Next Article in Journal
Recent Advances in the Extraction of Pittosporum angustifolium Lodd. Used in Traditional Aboriginal Medicine: A Mini Review
Next Article in Special Issue
Combined Therapy of Chitosan and Exercise Improves the Lipid Profile, Adipose Tissue and Hepatic Alterations in an In Vivo Model of Induced-Hyperlipidemia
Previous Article in Journal
Anti-Inflammatory and Neuroprotective Effect of the Anti-Obesity Dietary Supplement Dekosilhue® in an In Vitro Model of Neuroinflammation
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Goji Berry: Health Promoting Properties

by
Prodromos Skenderidis
*,
Stefanos Leontopoulos
and
Dimitrios Lampakis
Laboratory of Food and Biosystems Engineering, Department of Agrotechnology, University of Thessaly, 41110 Larissa, Greece
*
Author to whom correspondence should be addressed.
Nutraceuticals 2022, 2(1), 32-48; https://doi.org/10.3390/nutraceuticals2010003
Submission received: 8 February 2022 / Revised: 4 March 2022 / Accepted: 9 March 2022 / Published: 14 March 2022
(This article belongs to the Special Issue Functional Foods as a New Therapeutic Strategy)

Abstract

:
Since ancient times, it has been noticed that Goji berry fruit juice, roots and leaves consist of ingredients that contain a wide variety of bioactive substances. The consumption of goji berry fruits results in properties which improve the subjective feeling of general well-being. The aim of this work is to present the information from the existing literature on the possible role of goji berry plant parts and their extracts as a functional food. Lycium barbarum Polysaccharides (LBP) and polyphenols are the most researched aspects of fruits associated with the promotion of human health. Goji berry fruits demonstrated anti-oxidative properties that are associated with age-related diseases such as diabetes, atherosclerosis and antitumor and immunoregulatory activities. Bioactive secondary metabolites contained in fruit lead to positive effects for human vision, while other biochemicals contained in the root bark have shown hepatoprotective and inhibitory actions on the rennin/angiotensin system. The results presented so far in the literature verify their use in traditional medicine.

1. Introduction

Modern life-styles and dietary habits are the main cause of several human modern diseases such as diabetes, hepatitis and cardiovascular issues [1,2,3]. About 1/5 of the known plant species [4] that have participated in pharmaceutical studies cover a wide range of beneficial effects on human health, animal welfare and crop protection by enhancing human health against free radical damage [5,6,7,8,9,10,11,12,13]. The high concentrations of phytochemicals found in plants are accumulated mainly in their fruits and vegetables. Among beneficial phytochemicals, antioxidant compounds including phenolics, anthocyanins, carotenoids, and tocopherols may be used as a supplement for the human body by acting as natural antioxidants [14]. Thus, the consumption of fruit and vegetables has been linked with several health benefits, as a result of medicinal properties and high nutritional value [15] and is recommended by many scientists throughout the world [16]. In more detail, many studies mention the antioxidant and pharmacological activities of different plant extracts [17,18,19,20].
Among important plant species with significant biomedical issues is the Goji berry where fruit juice, roots and leaves contain ingredients that have a variety of bioactive properties [21,22,23,24].
The objective of this paper is to provide a review of phytochemical studies that have addressed the beneficial effects for human health of bioactive compounds contained in Goji berries.

Search Strategy

An electronic literature search was conducted using PubMed, Medline (OvidSP), and Google Scholar for the period between 1992 to 2022. Additional articles were identified from references in the retrieved articles. Search terms included combinations of the following: “goji berry”, “Lycium barbarum”, “health promoting effects”, “phytochemical”, “antioxidant”, “Lycium barbarum polysaccharides” and “pharmacological”. The search was restricted to articles in English that addressed the phytochemical constituents and pharmacological properties of goji berries.

2. Bioactivities

2.1. Antioxidant Activity

The most studied molecular mechanism of the oxidation of cellular components is that of lipid peroxidation. This is a circular feedback chain process, which, if started and not suspended in time, can oxidize all the biological material. DNA can tolerate a large number of different oxidative lesions, depending on the factors that cause them. Unlike oxidized proteins, which are usually fragmented and their amino acids reused, the oxidized DNA can be repaired in situ. Insufficient DNA repair can result in mutation and, ultimately, cell death by either necrosis or apoptosis.
The amino acids cysteine, methionine, tyrosine, phenylalanine, tryptophan and histidine are more susceptible to oxidative modifications. Relatively recent research results in this field commented on the fact that oxidative modifications of amino acid residues in proteins, besides the negative effects, may also play a positive role by participating in the redox signaling process.
Goji berries have been shown to possess antioxidant properties, neutralizing the oxidative action of free radicals and activating antioxidant mechanisms (Figure 1), such as an increase in superoxide dismutase (SOD), glutathione (GSH), glutathione peroxidase (GPx), catalase (CAT), and erythroid-derived 2-like 2 (Nrf2) expression of several antioxidant and cytoprotective enzymes [25]. Thus, L. barbarum extracts exhibited the binding of peroxide anion radicals and the subsequent reduction of their activity [26].
The protective effect on the inhibition of lipid peroxidation by goji berry extracts is probably due to the polyphenols of goji berry fruit (Figure 2) [27]. Caffeic acid, which is the main hydroxycinnamic acid in goji berries, not only has potent antioxidant effects but also has anti-inflammatory and anti-cancer effects, while recent studies have shown that caffeic acid in its free form or conjugated to other groups, such as quinic acid and sugars, has a protective effect against Alzheimer’s disease [28].
Moreover, ethanol extract (70% w/v) of L. chinense protects hepatic cells against oxidative stress-induced cell damage by removing intracellular ROS, SOD recovery, CAT and glutathione action, reducing lipid oxidation, DNA destruction and protein carbonyl values [29]. Further, Changbo et al. [30] have shown that the administration of LBP in mice can reduce the oxidative stress caused after exercise in swimming, increasing the antioxidant enzymes SOD, CAT and GPx.
An important ingredient that contributes to the antioxidant activity of fruits is also AA-2βG, which has similar antioxidant properties to vitamin C. Studies focusing on its effects showed that it exhibits strong binding activity against DPPH and H2O2 and inhibits H2O2-mediated hemolysis better than vitamin C. Studies have also demonstrated similar effects in the binding of OH radicals. Although the in vitro antioxidant capacity has shown that AA-2βG presented lower activity compared to vitamin C; on the contrary, in vivo studies demonstrated that AA-2βG protected mice liver from carbon tetrachloride-induced acute liver injury better than vitamin C [31].
Furthermore, several studies have identified the protective mechanisms of the biochemical action of goji berries in relation to the induction of the Nrf2 nuclear factor [25,32]. A recent study, suggested that goji berry aqueous extracts exhibit antimutagenic activity, protecting DNA against peroxyl and hydroxyl radicals [33]. In the context of the same study, substantial antioxidant activity of goji berry aqueous extracts in C2C12 muscle cells was also observed, indicated by increased glutathione (GSH) levels up to 189.5% and a decrease of protein carbonyls and lipid peroxidation by 29.1% and 21.8%, respectively [33].

2.2. Antiaging Activity

Aging is defined as the accumulation of various deleterious changes in cells and tissues [34], especially for elderly people [35].
Several studies have shown that genetic and environmental factors regulate specific pathways involved in hormone signaling, nutritional signaling and the detection of mitochondrial and ROS signaling and genomic survival. It is a common belief that the accumulation of the effects of oxidative stress contributes to the aging process [36,37,38]. For this reason, many of the experimental aging models use the pouring of D-galactose into mouse or rat tissues for a period of 6–8 weeks as a toxin in order to produce free radicals [39]. According to Deng et al. [40], the addition on a daily basis of 100 mg LBP/kg to the diet of mice reduced serum advanced glycation end products (AGE), retrieving the memory pointer back to experimental animals, increasing superoxide dismutase levels in erythrocytes and finally helping them to restore kinetic activity.
The life cycle of Drosophila melanogaster (fruit-fly) has been used as an alternative model for aging studies. Based on this model, the addition of 16 mg LBP/kg shows a statistically significant increase of the average life span of male insects [41].
Furthermore, studies conducted on elderly mice have shown that the consumption of 200–500 mg/kg of LBP promotes oxidative stress reduction, as it reduces the oxidative stress markers associated with the aging process [42]. It has also been reported that LBP activates the antioxidative pathways Nrf2/ARE and Nrf2/HO-1 by activating antioxidants and detoxifying enzymes. One of these enzymes is heme oxygenase-1 (HO-1), which is regulated by the factor associated with the nuclear factor erythroid 2–related factor 2 (Nrf2) [43].
In vivo studies on Factor Nrf2 have shown that it plays an important role in the endogenous antioxidant system by regulating the expression of important antioxidant enzymes, such as oxygenase-1 (HO-1), SOD and CAT. In particular, in oxidative stress or exogenous (pharmacological) activation, Nrf2 moves into the cell nucleus and induces the expression of antioxidant enzymes by blocking the antioxidant response (ARE) [44]. It has also been commented that activation of PI3K/AKT/Nrf2 not only prevents the development of oxidative stress but also prevents metabolic glucose abnormalities such as the occurrence of insulin resistance. Activation of Nrf2 by LBP offers a new alternative therapeutic approach to the prevention of insulin resistance caused by a long-term high-fat diet [45].
The effect of ultraviolet radiation (UVB) causes skin damage by inducing oxidative and inflammatory lesions and thus causes aging and carcinogenicity of the skin. The protective effect of LBPs through the induction of Nrf2 is likely to exert a protective effect against the negative effect of ultraviolet radiation on the skin by binding to the active radicals and reducing DNA damage, resulting in the suppression of the ultraviolet-induced P38 MAP pathway. Based on the previous beneficial effects, LBP could potentially be used as an ingredient in products intended to protect the skin against oxidative damage from environmental conditions [32].
A recent study investigating retinal protection from damage caused by I/R radiation showed that activation of the Nrf2/HO-1 antioxidant pathway was adapted to neutralize damage to the retina. The use of LBP not only reduced the production of ROS but also enhanced the activation of the Nrf2/HO-1 antioxidant pathway in retinas under the influence of I/R [46].
All of the previous studies support that LBP has positive anti-aging effects, while a clinical study indicates that dietary intake of a total of 500 mg of L. barbarum over 10 days can significantly reduce plasma triglyceride levels and increase levels of cyclic adenosine monophosphate (cAMP) and SOD [47].
As the anti-aging effects of L. barbarum display a wide range of target tissues, it is believed that it can overall protect cells from oxidative, hyperglycemic and hyperlipidemic conditions. According to the results of a previous clinical study conducted in alloxan-treated rabbits, the LBP group reduced the blood glucose levels [48].
In addition to polysaccharides, the presence of components in fruits, such as carotenes, betaine, polyphenols and vitamin C in the precursor form of 2-O-β-d-glucopyranosyl-l- ascorbic acid, contributes to antioxidant and anti-aging properties of the goji berry fruit. Thus, betaine has been shown to have a protective effect against skin aging by ultraviolet radiation by mouse-assisted research. Betaine’s protective effect is mediated by inhibition of the extracellular kinase signal transducer (ERP), protein kinase (MEK) and metalloproteinase 9 (MMP-9), resulting in a reduction in collagen wrinkles and damage caused by UVB [49].
Finally, the regulation of the operation of a basic organ, such as the liver or kidneys, results in the regulation of other organs or even of the entire body, according to the traditional Chinese medicine theory. Based on this theory, in traditional Chinese medicine, the use and consumption of L. barbarum fruits is recommended for the treatment of aging-related diseases due to the appearance of a wide range of positive effects, reducing all risk factors in aging-related diseases.

