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1.
Chinese Journal of Biotechnology ; (12): 4756-4764, 2022.
Article in Chinese | WPRIM | ID: wpr-970346

ABSTRACT

Selenium (Se) is an essential trace element for organisms. Se deficiency will cause diseases such as Keshan disease and Kashin-Beck in human being, and huge loss to animal husbandry. Currently available Se supplements have such problems as low Se content, poor bioavailability, and poor safety. Chlorella pyrenoidosa can produce bioavailable and safe organic Se under suitable conditions, which is thus a promising Se supplement. Therefore, in this study, we tried to improve the Se tolerance and accumulation of C. pyrenoidosa by directional adaptation. To be specific, we gradually increased the concentration of Na2SeO3 in medium to domesticate C. pyrenoidosa and optimized the adapting time and concentration gradient of Na2SeO3 during the adaptation. The results showed that the adapted C. pyrenoidosa was more tolerant to Se and had stronger Se enrichment ability. In 5 L fermenter, the adapted strains could tolerate 40 mg/L Na2SeO3 and the synthesis rate of organic Se was 175.6% higher. Then, Se addition method in the 5 L fermenter was optimized. The result demonstrated that addition of Na2SeO3 at 40 mg/L during heterotrophic culture achieved the final dry weight of C. pyrenoidosa cells at 106.4 g/L, content of organic Se at 1 227 mg/kg, and synthesis rate of organic Se at 1.36 mg/(L·h). Compared with the reported highest cell density of 75 g/L and the highest organic Se content of 560 mg/kg, the corresponding figures in this study were 41.9% and 119.1% higher, respectively. In conclusion, directional adaptation can remarkably improve the Se tolerance and enrichment of C. pyrenoidosa.


Subject(s)
Animals , Humans , Selenium/pharmacology , Chlorella , Heterotrophic Processes
2.
J. appl. oral sci ; 29: e20200414, 2021. tab, graf
Article in English | LILACS | ID: biblio-1154614

ABSTRACT

Abstract Objective The exposure to mercury (Hg) from dental amalgams is a suspected causative factor in neurological diseases. This study investigated the toxic effects of two different amalgam compositions related to Hg and the protective effects of selenium against the toxic effects of Hg through the TRPV1 channel in the human DBTRG glioblastoma cell line. Methodology Six groups of the cells were organized. Analyses of cell viability, apoptosis, caspase 3 and caspase 9 activities, mitochondrial membrane depolarization, reactive oxygen species (ROS) production, and Western Blotting for protein expression levels were performed. Results Cell viability values were lower in amalgam with high copper (HCu) and low copper (LCu) groups independently of time but were increased by selenium and capsazepine (p<0.001 and p<0.05). Conversely, apoptosis rates, caspase 3 and caspase 9 expression, ROS formation, mitochondrial membrane depolarization, and protein expression levels were higher in the HCu and LCu groups but were decreased by selenium (p<0.001 and p<0.05). Conclusions Selenium combined with an amalgam of either HCu or LCu decreases the toxic effects created by Hg in human DBTRG glioblastoma cells.


Subject(s)
Humans , Selenium/pharmacology , Glioblastoma , Cell Survival , Oxidative Stress , Dental Amalgam , TRPV Cation Channels
3.
Int. j. morphol ; 38(6): 1786-1796, Dec. 2020. graf
Article in English | LILACS | ID: biblio-1134512

