Showing 2 results for Microdialysis.
A Vahabzadeh, M Fillenz,
Volume 12, Issue 3 (11-1998)
Abstract
Microdialysis was used to measure the effect of benzodiazepines (BDZs) on
basal levels and on stress-induced increases of 5 -hydroxytryptamine (5 -HT), 5 -
hydroxyind oleacetic acid (5 -HIAA) , noradrenaline (NA), and
dihydroxyphenylacetic acid (DOP AC). The stressors used were a 5 min tail pinch
or a 10 min period of restraint. A subcutaneous injection of 5 mg/kg diazepam
decreased basal levels of 5 -HT, 5 -HIAA, and DOPAC, but not NA. There was no
effect on the stress-induced increase in 5 -HT, NA, and 5 -HIAA, while the increase
in DOPAC was completely abolished. Local infusion of 5 µM flurazepam
decteased the basal level of 5 - HT but not 5 -HIAA and abolished the stress-induced
increase of 5 -HIAA but not 5 -HT. These results suggest that the anxiolytic action
of BDZs is unlikely to be attributable to the suppression of stress-induced increases
in the release of NA or 5 -HT in the hippocampus.
H Alaei, M Huotari, Pt Piepponen, L Ahtee, O Hanninen, Pt Mannisto,
Volume 17, Issue 3 (11-2003)
Abstract
In vivo microdialysis was used to study the effects of morphine on glutamate
release from the ventral tegmentum area (VTA) in freely moving rats. Intraperitoneal
(i.p.) injection of acute and repeated morphine at increasing doses significantly
enhanced glutamate release. Only a minor tolerance developed to this dosage
of morphine. AP-S (2-amino-5-phosphonovaleric acid, 0.5 mg/kg i.p.), a
NMDA receptor antagonist, given 20 min before each repeated morphine injection,
did not have a significant effect on the stimulated glutamate release . Conversely,
injection of CNQX (6-cyano-7-nitroquinoxaline-2, 3-dione, 0.5 mg/kg
i.p.), an AMPA receptor antagonist, 20 min before each morphine dose was found
to markedly inhibit morphine-induced glutamate release in the VTA. In all experiments,
glutamate release reduced by time. These results show for the first
time that acute and repeated injection of morphine stimulates glutamate release in
the conscious rat VTA via AMPA receptors.