GABAA receptor modulation by neurosteroids in models of temporal lobe epilepsies
被引:42
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作者:
Ferando, Isabella
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机构:
Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Interdept Grad Program Mol Cellular & Integrat Ph, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
Ferando, Isabella
[1
,3
]
Mody, Istvan
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机构:
Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
Mody, Istvan
[1
,2
]
机构:
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Interdept Grad Program Mol Cellular & Integrat Ph, Los Angeles, CA 90095 USA
Temporal lobe epilepsy;
Neurosteroids;
GABA(A) receptors;
Tonic current;
SUBUNIT MESSENGER-RNAS;
IN-VIVO MICRODIALYSIS;
TONIC INHIBITION;
A RECEPTOR;
RAT HIPPOCAMPUS;
GRANULE CELLS;
STATUS EPILEPTICUS;
PILOCARPINE MODEL;
DELTA-SUBUNIT;
NEUROACTIVE STEROIDS;
D O I:
10.1111/epi.12038
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Epilepsies consist of a spectrum of neurologic disorders typically characterized by unpredictable and dysfunctional network behaviors in the central nervous system (CNS), which lead to discrete episodes of large bouts of uncontrolled neuronal synchrony that interfere with the normal functioning of the brain. Temporal lobe epilepsy (TLE) is accompanied by changes in interneuronal innervation and modifications in different ?-aminobutyric acid (GABA)A receptor subunits. Hormones play an important role in modulating the overall excitability of neurons, and at the same time hormonal pathways are frequently modified during epilepsy. This review focuses on TLE-correlated modifications of GABAergic transmission, and in particular on the implications of some of our own findings related to GABAARs containing the d subunits (d-GABAARs). These are extra- or perisynaptic GABAARs that mediate tonic inhibition, a major component of the inhibitory mechanism in the brain. The most potent endogenous modulators of d-GABAARs are neurosteroids, which act as positive allosteric modulators. Plasticity of d-GABAARs during TLE consists of down-regulation of the subunit in the dentate gyrus granule cells (DGGCs), while being up-regulated in interneurons. Surprisingly, the level of tonic inhibition in DGGCs remains unchanged, consistent with the idea that it becomes mediated by GABAARs containing other subunits. In parallel, tonic inhibition in a TLE model ceases to be sensitive to neurosteroid potentiation. In contrast, as predicted by the anatomic plasticity, interneuronal tonic current is increased, and remains sensitive to neurosteroids. These findings have important pharmacologic implications. Where neurosteroids normally have sedative and anticonvulsant effects, bimodal and cell-type specific modulations in their natural targets might weaken the inhibitory control on the dentate gate, under circumstances of altered neurosteroids levels (stress, ovarian cycle, or the postpartum period).
机构:
Tokyo Metropolitan Univ, Grad Sch Human Hlth Sci, Div Frontier Hlth Sci, Tokyo 158, JapanTokyo Metropolitan Univ, Grad Sch Human Hlth Sci, Div Frontier Hlth Sci, Tokyo 158, Japan
Murashima, Yoshiya L.
Yoshii, Mitsunobu
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Tokyo Metropolitan Univ, Grad Sch Human Hlth Sci, Div Frontier Hlth Sci, Tokyo 158, JapanTokyo Metropolitan Univ, Grad Sch Human Hlth Sci, Div Frontier Hlth Sci, Tokyo 158, Japan
机构:
Virginia Commonwealth Univ, Med Coll Virginia, Dept Neurol, Richmond, VA 23298 USAVirginia Commonwealth Univ, Med Coll Virginia, Dept Neurol, Richmond, VA 23298 USA
机构:
Univ Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, EnglandUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
Miller, Paul S.
Scott, Suzanne
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机构:
Univ Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
MRC Lab Mol Biol, Neurobiol Div, Cambridge, EnglandUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
Scott, Suzanne
Masiulis, Simonas
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Univ Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
MRC Lab Mol Biol, Neurobiol Div, Cambridge, EnglandUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
Masiulis, Simonas
De Colibus, Luigi
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Univ Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, EnglandUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
De Colibus, Luigi
Pardon, Els
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机构:
Vrije Univ Brussel, Struct Biol Brussels, Cambridge, England
VIB, VUB Ctr Struct Biol, Brussels, BelgiumUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
Pardon, Els
Steyaert, Jan
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机构:
Vrije Univ Brussel, Struct Biol Brussels, Cambridge, England
VIB, VUB Ctr Struct Biol, Brussels, BelgiumUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
Steyaert, Jan
Aricescu, A. Radu
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机构:
Univ Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England
MRC Lab Mol Biol, Neurobiol Div, Cambridge, EnglandUniv Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Oxford, England