ABSTRACT

SUMMARY: Bisphenol A (BPA) is an industrial chemical widely used to make polycarbonate plastics for packaging and epoxy resins. This study sought to examine how selenium (Se) affects BPA toxicity in terms of albino rats' histological structure, antioxidant enzymes and reproductive organs (seminiferous tubules). Twenty-four adult male rats were divided into four experimental groups: Group 1: Control; Group 2: Orally administered BPA; Group 3: Orally administered sodium selenite; Group 4: Treated daily with BPA followed by selenium (Se). All experiment done for 4 weeks. BPA exposure caused changes in the testicular histological structure, which consists apoptosis, and led to changes in several biochemical markers: Malondialdehyde, catalase, superoxide dismutase, and glutathione peroxidase. However, these BPA side effects may be ameliorated in rats treated with BPA-plus-Se. These protective effects of Se may attributable to its ability to remove potentially damaging oxidizing agents in living organisms. The results may confirm that Se countered the oxidant effects and increased the BPA-induced stress response in rats. So, Se promotes the healthy growth and development of mammals by protecting them from oxidative stress. As human are greatly exposed to BPA and it can accumulate in tissues, there is concern about human reproductive functions particularly for occupational workers exposed usually to greater levels of BPA. Thus, the use of BPA in multiple industries must be restricted and the inaccurate usage of plastic containers should be avoided to decrease the health hazards. Administration of Se may protect against the adverse effects of BPA on reproductive functions and structures.


RESUMEN: El bisfenol A (BPA) es un químico industrial ampliamente utilizado para fabricar plásticos de policarbonato para envases y resinas epoxi. Este estudio examinó el efecto de selenio (Se) en la toxicidad del BPA en términos de la estructura histológica, enzimas antioxidantes y los órganos reproductivos (túbulos seminíferos) de ratas albinas. Se dividieron veinticuatro ratas macho adultas en cuatro grupos experimentales: Grupo 1: control; Grupo 2: BPA administrado por vía oral; Grupo 3: BPA administrado por vía oral para; Grupo 4: tratado diariamente con BPA seguido de selenio (Se). El experimento se realizó durante cuatro semanas y se observó que la exposición al BPA provocó cambios en la estructura histológica testicular, incluyendo apoptosis, y alteraciones en varios marcadores bioquímicos:malondialdehído, catalasa, superóxido dismutasa y glutatión peroxidasa. Sin embargo, estos efectos secundarios del BPA pueden mejorar en ratas tratadas con BPA-plus-Se. Estos efectos protectores del Se pueden ser atribuidos a la capacidad de eliminar agentes oxidantes potencialmente dañinos en organismos vivos. Los resultados indicaron que se contrarrestaron los efectos oxidantes y aumentó la respuesta al estrés inducido por BPA en ratas, y favorece el crecimiento y desarrollo en los mamíferos al protegerlos del estrés oxidativo. Debido a la exposición al BPA en el ser humano, se puede acumular en los tejidos, por lo que existe una preocupación por el daño a las funciones reproductivas en particular de los trabajadores que generalmente están expuestos a niveles más altos de BPA. Por lo tanto, se debe restringir el uso de BPA en las industrias y evitar el uso incorrecto de envases de plástico para así disminuir los riesgos para la salud. La administración correcta de Se puede proteger contra los efectos adversos del BPA en las funciones y estructuras reproductivas.


Subject(s)
Animals , Male , Rats , Phenols/toxicity , Selenium/pharmacology , Testis/drug effects , Benzhydryl Compounds/toxicity , Antioxidants/pharmacology , Phenols/administration & dosage , Superoxide Dismutase/drug effects , Testis/pathology , Benzhydryl Compounds/administration & dosage , Microscopy, Electron , Biomarkers , Catalase/drug effects , Administration, Oral , Apoptosis/drug effects , Oxidative Stress , Glutathione Peroxidase/drug effects
4.
Braz. oral res. (Online) ; 32: e103, 2018. tab, graf
Article in English | LILACS | ID: biblio-974462

ABSTRACT

Abstract The aim of this study is to evaluate the expression of cytokines in response to mineral trioxide aggregate (MTA) plus selenium in germ-free mice with experimental furcal perforation. The first left maxillary molar was opened, and the furcal area was perforated and treated with post-MTA-Se (experimental group). The same surgical intervention was performed for the maxillary right first molar, which was treated with MTA (control group). Fifteen mice were sacrificed 7, 14, and 21 days after furcal perforation, and periapical tissue samples were collected. The mRNA expression levels of the cytokines TGF-β, TNF-α, IFN-γ, HPRT, IL-10, IL-4, RANK, RANKL, IL-1, and IL-17 were assessed by using real-time polymerase chain reaction. In the experimental group, at 21-days post-MTA-Se sealing, the mRNA levels of TNF-α and IL-10 were upregulated compared with those in the control group (p < 0.05). Futher assessment revealed basal mRNA expression levels of IL-1α, IFN-γ, RANK, RANKL, IL-17A, IL-4, and TGF-β, over long experimental times, in both the experimental and control groups (p > 0.05). In conclusion, MTA+Se sealing favoured increased expression of IL-10 and TNF-α at later time points (day 21).