2.3. Antitumor and Immunoregulatory Activity

The defensive mechanisms of vertebrates are also known as the immune system. The immune system recognizes and destroys foreign invaders and toxic substances by a process known as an immune response. The molecule that causes the immune response is called an antigen. In addition, these mechanisms are involved in the body’s effort to remove aged or damaged cells, as well as destroying cancer cells, while sometimes they cause damage against the tissues of the organism itself.
The two main groups of cells in the immune system are the cells of the medullary line and the lymphocytes. Lymphocytes include B-lymphocytes and T-lymphocytes as well as a large granular cell, NK (or natural killer cells). The medullary cells consist of monocytes/macrophages, dendritic cells, neutrophils, eosinophils and basophils. B lymphocytes have an antibody molecule in their membrane, whereas T lymphocytes have an antigen-binding receptor in their membrane. When a B cell encounters an antigen, it quickly divides and differentiates into a B-cell memory and a B-cell effector or plasmid cell. Plasmocytes produce a large number of antibodies (antibody, Ab) or immunoglobulin (immunoglobulin, Ig) that act on the antigen and destroy it. T-lymphocytes, when they meet an antigen or tumor, secrete cytokines (growth factors), directly killing the infected target cell (CD8 killer T cells) and also activating B-cells to make antibody responses and macrophages to destroy microorganisms that either invaded the macrophage or were ingested by it (CD4 helper T cell). There are two types of immunity—humoral and cellular. Humoral immunity is mediated by antibodies produced by B cells and is the main defensive mechanism against extracellular microbes and their toxins, with secreted antibodies binding to them by inducing their elimination. Cellular immunity is mediated by T cells, with dendritic cells playing an important role against antigens.
A clinical study completed by Cao et al. [50] examined the effect of a combination of lymphokine-activated killer (LAK)/IL-2 and LBP on advanced cancer patients (79 patients). The results of this study showed that the response rate and duration of mean tumor regression of patients treated with LAK/IL-2 plus LBPs was higher than those of patients receiving only LAK/IL-2. LAK/IL-2 plus LBP therapy resulted in a more pronounced increase in NK and LAK activity than LAK/IL-2 alone. Furthermore, a study carried out by Gan et al. [51] showed that the administration of LBP3p polysaccharide enhanced the immune system in S180-bearing mice by increasing spleen lymphocyte proliferation and cytotoxic T-lymphocyte activity (CTL).
However, results published by Zhang et al. [52] showed that LBP therapy inhibited growth of hepatoma cell line QGY7703, phase S, phase interruption and induction of apoptosis, as well as a simultaneous increase in the amount of cellular RNA and Ca2+ concentration in human tissues.
Clinical studies demonstrated the immunomodulatory effects of standardized L. barbarum (GoChi) fruit juice on elderly healthy people in China. The results showed that the GoChi group differed, statistically increasing the number of lymphocytes and levels of interleukin-2 and immunoglobulin G. This study concludes that daily consumption of GoChi significantly increases several immune responses and subjective feelings of general well-being without any undesirable effects [21,22].
Follicular helper CD4 T helper cells (Tfh) are the specialized help providers in B lymphocytes since they are necessary for their maintenance and for differentiation into plasmocytes and memory B cells. For this reason, the correlation of Tfh with the production of antibodies from B lymphocytes was studied. Su et al. [53] investigated whether LBP upregulated expression in such molecules on Tfh cells. BALB/c mice were administered 5 mg/kg, 25 mg/kg and 50 mg/kg LBP daily for 7 days, and the enhancement of the humoral immune response by the activation of Tfh cells using LBP was confirmed by the increase of the expression of numerous molecules, including CXCR5 and PD-1 surface markers. Furthermore, Yang et al. [54] showed in their study that LBPs can enhance the immune system against antigenic infection by enhancing phagocytosis in RAW264.7 phagocytes.
He et al. [55], by observing intracellular ROS production and DNA damage, reported a stimulation effect of LBB on the apoptosis of MCF-7 human breast carcinoma cells and the inhibition of the cell cycle in the G0/G1 phase.
Moreover, Huang et al. [56] investigated the mechanisms of LBP suppressive action against breast cancer in MCF-7 cells in vitro. The results of their study showed that LBP therapy can inhibit the proliferation of MCF-7 cells with insulin-like growth factor 1 (IGF-1) in a dose- and time-dependent manner to suppress phosphatidylinositol 3-kinase activity (PI3 K) and phosphorylated-PI3 K (p-PL3 K) inhibit protein-1 (HIF-1) accumulation caused by hypoxia and suppress the expression of vascular endothelial growth factor (VEGF) mRNA and protein production. These results indicated that LBPs could inhibit tumor cell growth by suppressing IGF-1-induced angiogenesis via the PI3 K/HIF-1/VEGF signaling pathways. In a recent study completed by Deng et al. [57] it was presented that LBP3 polysaccharide could reduce immune toxicity and enhance the antitumor activity of doxorubicin in mice. The results of the aforementioned study showed that LBP3 did not offer protection against body weight loss caused by dox, but it promoted the recovery of body weight starting 5 days after dox treatment in tumor-free mice. Furthermore, LBP3 was found to promote cell cycle recovery in bone marrow cells, improve peripheral blood lymphocyte counts, and restored the cytotoxicity of natural killer cells. Moreover, the antitumor activity of dox, peripheral blood and lymphocyte counts has been improved.
Apart from polysaccharides, phytochemical compounds mentioned previously contribute to the anti-aging activity exerting a protective effect against cancer cells. For example, betaine has been shown to have an inhibitory effect on colorectal cancer because of its anti-inflammatory action. Kim et al. [58] showed that adding betaine to a mouse diet could achieve a reduction of the incidence of colitis associated with cancer by reducing the levels of ROS and its ratio with oxidized glutathione (GSSG), related to the inflammation of cytokines such as IL-6, IL-1β and IL-22 and protein levels of COX-2 and iNOS with azoxymethane-induced colitis. In addition, Hsu et al. [22] demonstrated that the inhibition of colonic HT29 cancer cells from a mixture of nanoparticle and carotenoid extracts from L. barbarum was activated by increasing expression of P53 and P21, reducing the expression of CDK1, CDK2, cyclin A and cyclin B arresting cell cycle at G2/M.
The antitumor activity of goji berry extracts (primarily LBP-based studies) is mainly due to their ability to induce the disruption of cell cycle apoptosis and the inhibition of some important signaling pathways that act as carcinogenic protective agents by eliminating cancerous cells.

2.4. Antidiabetic Activity

The number of patients with diabetes worldwide has quadrupled over the last 30 years, and it is the ninth leading cause of death. One in 11 adults today has type II diabetes, accounting for 90% of diabetes cases, and the prediction is that by 2050, one in three will suffer from diabetes. The majority of people suffering from diabetes are aged between 45 and 64.
Sugar, a common constituent of diet, is also a major factor often responsible for elevating the glucose level in diabetic patients [59]. Diabetes mellitus is a metabolic disease characterized by an increase in blood sugar (hyperglycemia) and a metabolic disorder of glucose (C6H12O6), either as a result of decreased insulin secretion or due to a decrease in the sensitivity of cells to insulin. Insulin is a hormone produced in the pancreas that forces the liver and muscle cells to absorb blood glucose and store it as glycogen for future body energy needs. In case the insulin concentration in the body is low or zero and glucose absorption cannot take place, the body begins to use fat as a source of energy by transporting lipids from adipose tissue to the liver [60]. Nowadays, there are known various types of diabetes. The main diabetes types are type I and type II. In general, diabetes is associated with the risk of serious health complications, including myocardial infarction, stroke, kidney failure, vision loss and premature death. So required care for diabetics is likely to be needed for many years [61].
The effect of the antidiabetic action of goji berry extracts has been investigated in various studies. Goji berries may have a positive effect on blood glucose control, as documented in relevant studies described in a study published by Silva et al. [62]. Furthermore, in a study completed by Wu et al. [63] feeding of type 2 diabetic mice with goji berry extract for 4 weeks showed a decrease in blood glucose levels by 35%. Moreover, Zhang et al. [64] suggested that the fraction LBPF4-OL of the LBP promotes lymphocyte proliferation secreting TNF-α and IL-1β. Luo et al. [48] also showed that L. barbarum extracts have hypoglycemic and hypolipidemic effects as well as strong antioxidant activity in rabbits with diabetes and hyperlipidemia from aloxane.
One of the causative factors for insulin resistance development is oxidative stress. Oxidative stress is one of the factors that can activate the JNK pathway under the diabetes condition. Recent research presented that under an oxidative status, the nuclear factor Nrf2 plays a role in insulin-mediated glucose uptake [33]. The positive effects on insulin resistance from Nrf2 activation caused from the enhancement of insulin sensitivity due to the decrease of ROS production are presented in a study completed by Bagul et al. [65]. Nakatani et al. [66] showed also that activation of c-jun N-terminal kinase (JNK) leads to a decrease of insulin sensibility due to the increase of IRS-1 serine phosphorylation insulin target tissues, while insulin resistance status was improved in the JNK-KO of mice. Furthermore, studies done by Kaneto [67] commented that the activation of p38 mitogen-activated protein kinase (MAPK) and JNK signaling can directly or indirectly promote diabetes. It has been reported that the JNK pathway plays a crucial role in the progression of insulin resistance [68].
Another positive finding regarding the use of LBP was reported by Yang et al. [69]. According to the authors, there is a link between oxidative stress, Nrf2 activity and insulin resistance. According to the above-mentioned study, in vivo and in vitro studies demonstrated that high-fat induced-insulin resistance could be ameliorated by LBP by the upregulation of the PI3K/AKT/Nrf2 signaling pathway. Due to this reaction, it was suggested that LBP may have a promising role in managing insulin resistance-associated oxidative stress in acute or chronic liver damage. Furthermore, Cai et al. [70] studied 67 patients in vivo for three months and found protective effects against the two types of hypoglycemia, lowering the glucose levels in the blood and increasing insulin. Finally, Zhao et al. [71] researched the prophylactic effects of LBP using 25 Japanese male diabetic rabbits induced by Alloxan. Results of this study showed improvement in renal function and inflammation in diabetic rabbits. However, the effect was more effective in preventing disease rather than treating it.

