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N‐type calcium channels mediate a GABAB presynaptic modulation in the corticostriatal synapse in turtle's paleostriatum augmentatum
Authors:Eduardo Sánchez‐Mejorada  Guadalupe Sánchez‐Mondragon  Juan Carlos Pineda  Mónica González  Jaime Barral
Affiliation:1. Neurociencias (UIICSE), FES Iztacala, UNAM, México;2. Dept Neurociencias. CIR “Hideyo Noguchi”, UADY, Yucatán, México;3. Morfofisiología, FES Iztacala, UNAM, México
Abstract:
Spikes population evoked by a paired pulse protocol were used to assess the influence of GABAA and GABAB receptors agonists and antagonists on the synaptic potentials and in the S2/S1 ratio in a paired pulse (PP) protocol in the cortico‐paleostriatum augmentatum synapses of the turtle. GABAA agonist, muscimol, decreased the amplitude of synaptic responses whereas the facilitation produced with the PP protocol did not change, suggesting a postsynaptic action for GABAA receptors. GABAB agonist, baclofen, enhanced paired pulse ratio indicating a presynaptic modulation through the GABAB receptor. Selective antagonists for N‐ and P/Q‐type Ca2+‐channels also enhanced paired pulse ratio, suggesting that any of these channel types may be involved in neurotransmitter release. However, the strong paired pulse facilitation produced by baclofen was occluded by blocking the N‐type Ca2+ channels with ω‐conotoxin GVIA (1 μM), but not by the blockage of P/Q‐type Ca2+ channels with ω‐agatoxin TK (400 nM). These data suggest that N and P/Q channels participate in the neurotransmitter release, whereas only N‐type Ca2+ channels are involved in the presynaptic modulation of GABAB in the corticostriatal synapse of the turtle. Synapse 63:855–862, 2009. © 2009 Wiley‐Liss, Inc.
Keywords:paleostriatum augmentatum  field potential recording  GABAA  GABAB  presynaptic modulation  calcium channels  basal ganglia  turtle
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