Literature DB >> 2920772

Chronic diazepam treatment produces regionally specific changes in GABA-stimulated chloride influx.

R J Marley1, D W Gallager.   

Abstract

GABA-stimulated 36Cl- influx was used to investigate regional differences in response to chronic diazepam treatment by comparing cortical and cerebellar tissue from rats chronically treated with diazepam for 3 weeks. Using a treatment protocol which has previously been shown to produce behavioral tolerance and physical dependence, cortical membrane preparations from chronic diazepam-treated rats were found to exhibit a decreased responsiveness to the stimulation of 36Cl- influx by GABA and a corresponding decrease in the ability of flunitrazepam to enhance GABA-stimulated 36Cl-influx. This decrease in sensitivity to flunitrazepam, however, appears to reflect the underlying decrease in sensitivity to GABA. In contrast, in membrane vesicles prepared from cerebella of chronic diazepam-treated rats, there was no measurable effect on GABA-stimulated 36Cl--influx or on the enhancement of GABA-stimulated 36Cl- influx by flunitrazepam. These results support the suggestion that there is a regionally specific reduction in GABA/benzodiazepine receptor function following chronic benzodiazepine treatment.

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Year:  1989        PMID: 2920772     DOI: 10.1016/0014-2999(89)90151-9

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  13 in total

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8.  Subunit- and brain region-specific reduction of GABAA receptor subunit mRNAs during chronic treatment of rats with diazepam.

Authors:  Y Wu; H C Rosenberg; T H Chiu; T J Zhao
Journal:  J Mol Neurosci       Date:  1994       Impact factor: 3.444

9.  Chronic diazepam treatment in rats causes long-lasting changes in central [3H]-5-hydroxytryptamine and [14C]-gamma-aminobutyric acid release.

Authors:  P K Hitchcott; S E File; M Ekwuru; M J Neal
Journal:  Br J Pharmacol       Date:  1990-01       Impact factor: 8.739

10.  Imidazenil: a low efficacy agonist at alpha1- but high efficacy at alpha5-GABAA receptors fail to show anticonvulsant cross tolerance to diazepam or zolpidem.

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Journal:  Neuropharmacology       Date:  2008-05-09       Impact factor: 5.250

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