2.5. Hypertension and Heart Protective Effects

Hypertension is today one of the major public health problems due to its high incidence, its importance in cardiovascular disease and its correlation with a large number of health problems leading to death. Nearly one in two adults (about 103 million people) suffer from hypertension in the United States only [72]. Hypertension is influenced by factors such as genetics, lack of exercise and dietary intake of sodium, which is one of the most common causes of hypertension. It has been reported that the dietary sodium intake has been correlated with blood pressure, confirming the sensitivity of blood pressure to salt [73].
Regarding LBP’s protective positive effects on myocardial I/R damage Shao Ping and Pin-Ting [74] used in their study of Wistar adult male rats. In their study, it was presented that LBPs protected rat hearts from I/R injury via upregulation of heart Na+/K+-ATPase and inhibition of cardiomyocyte apoptosis concluding the cardioprotective effect of LBP stems caused by their antioxidant, anti-inflammatory and anti-apoptotic activities.
Prophylactic activity of LBP against cardiotoxic side effects of doxorubicin (DOX), which is a potent antitumor agent, has been also demonstrated in acute DOX-induced cardiotoxicity in rats [75,76] and beagle dogs [77]. Data of previous studies indicated that L. barbarum fruits and extracts may exert a potent protective effect on DOX-induced cardiomyocyte damage, mainly via antioxidative and free radical-scavenging pathways. Zhang et al. [78] in their study, related the anti-hypertensive effect of L. barbarum to down regulated expression of renal endothelial lncRNAs ONE in a rat model of salt-sensitive hypertension. In conclusion, their study commented that L. barbarum treatment can restore blood pressure to normal levels. At the same time, the expression of long noncoding RNA (lncRNA) was found to be reduced by the suppression of the antisense mRNA (sONE). Moreover, the improvement of endothelial nitric oxide synthase (eNOS) levels in the hypertensive model rats treated with L. barbarum compared with that receiving a high-salt diet was also observed. In addition, Guo et al. [79], using a meta-analysis of randomized controlled trials, presented that L. barbarum treatment significantly reduced fasting glucose concentrations while marginally reducing concentrations of total cholesterol and yielded no benefit in terms of bodyweight and blood pressure.

2.6. Hepatoprotective Activity

Alcohol use is the third leading risk factor contributing to the global burden of disease, after high blood pressure and tobacco smoking. According to a WHO report published in September 2018, alcohol causes 3 million annual deaths globally and accounts for 5.3% of all deaths. Despite the three above mentioned factors affecting liver Demori and Voci [80] commented that modern eating habits involving high-calorie diets that lead to obesity also can cause liver diseases such as hepatic steatosis. Chronic alcohol overdrinking (CAO) typically progresses through the stages of fatty liver or simple steatosis, alcoholic hepatitis and chronic hepatitis with hepatic fibrosis or cirrhosis [81].
The use of L. barbarum was originally proposed in traditional Chinese medicine for the treatment of liver diseases. Nowadays, studies done by Xiao et al. [82] have proved that feeding alcohol-induced liver injury rats with 300 mg/kg LBP for 30 days showed positive reverse effects, reducing liver injury, preventing the progression of alcohol-induced fatty liver and improving antioxidant function, in contrast with the ethanol group.
Pretreatment with 50 µg/mL LBP of rat normal hepatocyte line BRL-3A cells has shown a significant reduction of 24-hour ethanol-induced over expression of thioredoxin-interacting protein (TXNIP) increasing cellular apoptosis. Xiao et al. [83] also observed an activation of NOD-like receptor 3 (NLRP3) inflammasome and reduction of the antioxidant enzyme expression and ROS. Non-alcoholic fatty liver disease is an important factor in causing hepatocarcinoma and is associated with obesity, insulin resistance and metabolic syndrome. As mentioned previously, obesity leads to a decrease in insulin sensitivity (IR), a decrease in the antioxidant enzymes SOD, CAT and GSH-Px but also an increase in ROS, leading to liver dysfunction, hepatic steatosis and depletion of the hepatocyte population [80,84,85].
Cui et al. [27] examined the effects of L. barbarum aqueous (LBAE) and ethanol (LBEE) extracts on oxidative stress and antioxidant enzymes in the liver of rats fed with a high-fat diet (HFD). They concluded that LBAE and especially LBEE have strong antioxidant activities and can prevent or reduce the effects of HFD on several parameters of toxicity in HF rats. LBEE displayed stronger antioxidant and hepatoprotective effects than the aqueous extract of L. barbarum, a fact that probably has to do with the higher concentration of polyphenolic content that led to higher antioxidant activity and lipid peroxidation inhibition.
Protection against hepatotoxic effects of CCl4 has been documented by Kim et al. [86] using two cerebrosides isolated from L. chinense fruits (1-O-β-D-glucopyranosyl- (2S, 3R, 4E, 8Z)-2-N-palmitoyloctadecasphinga-4,8-dienine and 1-D-glucopyranosyl-(2S, 3R, 4E, 8Z)-2-N-(2′-hydroxypalmitoyl) octadecasphinga-4,8-dienine) in the culture of rat hepatocytes. Xiao et al. [87] also tested the effects of LBP on oxidative stress and liver necrosis of mice. Both studies showed significant sub-protective action, while in the second, it was shown that LBP reduced hepatic necrosis and alanine aminotransferase (ALT) levels in serum caused by CCl4, indicating that the beneficial effect on hepatotoxicity ought partly to reduce the activity of the kappa-B nuclear factor. Additionally, the use of LBP reduced hepatic inflammation by reducing pro-inflammatory mediators and chemokines.

2.7. Eye and Vision Activity

Zeaxanthin and lutein are two common carotenoids found in plants and are constituents of the yellow macular pigment in human retina [88]. Biological functions of these macular pigments include the absorption of spectra. The function of these pigments is to absorb the blue light that can cause harm to the retina, but this chronic process of absorption may affect these macular pigments [89].
Glaucoma is the second most common cause of blindness and is a degenerative disease of retinal ganglion cells (RGCs) and the optic nerve and is expected to affect about 111.8 million people between 40 and 80 years by 2040 [90]. The most common types of glaucoma are primary open angle glaucoma (POAG) and primary angle closure glaucoma (PACG) [91]. The appearance of glaucoma caused mainly by the progressive disruption of RGC axonal transport or with retinal ischemia. Pathologically, glaucoma is characterized by the death of RGCs and increased intraocular pressure (IOP) [92]. Increased IOP is an important contributor to POAG. Elevation of IOP could cause many changes that are involved in the pathogenesis of glaucoma, such as oxidative stress, glutamate toxicity and ischemia [91].
The positive effects of goji berries on eye diseases such as glaucoma, cataract and rhinitis pigmentosa (RP) have been proposed by Chinese herbalists due to their high concentration of zeaxanthin and their esters, which are ready absorbed into serum, resulting in protection of the retina against free radicals and blue light damage. Leung et al. [93] reported that the levels of these two carotenoids in the serum and tissues of rhesus monkeys after feeding with L. barbarum fruits were significantly higher against the control group. Furthermore, clinical studies focused on L. barbarum as a therapy for retinal diseases in humans exist in the scientific literature. Chan et al. [94], in a study involving retinitis pigmentosa patients, showed that L. barbarum treatment can provide a neuroprotective effect for the retina and could help delay or minimize cone degeneration in RP. The positive effect of goji berries on glaucoma is due to the activation of the microglia at a moderate level resulting RGCs protection against IOP regulating important intracellular pathways that stimulate the body’s defense under stress situations.
Chu et al. [95] studied the positive effects of LBP on preserving retinal function by multifocal electroretinogram (mfERG) analysis of 30 eyes of 30 Sprague-Dawley rats using a partial optic nerve transection (PONT) model in order to study secondary degeneration of retinal ganglion cells. The experimental results demonstrated that the feeding for 4 weeks with LBP, altered the functional reduction caused by PONT by regulating the signal from the outer retina. Li et al. [96] also suggested that LBP can reduce the loss of axons in the central optic nerves (ONs). Preservation of the g-ratio (axon diameter/fiber diameter) in the ventral Ons activates the microglia/macrophages in the Ons 12 h after PONT and finally decreases the magnitude response of microglia/macrophages 4 weeks after PONT. When the supply of blood to the retina is inadequate, the appearance of retinal ischemia due to lack of oxygen results in an altered metabolic function that eventually leads to irreversible cell death. An LBP diet of mice with acute ocular hypertension showed that it reduces the loss of RGC, protecting nerve fiber density, reducing immunoglobulin leakage and increasing blood vessel density [97,98,99]. Furthermore, similar studies in rats completed by He et al. [100] and Chu et al. [95] confirmed the protection of RGCs, commenting on the importance of Nrf2 activation that leads to an increase of heme oxygenase-1 (HO-1) expression. Thus, the induction of the antioxidant pathway plays an important role in maintaining the redox status of the retina.
The blood-retinal barrier (BRB) is a protective barrier that consists of the outer and inner BRB. The role of the BRB is to maintain the homeostatic condition of the retinal microenvironment and prevent harmful substances from getting into the retina. It has been presented that mice administered with LBP a week before retinal ischemia showed protection against neuronal cell death and to retinal oxidative stress by inhibition of lipid peroxidation and against disruption of the BRB 48 h after reperfusion [99].
Age-related macular degeneration may occur gradually over a period of years (dry AMD) or suddenly in weeks or months (wet AMD). The macula has a large number of light detection cells that provide acute central vision. It is located at the back of the eye and is the most sensitive part of the retina. These cells convert light into electrical signals, sending them through the optic nerve to the brain, where they are “translated” into the images we see. Any damage to the macula leads to a blurred, distorted or dark representation of the center of the field of vision [101]. Studies by Bucheli et al. [102] in elderly people have shown that daily goji berry consumption for a period of 90 days increases plasma zeoxanthine and antioxidant levels. In addition, it protects against hypopigmentation and soft drusen accumulation in the macula of elderly people. The deposition of extracellular amyloid beta (Aβ), oxidative stress, and inflammation have all been implicated in AMD. Yoshida et al. [103] has commented that retinal ganglion cells and retinal pigment epithelium also synthesize Aβ, which are secreted in the posterior eye. Age-related changes in the composition of Aβ as well as its degradative enzymes lead to an increase in the amount of deposition in the retina [104]. The protective effect of LBPs on macular neurons during the pathogenesis of AMD is due to the protection of these cell neurons from the stress caused by Aβ [97,98,105].
Finally, Chien et al. [106] examined goji berry effects on dry eye disease in a male Sprague-Dawley rat model. Their study indicated that in the group treated with goji berries, the severity of the kerato conjunctival staining decreased significantly and ameliorated dry eye disease symptoms appeared in a dose-dependent manner.
According to the above-mentioned studies it is believed that Goji berry consumption positively affects eye and vision activity in many ways.

