A model of atropine-resistant theta oscillations in rat hippocampal area CA1

被引:135
作者
Gillies, MJ
Traub, RD
LeBeau, FEN
Davies, CH
Gloveli, T
Buhl, EH
Whittington, MA
机构
[1] Univ Leeds, Sch Biomed Sci, Leeds LS2 9NQ, W Yorkshire, England
[2] GlaxoSmithKline, Harlow CM19 5AW, Essex, England
[3] SUNY Hlth Sci Ctr, Dept Physiol & Pharmacol, Brooklyn, NY 11203 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2002年 / 543卷 / 03期
基金
英国惠康基金;
关键词
D O I
10.1113/jphysiol.2002.024588
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Theta frequency oscillations are a predominant feature of rhythmic activity in the hippocampus. We demonstrate that hippocampal area CA1 generates atropine-resistant theta population oscillations in response to metabotropic glutamate receptor activation under conditions of reduced AMPA receptor activation. This activity occurred in the absence of inputs from area CA3 and extra-ammonic areas. Field theta oscillations were co-expressed with pyramidal distal apical dendritic burst spiking and were temporally related to trains of IPSPs with slow kinetics. Pyramidal somatic responses showed theta oscillations consisted of compound inhibitory synaptic potentials with initial IPSPs with slow kinetics followed by trains of smaller, faster IPSPs. Pharmacological modulation of IPSPs altered the theta oscillation suggesting an inhibitory network origin. Somatic IPSPs, dendritic burst firing and stratum pyramidale interneuron activity were all temporally correlated with spiking in stratum oriens interneurons demonstrating intrinsic theta-frequency oscillations. Disruption of spiking in these interneurons was accompanied by a loss of both field theta and theta frequency IPSP trains. We suggest that population theta oscillations can be generated as a consequence of intrinsic theta frequency spiking activity in a subset of stratum oriens interneurons controlling electrogenesis in pyramidal cell apical dendrites.
引用
收藏
页码:779 / 793
页数:15
相关论文
共 37 条
[1]  
Awad H, 2000, J NEUROSCI, V20, P7871
[2]   Interactions between distinct GABAA circuits in hippocampus [J].
Banks, MI ;
White, JA ;
Pearce, RA .
NEURON, 2000, 25 (02) :449-457
[3]  
BRAGIN A, 1995, J NEUROSCI, V15, P47
[4]   DIVERSE SOURCES OF HIPPOCAMPAL UNITARY INHIBITORY POSTSYNAPTIC POTENTIALS AND THE NUMBER OF SYNAPTIC RELEASE SITES [J].
BUHL, EH ;
HALASY, K ;
SOMOGYI, P .
NATURE, 1994, 368 (6474) :823-828
[5]   CELLULAR BASES OF HIPPOCAMPAL EEG IN THE BEHAVING RAT [J].
BUZSAKI, G ;
LEUNG, LWS ;
VANDERWOLF, CH .
BRAIN RESEARCH REVIEWS, 1983, 6 (02) :139-171
[6]   2-STAGE MODEL OF MEMORY TRACE FORMATION - A ROLE FOR NOISY BRAIN STATES [J].
BUZSAKI, G .
NEUROSCIENCE, 1989, 31 (03) :551-570
[7]   LAMINAR DISTRIBUTION OF HIPPOCAMPAL RHYTHMIC SLOW ACTIVITY (RSA) IN THE BEHAVING RAT - CURRENT SOURCE DENSITY ANALYSIS, EFFECTS OF URETHANE AND ATROPINE [J].
BUZSAKI, G ;
CZOPF, J ;
KONDAKOR, I ;
KELLENYI, L .
BRAIN RESEARCH, 1986, 365 (01) :125-137
[8]   Theta oscillations in the hippocampus [J].
Buzsáki, G .
NEURON, 2002, 33 (03) :325-340
[9]  
Chapman CA, 1999, J NEUROSCI, V19, P8637
[10]   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