Neurons located in the nucleus paragigantocellularis (PGi) in the rostral ventral medulla provide a strong opioid and excitatory amino acid projection to the nucleus locus coeruleus (LC) in the dorsal pontine tegmentum. The LC is solely responsible for providing norepinephrine to the forebrain and activation of neurons in this brain region has been correlated with changes in behavioral state and a general increase in sympathetic activity. Several lines of evidence have recently implicated the PGi/LC pathway in the mediation of the physical and adverse signs observed in animals upon withdrawal from opiates. Specifically, neurons in the LC of opiate dependent rats have been reported to have significant increases in their discharge rates following cessation of opiate administration or by precipitation of opiate withdrawal with an opiate antagonist. This increase in neuronal activity has been reported to be caused by an efflux of excitatory amino acids from axon terminals in the LC most likely deriving from the PGi. Activation of glutamate-containing neurons in the PGi may depend on direct synaptic activation of the morphine-like mu-opiate receptor by endogenous opioid peptides on LC-projecting neurons in the PGi which subsequently affect glutamate release in the LC. The recent production of antibodies directed against such receptors can be used to examine the sites of actions of their endogenous ligands.
The specific aims of the proposed studies address fundamental questions regarding anatomical substrates responsible for mediating LC activation during opiate withdrawal.
Aim 1 will examine whether the mu-selective opiate receptor is localized on (1) plasmalemmal sites of LC-projecting neurons in the PGi and (2) axon terminals which are presynaptic to LC-projecting neurons in the PGi.
Aim 1 1 will determine the cellular substrates for proposed inter-actions between PGi afferent terminals, enkephalin afferents and the mu- selective receptor. The methods include dual labeling immunocytochemistry and tract-tracing at the electron microscopic level in adult rat brain. Ultrastructural analysis is a powerful technique to determine directly whether receptors are neuronal or glial, as well as their pre- and postsynaptic locations on identified neurons. This methodology permits the direct visualization of sites representing the functional expression of identified receptors. Ultrastructural immunocytochemical localization of neuro-transmitters and receptors also complement pharmacological and physiological studies in which direct and indirect interactions are difficult, if not impossible, to differentiate. The results will serve to verify and qualify the cellular mechanisms through which opiate receptor activation and excitatory amino acids may regulate neuronal activity in the PGi/LC pathway. Elucidation of the anatomical substrates in the medullo-coerulear circuit may provide a model for our under-standing of the neural circuits involved in drug dependence in humans. These studies will lay the necessary groundwork for future studies directed at examing potential changes in mu-opiate receptor density and distribution in naive versus opiate dependent animals.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Small Research Grants (R03)
Project #
5R03DA010450-03
Application #
2517996
Study Section
Human Development Research Subcommittee (NIDA)
Project Start
1996-09-30
Project End
1999-08-31
Budget Start
1997-09-01
Budget End
1999-08-31
Support Year
3
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Pathology
Type
Schools of Medicine
DUNS #
061197161
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Valentino, R J; Van Bockstaele, E (2001) Opposing regulation of the locus coeruleus by corticotropin-releasing factor and opioids. Potential for reciprocal interactions between stress and opioid sensitivity. Psychopharmacology (Berl) 158:331-42
Van Bockstaele, E J; Peoples, J; Menko, A S et al. (2000) Decreases in endogenous opioid peptides in the rat medullo-coerulear pathway after chronic morphine treatment. J Neurosci 20:8659-66
Van Bockstaele, E J; Saunders, A; Commons, K G et al. (2000) Evidence for coexistence of enkephalin and glutamate in axon terminals and cellular sites for functional interactions of their receptors in the rat locus coeruleus. J Comp Neurol 417:103-14
Van Bockstaele, E J (2000) Multiple substrates for serotonergic modulation of rat locus coeruleus neurons and relationships with kainate receptors. Brain Res Bull 51:433-42
Van Bockstaele, E J; Peoples, J; Telegan, P (1999) Efferent projections of the nucleus of the solitary tract to peri-locus coeruleus dendrites in rat brain: evidence for a monosynaptic pathway. J Comp Neurol 412:410-28
Van Bockstaele, E J; Saunders, A; Telegan, P et al. (1999) Localization of mu-opioid receptors to locus coeruleus-projecting neurons in the rostral medulla: morphological substrates and synaptic organization. Synapse 34:154-67
Commons, K G; van Bockstaele, E J; Pfaff, D W (1999) Frequent colocalization of mu opioid and NMDA-type glutamate receptors at postsynaptic sites in periaqueductal gray neurons. J Comp Neurol 408:549-59
Van Bockstaele, E J; Colago, E E; Aicher, S (1998) Light and electron microscopic evidence for topographic and monosynaptic projections from neurons in the ventral medulla to noradrenergic dendrites in the rat locus coeruleus. Brain Res 784:123-38
Van Bockstaele, E J (1998) Morphological substrates underlying opioid, epinephrine and gamma-aminobutyric acid inhibitory actions in the rat locus coeruleus. Brain Res Bull 47:1-15
Lee, A; Rosin, D L; Van Bockstaele, E J (1998) alpha2A-adrenergic receptors in the rat nucleus locus coeruleus: subcellular localization in catecholaminergic dendrites, astrocytes, and presynaptic axon terminals. Brain Res 795:157-69

Showing the most recent 10 out of 13 publications