2.8. Pre-Biotic Activity

The term probiotic originates from the Greek words pre + bios and has been used with many different meanings in recent decades. Initially, the term “probiotic” was used to describe compounds produced by a protozoan that stimulated the growth of another [107]. Finally, experts from the Food and Agriculture Organization/World Health Organization have identified probiotics as “living microorganisms, which when consumed in sufficient quantities as part of the feed contribute to the beneficial effect of the host” [108].
The use of probiotics extends back to a time before the discovery of microbes. Fermented dairy products were depicted in Egyptian hieroglyphics, and buffalo milk fermentation was traditionally used by Mongolian nomads to preserve their milk during their long journeys [109]. So far, many microorganisms such as fungi, yeasts, bacteria or their mixed combination have been considered or used as probiotics. The two main bacterial genera mainly referred to as probiotics are those of Lactobacillus and Bifidobacterium [110].
Historically, during the 1800s, the positive effect on human health of the consumption of fermented dairy products was observed by scientists. Although Louis Pasteur identified bacteria and yeasts that were responsible for the fermentation process did not associate these microbes with any apparent health effects. In 1905, Elie Metchnikoff, who had worked with Pasteur in the 1860s, observed that Bulgarian shepherd’s longevity was mainly due to the lactobacilli used for yogurt fermentation and the presence of these lactobacilli in the sheep intestine in Bulgaria not with the yogurt they consumed but with [111]. In particular, Metchnikoff, in his study, “The Prologue of Life” in 1908, assumed that lactic acid bacteria detected in Bulgarian yogurts, the so-called Balkan Bulgarian, later known as Lactobacillus bulgaricus (now called L. delbrueckii subsp. bulgaricus) and Streptococcus thermophilus, are responsible for enhancing the intestinal system by inhibiting microbial fermentation, resulting in a reduction in unwanted by-products, such as amines and ammonia. Thus, for the first time, Metchnikoff highlighted the importance of specific micro-organisms and their contribution to human health and longevity.
Prebiotics are components of non-digestible foods that effectively affect the host by favoring growth and/or bacterial activity in the large intestine [112,113].
The term “symbiotic” is defined as a mixture of probiotics and prebiotics that beneficially affect the host by improving the survival of the beneficial microflora, enriching it with live beneficial bacteria found in dietary supplements in the gastrointestinal tract. These microorganisms promote health and thus improve welfare in the gastrointestinal tract. Symbiotics are aimed at enhancing the survival and activity of probiotics as proven in vivo, as well as stimulating Bifidobacterium species [111].
The prebiotic action of goji berries has been shown by its addition to yogurt [114], which resulted in maintenance the viability of lactic acid bacteria (LAB) at probiotic levels (106–107 log CFU/mL) during 21 days of storage compared to classic yogurt control. Similar results were presented in the study of Baba et al. [115], where the addition of aqueous extracts of L. barbarum to yogurt significantly improved the bioavailability of probiotic bacteria Lactobacillus spp. and Streptococcus thermophilus.
Furthermore, Liao et al. [116] demonstrated the beneficial prebiotic effect of the addition of L. barbarum to fermentation in Sichuan pickle (traditional Chinese pickle). According to the results presented in this study, L. barbarum addition not only increased the amount of LAB but also improved considerably the organoleptic quality and reduced the nitrite content of the pickle. Additionally, the results of a recent study completed by Zhou et al. [117] demonstrated that LBP improved the tolerance of B. longum subsp. infantis Bi-26 and L. acidophilus NCFM to the gastrointestinal environment. These results were also found to be in line with the study completed by Skenderidis et al. [19] that indices that LBP promotes the proliferation protecting Bifidobacterium and Lactobacillus strains by enhancing carbon and energy metabolism. These results also reported that the viability of L. casei was less affected, followed by B. lactis Bb12, which showed the greatest tolerance in the acidic environment, while the survival of B. longum 42 was low. Similar results were also confirmed by González-Rodríguez et al. [118], where B. longum 42 showed lower resistance in low pH conditions compared to B. lactis Bb12.
To confer a health benefit on the host, the LAB must be able to overcome the physical and chemical barriers of the gastrointestinal tract, especially acidic and proteolytic enzymes and bile stresses [119]. Consequently, the LAB should be resistant to the gastrointestinal environment.
The existence of an extracellular polysaccharide film produced by certain lactic bacteria or Bifidobacterium has also been reported in the literature [120,121]. This polysaccharide film protects probiotic bacterial cells from the environment and acts as a shield against the conditions prevailing in the gastrointestinal tract and helps them to survive. It has also been reported that Bifidobacterium longum strains produce larger amounts of this film than Bb12, resulting in higher bile strength [19]. This resistance is related to the binding of bile salts from the polysaccharide film, resulting in a reduction in its antimicrobial activity [116,120]. Finally, Skenderidis et al. [19] confirmed the increase of the Bb12 strain viability induced by goji berry extracts. This increase is probably related to goji berry polysaccharides, which consist of galactose, glucose, fructose, arabinose, mannose and xylose molecules, which are also the structural molecules of this extracellular polysaccharide antimicrobial [120,121,122,123].

2.9. Other Bioactivities

Additional bioactive effects of goji berries, such as skin protection and its synergistic potential within fertility treatment by inducing spermatogenesis, have been reported [25,33,124,125,126]. Studies carried out with phenolic compounds isolated from the fruits of L. barbarum showed that the extracts had a bactericidal effect against Gram positive and Gram-negative bacteria [10]. On the other hand, L. chinense leaf extracts were found to be more potent as antimicrobial agents than the fruit extracts, with the best microbiocidal activity exerted on Bacillus subtilis [127].

3. Conclusions

There are many scientific research results that support the positive effects of the consumption of goji berry fruits and their plant parts (bark, leaves) extracts. Their potential health benefits include protection against oxidative damage, antidiabetic, immunoregulatory, vision protective, hepatoprotective, and prebiotic activities that are associated with the promotion of risk reduction in the development of chronic diseases such as cancer, diabetes, cardiovascular disease, Alzheimer’s disease, cataracts, and age-related diseases. Therefore, the screening of individual constituents of bioactive goji berries that exhibit health-promoting properties requires further investigation. This is because a cause–effect relationship between the intake of goji berries and its health effects can only be established when the composition of goji berries is properly characterized and standardized. Furthermore, extensive investigation is needed to examine the effects of adding these beneficial bioactive phytochemicals from goji berries, using advanced technologies, into food systems. Further research is also needed to evaluate the effectiveness of goji berry extracts in the food ecosystem and to establish their role as a functional agent in the design of new fortified foods.

