L-arginine potentiates GABA-mediated synaptic transmission by a nitric oxide-independent mechanism in rat dopamine neurons

被引:15
作者
Shen, KZ
Cox, BA
Johnson, SW
机构
[1] OREGON HLTH SCI UNIV,DEPT NEUROL,PORTLAND,OR 97201
[2] OREGON HLTH SCI UNIV,DEPT PHYSIOL & PHARMACOL,PORTLAND,OR 97201
关键词
baclofen; GABA transporter; GABA(A) receptor; GABA(B) receptor; inhibitory postsynaptic current; substantia nigra;
D O I
10.1016/S0306-4522(97)00024-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Effects of L-arginine in the nervous system are often attributed to nitric oxide. Using whole-cell patch pipettes to record membrane currents in voltage-clamp from dopamine neurons in the rat midbrain slice, the present studies found that L-arginine potentiates GABA-dependent membrane currents via a nitric oxide-independent mechanism. L-Arginine (0.3-10 mM) increased the peak amplitude, half-width duration and time constant of decay of GABA(B) receptor-mediated inhibitory postsynaptic currents in a concentration-dependent manner. In the presence of CGP 35348 (300 mu M), a GABA(B) receptor antagonist, L-arginine also prolonged the duration of inhibitory postsynaptic currents mediated by GABA(A) receptors, but their amplitudes were reduced. L-Arginine (10 mM) also evoked 17 +/- 3 pA of outward current (at - 60 mV) which was significantly increased in the presence of exogenous GABA (100 mu M). Pressure-ejection of GABA from micropipettes produced outward currents mediated by GABA(B) receptors (recorded in bicuculline) or GABA(A) receptors (recorded in CGP 35348); both types of receptor-mediated currents were increased by L-arginine (10 mM). In contrast, outward currents evoked by baclofen, a GABA(B) receptor agonist, were not potentiated by L-arginine. The GABA transport inhibitors NO 711 (1 mu M) and nipecotic acid (1 mM) significantly increased the half-width duration and time-constant of decay of GABA(B)-mediated inhibitory postsynaptic currents, thus mimicking effects of L-arginine. However, nitric oxide donors failed to mimic effects of L-arginine on GABA(B) inhibitory postsynaptic currents, and inhibitors of nitric oxide synthesis failed to selectively block the action of L-arginine. These findings suggest that L-arginine potentiates GABA synaptic transmission by a nitric oxide-independent mechanism. Similarities between effects of L-arginine, NO 711 and nipecotic acid suggest that L-arginine inhibits a GABA transporter. (C) 1997 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:649 / 658
页数:10
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