The main theme of this proposal is to examine the mechanisms that contribute to plasticity of behavior in mammalian and invertebrate nervous systems. We will use a combination of behavioral, electrophysiological, biochemical, morphological, and molecular genetic techniques to study problems that are related to the four main types of plasticity: learning, motivation, recovery from damage, and development. Individual research projects have been designed to promote interdisciplinary collaboration between ten individual laboratories. To simplify the cell and molecular analysis of plasticity, three principal experimental systems will be employed: 1. semi-intact or reduced systems in which neuronal activity can be recorded while the organism exhibits behavioral responses; 2. isolated intact ganglia, and 3. cell culture and brain slice systems in which experimental control can be greatly increased. We will use semi-intact and reduced preparations of vertebrates as well as invertebrates to investigate two types of problems: a) plasticity of motor behavior, using a restrained cat engaged in a multijoint movement task; and b) alterations of motivational state, using a preparation of the marine mollusc Aplysia, that exhibits various types of plasticity and switching of motivational states involving feeding. Isolated ganglia of Aplysia will also be employed. We will use cell culture to study synaptic plasticity and axonal growth of both vertebrate (PC12 cells, and spinal cord neurons) and invertebrate (Aplysia) neurons. Finally, brain slices will be used to study long-term potentiation, a model of vertebrate learning. A comparison of the mechanisms of different forms of plasticity in vertebrate and invertebrate neural systems should provide insights into general mechanisms that contribute to plasticity of behavior.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM032099-11
Application #
3096176
Study Section
Special Emphasis Panel (SSS (P3))
Project Start
1982-05-01
Project End
1997-04-30
Budget Start
1993-05-01
Budget End
1994-04-30
Support Year
11
Fiscal Year
1993
Total Cost
Indirect Cost
Name
New York State Psychiatric Institute
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Tang, D; Goldberg, D J (2000) Bundling of microtubules in the growth cone induced by laminin. Mol Cell Neurosci 15:303-13
Rosen, S C; Miller, M W; Cropper, E C et al. (2000) Outputs of radula mechanoafferent neurons in Aplysia are modulated by motor neurons, interneurons, and sensory neurons. J Neurophysiol 83:1621-36
Rosen, S C; Miller, M W; Evans, C G et al. (2000) Diverse synaptic connections between peptidergic radula mechanoafferent neurons and neurons in the feeding system of Aplysia. J Neurophysiol 83:1605-20
Chain, D G; Casadio, A; Schacher, S et al. (1999) Mechanisms for generating the autonomous cAMP-dependent protein kinase required for long-term facilitation in Aplysia. Neuron 22:147-56
Baranes, D; Lederfein, D; Huang, Y Y et al. (1998) Tissue plasminogen activator contributes to the late phase of LTP and to synaptic growth in the hippocampal mossy fiber pathway. Neuron 21:813-25
Sun, Z Y; Schacher, S (1998) Binding of serotonin to receptors at multiple sites is required for structural plasticity accompanying long-term facilitation of Aplysia sensorimotor synapses. J Neurosci 18:3991-4000
Bailey, C H; Kaang, B K; Chen, M et al. (1997) Mutation in the phosphorylation sites of MAP kinase blocks learning-related internalization of apCAM in Aplysia sensory neurons. Neuron 18:913-24
Martin, K C; Casadio, A; Zhu, H et al. (1997) Synapse-specific, long-term facilitation of aplysia sensory to motor synapses: a function for local protein synthesis in memory storage. Cell 91:927-38
Zhu, H; Wu, F; Schacher, S (1997) Site-specific and sensory neuron-dependent increases in postsynaptic glutamate sensitivity accompany serotonin-induced long-term facilitation at Aplysia sensorimotor synapses. J Neurosci 17:4976-86
Teyke, T; Xin, Y; Weiss, K R et al. (1997) Ganglionic distribution of inputs and outputs of C-PR, a neuron involved in the generation of a food-induced arousal state in Aplysia. Invert Neurosci 2:235-44

Showing the most recent 10 out of 96 publications