Present knowledge of the structure and physiology of sensilla and their sensory neurons in the antennae of insects provide a basis for a detailed neurophysiological, anatomical, and ultrastructural study of neural pathways subserving olfaction and mechanosensation in the insect brain.
This research aims to trace the pathways of antennal afferent axons into the central nervous system; to characterize the electrophysiological responses of the neurons in the deutocerebrum to defined olfactory and mechanosensory antennal inputs; to prepare an inventory of types and projections of deutocerebral neurons; to classify synapses in the glomeruli of the deutocerebral antennal lobes on the basis of ultrastructure and the cellular elements participating in each type; to probe further the chemical composition and physiological actions of male and female pheromone systems; and to test the usefulness of methods of metabolic cell-marking to construct functional maps of neural activity in the central nervous system with various types of antennal stimulation. These studies will employ the large, easily reared, and experimentally tractable lepidopteran insect Manduca sexta. The central effort in this work will involve intracellular recording of synaptic and active potentials in, and intracellular dye-marking of, deutocerebral neurons with glass micro-electrodes in order to correlate cell responses with cell types. This research is expected to contribute knowledge about the brain mechanisms underlying olfactorily mediated behavior in insects and thereby to aid progress toward new and selective means of controlling insects that spread diseases and destroy food supplies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
7R01AI023253-01
Application #
3135142
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1985-09-01
Project End
1986-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Arizona
Department
Type
Organized Research Units
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85722
Heinbockel, Thomas; Shields, Vonnie D C; Reisenman, Carolina E (2013) Glomerular interactions in olfactory processing channels of the antennal lobes. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 199:929-46
Heinbockel, T; Christensen, T A; Hildebrand, J G (2004) Representation of binary pheromone blends by glomerulus-specific olfactory projection neurons. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 190:1023-37
Mercer, Alison R; Hildebrand, John G (2002) Developmental changes in the electrophysiological properties and response characteristics of Manduca antennal-lobe neurons. J Neurophysiol 87:2650-63
Mercer, Alison R; Hildebrand, John G (2002) Developmental changes in the density of ionic currents in antennal-lobe neurons of the sphinx moth, Manduca sexta. J Neurophysiol 87:2664-75
Kloppenburg, P; Heinbockel, T (2000) 5-Hydroxy-tryptamine modulates pheromone-evoked local field potentials in the macroglomerular complex of the sphinx moth Manduca sexta. J Exp Biol 203:1701-9
Lehman, H K; Murgiuc, C M; Hildebrand, J G (2000) Characterization and developmental regulation of tyramine-beta-hydroxylase in the CNS of the moth, Manduca sexta. Insect Biochem Mol Biol 30:377-86
Kloppenburg, P; Ferns, D; Mercer, A R (1999) Serotonin enhances central olfactory neuron responses to female sex pheromone in the male sphinx moth manduca sexta. J Neurosci 19:8172-81
Kent, K S; Oland, L A; Hildebrand, J G (1999) Development of the labial pit organ glomerulus in the antennal lobe of the moth Manduca sexta: the role of afferent projections in the formation of identifiable olfactory glomeruli. J Neurobiol 40:28-44
Heinbockel, T; Christensen, T A; Hildebrand, J G (1999) Temporal tuning of odor responses in pheromone-responsive projection neurons in the brain of the sphinx moth Manduca sexta. J Comp Neurol 409:1-12
Sun, X (1999) Combining laser scanning confocal microscopy and electron microscopy. Methods Enzymol 307:135-52

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