Abstract
Aging is characterized by an imbalance between damage inflicted by reactive oxygen species (ROS) and the antioxidative defenses of the organism. As a significant nutritional factor, the trace element selenium (Se) may remodel gradual and spontaneous physiological changes caused by oxidative stress, potentially leading to disease prevention and healthy aging. Se is involved in improving antioxidant defense, immune functions, and metabolic homeostasis. An inadequate Se status may reduce human life expectancy by accelerating the aging process or increasing vulnerability to various disorders, including immunity dysfunction, and cancer risk. This review highlights the available studies on the effective role of Se in aging mechanisms and shows the potential clinical implications related to its consumption. The main sources of organic Se and the advantages of its nanoformulations were also discussed.
Keywords: selenium, health benefit, human aging, antioxidant effect, immunoprotection, chemoprevention
1. Introduction
Aging is an important risk factor in the advancement of many age-related disorders [1]. Since there is a steady trend toward the aging of the human population on a global scale, the number of diseases associated with aging is also gradually increasing. The pathogenesis of various health disorders, including neurodegenerative diseases or cancer, is due to the accumulation of reactive oxygen species (ROS) that cause oxidative stress and inflammation, which are the main contributors to cellular senescence [1,2]. Generally, aging is characterized by an imbalance between damage inflicted by ROS and the organism’s antioxidant defenses [3]. Free radicals could be produced due to the influence of environmental pollutants, metal ions, radiation, or by-products of metabolized drugs [4]. ROS production and oxidative damage to biomacromolecules (nucleic acids, lipids, and proteins) can represent a suitable environment for developing age-related diseases [5,6]. Endogenous defense mechanisms of the human body cannot supply the full prevention of ROS damage, and different natural sources of dietary antioxidants are especially important for this purpose [7]. The antioxidant properties of many polyphenols, vitamins, and trace elements are well known [4,7,8,9,10,11]. The deficiency of micronutrients such as vitamins and minerals can suppress immunity and cause a predisposition to infectious diseases, cancer, neurodegeneration, cardiovascular disorders, and hormonal misbalance [12]. Natural antioxidants, as effective free radical scavengers, are indispensable in preventing and treating many age-related disorders [1,4].
The trace element selenium (Se) was regarded as a dietary supplement for improving health as it possesses valuable antioxidant properties [13]. It may remodel gradual and spontaneous biochemical and physiological changes, potentially leading to disease prevention and healthy aging, because it is involved in improving antioxidant defense, immune functions, and metabolic homeostasis [14]. Se is naturally found in water, soil, and food [15]. Amino acids, peptides, and enzymes are regarded as the main biologically important Se-containing organic compounds [13]. Selenocysteine, the S-to-Se substituted variant of amino acid cysteine, is a key component of selenoproteins [16]. Thus, the physiological effect of Se is mainly due to its incorporation in selenoproteins [17].
It should be noted that 25 selenoproteins have been discovered in humans [18]. Selenoproteins have been implicated in many metabolic and functional pathways, such as aging, cancer, or infection [19]. Thus, the Se-containing enzyme glutathione peroxidase can help lower free radical reactions to tolerable levels by reducing H2O2 to H2O and organic hydroperoxides (ROOH) to alcohol (ROH) [20,21]. The Se-dependent glutathione peroxidases (GPX1–4 and GPX6) and thioredoxin reductases (TrxR1-3) directly suppress oxidative stress; cytosolic GPX4 is essential for embryonic development and cell survival. GPX1 is the most abundant selenoprotein and a major metabolic form of body Se against severe oxidative stress [22]. Incidentally, GPX1 was the first selenoprotein discovered in the mammalian body [17]. GPX1 is a special mammalian selenoenzyme maintaining redox equilibrium by detoxifying ROS [17]. Several non-enzymatic selenoproteins are also known, such as selenoproteins F, H, I, K, etc. [17]. Avery and Hoffmann reported that Se deficiency could cause immune incompetence, significantly increasing susceptibility to pathogens or even cancer [17]. For instance, the health-promoting functions of selenoprotein K were proven in the example of the immune system functioning [23].
According to the WHO recommendations, the daily intake of Se by adults should be at 40–70 µg/day depending on gender and body condition (weight, pregnancy status in women, etc.) [24]. Nevertheless, the average content of Se in the daily diet quite often does not reach this level. The typical level of daily consumption varies in the range of 30–50 µg/day in different European countries [20]. It should be mentioned that Se in doses above 400 µg/day shows harmful actions. The uncontrolled intake of Se-enriched products may result in poisoning [20]. Therefore, Se could be considered a trace element characterized by a very narrow range of concentrations in the human body between deficiency, optimal physiological, and toxic levels [20]. The benefits of Se for the human body are most often evaluated during studies of its content in biological material (blood, plasma, urine, tissue) or glutathione peroxidase activity [25]. The normal range for plasma Se is about 120–160 ng/mL [26].
Se deficiency, which affects about one billion people worldwide, may significantly affect health [27]. In many countries, Se may be deficient because of its low concentration in the soils and, accordingly, in the plants that grow on this substrate [13]. Such famous endemic Asiatic diseases as Keshan and Kashin–Beck are due to Se deficiency. It should be mentioned that more than 50% of Chinese regions are characterized by Se deficiency in the soil [28]. Se has a narrow margin between its essential levels and the amounts associated with toxicity [13]. Generally, Se’s health effect (beneficial or toxic) is dose-dependent and related to the chemical form of this trace element and its bioavailability [29]. Slight excess in Se content can result in toxicity; thus, it must be taken carefully and cautiously [20,30]. Health outcomes occur when there is a lack or excess of Se in the body (Figure 1). In particular, Se deficiency leads to endocrine and immunity disorders, infections, chronic inflammation, neurodegeneration, cardiovascular disease, and cancer, which ultimately negatively affect longevity [31].
The excess of Se in some geographic regions can cause another disorder called ‘selenosis’ [13,32]. Clinical signs of selenosis include garlic odor of the breath and diarrhea, alopecia, nail peeling, pains, irritability, chills, tremors, and neurological damage. Extreme selenosis cases can show liver alterations, cirrhosis, pulmonary edema, lung lesions, or death [33].
The main form of Se ingested by humans is regarded as selenomethionine [17]. It is worth noting that organic selenomethionine could cause toxicity at concentrations much higher than inorganic Se [34]. Organic Se, especially SeMet, the major food species, is more beneficial than its inorganic form in the frame of a balanced diet [29].
This element, taken in excess as dietary supplementation or as a result of environmental pollution, may have a toxic effect in the form of joint diseases and disorders of the blood system [35]. Toenail health demonstrates Se’s nutritional status in epidemiological studies more significantly than other biomarkers [31].
The risk of Se deficiency seems to increase in proportion to age [36] and age-related diseases [22]. Se can be considered a longevity indicator in an elderly population since it plays a role in health maintenance in aging individuals [37]. Inadequate Se status may reduce human life expectancy by accelerating the aging process or increasing vulnerability to various age-related diseases. González et al. showed that maintaining good serum Se levels is important since it may affect the self-perception of health, physical activity, and, consequently, the quality of life in older adults [38]. This review highlights the available studies on the effective role of Se in aging mechanisms and shows the potential clinical implications related to its consumption. The main sources of organic Se were also discussed.
2. The Role of Se in the Prevention and Treatment of Health Disorders
2.1. Oxidative Stress, Inflammation, and Immunity
In the inevitable aging process provided by nature, there is an imbalance between antioxidative defense and ROS, irreversible changes in mitochondrial renewal, and stem cell exhaustion [39]. According to Alehagen et al., these disorders are closely associated with chronic inflammation, which accompanies age-related diseases [39]. Simonoff et al. claimed that the antioxidant status of older people could be evaluated by measuring blood Se and vitamin (A and E) levels [40]. Serum and plasma Se levels, glutathione peroxidase activity, and selenoprotein P concentrations are commonly used measures of a Se status in humans [17].
Se possesses antioxidant, immunostimulating, and anti-inflammatory effects [33]. Many selenoproteins are involved in the regulation of antioxidant activities [41]. The selenocysteine residue in selenoprotein K is regarded to be responsible for its bioactivity [23]. Selenoproteins such as GPXs 1–4 efficiently detoxify cellular peroxides that protect against ROS [13]. In vivo studies have shown that in mice treated with an abdominal injection of D-galactose to induce the aging model, selenoproteins extracted from Se-rich rice enhanced the enzymatic antioxidant capacity (GSH-Px and SOD) in the liver and serum of mice of Se-diet group, compared to the control group [42].
As a cofactor of enzymes involved in antioxidant protection, Se plays a significant role in regulating different inflammatory processes in the organism [35]. Insufficient Se level in the organism is associated with such inflammatory skin diseases as psoriasis and atopic dermatitis [43]. Generally, Se stimulates increasing antibody production in the immune system [20,44]. The optimal Se status (60–175 ng Se/mL plasma) can mitigate an inflammatory process and reduce complications in the lungs, intestines, etc. [17]. Espaladori et al. found that Se used for intracanal medication could potentiate the healing effects of calcium hydroxide in the anti-inflammatory response in periapical dental tissues [45]. According to Ceyan et al., Se demonstrated the protective effect against oxidative toxicity induced by dental amalgam [46].
A group of 16 centenarians, aged 101 to 105 years, living in the Upper Silesia district (Poland), had significantly higher red blood cell glutathione reductase and catalase activities than young, healthy female adults [47]. The increase in the activities of enzymes in the blood of the centenarians, mainly glutathione reductase and catalase, could be interpreted as a favorable response to oxidative stress, which enables the balance between the production of ROS and efficacy of antioxidant defenses in normal aging [47]. Se supplementation in respiratory distress syndrome patients can also modulate the inflammatory response by restoring the antioxidant capacity of the lungs through interleukin (IL)-1β and IL-6 levels [48]. Selenoproteins are very important for prostanoid metabolism due to their immunomodulatory effects [49].
