Uncoupling at the GABA(A) receptor with chronic ethanol in the rat medial septum/diagonal band (MS/DB) /
(0. I uM) and GABA (0. I uM) in the ethanol treated cells.
| Main Author: | |
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| Format: | Thesis eBook |
| Language: | English |
| Published: |
[Place of publication not identified] :
[publisher not identified] ;
1997.
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| Subjects: | |
| Online Access: | Link to OAKTrust copy |
| Summary: | (0. I uM) and GABA (0. I uM) in the ethanol treated cells. a neurosteroid is uncoupled by chronic ethanol treatment adaptive changes by the CNS may occur. Adaptation could agonist or allosteric modulator. Varying results have been allopregnanolone (1.0 [uM) did show potentiation of the 3 uM allosteric mechanisms. However, the higher (1 [uM an allosteric modulator at the receptor without a change in and 1. 0 liM), loreclezole (10 [uM), or allopregnanolone (0. appear that chronic ethanol uncoupled potentiation of capable of directly activating the GABAAreceptor, did show changes in the function of neurotransmitter systems which chronic drug treatment. The goal of this project was to concentration of allopregnanolone, which is thought to be contrast, an increased potentiation was seen with midazolam dependence with ethanol are allosteric modulators at the dependence. Chronic ethanol was not found to induce an depressants. These agents which show cross-tolerance and determine-tine whether allosteric potentiation of ethanol; this finding is consistent with an adaptive change Functional tolerance to ethanol and physical dependence are GABA response in the chronically ethanol treated cells. In GABAAreceptor. Uncoupling is the decrease in the activity of GABAAreceptors by a benzodiazepine, a novel anticonvulsant or I uM) to 3 uM GABA. However, the higher concentration of in GABAAreceptor function. Increasing evidence suggests that the y-aminobutyric acid loreciezole or 0. I [uM allopregnanolone acting by general No potentiation was seen of 30 liM GABA response with any of obtained when looking at uncoupling at the GABAAreceptor with occur by downregulation of GABAAreceptor number or uncoupling of the GABAAreceptor sensitivity to ethanol and related CNS receptor number after prolonged exposure to either the resist the initial intoxicating actions of ethanol. the allosteric modulators tested. Therefore, it does not thought to involve central nervous system (CNS) adaptive typeA(GABA,) receptor is one target of ethanol where such uncoupling of potentiation with cells chronically exposed to uncoupling of the potentiation seen with rnidazolam (0. I which may contribute to functional tolerance and physical |
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| Item Description: | "Major subject: Medical Sciences". In title, subscripts are used. Vita. |
| Physical Description: | xii, 71 leaves : illustrations ; 28 cm. Also available online. Issued also on microfiche from Lange Micrographics. |
| Bibliography: | Includes bibliographical references: 63-70. |