Musall Simon, Haiss Florent, Weber Bruno, von der Behrens Wolfger
Brain Research Institute.
Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
Cereb Cortex. 2017 Jan 1;27(1):863-876. doi: 10.1093/cercor/bhv283.
Stimulus-specific adaptation (SSA) to repetitive stimulation has been proposed to separate behaviorally relevant features from a stream of continuous sensory information. However, the exact mechanisms giving rise to SSA and cortical deviance detection are not well understood. We therefore used an oddball paradigm and multicontact electrodes to characterize single-neuron and local field potential responses to various deviant stimuli across the rat somatosensory cortex. Changing different single-whisker stimulus features evoked robust SSA in individual cortical neurons over a wide range of stimulus repetition rates (0.25-80 Hz). Notably, SSA was weakest in the granular input layer and significantly stronger in the supra- and infragranular layers, suggesting that a major part of SSA is generated within cortex. Moreover, we found a small subset of neurons in the granular layer with a deviant-specific late response, occurring roughly 200 ms after stimulus offset. This late deviant response exhibited true-deviance detection properties that were not explained by depression of sensory inputs. Our results show that deviant responses are actively amplified within cortex and contain an additional late component that is sensitive for context-specific sensory deviations. This strongly implicates deviance detection as a feature of intracortical stimulus processing beyond simple sensory input depression.
刺激特异性适应(SSA)对重复刺激的作用被认为是从连续的感觉信息流中分离出行为相关特征。然而,引发SSA和皮质偏差检测的确切机制尚未完全清楚。因此,我们采用了oddball范式和多触点电极来表征大鼠体感皮层中单个神经元和局部场电位对各种偏差刺激的反应。改变不同的单根触须刺激特征,在广泛的刺激重复率(0.25 - 80 Hz)范围内,能在单个皮质神经元中诱发强烈的SSA。值得注意的是,SSA在颗粒状输入层中最弱,而在颗粒上层和颗粒下层中明显更强,这表明SSA的主要部分是在皮质内产生的。此外,我们在颗粒层中发现了一小部分神经元具有偏差特异性的晚期反应,大约在刺激结束后200毫秒出现。这种晚期偏差反应表现出真正的偏差检测特性,并非由感觉输入的抑制所解释。我们的结果表明,偏差反应在皮质内被积极放大,并且包含一个额外的晚期成分,该成分对特定情境的感觉偏差敏感。这强烈暗示偏差检测是皮质内刺激处理的一个特征,而非简单的感觉输入抑制。