Impact of heterogeneous perisomatic IPSC populations on pyramidal cell firing rates

被引:15
作者
Aradi, I [1 ]
Santhakumar, V [1 ]
Soltesz, I [1 ]
机构
[1] Univ Calif Irvine, Dept Anat & Neurobiol, Irvine, CA 92697 USA
关键词
D O I
10.1152/jn.00916.2003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous computational modeling studies suggested a set of rules underlying the modulation of principal cell firing rates by heterogeneity in the synaptic parameters ( peak amplitude and decay kinetics) of populations of GABAergic inputs. Here we performed dynamic clamp experiments in CA1 hippocampal pyramidal cells to test these ideas in biological neurons. In agreement with the simulation studies, the effects of increasing the event-to-event variance in a population of perisomatically injected inhibitory postsynaptic current (IPSC) peak conductances caused either an increase, decrease, or no change in the firing rates of CA1 pyramidal cells depending on the mean around which the scatter was introduced, the degree of the scatter, the depolarization that the pyramidal cell received, and the IPSC reversal potential. In contrast to CA1 pyramidal cells, both model and biological CA3 pyramidal cells responded with bursts of action potentials to sudden, step-wise alterations in input heterogeneity. In addition, injections of 40-Hz IPSC conductances together with theta-modulated depolarizing current inputs to CA1 pyramidal cells demonstrated that the principles underlying the modulation of pyramidal cell excitability by heterogeneous IPSC populations also apply during membrane potential oscillations. Taken together, these experimental results and the computational modeling data show the existence of simple rules governing the interactions of heterogeneous interneuronal inputs and principal cells.
引用
收藏
页码:2849 / 2858
页数:10
相关论文
共 38 条
[1]   Postsynaptic effects of GABAergic synaptic diversity: regulation of neuronal excitability by changes in IPSC variance [J].
Aradi, I ;
Santhakumar, V ;
Chen, K ;
Soltesz, I .
NEUROPHARMACOLOGY, 2002, 43 (04) :511-522
[2]   Modulation of network behaviour by changes in variance in interneuronal properties [J].
Aradi, I ;
Soltesz, I .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 538 (01) :227-251
[3]   Rapid signaling at inhibitory synapses in a dentate gyrus interneuron network [J].
Bartos, M ;
Vida, I ;
Frotscher, M ;
Geiger, JRP ;
Jonas, P .
JOURNAL OF NEUROSCIENCE, 2001, 21 (08) :2687-2698
[4]   Gain modulation from background synaptic input [J].
Chance, FS ;
Abbott, LF ;
Reyes, AD .
NEURON, 2002, 35 (04) :773-782
[5]   Febrile seizures in the developing brain result in persistent modification of neuronal excitability in limbic circuits [J].
Chen, K ;
Baram, TZ ;
Soltesz, I .
NATURE MEDICINE, 1999, 5 (08) :888-894
[6]   Persistently modified h-channels after complex febrile seizures convert the seizure-induced enhancement of inhibition to hyperexcitability [J].
Chen, K ;
Aradi, I ;
Thon, N ;
Eghbal-Ahmadi, M ;
Baram, TZ ;
Soltesz, I .
NATURE MEDICINE, 2001, 7 (03) :331-337
[7]   SYNCHRONIZATION OF NEURONAL-ACTIVITY IN HIPPOCAMPUS BY INDIVIDUAL GABAERGIC INTERNEURONS [J].
COBB, SR ;
BUHL, EH ;
HALASY, K ;
PAULSEN, O ;
SOMOGYI, P .
NATURE, 1995, 378 (6552) :75-78
[8]   Distribution of spontaneous currents along the somato-dendritic axis of rat hippocampal CA1 pyramidal neurons [J].
Cossart, R ;
Hirsch, JC ;
Cannon, RC ;
Dinoncourt, C ;
Wheal, HV ;
Ben-Ari, Y ;
Esclapez, M ;
Bernard, C .
NEUROSCIENCE, 2000, 99 (04) :593-603
[9]   Synaptic background noise controls the input/output characteristics of single cells in an in vitro model of in vivo activity [J].
Fellous, JM ;
Rudolph, M ;
Destexhe, A ;
Sejnowski, TJ .
NEUROSCIENCE, 2003, 122 (03) :811-829
[10]   Interneuron diversity series: Rhythm and mood in perisomatic inhibition [J].
Freund, TF .
TRENDS IN NEUROSCIENCES, 2003, 26 (09) :489-495