Se deficiency has a negative effect on the condition of innate and adaptive immune responses [17]. The impact of Se on the immune system is multitargeted, i.e., modulating the activities of neutrophils, macrophages, natural killer cells, and T and B-lymphocytes [18]. The studies of the last decade showed that optimal Se supplementation could be used to effectively support the immune system during childhood leukemia [50]. The sufficient Se level improved the phagocytosis functions in macrophages and T-cells activity [51].
Many selenoenzymes and non-enzymatic selenoprotein K, an endoplasmic reticulum transmembrane protein important for calcium-dependent signaling, play an important role in the activation of immune cells [18,52]. Marciel and Hoffmann reported that calcium homeostasis might be altered when different types of cells transform into tumor cells. Selenoprotein K, playing a prominent role in regulating immunity as a cofactor for an enzyme involved in post-translational modifications and maturation of proteins in the endoplasmic reticulum, promotes the calcium flux in the endoplasmic reticulum of immune cells [23]. Thus, Se deficiency is related not only to disrupted antioxidant defense but also to calcium flux and protein folding in cells [53]. It could be concluded that Se supplementations can boost immunity against cancer or other diseases, creating an opportunity for healthy longevity.
2.2. Infections
As it is known, ROS are frequently produced in the human body during viral infections, and their excess can induce oxidative stress being one of the hallmarks of clinical symptoms for many diseases [54]. Among the essential micronutrients implicated in the progression of viral infection, Se plays an important role in redox homeostasis and antioxidant defense due to its incorporation, as already mentioned, in the vitally important selenoproteins [55,56]. For example, Se supplementation strongly affected viral suppression and T-cell recovery in HIV-infected patients in Rwanda [57]. Patients infected with tuberculosis and HIV had lower Se statuses when compared to healthy humans [17].
For the third year, the coronavirus disease COVID-2019 has been affecting millions of people and leading to periodic global pandemic outbreaks. A deficiency in Se was recorded in several health disorders caused by viruses, including COVID-19 [35,55]. Recent studies revealed that COVID-19 patients have lower circulating levels of iron (Fe), zinc (Zn), and Se [58]. Se supplementation in COVID-19 patients has been useful in preventing disease progression [59]. Hargreaves and Mantle found that coenzyme Q10 and Se could decrease oxidative stress and inflammation levels in COVID-19-infected patients [60]. Se-containing agents were regarded as important regulators of the defense mechanisms against COVID-19 due to their anti-inflammatory and immunomodulatory properties [61].
Antibiotic resistance and cancer are now considered the two most significant public health problems that are leading to significant mortality of the planet’s population due to the deaths of over 1.5 million people per year [62]. This suggests that antibiotics and available chemotherapeutics do not supply effective treatment for such serious health problems. Se nanoparticles demonstrated significant antibacterial activity against multidrug-resistant bacteria [63]. Se-containing sealant eliminated the biofilm formation in dental plaque caused by pathogenic bacteria Streptococcus mutans, S. sanguinis, and S. salivarius [64,65]. Seguya et al. compared the efficacy of an organoselenium sealant and chlorhexidine diacetate to prevent the formation of S. mutans biofilm on human teeth [66]. It was reported that chlorhexidine diacetate and organoselenium slightly inhibited S. mutants’ attachment to the teeth [66].
Se supplementation was beneficial during murine infection with a Brazil strain of Trypanosoma cruzi, resulting in decreased parasitemias and increased longevity. After 64 days of infection, groups receiving 4 ppm and 8 ppm Se as sodium selenate in drinking water exhibited 60% survival, and the group without Se demonstrated 0% survival [67].
2.3. Endocrine System Disorders
As it is known, the proper functioning of the thyroid gland requires several elements, including Se, Zn, and copper (Cu), in addition to iodine [68]. Se is one of the important regulators of metabolic processes, and optimal intake is necessary to maintain homeostasis [69].
As reported recently, 35 selenoproteins have been identified [70]. As it was noted by Schomburg [71], a significant number of selenoproteins are involved in the functioning of the thyroid gland. Se deficiency is crucial for developing Hashimoto’s thyroiditis and Graves’ disease [72]. A severe deficiency of Se in diet during pregnancy can cause the development of autoimmune thyroid disease [73].
Three of them are iodothyronine deiodinases, which play a key role in thyroid hormone metabolism. One of the critical roles of Se-enzymes is the involvement in the thyroid hormone synthesis and, therefore, in regulating basic metabolism in all body cells and tissues [74]. Iodothyronine deiodinases cleave iodine-carbon bonds in the thyroid hormone metabolism. Selenoproteins P and GPX 3, present in the human plasma, are often estimated as biomarkers for assessing the Se status of an organism [13,34]. Administration of Se in the case of autoimmune thyroiditis reduced autoimmune antibody titers and improved the well-being of patients [75].
Persistent Se deficiency may also cause infertility [35]. Many clinical studies implicate Se deficiency in several reproductive complications, such as male and female infertility, miscarriage, preterm labor, etc. [76,77].
As was concluded by Prabhu and Lei, both Se deficiency and oversupply seem to dysregulate glucose metabolism and potentiate the risk of type 2 diabetes in several animal studies, with less clear associations discovered in clinical studies [34].
2.4. Cancer
During the 5-year epidemiologic studies and clinical trials conducted by Japanese scientists, the significant effects of sufficient Se status were established in patients with different cancer types [78]. Razaghi et al. reported that nutritional doses of Se can stimulate the immune system against cancer [18]. The anti-cancer effects of selenoprotein K have been revealed in melanoma models in vivo and in human melanoma cell lines [23]. According to Varlamova et al., various mechanisms are involved in the anticarcinogenic effect of Se. Besides the prominent antioxidant effects, Se-containing compounds can maintain DNA stability, regulate inflammatory and immune responses, and inhibit the toxicity of heavy metals [79]. Thus, Se possesses anticarcinogenic properties, especially if administered in a preventive manner before the onset of a disease or at the early stage of its development [20,56,80]. However, its overdosing can act as pro-oxidant inducing cell death. As it is commonly known, the anticancer mechanism of Se is related to its significant antioxidant capacity [20]. Razaghi et al. noticed that Se status in cancer patients is highly correlated with concentrations of proinflammatory cytokines [18]. Varlamova and Turovsky described the main cytotoxic activities of methylseleninic acid on different cancer cells [81].
Considering that cancer cells are quite vulnerable to exposure to ROS, targeting the antioxidant capacity of tumor cells has been considered a promising strategy for anticancer therapy [82]. At increased but non-lethal doses, Se acts as a pro-oxidant and inhibits the growth of cancer cells without side effects on normal cells [53,83]. According to Wang et al., the detection by flow cytometry has shown decreased cancer cell viability of buffalo rat liver induced by Se nanoparticles (over 24 μM) [84]. It occurred mainly due to tumor cell apoptosis rather than necrosis. Thus, Se was regarded as a ‘double-edged sword’ due to its antioxidant properties at nutritional levels or prooxidant effects at supranutritional levels [18,85]. In tumor cells, due to the acidic pH state with redox imbalance, excessive Se-compounds cause ROS overproduction, leading to ER stress and disruption of the integrity of mitochondria [79]. The anti-cancer effects of Se-compounds are related to their ability to induce oxidative stress and subsequent DNA damage in cancer cells that lead to obligate apoptosis [17]. On the contrary, the Se intake at an optimal level could prevent damage to the DNA in healthy cells and, consequently, the occurrence of mutations.
As it is known, benign prostatic hyperplasia and adenocarcinoma are closely associated with the age of men. Daragó et al. found that deficiency of Zn, Cu, and Se caused disturbing homeostasis in the etiology of the abovementioned prostatic diseases [86]. Se nanoparticles with a size below 100 nm produced by a novel green process called pulsed laser ablation in liquids (PLAL) showed an anticancer effect on human glioblastoma and melanoma cells [62]. Se-nanoformulations’ anticancer effects inhibited cancer cells’ growth by interrupting the cell cycle at the synthetic phase [87]. Selenomethylselenocysteine, found in Se-enriched plants from the Brassica and Allium genera, was regarded as a compound possessing prominent anti-cancerous properties [25].
During the clinical study, 325 cases of Chinese patients with oral cancer were analyzed by Chen et al. [88]. The multiple interactions between Se intake, drinking/smoking status, and fish and fresh fruit intake frequencies were studied. The high level of serum Se was regarded as a protective factor for the risk of oral cancer. Appropriate diet and immunity are considered important modifiable factors in oral cancer [89]. Se and ceruloplasmin levels in serum were regarded as disease markers in squamous cell carcinoma. The effect of Se on the reduction of all-cause and cancer mortality was observed in the 12-year study carried out on 13,887 adults in the US population [90].
2.5. Intoxication
Se is an effective protective agent for the human body against various environmental pollutants and drug-related side effects [91]. Limaye A. et al. found that Se and polyphenol curcumin were quite effective against aflatoxicosis due to their prominent antioxidant properties [92]. Bjørklund [93] found that numerous studies have shown that many Se-containing foods protect the human body against mercury (Hg) exposure. It is due to the high affinity between Se and Hg. The appropriate intake of Se and Zn and some vitamins have been suggested to reduce As-induced toxicity [94].
3. The Role of Se in Longevity and Age-Related Disorders
Age-related disorders such as neurodegeneration, cardiovascular disease, immune dysfunction, formation of skin wrinkles, etc., are closely associated with Se deficiency [95]. Se concentration in healthy adults’ plasma is higher than in the elderly population [96].
