The essence of nervous system organization is the establishment of synaptic circuits. A great deal of precision is demanded in the construction of these circuits, and many of the disorders of behaviour that occur in humans and other animals are due to abnormalities in the development of synaptic connections. The long-term objectives of this research are to elucidate basic cellular and molecular mechanisms which underlie the formation and maintenance of specific synaptic connections, using the terminal ganglion of the cockroach as a model system. Many of the mechanisms which control other aspects of neuronal development have been shown to be conserved throughout evolution, which makes it likely that this work will contribute to our eventual understanding of how our own brains are assembled. The first specific aim of this project is to determine the sequence and specificity of synapse formation between identified neurons during embryonic development, using intracellular recording, dye injection and light and electron microscopy.
The second aim i s to assess the accuracy with which cercal afferents regenerate their arborization and synaptic connections, using a combination of intracellular recording, dye injection, and morphometric analysis. The third specific aim is to determine the physiological and anatomical basis for synaptic competition in mutant cockroaches with a supernumerary presynaptic neuron, using a combination of quantal analysis and quantitative electron microscopy. Intracellular dye injection will be used to find out whether the supernumerary axon arrives later in the terminal ganglion than the normal axons. The effect of synchronized regeneration on the relative synaptic efficacies will be investigated. Intracellular recording and dye injection will be used to pursue the fourth aim of this project; to determine the role of competitive interactions during postembryonic development of genetically wild-type animals.

Project Start
1998-09-30
Project End
1999-07-27
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
30
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Puerto Rico Med Sciences
Department
Type
DUNS #
City
San Juan
State
PR
Country
United States
Zip Code
00936
Delgado, Nadia; Vallejo, Deborah; Miller, Mark W (2012) Localization of serotonin in the nervous system of Biomphalaria glabrata, an intermediate host for schistosomiasis. J Comp Neurol 520:3236-55
Levi, Rafael; Selverston, Allen I (2006) Mechanisms underlying type I mGluR-induced activation of lobster gastric mill neurons. J Neurophysiol 96:3378-88
Diaz-Rios, Manuel; Oyola, Eduardo; Miller, Mark W (2002) Colocalization of gamma-aminobutyric acid-like immunoreactivity and catecholamines in the feeding network of Aplysia californica. J Comp Neurol 445:29-46
Duprey-Diaz, Mildred V; Soto, Ileana; Blagburn, Jonathan M et al. (2002) Changes in brain-derived neurotrophic factor and trkB receptor in the adult Rana pipiens retina and optic tectum after optic nerve injury. J Comp Neurol 454:456-69
Kuffler, D (2000) Can regeneration be promoted within the spinal cord? P R Health Sci J 19:241-52
Blanco, R E; Lopez-Roca, A; Soto, J et al. (2000) Basic fibroblast growth factor applied to the optic nerve after injury increases long-term cell survival in the frog retina. J Comp Neurol 423:646-58
Delgado, J Y; Oyola, E; Miller, M W (2000) Localization of GABA- and glutamate-like immunoreactivity in the cardiac ganglion of the lobster Panulirus argus. J Neurocytol 29:605-19
Zheng, M; Kuffler, D P (2000) Guidance of regenerating motor axons in vivo by gradients of diffusible peripheral nerve-derived factors. J Neurobiol 42:212-9
Hill, E S; Latalladi, G; Kuffler, D P (1999) Dissociated adult Rana pipiens motoneuron growth cones turn up concentration gradients of denervated peripheral nerve-released factors. Neurosci Lett 277:87-90
Blanco, R E; Rosado, J; Padilla, J et al. (1999) Ultrastructural studies of dorsal root axons regenerating through adult frog optic and sciatic nerves. Microsc Res Tech 46:310-8

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