of lipid peroxidation, the decreases of 21.8% and 9.4% after exposure to 25 µg/mL and 100 µg/mL, respectively, attested to the antioxidant capacity of goji berries extracts.
Despite the extensive research and the advances in cancer treatments made in recent years, cancer is still a worldwide problem [17,40]. The knowledge that several polyphenol-rich extracts from natural matrices have been suggested as promising anticancer agents with few side effects, being associated with lower risks of cancer and cancer mortality, has increased consumers&#; interest in fruits and natural matrices [5,6,35].
Kwaśnik et al. [17] performed a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay with human natural killer cells (NK-92) against human colon cancer cell line LS180 after 48 h of incubation in the presence or absence of an ethanolic extract of goji berries in different concentrations (1&#;500 µg/mL). According to the authors, in the absence of the extract, the strongest anticancer effect obtained (with the elimination of 91% of the cancer cells) occurs when LS180 and NK-92 were used in a ratio of 1:1. In the presence of extract, using the same ratio, 94.8% of the LS180 cells were eliminated. Therefore, goji berries extract reduced by 5%, 12.8% and 20.6%, respectively, the proliferation of LS180 using concentrations of 1, 2.5 and 5 μg/mL. When LS180 and NK-92 cells, in a ratio of 2:3, are exposed to goji berries extract in concentrations of 2.5 and 5 μg/mL, the viability of LS180 cells is reduced to 96.5% and 98.1%, respectively. These results support the chemopreventive properties of goji berry extract, depending on the dose and number of lymphocytes used. Probably, this is due to the immunomodulatory properties of goji berries, which increase the viability and proliferation of NK cells and promote their recognition and elimination capacity.
Another study assessed the proliferation and apoptotic and necrotic effects of different concentrations of an ethanolic extract of goji berries in the T47D human breast cancer cell line [44]. The MTT assay results attested to a strong decrease in cell proliferation after exposure to the highest extract concentration (1 mg/mL) (70%, 55.7%, and 51.4% after 24, 48, and 96 h, respectively). The bromodeoxyuridine (BrdU) cell proliferation assay supported these results, showing a sharp decrease in the proliferation of T47D cells, similar to the Neutral Red (NR) cell viability assay, which demonstrated a slight decrease in the T47D cell viability. The Western blotting analyses employed to evaluate the expression of p21 and p53 proteins, cyclin-dependent kinase 6 (CDK6), and cyclin D1 highlighted the significant increase in p21 and p53 protein expression as well as a slight decrease in CDK6 and cyclin D1 expression. Regarding T47D cells, an increase in the apoptotic percentage was detected (37%, 61.6%, and 88% when treated with 0.1, 0.5, and 1 mg/mL of extract, respectively), as well as a significant necrotic change at 0.5 mg/mL of extract for propidium iodide and Hoechst solution staining. These results attested that the anticancer activity of goji berries extract is due to apoptotic effects through the mitochondrial pathway. To confirm these results using Western blotting, the authors demonstrated a dose-dependent significant increase in pro-apoptotic Bax protein expression and a decrease in anti-apoptotic BclxL protein expression after treatment of T47D cells with the extract for 48 h when compared to the control.
