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Modulation of Antioxidant Enzymatic Activities by Certain Antiepileptic Drugs (Valproic Acid, Oxcarbazepine, and Topiramate): Evidence in Humans and Experimental Models
Author(s) -
Noemí CárdenasRodríguez,
Elvia Coballase-Urrutía,
Liliana Rivera-Espinosa,
Arantxa Romero-Toledo,
Aristides Iii Sampieri,
Daniel OrtegaCuellar,
Hortencia Montesinos-Correa,
Esaú Floriano-Sánchez,
Liliana CarmonaAparicio
Publication year - 2013
Publication title -
oxidative medicine and cellular longevity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.494
H-Index - 93
eISSN - 1942-0900
pISSN - 1942-0994
DOI - 10.1155/2013/598493
Subject(s) - topiramate , excitotoxicity , oxcarbazepine , valproic acid , pharmacology , glutamate receptor , epilepsy , chemistry , oxidative stress , neuroprotection , nmda receptor , biochemistry , medicine , receptor , neuroscience , biology , carbamazepine
It is estimated that at least 100 million people worldwide will suffer from epilepsy at some point in their lives. This neurological disorder induces brain death due to the excessive liberation of glutamate, which activates the postsynaptic N-methyl-D-aspartic acid (NMDA) receptors, which in turn cause the reuptake of intracellular calcium (excitotoxicity). This excitotoxicity elicits a series of events leading to nitric oxide synthase (NOS) activation and the generation of reactive oxygen species (ROS). Several studies in experimental models and in humans have demonstrated that certain antiepileptic drugs (AEDs) exhibit antioxidant effects by modulating the activity of various enzymes associated with this type of stress. Considering the above-mentioned data, we aimed to compile evidence elucidating how AEDs such as valproic acid (VPA), oxcarbazepine (OXC), and topiramate (TPM) modulate oxidative stress.

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