Navegando por Assunto "Stress oxidativo"

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Acesso aberto (Open Access)
Alterações oxidativas e inflamatórias induzidas pela dapsona no sangue e no córtex pré-frontal de camundongos: efeitos do ácido alfa-lipóico
(Universidade Federal do Pará, 2018-12-14) GOMES, Bruno Alexandre Quadros; MONTEIRO, Marta Chagas; http://lattes.cnpq.br/6710783324317390
Dapsone (DDS), a drug used in leprosy multidrug therapy, can cause many adverse reactions and intoxications, inducing the generation of reactive oxygen species (ROS) and imbalance in the redox state, increase methemoglobin (MetHb) formation, hemolysis and release of heme and iron free, which may interfere with redox homeostasis in more vulnerable regions, such as prefrontal cortex (PFC), causing neurotoxicity and even neuroinflammation. In this sense, antioxidant compounds with chelating properties such as α-lipoic acid (ALA) may play a key role in combating or preventing these alterations. Thus, this work aims to evaluate the effect of DDS on MetHb formation, peripheral oxidative stress, and oxidative changes and neuroinflammation in PFC, as well as, effects of ALA. For this, was induced MetHb formation in Swiss mice with DDS 40mg/kg ip for 5 days. Two hours after DDS administration, ALA was given at two concentrations (12.5 and 25 mg/kg). Besides MetHb percentage, total equivalent antioxidant capacity (TEAC), reduced glutathione (GSH), superoxide dismutase (SOD), catalase (CAT) thiobarbituric acid reactive substances (TBARS), and iron concentrations in blood and PFC were evaluated, as well as, IL-1β, IL-17, and IL-4 cytokine concentrations, and de F4/80+, GFAP, and BDNF expression in PFC. Our results show that DDS induces the MetHb formation in red blood cells of mice, however, ALA was able to prevent or reverse the oxidation of hemoglobin induced by DDS at two used concentrationns. DDS reduced antioxidant capacity (TEAC) in plasma and red blood cells; decreased erythrocyte GSH, CAT, and SOD; and increased TBARS and plasma iron; however, ALA at two concentrations increased or reestablished TEAC in plasma and red blood cells at baseline levels. In addition to increasing or reestablishing GSH levels, SOD, and CAT in red blood cells, and decreased TBARS and iron levels, mainly in euthanized animals 4h after treatment. Curiously ALA 50mg/kg increased plasma iron concentrations. The treatment with DDS 40mg/kg also reduced TEAC, GSH, SOD e CAT in the PFC of the mice and increased TBARS and iron, characterizing oxidative stress, mainly in euthanized animals in 24h after treatment. Treatment with ALA increased or restored TEAC and GSH; and increased SOD and CAT in 12,5mg/kg concentration in euthanized animals 4h after treatment, as well as reducing TBARS levels and decreasing or preventing iron overload, mainly in euthanized animals 24h after treatment. DDS also promoting microglial and astrocyte activation in PFC, through F4/80+ e GFAP expression., with increased IL-1β and IL-4 production, and BDNF reduction, on the other hand, ALA 25mg/kg reduced GFAP and IL-1β expression, besides increased BDNF, suggesting that DDS also can cause neuroinflammation, and ALA presents antioxidant and anti-inflammatory properties against toxicity caused by DDS. These results suggest that ALA is promising and plays an important role in the prevention and/or formation of MetHb, reestablishment of redox balance and iron concentrations in both blood and PFC. Thus, ALA may be a usefull adjuvant therapy in DDS-induced toxicity, with lower toxicity and increasing adherence to treatment of leprosy patients.
Acesso aberto (Open Access)
Avaliação dos efeitos decorrentes da exposição ao cloreto de alumínio sobre parâmetros motores, cognitivos e de estresse oxidativo em ratos
(Universidade Federal do Pará, 2018-12-18) FERNANDES, Rafael Monteiro; LIMA, Rafael Rodrigues; http://lattes.cnpq.br/6791765554367432
Aluminum (Al) is the third most abundant metal in the earth's crust, being present in large amounts in soil and water, its high bioavailability makes it an important environmental contaminant. Al is considered a neurotoxic agent and accumulates in the nervous system, being this behavior associated with several neurodegenerative diseases. However, little is known about its effects at doses similar to human consumption in the nervous and biochemical systems. Thus, this study investigated the effects of chronic exposure to aluminum chloride (AlCl3) on cognition, motor behavior and oxidative stress. For this, adult Wistar rats were divided into three groups: Al1 (8.3 mg / kg / day), Al2 (5.2 mg / kg / day) and Control (Distilled water) being exposed orally for 60 days. After the exposure period, behavioral, histological, oxidative stress parameters and quantification of aluminum levels in the blood were performed. There were no changes in motor behavior, there was change in only one exploratory parameter and in cognition. No differences were found in the population of the purkinje neurons between the experimental groups. Exposure to Al increased levels of this metal in the blood, also altering the parameters of oxidative biochemistry. Thus, we can affirm that exposure to Al in rats, at doses equivalent to urban exposure and in potentially safe doses are capable of promoting breakage of blood homeostasis, altering hippocampal biochemical balance, generating a state of oxidative stress and cognitive damage, not being able to promote significant changes in the cerebellum and motor parameters.
