THE EFFECT OF INTERMITTENT HYPOXIC TRAINING UNDER OXIDATIVE STRESS PARAMETERS IN WISTAR RATS FED ON STANDARD AND HIGH FAT DIET

Considerando-se que dietas ricas em gordura levam ao estresse oxidativo, causando lesões nas células e que o treinamento hipóxico intermitente (THI) aumenta as defesas antioxidantes endógenas em diversas situações, o objetivo deste estudo foi avaliar o efeito do THI em parâmetros de estresse oxidativo e defesas antioxidantes em fígado de ratos Wistar alimentados com dieta rica em gordura e/ou dieta padrão. Ratos Wistar foram divididos em grupos alimentados com dieta padrão ou rica em gordura. Os grupos foram submetidos a hipóxia intermitente (HI), 15 minutos HI (14-11% O2) intercalados com cinco minutos de re-oxigenação ou sessões de normóxia (N) (21% O2), por um período de duas horas diárias durante 30 dias. Os ratos Wistar alimentados com dieta padrão, e submetidas a HI, apresentaram uma redução de 37,7% na concentração de substâncias reativas ao ácido tiobarbitúrico (TBARS) e aumento de 34,66% e 39,8% no conteúdo de superóxido dismutase (SOD) e catalase (CAT), respectivamente, em comparação com o seu controlo (normoxia). No grupo com dieta rica em gordura, não houve diferença estatística entre os subgrupos HI e N. Nossos dados, que demonstram que o THI possui efeito antioxidante no fígado de ratos Wistar, argumentam em favor do uso alternativo de protocolos de hipoxia intermitente no tratamento de determinadas patologias

La correspondencia de Valencia : diario de noticias : eco imparcial de la opinión y de la prensa: Año XLI Número 17420 - 1918 Mayo 05

Copia digital. Madrid : Ministerio de Cultura. Subdirección General de Coordinación Bibliotecaria, 200

Long-Term Aspartame Administration Leads to Fibrosis, Inflammasome Activation, and Gluconeogenesis Impairment in the Liver of Mice

Background: Aspartame is an artificial sweetener used in foods and beverages worldwide. However, it is linked to oxidative stress, inflammation, and liver damage through mechanisms that are not fully elucidated yet. This work aimed to investigate the effects of long-term administration of aspartame on the oxidative and inflammatory mechanisms associated with liver fibrosis progression in mice. Methods: Mice were divided into two groups with six animals each: control and aspartame. Aspartame (80 mg/kg, via oral) or vehicle was administrated for 12 weeks. Results: Aspartame caused liver damage and elevated serum transaminase levels. Aspartame also generated liver fibrosis, as evidenced by histology analysis, and pro-fibrotic markers’ upregulation, including transforming growth factor β 1, collagen type I alpha 1, and alpha-smooth muscle actin. Furthermore, aspartame reduced nuclear factor erythroid 2-related factor 2 (Nrf2) activation and enzymatic antioxidant activity and increased lipid peroxidation, which triggered NOD-like receptor containing protein 3 (NLRP3) inflammasome activation and p53 induction. Furthermore, aspartame reduced peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1α) levels, possibly through p53 activation. This PGC-1α deficiency could be responsible for the changes in lipid profile in serum, total lipid accumulation, and gluconeogenesis impairment in liver, evidenced by the gluconeogenic enzymes’ downregulation, thus causing hypoglycemia. Conclusions: This work provides new insights to understand the mechanisms related to the adverse effects of aspartame on liver tissue

Chronic aspartame intake causes changes in the trans-sulphuration pathway, glutathione depletion and liver damage in mice