Author Contributions

Conceptualization, P.S.; investigation, P.S. and S.L.; writing—original draft preparation, P.S.; writing—review and editing, P.S., S.L. and D.L.; visualization, P.S.; supervision, P.S.; All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Knight, K.; Badamgarav, E.; Henning, J.M.; Hasselblad, V.; Anacleto, P.; Gano, P.; Ofman, J.J.; Weingarten, S.R. A Systematic review of diabetes disease management programs. Am. J. Manag. Care 2005, 11, 242–250. [Google Scholar] [PubMed]
  2. Kannel, W.B. Diabetes and cardiovascular disease. The Framingham study. JAMA 1979, 241, 2035–2038. [Google Scholar] [CrossRef] [PubMed]
  3. Sowers, J.R.; Epstein, M.; Frohlich, E.D. Diabetes, hypertension, and cardiovascular disease. Hypertension 2001, 37, 1053–1059. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Naczk, M.; Shahidi, F. Phenolics in cereals, fruits and vegetables: Occurrence, extraction and analysis. J. Pharm. Biomed. Anal. 2006, 41, 1523–1542. [Google Scholar] [CrossRef] [PubMed]
  5. Altemimi, A.; Lakhssassi, N.; Baharlouei, A.; Watson, D.G.; Lightfoot, D.A. Phytochemicals: Extraction, isolation, and identification of bioactive compounds from plant extracts. Plants 2017, 6, 42. [Google Scholar] [CrossRef] [PubMed]
  6. Leontopoulos, S.; Skenderidis, P.; Kalorizou, H.; Petrotos, K. Bioactivity potential of polyphenolic compounds in human health and their effectiveness against various food borne and plant pathogens. A review. J. Food Biosyst. Eng. 2017, 7, 1–19. [Google Scholar]
  7. Lampakis, D.; Skenderidis, P.; Leontopoulos, S. Technologies and extraction methods of polyphenolic compounds derived from pomegranate (Punica granatum) peels. A mini review. Processes 2021, 9, 236. [Google Scholar] [CrossRef]
  8. Leontopoulos, S.; Skenderidis, P.; Vagelas, I.K. Potential use of polyphenolic compounds obtained from olive mill waste waters on plant pathogens and plant parasitic nematodes. In Plant Defence: Biological Control; Mérillon, J.-M., Ramawat, K.G., Eds.; Springer International Publishing: Cham, Switzerland, 2020; pp. 137–177. ISBN 978-3-030-51034-3. [Google Scholar]
  9. Greathead, H. Plants and plant extracts for improving animal productivity. Proc. Nutr. Soc. 2003, 62, 279–290. [Google Scholar] [CrossRef]
  10. Skenderidis, P.; Mitsagga, C.; Giavasis, I.; Petrotos, K.; Lampakis, D.; Leontopoulos, S.; Hadjichristodoulou, C.; Tsakalof, A. The in vitro antimicrobial activity assessment of ultrasound assisted Lycium barbarum fruit extracts and pomegranate fruit peels. J. Food Meas. Charact. 2019, 13, 2017–2031. [Google Scholar] [CrossRef]
  11. Leontopoulos, S.; Skenderidis, P.; Petrotos, K.; Giavasis, I. Corn silage supplemented with pomegranate (Punica granatum) and avocado (Persea americana) pulp and seed wastes for improvement of meat characteristics in poultry production. Molecules 2021, 26, 5901. [Google Scholar] [CrossRef]
  12. Zengin, Z.B.; Meza, L.; Pal, S.K.; Grivas, P. Chemoimmunotherapy in urothelial cancer: Concurrent or sequential? Lancet Oncol. 2021, 22, 894–896. [Google Scholar] [CrossRef]
  13. Negi, G.; Kumar, A.; Joshi, R.P.; Sharma, S.S. Oxidative stress and Nrf2 in the pathophysiology of diabetic neuropathy: Old perspective with a new angle. Biochem. Biophys. Res. Commun. 2011, 408, 1–5. [Google Scholar] [CrossRef]
  14. Boots, A.W.; Haenen, G.R.; Bast, A. Health effects of quercetin: From antioxidant to nutraceutical. Eur. J. Pharmacol. 2008, 585, 325–337. [Google Scholar] [CrossRef] [PubMed]
  15. Valko, M.; Rhodes, C.J.; Moncol, J.; Izakovic, M.; Mazur, M. Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem. Biol. Interact. 2006, 160, 1–40. [Google Scholar] [CrossRef] [PubMed]
  16. Vivekananthan, D.P.; Penn, M.S.; Sapp, S.K.; Hsu, A.; Topol, E. Use of antioxidant vitamins for the prevention of cardiovascular disease: Meta-analysis of randomised trials. Lancet 2003, 361, 2017–2023. [Google Scholar] [CrossRef]
  17. Rocchetti, G.; Senizza, B.; Putnik, P.; Kovačević, D.B.; Barba, F.J.; Trevisan, M.; Lucini, L. Untargeted screening of the bound/free phenolic composition in tomato cultivars for industrial transformation. J. Sci. Food Agric. 2019, 99, 6173–6181. [Google Scholar] [CrossRef]
  18. Rocchetti, G.; Lucini, L.; Corrado, G.; Colla, G.; Cardarelli, M.; De Pascale, S.; Rouphael, Y. Phytochemical profile, mineral content, and bioactive compounds in leaves of seed-propagated artichoke hybrid cultivars. Molecules 2020, 25, 3795. [Google Scholar] [CrossRef]
  19. Skenderidis, P.; Mitsagga, C.; Lampakis, D.; Petrotos, K.; Giavasis, I. The effect of encapsulated powder of goji berry (Lycium barbarum) on growth and survival of probiotic bacteria. Microorganisms 2020, 8, 57. [Google Scholar] [CrossRef] [Green Version]
  20. Skenderidis, P.; Leontopoulos, S.; Petrotos, K.; Giavasis, I. Vacuum microwave-assisted aqueous extraction of polyphenolic compounds from avocado (Persea Americana) solid waste. Sustainability 2021, 13, 2166. [Google Scholar] [CrossRef]
  21. Amagase, H.; Sun, B.; Borek, C. Lycium barbarum (goji) juice improves in vivo antioxidant biomarkers in serum of healthy adults. Nutr. Res. 2009, 29, 19–25. [Google Scholar] [CrossRef]
  22. Hsu, C.-H.; Nance, D.M.; Amagase, H. A meta-analysis of clinical improvements of general well-being by a standardized Lycium barbarum. J. Med. Food 2012, 15, 1006–1014. [Google Scholar] [CrossRef]
  23. Yao, R.; Heinrich, M.; Zou, Y.; Reich, E.; Zhang, X.; Chen, Y.; Weckerle, C. Quality variation of goji (Fruits of Lycium spp.) in China: A comparative morphological and metabolomic analysis. Front. Pharmacol. 2018, 9, 151. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Skenderidis, P.; Lampakis, D.; Giavasis, I.; Leontopoulos, S.; Petrotos, K.; Hadjichristodoulou, C.; Tsakalof, A. Chemical properties, fatty-acid composition, and antioxidant activity of goji berry (Lycium barbarum L. and Lycium chinense Mill.) Fruits. Antioxidants 2019, 8, 60. [Google Scholar] [CrossRef] [Green Version]
  25. Cao, S.; Du, J.; Hei, Q. Lycium barbarum polysaccharide protects against neurotoxicity via the Nrf2-HO-1 pathway. Exp. Ther. Med. 2017, 14, 4919–4927. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Ahmed, N.; Wang, M.; Shu, S. Effect of commercial Bacillus thuringiensis toxins on Tyrophagus putrescentiae (Schrank) fed on wolfberry (Lycium barbarum L.). Int. J. Acarol. 2016, 42, 1–6. [Google Scholar] [CrossRef]
  27. Cui, B.; Liu, S.; Lin, X.; Wang, J.; Li, S.; Wang, Q.; Li, S. Effects of Lycium barbarum aqueous and ethanol extracts on high-fat-diet induced oxidative stress in rat liver tissue. Molecules 2011, 16, 9116–9128. [Google Scholar] [CrossRef] [PubMed]
  28. Habtemariam, S. Protective effects of caffeic acid and the Alzheimer’s brain: An update. Mini-Rev. Med. Chem. 2017, 17, 667–674. [Google Scholar] [CrossRef]
  29. Zhang, R.; Kang, K.A.; Piao, M.J.; Kim, K.C.; Kim, A.D.; Chae, S.; Park, J.S.; Youn, U.J.; Hyun, J.W. Cytoprotective effect of the fruits of Lycium chinense Miller against oxidative stress-induced hepatotoxicity. J. Ethnopharmacol. 2010, 130, 299–306. [Google Scholar] [CrossRef]
  30. Changbo, D. Supplementation of Lycium barbarum polysaccharides protection of skeletal muscle from exercise-induced oxidant stress in mice. Afr. J. Pharm. Pharmacol. 2012, 6, 643–647. [Google Scholar] [CrossRef]
  31. Zhang, Z.; Liu, X.; Zhang, X.; Liu, J.; Hao, Y.; Yang, X.; Wang, Y. Comparative evaluation of the antioxidant effects of the natural vitamin C analog 2-O-β-D-glucopyranosyl-L-ascorbic acid isolated from Goji berry fruit. Arch. Pharmacal. Res. 2011, 34, 801–810. [Google Scholar] [CrossRef]
  32. Li, H.; Li, Z.; Peng, L.; Jiang, N.; Liu, Q.; Zhang, E.; Liang, B.; Li, R.; Zhu, H. Lycium barbarum polysaccharide protects human keratinocytes against UVB-induced photo-damage. Free Radic. Res. 2017, 51, 200–210. [Google Scholar] [CrossRef] [PubMed]
  33. Skenderidis, P.; Kerasioti, E.; Karkanta, E.; Stagos, D.; Kouretas, D.; Konstantinos, P.; Hadjichristodoulou, C. Assessment of the antioxidant and antimutagenic activity of extracts from goji berry of Greek cultivation. Toxicol. Rep. 2018, 5, 251–257. [Google Scholar] [CrossRef]
