“…On the postsynaptic terminal, A 1 Rs enhance the activity of G-protein-coupled Kir channels, which cause hyperpolarization and consequently reduced excitability (Boison, 2012;Aronica et al, 2013). Consistently, A 1 R agonists possess anticonvulsant and neuroprotective effects (Dunwiddie and Worth, 1982;Barraco et al, 1984;Gouder et al, 2003;Li et al, 2013), while antagonists promote seizures and aggravates neuronal damage (Ault et al, 1987;Dunwiddie, 1990;Avsar and Empson, 2004;Vianna et al, 2005). Consistently, A 1 R agonists possess anticonvulsant and neuroprotective effects (Dunwiddie and Worth, 1982;Barraco et al, 1984;Gouder et al, 2003;Li et al, 2013), while antagonists promote seizures and aggravates neuronal damage (Ault et al, 1987;Dunwiddie, 1990;Avsar and Empson, 2004;Vianna et al, 2005).…”