The items related to the possible effects of Se application for increasing animals’ longevity were widely investigated [97,98,99,100]. The activity of GSH-Px in the female and male flies Drosophila melanogaster was elevated with the increased sodium selenite in the medium. The average life span and the average maximum life span of flies in the Se groups improved significantly compared with the control group [100]. Another animal study showed that the survival rate of flies fed a diet deficient in Se was one-half that of flies fed a diet supplemented with optimal amounts of Se [99]. Administration of sodium selenite for seven days significantly increased the longevity of mice inoculated with 10(5) L797 cells. These outcomes suggest that the anti-leukemic effect of sodium selenite is associated with the inhibition of DNA replication, transcription, and translation [97]. In their recent publication, Wu et al. suggested a novel aging model by which Se at low levels may be considered a hormetic chemical and decouple health span and longevity [22]. The authors’ experimental data revealed that dietary Se deprivation increased the incidence of osteoporosis, gray hair, alopecia, and cataract but surprisingly promoted longevity in mice; deprivation also accelerated age-dependent declines in glucose tolerance, insulin sensitivity, and glucose-stimulated insulin production.
Steinbrenner and Klotz analyzed the epidemiological studies [101]. They revealed that the insufficient dietary intake of Zn and Se can cause cognitive dysfunctions in aged persons. Se supplementation effectively restored cognitive decline associated with aging [2]. Even though Se is crucial to brain health, at the same time, it can exhibit neurotoxicity, depending on speciation and dosage [102]. The valuable skincare and anti-aging effects were recorded by Wei et al. after the external application of Se-enriched fermented mung beans [103].
Ischemic heart death correlated inversely with blood Se in 25 US cities in 22 states [104]. The association between serum Se and hand grip strength among 676 moderately to severely disabled community-dwelling women in Baltimore, Maryland, was established [105]. Population-based studies showed that low serum Se and total carotenoid concentrations were associated with an increased risk of death among older women in the US population [106]. According to Al-Mubarak et al., insufficient Se intake was discovered in 30–50% of patients with heart failure [107].
Body Se in centenarians is maintained at a nutritionally adequate level, suggesting a positive association between selenoprotein expression and longevity. Elevated ROS levels contributed to the pathologies of Alzheimer’s and Parkinson’s diseases, which antioxidative selenoproteins can suppress. Selenoprotein p (SelP) is essential for the normal function of neuronal cells and protects against Alzheimer’s disease [22].
Scientists conducted several investigations concerning environmental and nutritional factors, including Se consumption, relating to human longevity in Chinese areas [104,108,109,110,111,112]. In 446 oldest elderly from longevity areas in China (5 provinces), the median (interquartile range) of the content of plasma Se was 1.44 (0.91) μmol/L. The contents of plasma Se, Fe, and Cu in centenarians were higher than in those aged 90 and over; the contents of plasma Se increased with age. The concentrations of plasma Se were high in the oldest elderly in the longevity areas [111]. The centenarians from seven longevity areas in China, who participated in another longitudinal survey [111], had lower chronic disease risks and higher antioxidant activity compared with other age groups and had a higher level of nutritional elements compared with those aged 90 and over. A cross-sectional study [108] in all 18 cities and counties in Hainan Province revealed a positive correlation between daily intake of Cu, Se, and Zn from food and water and aging and longevity indexes. Another Chinese study confirmed that the percentage of long-lived people in the Zhongxiang area, where the inhabitants commonly have long life spans, was closely related to the macro- and microelement contents of their staple food, rice [110]. The study’s authors classified the elements of rice based on their effect on longevity, indicating that Se showed a positive correlation with it. Foster and Zhang determined that fewer people of advanced age reside in Chinese counties where Kaschin-Beck and Keshan diseases are endemic than in unaffected counties [112]. These researchers substantiate it by elevated mortality from endemic and chronic diseases in Se-deficient areas and accelerated aging due to excessive cellular damage. In Se deficient areas of China, the life span of adults was lowered severely, with the occurrence of heart muscle damage [104]. Huang et al. [113] found higher 85+/65+ distribution ratios, indicating enhanced longevity in the coastal southern and eastern regions of China, whereas higher levels of Se distribution in soil occur [109]. Nutritional factors such as Se and omega-3 fatty acids in sea fish were crucial to longevity there.
A cohort study of 227 older adults residing in 14 nursing homes in Asturias (Spain) revealed that subjects with the upper tertile of serum Se had more than twice as much probability of reporting good health status, good chewing ability, and of doing more than 60 min of exercise/day [38]. Researchers who designed a 9-year longitudinal EVA study in France involving 1389 free-living participants aged 59–71 years [37] investigated the relationships between plasma Se and longevity. They concluded that inadequate plasma Se could adversely affect the maintenance of optimal health in an aging population. Comparisons of survival distributions among quartiles of plasma Se showed that mortality increased in subgroups with low plasma Se concentrations at baseline; a 0.2 µmol/L decrease in plasma Se was significantly associated with higher mortality risk.
The low percentages of Se deficiencies were reported as a possible explanation for longevity in Italian scientists’ nonagenarian–centenarian studies. A significant decrease in Se values was demonstrated in a group of nonagenarians/centenarians (91–110 years) compared to a group of elderly subjects (60–90 years). Another study [114] involved subjects who lived in Sardinia, an Italian island with a higher prevalence of centenarians than in other European countries. Significant depletion of Se concentration in plasma of nonagenarians (89.0 ± 6.3 years) and centenarians (101 ± 1 years) with respect to controls (61.2 ± 1.1 years) was shown; the geometric mean values of Se were: 111 µg/mL in controls, 88.9 µg/mL in nonagenarians, 81.9 µg/mL in centenarians.
4. Sources of Se in the Human Diet
Organic Se from food is considered a safe and efficient source of supporting human health [115]. Among the sources of organic Se for humans, we find foods of animal, vegetable, and mushroom origin [13,116]. The main animal sources of Se are red meats, poultry, beef or sheep liver, seafood, eggs, and dairy products [31,35,117]. The main kinds of food containing Se in comparatively high amounts are shown in Figure 2.
Plants can absorb inorganic Se from soil and transform it into an organic form such as selenomethionine or selenocysteine, which are much more accessible for animals and humans than inorganic ones [25,118]. Consumed by humans, organic Se changes by joining amino acids and proteins [25].
The extremely high Se content, mainly in the form of selenomethionine, is a characteristic feature of Brazilian nuts [20]. Broccoli, which can accumulate Se many-fold higher than other plants, is associated with a reduced risk of some cancer types [119]. Consumption of Se-enriched broccoli led to activation of human leukocytes and increased cytokine production during immune response [120]. It should be noted that consumed vegetables (garlic, broccoli, etc.) should contain methylated forms of organic Se to be effective in the prevention of cancer [25,117]. Methylseleninic acid can cause stress in the functioning endoplasmic reticulum through modulation of the membrane selenoproteins and activating the apoptosis of cancer [52,61,121].
The cluster analysis of average Se amounts in raw material of different medicinal plants demonstrated that the Apiaceae and Lamiaceae representatives are more Se-rich than species from other botanical families [122]. Thus, Majoranae herba (Lamiaceae) contained more than 50 μg/kg Se. An organic Se-compounds from mushroom Grifola frondosa formed by its combination of polysaccharides was very effective in immune regulation and had antitumor and anti-aging effects [123]. Se-containing yeasts are a valuable source of easily assimilable Se [20]. Fordyce reported that the bioavailability of Se was reduced in dairy products, mushrooms, and vegetables as a result of cooking, which causes losing about 50% of Se compounds, especially when vinegar and salt are added [124].
In recent decades, biofortification strategies have been widely applied to produce Se-enriched edible plants [125]. Enrichment of soil with fertilizers such as inorganic Se compounds leads to a rapid increase in crops’ organic Se levels [118]. It was also demonstrated that the plant biomass, bacteria, and yeast enriched in Se from the culture medium containing its inorganic sources were considered a prospect for this trace element supplementation [126]. Se-enriched yeast is the cheapest organic Se supplementation [25]. The concentration of Se in plants usually reflects its soil content and can vary in a very wide range, from 0.005 mg/kg to 5500 mg/kg [13,127]. Se-containing yeast used as a feed supplementation for livestock is currently approved in European countries to enrich animal food with this element [128].
5. Nanoformulations of Se in Age-Related Disorders
Nanoscale Se provides increased bioavailability and controlled release of various drugs into the body at the site of action. [129,130]. Nanoparticles supply a low dosage to restore the Se serum levels [131]. Various studies demonstrated that Se nanoparticles possess lower toxicity and higher bioavailability than organic or inorganic Se [84,132]. They are characterized by high adsorption capacity as the charges on their surface can conjugate and interact through various functional groups (C=O, COO−, NH, C–N, etc.), both positively and negatively charged [133].
Se nanoparticles with chitosan/citrate complex have protected experimental mice against ROS in galactose-induced aging [134]. Mamgain et al. reported the antioxidant activity of diverse Se-based nanoparticles [135]. The antioxidant, anti-carcinogenic, and immunomodulatory efficacy of nano-Se applications for enhancing stress resilience and productivity of livestock and fish were proven by Sarkar et al. [136]. The activation of oxidative stress in cancer cells was regarded as a key point in treating oncological disorders with Se nanoparticles [79].
