Comparação dos efeitos de compostos de selênio sobre parâmetros bioquímicos e de viabilidade celular em fatias de córtex de ratos jovens

• Autor(a) principal: Bitencourt, Paula Eliete Rodrigues
• Data de Publicação: 2014
• Tipo de documento: Dissertação
• Idioma: por
• Título da fonte: Manancial - Repositório Digital da UFSM
• Texto Completo: http://repositorio.ufsm.br/handle/1/5951
• topic: 3-metil-1-fenil-2-(fenilseleno) oct-2-en-1-um; Selenato de sódio; NP-SH; ADA; Citotoxicidade; Lipoperoxidação; 3-methyl-1-phenyl-2-(phenylselenium)oct-2-en-1-um; Sodium selenate; Cytotoxicity; Lipoperoxidation; CNPQ::CIENCIAS DA SAUDE::FARMACIA

Selenium (Se) is an oligoelement crucial for various biological processes. Se has anti-inflammatory and antioxidant properties and plays a key role in brain development. Adenosine deaminase (ADA, EC 3.5.4.4) is a key enzyme in purine metabolism because it helps in the regulation of intracellular and extracellular levels of adenosine, an important nucleoside that acts in the neuromodulation of the immune and nervous systems. Oxidative stress occurs when there is an imbalance between the production of reactive species and their detoxification by systems that remove or repair the resulting damage. In this context, several Se compounds have been developed and studied, among them the 3-methyl-1-phenyl-2-(phenylseleno)oct-2-en-1-one (C12H2HOSe), which is an α, β-unsaturated ketone functionalized vinyl chalcogenide, and sodium selenate (Na2SeO4), the main inorganic form of Se found in animals and plants. The aim of this study was to compare the effects of C12H2HOSe (organic Se) and Na2SeO4 (inorganic Se) on the cell viability, lipoperoxidation and ADA activity in cortex slices of young rats. The results showed that only organic Se caused a reduction in ADA activity at the concentrations of 1, 10 and 30μM in the cerebral cortex slices of the rats tested. However, this result is not related to the oxidation of the thiol groups, since this compound did not alter the NP-SH and LDH levels. Both compounds did not affect the lipoperoxidation levels, although the organic Se was capable of sequestering NO radicals at the highest concentration tested. The inorganic Se protected the cerebral cortex slices against the sodium nitroprusside-induced damage and increased the NP-SH levels. The tests used to evaluate cell viability (LDH and MTT) suggest the maintenance of the cell integrity of the cortex slices exposed to Se compounds. Therefore, our results suggest that organic Se has immunomodulatory properties, due to the reduction in ADA activity, and acted in the maintenance of the cell integrity. In turn, the antioxidant activity of inorganic Se was reaffirmed. Hence, the results of this study paved the way to explore both Se compounds in the CNS.