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Frequency-Dependent Inversion of Net Striatal Output by Endocannabinoid-Dependent Plasticity at Different Synaptic Inputs

机译:内源性大麻素可塑性在不同突触输入下的净纹状体输出的频率相关反转

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摘要

Understanding how striatal neurons integrate glutamatergic and GABAergic inputs is essential for understanding the control of movement and the formation of striatal-based memories. Here we show that GABAergic synapses on striatal medium spiny neurons (MSNs) are more sensitive than glutamatergic synapses on the same cells to endocannabinoid (eCB) signaling, and that protocols that induce short-lasting cannabinoid 1 receptor (CB1R)-dependent depression at glutamatergic synapses are sufficient to induce long-term depression (LTD) at GABAergic synapses. We also show that the frequency and duration of glutamatergic input are strong determinants of the net effect of eCB signaling, and key factors in determining if LTD has a net disinhibitory or inhibitory action in striatum. Plastic changes in net output from striatal MSNs are thus a complex function of disinhibitory and inhibitory LTD combined with other forms of synaptic plasticity such as long-term potentiation at excitatory synapses.
机译:了解纹状体神经元如何整合谷氨酸能和GABA能量输入对于理解运动的控制和基于纹状体的记忆的形成至关重要。在这里我们显示,纹状体中棘神经元(MSNs)上的GABA能突触比内细胞上的谷氨酸能突触对内源性大麻素(eCB)信号更敏感,并且该协议在谷氨酸能诱导短时大麻素1受体(CB1R)依赖性抑郁突触足以诱发GABA能突触的长期抑郁症(LTD)。我们还表明,谷氨酸能输入的频率和持续时间是eCB信号净效应的强力决定因素,也是确定LTD在纹状体中是否具有净抑制作用或抑制作用的关键因素。因此,纹状体MSN净输出的塑性变化是去抑制和抑制LTD与其他形式的突触可塑性(例如在兴奋性突触中的长期增强)结合的复杂功能。

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