Abstract

BackgroundNeurological disorders suggest that the excitotoxicity involves a drastic increase in intracellular Ca2+ concentrations and the formation of reactive oxygen species. The presence of these free radicals may also affect the dopaminergic system. The aim of this work was to determine if riboflavin (B2) and pyridoxine (B6) provide protection to the brain against free radicals generated by 3-nitropropionic acid (3-NPA) by measuring the levels of dopamine (DA) and selected oxidative stress markers.MethodsMale Fisher rats were grouped (n = 6) and treated as follows: group 1, control (NaCl 0.9%); group 2, 3-NPA (20 mg/kg); group 3, B2 (10 mg/kg); group 4, B2 (10 mg/kg) + 3-NPA (20 mg/kg); group 5, B6 (10 mg/kg) and group 6, B6 + 3-NPA. All treatments were administered every 24 h for 5 days by intraperitoneal route. After sacrifice, the brain was obtained to measure DA, GSH, and lipid peroxidation, Ca2+, Mg2+, ATPase and H2O2.Main findingsLevels of dopamine increased in cortex, striatum and cerebellum/medulla oblongata of animals that received 3-NPA alone. The lipid peroxidation increased in cortex, striatum, and cerebellum/medulla oblongata, of animals treated with B2 vitamin alone. ATPase dependent on Ca+2, Mg+2 and H2O2 increased in all regions of animals that received 3-NPA alone.ConclusionThe results confirm the capacity of 3-NPA to generate oxidative stress. Besides, the study suggests that B2 or B6 vitamins restored the levels of DA and reduced oxidative stress in brain of rats. We believe that these results would help in the study of neurodegenerative diseases.

Highlights

  • Neurological disorders suggest that the excitotoxicity involves a drastic increase in intracellular C­ a2+ concentrations and the formation of reactive oxygen species

  • The study suggests that ­B2 or ­B6 vitamins restored the levels of DA and reduced oxidative stress in brain of rats

  • The aim of this work was to determine if riboflavin ­(B2) and pyridoxine ­(B6) provide protection to the brain against free radicals generated by 3-nitropropionic acid (3-NPA) by measuring the levels of dopamine (DA) and selected oxidative stress markers

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Summary

Introduction

Neurological disorders suggest that the excitotoxicity involves a drastic increase in intracellular C­ a2+ concentrations and the formation of reactive oxygen species. The presence of these free radicals may affect the dopaminergic system. The aim of this work was to determine if riboflavin ­(B2) and pyridoxine ­(B6) provide protection to the brain against free radicals generated by 3-nitropropionic acid (3-NPA) by measuring the levels of dopamine (DA) and selected oxidative stress markers. There is evidence that metabolism of transmitter dopamine by monoamine oxidase enzyme may promote striatal damage in mitochondrial toxin induced models of Huntington’s disease (HD) [4], and that HD is a devastating neurodegenerative disorder that reflect neuronal dysfunction and death in selected brain regions with striatum and cerebral cortex being the principal targets [5]. Both compounds are water-soluble vitamins that possess antioxidant activity [8]

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