Synaptic plastic processes such as long-term potentiation (LTP) and long-term depression (LTD) play a central role in virtually all models that seek to explain learning and memory at a cellular level. Beyond even that, LTP and LTD are found in many brain areas and have been proposed to play a role in a wide range of neural functions and disorders. Neural functions from fear and emotion, through memory to addiction have been proposed to have a basis in these plastic processes. Therefore, the understanding of the mechanisms that underlie this plasticity will provide wide-ranging benefits not only to understanding normal brain function, but also to many neurological disorders. The study of LTP and LTD have been plagued by conflicting theories and experimental results that has in many cases slowed progress in understanding the underlying mechanism of these neuronal properties. Much of this confusion, we believe, has arisen from technical limitations of experiments that have, by necessity, relied exclusively on measures of synaptic plasticity in large populations of synapses. Since synapses can be found in a variety of plastic states, e.g. naive, potentiated, depressed, and populations of synapses almost certainly contain all these states and more, experimental manipulations may provide confusing results. Much as patch clamp recording, where the activity of a small number of ion channels could be recorded in isolation, revolutionized the study of ion channel function. the field of synaptic plasticity could benefit from experiments where very small numbers of synapses could be selectively studied and manipulated. In this proposal, we employ a method where we can record the activity of small numbers of synapses (1-10) identify their plastic state, and experimentally manipulate that state. By doing so, we can study the transitions between different plastic states in cases where we know the history of the synapses under study. In our preliminary studies, we have already clarified several issues relating to the mechanisms of synaptic plasticity and expect that the experiments in this proposal will greatly expand our knowledge of these mechanisms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH065541-04
Application #
6914952
Study Section
Special Emphasis Panel (ZRG1-MDCN-4 (01))
Program Officer
Asanuma, Chiiko
Project Start
2002-06-01
Project End
2007-05-31
Budget Start
2005-06-01
Budget End
2006-05-31
Support Year
4
Fiscal Year
2005
Total Cost
$275,053
Indirect Cost
Name
Stanford University
Department
Biophysics
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Valenzuela, Ricardo A; Micheva, Kristina D; Kiraly, Marianna et al. (2016) Array tomography of physiologically-characterized CNS synapses. J Neurosci Methods 268:43-52
Chang, Andy J; Ortega, Fabian E; Riegler, Johannes et al. (2015) Oxygen regulation of breathing through an olfactory receptor activated by lactate. Nature 527:240-4
Orr, Adrienne L; Hanson, Jesse E; Li, Dong et al. (2014) ?-Amyloid inhibits E-S potentiation through suppression of cannabinoid receptor 1-dependent synaptic disinhibition. Neuron 82:1334-45
Stephan, Alexander H; Madison, Daniel V; Mateos, José María et al. (2013) A dramatic increase of C1q protein in the CNS during normal aging. J Neurosci 33:13460-74
Mitra, Ananya; Blank, Martina; Madison, Daniel V (2012) Developmentally altered inhibition in Ts65Dn, a mouse model of Down syndrome. Brain Res 1440:1-8
Selcher, Joel C; Xu, Weifeng; Hanson, Jesse E et al. (2012) Glutamate receptor subunit GluA1 is necessary for long-term potentiation and synapse unsilencing, but not long-term depression in mouse hippocampus. Brain Res 1435:8-14
Salih, Dervis A M; Rashid, Asim J; Colas, Damien et al. (2012) FoxO6 regulates memory consolidation and synaptic function. Genes Dev 26:2780-801
Hanson, Jesse E; Orr, Adrienne L; Madison, Daniel V (2010) Altered hippocampal synaptic physiology in aged parkin-deficient mice. Neuromolecular Med 12:270-6
Hanson, Jesse E; Madison, Daniel V (2010) Imbalanced pattern completion vs. separation in cognitive disease: network simulations of synaptic pathologies predict a personalized therapeutics strategy. BMC Neurosci 11:96
Emond, Michelle R; Montgomery, Johanna M; Huggins, Matthew L et al. (2010) AMPA receptor subunits define properties of state-dependent synaptic plasticity. J Physiol 588:1929-46

Showing the most recent 10 out of 14 publications