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Molecular Pharmacology

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Research ArticleArticle

Steroid Interaction with a Single Potentiating Site Is Sufficient to Modulate GABA-A Receptor Function

John R. Bracamontes and Joe Henry Steinbach
Molecular Pharmacology April 2009, 75 (4) 973-981; DOI: https://doi.org/10.1124/mol.108.053629
John R. Bracamontes
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Joe Henry Steinbach
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Abstract

Neuroactive steroids are efficacious potentiators of GABA-A receptors. Recent work has identified a site in the α1 subunit of the GABA-A receptor, that is essential for potentiation by steroids. However, each receptor contains two copies of the α1 subunit. We generated concatemers of subunits so that the α1 subunits could be mutated separately and examined the consequences of mutations that remove potentiation by most neurosteroids (α1 Q241L, α1 Q241W). Concatemers were expressed in Xenopus laevis oocytes, and activation by GABA, potentiation by neurosteroids, and the agonist activity of piperidine-4-sulfonic acid (P4S) were determined. When the α1 Q241L mutation is present in α1 subunits the EC50 for activation by GABA is shifted to higher concentration and potentiation by neurosteroids is diminished. When the α1 Q241W mutation is expressed, the EC50 for GABA is shifted to lower concentration, the relative efficacy of P4S is increased, and potentiation by neurosteroids is diminished. Mutation of only one α1 subunit does not produce the full effect of mutating both sites. Overall, the data demonstrate that at a macroscopic level, the presence of a single wild-type steroid-binding site is sufficient to mediate responses to steroid, but both must be mutated to completely remove the effects of steroids. Differences between the two sites seem to be relatively subtle.

Footnotes

  • This work was supported by the National Institutes of Health National Institute of General Medical Sciences [GM47969].

  • ABBREVIATIONS: 3α5αPOH, (3α,5α)-3,21-dihydroxypregnan-20-one; 3α5αP, (3α,5α)-3-hydroxypregnan-20-one; 3α5βPOH, (3α,5β)-3,21-dihydroxypregnan-20-one; P4S, piperidine-4-sulfonic acid; γβα(Q241L), γ2L-β2-α1(Q241L).

  • ↵ Embedded Image The online version of this article (available at http://molpharm.aspetjournals.org) contains supplemental material.

    • Received November 21, 2008.
    • Accepted January 28, 2009.
  • The American Society for Pharmacology and Experimental Therapeutics
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Molecular Pharmacology: 75 (4)
Molecular Pharmacology
Vol. 75, Issue 4
1 Apr 2009
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Research ArticleArticle

Steroid Interaction with a Single Potentiating Site Is Sufficient to Modulate GABA-A Receptor Function

John R. Bracamontes and Joe Henry Steinbach
Molecular Pharmacology April 1, 2009, 75 (4) 973-981; DOI: https://doi.org/10.1124/mol.108.053629

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Research ArticleArticle

Steroid Interaction with a Single Potentiating Site Is Sufficient to Modulate GABA-A Receptor Function

John R. Bracamontes and Joe Henry Steinbach
Molecular Pharmacology April 1, 2009, 75 (4) 973-981; DOI: https://doi.org/10.1124/mol.108.053629
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