NMDA receptor activation is associated with many critical physiological and pathophysiological processes in the brain. Consequently, several endogenous modulating agents tightly regulate NMDA receptor function. Studies that investigate the molecular mechanisms of NMDA receptor modulation are important for characterizing the structural and functional properties of this protein. These investigations can also lead to the development of novel drugs to treat neuronal disorders in which abnormal NMDA receptor activation has been implicated. In this proposal, we expand our studies of NMDA receptor modulation to a novel form of functional regulation of this ion channel. We have observed that brief focal pulses of light potentiate NMDA receptor-mediated physiological responses in cultured neurons. In order to characterize this phenomenon, we have designed a series of studies to address the following Specific Aims: (1) To define the properties of light modulation of NMDA receptor function; (2) To establish whether light alteration of NMDA receptor function is mediated via a novel modulatory site; (3) To determine the properties of light modulation in recombinant NMDA receptors; and (4) To assess whether light modulation of the NMDA receptor has physiological significance in retinal function. Experiments outlined here utilize well-defined culture systems of rat cerebral cortex and retinal ganglion cells. We will perform electrophysiological measurements in these preparations, as in well as in non-neuronal mammalian cell lines that transiently express recombinant NMDA receptors. Additional studies will be performed on retinal slices. The long-term goals of this research program are to characterize fully NMDA receptor function. Results from these studies could facilitate the design of new therapeutic strategies to block NMDA receptor-mediated excitotoxicity. In addition, the investigations proposed here will focus on a novel form of modulation of NMDA receptor function, which may be important in retinal physiology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS029365-10
Application #
6096997
Study Section
Special Emphasis Panel (ZRG1-BDCN-2 (01))
Project Start
1991-04-01
Project End
2004-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
10
Fiscal Year
2000
Total Cost
$312,250
Indirect Cost
Name
University of Pittsburgh
Department
Biology
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Lee, Hanmi; Chen, Carol Xiu-Qing; Liu, Yong-Jian et al. (2005) KCC2 expression in immature rat cortical neurons is sufficient to switch the polarity of GABA responses. Eur J Neurosci 21:2593-9
Herin, Greta Ann; Aizenman, Elias (2004) Amino terminal domain regulation of NMDA receptor function. Eur J Pharmacol 500:101-11
Leszkiewicz, Daniel N; Aizenman, Elias (2003) Reversible modulation of GABA(A) receptor-mediated currents by light is dependent on the redox state of the receptor. Eur J Neurosci 17:2077-83
McLaughlin, BethAnn; Hartnett, Karen A; Erhardt, Joseph A et al. (2003) Caspase 3 activation is essential for neuroprotection in preconditioning. Proc Natl Acad Sci U S A 100:715-20
Leszkiewicz, Daniel N; McLaughlin, Beth Ann; Aizenman, Elias (2002) Protein kinases and light: unlikely partners in a receptor localization puzzle. Physiol Behav 77:533-6
Du, Shen; McLaughlin, BethAnn; Pal, Sumon et al. (2002) In vitro neurotoxicity of methylisothiazolinone, a commonly used industrial and household biocide, proceeds via a zinc and extracellular signal-regulated kinase mitogen-activated protein kinase-dependent pathway. J Neurosci 22:7408-16
Leszkiewicz, Daniel; Aizenman, Elias (2002) A role for the redox site in the modulation of the NMDA receptor by light. J Physiol 545:435-40
Santos, S; Aizenman, E (2002) Functional expression of muscle-type nicotinic acetylcholine receptors in rat forebrain neurons in vitro. Methods Find Exp Clin Pharmacol 24:63-6
McLaughlin, B; Pal, S; Tran, M P et al. (2001) p38 activation is required upstream of potassium current enhancement and caspase cleavage in thiol oxidant-induced neuronal apoptosis. J Neurosci 21:3303-11
Herin, G A; Du, S; Aizenman, E (2001) The neuroprotective agent ebselen modifies NMDA receptor function via the redox modulatory site. J Neurochem 78:1307-14

Showing the most recent 10 out of 41 publications