Long term potentiation (LTP) of synaptic transmission is a form of synaptic plasticity that is observed in all principal neurons in the hippocampus-a brain structure implicated in certain forms of long-term memory. LTP has been extensively studied at Schaffer collateral and perforant path synapses, while, for technical reasons, relatively less attention has been paid to mossy fiber synapses in the hippocampus. The mossy fiber synapse has a number of unusual features, including LTP that does not depend on the NMDA type of glutamate receptor, and the mechanisms for the induction and expression of LTP at this synapse are not well understood. In this renewal application we propose to utilize visual patch-clamp techniques, pre- and postsynaptic Ca2+ imaging, focal stimulation of mossy fibers, and whole-cell recordings from single, mossy fiber boutons, all in acute slices of rat hippocampus, to investigate a number of hypotheses derived from our previous studies of this synapse.
The aims of this proposal are: 1) To test the hypothesis that Ca2+ is released from stores inside mossy fiber boutons during stimulus protocols that induce LTP; 2) To test the hypothesis that Ca2+ released from intracellular stores postsynaptically during certain stimulus protocols is required for LTP induction; 3) To test the hypothesis that activation of protein kinases A, C, CaMKII, and MAPK is required for LTP induction or expression; 4) To test the hypothesis that brief-train LTP is associative and requires concomitant activity of other pathways for induction, while long-train LTP does not require co-activity of other afferents; and 5) To test hypotheses for a role of mossy fiber activity in the induction of LTP at commissural/associational and perforant path synapses onto CA3 neurons. The so-called """"""""detonator synapse"""""""" hypothesis will be tested as part of this aim. We will also test for associative and/or heterosynaptic plasticity between the other synaptic inputs to CA3 neurons and the mossy fibers. We believe that the results of these studies will add significantly to our understanding of the computational properties of the hippocampus and the role of the hippocampus in learning and memory and diseases of cognition.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
2R37MH044754-11
Application #
2911115
Study Section
Special Emphasis Panel (ZRG1-IFCN-7 (01))
Program Officer
Asanuma, Chiiko
Project Start
1989-09-01
Project End
2004-07-31
Budget Start
1999-08-01
Budget End
2000-07-31
Support Year
11
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Neurosciences
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Narayanan, Rishikesh; Dougherty, Kevin J; Johnston, Daniel (2010) Calcium store depletion induces persistent perisomatic increases in the functional density of h channels in hippocampal pyramidal neurons. Neuron 68:921-35
Dembrow, Nikolai C; Chitwood, Raymond A; Johnston, Daniel (2010) Projection-specific neuromodulation of medial prefrontal cortex neurons. J Neurosci 30:16922-37
Narayanan, Rishikesh; Johnston, Daniel (2010) The h current is a candidate mechanism for regulating the sliding modification threshold in a BCM-like synaptic learning rule. J Neurophysiol 104:1020-33
Routh, Brandy N; Johnston, Daniel; Harris, Kristen et al. (2009) Anatomical and electrophysiological comparison of CA1 pyramidal neurons of the rat and mouse. J Neurophysiol 102:2288-302
Shin, Minyoung; Brager, Darrin; Jaramillo, Thomas C et al. (2008) Mislocalization of h channel subunits underlies h channelopathy in temporal lobe epilepsy. Neurobiol Dis 32:26-36
Narayanan, Rishikesh; Johnston, Daniel (2008) The h channel mediates location dependence and plasticity of intrinsic phase response in rat hippocampal neurons. J Neurosci 28:5846-60
Narayanan, Rishikesh; Johnston, Daniel (2007) Long-term potentiation in rat hippocampal neurons is accompanied by spatially widespread changes in intrinsic oscillatory dynamics and excitability. Neuron 56:1061-75
Gasparini, Sonia; Losonczy, Attila; Chen, Xixi et al. (2007) Associative pairing enhances action potential back-propagation in radial oblique branches of CA1 pyramidal neurons. J Physiol 580:787-800
Brager, Darrin H; Johnston, Daniel (2007) Plasticity of intrinsic excitability during long-term depression is mediated through mGluR-dependent changes in I(h) in hippocampal CA1 pyramidal neurons. J Neurosci 27:13926-37
Yuan, Li-Lian; Chen, Xixi; Kunjilwar, Kumud et al. (2006) Acceleration of K+ channel inactivation by MEK inhibitor U0126. Am J Physiol Cell Physiol 290:C165-71

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