No-caloric sweeteners, such as aspartame, are widely used in various food and beverages to prevent the increasing rates of obesity and diabetes mellitus, acting as tools in helping control caloric intake. Aspartame is metabolized to phenylalanine, aspartic acid, and methanol. Our aim was to study the effect of chronic administration of aspartame on glutathione redox status and on the trans-sulphuration pathway in mouse liver. Mice were divided into three groups: control; treated daily with aspartame for 90 days; and treated with aspartame plus N-acetylcysteine (NAC). Chronic administration of aspartame increased plasma alanine aminotransferase (ALT) and aspartate aminotransferase activities and caused liver injury as well as marked decreased hepatic levels of reduced glutathione (GSH), oxidized glutathione (GSSG), γ-glutamylcysteine ​​(γ-GC), and most metabolites of the trans-sulphuration pathway, such as cysteine, S-adenosylmethionine (SAM), and S-adenosylhomocysteine ​​(SAH). Aspartame also triggered a decrease in mRNA and protein levels of the catalytic subunit of glutamate cysteine ligase (GCLc) and cystathionine γ-lyase, and in protein levels of methionine adenosyltransferase 1A and 2A. N-acetylcysteine prevented the aspartame-induced liver injury and the increase in plasma ALT activity as well as the decrease in GSH, γ-GC, cysteine, SAM and SAH levels and GCLc protein levels. In conclusion, chronic administration of aspartame caused marked hepatic GSH depletion, which should be ascribed to GCLc down-regulation and decreased cysteine levels. Aspartame triggered blockade of the trans-sulphuration pathway at two steps, cystathionine γ-lyase and methionine adenosyltransferases. NAC restored glutathione levels as well as the impairment of the trans-sulphuration pathway. Keywords: Aspartame, Cysteine, S-adenosylmethionine, N-acetylcystein

Oxidative stress parameters in juvenile Brazilian flounder Paralichthys orbignyanus (Valenciennes, 1839) (Pleuronectiformes: Paralichthyidae) exposed to cold and heat shocks

The aim of this study was to determine oxidative stress parameters in the liver and gill of Brazilian flounder juveniles (307.0 ± 16.0 g and 30.0 ± 4.0 cm) submitted to different water temperature (17.1, 23.0 and 28.8ºC) for 72 h and maintained at salinity 25‰. After the acclimation of 7 days, in 23ºC, fish were transferred to 200 L tanks containing seawater (salinity 25‰) at 28.8ºC (heat shock), 17.1ºC (cold shock) or 23.0ºC (control), five replicates (five fish tank-1). The sampled collection occurred in 0 (pre-challenge), 3, 24, 48 and 72 h after temperature shock. Flounder exposed to 17.1ºC and 28.8ºC showed significantly higher TBARS levels and GST activity in the liver post-exposition (PE) in relation to the control (23ºC). CAT activity in liver present a significantly increase at 17.1ºC, in first 48 h, and subsequently decrease in 72 h PE in relation to 28.8ºC. The gills of flounder showed significantly higher TBARS levels, GST and CAT activity when submitted at 17.1 and 28.8ºC in relation to 23.0ºC. There were observed changes in lipid peroxidation levels (LPO), CAT and GST activities in the liver and gill of Brazilian flounder in response to reactive oxygen species (ROS) produced by thermal shocks

Oxidative stress parameters in juvenile Brazilian flounder Paralichthys orbignyanus (Valenciennes, 1839) (Pleuronectiformes: Paralichthyidae) exposed to cold and heat shocks

The aim of this study was to determine oxidative stress parameters in the liver and gill of Brazilian flounder juveniles (307.0 ± 16.0 g and 30.0 ± 4.0 cm) submitted to different water temperature (17.1, 23.0 and 28.8ºC) for 72 h and maintained at salinity 25‰. After the acclimation of 7 days, in 23ºC, fish were transferred to 200 L tanks containing seawater (salinity 25‰) at 28.8ºC (heat shock), 17.1ºC (cold shock) or 23.0ºC (control), five replicates (five fish tank-1). The sampled collection occurred in 0 (pre-challenge), 3, 24, 48 and 72 h after temperature shock. Flounder exposed to 17.1ºC and 28.8ºC showed significantly higher TBARS levels and GST activity in the liver post-exposition (PE) in relation to the control (23ºC). CAT activity in liver present a significantly increase at 17.1ºC, in first 48 h, and subsequently decrease in 72 h PE in relation to 28.8ºC. The gills of flounder showed significantly higher TBARS levels, GST and CAT activity when submitted at 17.1 and 28.8ºC in relation to 23.0ºC. There were observed changes in lipid peroxidation levels (LPO), CAT and GST activities in the liver and gill of Brazilian flounder in response to reactive oxygen species (ROS) produced by thermal shocks

The Protective Effect of N-Acetylcysteine on Oxidative Stress in the Brain Caused by the Long-Term Intake of Aspartame by Rats