Varlamova et al. summarized the data of many researchers who described the positive physiological effect of nano-scale Se in the case of neurodegenerative disorders [79]. Nano-Se dietary supplementation improved the Se deposition in the testis and ovary of Japanese quail and their reproductive performance, thus prolonging their youth [137]. Se nanoparticles effectively prevented the progression of diabetic nephropathy [138]. Se nanosupplementations reduced the formation of advanced glycation end products by slowing down the process of protein glycation [139]. Se-nanoparticles demonstrated valuable cytotoxic potential in treating cancer in different cell lines [140,141]. Wang et al. reported that nanoscale Se supplementation possesses significant chemopreventive properties [142]. Turovsky and Varlamova comprehensively described the mechanism of calcium-dependent pro-apoptotic action of Se nanoparticles [143]. It was concluded that instead of systemic supplementation of Se, nano-formulations could be developed for targeted delivery of Se to tumors and decrease its dosage to minimize the adverse side effects [18,144].
6. Determination of Se in Foods
Se appears in the environment in a trace amount. Thus, determining the Se amount in food samples demands appropriate measurement methods, including sample preparation, separation technique, and detection [25]. Se speciation in food is not an easy goal because of its very low concentrations and availability of many different forms, as well as the lack of appropriate reference materials for its speciation that generates problems with validation. That is why speciation of Se has been conducted only for a few foods [25,145].
Bodnar et al. summarized that among different sample preparation techniques for Se determination, cryogenic trapping, wet/dry mineralization, and extraction methods (solid-phase, liquid–liquid, liquid–solid, and enzymatic) are the most used [25]. A UV-oxidation procedure was developed to completely digest food samples for the evaluation of trace levels of Se [146].
The chromatographic methods (liquid and gas chromatography) are more frequently used than capillary electrophoresis or isotachophoresis in the field of separation techniques. Gilbert-López et al. reported that more than 100 Se metabolites were identified in the Se-enriched yeast using the liquid chromatography-mass spectrometry method [147]. Among the detection systems, spectroscopic, spectrophotometric, and electroanalytical methods are mostly applied [25,148,149]. Thus, the detection limits for Se in the plant food using atomic absorption spectrometry were 35–40 ng/g [146].
7. Conclusions
The oxidative damage to macromolecules in the human body represents a suitable environment for developing age-related diseases. The trace element Se in the form of selenoproteins improves antioxidant defense, immune functions, and metabolic homeostasis. Se deficiency affects about one billion people in the world and may have a significant adverse effect on human health. Se-containing organic compounds play a key role in the health maintenance of aging individuals. The nutritional doses of Se can efficiently stimulate the immune system against infectious diseases or cancer. A deficiency in Se is evidenced in some disorders caused by viruses or pathogenic bacteria. It discusses the important roles of Se-enzymes according to their involvement in the thyroid hormones’ metabolism. Insufficient dietary intake of Se can cause cognitive dysfunctions and heart failure in aged persons. Organic Se from food of animal, plant, or mushroom origin is considered a safe and efficient source of supporting human health. Bio-fortification strategies are widely applied to produce Se-enriched edible plants and mushrooms. Nanoscale Se provides increased bioavailability and controlled release in the organism to the site of action. Generally, the health effect of Se is dose-dependent, and there is a narrow margin between its essential levels and the amounts associated with toxicity. Se possesses antioxidant properties at nutritional levels and prooxidant effects at supranutritional levels.
Author Contributions
Conceptualization, G.B., M.S., R.L. and H.A.; writing—original draft preparation, M.S., R.L., H.A. and I.K.; writing—review and editing, G.B., M.S., V.S. and M.P.; visualization V.S, M.P., G.B., V.S. and M.P. contributed to the final version of the manuscript and revised the manuscript. G.B. supervised the project. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Conflicts of Interest
The authors declare no conflict of interest.
Sample Availability
Not applicable.
Funding Statement
This research received no external funding.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Rusu M., Fizesan I., Vlase L., Popa D.-S. Antioxidants in Age-Related Diseases and Anti-Aging Strategies. Antioxidants. 2022;11:1868. doi: 10.3390/antiox11101868. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Leiter O., Zhuo Z., Rust R., Wasielewska J.M., Grönnert L., Kowal S., Overall R.W., Adusumilli V.S., Blackmore D.G., Southon A., et al. Selenium mediates exercise-induced adult neurogenesis and reverses learning deficits induced by hippocampal injury and aging. Cell Metab. 2022;34:408–423.e8. doi: 10.1016/j.cmet.2022.01.005. [DOI] [PubMed] [Google Scholar]
- 3.Afanas’ev I.B. Free radical mechanisms of aging processes under physiological conditions. Biogerontology. 2005;6:283–290. doi: 10.1007/s10522-005-2626-z. [DOI] [PubMed] [Google Scholar]
- 4.Alkadi H. A Review on Free Radicals and Antioxidants. Infect. Disord. Drug Targets. 2020;20:16–26. doi: 10.2174/1871526518666180628124323. [DOI] [PubMed] [Google Scholar]
- 5.Lee J., Koo N., Min D.B. Reactive oxygen species, aging, and antioxidative nutraceuticals. Compr. Rev. Food Sci. Food Saf. 2004;3:21–33. doi: 10.1111/j.1541-4337.2004.tb00058.x. [DOI] [PubMed] [Google Scholar]
- 6.Gasmi A., Chirumbolo S., Peana M., Mujawdiya P.K., Dadar M., Menzel A., Bjørklund G. Biomarkers of Senescence during Aging as Possible Warnings to Use Preventive Measures. Curr. Med. Chem. 2021;28:1471–1488. doi: 10.2174/0929867327999200917150652. [DOI] [PubMed] [Google Scholar]
- 7.Landete J.M. Dietary intake of natural antioxidants: Vitamins and polyphenols. Crit. Rev. Food Sci. Nutr. 2013;53:706–721. doi: 10.1080/10408398.2011.555018. [DOI] [PubMed] [Google Scholar]
- 8.Gasmi A., Mujawdiya P.K., Lysiuk R., Shanaida M., Peana M., Gasmi Benahmed A., Beley N., Kovalska N., Bjørklund G. Quercetin in the Prevention and Treatment of Coronavirus Infections: A Focus on SARS-CoV-2. Pharmaceuticals. 2022;15:1049. doi: 10.3390/ph15091049. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Shanaida M., Adamiv S., Yaremchuk O., Ivanusa I. Pharmacological study of the polyphenol-containing phytosubstance obtained from the anise hyssop herb. PharmacologyOnLine. 2021;2:105–112. [Google Scholar]
- 10.Gons’kyi Ia I., Korda M.M., Klishch I.M. Status of the free radical oxidation and antioxidant system in rats with toxic liver damage; effect of tocopherol and dimethylsulfoxide. Ukr. Biokhimicheskii Zhurnal. 1991;63:112–116. [PubMed] [Google Scholar]
- 11.Gasmi A., Mujawdiya P.K., Noor S., Lysiuk R., Darmohray R., Piscopo S., Lenchyk L., Antonyak H., Dehtiarova K., Shanaida M., et al. Polyphenols in Metabolic Diseases. Molecules. 2022;27:6280. doi: 10.3390/molecules27196280. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Ćurko-Cofek B. Micronutrients in Ageing and Longevity. In: Rattan S.I.S., Kaur G., editors. Nutrition, Food and Diet in Ageing and Longevity. Springer International Publishing; Cham, Switzerland: 2021. pp. 63–83. [DOI] [Google Scholar]
- 13.Antonyak H., Iskra R., Panas N., Lysiuk R. Selenium. In: Malavolta M., Mocchegiani E., editors. Trace Elements and Minerals in Health and Longevity. Springer International Publishing; Cham, Switzerland: 2018. pp. 63–98. [DOI] [Google Scholar]
- 14.Mocchegiani E., Malavolta M., Muti E., Costarelli L., Cipriano C., Piacenza F., Tesei S., Giacconi R., Lattanzio F. Zinc, metallothioneins and longevity: Interrelationships with niacin and selenium. Curr. Pharm. Des. 2008;14:2719–2732. doi: 10.2174/138161208786264188. [DOI] [PubMed] [Google Scholar]
