TY - JOUR
T1 - An analysis of the effects of acute and chronic fluexetine on extracellular norepinephrine in the rat hippocampus during stress
AU - Page, Michelle E.
AU - Abercrombie, Elizabeth D.
N1 - Funding Information:
We thank Eli Lilly for the gift of Fluoxetine. This work was supported by PHS DA08086 (EDA) and MH10969 (MEP). EDA is an Alfred P. Sloan Foundation ResearchF ellow.
PY - 1997/6
Y1 - 1997/6
N2 - The locus coerulens (LC) noradrenergic system is activated by a range of arousing and stressful stimuli. The serotonergic inputs to this structure have been shown to attenuate LC activation under some conditions. The present study examined the effect of fluoxetine, a selective serotonin reuptake inhibitor (SSRI) known to be a clinically effective antidepressant, on basal and stress-induced norepinephrine (NE) release. Basal and stress-induced NE efflux in the rat hippocampus were assessed using in viva microdialysis techniques. The effect of a 30 minute tailpinch stressor on extracellular concentration of NE was compared in rats treated with fluoxetine either once prior to tailpinch or twice daily of 14 days and, respectively, in unhandled controls and vehicle-treated control animals. A single fluoxetine injection prior to tailpinch did not significantly alter the tailpinch-induced increase of extracellular NE as compared to naive controls. However, there was an enhanced NE response to tailpinch in chronic fluoxetine versus chronic vehicle-treated control rats. Thus, acute blockade of 5-HT uptake by fluoxetine does not affect NE release in response tailpinch stress. Chronic fluoxetine administration, however, results in a potentiated evoked response of the LC-NE system. One action of chronic fluoxetine, which may relate to therapeutic efficacy, is an increase in responsivity of LC neurons.
AB - The locus coerulens (LC) noradrenergic system is activated by a range of arousing and stressful stimuli. The serotonergic inputs to this structure have been shown to attenuate LC activation under some conditions. The present study examined the effect of fluoxetine, a selective serotonin reuptake inhibitor (SSRI) known to be a clinically effective antidepressant, on basal and stress-induced norepinephrine (NE) release. Basal and stress-induced NE efflux in the rat hippocampus were assessed using in viva microdialysis techniques. The effect of a 30 minute tailpinch stressor on extracellular concentration of NE was compared in rats treated with fluoxetine either once prior to tailpinch or twice daily of 14 days and, respectively, in unhandled controls and vehicle-treated control animals. A single fluoxetine injection prior to tailpinch did not significantly alter the tailpinch-induced increase of extracellular NE as compared to naive controls. However, there was an enhanced NE response to tailpinch in chronic fluoxetine versus chronic vehicle-treated control rats. Thus, acute blockade of 5-HT uptake by fluoxetine does not affect NE release in response tailpinch stress. Chronic fluoxetine administration, however, results in a potentiated evoked response of the LC-NE system. One action of chronic fluoxetine, which may relate to therapeutic efficacy, is an increase in responsivity of LC neurons.
KW - Fluoxetine
KW - In vivo microdialysis
KW - Locus coeruleus
KW - Norepinephrine
KW - Stress
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U2 - 10.1016/S0893-133X(96)00281-3
DO - 10.1016/S0893-133X(96)00281-3
M3 - Article
C2 - 9165497
AN - SCOPUS:0030958457
SN - 0893-133X
VL - 16
SP - 419
EP - 425
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 6
ER -