Long-term intake of aspartame at the acceptable daily dose causes oxidative stress in rodent brain mainly due to the dysregulation of glutathione (GSH) homeostasis. N-Acetylcysteine provides the cysteine that is required for the production of GSH, being effective in treating disorders associated with oxidative stress. We investigated the effects of N-acetylcysteine treatment (150 mg kg(-1), i.p.) on oxidative stress biomarkers in rat brain after chronic aspartame administration by gavage (40 mg kg(-1)). N-Acetylcysteine led to a reduction in the thiobarbituric acid reactive substances, lipid hydroperoxides, and carbonyl protein levels, which were increased due to aspartame administration. N-Acetylcysteine also resulted in an elevation of superoxide dismutase, glutathione peroxidase, glutathione reductase activities, as well as non-protein thiols, and total reactive antioxidant potential levels, which were decreased after aspartame exposure. However, N-acetylcysteine was unable to reduce serum glucose levels, which were increased as a result of aspartame administration. Furthermore, catalase and glutathione S-transferase, whose activities were reduced due to aspartame treatment, remained decreased even after N-acetylcysteine exposure. In conclusion, N-acetylcysteine treatment may exert a protective effect against the oxidative damage in the brain, which was caused by the long-term consumption of the acceptable daily dose of aspartame by rats.Fil: Finamor, Isabela A.. Universidade Federal de Santa Maria; BrasilFil: Ourique, Giovana M.. Universidade Federal de Santa Maria; BrasilFil: Pês, Tanise S.. Universidade Federal de Santa Maria; BrasilFil: Saccol, Etiane M. H.. Universidade Federal de Santa Maria; BrasilFil: Bressan, Caroline A.. Universidade Federal de Santa Maria; BrasilFil: Scheid, Taína. Universidade Federal do Rio Grande do Sul; BrasilFil: Baldisserotto, Bernardo. Universidade Federal de Santa Maria; BrasilFil: Llesuy, Susana Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Bioquímica y Medicina Molecular; ArgentinaFil: Partata, Wânia A.. Universidade Federal do Rio Grande do Sul; BrasilFil: Pavanato, Maria A.. Universidade Federal do Rio Grande do Sul; Brasi

Myrcia sylvatica essential oil in the diet of gilthead sea bream (Sparus aurata L.) attenuates the stress response induced by high stocking density

The effects of diet supplemented with Myrcia sylvatica essential oil (EOMS) on growth and stress tolerance to different stocking densities were assessed in Sparus aurata. Initially, three experimental groups were established: (i) control, (ii) 1.0 and (iii) 2.0 ml EOMS/kg dry feed. After 90 days, nine fish per group were anaesthetized, weighed and sampled for metabolic analysis. The remaining fish were divided into two different conditions: low (LD—5 kg/m3) and high (HD—40 kg/m3) stocking densities, constituting a final experimental setup with six treatments. After 22 days, 10 individuals per treatment were anaesthetized and sampled for biochemical analysis. EOMS feeding for 90 days did not interfere with growth, although it was effective in reducing cortisol levels and the activation of lipid and carbohydrate metabolism. The HD interfered in growth performance, increased the lactate levels in the control group, reducing also hepatic glycogen levels without dependence on diet supplementation. The 2.0 ml EOMS + LD group increased the growth parameters and decreased the cortisol and triglycerides levels. Additionally, metabolism adjustment was observed to provide energy during LD and HD conditions, indicating that diets supplemented with EOMS produce metabolic reorganization to maintain body homeostasis, suggesting its use as a beneficial supplement in fish.Spanish Ministry of Science and Education, Grant/Award Number: AGL2013-48835-C2-R and AGL2016-76069-C2-1-R; Spanish Ministry of Education, Economy and Competitiveness (MINECO); CAPES (Ministry of Education of Brazil, Brazil); PDSE-CAPES (Programa Institucional de Bolsas de Doutorado Sanduíche no Exterior, Grant/Award Number: 5055/14-8); CNPq research fellowshipPeer reviewe

Effects of parboiled rice diet on oxidative stress parameters in kidney of rats with streptozotocin-induced diabetes

