Ascending neurotransmitter systems from the brainstem and basal forebrain regulate activities in cortical networks through direct actions on GABAergic inhibitory interneurons. Data suggest that neurotransmitters such as acetylcholine (ACh) and serotonin (5-HT) can selectively activate particular subgroups of inhibitory interneurons through different classes of postsynaptic receptors and thus modify the flow of information in cortical circuits. These experiments will examine effects of ACh and 5-HT on low threshold spike (LTS) and fast spiking aboutS) GABAergic interneurons in layer V of rat visual cortex. about Patch-clamp techniques will be used to obtain whole cell recordings to evaluate the subtypes of cholinergic and serotonergic receptors on different subclasses of interneurons and the nature of the postsynaptic responses. In paired recordings, unitary inhibitory postsynaptic currents will be evoked on pyramidal neurons and presynaptic effects of cholinergic and serotonergic agonists will be assessed. Intracellular labeling with biocytin combined with immunocytochemistry for calcium binding proteins and neuropeptides will be used along with electrophysiological behavior to classify interneurons to further test the hypothesis that subgroups of interneurons are selectively modulated by ACh and 5-HT. Given the importance of the GABAergic inhibitory network in information processing and pathophysiologic processes such as epileptogenesis, and the observation that these ascending neurotransmitter systems may be altered anatomically following cortical lesions, information regarding action of modulators like ACh and serotonin is critical to our understanding of normal and disordered cortical function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS039579-01A1
Application #
6200778
Study Section
Special Emphasis Panel (ZRG1-BDCN-2 (01))
Program Officer
Jacobs, Margaret
Project Start
2000-07-10
Project End
2004-06-30
Budget Start
2000-07-10
Budget End
2001-06-30
Support Year
1
Fiscal Year
2000
Total Cost
$337,210
Indirect Cost
Name
Stanford University
Department
Neurology
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Gu, Feng; Parada, Isabel; Shen, Fran et al. (2017) Structural alterations in fast-spiking GABAergic interneurons in a model of posttraumatic neocortical epileptogenesis. Neurobiol Dis 108:100-114
Brill, Julia; Mattis, Joanna; Deisseroth, Karl et al. (2016) LSPS/Optogenetics to Improve Synaptic Connectivity Mapping: Unmasking the Role of Basket Cell-Mediated Feedforward Inhibition. eNeuro 3:
Takahashi, D Koji; Gu, Feng; Parada, Isabel et al. (2016) Aberrant excitatory rewiring of layer V pyramidal neurons early after neocortical trauma. Neurobiol Dis 91:166-81
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Jin, Xiaoming; Jiang, Kewen; Prince, David A (2014) Excitatory and inhibitory synaptic connectivity to layer V fast-spiking interneurons in the freeze lesion model of cortical microgyria. J Neurophysiol 112:1703-13
Mantoan Ritter, Laura; Golshani, Peyman; Takahashi, Koji et al. (2014) WONOEP appraisal: optogenetic tools to suppress seizures and explore the mechanisms of epileptogenesis. Epilepsia 55:1693-702
Ma, Yunyong; Ramachandran, Anu; Ford, Naomi et al. (2013) Remodeling of dendrites and spines in the C1q knockout model of genetic epilepsy. Epilepsia 54:1232-9
Mao, Rong; Schummers, James; Knoblich, Ulf et al. (2012) Influence of a subtype of inhibitory interneuron on stimulus-specific responses in visual cortex. Cereb Cortex 22:493-508
Ma, Yunyong; Prince, David A (2012) Functional alterations in GABAergic fast-spiking interneurons in chronically injured epileptogenic neocortex. Neurobiol Dis 47:102-13
Faria, Leonardo C; Parada, Isabel; Prince, David A (2012) Interneuronal calcium channel abnormalities in posttraumatic epileptogenic neocortex. Neurobiol Dis 45:821-8

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