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L-type Ca2+ channel activity determines modulation of GABA release by dopamine in the substantia nigra reticulata and the globus pallidus of the rat

2013; Elsevier BV; Volume: 256; Linguagem: Inglês

10.1016/j.neuroscience.2013.10.037

1873-7544

S. Recillas-Morales, Lizzette Sanchez‐Vega, N. Ochoa-Sánchez, Isaac H. Caballero‐Florán, Francisco Paz‐Bermúdez, I. Silva, Jorge Aceves, David Erlij, Benjamí­n Florán,

Neurological disorders and treatments

Modulation of L-type Ca2+-channel function by dopamine is a major determinant of the rate of action potential firing by striatal medium spiny neurons. However, the role of these channels in modulating GABA release by nerve terminals in the basal ganglia is unknown. We found that depolarization-induced [3H]GABA release in both the substantia nigra reticulata and the external globus pallidus (GPe), was depressed by about 50% by either the selective L-channel dihydropyridine blocker nifedipine or the P/Q channel blocker ω-agatoxin TK. The effects of these blockers were additive and together eliminated about 90% of depolarization-induced [3H]GABA release. In addition, in the substantia nigra reticulata, dihydropyridines prevented both the stimulation of [3H]GABA release produced by dopamine D1 receptor activation and the inhibition caused by D4 receptor activation. In the GP nifedipine blocked the effects of D2 and A2A receptor coactivation as well as the effects of activating adenylyl cyclase with forskolin. ω-Agatoxin TK did not interfere with the action of these modulatory agents. The L-type Ca2+-channel agonist BAYK 8644 stimulated GABA release in both substantia nigra reticulata and GP. Because dihydropyridine sensitivity is a key criterion to identify L-type Ca2+-channel activity, our results imply that these channels are determinant of GABA release modulation by dopamine in striatonigral, striatopallidal and pallidonigral terminals.