Subject(s)
Animals , Male , Female , Oxides/pharmacology , Root Canal Filling Materials/pharmacology , Selenium/pharmacology , Cytokines/analysis , Silicates/pharmacology , Furcation Defects/drug therapy , Calcium Compounds/pharmacology , Aluminum Compounds/pharmacology , Dental Pulp Cavity/injuries , Root Canal Therapy/methods , Time Factors , Reproducibility of Results , Treatment Outcome , Furcation Defects/immunology , Dental Pulp Cavity/drug effects , Dental Pulp Cavity/immunology , Drug Combinations , Real-Time Polymerase Chain Reaction , Molar/drug effects , Molar/injuries
5.
São Paulo; s.n; s.n; 2018. 127 p. tab, ilus, graf.
Thesis in Portuguese | LILACS | ID: biblio-913414

ABSTRACT

A inflamação e o estresse oxidativo são processos que ocorrem simultaneamente na obesidade e contribuem para o aumento da síntese de mediadores inflamatórios e de espécies reativas de oxigênio e nitrogênio. O mineral selênio (Se), cuja principal fonte alimentar é a castanha-do-brasil, possui propriedades antioxidantes e anti-inflamatórias. Considerando a importância do processo inflamatório na obesidade e o potencial papel do Se como anti-inflamatório por meio da atuação de selenoproteínas, o estudo da influência deste micronutriente neste contexto é de grande relevância. Desse modo, o objetivo deste estudo foi avaliar o efeito do consumo da castanha-do-brasil sobre os biomarcadores inflamatórios e o estado nutricional relativo ao Se de mulheres obesas. No total, foram recrutadas 72 participantes alocadas randomicamente no grupo que consumiu a castanha-dobrasil (BN) ou no grupo controle (CO) e, acompanhadas por um período de 2 meses. O grupo BN consumiu 1 unidade de castanha-do-brasil (~409,5 µg/Se) por dia e o grupo CO não recebeu nenhum tipo de intervenção. Antes e após o período da intervenção, foram realizadas as avaliações antropométrica e do consumo alimentar, e dos parâmetros bioquímicos relacionados ao Se, estresse oxidativo, perfil lipídico e biomarcadores inflamatórios. Completaram o estudo 29 participantes do grupo BN e 26 do grupo CO com idade média de 40,3 (9,0) e 39,4 (9,5) anos (p=0,714), respectivamente. No baseline do estudo, observou-se que a população estudada não apresentava deficiência de Se. No grupo BN, verificou-se um aumento de todos biomarcadores de Se avaliados. Após 8 semanas de intervenção, um aumento significativo foi observado na expressão gênica de diversos parâmetros pró-inflamatórios no grupo BN (IL-6, TNF-α, TLR2 e TLR4). Apesar de não ter havido mudanças nas concentrações plasmáticas referentes a estes parâmetros, o aumento significativo da expressão gênica pode ser um indicativo de estímulo pró-inflamatório induzido pelo consumo da castanha-do-brasil com altas concentrações de Se


