Short-term Depression of External Globus Pallidus-Subthalamic Nucleus Synaptic Transmission and Implications for Patterning Subthalamic Activity

被引:28
作者
Atherton, Jeremy F. [1 ]
Menard, Ariane [1 ]
Urbain, Nadia [2 ]
Bevan, Mark D. [1 ]
机构
[1] Northwestern Univ, Dept Physiol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Univ Lyon 1, INSERM CNRS UMR5292 U1028, Lab Physiopathol Reseaux Neuronaux Cycle Veille S, F-69372 Lyon 08, France
基金
美国国家卫生研究院;
关键词
PRESYNAPTIC CALCIUM CURRENT; NEURONS IN-VITRO; BASAL GANGLIA; POSTSYNAPTIC MECHANISMS; BETA OSCILLATIONS; RAT; SYNAPSES; GABA; PARKINSONISM; RECEPTOR;
D O I
10.1523/JNEUROSCI.3576-12.2013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The frequency and pattern of activity in the reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthalamic nucleus (STN) are closely related to motor function. Although phasic, unitary GPe-STN inputs powerfully pattern STN activity ex vivo, correlated GPe-STN activity is not normally observed in vivo. To test the hypothesis that the GPe's influence is constrained by short-term synaptic depression, unitary GPe-STN inputs were stimulated in rat and mouse brain slices at rates and in patterns that mimicked GPe activity in vivo. Together with connectivity estimates these data were then used to simulate GPe-STN transmission. Unitary GPe-STN synaptic connections initially generated large conductances and transmitted reliably. However, the amplitude and reliability of transmission declined rapidly (tau = 0.6 +/- 0.5s) to <10% of their initial values when connections were stimulated at the mean rate of GPe activity in vivo (33 Hz). Recovery from depression (tau = 17.3 +/- 18.9s) was also longer than pauses in tonic GPe activity in vivo. Depression was the result of the limited supply of release-ready vesicles and was in sharp contrast to Calyx of Held transmission, which exhibited 100% reliability. Injection of simulated GPe-STN conductances revealed that synaptic depression caused tonic, nonsynchronized GPe-STN activity to disrupt rather than abolish autonomous STN activity. Furthermore, synchronous inhibition of tonically active GPe-STN neurons or phasic activity of GPe-STN neurons reliably patterned STN activity through disinhibition and inhibition, respectively. Together, these data argue that the frequency and pattern of GPe activity profoundly influence its transmission to the STN.
引用
收藏
页码:7130 / +
页数:16
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