A study using hepatoma cells (SMMC- and HepG2), cervical cancer cells (HeLa), gastric carcinoma cells (SGC-), and human breast cancer cells (MCF-7) determined the influence of L. barbarum fruits&#; crude polysaccharides on the inhibition of cancer cell growth via cell arrest and apoptosis [40]. According to the authors, the fruits&#; crude polysaccharides were obtained by water extraction, alcohol precipitation and deproteinization, and fractional precipitation with gradient concentrations of ethanol (30%, 50%, and 70%), originating different fractions (LBGP-I-1, LBGP-I-2, and LBGP-I-3). Through an MTT assay, all L. barbarum fruit polysaccharide fractions showed a remarkable inhibition of SMMC-, HeLa, and MCF-7 cell growth in a dose-dependent manner, with MCF-7 cells being more sensitive to the LBGP-I-3 fraction (with a cell viability reduction to 48.96%). To study the inhibitory mechanism behind this result, the cell cycle of MCF-7 cells treated with LBGP-I-3 at µg/mL was analyzed by flow cytometry. The results showed a percentage of 72.76%, 24.21%, and 3.04% of cells in the G0/G1, S, and G2/M phase, respectively, suggesting that LBGP-I-3 arrested the MCF-7 cell cycle at the G0/G1 phase. AO-EB and DAPI staining were used to detect basic morphological changes in apoptotic cells, with the results attesting that the LBGP-I-3 fraction induces the MCF-7 apoptosis. The results also supported that the apoptotic effect was caused by the increased expression of pro-apoptotic Caspase-3, 8, and 9 proteins as well as the decrease in the Bcl-2/Bax ratio and mitochondrial membrane potential. A significant decrease in T-SOD and CAT activities, as well as GSH-Px activity and GSH content, coupled with the enhancement of the MAPK signaling pathway, down-regulating p-ErK1/2 levels and up-regulating p-JKN and p-p38 levels, was also observed.
The phytochemicals present in plants, particularly phenolic acids, flavonoids, and tannins, exert their antimicrobial effects by complexing with extracellular and soluble proteins, leading to the disruption of the microbial membrane, metal ion deprivation, and interactions with enzymes [30,45]. Another way of explaining the antimicrobial activity of polyphenols is their structural features, as well as the pH and sodium chloride concentration, which results in physiological changes in the microorganisms and, eventually, cell death [45].
A study carried out by Kabir et al. [45] confirmed that chlorogenic acid, one of the principal phenolic acids detected in goji berries, exhibited a bacteriostatic and bactericidal effect against Escherichia coli. The bacteriostatic effect was assessed by measuring the optical density by determining the growth inhibition of chlorogenic acid when added to a culture of E. coli. Regarding the bactericidal effect, it was assessed by using mid-logarithmic phase cell cultures (106 cells/mL) at different doses (2.5, 5.0, and 10 mM), treatment times (0, 1, 3, and 6 h), temperatures (20, 37, 45, and 50 &#;C), and pH conditions (8.0, 7.0, 6.0, 5.0, and 4.0). The overall results demonstrated a synergetic antimicrobial effect expressed by chlorogenic acid and related compounds and a dose, temperature, and time-dependent bactericidal effect. The authors stated that the bactericidal effect shown by chlorogenic acid may be due to the capacity to promote physiological changes on the microbial cell membrane that result in cell death. This study corroborated the results achieved by Ilić et al. [33], which evaluated the antimicrobial activity of goji berries from Serbia. According to the authors, the methanolic extract of goji berries presented mild antimicrobial activity against Gram-positive and Gram-negative bacteria as well as yeast, with remarkable activity against Klebsiella pneumoniae, Salmonella abony, and Pseudomonas aeruginosa. In another study, Mocan et al. [46] also explored the antimicrobial activity of L. barbarum flowers. According to the authors, the antimicrobial activity was mild against Gram-positive (namely Staphylococcus aureus, Bacillus subtilis, and Listeria monocytogenes) and Gram-negative (Salmonella typhimurium) bacteria and lacking against E. coli, oppositely to what was observed for goji berries.
The inflammatory response is initiated by the stimulation of innate immunity, the release of immune effectors, the inhibition of enzymes, and the production of pro-inflammatory mediators, such as tumor necrosis factor-α (TNF-α), interleukins (IL), and transcription factor nuclear factor kappa B (NF-kB) [3]. If over-expressed, inflammation can cause numerous complications in patients, being an important hallmark of diseases or pathological conditions, such as cancer, neurodegenerative diseases, respiratory pathologies, and several autoimmune diseases [3,5]. Natural extracts, typically rich in alkaloids, flavonoids, terpenoids and tannins, have been associated with anti-inflammatory effects [5]. A study conducted by Nardi et al. [3] addressed the anti-inflammatory effect of L. barbarum berries using paw edema carrageenan, an acute model of inflammation widely employed to evaluate the anti-inflammatory effect of natural products. Briefly, the right paw of mice was injected with 450 µg of carrageenan, and the left paw was injected with the same volume of sterile phosphate-buffered saline (PBS) (control). After established conditions, the animals were orally administered with a methanolic extract of goji berries in doses of 50 mg/kg and 200 mg/kg, 12 h after 12 h, for 10 days. The authors stated that after the carrageenan injection, neutrophils migrate to the inflamed paw and release enzymes, such as myeloperoxidase, which increase ROS production and induce an inflammatory state. The results attested to the anti-inflammatory capacity of the compounds present in goji berries, with the doses of 50 mg/kg and 200 mg/kg leading to a reduction of paw edema in 38% and 63.8% of mice, respectively.
