Topic: apical dendrites

Pyramidal neurons have apical dendrites that are both physically and electrically segregated from their cell bodies. In sensory cortex, these apical dendrites receive primarily top-down signals from associative and motor regions, while the cell bodies and nearby dendrites of these same pyramidal neurons are mostly targeted by bottom-up or locally recurrent inputs from the sensory periphery. Due to these differences, a number of theories in computational neuroscience postulate a unique role for apical dendrites in shaping sensory processing and plasticity in the face of new or surprising stimul

Synaptic plasticity is believed to be a key physiological mechanism for learning. It is well-established that it depends on pre and postsynaptic activity. However, models that rely solely on pre and postsynaptic activity for synaptic changes have, to date, not been able to account for learning complex tasks that demand hierarchical networks. Here, we show that if synaptic plasticity is regulated by high-frequency bursts of spikes, then neurons higher in the hierarchy can coordinate the plasticity of lower-level connections. Using simulations and mathematical analyses, we demonstrate that, when

Synaptic plasticity is believed to be a key physiological mechanism for learning. It is well-established that it depends on pre and postsynaptic activity. However, models that rely solely on pre and postsynaptic activity for synaptic changes have, to date, not been able to account for learning complex tasks that demand hierarchical networks. Here, we show that if synaptic plasticity is regulated by high-frequency bursts of spikes, then neurons higher in the hierarchy can coordinate the plasticity of lower-level connections. Using simulations and mathematical analyses, we demonstrate that, when

Artificial recurrent neural networks (RNNs) are difficult to train due to their tendency towards instability, and common training algorithms that tame such networks are not biologically plausible, i.e., back-propagation through time (BPTT). Node perturbation learning in combination with local Hebbian weight updates has been shown to approximate BPTT [1] and, thus, could achieve similar performance while being biologically plausible. However, where these perturbations could arise from and how they are utilized within neurons remains obscure. For years, the neuroscientific community has known ab