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Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress

BACKGROUND: Oxidative stress has been implicated in various disorders including epilepsy. We studied the antioxidant status in patients with epilepsy and aimed at determining whether there was any difference in the antioxidant levels between patients and controls, patients who are not on antiepilept...

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Autores principales: Menon, Bindu, Ramalingam, Krishnan, Kumar, Rajendiran Vinoth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4251012/
https://www.ncbi.nlm.nih.gov/pubmed/25506160
http://dx.doi.org/10.4103/0972-2327.144008
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author Menon, Bindu
Ramalingam, Krishnan
Kumar, Rajendiran Vinoth
author_facet Menon, Bindu
Ramalingam, Krishnan
Kumar, Rajendiran Vinoth
author_sort Menon, Bindu
collection PubMed
description BACKGROUND: Oxidative stress has been implicated in various disorders including epilepsy. We studied the antioxidant status in patients with epilepsy and aimed at determining whether there was any difference in the antioxidant levels between patients and controls, patients who are not on antiepileptic drugs (AEDs), and on treatment, between individual AEDs and patients on monotherapy and polytherapy. MATERIALS AND METHODS: Antioxidant levels like catalase, glutathione peroxidase (GPx), vitamin E, glutathione (GSH), thiol group (SH), uric acid, and total antioxidant capacity (TAC) were compared between 100 patients with epilepsy and equal number of controls. Twenty-five patients who were not on AEDs were compared with patients on AEDs and the control group. Patients were divided into monotherapy and polytherapy group and antioxidant status was compared between the two groups and between individual drugs. RESULTS: Catalase, SH, vitamin E, and TAC were significantly low in patients with epilepsy than those in the control group (P < 0.001). GSH and uric acid did not show any difference; GPx in patients was significantly higher than those in the control group There were no differences in the antioxidant levels between the treated and the untreated groups; however, it was lower in untreated patients than controls (P < 0.001), suggesting that AEDs do not modify the oxidative stress. Patients on Valproate (VPA) showed higher catalase and GPx levels. Catalase was higher in the monotherapy than polytherapy group (P < 0.04). CONCLUSION: Our study found significantly low levels of antioxidant in patients as compared to controls. AED did not influence the antioxidant status suggesting that seizures induce oxidative stress.
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spelling pubmed-42510122014-12-12 Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress Menon, Bindu Ramalingam, Krishnan Kumar, Rajendiran Vinoth Ann Indian Acad Neurol Original Article BACKGROUND: Oxidative stress has been implicated in various disorders including epilepsy. We studied the antioxidant status in patients with epilepsy and aimed at determining whether there was any difference in the antioxidant levels between patients and controls, patients who are not on antiepileptic drugs (AEDs), and on treatment, between individual AEDs and patients on monotherapy and polytherapy. MATERIALS AND METHODS: Antioxidant levels like catalase, glutathione peroxidase (GPx), vitamin E, glutathione (GSH), thiol group (SH), uric acid, and total antioxidant capacity (TAC) were compared between 100 patients with epilepsy and equal number of controls. Twenty-five patients who were not on AEDs were compared with patients on AEDs and the control group. Patients were divided into monotherapy and polytherapy group and antioxidant status was compared between the two groups and between individual drugs. RESULTS: Catalase, SH, vitamin E, and TAC were significantly low in patients with epilepsy than those in the control group (P < 0.001). GSH and uric acid did not show any difference; GPx in patients was significantly higher than those in the control group There were no differences in the antioxidant levels between the treated and the untreated groups; however, it was lower in untreated patients than controls (P < 0.001), suggesting that AEDs do not modify the oxidative stress. Patients on Valproate (VPA) showed higher catalase and GPx levels. Catalase was higher in the monotherapy than polytherapy group (P < 0.04). CONCLUSION: Our study found significantly low levels of antioxidant in patients as compared to controls. AED did not influence the antioxidant status suggesting that seizures induce oxidative stress. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4251012/ /pubmed/25506160 http://dx.doi.org/10.4103/0972-2327.144008 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Menon, Bindu
Ramalingam, Krishnan
Kumar, Rajendiran Vinoth
Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
title Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
title_full Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
title_fullStr Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
title_full_unstemmed Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
title_short Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
title_sort low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4251012/
https://www.ncbi.nlm.nih.gov/pubmed/25506160
http://dx.doi.org/10.4103/0972-2327.144008
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