Literature DB >> 6308160

Modulation of [3H]muscimol binding in rat cerebellar and cerebral cortical membranes by picrotoxin, pentobarbitone, and etomidate.

U Quast, O Brenner.   

Abstract

Modulation of [3H]muscimol binding by picrotoxin, pentobarbitone, and etomidate was investigated in rat cerebellar and cerebral cortical membranes. In cerebellum, at 37 degrees C in the presence of chloride ions (150 mM), picrotoxin and picrotoxinin decreased specific [3H]muscimol binding to 43 +/- 3% of control, with an EC50 of 1.2 +/- 0.1 microM. [3H]Muscimol saturation experiments in the presence and absence of picrotoxin indicated that the picrotoxin effect was primarily due to a loss of high-affinity muscimol sites with KD approximately equal to 10 nM. Pentobarbitone enhanced specific [3H]muscimol binding to 259 +/- 3% of control, with EC50 = 292 +/- 37 microM, and etomidate increased binding to 298 +/- 18%, with EC50 = 7.1 +/- 1.0 microM. The influence of temperature and chloride ion concentration on these effects was investigated by comparing experiments at 37 and 0 degrees C in the presence or absence of chloride at constant ionic strength. The results indicate that studies at 0 degrees C underestimate the coupling between GABA receptors and barbiturate sites and that they greatly overestimate the importance of chloride ions in this phenomenon. In cerebral cortical membranes (37 degrees C, 150 mM Cl-), the effect of picrotoxin was similar to that observed in cerebellum, whereas the effects of pentobarbitone and etomidate were greater, but occurred at higher concentrations.

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Year:  1983        PMID: 6308160     DOI: 10.1111/j.1471-4159.1983.tb04758.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  7 in total

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2.  A Multifaceted GABAA Receptor Modulator: Functional Properties and Mechanism of Action of the Sedative-Hypnotic and Recreational Drug Methaqualone (Quaalude).

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Journal:  Mol Pharmacol       Date:  2015-06-08       Impact factor: 4.436

Review 3.  Lipid bilayer regulation of membrane protein function: gramicidin channels as molecular force probes.

Authors:  Jens A Lundbaek; Shemille A Collingwood; Helgi I Ingólfsson; Ruchi Kapoor; Olaf S Andersen
Journal:  J R Soc Interface       Date:  2009-11-25       Impact factor: 4.118

4.  Positive and Negative Allosteric Modulation of an α1β3γ2 γ-Aminobutyric Acid Type A (GABAA) Receptor by Binding to a Site in the Transmembrane Domain at the γ+-β- Interface.

Authors:  Selwyn S Jayakar; Xiaojuan Zhou; Pavel Y Savechenkov; David C Chiara; Rooma Desai; Karol S Bruzik; Keith W Miller; Jonathan B Cohen
Journal:  J Biol Chem       Date:  2015-07-30       Impact factor: 5.157

5.  Lipid bilayer-mediated regulation of ion channel function by amphiphilic drugs.

Authors:  Jens A Lundbaek
Journal:  J Gen Physiol       Date:  2008-04-14       Impact factor: 4.086

6.  Modulation of the GABAA receptor by depressant barbiturates and pregnane steroids.

Authors:  J A Peters; E F Kirkness; H Callachan; J J Lambert; A J Turner
Journal:  Br J Pharmacol       Date:  1988-08       Impact factor: 8.739

7.  On the mechanism of action of picrotoxin on GABA receptor channels in dissociated sympathetic neurones of the rat.

Authors:  C F Newland; S G Cull-Candy
Journal:  J Physiol       Date:  1992-02       Impact factor: 5.182

  7 in total

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