Inhibitory neuronal networks broaden with age and experience
Prior to this study, scientists had very little understanding of how sensory maps of inhibitory circuits develop or mature.
All animals, including humans, encounter various external stimuli such as smell, vision, taste and touch, all of which are systematically represented in different regions of the brain as distinct sensory maps.
Currently, it is believed that sensory neuronal maps are diffusely laid down during gestation and then fine-tuned during a critical period in development and later on in life depending on an individual’s sensorial experiences. For instance, since rodents rely heavily on smell to navigate their environment, every mouse whisker is represented as a distinct segment in the brain cortex.
Using a combination of optogenetics and calcium imaging, scientists found that inhibitory neurons in the mice olfactory system also exhibit changes in network organization and function when exposed to different scents. However, surprisingly, contrary to excitatory circuits, inhibitory networks broaden as they age and in response to various sensory stimuli.
Mice have a keen sense of smell. They are able to discern individual scents from a large array of olfactory inputs, largely due to the complex populations of inhibitory neurons they possess. Inhibitory neurons in the olfactory circuit are among the few neurons that continue to be added and integrated into existing circuits after birth.
It was found that mature granule cell neurons receive stronger connections than immature neurons do. Moreover, mature inhibitory neurons were far more responsive to a wider range of complex odors.
This developmental broadening of inhibitory neurons also helped to regulate the activity of excitatory neurons. The authors compare inhibitory neuronal networks to the web of traffic lights that help to optimally control the flow of traffic on roads (excitatory sensory maps) in a neighborhood or city (brain).
By identifying the fundamental principle that govern the formation and regulation of inhibitory networks, Arenkiel and colleagues have now provided researchers with a framework to understand how brain circuits respond in a normal situation. This will serve as a critical baseline to understand what goes wrong in many neurological diseases, and will help to identify specific strategies to restore excitatory and/ inhibitory network imbalances.