H2020Individual fellowship2018–2021

CoDEC · Decoding the development of physiologic and epileptic cognitive neural networks

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2018-06-01 → 2021-05-31
EU contribution
€239,861
Participants
2
Scheme
MSCA-IF-GF

Lines connect the coordinator with its partners.

Results in brief

Decoding the development of physiologic and epileptic cognitive neural networks

Cognitive dysfunction is a hallmark of many neuropsychiatric diseases, with potentially devastating effects on functional outcomes and quality of life in affected patients. The neural networks underlying cognitive processes are characterized by bidirectional communication between numerous brain regions, allowing integration and advanced processing of multimodal sensory information. Our main objective is to gain insight into the operations of these cognitive neuronal networks by examining intra- and inter-cortical communication across development. Effective communication between brain regions requires the creation of discrete temporal windows for dynamic routing of neural signals. Oscillatory activity is an efficient means of creating epochs of synchrony within and between neural networks, providing a means to boost or suppress information transfer. This precisely coordinated interplay of inter-cortical oscillations is not an inborn property of the brain’s neural networks. Maturation of the cortical networks in a developing organism is highly activity-dependent, with synchronized neural activity playing a crucial role in the establishment of stable structural and functional connections. The emergence and refinement of cognitive functions in humans is associated with the appearance of oscillations in specific frequency bands and enhanced long-range synchronization of this oscillatory activity. Preterm babies between the 24th and 37th gestational weeks exhibit a fast frequency alpha-beta spindle-like (8–25 Hz) rhythmic activity superimposed on 0.3–1.5 Hz slow delta waves called delta brush. This pattern is involved in inaugurating synchrony within and between cortical areas, and abnormalities in its occurrence are associated with improper cortical maturation. Mice are a useful model for studying the development of brain activity, since a substantial portion of cortical development that occurs prior to birth in humans occurs after birth in mice. However, to date, in vivo study of rodent electrophysiology has been severely challenged due to the size and fragility of the mouse pup’s brain. Our second objective was the technological development and use of a novel electrocorticography (ECoG) array called NeuroGrid, which allows us an unprecedented spatiotemporal resolution in our recordings, while acquiring neural data simultaneously from multiple functionally diverse cortical regions. The technological advantages of NeuroGrid and the outstanding options when combining it with other techniques positions us perfectly to initiate a novel characterization of rodent neurophysiology, with important potential applications for human health.

Data: CORDIS, © European Union

Project objective

The neuronal networks that comprise the mammalian brain are immature at the time of birth, and are shaped by genetic and environmental influences over the course of postnatal development. Human brain maturation occurs over a particularly extended period of time, especially in cortical areas involved in integrated information processing and cognition. The proper maturation of intra- and inter-cortical networks is necessary for efficient and appropriate brain function. Thus, when brain development goes awry, neuropsychiatric disorders such as epilepsy, intellectual disability, and autism can result.Direct investigation of immature neural networks would allow us to better understand the physiological and pathological processes that occur during development. In vivo neurophysiology in animal models is a powerful method to explore both the population synaptic activity and neural spiking of intact neural networks. However, this approach is challenging in developing organisms due to the small size and fragile nature of the brain. Here, we bring together advancements in neural interface design and neurophysiological recording to overcome this challenge and realize the principal goal of this project: to determine the neurophysiologic patterns that characterize normal maturation of inter-cortical communication and identify how these patterns are deranged in the presence of genetic predisposition to neuropsychiatric disease. Data generated using this approach has the potential to improve diagnosis of developmental neuropsychiatric disorders, identify the earliest window for therapeutic intervention, and suggest novel therapeutic strategies.

Original text from CORDIS.

Participants

  • UNIVERSITAETSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAET MAINZ · MainzCoordinatorGermany
  • TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK · New YorkUnited States

Links

Data: CORDIS, © European Union