Grant: Discovery Grants Program - Individual
University of Western Ontario
$55,000.00
The Neural Basis of Audiovisual Temporal Processing and Perception: From Cortical Networks to Cellular Mechanisms
FY 2019-20
Summary
In providing us with a more complete sensory experience, our brains naturally merge information from our different senses. In situations when an auditory and visual stimulus occur within ~100 ms of each other, we often perceive that they happened at the same moment, even though they were actually offset in time. Although this integration of closely-timed audiovisual stimuli can offer certain behavioural advantages, such as improved detection, identification and localization of objects in the environment, an overly broad window of temporal integration can be problematic, as information from truly separate events may not be correctly perceived as such. Recent human studies have suggested that the precision of perceptual binding of audiovisual stimuli is regulated by neural oscillations, especially in the gamma-band (>30 Hz), within the audiovisual cortex; a phenomenon that has been suggested to depend on local GABAergic neurotransmission. At present, however, the specific brain circuits and cellular mechanisms that regulate the putative oscillatory activity subserving audiovisual perceptual binding remain elusive, in part because the field has lacked suitable animal models for invasive studies. Toward that goal, my lab has recently established that rats represent an excellent model to study the neural basis of audiovisual temporal processing at the level of single neurons, local microcircuits and sensory perception. For example, using pharmacological manipulations, we revealed that GABAergic neurotransmission in the rat audiovisual cortex (V2L) not only controls the precise timing of audiovisual integration, but it also affects the window of time over which perceptual binding occurs. That said, given the complexity of the local GABAergic microcircuits and the various GABA-A receptor subunits expressed at specific locations on cortical pyramidal neurons, additional work is needed to uncover the cellular mechanisms by which GABAergic neurotransmission controls the temporal integration of audiovisual stimuli into a unified percept. In this proposal, we will use an advanced approach combining optogenetics/shRNA manipulation + in vivo electrophysiological recordings in behaving rats to address the following objectives: (1) To identify how unisensory vs. multisensory thalamocortical projections to the V2L cortex contribute to audiovisual temporal processing and perception; (2) To investigate the role of GABAergic interneurons within the V2L cortex on audiovisual temporal processing and perception, and; (3) To determine which of the specific GABA-A receptor subunits expressed on pyramidal neurons in V2L cortex are responsible for fine-tune audiovisual temporal processing and perception. Ultimately, given my lab's expertise, infrastructure and recent progress, no other lab in the world is as well-positioned to tackle the long-standing question: How does the mammalian brain integrate closely-timed auditory and visual stimuli into a unified percept?
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2019-06085
Name nom
Allman, Brian
Department département
Anatomy and Cell Biology
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2019
Competition year année de concours
2019
Award amount
55000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1210
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Psychology
Area of application fr
Psychologie
Research subject code
6301
Research subject group en
Psychology
Research subject group fr
Psychologie
Research subject en
Sensory systems and perception
Research subject fr
Systèmes sensoriels et perception
Installment
inst:1 - 5
Partie
1
Nb partie
5
Application title
The Neural Basis of Audiovisual Temporal Processing and Perception: From Cortical Networks to Cellular Mechanisms
Keyword
NSERC
Application summary
In providing us with a more complete sensory experience, our brains naturally merge information from our different senses. In situations when an auditory and visual stimulus occur within ~100 ms of each other, we often perceive that they happened at the same moment, even though they were actually offset in time. Although this integration of closely-timed audiovisual stimuli can offer certain behavioural advantages, such as improved detection, identification and localization of objects in the environment, an overly broad window of temporal integration can be problematic, as information from truly separate events may not be correctly perceived as such. Recent human studies have suggested that the precision of perceptual binding of audiovisual stimuli is regulated by neural oscillations, especially in the gamma-band (>30 Hz), within the audiovisual cortex; a phenomenon that has been suggested to depend on local GABAergic neurotransmission. At present, however, the specific brain circuits and cellular mechanisms that regulate the putative oscillatory activity subserving audiovisual perceptual binding remain elusive, in part because the field has lacked suitable animal models for invasive studies. Toward that goal, my lab has recently established that rats represent an excellent model to study the neural basis of audiovisual temporal processing at the level of single neurons, local microcircuits and sensory perception. For example, using pharmacological manipulations, we revealed that GABAergic neurotransmission in the rat audiovisual cortex (V2L) not only controls the precise timing of audiovisual integration, but it also affects the window of time over which perceptual binding occurs. That said, given the complexity of the local GABAergic microcircuits and the various GABA-A receptor subunits expressed at specific locations on cortical pyramidal neurons, additional work is needed to uncover the cellular mechanisms by which GABAergic neurotransmission controls the temporal integration of audiovisual stimuli into a unified percept. In this proposal, we will use an advanced approach combining optogenetics/shRNA manipulation + in vivo electrophysiological recordings in behaving rats to address the following objectives: (1) To identify how unisensory vs. multisensory thalamocortical projections to the V2L cortex contribute to audiovisual temporal processing and perception; (2) To investigate the role of GABAergic interneurons within the V2L cortex on audiovisual temporal processing and perception, and; (3) To determine which of the specific GABA-A receptor subunits expressed on pyramidal neurons in V2L cortex are responsible for fine-tune audiovisual temporal processing and perception. Ultimately, given my lab's expertise, infrastructure and recent progress, no other lab in the world is as well-positioned to tackle the long-standing question: How does the mammalian brain integrate closely-timed auditory and visual stimuli into a unified percept?