The long-term goal of the experiments described in this proposal is to identify sources of plasticity of voltage-activated calcium (Ca) channels. The N-type Ca channel has been found only in nerve cells and neuronally-derived tissues, is associated with the regulation of neurotransmitter synthesis and release from presynaptic nerve endings, and in turn, is modulated by many of these same neurotransmitters. N-type Ca channels are the most highly modulated Ca channel in the brain in that more pathways exist for modulation of this Ca channel than for any other, and because of this, are thought to play a special role in the brain. N-type Ca channels display endogeous, heterogeneous activity, called modes, where measured unitary conductance and kinetics vary from mode to mode. Each mode can last for seconds to minutes. At least six modes have been identified and are a source of neural plasticity at the level of the N-type Ca channel.
The specific aims of this project are to 1) identify the causes of modal gating and permeation of N-type Ca currents that give rise to channel plasticity, 2) determine whether modulation of N-type Ca channel behavior by neurotransmitters and cellular signals alters the frequency of occurrence and/or the biophysical characteristics of these modes, and 3) identify differences between the subunit composition of N-type Ca channels in sympathetic neurons and in the brain and determine whether differences in the expression level of the subunits is an additional source of plasticity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29NS034195-05
Application #
2891986
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Program Officer
Chiu, Arlene Y
Project Start
1995-06-01
Project End
2001-07-31
Budget Start
1999-06-01
Budget End
2001-07-31
Support Year
5
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Physiology
Type
Schools of Medicine
DUNS #
660735098
City
Worcester
State
MA
Country
United States
Zip Code
01655
Roberts-Crowley, Mandy L; Rittenhouse, Ann R (2009) Arachidonic acid inhibition of L-type calcium (CaV1.3b) channels varies with accessory CaVbeta subunits. J Gen Physiol 133:387-403
Mitra-Ganguli, Tora; Vitko, Iuliia; Perez-Reyes, Edward et al. (2009) Orientation of palmitoylated CaVbeta2a relative to CaV2.2 is critical for slow pathway modulation of N-type Ca2+ current by tachykinin receptor activation. J Gen Physiol 134:385-96
Roberts-Crowley, Mandy L; Mitra-Ganguli, Tora; Liu, Liwang et al. (2009) Regulation of voltage-gated Ca2+ channels by lipids. Cell Calcium 45:589-601
Heneghan, John F; Mitra-Ganguli, Tora; Stanish, Lee F et al. (2009) The Ca2+ channel beta subunit determines whether stimulation of Gq-coupled receptors enhances or inhibits N current. J Gen Physiol 134:369-84
Liu, Liwang; Gonzalez, Pamela K; Barrett, Curtis F et al. (2003) The calcium channel ligand FPL 64176 enhances L-type but inhibits N-type neuronal calcium currents. Neuropharmacology 45:281-92
Liu, Liwang; Rittenhouse, Ann R (2003) Arachidonic acid mediates muscarinic inhibition and enhancement of N-type Ca2+ current in sympathetic neurons. Proc Natl Acad Sci U S A 100:295-300
N'Gouemo, P; Rittenhouse, A R (2000) Biophysical and pharmacological characterization of voltage-sensitive calcium currents in neonatal rat inferior colliculus neurons. Neuroscience 96:753-65