Inflammation and oxidative stress are processes that occur simultaneously in obesity and contribute to an increase in the synthesis of inflammatory mediators and reactive oxygen and nitrogen species. The mineral selenium (Se), whose main food source is the Brazil nut, has antioxidant and anti-inflammatory properties. Considering the importance of the inflammatory process in obesity and the potential role of Se as an anti-inflammatory by means of selenoproteins, the study of the influence of this micronutrient in this context is of great relevance. Thus, the aim of this study was to evaluate the effect of Brazil nut intake on inflammatory biomarkers and nutritional status of Se in obese women. In total, 72 participants randomly assigned to Brazil nut group (BN) or control group (CO) were recruited and followed up for 2 months. The BN group consumed 1 unit of Brazil nut (~ 409.5 µg/Se) per day and the CO group did not received any intervention. On baseline and after two months of follow-up, the evaluation of anthropometry and food consumption, and of the biochemical parameters related to Se, oxidative stress, lipid profile and inflammatory biomarkers were performed. Twenty-nine participants of BN group and twenty-six of the CO group completed the trial, with a mean age of 40.3 (9.0) and 39.4 (9.5) years (p= 0.714), respectively. At the baseline of the study, it was observed that this population did not present Se deficiency. In BN group, there was an increase in all Se biomarkers evaluated. After 8 weeks of intervention, a significant increase was observed in gene expression of several pro-inflammatory parameters in BN group (IL-6, TNF-α, TLR2 and TLR4). Although there have been no changes in plasma concentrations related to these parameters, a significant increase in gene expression may be an indicative of a pro-inflammatory stimulus induced by the intake of Brazil nuts with high Se concentrations


Subject(s)
Humans , Female , Middle Aged , Selenium/pharmacology , Bertholletia/adverse effects , Obesity/complications , Nutritional Status , Oxidative Stress , Inflammation/classification
6.
An. acad. bras. ciênc ; 89(1,supl): 457-467, May. 2017. graf
Article in English | LILACS | ID: biblio-886663

ABSTRACT

ABSTRACT The present study investigated the antioxidant effect of a new class of quinoline derivatives (a-d) on assays in vitro. Lipid peroxidation, thiol peroxidase-like and free radical scavenging activities were determined to evaluate antioxidant activity of compounds. Thiol oxidase-like and δ-aminolevulinate dehydratase activities were performed as a toxicological parameter. A second objective of this study was to evaluate the in vivo antinociceptive effect of the compound with better antioxidant effect and without toxic effects in a model of nociception induced by formalin in mice. In liver, at 100 µM, compound a reduced the lipid peroxidation to the control levels, while compounds c and d partially reduced it. In brain, only compound d partially reduced the lipid peroxidation at 50 and 100 µM. Compound b did not have an effect on the lipid peroxidation. Thiol peroxidase-like and free radical scavenging activities are not involved in the antioxidant mechanisms of these compounds. Compounds did not present thiol oxidase-like activity and effect on the δ-aminolevulinate dehydratase. In vivo experiments showed that compound a caused an inhibition of licking time in the first and second phases, and edema formation induced by formalin. In conclusion, quinoline derivative without selenium presented better in vitro antioxidant effect and in vivo antinociceptive activity.


Subject(s)
Animals , Male , Rats , Quinolines/pharmacology , Selenium/pharmacology , Oxidative Stress/drug effects , Analgesics/pharmacology , Antioxidants/pharmacology , Oxidation-Reduction , Quinolines/chemistry , Pain Measurement , Free Radical Scavengers , Disease Models, Animal , Oxidoreductases Acting on Sulfur Group Donors/pharmacology , Porphobilinogen Synthase/pharmacology
7.
IJEM-Iranian Journal of Endocrinology and Metabolism. 2017; 19 (2): 116-125
in Persian | IMEMR | ID: emr-189250

ABSTRACT

Introduction: The liver is known as a tissue highly sensitive to immunological changes such as cytokines activity. It has been shown that using selenium nanoparticle supplementation and exercise training separately can effectively decrease tumor volume and improve immune responses. The aim of this study was to examine the effects of aerobic interval training and supplementation of selenium nanoparticles on protein expression of cytokines in liver tissue in mice with breast cancer


Materials and Methods: Sixty-four Balbc mice were divided into eight groups. Experimental groups received aerobic interval training and selenium nanoparticles supplementation orally for 6 weeks, before and after cancer induction. At the end of the sixth week, after tumor injection, proteins levels of IL-6, IL-4, TNF-alpha and INF-gamma were measured in liver tissue by the enzyme-linked immunosorbent assay [ELISA] method


