2019
DOI: 10.1007/s11062-019-09786-9
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Peroxisomal Proliferator-Activated γ-Receptors: Participation in the Anti-Seizure Effects of Transcranial DC Stimulation of the Cerebellum

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Cited by 3 publications
(3 citation statements)
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“…Agonists of γ-receptors that activate peroxisomal proliferator (PPARγ) also show anticonvulsant properties, including in models of PTZ -induced kindling, pilocarpine-induced and febrile seizures [10,11,12]. In our studies, it was determined that blocking PPARγ using BADGE ensured a reduction in the expressiveness of the anticonvulsant effects of noninvasive irritations of cerebellar structures [13]. However, until recently, the effectiveness of the combined use of H3 histamine receptor blockers and PPARγ agonists in relation to the manifestations of chronic epileptic syndrome -PTZ-induced kindling, which allows to reproduce resistance to the effects of antiepileptic drugs, has not been studied [5,14].…”
mentioning
confidence: 92%
“…Agonists of γ-receptors that activate peroxisomal proliferator (PPARγ) also show anticonvulsant properties, including in models of PTZ -induced kindling, pilocarpine-induced and febrile seizures [10,11,12]. In our studies, it was determined that blocking PPARγ using BADGE ensured a reduction in the expressiveness of the anticonvulsant effects of noninvasive irritations of cerebellar structures [13]. However, until recently, the effectiveness of the combined use of H3 histamine receptor blockers and PPARγ agonists in relation to the manifestations of chronic epileptic syndrome -PTZ-induced kindling, which allows to reproduce resistance to the effects of antiepileptic drugs, has not been studied [5,14].…”
mentioning
confidence: 92%
“…Критерієм включення щурів до спостереження було виникнення генералізованих клоніко-тонічних судомних нападів у відповідь на останні дві ін'єкції епілептогену. Тяжкість судом оцінювали за 6бальною шкалою [6].…”
unclassified
“…В наших дослідженнях визначено, що блокування PPARγ застосуванням BADGE забезпечувало зниження виразності протисудомних впливів неінвазивних подразнень структур мозочка [6]. Також встановлено, що гальмування тирозин-кінази на моделі ПТЗ-кіндлінгу супроводжується розвитком протисудомних ефектів [5,12].…”
unclassified