Abstract
To test the importance of a certain cell type or brain area it is common to make a “lack of function” experiment in which the neuronal population of interest is inhibited. Here we review physiological and methodological constraints for making controlled perturbations using the corticothalamic circuit as an example. The brain with its many types of cells and rich interconnectivity offers many paths through which a perturbation can spread within a short time. To understand the side effects of the perturbation one should record from those paths. We find that ephaptic effects, gap-junctions, and fast chemical synapses are so fast that they can react to the perturbation during the few milliseconds it takes for an opsin to change the membrane potential. The slow chemical synapses, astrocytes, extracellular ions and vascular signals, will continue to give their physiological input for around 20 ms before they also react to the perturbation. Although we show that some pathways can react within milliseconds the strength/speed reported in this review should be seen as an upper bound since we have omitted how polysynaptic signals are attenuated. Thus the number of additional recordings that has to be made to control for the perturbation side effects is expected to be fewer than proposed here. To summarize, the reviewed literature not only suggests that it is possible to make controlled “lack of function” experiments, but, it also suggests that such a “lack of function” experiment can be used to measure the context of local neural computations.
Highlights
Many times in neuroscience it is necessary to prove the importance of one type of population of neurons
As a result of inhibiting the source population (S) the activity in a downstream target population (T) will be modified (Figure 1A). This remaining activity resembles the background activity that is coming from all over the brain except from the inhibited area. Since this remaining background activity defines the context of neural computations we propose that it should be estimated
Before we review the latency of those side-effects we first examine the speed of optogenetic inhibition
Summary
Comparison between Inhibitory Opsins and Neural Circuits. Front. We review physiological and methodological constraints for making controlled perturbations using the corticothalamic circuit as an example. The brain with its many types of cells and rich interconnectivity offers many paths through which a perturbation can spread within a short time. To understand the side effects of the perturbation one should record from those paths. We find that ephaptic effects, gap-junctions, and fast chemical synapses are so fast that they can react to the perturbation during the few milliseconds it takes for an opsin to change the membrane potential. The slow chemical synapses, astrocytes, extracellular ions and vascular signals, will continue to give their physiological input for around 20 ms before they react to the perturbation. The number of additional recordings that has to be made to control for the perturbation side effects is expected to be fewer than proposed here.
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