Acesso aberto (Open Access)
Efeitos do exercício físico sore parâmetros cognitivos e bioquímicos em ratos expostos ao etanol de forma intensa e episódica (Binge Drinking)
(Universidade Federal do Pará, 2018-12-21) TEMBRA, Dinair Pamplona dos Santos; LIMA, Rafael Rodrigues; http://lattes.cnpq.br/3512648574555468
The consumption pattern of heavy and episodic ethanol, weekend consumption, characterizes the pattern of excessive alcohol consumption or binge drinking that promotes an imbalance of brain metabolic functions, contributing to neurodegeneration and cerebral dysfunction. And because it is a legal drug, it has global relevance in public and social health. In this way, we aimed to investigate the effects of physical training of moderate intensity, in treadmill, on the deleterious effects of ethanol on hippocampus functions related to memory and learning. For this, 80 Wistar rats were divided into four groups: Control group; Trained group (animals trained and treated with distilled water); Ethanol group (animals not trained and treated with doses of 3 g / kg / day of ethanol, 20% w / v); and ethanol + trained group (animals trained and exposed to ethanol). Physical exercise was performed on a treadmill for 5 days a week for 4 weeks and all doses of ethanol and distilled water were administered by intragastric gavage (three days a week) in four repeated cycles. After the experimental period, the animals were submitted to the task of object recognition and Morris aquatic labyrinth test, and after euthanasia, blood and hippocampus were collected to measure levels of antioxidant capacity equivalent to trolox (TEAC), content of reduced glutathione (GSH), nitrite and lipid peroxidation. (LPO). Our results showed that EtOH caused marked oxidative stress and mnemonic damage, and physical exercise promoted neuroprotective effects, including modulation of oxidative plasma biochemistry (by restoration of GSH levels) and hippocampus (reducing levels of LPO and increasing antioxidant parameters) and improving cognitive function. Therefore, physical exercise may be an important prophylactic and therapeutic tool to improve and even prevent the deleterious effects of ethanol on cognitive functions.
Acesso aberto (Open Access)
Marcadores de estresse oxidativo e concentrações de primaquina e carboxiprimaquina em pacientes com malária por Plasmodium vivax
(Universidade Federal do Pará, 2014-11-06) RODRIGUES, Luiz Carlos de Souza; VIEIRA, José Luiz Fernandes; http://lattes.cnpq.br/2739079559531098
The changes in redox cycle has been associated with the physiopathology of severity of malaria in experimental models and in humans. However, a few studies evaluated the changes in redox equilibrium of patients with no severe malaria by P.vivax, which comprise the majority of the cases of disease. The variations of oxidative damage and the respective antioxidant response of human host were not compared before, during and after chemotherapy. Also, the mechanisms responsible by the generation of free radical in each phase that is, the heme degradation, respiratory burst of macrophages or antimalarials uses, were not determined. The objective of this study was to estimate the levels of biomarkers of oxidative damage and the respective antioxidant response, as well as primaquine and carboxyprimaquine whole blood levels in malaria by P. vivax. Therefore, were enrolled 38 patients with slide confirmed infection by P. vivax followed by 28 days. Serial blood samples were collected on pre-doses samples (D0) and on D2, D7 and D14. The oxidative damage and the antioxidant defense were estimated by the spectrophotometric measures of thiobarbituric acid reatives substances and methemoglobinemia, and by total antioxidant capacity and reduced glutathione, respectively. The control group consisted of 19 healthy volunteers matched for age and gender ratio. Primaquine and its major metabolite were determined by high performance liquid chromatography. The results revealed that the disease occurred in male patients of working age. Haematological parameters remained constant during the study. Biochemical evaluation showed a significant decrease in HDL-cholesterol levels during the study. Methemoglobinemia was associated with antimalarials uses, because the levels were similar to control group and increased significantly during the treatment. The levels of thiobarbituric acid reatives substances were associated with plasmodium and probably respiratory burst of macrophages, because they were higher than control group on D0, and no significant changes were observed after antimalarials usage. Total antioxidant capacity and oxidative stress levels were similar during the study as well as in the control group. The levels of reduced glutathione decreased significantly during the study and doesn’t be associated with both parasitaemia. Primaquine does not show a significant accumulation, and the concentrations of parent drug and its carboxyl metabolite were not associated with methemoglobinemia and thiobarbituric acid reatives substances levels.