EFFECTS OF CHRONIC TREATMENT WITH ETHANOL AND WITHDRAWAL ON LEVELS OFMONOAMINES IN RAT CEREBRAL-CORTEX AND STRIATUM - INFLUENCE OF MIDAZOLAM, THIOPENTHAL AND SOMATOSTATIN
E. Gilmartin et al., EFFECTS OF CHRONIC TREATMENT WITH ETHANOL AND WITHDRAWAL ON LEVELS OFMONOAMINES IN RAT CEREBRAL-CORTEX AND STRIATUM - INFLUENCE OF MIDAZOLAM, THIOPENTHAL AND SOMATOSTATIN, International journal of biochemistry & cell biology, 27(12), 1995, pp. 1267-1276
It is accepted that ethanol affects the central neurotransmission, Thi
s paper deals with the effects of chronic ethanol treatment and withdr
awal on cortical and striatal levels of several neurotransmitters, The
influence of barbiturate, benzodiazepine and somatostatin has been st
udied in order to establish possible cross-interactions. Serotonin, 5-
hydroxyindoleacetic acid, dopamine and norepinephrine levels from rat
cerebral cortex and striatum were determined by high performance Liqui
d chromatography (HPLC) with electrochemical detection, Rats were chro
nically treated with ethanol (11-12 g/kg/day) for 6 weeks. The chronic
ethanol treatment decreased the cortical serotonin (P < 0.01) and 5-h
ydroxyindoleacetic acid (P < 0.01) concentrations, while ethanol withd
rawal decreased them in cortex and striatum, A single dose of differen
t drugs produced an increase of serotonin and 5-hydroxyindoleacetic ac
id striatal-but not cortical-levels. The chronic ethanol treatment or
48 hr of ethanol-withdrawal produced a depletion of striatal serotoner
gic system when barbiturate thiopenthal was administered. The benzodia
zepine midazolam elicited a decrease of striatal serotonin (P < 0.01)
and 5-hydroxyindoleacetic acid (P < 0.05) levels in 48 hr ethanol-with
drawn and chronically ethanol-treated rats, respectively, Somatostatin
injected to chronically ethanol-exposed rats resulted in decreased (P
< 0.05) striatal serotonin concentrations, Cortical norepinephrine le
vels decreased after 24 and 48 hr of ethanol-withdrawal (P < 0.05 and
P < 0.01, respectively), The depletion of striatal and cortical seroto
nergic systems after both chronic ethanol treatment and withdrawal, co
uld be explained as an environment-dependent tolerance response, It ca
n be concluded that ethanol and/or psychotropic drugs interact with ne
urotransmission systems in specific ways in different regions of the b
rain.