- 15.Wang N., Tan H.Y., Li S., Xu Y., Guo W., Feng Y. Supplementation of Micronutrient Selenium in Metabolic Diseases: Its Role as an Antioxidant. Oxidative Med. Cell Longev. 2017;2017:7478523. doi: 10.1155/2017/7478523. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Arnér E.S.J. Common modifications of selenocysteine in selenoproteins. Essays Biochem. 2020;64:45–53. doi: 10.1042/EBC20190051. [DOI] [PubMed] [Google Scholar]
- 17.Avery J.C., Hoffmann P.R. Selenium, Selenoproteins, and Immunity. Nutrients. 2018;10:1203. doi: 10.3390/nu10091203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Razaghi A., Poorebrahim M., Sarhan D., Björnstedt M. Selenium stimulates the antitumour immunity: Insights to future research. Eur. J. Cancer. 2021;155:256–267. doi: 10.1016/j.ejca.2021.07.013. [DOI] [PubMed] [Google Scholar]
- 19.Vinceti M., Filippini T., Del Giovane C., Dennert G., Zwahlen M., Brinkman M., Zeegers M.P., Horneber M., D’Amico R., Crespi C.M. Selenium for preventing cancer. Cochrane Database Syst. Rev. 2018;1:CD005195. doi: 10.1002/14651858.CD005195.pub4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Kieliszek M., Blazejak S. Current Knowledge on the Importance of Selenium in Food for Living Organisms: A Review. Molecules. 2016;21:609. doi: 10.3390/molecules21050609. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Harman D. The aging process. Proc. Natl. Acad. Sci. USA. 1981;78:7124–7128. doi: 10.1073/pnas.78.11.7124. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Wu M., Porres J., Cheng W.H. Selenium, Selenoproteins, and Age-Related Disorders. Bioact. Food Diet. Interv. Aging Popul. 2013:227–239. doi: 10.1016/B978-0-12-397155-5.00019-2. [DOI] [Google Scholar]
- 23.Marciel M., Hoffmann P. Molecular Mechanisms by Which Selenoprotein K Regulates Immunity and Cancer. Biol. Trace Elem. Res. 2019;192:60–68. doi: 10.1007/s12011-019-01774-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Institute of Medicine (US) Dietary Reference Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids. The National Academies Press; Washington, DC, USA: 2000. Panel on Dietary Antioxidants and Related Compounds. [DOI] [PubMed] [Google Scholar]
- 25.Bodnar M., Szczyglowska M., Konieczka P., Namiesnik J. Methods of Selenium Supplementation: Bioavailability and Determination of Selenium Compounds. Crit. Rev. Food Sci. Nutr. 2016;56:36–55. doi: 10.1080/10408398.2012.709550. [DOI] [PubMed] [Google Scholar]
- 26.Wimmer I., Hartmann T., Brustbauer R., Minear G., Dam K. Selenium levels in patients with autoimmune thyroiditis and controls in lower Austria. Horm. Metab. Res. 2014;46:707–709. doi: 10.1055/s-0034-1377029. [DOI] [PubMed] [Google Scholar]
- 27.Kieliszek M. Selenium–Fascinating Microelement, Properties and Sources in Food. Molecules. 2019;24:1298. doi: 10.3390/molecules24071298. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Dinh Q.T., Cui Z., Huang J., Tran T.A.T., Wang D., Yang W., Zhou F., Wang M., Yu D., Liang D. Selenium distribution in the Chinese environment and its relationship with human health: A review. Environ. Int. 2018;112:294–309. doi: 10.1016/j.envint.2017.12.035. [DOI] [PubMed] [Google Scholar]
- 29.Thiry C., Ruttens A., De Temmerman L., Schneider Y.-J., Pussemier L. Current knowledge in species-related bioavailability of selenium in food. Food Chem. 2012;130:767–784. doi: 10.1016/j.foodchem.2011.07.102. [DOI] [Google Scholar]
- 30.Brozmanová J., Mániková D., Vlčková V., Chovanec M. Selenium: A double-edged sword for defense and offence in cancer. Arch. Toxicol. 2010;84:919–938. doi: 10.1007/s00204-010-0595-8. [DOI] [PubMed] [Google Scholar]
- 31.Hu W., Zhao C., Hu H., Yin S. Food Sources of Selenium and Its Relationship with Chronic Diseases. Nutrients. 2021;13:1739. doi: 10.3390/nu13051739. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Huang L., Shi Y., Lu F., Zheng H., Liu X., Gong B., Yang J., Lin Y., Cheng J., Ma S., et al. Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan population. PLoS ONE. 2013;8:e71411. doi: 10.1371/journal.pone.0071411. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Joshi T., Durgapal S., Juyal V., Jantwal A., Rana M., Kumar A. Chapter4.15—Selenium. In: Nabavi S.M., Silva A.S., editors. Antioxidants Effects in Health. Elsevier; Amsterdam, The Netherlands: 2022. pp. 461–474. [DOI] [Google Scholar]
- 34.Prabhu K.S., Lei X.G. Selenium. Adv. Nutr. 2016;7:415–417. doi: 10.3945/an.115.010785. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Kieliszek M. Chapter Eleven—Selenium. In: Eskin N.A.M., editor. Advances in Food and Nutrition Research. Volume 96. Academic Press; Cambridge, MA, USA: 2021. pp. 417–429. [DOI] [PubMed] [Google Scholar]
- 36.Savarino L., Granchi D., Ciapetti G., Cenni E., Ravaglia G., Forti P., Maioli F., Mattioli R. Serum concentrations of zinc and selenium in elderly people: Results in healthy nonagenarians/centenarians. Exp. Gerontol. 2001;36:327–339. doi: 10.1016/S0531-5565(00)00218-7. [DOI] [PubMed] [Google Scholar]
- 37.Akbaraly N.T., Arnaud J., Hininger-Favier I., Gourlet V., Roussel A.M., Berr C. Selenium and mortality in the elderly: Results from the EVA study. Clin. Chem. 2005;51:2117–2123. doi: 10.1373/clinchem.2005.055301. [DOI] [PubMed] [Google Scholar]
- 38.González S., Huerta J.M., Fernández S., Patterson A.M., Lasheras C. Life-quality indicators in elderly people are influenced by selenium status. Aging Clin. Exp. Res. 2007;19:10–15. doi: 10.1007/BF03325205. [DOI] [PubMed] [Google Scholar]
- 39.Alehagen U., Opstad T.B., Alexander J., Larsson A., Aaseth J. Impact of Selenium on Biomarkers and Clinical Aspects Related to Ageing. A Review. Biomolecules. 2021;11:1478. doi: 10.3390/biom11101478. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Simonoff M., Sergeant C., Garnier N., Moretto P., Llabador Y., Simonoff G., Conri C. Free Radicals and Aging. Springer; Berlin/Heidelberg, Germany: 1992. Antioxidant Status (Selenium, Vitamins A and E) and Aging; pp. 368–397. [DOI] [PubMed] [Google Scholar]
- 41.Cai Z., Zhang J., Li H. Selenium, aging and aging-related diseases. Aging Clin. Exp. Res. 2019;31:1035–1047. doi: 10.1007/s40520-018-1086-7. [DOI] [PubMed] [Google Scholar]
- 42.Zeng R., Farooq M.U., Zhang G., Tang Z., Zheng T., Su Y., Hussain S., Liang Y., Ye X., Jia X., et al. Dissecting the Potential of Selenoproteins Extracted from Selenium-Enriched Rice on Physiological, Biochemical and Anti-Ageing Effects In Vivo. Biol. Trace Elem. Res. 2020;196:119–130. doi: 10.1007/s12011-019-01896-z. [DOI] [PubMed] [Google Scholar]
- 43.Lv J., Ai P., Lei S., Zhou F., Chen S., Zhang Y. Selenium levels and skin diseases: Systematic review and meta-analysis. J. Trace Elem. Med. Biol. 2020;62:126548. doi: 10.1016/j.jtemb.2020.126548. [DOI] [PubMed] [Google Scholar]
- 44.Ma C., Hoffmann P.R. Selenoproteins as regulators of T cell proliferation, differentiation, and metabolism. Semin. Cell Dev. Biol. 2021;115:54–61. doi: 10.1016/j.semcdb.2020.11.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Espaladori M.C., Diniz J.M.B., de Brito L.C.N., Tavares W.L.F., Kawai T., Vieira L.Q., Sobrinho A.P.R. Selenium intracanal dressing: Effects on the periapical immune response. Clin. Oral Investig. 2021;25:2951–2958. doi: 10.1007/s00784-020-03615-8. [DOI] [PubMed] [Google Scholar]
- 46.Ceyhan D., Guzel K.G.U., Cig B. The protective role of selenium against dental amalgam-induced intracellular oxidative toxicity through the TRPV1 channel in DBTRG glioblastoma cells. J. Appl. Oral Sci. 2021;29:e20200414. doi: 10.1590/1678-7757-2020-0414. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Klapcinska B., Derejczyk J., Wieczorowska-Tobis K., Sobczak A., Sadowska-Krepa E., Danch A. Antioxidant defense in centenarians (a preliminary study) Acta Biochim. Pol. 2000;47:281–292. doi: 10.18388/abp.2000_4008. [DOI] [PubMed] [Google Scholar]
- 48.Mahmoodpoor A., Hamishehkar H., Shadvar K., Ostadi Z., Sanaie S., Saghaleini S.H., Nader N.D. The Effect of Intravenous Selenium on Oxidative Stress in Critically Ill Patients with Acute Respiratory Distress Syndrome. Immunol. Investig. 2019;48:147–159. doi: 10.1080/08820139.2018.1496098. [DOI] [PubMed] [Google Scholar]
- 49.Qian F., Misra S., Prabhu K.S. Selenium and selenoproteins in prostanoid metabolism and immunity. Crit. Rev. Biochem. Mol. Biol. 2019;54:484–516. doi: 10.1080/10409238.2020.1717430. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Radhakrishnan N., Dinand V., Rao S., Gupta P., Toteja G., Kalra M., Yadav S.P., Sachdeva A. Antioxidant Levels at Diagnosis in Childhood Acute Lymphoblastic Leukemia. Indian J. Pediatr. 2012;80:292–296. doi: 10.1007/s12098-012-0892-8. [DOI] [PubMed] [Google Scholar]
