TY - JOUR
T1 - Potentiation of GABAA receptors by neurosteroids
T2 - Mechanisms and sites
AU - Steinbach, Joseph H.
AU - Akk, Gustav
N1 - Funding Information:
We thank all the members of our Program Project Grant for advice and assistance. In particular, we thank Doug Covey for steroids, Alex Evers for sharing results from binding experiments, Steve Mennerick and Chuck Zorumski for sharing results from experiments with other cell types, and John Bracamontes for molecular biological manipulations and cell culture work. This work supported by NIH P01 GM-47969.
PY - 2005/11
Y1 - 2005/11
N2 - Neurosteroids increase the strength of neuronal inhibition by enhancing the activity of GABA-A receptors. The response to lower concentrations of GABA is increased in the presence of these drugs. One question is the nature of the basis for the potentiation - is there a change in the affinity of the receptor for GABA or an increase in the efficacy of activation? The answer for these drugs is that the major change occurs in the efficacy of activation, with no change in channel opening but a decrease in rates for entering states with a closed channel. There are at least 2 sites of action, which can be distinguished by the activity of steroid analogues with different structures. There are at least 3 mechanisms of action. Mutations of GABAA receptor subunits indicate that at least one site for steroid action is likely to be at the extreme carboxyl end of the γ2 subunit. Analysis of data obtained at a low concentration of GABA suggests that the ability of steroids to potentiate the GABAA receptor may be affected by the extent of ligation with GABA.
AB - Neurosteroids increase the strength of neuronal inhibition by enhancing the activity of GABA-A receptors. The response to lower concentrations of GABA is increased in the presence of these drugs. One question is the nature of the basis for the potentiation - is there a change in the affinity of the receptor for GABA or an increase in the efficacy of activation? The answer for these drugs is that the major change occurs in the efficacy of activation, with no change in channel opening but a decrease in rates for entering states with a closed channel. There are at least 2 sites of action, which can be distinguished by the activity of steroid analogues with different structures. There are at least 3 mechanisms of action. Mutations of GABAA receptor subunits indicate that at least one site for steroid action is likely to be at the extreme carboxyl end of the γ2 subunit. Analysis of data obtained at a low concentration of GABA suggests that the ability of steroids to potentiate the GABAA receptor may be affected by the extent of ligation with GABA.
KW - Anesthetic mechanism
KW - GABA-A receptor
KW - Neurosteroid
KW - Potentiation
UR - http://www.scopus.com/inward/record.url?scp=33646444756&partnerID=8YFLogxK
U2 - 10.1016/j.ics.2005.07.077
DO - 10.1016/j.ics.2005.07.077
M3 - Article
AN - SCOPUS:33646444756
SN - 0531-5131
VL - 1283
SP - 21
EP - 25
JO - International Congress Series
JF - International Congress Series
ER -