PPAR-Alpha Agonists as Novel Antiepileptic Drugs: Preclinical Findings (Articolo in rivista)

Type
Label
  • PPAR-Alpha Agonists as Novel Antiepileptic Drugs: Preclinical Findings (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1371/journal.pone.0064541 (literal)
Alternative label
  • Puligheddu M., Pillolla G., Melis M., Lecca S., Marrosu F., De Montis M.G., Scheggi S., Carta G., Murru E., Aroni S., Muntoni A.L., Pistis M. (2013)
    PPAR-Alpha Agonists as Novel Antiepileptic Drugs: Preclinical Findings
    in PloS one
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Puligheddu M., Pillolla G., Melis M., Lecca S., Marrosu F., De Montis M.G., Scheggi S., Carta G., Murru E., Aroni S., Muntoni A.L., Pistis M. (literal)
Pagina inizio
  • 1 (literal)
Pagina fine
  • 10 (literal)
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  • 8 (literal)
Rivista
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  • 5 (literal)
Note
  • ISI Web of Science (WOS) (literal)
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  • Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Cagliari, Italy; Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy; Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy; C.N.R. Neuroscience Institute, Cagliari, Italy (literal)
Titolo
  • PPAR-Alpha Agonists as Novel Antiepileptic Drugs: Preclinical Findings (literal)
Abstract
  • Nicotinic acetylcholine receptors (nAChRs) are involved in seizure mechanisms. Hence, nocturnal frontal lobe epilepsy was the first idiopathic epilepsy linked with specific mutations in a4 or b2 nAChR subunit genes. These mutations confer gain of function to nAChRs by increasing sensitivity toward acetylcholine. Consistently, nicotine elicits seizures through nAChRs and mimics the excessive nAChR activation observed in animal models of the disease. Treatments aimed at reducing nicotinic inputs are sought as therapies for epilepsies where these receptors contribute to neuronal excitation and synchronization. Previous studies demonstrated that peroxisome proliferator-activated receptors-a (PPARa), nuclear receptor transcription factors, suppress nicotine-induced behavioral and electrophysiological effects by modulating nAChRs containing b2 subunits. On these bases, we tested whether PPARa agonists were protective against nicotine-induced seizures. To this aim we utilized behavioral and electroencephalographic (EEG) experiments in C57BL/J6 mice and in vitro patch clamp recordings from mice and rats. Convulsive doses of nicotine evoked severe seizures and bursts of spike-waves discharges in ,100% of mice. A single dose of the synthetic PPARa agonist WY14643 (WY, 80 mg/kg, i.p.) or chronic administration of fenofibrate, clinically available for lipid metabolism disorders, in the diet (0.2%) for 14 days significantly reduced or abolished behavioral and EEG expressions of nicotine-induced seizures. Acute WY effects were reverted by the PPARa antagonist MK886 (3 mg/kg, i.p.). Since neocortical networks are crucial in the generation of ictal activity and synchrony, we performed patch clamp recordings of spontaneous inhibitory postsynaptic currents (sIPSCs) from frontal cortex layer II/III pyramidal neurons. We found that both acute and chronic treatment with PPARa agonists abolished nicotine-induced sIPSC increases. PPARa within the CNS are key regulators of neuronal activity through modulation of nAChRs. These effects might be therapeutically exploited for idiopathic or genetically determined forms of epilepsy where nAChRs play a major role. (literal)
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