Neurosteroids have important roles in mental health-related disorders and these compounds have great potential for neuropsychopharmacological applications. Neurosteroids affect ligand-gated ion channels and metabotropic receptors by nongenomic mechanisms, but their mechanism of action is not completely understood. We have convincing preliminary evidence of a novel effect of the neurosteroids. We found that these compounds act at a presynaptic site to dramatically enhance glutamatergic paired-pulse facilitation, which is a model of short-term presynaptic plasticity. Additionally we observed an increase spontaneous miniature glutamatergic excitatory postsynaptic currents. We thus propose the following hypothesis: HYPOTHESIS: Neurosteroid actions in the CNS are due in part to enhancement of glutamate release in the hippocampus. To test this hypothesis we will address the following two specific aims:
Specific Aim #1. Investigate the modulation of glutamate release by neurosteroids. We will use hippocampal slices and sharp-electrode electrophysiological techniques to study effect of two physiologically important neurosteroids, pregnenolone sulfate and dehydroapiandrosterone sulfate, on paired pulse facilitation. We will also examine effects of these compounds on spontaneous miniature glutamatergic excitatory postsynaptic currents. We will use hippocampal slices and whole-cell patch-clamp electrophysiological techniques for these studies.
Specific Aim #2. Investigate the mechanisms by which neurosteroids modulate glutamate release. We will consider the role of presynaptic metabotropic receptors and ion channels in the modulation of glutamate release by neurosteroids. Specifically we will test a role of sigma receptors, voltage-gated calcium channels and potassium channels. The proposed studies will increase our understanding of the mechanism of action of these compounds in the brain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21MH063126-01A1
Application #
6467715
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Winsky, Lois M
Project Start
2002-05-01
Project End
2004-04-30
Budget Start
2002-05-01
Budget End
2003-04-30
Support Year
1
Fiscal Year
2002
Total Cost
$148,750
Indirect Cost
Name
University of New Mexico
Department
Neurosciences
Type
Schools of Medicine
DUNS #
829868723
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Thomas, Michael J; Mameli, Manuel; Carta, Mario et al. (2005) Neurosteroid paradoxical enhancement of paired-pulse inhibition through paired-pulse facilitation of inhibitory circuits in dentate granule cells. Neuropharmacology 48:584-96
Schiess, Adrian R; Partridge, L Donald (2005) Pregnenolone sulfate acts through a G-protein-coupled sigma1-like receptor to enhance short term facilitation in adult hippocampal neurons. Eur J Pharmacol 518:22-9
Bustillo, Juan; Wolff, Christina; Myers-y-Gutierrez, Adan et al. (2004) Treatment of rats with antipsychotic drugs: lack of an effect on brain N-acetyl aspartate levels. Schizophr Res 66:31-9
Meyer, Douglas A; Carta, Mario; Partridge, L Donald et al. (2002) Neurosteroids enhance spontaneous glutamate release in hippocampal neurons. Possible role of metabotropic sigma1-like receptors. J Biol Chem 277:28725-32