Development of GABAA receptor-mediated inhibitory postsynaptic currents in hippocampus

被引:52
作者
Banks, MI
Hardie, JB
Pearce, RA
机构
[1] Univ Wisconsin, Dept Anesthesiol, Madison, WI 53706 USA
[2] Univ Wisconsin, Neurosci Training Program, Madison, WI 53706 USA
关键词
D O I
10.1152/jn.00026.2002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Hippocampal CA1 pyramidal cells receive two kinetic classes of GABA(A) receptor-mediated inhibition: slow dendritic inhibitory postsynaptic currents (GABA(A,slow) IPSCs) and fast perisomatic (GABA(A,fast)) IPSCs. These two classes of IPSCs are likely generated by two distinct groups of interneurons, and we have previously shown that the kinetics of the IPSCs have important functional consequences for generating synchronous firing patterns. Here, we studied developmental changes in the properties of GABA(A,fast) and GABA(A,slow) spontaneous, miniature, and evoked IPSCs (sIPSCs, mIPSCs, and eIPSCs, respectively) using whole cell voltage-clamp recordings in brain slices from animals aged P10-P35. We found that the rate of GABA(A,slow) sIPSCs increased by over 70-fold between P11 and P35 (from 0.0017 to 0.12 s(-1)). Over this same age range, we observed a >15-fold increase in the maximal amplitude of GABA(A,slow) eIPSCs evoked by stratum lacunosum-moleculare (SL-M) stimuli. However, the rate and amplitude of GABA(A,slow) mIPSCs remained unchanged between P10 and P30, suggesting that the properties of GABA(A,slow) synapses remained stable over this age range, and that the increase in sIPSC rate and in eIPSC amplitude was due to increased excitability or excitation of GABA(A,slow) interneurons. This hypothesis was tested using bath application of norepinephrine (NE), which we found at low concentrations (1 muM) selectively increased the rate of GABA(A,slow) SIPSCS while leaving GABA(A,fast) sIPSCs unchanged. This effect was observed in animals as young as P13 and was blocked by coapplication of tetrodotoxin, suggesting that NE was acting to increase the spontaneous firing rate of GABA(A,slow) interneurons and consistent with our hypothesis that developmental changes in GABA(A,slow) IPSCs are due to changes in presynaptic excitability. In contrast to the changes we observed in GABA(A,slow) IPSCs, the properties of GABA(A,fast) sIPSCs remained largely constant between P11 and P35, whereas the rate, amplitude, and kinetics of GABA(A,fast) mIPSCs showed significant changes between P10 and P30, suggesting counter-balancing changes in action potential-dependent GABA(A,fast) sIPSCs. These observations suggest differential developmental regulation of the firing properties of GABA(A,fast) and GABA(A,slow) interneurons in CA1 between P10 and P35.
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页码:3097 / 3107
页数:11
相关论文
共 42 条
[1]   Properties of a calcium-activated K+ current on interneurons in the developing rat hippocampus [J].
Aoki, T ;
Baraban, SC .
JOURNAL OF NEUROPHYSIOLOGY, 2000, 83 (06) :3453-3461
[2]   Interactions between distinct GABAA circuits in hippocampus [J].
Banks, MI ;
White, JA ;
Pearce, RA .
NEURON, 2000, 25 (02) :449-457
[3]  
Banks MI, 1998, J NEUROSCI, V18, P1305
[4]  
BENARI Y, 1990, PROG BRAIN RES, V83, P313
[5]  
Bergles DE, 1996, J NEUROSCI, V16, P572
[6]   THE FORMATION AND MATURATION OF SYNAPSES IN THE VISUAL-CORTEX OF THE RAT .2. QUANTITATIVE-ANALYSIS [J].
BLUE, ME ;
PARNAVELAS, JG .
JOURNAL OF NEUROCYTOLOGY, 1983, 12 (04) :697-712
[7]   CNQX increases GABA-mediated synaptic transmission in the cerebellum by an AMPA/kainate receptor-independent mechanism [J].
Brickley, SG ;
Farrant, M ;
Swanson, GT ;
Cull-Candy, SG .
NEUROPHARMACOLOGY, 2001, 41 (06) :730-736
[8]   GABA - AN EXCITATORY TRANSMITTER IN EARLY POSTNATAL LIFE [J].
CHERUBINI, E ;
GAIARSA, JL ;
BENARI, Y .
TRENDS IN NEUROSCIENCES, 1991, 14 (12) :515-519
[9]   Protracted postnatal development of inhibitory synaptic transmission in rat hippocampal area CA1 neurons [J].
Cohen, AS ;
Lin, DD ;
Coulter, DA .
JOURNAL OF NEUROPHYSIOLOGY, 2000, 84 (05) :2465-2476
[10]   Effects of a naturally occurring neurosteroid on GABAA IPSCs during development in rat hippocampal or cerebellar slices [J].
Cooper, EJ ;
Johnston, GAR ;
Edwards, FA .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 521 (02) :437-449