Immune response suppression is usually associated with the development of immunological diseases. The actual research is focused on finding immunomodulating agents capable of preventing and treating these disorders [47]. Goji berries have been reported as a support to the immune system [6,47], either by regulating the expression of immune factors, such as cytokines and cell adhesion molecules [16,39], or by promoting the proliferation and activity of immune cells, such as natural killer cells [17] and lymphocytes [47].
Different authors [16,24,39,47] stated that the immunomodulatory effects of L. barbarum fruits are greatly related to LBP, one of the major active ingredients isolated from berries. LBP is a mixture of proteoglycans and polysaccharides that mainly consists of arabinose, galactose, glucose, xylose, and a small amount of rhamnose, mannose, and galacturonic acid as its glycosidic part. It was reported that LBP is an adjuvant that improves the immune responses against vaccines and increases humoral immunity [39], probably due to an increased expression of IL-2 and TNF-α, molecules involved in immunomodulation [16]. To assess the immune function alteration during the administration of LBP, Zhu et al. [39] divided fourteen mice into two groups and administered a dose of 0.1 mL/10 g body weight of LBP powder for 14 days in the first group, the experimental group, and the same volume of physiological saline via intragastric administration in the second group, the control group. After the experimental period, blood samples were collected, and the animals were sacrificed to excise the spleen and thymus. The viscera indices were measured (thymus or spleen index = weight of thymus or spleen (mg)/body weight ( mg)), and the concentrations of immune factors (namely, transforming growth factor-β (TGF-β), interferon-γ (IFN-γ), and IL-6) in the serum were detected using a commercial enzyme-linked immunosorbent assay (ELISA) kit. The results supported the theory that LBP can enhance the innate immune response since the spleen and thymus index of mice from the experimental group (5.12 mg/ mg and 4.12 mg/ mg, respectively) were significantly higher (p < 0.05) when compared to the control group (namely 4.19 mg/ mg and 2.86 mg/ mg). Moreover, the concentration of the immune factors TGF-β and IL-6 in the experimental group (namely, > 500 pg/mL and &#; 100 pg/mL) were also significantly higher (p < 0.05) when compared to the control group.
It has also been reported that phenolic amides from the nonpolysaccharide fraction of L. barbarum fruits can not only in vitro modulate the proliferation of B and T cells but also enhance the immune cell factors (IFN-γ, IL-2, and IL-10) [47]. Prednisone-induced immunodeficient mice were intragastrically administered with a phenolic amid extract, showing a significant spleen cell proliferation (p < 0.01) when compared to the prednisone-induced immunodeficient mice intragastrically administered with an ethanolic extract of goji berries or an LBP extract. The immunological cytokines (IFN-γ, IL-2, and IL-10) were also significantly enhanced (p < 0.01) in mice treated with the ethanolic goji berries extract, LBP extract, and phenolic amide extract when compared to the control. Overall, the total phenolic amides had the strongest immunity-activating effects.
Since natural killer cells are one of the first elements from the innate immune system to act, Kwaśnik et al. [17] studied the cell viability and proliferation of human natural killer cells (NK-92) in the presence of an ethanolic goji berry extract. The authors highlighted that goji berry extract has the capacity to enhance NK cell proliferation by 61.0% in concentrations ranging between 1 and 250 µg/mL.