  34. Bucheli, P.; Gao, Q.; Redgwell, R.; Karine, V.; Wang, J.; Zhang, W.; Nong, S.; Cao, B. Chapter 14 Wolfberry biomolecular and clinical aspects of Chinese. In Herbal Medicine: Biomolecular and Clinical Aspects; CRC Press: Boca Raton, FL, USA, 2013; pp. 1–17. [Google Scholar]
  35. Kaur, D.; Rasane, P.; Singh, J.; Kaur, S.; Kumar, V.; Mahato, D.K.; Dey, A.; Dhawan, K.; Kumar, S. Nutritional interventions for elderly and considerations for the development of geriatric Foods. Curr. Aging Sci. 2019, 12, 15–27. [Google Scholar] [CrossRef] [PubMed]
  36. Li, X.; Zhou, A. Evaluation of antioxidant activity of the polysaccharides extracted from Lycium barbarum fruits in vitro. Eur. Polym. J. 2007, 43, 488–497. [Google Scholar] [CrossRef]
  37. Yi, R.; Liu, X.-M.; Dong, Q. A study of Lycium barbarum polysaccharides (LBP) extraction technology and its anti-aging effect. Afr. J. Tradit. Complement. Altern. Med. 2013, 10, 171–174. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Xia, G.; Xin, N.; Liu, W.; Yao, H.; Hou, Y.; Qi, J. Inhibitory effect of Lycium barbarum polysaccharides on cell apoptosis and senescence is potentially mediated by the p53 signaling pathway. Mol. Med. Rep. 2014, 9, 1237–1241. [Google Scholar] [CrossRef] [PubMed]
  39. Ho, S.-C.; Liu, J.-H.; Wu, R.-Y. Establishment of the mimetic aging effect in mice caused by D-galactose. Biogerontology 2003, 4, 15–18. [Google Scholar] [CrossRef]
  40. Deng, H.-B.; Cui, D.-P.; Jiang, J.-M.; Feng, Y.-C.; Cai, N.-S.; Li, D.-D. Inhibiting effects of Achyranthes bidentata polysaccharide and Lycium barbarum polysaccharide on non-enzyme glycation in D-galactose induced mouse aging model. Biomed. Environ. Sci. 2003, 16, 267–275. [Google Scholar]
  41. Wang, Y.; Zhao, H.; Sheng, X.; Gambino, P.E.; Costello, B.; Bojanowski, K. Protective effect of Fructus lycii polysaccharides against time and hyperthermia-induced damage in cultured seminiferous epithelium. J. Ethnopharmacol. 2002, 82, 169–175. [Google Scholar] [CrossRef]
  42. Ji, L.L. Antioxidant signaling in skeletal muscle: A brief review. Exp. Gerontol. 2007, 42, 582–593. [Google Scholar] [CrossRef]
  43. Ma, Q. Role of Nrf2 in Oxidative stress and toxicity. Annu. Rev. Pharmacol. Toxicol. 2013, 53, 401–426. [Google Scholar] [CrossRef] [Green Version]
  44. David, J.A.; Rifkin, W.J.; Rabbani, P.S.; Ceradini, D.J. The Nrf2/Keap1/ARE Pathway and oxidative stress as a therapeutic target in type II diabetes mellitus. J. Diabetes Res. 2017, 2017, 4826724. [Google Scholar] [CrossRef] [PubMed]
  45. Yang, P.; Li, D.; Jin, S.; Ding, J.; Guo, J.; Shi, W.; Wang, C. Stimuli-responsive biodegradable poly (methacrylic acid) based nano-capsules for ultrasound traced and triggered drug delivery system. Biomaterials 2014, 35, 2079–2088. [Google Scholar] [CrossRef]
  46. Gao, Y.; Wei, Y.; Wang, Y.; Gao, F.; Chen, Z. Lycium barbarum: A traditional Chinese herb and a promising anti-aging agent. Aging Dis. 2017, 8, 778–791. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Ming, M.; Guanhua, L.; Zhanhai, Y.; Guang, C.; Xuan, Z. Effect of the Lycium barbarum polysaccharides administration on blood lipid metabolism and oxidative stress of mice fed high-fat diet in vivo. Food Chem. 2009, 113, 872–877. [Google Scholar] [CrossRef]
  48. Luo, Q.; Cai, Y.; Yan, J.; Sun, M.; Corke, H. Hypoglycemic and hypolipidemic effects and antioxidant activity of fruit extracts from Lycium barbarum. Life Sci. 2004, 76, 137–149. [Google Scholar] [CrossRef] [PubMed]
  49. Im, A.-R.; Lee, H.J.; Youn, U.J.; Hyun, J.W.; Chae, S. Orally administered betaine reduces photodamage caused by UVB irradiation through the regulation of matrix metalloproteinase-9 activity in hairless mice. Mol. Med. Rep. 2016, 13, 823–828. [Google Scholar] [CrossRef]
  50. Cao, G.; Yang, W.; Du, P. Observation of the effects of LAK/IL-2 Therapy combining with Lycium barbarium polysaccharides in the treatment of 75 cancer patients. Chin. J. Oncol. 1994, 16, 428–431. [Google Scholar]
  51. Gan, L.; Zhang, S.H.; Yang, X.L.; Xu, H.B. Immunomodulation and antitumor activity by a polysaccharide À protein complex from Lycium barbarum. Int. Immunopharmacol. 2004, 4, 563. [Google Scholar] [CrossRef]
  52. Zhang, M.; Chen, H.; Huang, J.; Li, Z.; Zhu, C.; Zhang, S. Effect of Lycium barbarum polysaccharide on human hepatoma QGY7703 cells: Inhibition of proliferation and induction of apoptosis. Life Sci. 2005, 76, 2115–2124. [Google Scholar] [CrossRef]
  53. Su, C.-X.; Duan, X.-G.; Liang, L.-J.; Wang, F.; Zheng, J.; Fu, X.-Y.; Yan, Y.-M.; Huang, L.; Wang, N.-P. Lycium barbarum polysaccharides as an adjuvant for recombinant vaccine through enhancement of humoral immunity by activating Tfh cells. Veter-Immunol. Immunopathol. 2014, 158, 98–104. [Google Scholar] [CrossRef] [PubMed]
  54. Yang, R.-F.; Zhao, C.; Chen, X.; Chan, S.-W.; Wu, J.-Y. Chemical properties and bioactivities of Goji (Lycium barbarum) polysaccharides extracted by different methods. J. Funct. Foods 2015, 17, 903–909. [Google Scholar] [CrossRef]
  55. He, N.; Yang, X.; Jiao, Y.; Tian, L.; Zhao, Y. Characterisation of antioxidant and antiproliferative acidic polysaccharides from Chinese wolfberry fruits. Food Chem. 2012, 133, 978–989. [Google Scholar] [CrossRef]
  56. Huang, X.; Zhang, Q.-Y.; Jiang, Q.-Y.; Kang, X.-M.; Zhao, L. Polysaccharides derived from Lycium barbarum suppress IGF-1-induced angiogenesis via PI3K/HIF-1α/VEGF signalling pathways in MCF-7 cells. Food Chem. 2012, 131, 1479–1484. [Google Scholar] [CrossRef]
  57. Deng, X.; Luo, S.; Luo, X.; Hu, M.; Ma, F.; Wang, Y.; Zhou, L.; Huang, R. Fraction From Lycium barbarum Polysaccharides Reduces Immunotoxicity and Enhances Antitumor Activity of Doxorubicin in Mice. Integr. Cancer Ther. 2018, 17, 860–866. [Google Scholar] [CrossRef] [Green Version]
  58. Kim, N.H.; Sung, B.; Kang, Y.J.; Jang, J.Y.; Hwang, S.Y.; Lee, Y.; Kim, M.; Im, E.; Yoon, J.-H.; Kim, C.M.; et al. Anti-inflammatory effects of betaine on AOM/DSS-induced colon tumorigenesis in ICR male mice. Int. J. Oncol. 2014, 45, 1250–1256. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Singh, J.; Rasane, P.; Kaur, S.; Kumar, V.; Dhawan, K.; Mahato, D.K.; Malhotra, S.; Sarma, C.; Kaur, D.; Bhattacharya, J. Nutritional interventions and considerations for the development of low calorie or sugar free foods. Curr. Diabetes Rev. 2020, 16, 301–312. [Google Scholar] [CrossRef]
  60. Zheng, Y.; Ley, S.H.; Hu, F.B. Global aetiology and epidemiology of type 2 diabetes mellitus and its complications. Nat. Rev. Endocrinol. 2018, 14, 88–98. [Google Scholar] [CrossRef]
  61. Wild, S.; Roglic, G.; Green, A.; Sicree, R.; King, H. Global prevalence of diabetes: Estimates for the Year 2000 and projections for 2030. Diabetes Care 2004, 27, 1047–1053. [Google Scholar] [CrossRef] [Green Version]
  62. Silva, C.; Alves, B.; Azzalis, L.; Junqueira, V.; Fonseca, R.; Fonseca, A.; Fonseca, F. Goji Berry (Lycium Barbarum) in the treatment of diabetes melitus: A systematic review. Food Res. 2017, 1, 221–224. [Google Scholar] [CrossRef]
  63. Wu, H.; Guo, H.; Zhao, R. Effect of Lycium barbarum Polysaccharide on the improvement of antioxidant ability and DNA damage in NIDDM Rats. Yakugaku Zasshi 2006, 126, 365–371. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Zhang, M.; Tang, X.; Wang, F.; Zhang, Q.; Zhang, Z. Characterization of Lycium barbarum polysaccharide and its effect on human hepatoma cells. Int. J. Biol. Macromol. 2013, 61, 270–275. [Google Scholar] [CrossRef] [PubMed]
  65. Bagul, P.K.; Middela, H.; Matapally, S.; Padiya, R.; Bastia, T.; Madhusudana, K.; Reddy, B.R.; Chakravarty, S.; Banerjee, S.K. Attenuation of insulin resistance, metabolic syndrome and hepatic oxidative stress by resveratrol in fructose-fed rats. Pharmacol. Res. 2012, 66, 260–268. [Google Scholar] [CrossRef] [PubMed]
  66. Nakatani, Y.; Kaneto, H.; Kawamori, D.; Hatazaki, M.; Miyatsuka, T.; Matsuoka, T.-A.; Kajimoto, Y.; Matsuhisa, M.; Yamasaki, Y.; Hori, M. Modulation of the JNK pathway in liver affects insulin resistance status. J. Biol. Chem. 2004, 279, 45803–45809. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Kaneto, H. The JNK pathway as a therapeutic target for diabetes. Expert Opin. Ther. Targets 2005, 9, 581–592. [Google Scholar] [CrossRef]
  68. Kaneto, H.; Matsuoka, T.-A.; Nakatani, Y.; Kawamori, D.; Miyatsuka, T.; Matsuhisa, M.; Yamasaki, Y. Oxidative stress, ER stress, and the JNK pathway in type 2 diabetes. Klin. Wochenschr. 2005, 83, 429–439. [Google Scholar] [CrossRef] [PubMed]
