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Grant: Research Tools and Instruments - Category 1 (<$150,000)

York University

$60,750.00

Measuring functional networks of multiple brain cells with a fine-scale triade electrode system during higher attentional task performance

FY 2011-12

Summary
The brain contains billions of cells, but at any moment in time only small subsets of these cells become co-active. These subsets of cells form functional networks that co-activate only over few hundreds of milliseconds when the brain engages in focused attention towards particular stimuli in our environment. Our research equipment promises to elucidate the mechanisms that underlie the dynamic formation of these selective functional networks of cells in the brain by using recently developed fine-scale electrophysiological techniques. To understand the temporal dynamics of network formation, it is pivotal to record from many, isolated cells at the same time as animals switch from a non-selective state (e.g. none-attentive idling), to a selective state (e.g. focused attention). During this switching of states, cells exchange information and become co-active, but it has remained one of the big challenges in systems neuroscience to measure many co-active cells while animals perform higher attentional functions. The major challenges lie at three fronts: First, the small subset of cells whose activity carries relevant information need to be identified. Second, these cells need to be clearly isolated from the dense matrix of neighboring cells by using electrophysiological probes with a high signal-to-noise ratio. And thirdly, these cells need to be kept isolated for prolonged times to be able to infer network mechanisms and their functional importance for behavior in controlled attention experiments. This application proposes the use of a triade electrode drive system that surmounts these challenges with maximal efficiency. Each triade system allows to manipulate independently the depth of three high signal-to-noise electrodes. By combining several triade systems, it becomes feasible to identify, isolate and stabilize multiple single cells at the same time. The time-efficiency of the system allows to measure networks of single cells for prolonged times while subjects perform well controlled attention experiments - promising unprecedented insights into the mechanisms underlying the formation of selective functional networks.
Program
Research Tools and Instruments - Category 1 (<$150,000)
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
423394-2012
Name nom
Womelsdorf, Thilo
Department département
Biology
Organization id
38
Institution établissement
York University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2011
Competition year année de concours
2012
Award amount
60750
Program id
EQPEQ
Program nane en
Research Tools and Instruments - Category 1 (<$150,000)
Program name fr
Outils et instruments de recherche - catégorie 1 (<150 000$)
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5501
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Neurophysiology
Research subject fr
Neurophysiologie
Partie
1
Nb partie
1
Application title
Measuring functional networks of multiple brain cells with a fine-scale triade electrode system during higher attentional task performance
Keyword
NSERC
Application summary
The brain contains billions of cells, but at any moment in time only small subsets of these cells become co-active. These subsets of cells form functional networks that co-activate only over few hundreds of milliseconds when the brain engages in focused attention towards particular stimuli in our environment. Our research equipment promises to elucidate the mechanisms that underlie the dynamic formation of these selective functional networks of cells in the brain by using recently developed fine-scale electrophysiological techniques. To understand the temporal dynamics of network formation, it is pivotal to record from many, isolated cells at the same time as animals switch from a non-selective state (e.g. none-attentive idling), to a selective state (e.g. focused attention). During this switching of states, cells exchange information and become co-active, but it has remained one of the big challenges in systems neuroscience to measure many co-active cells while animals perform higher attentional functions. The major challenges lie at three fronts: First, the small subset of cells whose activity carries relevant information need to be identified. Second, these cells need to be clearly isolated from the dense matrix of neighboring cells by using electrophysiological probes with a high signal-to-noise ratio. And thirdly, these cells need to be kept isolated for prolonged times to be able to infer network mechanisms and their functional importance for behavior in controlled attention experiments. This application proposes the use of a triade electrode drive system that surmounts these challenges with maximal efficiency. Each triade system allows to manipulate independently the depth of three high signal-to-noise electrodes. By combining several triade systems, it becomes feasible to identify, isolate and stabilize multiple single cells at the same time. The time-efficiency of the system allows to measure networks of single cells for prolonged times while subjects perform well controlled attention experiments - promising unprecedented insights into the mechanisms underlying the formation of selective functional networks.