Results: Results of the current study showed that IL-6, TNF-alpha and IL-4 protein levels decreased in liver tissue of the breast cancer tumor [P<0.05]. Aerobic interval training caused significant increase in IL-6 and TNF-alpha protein levels in liver tissue [P<0.05]. Increase in INF-gamma cytokine levels in liver tissue was also observed, following selenium nanoparticle supplementation [P<0.05]. Results also showed that tumor volume decreased following exercise training and administration of selenium nanoparticles administration


Conclusion: Cytokines changes in liver tissue occurred in conjunction with decrease in tumor volume. It is possible that simultaneously using selenium nanoparticles and exercise training with immune system reinforcement could help in reducing tumor volume and modulating cytokine levels in liver


Subject(s)
Animals, Laboratory , Selenium/pharmacology , Nanoparticles , Cytokines , Liver , Breast Neoplasms , Mice , Mice, Inbred BALB C
8.
Acta cir. bras ; 30(6): 394-400, 06/2015. tab, graf
Article in English | LILACS | ID: lil-749642

ABSTRACT

PURPOSE: To evaluate the central nervous system toxicity of cisplatin and neuroprotective effect of selenium. METHODS: Twenty-one male Wistar albino rats were divided into three groups: control (C), cisplatin (CS), cisplatin and selenium (CSE, n=7 in each group). Cisplatin (12 mg/kg/day, i.p.) was administered to CS and CSE groups for three days. Furthermore, CSE group received 3mg/kg/day (twice-a-day as 1.5 mg/kg) selenium via oral gavage five days before cisplatin injection and continued for 11 consecutive days. The same volumes of saline were administered to C group intraperitoneally and orally at same time. RESULTS: Heterochromatic and vacuolated neurons and dilated capillary vessels in the brain were observed in the histochemical examinations of cisplatin treated group. Rats that were given a dose of 3mg/kg/day selenium decreased the cisplatin induced histopathological changes in the brain, indicating a protective effect. In addition, cytoplasmic staining of the cell for bcl-2, both cytoplasmic and nuclear staining for bax were determined to be positive in the all groups. Bax positive cells were increased in the CS group compared to C group, in contrast to decreased bcl-2 positivity. CONCLUSION: Selenium limited apototic activity and histological changes due to the cisplatin related central neurotoxicity. .


Subject(s)
Animals , Male , Antineoplastic Agents/toxicity , Antioxidants/pharmacology , Brain/drug effects , Cisplatin/toxicity , Neurons/drug effects , Selenium/pharmacology , Apoptosis/drug effects , Brain/pathology , Immunohistochemistry , Models, Animal , Neuroprotective Agents/pharmacology , Rats, Wistar , Reproducibility of Results , Time Factors
9.
Nutrire Rev. Soc. Bras. Aliment. Nutr ; 40(2): 237-245, 2015. ilus
Article in Portuguese | LILACS | ID: biblio-881947

ABSTRACT

OBJECTIVE: This review aims to bring updated information on the relationship between oxidative stress and the role of selenium as antioxidant nutrient in mechanisms involved in the pathogenesis of type 2 diabetes mellitus. Data source: The bibliographic survey was conducted in PubMed, SciELO and Lilacs, considering the 2002-2014 period, and included the following types of studies: randomized or quasi-randomized controlled trials, cohort, case-control study, case series and case report. Forty-nine pertinent scientific studies were selected. Data synthesis: Several studies have demonstrated the contribution of acute and/or chronic hyperglycemia to the manifestation of oxidative stress in type 2 diabetic patients. Accordingly, selenium has an important participation in controlling this disease due to its antioxidant role in the elimination of free radicals, present in excess, and because it blocks the activation of nuclear transcription factor kappa B, a regulator sensitive to oxidants that stimulates the production of inflammatory mediators (cytokines) and adhesion molecules. CONCLUSIONS: There is convincing experimental evidence demonstrating the involvement of selenium in glycemic control. However, current information is still scarce and inconsistent, and it is necessary to conduct further studies on the subject to determine the selenium intake safety range as well as clarify the influence of this mineral on the manifestation of type 2 diabetes mellitus and its associated disorders