  69. Yang, Y.; Li, W.; Li, Y.; Wang, Q.; Gao, L.; Zhao, J. Dietary Lycium barbarum Polysaccharide induces Nrf2/ARE pathway and ameliorates insulin resistance induced by high-fat via activation of PI3K/AKT signaling. Oxidative Med. Cell. Longev. 2014, 2014, 1–10. [Google Scholar] [CrossRef] [Green Version]
  70. Cai, H.; Liu, F.; Zuo, P.; Huang, G.; Song, Z.; Wang, T.; Lu, H.; Guo, F.; Han, C.; Sun, G. Practical application of antidiabetic efficacy of Lycium barbarum polysaccharide in patients with Type 2 diabetes. Med. Chem. 2015, 11, 383–390. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Zhao, R.; Gao, X.; Zhang, T.; Li, X. Effects of Lycium barbarum. polysaccharide on type 2 diabetes mellitus rats by regulating biological rhythms. Iran. J. Basic Med. Sci. 2016, 19, 1024–1030. [Google Scholar] [CrossRef]
  72. Finegold, J.A.; Asaria, P.; Francis, D.P. Mortality from ischaemic heart disease by country, region, and age: Statistics from World Health Organisation and United Nations. Int. J. Cardiol. 2013, 168, 934–945. [Google Scholar] [CrossRef] [Green Version]
  73. Levy, D.; Ehret, G.B.; Rice, K.; Verwoert, G.C.; Launer, L.J.; Dehghan, A.; Glazer, N.L.; Morrison, A.C.; Johnson, A.D.; Aspelund, T.; et al. Genome-wide association study of blood pressure and hypertension. Nat. Genet. 2009, 41, 677–687. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Lu, S.-P.; Zhao, P.-T. Chemical characterization of Lycium barbarum polysaccharides and their reducing myocardial injury in ischemia/reperfusion of rat heart. Int. J. Biol. Macromol. 2010, 47, 681–684. [Google Scholar] [CrossRef] [PubMed]
  75. Xin, Y.-F.; Zhou, G.-L.; Deng, Z.-Y.; Chen, Y.-X.; Wu, Y.-G.; Xu, P.-S.; Xuan, Y.-X. Protective effect of Lycium barbarum on doxorubicin-induced cardiotoxicity. Phytother. Res. 2007, 21, 1020–1024. [Google Scholar] [CrossRef]
  76. Xin, Y.-F.; Wan, L.-L.; Peng, J.-L.; Guo, C. Alleviation of the acute doxorubicin-induced cardiotoxicity by Lycium barbarum polysaccharides through the suppression of oxidative stress. Food Chem. Toxicol. 2011, 49, 259–264. [Google Scholar] [CrossRef]
  77. Xin, Y.; Zhang, S.; Gu, L.; Liu, S.; Gao, H.; You, Z.; Zhou, G.; Wen, L.; Yu, J.; Xuan, Y. Electrocardiographic and Biochemical evidence for the cardioprotective effect of antioxidants in acute doxorubicin-induced cardiotoxicity in the beagle dogs. Biol. Pharm. Bull. 2011, 34, 1523–1526. [Google Scholar] [CrossRef] [Green Version]
  78. Zhang, X.; Yang, X.; Lin, Y.; Suo, M.; Gong, L.; Chen, J.; Hui, R. Anti-hypertensive effect of Lycium barbarum L. with down-regulated expression of renal endothelial lncRNA sONE in a rat model of salt-sensitive hypertension. Int. J. Clin. Exp. Pathol. 2015, 8, 6981–6987. [Google Scholar]
  79. Guo, X.F.; Li, Z.H.; Cai, H.; Li, D. The Effects of Lycium Barbarum L. (L. Barbarum) on cardiometabolic risk factors: A me-ta-analysis of randomized controlled trials. Food Funct. 2017, 8, 1741–1748. [Google Scholar] [CrossRef] [PubMed]
  80. Demori, I.; Voci, A.; Fugassa, E.; Burlando, B. Combined effects of high-fat diet and ethanol induce oxidative stress in rat liver. Alcohol 2006, 40, 185–191. [Google Scholar] [CrossRef] [PubMed]
  81. Orman, E.S.; Odena, G.; Bataller, R. Alcoholic liver disease: Pathogenesis, management, and novel targets for therapy. J. Gastroenterol. Hepatol. (Aust.) 2013, 28, 77–84. [Google Scholar] [CrossRef] [Green Version]
  82. Xiao, J.; Wang, J.; Xing, F.; Han, T.; Jiao, R.; Liong, E.C.; Fung, M.-L.; So, K.-F.; Tipoe, G.L. Zeaxanthin Dipalmitate therapeutically improves hepatic functions in an alcoholic fatty liver disease model through modulating MAPK pathway. PLoS ONE 2014, 9, e95214. [Google Scholar] [CrossRef] [Green Version]
  83. Xiao, J.; Zhu, Y.; Liu, Y.; Tipoe, G.L.; Xing, F.; So, K.-F. Lycium barbarum polysaccharide attenuates alcoholic cellular injury through TXNIP-NLRP3 inflammasome pathway. Int. J. Biol. Macromol. 2014, 69, 73–78. [Google Scholar] [CrossRef] [Green Version]
  84. Assy, N.; Kaita, K.; Mymin, D.; Levy, C.; Rosser, B.; Minuk, G. Fatty infiltration of liver in hyperlipidemic patients. Am. J. Dig. Dis. Sci. 2000, 45, 1929–1934. [Google Scholar] [CrossRef] [PubMed]
  85. Lee, Y.M.; Choi, J.S.; Kim, M.H.; Jung, M.H.; Lee, Y.S.; Song, J. Effects of dietary genistein on hepatic lipid metabolism and mitochondrial function in mice fed high-fat diets. Nutrition 2006, 22, 956–964. [Google Scholar] [CrossRef] [PubMed]
  86. Kim, S.Y.; Lee, E.J.; Kim, H.P.; Kim, Y.C.; Moon, A. A novel cerebroside from Lycii fructus preserves the hepatic glutathione redox system in primary cultures of rat hepatocytes. Biol. Pharm. Bull. 1999, 22, 873–875. [Google Scholar] [CrossRef]
  87. Xiao, J.; Liong, E.C.; Ching, Y.P.; Chang, R.C.C.; So, K.F.; Fung, M.L.; Tipoe, G.L. Lycium barbarum polysaccharides protect mice liver from carbon tetrachloride-induced oxidative stress and necroinflammation. J. Ethnopharmacol. 2012, 139, 462–470. [Google Scholar] [CrossRef] [PubMed]
  88. Krinsky, N.I.; Landrum, J.T.; Bone, R.A. Biologic mechanisms of the protective role of Iutein and Zeaxanthin in the eye. Annu. Rev. Nutr. 2003, 23, 171. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. Taylor, H.R.; West, S.; Muñoz, B.; Rosenthal, F.S.; Bressler, S.B.; Bressler, N.M. The Long-term effects of visible light on the eye. Arch. Ophthalmol. 1992, 110, 99–104. [Google Scholar] [CrossRef]
  90. Tham, Y.-C.; Li, X.; Wong, T.Y.; Quigley, H.A.; Aung, T.; Cheng, C.-Y. Global prevalence of glaucoma and projections of glaucoma burden through 2040: A systematic review and meta-analysis. Ophthalmology 2014, 121, 2081–2090. [Google Scholar] [CrossRef]
  91. Quigley, H.; Broman, A.T. The number of people with glaucoma worldwide in 2010 and 2020. Br. J. Ophthalmol. 2006, 90, 262–267. [Google Scholar] [CrossRef] [Green Version]
  92. Prasanna, G.; Hulet, C.; Desai, D.; Krishnamoorthy, R.R.; Narayan, S.; Brun, A.-M.; Suburo, A.M.; Yorio, T. Effect of elevated intraocular pressure on endothelin-1 in a rat model of glaucoma. Pharmacol. Res. 2005, 51, 41–50. [Google Scholar] [CrossRef]
  93. Leung, I.; Tso, M.; Li, W.; Lam, T. Absorption and tissue distribution of Zeaxanthin and Iutein in rhesus monkeys after taking Fructus lycii (Gou Qi Zi) extract. Investig. Ophthalmol. Vis. Sci. 2001, 42, 466. [Google Scholar]
  94. Chan, H.H.-L.; Lam, C.H.-I.; Choi, K.-Y.; Li, S.Z.-C.; Lakshmanan, Y.; Yu, W.-Y.; Chang, R.C.-C.; Lai, J.S.-M.; So, K.-F. Delay of cone degeneration in retinitis pigmentosa using a 12-month treatment with Lycium barbarum supplement. J. Ethnopharmacol. 2019, 236, 336–344. [Google Scholar] [CrossRef] [PubMed]
  95. Chu, P.H.W.; Li, H.-Y.; Chin, M.-P.; So, K.-F.; Chan, H.H.L. Effect of Lycium barbarum (Wolfberry) polysaccharides on preserving retinal function after partial optic nerve transection. PLoS ONE 2013, 8, e81339. [Google Scholar] [CrossRef] [Green Version]
  96. Li, H.-Y.; Ruan, Y.-W.; Kau, P.W.-F.; Chiu, K.; Chang, R.C.-C.; Chan, H.H.L.; So, K.-F. Effect of Lycium barbarum (Wolfberry) on alleviating axonal degeneration after partial optic nerve transection. Cell Transplant. 2015, 24, 403–417. [Google Scholar] [CrossRef] [Green Version]
  97. Mi, X.-S.; Feng, Q.; Lo, A.C.Y.; Chang, R.C.-C.; Lin, B.; Chung, S.K.; So, K.-F. Protection of retinal ganglion cells and retinal vasculature by Lycium barbarum polysaccharides in a mouse model of acute ocular hypertension. PLoS ONE 2012, 7, e45469. [Google Scholar] [CrossRef] [Green Version]
  98. Mi, X.S.; Chiu, K.; Van, G.; Leung, J.W.; Lo, A.C.; Chung, S.K.; Chang, R.C.; So, K.F. Effect of Lycium barbarum polysaccharides on the expression of endothelin-1 and its receptors in an ocular hypertension model of rat glaucoma. Neural Regen. Res. 2012, 7, 645–651. [Google Scholar] [CrossRef] [PubMed]
  99. Li, S.-Y.; Yang, D.; Yeung, C.-M.; Yu, W.Y.; Chang, R.C.-C.; So, K.-F.; Wong, D.; Lo, A.C.Y. Lycium barbarum polysaccharides reduce neuronal damage, blood-retinal barrier disruption and oxidative stress in retinal ischemia/reperfusion injury. PLoS ONE 2011, 6, e16380. [Google Scholar] [CrossRef] [Green Version]
