Search bioRxiv⌕ Search

Biology subjects

Miehl, C.

Publications and source records attributed to Miehl, C..

2 recordsLinked to original sources

Stability and learning in excitatory synapses by nonlinear inhibitory plasticity

Synaptic changes underlie learning and memory formation in the brain. But synaptic plasticity of excitatory synapses on its own is unstable, leading to unlimited growth of synaptic strengths without additional homeostatic mechanisms. To control excitatory synaptic strengths we propose a novel form of synaptic plasticity at inhibitory synapses. We identify two key features of inhibitory plasticity, dominance of inhibition over excitation and a nonlinear dependence on the firing rate of postsynaptic excitatory neurons whereby inhibitory synaptic strengths change in the same direction as excitatory synaptic strengths. We demonstrate that the stable synaptic strengths realized by this novel inhibitory plasticity achieve a fixed excitatory/inhibitory set-point in agreement with experimental results. Applying a disinhibitory signal can gate plasticity and lead to the generation of receptive fields and strong bidirectional connectivity in a recurrent network. Hence, a novel form of nonlinear inhibitory plasticity can simultaneously stabilize excitatory synaptic strengths and enable learning upon disinhibition.

neuroscience↗

The generation of cortical novelty responses through inhibitory plasticity

Animals depend on fast and reliable detection of novel stimuli in their environment. Indeed, neurons in multiple sensory areas respond more strongly to novel in comparison to familiar stimuli. Yet, it remains unclear which circuit, cellular and synaptic mechanisms underlie those responses. Here, we show that inhibitory synaptic plasticity readily generates novelty responses in a recurrent spiking network model. Inhibitory plasticity increases the inhibition onto excitatory neurons tuned to familiar stimuli, while inhibition for novel stimuli remains low, leading to a network novelty response. Generated novelty responses do not depend on the exact temporal structure but rather on the distribution of presented stimuli. By including tuning of inhibitory neurons, the network further captures stimulus-specific adaptation. Finally, we suggest that disinhibition can control the amplification of novelty responses. Therefore, inhibitory plasticity provides a flexible, biologically-plausible mechanism to detect the novelty of bottom-up stimuli, enabling us to make numerous experimentally testable predictions.

neuroscience↗