OBJETIVO: Esta revisão visa trazer informações atualizadas sobre a relação entre o estresse oxidativo e o papel do selênio como nutriente antioxidante em mecanismos envolvidos na patogênese do diabetes mellitus tipo 2. Fonte de dados: O levantamento bibliográfico foi realizado nas bases de dados Pubmed, SciELO e Lilacs considerando o período de 2002 a 2014 e abrangeu os seguintes tipos de estudos: ensaios clínicos controlados randomizados ou quase-randomizados, coorte, estudo caso-controle, série de casos e relato de caso. Foram selecionados 49 que se relacionavam com esta pesquisa bibliográfica. Síntese dos dados: Várias pesquisas têm demonstrado a contribuição do estado hiperglicêmico agudo e/ou crônico na manifestação do estresse oxidativo em pacientes diabéticos tipo 2. Nesse sentido, o selênio possui participação importante no controle dessa doença, devido ao seu papel antioxidante na eliminação dos radicais livres, presentes em excesso, e por bloquear a ativação do fator de transcrição nuclear kappa B, um regulador sensível a oxidantes que estimula a produção de mediadores inflamatórios (citocinas) e de moléculas de adesão. CONCLUSÕES: Existem evidências experimentais convincentes que demonstram a participação do selênio no controle glicêmico. No entanto, as informações atuais ainda são bastante escassas e inconsistentes e faz-se necessária a realização de novos estudos sobre o tema a fim de determinar a faixa de segurança de ingestão de selênio, além de obter esclarecimentos acerca da influência do mineral sobre a manifestação do diabetes mellitus tipo 2 e das desordens a ele associadas


Subject(s)
Humans , Male , Female , Diabetes Mellitus, Type 2/diagnosis , Diabetes Mellitus, Type 2/metabolism , Oxidative Stress/physiology , Selenium/therapeutic use , Selenium/analysis , Selenium/pharmacology
10.
BCCR-Basic and Clinical Cancer Research. 2011; 3 (1): 14-22
in English | IMEMR | ID: emr-137510

ABSTRACT

The present study was performed to investigate the effects of trace elements particularity Se, Zn and Cu on tumor genesis in breast cancer. The inhibitory effect of Se, Zn and Cu, on telomerase activity was analyzed in human breast tumor tissues and breast cancer [T47D] cells. Tissue specimens from 24 women with benign breast disease and 32 women with breast cancer specimens [ductal carcinoma, lobular carcinoma] were collected during surgery. In addition venous blood samples were obtained for assessing the trace elements. T47D cell line was cultured and treated with trace elements. Telomerase activity then was measured with TRAP assay in cell line and tissue extracts. There was a significant difference between tissue and serum levels of Cu, Se and the ratio of Cu/Zn in patients and controls [P<0.001]. After treating with 100 microm/L Zn So4, 10 um /L Cu So4 for 6 hours, telomerase activity of T47D cells was markedly increased. But after treating with 10, and 30 um /L selenium-L- methionin, telomerase activity was markedly inhibited. Telomerase activity of T47D cells for 24 hours were 0.93, 0.60 and for 48 hours were 0.76, 0.12 respectively [control 49.2%]. There were variations in serum level of Zn and Cu in breast cancer patients. Association between trace elements level and telomerase activity level can be exploited as prognostic and diagnostic marker for breast cancer


Subject(s)
Humans , Female , Breast Neoplasms/enzymology , Telomerase/genetics , Selenium/pharmacology , Zinc/pharmacology , Copper/pharmacology , Cell Line , Tissue Extracts , Tumor Cells, Cultured , Gene Expression Regulation, Enzymologic/drug effects , Gene Expression Regulation, Neoplastic/drug effects
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