Serotonin, acting as a chemical neurotransmitter in the central nervous system (CNS), is importantly implicated in a variety of human neuro- and psychopathologies. However, its basic neurobiological role remains somewhat obscure. A true appreciation of how serotonin functions in disease processes, and treatment of them, presupposes an understanding of its actions in normal mammalian physiology and behavior. To that end, the present research is aimed at furthering knowledge of the basic functioning of the CNS serotonin system primarily through recording the electrical activity of brain serotonin neurons in behaving animals. Recordings will be made in both the rostral/ascending group of serotonin neurons (in the dorsal raphe nucleus) as well as the caudal/descending group (in the nuclei raphe obscurus and pallidus). The proposed studies are an outgrowth of our basic hypothesis that the activity of serotonin neurons is closely linked to level of behavioral activation/tonic motor activity, and especially to repetitive motor activity (central pattern generator-mediated). Two major groups of experiments are proposed: 1) environmental and behavioral factors that may modulate the basic activity of these brain cells, and the neurochemicals that mediate these effects; 2) the role of brain serotonin neurons in central fatigue. The importance of this latter issue derives from the fact that fatigue is considered an important component in a number of disease processes (e.g., chronic fatigue syndrome, multiple sclerosis, and depression). In addition to single unit recordings in behaving animals, the experiments will employ: 1) In vivo microdialysis measures of brain serotonin and dopamine; 2) Local drug administration by means of reverse microdialysis; 3) c-Fos expression (in conjunction with double labeling) as an indicator of serotonin neurons activated under specific conditions; and 4) Computer-generated spike train analyses.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
2R01MH023433-28
Application #
6370595
Study Section
Special Emphasis Panel (ZRG1-IFCN-3 (01))
Project Start
1976-06-01
Project End
2006-06-30
Budget Start
2001-08-20
Budget End
2002-06-30
Support Year
28
Fiscal Year
2001
Total Cost
$349,659
Indirect Cost
Name
Princeton University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
Kochman, Linda J; Fornal, Casimir A; Jacobs, Barry L (2009) Suppression of hippocampal cell proliferation by short-term stimulant drug administration in adult rats. Eur J Neurosci 29:2157-65
Fornal, Casimir A; Stevens, Joanne; Barson, Jessica R et al. (2007) Delayed suppression of hippocampal cell proliferation in rats following inescapable shocks. Brain Res 1130:48-53
Yap, Jasmine J; Takase, Luiz F; Kochman, Linda J et al. (2006) Repeated brief social defeat episodes in mice: effects on cell proliferation in the dentate gyrus. Behav Brain Res 172:344-50
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Martin-Cora, Francisco J; Fornal, Casimir A; Jacobs, Barry L (2005) Single-unit responses of serotonergic medullary raphe neurons to cardiovascular challenges in freely moving cats. Eur J Neurosci 22:3195-204
Takase, Luiz F; Nogueira, Maria Ines; Bland, Sondra T et al. (2005) Effect of number of tailshocks on learned helplessness and activation of serotonergic and noradrenergic neurons in the rat. Behav Brain Res 162:299-306
Takase, Luiz F; Nogueira, Maria Ines; Baratta, Michael et al. (2004) Inescapable shock activates serotonergic neurons in all raphe nuclei of rat. Behav Brain Res 153:233-9
Jacobs, Barry L; Martin-Cora, Francisco J; Fornal, Casimir A (2002) Activity of medullary serotonergic neurons in freely moving animals. Brain Res Brain Res Rev 40:45-52

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