Prebiotics are non-digestible ingredients that can selectively promote the growth and activity of specific bacteria, modulating the gut microbiota [39]. Goji berries have demonstrated a gut microbiota positive modulating effect [18,39], probably due to phenolic compounds or polysaccharides present, such as LBP [43]. The prebiotic activity of goji berries was attested to by Skenderidis et al. [18], who cultivated strains of Bifidobacterium and Lactobacillus in the presence and absence of different encapsulated goji berry extracts. According to the authors, the extract with higher amounts of polyphenols and polysaccharides stimulated the growth and proliferation of probiotic strains on a larger scale, mostly Bifidobacterium strains, when the cultures were submitted to a gastrointestinal environment (simulated gastric and intestinal juices). Another study [39] assessed the prebiotic activity of LBP in vitro through the growth of L. acidophilus and B. longum. Both strains were properly cultivated, and different concentrations of LBP powder (experimental group) and glucose (control group) were administered. These experiments highlighted the positive effect of LBP on the growth of both strains when compared to the control group. The authors also evaluated the effects of LBP intake on the composition of cecal gut microbiota [39]. After mice were administered a dose of 0.1 mL/10 g body weight of LBP powder for 14 days, the cecal content samples were collected, and the microbial DNA was extracted and amplified. The results showed a clear modification of the gut microbiota after treatment, with the dominant bacterial communities being Firmicutes and Proteobacteria. Furthermore, the percentage of beneficial bacteria, such as Akkermansia, Lactobacillus and Prevotellaceae, significantly increased when compared to the control.
Since neurological damage may occur as a consequence of oxidative stress and inflammation, goji berries have been associated with neuroprotective effects [43]. A study conducted by Fernando et al. [19] assessed the neuroprotective activity of a goji berry powder (GBP) against the development of Alzheimer&#;s disease (AD). The authors observed that diets rich in antioxidants can directly affect amyloid beta levels and influence the development of AD. To test this theory, human neuroblastoma BE(2)-M17 cells were treated with and without 20 µM of amyloid beta 42 and exposed to different concentrations of GBP (0.6, 0.9, 1.2, 1.5 and 1.8 µg/mL). The GBP significantly increased the cell viability up to 105% (GBP at 1.2 µg/mL), while the Western blot analysis showed a significant reduction in the amyloid beta up to 20% (GBP at 1.5 µg/mL). Furthermore, the ELISA attested to a 17% reduction of the amyloid beta in amyloid beta-induced neuronal cells when compared to the control (GBP at 1.5 µg/mL). Other authors [16,24] also stated that the major active ingredient isolated from goji berries, LBP, has ocular and neuroprotective effects [20]. In another study, Pehlİvan Karakaçs et al. [20] reported that LBP has a neuroprotection effect in female rats by performing behavioral tests and immunohistochemistry analyses. The animals were submitted to ovariectomy and daily treated with oral low and high doses of polysaccharides obtained from L. barbarum fruits (20 and 200 mg/kg) for 4 weeks. According to the behavioral test performed, the LBP present in goji berries can decrease stress-induced anxious behavior in rats. The behavioral disruption could be caused by the accumulation of ROS in the brain, which increases oxidative stress, leading to mitochondrial dysfunction in neuronal cells and apoptosis. However, behavioral disruption can also be caused by variations in neurotransmitter levels in some brain regions, such as the hippocampus. The neuroprotective effect of LBP was demonstrated by the increased levels of brain-derived neurotrophic factor, which promotes neuronal proliferation, survival, and maintenance of neuron structure and function in the hippocampus region.
Diabetes is a complex chronic disease caused by metabolic disorders of carbohydrates, lipids, lipoproteins, and increased oxidative stress [43]. It is characterized by the inability to maintain blood glucose levels within healthy ranges, leading to hyperglycemia [36]. Drug treatment is inevitable; however, it is often expensive or unavailable [36]. In these cases, a change in patient lifestyle and eating habits is extremely important [21,38,43]. Therefore, industries are encouraged to find alternative compounds with antihyperglycemic properties, mostly from natural sources, such as goji berries [5,10]. Enzyme inhibitors are good candidates for the treatment of non-insulin-dependent diabetic patients [36]. Since pancreatic α-amylase and intestinal α-glucosidase are enzymes responsible for the hydrolysis of carbohydrates into monosaccharides, such as glucose, the capacity of goji berries to inhibit these enzymes proves the antihyperglycemic effect of this fruit [36]. According to Wojdyło et al. [36], the inhibition of α-amylase and α-glucosidase was, on average, 63% and 10%, respectively.
