Abstract
A leading theory holds that neurodevelopmental brain disorders arise from imbalances in excitatory and inhibitory (E/I) brain circuitry. However, it is unclear whether this one-dimensional model is rich enough to capture the multiple neural circuit alterations underlying brain disorders. Here, we combined computational simulations with analysis of in vivo two-photon Ca2+ imaging data from somatosensory cortex of Fmr1 knock-out (KO) mice, a model of Fragile-X Syndrome, to test the E/I imbalance theory. We found that: (1) The E/I imbalance model cannot account for joint alterations in the observed neural firing rates and correlations; (2) Neural circuit function is vastly more sensitive to changes in some cellular components over others; (3) The direction of circuit alterations in Fmr1 KO mice changes across development. These findings suggest that the basic E/I imbalance model should be updated to higher dimensional models that can better capture the multidimensional computational functions of neural circuits.
Original language | English |
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Journal | eLife |
Volume | 6 |
DOIs | |
Publication status | Published (in print/issue) - 31 Oct 2017 |
Keywords
- Action Potentials
- Animals
- Calcium/analysis
- Computer Simulation
- Fragile X Mental Retardation Protein/genetics
- Fragile X Syndrome/pathology
- Mice
- Mice, Knockout
- Neural Inhibition
- Neural Pathways/pathology
- Optical Imaging
- Somatosensory Cortex/pathology