- 51.Carlson B.A., Yoo M.H., Shrimali R.K., Irons R., Gladyshev V.N., Hatfield D.L., Park J.M. Role of selenium-containing proteins in T-cell and macrophage function. Proc. Nutr. Soc. 2010;69:300–310. doi: 10.1017/S002966511000176X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Varlamova E. Participation of selenoproteins localized in the ER in the processes occurring in this organelle and in the regulation of carcinogenesis-associated processes. J. Trace Elem. Med. Biol. 2018;48:172–180. doi: 10.1016/j.jtemb.2018.04.005. [DOI] [PubMed] [Google Scholar]
- 53.Huang Z., Rose A.H., Hoffmann P.R. The role of selenium in inflammation and immunity: From molecular mechanisms to therapeutic opportunities. Antioxid. Redox Signal. 2012;16:705–743. doi: 10.1089/ars.2011.4145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Guillin O.M., Vindry C., Ohlmann T., Chavatte L. Selenium, Selenoproteins and Viral Infection. Nutrients. 2019;11:2101. doi: 10.3390/nu11092101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Zhang J., Saad R., Taylor E.W., Rayman M.P. Selenium and selenoproteins in viral infection with potential relevance to COVID-19. Redox Biol. 2020;37:101715. doi: 10.1016/j.redox.2020.101715. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Ali W., Benedetti R., Handzlik J., Zwergel C., Battistelli C. The innovative potential of selenium-containing agents for fighting cancer and viral infections. Drug Discov. Today. 2021;26:256–263. doi: 10.1016/j.drudis.2020.10.014. [DOI] [PubMed] [Google Scholar]
- 57.Kamwesiga J., Mutabazi V., Kayumba J., Tayari J.C., Uwimbabazi J.C., Batanage G., Uwera G., Baziruwiha M., Ntizimira C., Murebwayire A., et al. Effect of selenium supplementation on CD4+ T-cell recovery, viral suppression and morbidity of HIV-infected patients in Rwanda: A randomized controlled trial. AIDS. 2015;29:1045–1052. doi: 10.1097/QAD.0000000000000673. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Li Y., Luo W., Liang B. Circulating trace elements status in COVID-19 disease: A meta-analysis. Front. Nutr. 2022;9:982032. doi: 10.3389/fnut.2022.982032. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Fakhrolmobasheri M., Mazaheri-Tehrani S., Kieliszek M., Zeinalian M., Abbasi M., Karimi F., Mozafari A.M. COVID-19 and Selenium Deficiency: A Systematic Review. Biol. Trace Elem. Res. 2022;200:3945–3956. doi: 10.1007/s12011-021-02997-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Hargreaves I.R., Mantle D. COVID-19, Coenzyme Q10 and Selenium. Adv. Exp. Med. Biol. 2021;1327:161–168. doi: 10.1007/978-3-030-71697-4_13. [DOI] [PubMed] [Google Scholar]
- 61.Mal’tseva V.N., Goltyaev M.V., Turovsky E.A., Varlamova E.G. Immunomodulatory and Anti-Inflammatory Properties of Selenium-Containing Agents: Their Role in the Regulation of Defense Mechanisms against COVID-19. Int. J. Mol. Sci. 2022;23:2360. doi: 10.3390/ijms23042360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Geoffrion L.D., Hesabizadeh T., Medina-Cruz D., Kusper M., Taylor P., Vernet-Crua A., Chen J., Ajo A., Webster T.J., Guisbiers G. Naked Selenium Nanoparticles for Antibacterial and Anticancer Treatments. ACS Omega. 2020;5:2660–2669. doi: 10.1021/acsomega.9b03172. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Han H.W., Patel K.D., Kwak J.H., Jun S.K., Jang T.S., Lee S.H., Knowles J.C., Kim H.W., Lee H.H., Lee J.H. Selenium Nanoparticles as Candidates for Antibacterial Substitutes and Supplements against Multidrug-Resistant Bacteria. Biomolecules. 2021;11:1028. doi: 10.3390/biom11071028. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Tran P., Hamood A., Mosley T., Gray T., Jarvis C., Webster D., Amaechi B., Enos T., Reid T. Organo-selenium-containing dental sealant inhibits bacterial biofilm. J. Dent. Res. 2013;92:461–466. doi: 10.1177/0022034513482141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Tran P., Kopel J., Ray C., Reed J., Reid T.W. Organo-selenium containing dental sealant inhibits biofilm formation by oral bacteria. Dent. Mater. 2022;38:848–857. doi: 10.1016/j.dental.2022.04.006. [DOI] [PubMed] [Google Scholar]
- 66.Seguya A., Mowafy M., Gaballah A., Zaher A. Chlorhexidine versus organoselenium for inhibition of S. mutans biofilm, an in vitro study. BMC Oral Health. 2022;22:14. doi: 10.1186/s12903-022-02049-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Davis C.D., Brooks L., Calisi C., Bennett B.J., McElroy D.M. Beneficial effect of selenium supplementation during murine infection with Trypanosoma cruzi. J. Parasitol. 1998;84:1274–1277. doi: 10.2307/3284689. [DOI] [PubMed] [Google Scholar]
- 68.Stuss M., Michalska-Kasiczak M., Sewerynek E. The role of selenium in thyroid gland pathophysiology. Endokrynol. Pol. 2017;68:440–465. doi: 10.5603/EP.2017.0051. [DOI] [PubMed] [Google Scholar]
- 69.Méplan C. Trace elements and ageing, a genomic perspective using selenium as an example. J. Trace Elem. Med. Biol. 2011;25((Suppl. 1)):S11–S16. doi: 10.1016/j.jtemb.2010.10.002. [DOI] [PubMed] [Google Scholar]
- 70.Shreenath A.P., Ameer M.A., Dooley J. Selenium Deficiency. StatPearls Publishing; Treasure Island, FL, USA: 2021. [Google Scholar]
- 71.Schomburg L. Selenium, selenoproteins and the thyroid gland: Interactions in health and disease. Nat. Rev. Endocrinol. 2011;8:160–171. doi: 10.1038/nrendo.2011.174. [DOI] [PubMed] [Google Scholar]
- 72.Gorini F., Sabatino L., Pingitore A., Vassalle C. Selenium: An Element of Life Essential for Thyroid Function. Molecules. 2021;26:7084. doi: 10.3390/molecules26237084. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Ambroziak U., Hybsier S., Shahnazaryan U., Krasnodebska-Kiljanska M., Rijntjes E., Bartoszewicz Z., Bednarczuk T., Schomburg L. Severe selenium deficits in pregnant women irrespective of autoimmune thyroid disease in an area with marginal selenium intake. J. Trace Elem. Med. Biol. 2017;44:186–191. doi: 10.1016/j.jtemb.2017.08.005. [DOI] [PubMed] [Google Scholar]
- 74.Minich W.B. Selenium Metabolism and Biosynthesis of Selenoproteins in the Human Body. Biochemistry. 2022;87((Suppl. 1)):S168–S177. doi: 10.1134/S0006297922140139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75.Köhrle J. Selenium and the thyroid. Curr. Opin. Endocrinol. Diabetes Obes. 2013;20:441–448. doi: 10.1097/01.med.0000433066.24541.88. [DOI] [PubMed] [Google Scholar]
- 76.Mistry H.D., Broughton Pipkin F., Redman C.W., Poston L. Selenium in reproductive health. Am. J. Obstet. Gynecol. 2012;206:21–30. doi: 10.1016/j.ajog.2011.07.034. [DOI] [PubMed] [Google Scholar]
- 77.Mojadadi A., Au A., Salah W., Witting P., Ahmad G. Role for Selenium in Metabolic Homeostasis and Human Reproduction. Nutrients. 2021;13:3256. doi: 10.3390/nu13093256. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Ujiie S., Kikuchi H. The Relation between Serum Selenium Value and Cancer in Miyagi, Japan: 5-Year Follow up Study. Tohoku J. Exp. Med. 2002;196:99–109. doi: 10.1620/tjem.196.99. [DOI] [PubMed] [Google Scholar]
- 79.Varlamova E., Turovsky E., Blinova E. Therapeutic Potential and Main Methods of Obtaining Selenium Nanoparticles. Int. J. Mol. Sci. 2021;22:10808. doi: 10.3390/ijms221910808. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Radomska D., Czarnomysy R., Radomski D., Bielawska A., Bielawski K. Selenium as a Bioactive Micronutrient in the Human Diet and Its Cancer Chemopreventive Activity. Nutrients. 2021;13:1649. doi: 10.3390/nu13051649. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Varlamova E., Turovsky E. The main cytotoxic effects of methylseleninic acid on various cancer cells. Int. J. Mol. Sci. 2021;22:6614. doi: 10.3390/ijms22126614. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Cairns R.A., Harris I.S., Mak T.W. Regulation of cancer cell metabolism. Nat. Rev. Cancer. 2011;11:85–95. doi: 10.1038/nrc2981. [DOI] [PubMed] [Google Scholar]
- 83.Weekley C., Harris H. Which form is that? The importance of selenium speciation and metabolism in the prevention and treatment of disease. Chem. Soc. Rev. 2013;42:8870–8894. doi: 10.1039/c3cs60272a. [DOI] [PubMed] [Google Scholar]
- 84.Wang H., He Y., Liu L., Tao W., Sun W., Pei X., Xiao Z., Jin Y., Wang M. Prooxidation and Cytotoxicity of Selenium Nanoparticles at Nonlethal Level in Sprague-Dawley Rats and Buffalo Rat Liver Cells. Oxidative Med. Cell Longev. 2020;2020:7680276. doi: 10.1155/2020/7680276. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Lee K.H., Jeong D. Bimodal actions of selenium essential for antioxidant and toxic pro-oxidant activities: The selenium paradox (Review) Mol. Med. Rep. 2012;5:299–304. doi: 10.3892/mmr.2011.651. [DOI] [PubMed] [Google Scholar]
