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Antioxidant effect of buspirone in epilepsy: is the case closed?

Efeito antioxidante de buspirona nas epilepsias: o caso está encerrado?

LETTER TO THE EDITOR

Antioxidant effect of buspirone in epilepsy : is the case closed?

Efeito antioxidante de buspirona nas epilepsias: o caso está encerrado?

Fulvio Alexandre Scorza

Disciplina de Neurologia Experimental, Departamento de Neurologia e Neurocirurgia, Escola Paulista de Medicina, Universidade Federal de São Paulo (EPM/Unifesp), São Paulo, SP, Brazil

Correspondence to Correspondence to: Fulvio Alexandre Scorza Departamento de Neurologia/Neurocirurgia, Disciplina de Neurologia Experimental, Universidade Federal de São Paulo Rua Botucatu, 862 - Vila Clementino 04023-900 - São Paulo, SP, Brazil Phone: (55 11) 5549-2064 E-mail: scorza.nexp@epm.br

I read with interest a very comprehensive article titled "Antioxidant effect of buspirone in epilepsy model induced by pilocarpine" by Ferreira et al.1 published in the December issue of Revista de Psiquiatria Clínica. In brief, the authors demonstrated that the pretreatment with buspirone has an anticonvulsant and antioxidant effect during the acute period of pilocarpine model of temporal lobe epilepsy. Given the dearth of published data about the relation of buspirone and epilepsy, we applaud Dr. Ferreira et al. for pursuing this topic, but I also find it necessary to address some purposes regarding their comments.

Initially developed for use in the treatment of generalised anxiety disorder, it appears that buspirone may be useful in various other psychiatric and neurological disorders, such as attenuating side effects of Parkinson's disease therapy, ataxia, depression, social phobia, and behaviour disturbances following brain injury, and those accompanying Alzheimer's disease, dementia and attention deficit disorder2. Concerning epilepsy, few studies have accurately assessed the relationship between buspirone, seizures, and chronic epilepsy. Following a chronological sequence, Pranzatelli et al. showed in 1993 some inspiring proposals after evaluating the effects of buspirone administration in four individuals with progressive myoclonus epilepsy3. From experimental point of view, it was shown two years later that buspirone, using the low Mg2+ induced model epilepsy, was effective in reducing the frequency of occurrence of low magnesium induced field potentials in CA1 and CA3 areas of the hippocampus slice preparation (guinea pigs) in a dose dependent manner4. In 2004, Macêdo et al. demonstrated that small doses of buspirone protected against cocaine-induced seizures and/or mortality5. Recently, the research group led by De Freitas showed that buspirone exerted anticonvulsant effects associated with the inhibition of the development of oxidative stress caused by pilocarpine-induced seizures, suggesting a therapeutic use potential of buspirone in epilepsy treatment6.

In sum, the data presented by Ferreira et al.1 open up new avenues of research in epilepsy field. Obviously, many question still to be answered, such as: What are the effects of buspirone during epileptogenesis process in the pilocarpine model? Buspirone exerts antioxidant action in other brain structures, beyond the hippocampal formation? What is the effect of buspirone in animals with refractory epilepsy?

Finally, while these and other questions have not been answered, I express my congratulations to Ferreira et al. for the stimulating article and I am sure that the integration of the advancements in basic science with clinical trials allows us to create highly effective pharmacological strategies against uncontrolled epilepsy.

Received: 11/3/2012

Accepted: 11/3/2012

Comment about "Antioxidant effect of buspirone in epilepsy model induced by pilocarpine"

  • 1. Ferreira PB, de Almeida AAC, de Freitas RM. Antioxidant effect of buspirone in epilepsy model induced by pilocarpine. Rev Psiq Clín. 2012;39:153-6.
  • 2. Loane C, Politis M. Buspirone: what is it all about? Brain Res. 2012;1461:111-8.
  • 3. Pranzatelli MR, Franz D, Tate E, Martens JM. Buspirone in progressive myoclonus epilepsy. J Neurol Neurosurg Psychiatry. 1993;56:114-5.
  • 4. Walden J, Von Wegerer J, Roed I, Berger M. Effects of the serotonin-1A agonists buspirone and ipsapirone on field potentials in the hippocampus slice: comparison with carbamzepine and verapamil. Eur Neuropsychopharmacol. 1995;5:57-61.
  • 5. Macêdo DS, Santos RS, Belchior LD, Neto MA, Vasconcelos SM, Lima VT, et al. Effect of anxiolytic, antidepressant, and antipsychotic drugs on cocaine-induced seizures and mortality. Epilepsy Behav. 2004;5:852-6.
  • 6. De Freitas RL, Santos IM, de Souza GF, Tomé Ada R, Saldanha GB, De Freitas RM. Oxidative stress in rat hippocampus caused by pilocarpine-induced seizures is reversed by buspirone. Brain Res Bull. 2010;16(81):505-9.
  • Correspondence to:

    Fulvio Alexandre Scorza
    Departamento de Neurologia/Neurocirurgia, Disciplina de Neurologia Experimental, Universidade Federal de São Paulo
    Rua Botucatu, 862 - Vila Clementino
    04023-900 - São Paulo, SP, Brazil
    Phone: (55 11) 5549-2064
    E-mail:
  • Publication Dates

    • Publication in this collection
      02 Jan 2013
    • Date of issue
      2012
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