TY - JOUR
T1 - Sustained GABA-induced regulation of the L-type Ca2+ conductance in crustacean muscle fibers
AU - Castellote, Juan
AU - Araque, Alfonso
AU - Buño, Washington
PY - 1997
Y1 - 1997
N2 - The sustained effects of γ-aminobutyric acid (GABA) on voltage-gated conductances, and excitatory and inhibitory postsynaptic currents (EPSC and IPSC, respectively) in crayfish opener muscle fibers were analyzed using the two-electrode voltage-clamp technique. GABA (1.0 mM) was applied for 1-2 min and measurements were performed 30 min after restoring control Ringer solution. The L-type Ca2+ current (I(Ca)) was reduced by > 33%. The I(Ca) conductance (g(Ca)) was reduced and the activation and inactivation were slowed down by GABA. The I(Ca) regulation outlasted GABA superfusion (150 min). A small decrease (< 19%) of the Ca2+-activated K+ current (I(Kca)), due to the I(Ca) reduction, was also recorded. The leak (I(L)), the delayed-rectifier (I(K)) and the hyperpolarization-activated (I(AB)) currents were not af fected. Picrotoxin (0.5 mM) and bicuculline (0.2 mM) blocked the I(Ca) reduction. Neither the GABA(B) antagonist saclofen (1.0 mM) nor the agonist baclofen (1.0 mM) had any effect. Therefore, the I(Ca) regulation was probably mediated through GABA(A) receptors. EPSCs, but not IPSCs, were reduced (30%) for prolonged periods (> 100 min.) after GABA application. We describe a new, potentially functional, role for GABA receptors in the mediation of a sustained reduction of presynaptic and postsynaptic excitability in crustacean muscle.
AB - The sustained effects of γ-aminobutyric acid (GABA) on voltage-gated conductances, and excitatory and inhibitory postsynaptic currents (EPSC and IPSC, respectively) in crayfish opener muscle fibers were analyzed using the two-electrode voltage-clamp technique. GABA (1.0 mM) was applied for 1-2 min and measurements were performed 30 min after restoring control Ringer solution. The L-type Ca2+ current (I(Ca)) was reduced by > 33%. The I(Ca) conductance (g(Ca)) was reduced and the activation and inactivation were slowed down by GABA. The I(Ca) regulation outlasted GABA superfusion (150 min). A small decrease (< 19%) of the Ca2+-activated K+ current (I(Kca)), due to the I(Ca) reduction, was also recorded. The leak (I(L)), the delayed-rectifier (I(K)) and the hyperpolarization-activated (I(AB)) currents were not af fected. Picrotoxin (0.5 mM) and bicuculline (0.2 mM) blocked the I(Ca) reduction. Neither the GABA(B) antagonist saclofen (1.0 mM) nor the agonist baclofen (1.0 mM) had any effect. Therefore, the I(Ca) regulation was probably mediated through GABA(A) receptors. EPSCs, but not IPSCs, were reduced (30%) for prolonged periods (> 100 min.) after GABA application. We describe a new, potentially functional, role for GABA receptors in the mediation of a sustained reduction of presynaptic and postsynaptic excitability in crustacean muscle.
KW - Crayfish muscle
KW - EPSC depression
KW - I(Ca) regulation
KW - L-type current
KW - Pre- and postsynaptic excitability
KW - Sustained GABA effects
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U2 - 10.1007/s004240050396
DO - 10.1007/s004240050396
M3 - Article
C2 - 9178626
AN - SCOPUS:0030952196
SN - 0031-6768
VL - 434
SP - 272
EP - 279
JO - Pflugers Archiv European Journal of Physiology
JF - Pflugers Archiv European Journal of Physiology
IS - 3
ER -