Effect of GABA on GnRH neurons switches from depolarization to hyperpolarization at puberty in the female mouse

被引:139
作者
Han, SK [1 ]
Abraham, IM [1 ]
Herbison, AE [1 ]
机构
[1] Babraham Inst, Neuroendocrinol Lab, Cambridge CB2 4AT, England
关键词
D O I
10.1210/en.143.4.1459
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The amino acid gamma-aminobutyric acid (GABA) plays an important role in the regulation of the GnRH neurons. We examined whether GABA depolarizes or hyperpolarizes GnRH neurons over postnatal development using gramicidin, perforated-patch electrophysiology combined with GnRH-LacZ transgenic mice in whom GnRH neurons can be made to fluoresce. The basic membrane properties and GABA responsiveness of GnRH neurons were not altered by transgene expression or fluorescence. Ten of 12 immature GnRH neurons (10-17 d) were depolarized by GABA in a direct and dose-dependent manner that was blocked by a GABA(A) receptor antagonist. In peripubertal GnRH neurons (25-30 d), GABA exerted depolarizing (4/11) as well as hyperpolarizing (5/11) effects on GnRH neurons. In adult female mice, GABA was found to exert exclusively hyperpolarizing actions on GnRH neurons (9/10) that were direct and mediated by the GABA(A) receptor. GABA switched from depolarizing to hyperpolarizing actions around postnatal d 31, the time of vaginal opening. Unidentified preoptic area neurons exhibited predominantly hyperpolarizing responses to GABA at all three postnatal stages. These findings demonstrate that GnRH neurons display an unusually late postnatal switch in their response to GABA. They also provide the first direct evidence that GABA inhibits the electrical activity of postpubertal GnRH neurons.
引用
收藏
页码:1459 / 1466
页数:8
相关论文
共 59 条
[1]   GABA(A), NMDA and AMPA receptors: a developmentally regulated 'menage a trois' [J].
BenAri, Y ;
Khazipov, R ;
Leinekugel, X ;
Caillard, O ;
Gaiarsa, JL .
TRENDS IN NEUROSCIENCES, 1997, 20 (11) :523-529
[2]   A conditional tetracycline-regulated increase in gamma amino butyric acid production near luteinizing hormone-releasing hormone nerve terminals disrupts estrous cyclicity in the rat [J].
Bilger, M ;
Heger, S ;
Brann, DW ;
Paredes, A ;
Ojeda, SR .
ENDOCRINOLOGY, 2001, 142 (05) :2102-2114
[3]   Effects of γ-aminobutyric acidA receptor manipulation on migrating gonadotropin-releasing hormone neurons through the entire migratory route in vivo and in vitro [J].
Bless, EP ;
Westaway, WA ;
Schwarting, GA ;
Tobet, SA .
ENDOCRINOLOGY, 2000, 141 (03) :1254-1262
[4]   Shunting versus inactivation: Analysis of presynaptic inhibitory mechanisms in primary afferents of the crayfish [J].
Cattaert, D ;
El Manira, A .
JOURNAL OF NEUROSCIENCE, 1999, 19 (14) :6079-6089
[5]   GABA - AN EXCITATORY TRANSMITTER IN EARLY POSTNATAL LIFE [J].
CHERUBINI, E ;
GAIARSA, JL ;
BENARI, Y .
TRENDS IN NEUROSCIENCES, 1991, 14 (12) :515-519
[6]   Correlation between electrophysiological and morphological characteristics during maturation of rat supraoptic neurons [J].
Chevaleyre, V ;
Moos, FC ;
Desarménien, MG .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 13 (06) :1136-1146
[7]   Developmental expression of ClC-2 in the rat nervous system [J].
Clayton, GH ;
Staley, KJ ;
Wilcox, CL ;
Owens, GC ;
Smith, RL .
DEVELOPMENTAL BRAIN RESEARCH, 1998, 108 (1-2) :307-318
[8]   BIPHASIC GABAERGIC REGULATION OF GNRH SECRETION IN GT(1) CELL-LINES [J].
DELAESCALERA, GM ;
CHOI, ALH ;
WEINER, RI .
NEUROENDOCRINOLOGY, 1994, 59 (05) :420-425
[9]   GRAMICIDIN-PERFORATED PATCH RECORDING - GABA RESPONSE IN MAMMALIAN NEURONS WITH INTACT INTRACELLULAR CHLORIDE [J].
EBIHARA, S ;
SHIRATO, K ;
HARATA, N ;
AKAIKE, N .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 484 (01) :77-86
[10]  
Fueshko SM, 1998, J NEUROSCI, V18, P2560