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Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations

机译:乙酰胆碱和多巴胺信号模型差异改善神经表征。

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摘要

Biological and artificial neural networks (ANNs) represent input signals as patterns of neural activity. In biology, neuromodulators can trigger important reorganizations of these neural representations. For instance, pairing a stimulus with the release of either acetylcholine (ACh) or dopamine (DA) evokes long lasting increases in the responses of neurons to the paired stimulus. The functional roles of ACh and DA in rearranging representations remain largely unknown. Here, we address this question using a Hebbian-learning neural network model. Our aim is both to gain a functional understanding of ACh and DA transmission in shaping biological representations and to explore neuromodulator-inspired learning rules for ANNs. We model the effects of ACh and DA on synaptic plasticity and confirm that stimuli coinciding with greater neuromodulator activation are over represented in the network. We then simulate the physiological release schedules of ACh and DA. We measure the impact of neuromodulator release on the network's representation and on its performance on a classification task. We find that ACh and DA trigger distinct changes in neural representations that both improve performance. The putative ACh signal redistributes neural preferences so that more neurons encode stimulus classes that are challenging for the network. The putative DA signal adapts synaptic weights so that they better match the classes of the task at hand. Our model thus offers a functional explanation for the effects of ACh and DA on cortical representations. Additionally, our learning algorithm yields performances comparable to those of state-of-the-art optimisation methods in multi-layer perceptrons while requiring weaker supervision signals and interacting with synaptically-local weight updates.
机译:生物和人工神经网络(ANN)将输入信号表示为神经活动的模式。在生物学中,神经调节剂可以触发这些神经表征的重要重组。例如,将刺激物与乙酰胆碱(ACh)或多巴胺(DA)的释放配对会引起神经元对配对刺激物的响应的长期持续增长。 ACh和DA在重新排列表示形式中的功能作用仍然未知。在这里,我们使用Hebbian学习神经网络模型解决此问题。我们的目的是在塑造生物表征时获得对ACh和DA传递的功能性理解,并探索神经调节剂启发的ANN的学习规则。我们模拟了乙酰胆碱和DA对突触可塑性的影响,并确认与更大的神经调节剂激活相吻合的刺激在网络中被过度代表。然后,我们模拟ACh和DA的生理释放时间表。我们测量神经调节剂释放对网络表示及其对分类任务的性能的影响。我们发现,ACh和DA触发神经表示形式的明显变化,均改善了性能。假定的ACh信号会重新分配神经偏好,以便更多神经元编码对网络具有挑战性的刺激类别。推定的DA信号会适应突触权重,以便它们更好地匹配手头任务的类别。因此,我们的模型为ACh和DA对皮层表征的作用提供了功能上的解释。此外,我们的学习算法所产生的性能可与多层感知器中最先进的优化方法相媲美,同时需要较弱的监督信号并与突触局部权重更新进行交互。

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