ABSTRACT
Gamma oscillations are believed to underlie cognitive processes by shaping the formation of transient neuronal partnerships on a millisecond scale. These oscillations are coupled to the phase of breathing cycles in several brain areas, possibly reflecting local computations driven by sensory inputs sampled at each breath. Here, we investigated the mechanisms and functions of gamma oscillations in the piriform (olfactory) cortex of awake mice to understand their dependence on breathing and how they relate to local spiking activity. Mechanistically, we find that respiration drives gamma oscillations in the piriform cortex, which correlate with local feedback inhibition and result from recurrent connections between local excitatory and inhibitory neuronal populations. Moreover, respiration-driven gamma oscillations are triggered by the activation of mitral/tufted cells in the olfactory bulb and are abolished during ketamine/xylazine anesthesia. Functionally, we demonstrate that they locally segregate neuronal assemblies through a winner-take-all computation leading to sparse odor coding during each breathing cycle. Our results shed new light on the mechanisms of gamma oscillations, bridging computation, cognition, and physiology.
The cerebral cortex is the most recently evolved region of the mammalian brain. There, millions of neurons can synchronize their activity to create brain waves, a series of electric rhythms associated with various cognitive functions. Gamma waves, for example, are thought to be linked to brain processes which require distributed networks of neurons to communicate and integrate information. These waves were first discovered in the 1940s by researchers investigating brain areas involved in olfaction, and they are thought to be important for detecting and recognizing smells. Yet, scientists still do not understand how these waves are generated or what role they play in sensing odors. To investigate these questions, González et al. used a battery of computational approaches to analyze a large dataset of brain activity from awake mice. This revealed that, in the cortical region dedicated to olfaction, gamma waves arose each time the animals completed a breathing cycle that is, after they had sampled the air by breathing in. Each breath was followed by certain neurons relaying olfactory information to the cortex to activate complex cell networks; this included circuits of cells known as feedback interneurons, which can switch off weakly activated neurons, including ones that participated in activating them in the first place. The respiration-driven gamma waves derived from this 'feedback inhibition' mechanism. Further work then examined the role of the waves in olfaction. Smell identification relies on each odor activating a unique set of cortical neurons. The analyses showed that gamma waves acted to select and amplify the best set of neurons for representing the odor sensed during a sniff, and to quieten less relevant neurons. Loss of smell is associated with many conditions which affect the brain, such as Alzheimer's disease or COVID-19. By shedding light on the neuronal mechanisms that underpin olfaction, the work by González et al. could help to better understand how these impairments emerge, and how the brain processes other types of complex information.
Subject(s)
Olfactory Cortex , Piriform Cortex , Mice , Animals , Smell/physiology , Olfactory Bulb/physiology , Respiration , OdorantsABSTRACT
This work experimentally analyzes the learning and retrieval capabilities of the diluted metric attractor neural network when applied to collections of fingerprint images. The computational cost of the network decreases with the dilution, so we can increase the region of interest to cover almost the complete fingerprint. The network retrieval was successfully tested for different noisy configurations of the fingerprints, and proved to be robust with a large basin of attraction. We showed that network topologies with a 2D-Grid arrangement adapt better to the fingerprints spatial structure, outperforming the typical 1D-Ring configuration. An optimal ratio of local connections to random shortcuts that better represent the intrinsic spatial structure of the fingerprints was found, and its influence on the retrieval quality was characterized in a phase diagram. Since the present model is a set of nonlinear equations, it is possible to go beyond the naïve static solution (consisting in matching two fingerprints using a fixed distance threshold value), and a crossing evolution of similarities was shown, leading to the retrieval of the right fingerprint from an apparently more distant candidate. This feature could be very useful for fingerprint verification to discriminate between fingerprints pairs.