Four investigators with long standing interest in ion channels and synaptic biology have come together to study effects of acetylcholine (ACh) on the activation and modulation of ion channels in the central nervous system. Changes in the effective concentration of ACh or in the number of ACh receptors (AChRs) have been associated with cognitive disorders, attention deficits, memory loss in normal subjects and in Alzheimer's patients, in Parkinson's Disease and in drug seeking behaviors. Work described in this Program Project includes analyses of nicotinic and muscarinic mechanisms that may shed light on these disorders. The Program developed naturally out of collaborative projects already begun by the four investigators. Together, we plan to investigate the regulation of nicotinic AChRs by neuregulins, a family of trophic factors expressed in the brain; the role of nicotinic and muscarinic receptors in modulating synaptic transmission; the modulation by ACh of several types of voltage gated ion channels; the distribution and role of G-protein coupled potassium channels (GIRKs) in regulating neuronal firing. Several different regions of the brain will be studied including the hippocampus, substantia nigra, ventral tegmental area, globus pallidus, medial habenula, interpeduncular nucleus, and cerebellum. Several preparations will be employed including freshly dissociated neurons, nerve cell cultures, brain slices and genetically altered mice. The primary tools are electrophysiological as we are primarily concerned with ACh induced changes in synaptic function and neuronal firing patterns. The projects are closely related and interactions have already emerged that greatly facilitate progress in each area. These interactions will broaden the scope of our work in the future.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS038312-05
Application #
6625533
Study Section
Special Emphasis Panel (ZNS1-SRB-W (01))
Project Start
1998-12-01
Project End
2004-11-30
Budget Start
2002-12-01
Budget End
2004-11-30
Support Year
5
Fiscal Year
2003
Total Cost
$1,019,523
Indirect Cost
Name
Harvard University
Department
Biology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Richards, Kathryn S; Swensen, Andrew M; Lipscombe, Diane et al. (2007) Novel CaV2.1 clone replicates many properties of Purkinje cell CaV2.1 current. Eur J Neurosci 26:2950-61
McDonough, Stefan I; Mori, Yasuo; Bean, Bruce P (2005) FPL 64176 modification of Ca(V)1.2 L-type calcium channels: dissociation of effects on ionic current and gating current. Biophys J 88:211-23
Martina, Marco; Yao, Gui Lan; Bean, Bruce P (2003) Properties and functional role of voltage-dependent potassium channels in dendrites of rat cerebellar Purkinje neurons. J Neurosci 23:5698-707
Swensen, Andrew M; Bean, Bruce P (2003) Ionic mechanisms of burst firing in dissociated Purkinje neurons. J Neurosci 23:9650-63
Blitz, Dawn M; Regehr, Wade G (2003) Retinogeniculate synaptic properties controlling spike number and timing in relay neurons. J Neurophysiol 90:2438-50
Blair, Nathaniel T; Bean, Bruce P (2003) Role of tetrodotoxin-resistant Na+ current slow inactivation in adaptation of action potential firing in small-diameter dorsal root ganglion neurons. J Neurosci 23:10338-50
Do, Michael Tri H; Bean, Bruce P (2003) Subthreshold sodium currents and pacemaking of subthalamic neurons: modulation by slow inactivation. Neuron 39:109-20
Mitterdorfer, Jorg; Bean, Bruce P (2002) Potassium currents during the action potential of hippocampal CA3 neurons. J Neurosci 22:10106-15
Blair, Nathaniel T; Bean, Bruce P (2002) Roles of tetrodotoxin (TTX)-sensitive Na+ current, TTX-resistant Na+ current, and Ca2+ current in the action potentials of nociceptive sensory neurons. J Neurosci 22:10277-90
Chen, Chinfei; Blitz, Dawn M; Regehr, Wade G (2002) Contributions of receptor desensitization and saturation to plasticity at the retinogeniculate synapse. Neuron 33:779-88

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