Neurosteroid interactions with synaptic and extrasynaptic GABAA receptors: regulation of subunit plasticity, phasic and tonic inhibition, and neuronal network excitability

被引:196
作者
Carver, Chase Matthew [1 ]
Reddy, Doodipala Samba [1 ]
机构
[1] Texas A&M Univ, Hlth Sci Ctr, Coll Med, Dept Neurosci & Expt Therapeut, Bryan, TX 77807 USA
基金
美国国家卫生研究院;
关键词
GABA; GABA(A) receptor; Neurosteroid; Allopregnanolone; delta-Subunit; Tonic inhibition; Phasic inhibition; Extrasynaptic receptors; GAMMA-AMINOBUTYRIC-ACID; DENTATE GRANULE CELLS; ENHANCED ANTICONVULSANT ACTIVITY; POSITIVE ALLOSTERIC MODULATOR; HIPPOCAMPUS KINDLING MODEL; DISEASE-MODIFYING ACTIVITY; TRAUMATIC BRAIN-INJURY; CA1 PYRAMIDAL NEURONS; PROTEIN; 18; KDA; A-RECEPTOR;
D O I
10.1007/s00213-013-3276-5
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Neurosteroids are steroids synthesized within the brain with rapid effects on neuronal excitability. Allopregnanolone, allotetrahydrodeoxycorticosterone, and androstanediol are three widely explored prototype endogenous neurosteroids. They have very different targets and functions compared to conventional steroid hormones. Neuronal gamma-aminobutyric acid (GABA) type A (GABA(A)) receptors are one of the prime molecular targets of neurosteroids. This review provides a critical appraisal of recent advances in the pharmacology of endogenous neurosteroids that interact with GABA(A) receptors in the brain. Neurosteroids possess distinct, characteristic effects on the membrane potential and current conductance of the neuron, mainly via potentiation of GABA(A) receptors at low concentrations and direct activation of receptor chloride channel at higher concentrations. The GABA(A) receptor mediates two types of inhibition, now characterized as synaptic (phasic) and extrasynaptic (tonic) inhibition. Synaptic release of GABA results in the activation of low-affinity gamma 2-containing synaptic receptors, while high-affinity delta-containing extrasynaptic receptors are persistently activated by the ambient GABA present in the extracellular fluid. Neurosteroids are potent positive allosteric modulators of synaptic and extrasynaptic GABA(A) receptors and therefore enhance both phasic and tonic inhibition. Tonic inhibition is specifically more sensitive to neurosteroids. The resulting tonic conductance generates a form of shunting inhibition that controls neuronal network excitability, seizure susceptibility, and behavior. The growing understanding of the mechanisms of neurosteroid regulation of the structure and function of the synaptic and extrasynaptic GABA(A) receptors provides many opportunities to create improved therapies for sleep, anxiety, stress, epilepsy, and other neuropsychiatric conditions.
引用
收藏
页码:151 / 188
页数:38
相关论文
共 350 条
[1]
Protein Kinase C Phosphorylation Regulates Membrane Insertion of GABAA Receptor Subtypes That Mediate Tonic Inhibition [J].
Abramian, Armen M. ;
Comenencia-Ortiz, Eydith ;
Vithlani, Mansi ;
Tretter, Eva Verena ;
Sieghart, Werner ;
Davies, Paul A. ;
Moss, Stephen J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (53) :41795-41805
[2]
Characterization of brain neurons that express enzymes mediating neurosteroid biosynthesis [J].
Agis-Balboa, Roberto C. ;
Pinna, Graziano ;
Zhubi, Adrian ;
Maloku, Ekrem ;
Veldic, Marin ;
Costa, Erminio ;
Guidotti, Alessandro .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (39) :14602-14607
[3]
Neurosteroid access to the GABAA receptor [J].
Akk, G ;
Shu, HJ ;
Wang, C ;
Steinbach, JH ;
Zorumski, CF ;
Covey, DF ;
Mennerick, S .
JOURNAL OF NEUROSCIENCE, 2005, 25 (50) :11605-11613
[4]
Pregnenolone sulfate block of GABAA receptors:: mechanism and involvement of a residue in the M2 region of the α subunit [J].
Akk, G ;
Bracamontes, J ;
Steinbach, JH .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 532 (03) :673-684
[5]
Akk Gustav, 2009, Psychoneuroendocrinology, V34 Suppl 1, pS59, DOI 10.1016/j.psyneuen.2009.05.020
[6]
[Anonymous], 1981, Steroid Hormone Regulation of the Brain
[7]
L-655,708 enhances cognition in rats but is not proconvulsant at a dose selective for α5-containing GABAA receptors [J].
Atack, John R. ;
Bayley, Peter J. ;
Seabrook, Guy R. ;
Wafford, Keith A. ;
McKernan, Ruth M. ;
Dawson, Gerard R. .
NEUROPHARMACOLOGY, 2006, 51 (06) :1023-1029
[8]
NONVESICULAR RELEASE OF NEUROTRANSMITTER [J].
ATTWELL, D ;
BARBOUR, B ;
SZATKOWSKI, M .
NEURON, 1993, 11 (03) :401-407
[9]
Distinct functional and pharmacological properties of tonic and quantal inhibitory postsynaptic currents mediated by γ-aminobutyric acidA receptors in hippocampal neurons [J].
Bai, DL ;
Zhu, GY ;
Pennefather, P ;
Jackson, MF ;
Macdonald, JF ;
Orser, BA .
MOLECULAR PHARMACOLOGY, 2001, 59 (04) :814-824
[10]
Multiple roles for the first transmembrane domain of GABAA receptor subunits in neurosteroid modulation and spontaneous channel activity [J].
Baker, Carrie ;
Sturt, Brianne L. ;
Bamber, Bruce A. .
NEUROSCIENCE LETTERS, 2010, 473 (03) :242-247