  100. He, M.; Pan, H.; Chang, R.C.-C.; So, K.-F.; Brecha, N.C.; Pu, M. Activation of the Nrf2/HO-1 antioxidant pathway contributes to the protective effects of Lycium barbarum polysaccharides in the rodent retina after ischemia-reperfusion-induced damage. PLoS ONE 2014, 9, e84800. [Google Scholar] [CrossRef] [Green Version]
  101. Flammer, J.; Mozaffarieh, M. What is the present pathogenetic concept of glaucomatous optic neuropathy? Surv. Ophthalmol. 2007, 52, S162–S173. [Google Scholar] [CrossRef] [PubMed]
  102. Bucheli, P.; Vidal, K.; Shen, L.; Gu, Z.; Zhang, C.; Miller, L.; Wang, J. Goji berry effects on macular characteristics and plasma antioxidant levels. Optom. Vis. Sci. 2011, 88, 257–262. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  103. Yoshida, A.; Ishiko, S.; Akiba, J.; Kitaya, N.; Nagaoka, T. Radiating retinal folds detected by scanning laser ophthalmoscopy using a diode laser in a dark-field mode in idiopathic macular holes. Graefe’s Arch. Clin. Exp. Ophthalmol. 1998, 236, 445–450. [Google Scholar] [CrossRef] [PubMed]
  104. Prasad, T.; Zhu, P.; Verma, A.; Chakrabarty, P.; Rosario, A.M.; Golde, T.E.; Li, Q. Amyloid β peptides overexpression in retinal pigment epithelial cells via AAV-mediated gene transfer mimics AMD-like pathology in mice. Sci. Rep. 2017, 7, 3222. [Google Scholar] [CrossRef] [PubMed]
  105. Ho, Y.-S.; Yu, M.-S.; Lai, C.S.-W.; So, K.-F.; Yuen, W.-H.; Chang, R.C.-C. Characterizing the neuroprotective effects of alkaline extract of Lycium barbarum on β-amyloid peptide neurotoxicity. Brain Res. 2007, 1158, 123–134. [Google Scholar] [CrossRef] [PubMed]
  106. Chien, K.; Horng, C.; Huang, Y.; Hsieh, Y.; Wang, C.; Yang, J.; Lu, C.; Chen, F. Effects of Lycium barbarum (goji berry) on dry eye disease in rats. Mol. Med. Rep. 2018, 17, 809–818. [Google Scholar] [CrossRef] [PubMed]
  107. Lilly, D.M.; Stillwell, R.H. Probiotics: Growth-promoting factors produced by microorganisms. Science 1965, 147, 747–748. [Google Scholar] [CrossRef] [PubMed]
  108. FAO/WHO. Probiotics in Food Health and Nutritional Properties and Guidelines for Evaluation; Food and Nutrition Paper; FAO: Rome, Italy, 2001; Volume 85. [Google Scholar]
  109. Guo, L.; Li, T.; Tang, Y.; Yang, L.; Huo, G. Probiotic properties of Enterococcus strains isolated from traditional naturally fermented cream in China. Microb. Biotechnol. 2015, 9, 737–745. [Google Scholar] [CrossRef] [PubMed]
  110. Ohimain, E.I.; Ofongo, R.T.S. The Effect of probiotic and prebiotic feed supplementation on chicken health and gut microflora: A Review. Int. J. Anim. Vet. Adv. 2012, 4, 135–143. [Google Scholar]
  111. Gibson, G.R.; Roberfroid, M.B. Dietary modulation of the human colonic microbiota: Introducing the concept of prebiotics. J. Nutr. 1995, 125, 1401–1412. [Google Scholar] [CrossRef]
  112. Gibson, G.R.; Scott, K.P.; Rastall, R.A.; Tuohy, K.M.; Hotchkiss, A.; Dubert-Ferrandon, A.; Gareau, M.; Murphy, E.F.; Saulnier, D.; Loh, G.; et al. Dietary prebiotics: Current status and new definition. Food Sci. Technol. Bull. Funct. Foods 2010, 7, 1–19. [Google Scholar] [CrossRef] [Green Version]
  113. Trowell, H.; Southgate, D.A.T.; Wolever, T.M.S.; Leeds, A.R.; Gassull, M.A.; Jenkins, D.J.A. Dietary fibre redefined. Lancet 1976, 307, 967. [Google Scholar] [CrossRef]
  114. Schweizer, T.F.; Würsch, P. The physiological and nutritional importance of dietary fibre. Experientia 1991, 47, 181–186. [Google Scholar] [CrossRef] [PubMed]
  115. Baba, A.S.; Najarian, A.; Shori, A.B.; Lit, K.W.; Keng, G.A. Viability of lactic acid bacteria, Antioxidant activity and in vitro inhibition of angiotensin-I-converting enzyme of Lycium barbarum yogurt. Arab. J. Sci. Eng. 2014, 39, 5355–5362. [Google Scholar] [CrossRef]
  116. Liao, M.; Wu, Z.Y.; Yu, G.H.; Zhang, W.X. Improving the quality of Sichuan pickle by adding a traditional Chinese medicinal herb Lycium barbarumin its fermentation. Int. J. Food Sci. Technol. 2017, 52, 936–943. [Google Scholar] [CrossRef]
  117. Zhou, F.; Jiang, X.; Wang, T.; Zhang, B.; Zhao, H. Lycium barbarum polysaccharide (LBP): A novel prebiotics candidate for Bifidobacterium and Lactobacillus. Front. Microbiol. 2018, 9, 1034. [Google Scholar] [CrossRef]
  118. González-Rodríguez, I.; Sánchez, B.; Ruiz, L.; Turroni, F.; Ventura, M.; Ruas-Madiedo, P.; Gueimonde, M.; Margolles, A. Role of extracellular transaldolase from Bifidobacterium bifidum in mucin adhesion and aggregation. Appl. Environ. Microbiol. 2012, 78, 3992–3998. [Google Scholar] [CrossRef] [Green Version]
  119. Nami, Y.; Abdullah, N.; Haghshenas, B.; Radiah, D.; Rosli, R.; Khosroushahi, A.Y. Probiotic potential and biotherapeutic effects of newly isolated vaginal Lactobacillus acidophilus 36YL strain on cancer cells. Anaerobe 2014, 28, 29–36. [Google Scholar] [CrossRef]
  120. Alp, G.; Aslim, B.; Suludere, Z.; Akca, G. The role of hemagglutination and effect of exopolysaccharide production on bifidobacteria adhesion to Caco-2 cells in vitro. Microbiol. Immunol. 2010, 54, 658–665. [Google Scholar] [CrossRef]
  121. Al-Sheraji, S.H.; Ismail, A.; Manap, M.Y.; Mustafa, S.; Yusof, R.M. Viability and activity of Bifidobacteria during refrigerated storage of yoghurt containing Mangifera pajang fibrous polysaccharides. J. Food. Sci. 2012, 77, 624–630. [Google Scholar] [CrossRef] [PubMed]
  122. Redgwell, R.J.; Curti, D.; Wang, J.; Dobruchowska, J.M.; Gerwig, G.J.; Kamerling, J.P.; Bucheli, P. Cell wall polysaccharides of Chinese Wolfberry (Lycium barbarum): Part Characterisation of arabinogalactan-proteins. Carbohydr. Polym. 2011, 84, 1075–1083. [Google Scholar] [CrossRef]
  123. Redgwell, R.J.; Curti, D.; Wang, J.; Dobruchowska, J.M.; Gerwig, G.J.; Kamerling, J.P.; Bucheli, P. Cell wall polysaccharides of Chinese Wolfberry (Lycium barbarum): Part Characterization of soluble and insoluble polymer fractions. Carbohydr. Polym. 2011, 84, 1344–1349. [Google Scholar] [CrossRef]
  124. Reeve, V.E.; Allanson, M.; Arun, S.J.; Domanski, D.; Painter, N. Mice drinking goji berry juice (Lycium barbarum) are protected from UV radiation-induced skin damage via antioxidant pathways. Photochem. Photobiol. Sci. 2010, 9, 601–607. [Google Scholar] [CrossRef] [PubMed]
  125. Shi, G.-J.; Zheng, J.; Wu, J.; Qiao, H.-Q.; Chang, Q.; Niu, Y.; Sun, T.; Li, Y.-X.; Yu, J.-Q. Beneficial effects of Lycium barbarum polysaccharide on spermatogenesis by improving antioxidant activity and inhibiting apoptosis in streptozotocin-induced diabetic male mice. Food Funct. 2017, 8, 1215–1226. [Google Scholar] [CrossRef] [PubMed]
  126. Vidović, B.B.; Milinčić, D.D.; Marčetić, M.D.; Djuriš, J.D.; Ilić, T.D.; Kostić, A.Ž.; Pešić, M.B. Health benefits and applications of goji berries in functional food products development: A review. Antioxidants 2022, 11, 248. [Google Scholar] [CrossRef] [PubMed]
  127. Mocan, A.; Vlase, L.; Vodnar, D.C.; Bischin, C.; Hanganu, D.; Gheldiu, A.-M.; Oprean, R.; Silaghi-Dumitrescu, R.; Crișan, G. Polyphenolic content, antioxidant and antimicrobial activities of Lycium barbarum L. and Lycium chinense Mill. leaves. Molecules 2014, 19, 10056–10073. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Health-promoting properties of goji berry fruits and extracts.
Figure 1. Health-promoting properties of goji berry fruits and extracts.
Nutraceuticals 02 00003 g001
Figure 2. The chemical structure of the polyphenols contained in “Goji berries”.
Figure 2. The chemical structure of the polyphenols contained in “Goji berries”.
Nutraceuticals 02 00003 g002
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Skenderidis, P.; Leontopoulos, S.; Lampakis, D. Goji Berry: Health Promoting Properties. Nutraceuticals 2022, 2, 32-48. https://doi.org/10.3390/nutraceuticals2010003

AMA Style

Skenderidis P, Leontopoulos S, Lampakis D. Goji Berry: Health Promoting Properties. Nutraceuticals. 2022; 2(1):32-48. https://doi.org/10.3390/nutraceuticals2010003

Chicago/Turabian Style

Skenderidis, Prodromos, Stefanos Leontopoulos, and Dimitrios Lampakis. 2022. "Goji Berry: Health Promoting Properties" Nutraceuticals 2, no. 1: 32-48. https://doi.org/10.3390/nutraceuticals2010003

APA Style

Skenderidis, P., Leontopoulos, S., & Lampakis, D. (2022). Goji Berry: Health Promoting Properties. Nutraceuticals, 2(1), 32-48. https://doi.org/10.3390/nutraceuticals2010003

Article Metrics

Back to TopTop