The effect of parboiled rice (PR) and white rice (WR) diets on oxidative stress (OS) parameters was investigated in the kidneys of rats with streptozotocin-induced diabetes (40mg kg-1, iv). The experimental groups (n=8) were control fed with PR (CPR), control fed with WR, diabetic fed with PR, and diabetic fed with WR. After 30 days of treatment, all animals were anesthetized and exsanguinated before removal of kidneys, which were used to determine thiobarbituric acid reactive substances (TBARS), lipid hydroperoxides, carbonyl protein, superoxide dismutase, catalase, glutathione peroxidase (GPx), glutathione reductase, glutathione-S-transferase activities, and levels of glutathione (GSH). Total phenolic compounds were determined in WR and PR grains. Our data indicated that diabetes induced increase in TBARS and lipid hydroperoxides levels. Although PR has not prevented the rise in the levels of these measurements, its consumption by our animals resulted in higher GPx activity and GSH content than that of the CPR. Moreover, PR also presented concentration of total phenolic compounds 127% higher than WR grains. Thus, its consumption in this diabetic condition is suggested because this seems to confer greater protection against OS in the renal tissue of diabetic animals. © Copyright 2012, Mary Ann Liebert, Inc.Fil: Finamor, Isabela A.. Federal University of Santa Maria; BrasilFil: Saccol, Etiane M. H.. Federal University of Santa Maria; BrasilFil: Gabriel, Diogo. Federal University of Santa Maria; BrasilFil: Ourique, Giovana M.. Federal University of Santa Maria; BrasilFil: Riffel, Ana P.K.. Federal University of Santa Maria; BrasilFil: Konrad, Signorá P.. University of Vale do Rio dos Sinos; BrasilFil: Belló Klein, Adriane. Universidade Federal do Rio Grande do Sul; BrasilFil: Partata, Wania. Universidade Federal do Rio Grande do Sul; BrasilFil: Baldisserotto, Bernardo. Federal University of Santa Maria; BrasilFil: Llesuy, Susana Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Analítica y Fisicoquímica; ArgentinaFil: Pavanato, Maria A.. Federal University of Santa Maria; Brasi

Bioaccumulation and oxidative stress parameters in silver catfish (Rhamdia quelen) exposed to different thorium concentrations

The objective of this study was to evaluate the effect of chronic thorium (Th) exposure on bioaccumulation, metabolism (through biochemical parameters of the muscle) and oxidative parameters (lipidic peroxidation levels and antioxidant enzymes in the gills and in the hepatic and muscular tissues) of silver catfish (Rhamdia quelen). Silver catfish juveniles were exposed to different waterborne Th levels (in lg L1 ): 0 (control), 25.3 ± 3.2, 80.6 ± 12.0, 242.4 ± 35.6, and 747.2 ± 59.1 for 30 d. The gills and skin were the organs that accumulated the highest Th levels. The increase in the waterborne Th concentration corresponded to a progressive increase in the Th levels in the gills and kidney. Chronic Th exposure causes alterations in the oxidative parameters of silver catfish gills, which are correlated with the Th accumulation in this organ. The levels of GST decreased in the gills of fish exposed to 747.2 lg L1 Th and SOD activity decreased in silver catfish exposed to 242.4 and 747.2 lg L1 Th. In addition, the increase in the LPO in the gills exposed to 242.4 and 747.2 lg L1 Th suggests that higher oxidative damage occurred in the gills. However, in the liver and muscle, these alterations occurred mainly in the lowest waterborne Th level. Metabolic intermediates in the muscle were altered by Th exposure, but no clear relationship was found.Fil: Kochhann, Daiani. Universidade Federal de Santa Maria.; BrasilFil: Pavanato, Maria A.. Universidade Federal de Santa Maria.; BrasilFil: Llesuy, Susana Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Analítica y Fisicoquímica; ArgentinaFil: Correa, Lizelia M.. Universidade Federal de Santa Maria.; BrasilFil: Konzen Riffel, Ana P.. Universidade Federal de Santa Maria.; BrasilFil: Loro, Vania L.. Universidade Federal de Santa Maria.; BrasilFil: Mesko, Márcia F.. Universidade Estadual do Rio Grande do Sul ; Brasil. Universidade Federal de Santa Maria.; BrasilFil: Flores, Érico M.M.. Universidade Federal de Santa Maria.; BrasilFil: Dressler, Valderi L.. Universidade Federal de Santa Maria.; BrasilFil: Baldisserotto, Bernardo. Universidade Federal de Santa Maria.; Brasi