We propose to examine the impact of acute and chronic stress on the functional capacity of central noradrenergic neurons. Our studies may be divided into three groups:. (1) We wish to determine whether changes in tyrosine hydroxylase (TH) activity within locus coeruleus (LC) neurons during chronic cold stress are indicative of alterations in norepinephrine (NE) efflux. Release will be monitored using in vitro slices, in vivo voltammetry, and local perfusion in situ via dialysis tubing. The LC and two of its terminal fields will be examined, cerebellum and hippocampus will be examined. Among the questions to be studied are the following: Does acute, severe stress lead to an initial depletion of releasable NE? Does the activation of TH, which occurs within a few minutes of stimulation, increase the capacity for subsequent release? Does TH induction lead to a still greater capacity for release? (2) We wish to determine the extent to which increases in NE release during stress are due to alterations in the firing rate of LC neurons. We will record from LC neurons and determine the impact of stress on the firing rate of these cells. In addition, we will measure the amount of transmitter released from slices per impulse. (3) We wish to determine the degree to which adaptive changes occurring in central NE neurons in response to chronic stress affect the functioning of post-synaptic cells. We will record from single hippocampal granule cells and cerebellar Purkinje neurons during electrical stimulation of the LC to determine if exposure to chronic stress alters the inhibitory effect of release of endogenous NE on the spontaneous firing rates of these target neurons. In addition, electrical stimulation of glutaminergic, perforant path input to granule cells during electrical stimulation of the LC will be used to determine if exposure to chronic stress alters the modulatory effect of NE on other, non-NE inputs to target neurons. This work will be related to the basic neurobiology of monoaminergic neurons and their targets and to the relation between stress and depression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH043947-02
Application #
3383380
Study Section
(SRCM)
Project Start
1988-06-01
Project End
1993-05-31
Budget Start
1989-06-01
Budget End
1990-05-31
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
Schools of Arts and Sciences
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Zigmond, M J (1994) Chemical transmission in the brain: homeostatic regulation and its functional implications. Prog Brain Res 100:115-22
Gresch, P J; Sved, A F; Zigmond, M J et al. (1994) Stress-induced sensitization of dopamine and norepinephrine efflux in medial prefrontal cortex of the rat. J Neurochem 63:575-83
Keefe, K A; Sved, A F; Zigmond, M J et al. (1993) Stress-induced dopamine release in the neostriatum: evaluation of the role of action potentials in nigrostriatal dopamine neurons or local initiation by endogenous excitatory amino acids. J Neurochem 61:1943-52
Nisenbaum, L K; Abercrombie, E D (1993) Presynaptic alterations associated with enhancement of evoked release and synthesis of norepinephrine in hippocampus of chronically cold-stressed rats. Brain Res 608:280-7
Robinson, G B; Fluharty, S J; Zigmond, M J et al. (1993) Recovery of hippocampal dentate granule cell responsiveness to entorhinal cortical input following norepinephrine depletion. Brain Res 614:21-8
Keefe, K A; Zigmond, M J; Abercrombie, E D (1993) In vivo regulation of extracellular dopamine in the neostriatum: influence of impulse activity and local excitatory amino acids. J Neural Transm Gen Sect 91:223-40
Keefe, K A; Zigmond, M J; Abercrombie, E D (1992) Extracellular dopamine in striatum: influence of nerve impulse activity in medial forebrain bundle and local glutamatergic input. Neuroscience 47:325-32
Nisenbaum, L K; Abercrombie, E D (1992) Enhanced tyrosine hydroxylation in hippocampus of chronically stressed rats upon exposure to a novel stressor. J Neurochem 58:276-81
Lonart, G; Zigmond, M J (1991) Incubation of tissue slices in the absence of Ca2+ and Mg2+ can cause nonspecific damage. J Neurochem 56:1445-8
Lonart, G; Zigmond, M J (1991) High glutamate concentrations evoke Ca(++)-independent dopamine release from striatal slices: a possible role of reverse dopamine transport. J Pharmacol Exp Ther 256:1132-8

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