- 86.Daragó A., Klimczak M., Stragierowicz J., Jobczyk M., Kilanowicz A. Age-Related Changes in Zinc, Copper and Selenium Levels in the Human Prostate. Nutrients. 2021;13:1403. doi: 10.3390/nu13051403. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87.Luo H., Wang F., Bai Y., Chen T., Zheng W. Selenium nanoparticles inhibit the growth of HeLa and MDA-MB-231 cells through induction of S phase arrest. Colloids Surf. B. 2012;94:304–308. doi: 10.1016/j.colsurfb.2012.02.006. [DOI] [PubMed] [Google Scholar]
- 88.Chen Q., Lin L.S., Chen L., Lin J., Ding Y., Bao X.D., Wu J.F., Lin L.K., Yan L.J., Wang R., et al. Relationship between selenium and the risk for oral cancer: A case-control study. Zhonghua Liuxingbingxue Zazhi. 2019;40:810–814. doi: 10.3760/cma.j.issn.0254-6450.2019.07.015. [DOI] [PubMed] [Google Scholar]
- 89.Mampilly M.O., Ravindran N., Parambil M.S., Nilesh K., Jayagopalan P., Dhamali D. Assessment of Serum Selenium and Ceruloplasmin in Potentially Malignant Disorders and Oral Cancer. J. Pharm. Bioallied Sci. 2021;13:S989–S992. doi: 10.4103/jpbs.jpbs_380_21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Bleys J., Navas-Acien A., Stranges S., Menke A., Miller E.R., Guallar E. Serum selenium and serum lipids in US adults. Am. J. Clin. Nutr. 2008;88:416–423. doi: 10.1093/ajcn/88.2.416. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Kielczykowska M., Kocot J., Pazdzior M., Musik I. Selenium—A fascinating antioxidant of protective properties. Adv. Clin. Exp. Med. 2018;27:245–255. doi: 10.17219/acem/67222. [DOI] [PubMed] [Google Scholar]
- 92.Limaye A., Yu R.C., Chou C.C., Liu J.R., Cheng K.C. Protective and Detoxifying Effects Conferred by Dietary Selenium and Curcumin against AFB1-Mediated Toxicity in Livestock: A Review. Toxins. 2018;10:25. doi: 10.3390/toxins10010025. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 93.Bjørklund G. Selenium as an antidote in the treatment of mercury intoxication. Biometals. 2015;28:605–614. doi: 10.1007/s10534-015-9857-5. [DOI] [PubMed] [Google Scholar]
- 94.Bjørklund G., Rahaman M.S., Shanaida M., Lysiuk R., Oliynyk P., Lenchyk L., Chirumbolo S., Chasapis C.T., Peana M. Natural Dietary Compounds in the Treatment of Arsenic Toxicity. Molecules. 2022;27:4871. doi: 10.3390/molecules27154871. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.McCann J.C., Ames B.N. Adaptive dysfunction of selenoproteins from the perspective of the triage theory: Why modest selenium deficiency may increase risk of diseases of aging. FASEB J. 2011;25:1793–1814. doi: 10.1096/fj.11-180885. [DOI] [PubMed] [Google Scholar]
- 96.Robberecht H., De Bruyne T., Davioud-Charvet E., Mackrill J., Hermans N. Selenium Status in Elderly People: Longevity and Age-Related Diseases. Curr. Pharm. Des. 2019;25:1694–1706. doi: 10.2174/1381612825666190701144709. [DOI] [PubMed] [Google Scholar]
- 97.Jiang X.R., Macey M.G., Lin H.X., Newland A.C. The anti-leukaemic effects and the mechanism of sodium selenite. Leuk. Res. 1992;16:347–352. doi: 10.1016/0145-2126(92)90136-U. [DOI] [PubMed] [Google Scholar]
- 98.Kondrat’eva A.V., Kovan’ko E.G., Liutinskiĭ S.I., Ivanov S.D. Effect of selenium on reactions of elderly rats affected by low doses of radiochemical exposures. Adv. Gerontol. 2004;15:91–95. [PubMed] [Google Scholar]
- 99.Martin-Romero F.J., Kryukov G.V., Lobanov A.V., Carlson B.A., Lee B.J., Gladyshev V.N., Hatfield D.L. Selenium metabolism in Drosophila: Selenoproteins, selenoprotein mRNA expression, fertility, and mortality. J. Biol. Chem. 2001;276:29798–29804. doi: 10.1074/jbc.M100422200. [DOI] [PubMed] [Google Scholar]
- 100.Zhang X., Wang X., Bai L., Li Z. Effects of sodium selenite on the activity of GSH-Px and the life-span of Drosophila. Wei Sheng Yan Jiu. 2000;29:166–167. [PubMed] [Google Scholar]
- 101.Steinbrenner H., Klotz L.O. Selenium and zinc: “antioxidants” for healthy aging? Z. Gerontol. Geriatr. 2020;53:295–302. doi: 10.1007/s00391-020-01735-0. [DOI] [PubMed] [Google Scholar]
- 102.Solovyev N., Drobyshev E., Bjørklund G., Dubrovskii Y., Lysiuk R., Rayman M.P. Selenium, selenoprotein P, and Alzheimer’s disease: Is there a link? Free Radic. Biol. Med. 2018;127:124–133. doi: 10.1016/j.freeradbiomed.2018.02.030. [DOI] [PubMed] [Google Scholar]
- 103.Wei K., Guo C., Zhu J., Wei Y., Wu M., Huang X., Zhang M., Li J., Wang X., Wang Y., et al. The Whitening, Moisturizing, Anti-aging Activities, and Skincare Evaluation of Selenium-Enriched Mung Bean Fermentation Broth. Front. Nutr. 2022;9:837168. doi: 10.3389/fnut.2022.837168. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 104.Jackson M.L. Selenium: Geochemical distribution and associations with human heart and cancer death rates and longevity in China and the United States. Biol. Trace Elem. Res. 1988;15:13–21. doi: 10.1007/BF02990124. [DOI] [PubMed] [Google Scholar]
- 105.Beck J., Ferrucci L., Sun K., Walston J., Fried L.P., Varadhan R., Guralnik J.M., Semba R.D. Low serum selenium concentrations are associated with poor grip strength among older women living in the community. Biofactors. 2007;29:37–44. doi: 10.1002/biof.5520290104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 106.Ray A.L., Semba R.D., Walston J., Ferrucci L., Cappola A.R., Ricks M.O., Xue Q.L., Fried L.P. Low serum selenium and total carotenoids predict mortality among older women living in the community: The women’s health and aging studies. J. Nutr. 2006;136:172–176. doi: 10.1093/jn/136.1.172. [DOI] [PubMed] [Google Scholar]
- 107.Al-Mubarak A.A., van der Meer P., Bomer N. Selenium, Selenoproteins, and Heart Failure: Current Knowledge and Future Perspective. Curr. Heart Fail. Rep. 2021;18:122–131. doi: 10.1007/s11897-021-00511-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 108.Hao Z., Liu Y., Li Y., Song W., Yu J., Li H., Wang W. Association between Longevity and Element Levels in Food and Drinking Water of Typical Chinese Longevity Area. J. Nutr. Health Aging. 2016;20:897–903. doi: 10.1007/s12603-016-0690-5. [DOI] [PubMed] [Google Scholar]
- 109.Huang Y., Rosenberg M., Hou L., Hu M. Relationships among Environment, Climate, and Longevity in China. Int. J. Environ. Res. Public Health. 2017;14:1195. doi: 10.3390/ijerph14101195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Lv J., Wang W., Krafft T., Li Y., Zhang F., Yuan F. Effects of several environmental factors on longevity and health of the human population of Zhongxiang, Hubei, China. Biol. Trace Elem. Res. 2011;143:702–716. doi: 10.1007/s12011-010-8914-8. [DOI] [PubMed] [Google Scholar]
- 111.Shi X.M., Yin Z.X., Qian H.Z., Zhai Y., Liu Y.Z., Xu J.W., Zeng Y. A study on chronic diseases and other related health indicators of centenarians in longevity areas in China. Zhonghua Yu Fang Yi Xue Za Zhi. 2010;44:101–107. [PubMed] [Google Scholar]
- 112.Foster H.D., Zhang L. Longevity and selenium deficiency: Evidence from the People’s Republic of China. Sci. Total Environ. 1995;170:133–139. doi: 10.1016/0048-9697(95)04626-C. [DOI] [PubMed] [Google Scholar]
- 113.Huang Y., He L., Liu W., Fan C., Zheng W., Wong Y.S., Chen T. Selective cellular uptake and induction of apoptosis of cancer-targeted selenium nanoparticles. Biomaterials. 2013;34:7106–7116. doi: 10.1016/j.biomaterials.2013.04.067. [DOI] [PubMed] [Google Scholar]
- 114.Forte G., Deiana M., Pasella S., Baralla A., Occhineri P., Mura I., Madeddu R., Muresu E., Sotgia S., Zinellu A., et al. Metals in plasma of nonagenarians and centenarians living in a key area of longevity. Exp. Gerontol. 2014;60:197–206. doi: 10.1016/j.exger.2014.10.016. [DOI] [PubMed] [Google Scholar]
- 115.Ye M., Li J., Yu R., Cong X., Huang D., Li Y., Chen S., Zhu S. Selenium Speciation in Selenium-Enriched Plant Foods. Food Anal. Methods. 2022;15:1377–1389. doi: 10.1007/s12161-021-02208-9. [DOI] [Google Scholar]
- 116.Lei X.G., Combs G.F., Sunde R.A., Caton J.S., Arthington J.D., Vatamaniuk M.Z. Dietary Selenium Across Species. Annu. Rev. Nutr. 2022;42:337–375. doi: 10.1146/annurev-nutr-062320-121834. [DOI] [PubMed] [Google Scholar]
- 117.Finley J.W. Selenium accumulation in plant foods. Pt 1Nutr. Rev. 2005;63:196–202. doi: 10.1111/j.1753-4887.2005.tb00137.x. [DOI] [PubMed] [Google Scholar]
