Montelukast reduces seizures in pentylenetetrazol-kindled mice

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Abstract

Cysteinyl leukotrienes (CysLTs) have been implicated in seizures and kindling; however, the effect of CysLT receptor antagonists on seizure frequency in kindled animals and changes in CysLT receptor expression after pentylenetetrazol (PTZ)-induced kindling have not been investigated. In this study, we evaluated whether the CysLT1 inverse agonist montelukast, and a classical anticonvulsant, phenobarbital, were able to reduce seizures in PTZ-kindled mice and alter CysLT receptor expression. Montelukast (10 mg/kg, sc) and phenobarbital (20 mg/kg, sc) increased the latency to generalized seizures in kindled mice. Montelukast increased CysLT1 immunoreactivity only in non-kindled, PTZ-challenged mice. Interestingly, PTZ challenge decreased CysLT2 immunoreactivity only in kindled mice. CysLT1 antagonists appear to emerge as a promising adjunctive treatment for refractory seizures. Nevertheless, additional studies are necessary to evaluate the clinical implications of this research.

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Fleck, J., Temp, F. R., Marafiga, J. R., Jesse, A. C., Milanesi, L. H., Rambo, L. M., & Mello, C. F. (2016). Montelukast reduces seizures in pentylenetetrazol-kindled mice. Brazilian Journal of Medical and Biological Research, 49(4). https://doi.org/10.1590/1414-431X20155031

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