Most of the experiments that report the antihyperglycemic activity of goji berries have attributed this property to LBP [21,25,38]. Cai et al. [21] performed a clinical trial to study the antidiabetic efficacy of LBP. Sixty-seven patients diagnosed with type II diabetes were divided into two groups and treated twice daily, for three consecutive months, with capsules of 300 mg of microcrystalline cellulose in the control group and capsules with 150 mg of LBP power and 150 mg microcrystalline cellulose in the experimental group. The results of the oral metabolic tolerance test reported a significant decrease in serum glucose levels when compared to the control (&#;7.86% vs. 1.61%), as well as serum insulin (&#;56.71% vs. &#;8.73%). Regarding the insulinogenic index (insulin/glucose), the results attested to a noticeable increase (&#;0.98% vs. 0.04%, respectively, for the experimental and control groups). During the experimental period, the patients were asked not to change their previous therapies in order to compare the antidiabetic effect of LBP with or without the hypoglycemic medicines. After 3 months of treatment, the patients without hypoglycemic drugs showed a significant decrease in serum glucose, serum insulin, and the homeostasis model assessment index of insulin resistance, while the patients with hypoglycemic drugs did not present significant alterations, demonstrating that LBP has profound hypoglycemic efficacy when disassociated from hypoglycemic drugs.
The study developed by Zhao et al. [38] focused on the effect of LBP extract on diabetic rabbits (induced by Alloxan), evaluating the extract&#;s effect on diabetic nephropathy (DN). The experimental period lasted for 12 weeks, in which twenty-five rabbits were divided into five groups: group (I)&#;control group; group (II)&#;DN control group; group (III)&#;LBP prevention group from developing DN; group (IV)&#;positive DN control group using Telmisartan drug (10 mg/kg/day in 3 mL); group (V)&#;LBP treatment group using the LBP (10 mg/kg/day in 3 mL) as DN treatment. The results demonstrated that LBP not only helps after the development of DN but also benefits the prevention of complications since group (V) showed improvements in fasting glucose tolerance when compared to group (II), while group (III) had better results than group (V). This study also highlighted that LBP can be more efficient in the treatment of DN than standard drugs (in group (V), the kidney weight index (KWI) was significantly higher (p < 0.01) than in group (IV)). As for kidney function, even though LBP may be able to protect this organ from injuries, it cannot entirely treat it since the serum urea nitrogen and creatinine levels from groups (III), (IV) and (V) were significantly lower (p < 0.01) that in group (II). No significant changes were observed regarding group (I).
In addition to the biological activities described above, the antihyperlipidemic effect of goji berries has also been reported. Pai et al. [14] fed murine models with a high-fat diet (5 g of deoxycholic acid and 300 g of warm coconut oil mixed with 700 g of powdered rat chow per day) for 45 days to induce a state of hyperlipidemia. In the last 30 days of the study, a group of animals was orally treated daily with 10 mg/kg and 20 mg/kg of a 50% hydroalcoholic extract of L. barbarum fruits. The results showed a positive antihyperlipidemic activity, with the extract promoting a significant decrease in the triglyceride levels for both doses as well as a significant decrease in very low-density lipoprotein cholesterol at the highest dose, a significant increase in the high-density lipoprotein cholesterol at the lowest dose, and a dose-dependent decrease in the total cholesterol and low-density lipoprotein cholesterol levels. Additionally, the results obtained with the animals treated with the L. barbarum fruits and the animals treated with the standard antihyperlipidemic drug atorvastatin were similar, reinforcing the positive antihyperlipidemic activity of goji berries. The authors explained that this effect may be caused by more than one compound present in goji berries, namely polysaccharides and vitamins, such as vitamin C. Additionally, riboflavin, ascorbic acid, and coumarin and their synergistic effects may contribute to the hypolipidemic effect observed.
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