- 118.Navarro-Alarcon M., Cabrera-Vique C. Selenium in food and the human body: A review. Sci. Total Environ. 2008;400:115–141. doi: 10.1016/j.scitotenv.2008.06.024. [DOI] [PubMed] [Google Scholar]
- 119.Finley J.W. Reduction of cancer risk by consumption of selenium-enriched plants: Enrichment of broccoli with selenium increases the anticarcinogenic properties of broccoli. J. Med. Food. 2003;6:19–26. doi: 10.1089/109662003765184714. [DOI] [PubMed] [Google Scholar]
- 120.Bentley-Hewitt K.L., Chen R.K., Lill R.E., Hedderley D.I., Herath T.D., Matich A.J., McKenzie M.J. Consumption of selenium-enriched broccoli increases cytokine production in human peripheral blood mononuclear cells stimulated ex vivo, a preliminary human intervention study. Mol. Nutr. Food Res. 2014;58:2350–2357. doi: 10.1002/mnfr.201400438. [DOI] [PubMed] [Google Scholar]
- 121.Goltyaev M., Mal’tseva V.N., Novoselov V.I., Varlamova E. Expression patterns of er-resident selenoproteins in er- stress conditions caused by methylseleninic acid in different human cancer cells. Gene. 2020;755:144884. doi: 10.1016/j.gene.2020.144884. [DOI] [PubMed] [Google Scholar]
- 122.Ulewicz-Magulska B., Wesolowski M. A chemometric approach to distribution of selenium in medicinal plants cultivated in poland. J. Med. Food. 2013;16:460–466. doi: 10.1089/jmf.2012.0191. [DOI] [PubMed] [Google Scholar]
- 123.Huang S., Yang W., Huang G. Preparation and activities of selenium polysaccharide from plant such as Grifola frondosa. Carbohydr. Polym. 2020;242:116409. doi: 10.1016/j.carbpol.2020.116409. [DOI] [PubMed] [Google Scholar]
- 124.Fordyce F. Selenium Deficiency and Toxicity in the Environment. Elsevier—Academic Press; London, UK: 2005. pp. 373–415. [Google Scholar]
- 125.Zhang X., He H., Xiang J., Yin H., Hou T. Selenium-Containing Proteins/Peptides from Plants: A Review on the Structures and Functions. J. Agric. Food Chem. 2020;68:15061–15073. doi: 10.1021/acs.jafc.0c05594. [DOI] [PubMed] [Google Scholar]
- 126.Diowksz A., Pęczkowska B., Wŀodarczyk M., Ambroziak W. Bacteria/Yeast and Plant Biomass Enriched in Se via Bioconversion Process as a Source of Se Supplementation in Food. In: Bielecki S., Tramper J., Polak J., editors. Progress in Biotechnology. Volume 17. Elsevier; Amsterdam, The Netherlands: 2000. pp. 295–300. [DOI] [Google Scholar]
- 127.Arnault I., Auger J. Seleno-compounds in garlic and onion. J. Chromatogr. A. 2006;1112:23–30. doi: 10.1016/j.chroma.2006.01.036. [DOI] [PubMed] [Google Scholar]
- 128.Schrauzer G.N. Selenium yeast: Composition, quality, analysis, and safety. Pure Appl. Chem. 2006;78:105–109. doi: 10.1351/pac200678010105. [DOI] [Google Scholar]
- 129.Hosnedlova B., Kepinska M., Skalickova S., Fernandez C., Ruttkay-Nedecky B., Peng Q., Baron M., Melcova M., Opatrilova R., Zidkova J., et al. Nano-selenium and its nanomedicine applications: A critical review. Int. J. Nanomed. 2018;13:2107–2128. doi: 10.2147/IJN.S157541. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130.Chen N., Yao P., Zhang W., Zhang Y., Xin N., Wei H., Zhang T., Zhao C. Selenium nanoparticles: Enhanced nutrition and beyond. Crit. Rev. Food Sci. Nutr. 2022:1–12. doi: 10.1080/10408398.2022.2101093. [DOI] [PubMed] [Google Scholar]
- 131.Alhasan R., Kharma A., Leroy P., Jacob C., Gaucher C. Selenium Donors at the Junction of Inflammatory Diseases. Curr. Pharm. Des. 2019;25:1707–1716. doi: 10.2174/1381612825666190701153903. [DOI] [PubMed] [Google Scholar]
- 132.Khurana A., Tekula S., Saifi M.A., Venkatesh P., Godugu C. Therapeutic applications of selenium nanoparticles. Biomed. Pharmacother. 2019;111:802–812. doi: 10.1016/j.biopha.2018.12.146. [DOI] [PubMed] [Google Scholar]
- 133.Guan B., Yan R., Li R., Zhang X. Selenium as a pleiotropic agent for medical discovery and drug delivery. Int. J. Nanomed. 2018;13:7473–7490. doi: 10.2147/IJN.S181343. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 134.Bai K., Hong B., Hong Z., Sun J., Wang C. Selenium nanoparticles-loaded chitosan/citrate complex and its protection against oxidative stress in D-galactose-induced aging mice. J. Nanobiotechnol. 2017;15:92. doi: 10.1186/s12951-017-0324-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 135.Mamgain R., Kostic M., Singh F.V. Synthesis and Antioxidant Properties of Organoselenium Compounds. Curr. Med. Chem. 2022;29 doi: 10.2174/0929867329666220801165849. [DOI] [PubMed] [Google Scholar]
- 136.Sarkar B., Bhattacharjee S., Daware A., Tribedi P., Krishnani K.K., Minhas P.S. Selenium Nanoparticles for Stress-Resilient Fish and Livestock. Nanoscale Res. Lett. 2015;10:371. doi: 10.1186/s11671-015-1073-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 137.El-Kazaz S.E., Abo-Samaha M.I., Hafez M.H., El-Shobokshy S.A., Wirtu G. Dietary supplementation of nano-selenium improves reproductive performance, sexual behavior and deposition of selenium in the testis and ovary of Japanese quail. J. Adv. Vet. Anim. Res. 2020;7:597–607. doi: 10.5455/javar.2020.g457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 138.Kumar G.S., Kulkarni A., Khurana A., Kaur J., Tikoo K. Selenium nanoparticles involve HSP-70 and SIRT1 in preventing the progression of type 1 diabetic nephropathy. Chem. Biol. Interact. 2014;223:125–133. doi: 10.1016/j.cbi.2014.09.017. [DOI] [PubMed] [Google Scholar]
- 139.Du P.C., Tu Z.C., Wang H., Hu Y.M. Mechanism of Selenium Nanoparticles Inhibiting Advanced Glycation End Products. J. Agric. Food Chem. 2020;68:10586–10595. doi: 10.1021/acs.jafc.0c03229. [DOI] [PubMed] [Google Scholar]
- 140.Al-Otaibi A.M., Al-Gebaly A.S., Almeer R., Albasher G., Al-Qahtani W.S., Abdel Moneim A.E. Potential of green-synthesized selenium nanoparticles using apigenin in human breast cancer MCF-7 cells. Environ. Sci. Pollut. Res. Int. 2022;29:47539–47548. doi: 10.1007/s11356-022-19166-2. [DOI] [PubMed] [Google Scholar]
- 141.Nath D., Kaur L., Sohal H.S., Malhi D.S., Garg S., Thakur D. Application of Selenium Nanoparticles in Localized Drug Targeting for Cancer Therapy. Anticancer Agents Med. Chem. 2022;22:2715–2725. doi: 10.2174/1871520622666220215122756. [DOI] [PubMed] [Google Scholar]
- 142.Wang X., Xu T.T. Elemental Selenium at Nano Size (Nano-Se) as a Potential Chemopreventive Agent with Reduced Risk of Selenium Toxicity: Comparison with Se-Methylselenocysteine in Mice. Toxicol. Sci. 2008;101:22–31. doi: 10.1093/toxsci/kfm221. [DOI] [PubMed] [Google Scholar]
- 143.Turovsky E.A., Varlamova E.G. Mechanism of Ca2+-Dependent Pro-Apoptotic Action of Selenium Nanoparticles, Mediated by Activation of Cx43 Hemichannels. Biology. 2021;10:743. doi: 10.3390/biology10080743. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 144.Vahidi H., Barabadi H., Muthupandian S. Emerging Selenium Nanoparticles to Combat Cancer: A Systematic Review. J. Clust. Sci. 2020;31:301–309. doi: 10.1007/s10876-019-01671-z. [DOI] [Google Scholar]
- 145.Thavarajah D., Vandenberg A., George G., Pickering I. Chemical Form of Selenium in Naturally Selenium-Rich Lentils (Lens culinaris L.) from Saskatchewan. J. Agric. Food Chem. 2007;55:7337–7341. doi: 10.1021/jf070681i. [DOI] [PubMed] [Google Scholar]
- 146.Ranjit M., Dash K., Dheram K. UV-photolysis assisted digestion of food samples for the determination of selenium by electrothermal atomic absorption spectrometry (ETAAS) Food Chem. 2007;105:260–265. doi: 10.1016/j.foodchem.2006.11.011. [DOI] [Google Scholar]
- 147.Gilbert-Lopez B., Dernovics M., Moreno-Gonzalez D., Molina-Diaz A., Garcia-Reyes J.F. Detection of over 100 selenium metabolites in selenized yeast by liquid chromatography electrospray time-of-flight mass spectrometry. J. Chromatogr. B Anal. Technol. Biomed. Life Sci. 2017;1060:84–90. doi: 10.1016/j.jchromb.2017.06.001. [DOI] [PubMed] [Google Scholar]
- 148.Rievaj M., Culková E., Šandorová D., Lukáčová-Chomisteková Z., Bellová R., Durdiak J., Tomčík P. Electroanalytical Techniques for the Detection of Selenium as a Biologically and Environmentally Significant Analyte—A Short Review. Molecules. 2021;26:1768. doi: 10.3390/molecules26061768. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 149.Otilia B., Nartiță R., Rogobete A., Negrea A., Stroescu R., Teofana-Otilia B., Ilie C., Marginean O. Spectrophotometric Determination of Selenium Through Triiodide Anion. Clin. Lab. 2017;63:887–899. doi: 10.7754/Clin.Lab.2016.160905. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Not applicable.