STRESS-INDUCED CHANGES OF EXTRACELLULAR 5-HYDROXYINDOLEACETIC ACID CONCENTRATIONS FOLLOWED IN THE NUCLEUS-RAPHE-DORSALIS AND THE FRONTAL-CORTEX OF THE RAT
Hw. Clement et al., STRESS-INDUCED CHANGES OF EXTRACELLULAR 5-HYDROXYINDOLEACETIC ACID CONCENTRATIONS FOLLOWED IN THE NUCLEUS-RAPHE-DORSALIS AND THE FRONTAL-CORTEX OF THE RAT, Brain research, 614(1-2), 1993, pp. 117-124
In the present paper, the effect of different stressors on extracellul
ar 5-hydroxyindoleacetic acid (5-HIAA) concentrations in the frontal c
ortex and the N. raphe dorsalis (NRD) of the rat were studied. The fol
lowing stressful procedures were used: Immobilization, 10 min, cold, 2
0 min, and forced exercise in a rotating wheel, 2h. These procedures w
ere compared with a handling procedure, 10 min. The extracellular 5-HI
AA concentration was followed by in vivo voltammetry with carbon multi
fibre electrodes in the awake animal. Handling had no significant effe
ct on extracellular 5-HIAA concentrations neither in the frontal corte
x nor the NRD, whereas immobilization and cold evoked significant incr
eases in both brain areas. During and after forced exercise a signific
ant increase was measurable only in the frontal cortex, while extracel
lular 5-HIAA concentrations were unchanged in the NRD. Since it is ver
y likely that the modulation of the activity of the central serotonine
rgic system under stressful conditions is closely connected with chang
es in behaviour and temperature regulation, we compared our findings o
n extracellular 5-HIAA levels during stress with the effect of the 5-H
T1A agonist (+)-8-hydroxy-2-(di-n-propylamino)tetraline (8-OH-DPAT), a
substance known to reduce body temperature. The i.p. injection of a l
ow dose decreased significantly both, the extracellular 5-HIAA concent
ration in the NRD and body temperature. Our results suggest that the s
erotoninergic activation in the frontal cortex may prove to be a gener
al response to stress which could function perhaps as a part of the ce
ntral coping mechanism, whereas serotonin (5-HT) in the NRD may modula
te specific regulatory responses such as body temperature.