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Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;49(4): e5031, 2016. tab, graf
文章 在 英语 | LILACS | ID: lil-774523

摘要

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.


Subject(s)
Animals , Male , Mice , Acetates/pharmacology , Anticonvulsants/pharmacology , Leukotriene Antagonists/pharmacology , Quinolines/pharmacology , Seizures/drug therapy , Acetates/therapeutic use , Anticonvulsants/therapeutic use , Blotting, Western , Convulsants , Kindling, Neurologic/drug effects , Leukotriene Antagonists/therapeutic use , Pentylenetetrazole , Phenobarbital/pharmacology , Phenobarbital/therapeutic use , Quinolines/therapeutic use , Receptors, Leukotriene/drug effects , Seizures/chemically induced , Time Factors , Treatment Outcome
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