GABAergic control of synaptic summation in hippocampal CA1 pyramidal neurons
- PMID: 11811662
- DOI: 10.1002/hipo.1083
GABAergic control of synaptic summation in hippocampal CA1 pyramidal neurons
Abstract
The primary function of neurons is to integrate synaptic inputs and to transmit the results to other cells. It was shown previously that separate excitatory inputs to hippocampal pyramidal neurons are summated nonlinearly. In the hippocampus, responses of pyramidal neurons are influenced by GABAergic inputs in feed-forward or feedback manner, and also by oscillatory network activities. It is likely that these GABAergic inputs regulate the way synaptic inputs are summated. To examine the roles of GABAergic inputs on synaptic summation, we made whole-cell recordings from the cell bodies of CA1 pyramidal neurons in rat hippocampal slices while stimulating two independent input pathways with short interstimulus intervals, and examined the manner by which postsynaptic potentials were summated. We found that: 1) the summation of the perforant pathway and the Schaffer collateral pathway inputs was sublinear when the interval between two inputs was shorter than 30 ms, 2) the blockade of GABA(A) receptors partially suppressed the sublinearity, and 3) further blockade of GABA(B) receptors removed the sublinearity totally. We also found that 4) the summation was superlinear under the concomitant blockade of GABA(A) and GABA(B) receptors when the two inputs arrived with no delay. Thus our study demonstrates that GABAergic inputs are responsible for keeping the summation of two separate inputs on CA1 pyramidal neurons sublinear.
Similar articles
-
Inhibitory synaptic plasticity regulates pyramidal neuron spiking in the rodent hippocampus.Neuroscience. 2008 Jul 31;155(1):64-75. doi: 10.1016/j.neuroscience.2008.05.009. Epub 2008 May 21. Neuroscience. 2008. PMID: 18562122
-
Synchronization of GABAergic inputs to CA3 pyramidal cells precedes seizure-like event onset in juvenile rat hippocampal slices.J Neurophysiol. 2009 Oct;102(4):2538-53. doi: 10.1152/jn.91318.2008. Epub 2009 Aug 12. J Neurophysiol. 2009. PMID: 19675286
-
Conditional dendritic spike propagation following distal synaptic activation of hippocampal CA1 pyramidal neurons.Nat Neurosci. 2005 Dec;8(12):1667-76. doi: 10.1038/nn1599. Epub 2005 Nov 20. Nat Neurosci. 2005. PMID: 16299501
-
Neuronal diversity and temporal dynamics: the unity of hippocampal circuit operations.Science. 2008 Jul 4;321(5885):53-7. doi: 10.1126/science.1149381. Science. 2008. PMID: 18599766 Free PMC article. Review.
-
Possible physiological role of the perforant path-CA1 projection.Hippocampus. 1995;5(2):141-6. doi: 10.1002/hipo.450050210. Hippocampus. 1995. PMID: 7633517 Review. No abstract available.
Cited by
-
Ultrafast simulation of large-scale neocortical microcircuitry with biophysically realistic neurons.Elife. 2022 Nov 7;11:e79535. doi: 10.7554/eLife.79535. Elife. 2022. PMID: 36341568 Free PMC article.
-
Mu opioid receptor activation normalizes temporo-ammonic pathway driven inhibition in hippocampal CA1.Neuropharmacology. 2011 Feb-Mar;60(2-3):472-9. doi: 10.1016/j.neuropharm.2010.10.029. Epub 2010 Nov 4. Neuropharmacology. 2011. PMID: 21056047 Free PMC article.
-
Cholinergic modulation of excitatory synaptic input integration in hippocampal CA1.J Physiol. 2010 Oct 1;588(Pt 19):3727-42. doi: 10.1113/jphysiol.2010.188581. Epub 2010 Aug 6. J Physiol. 2010. PMID: 20693290 Free PMC article.
-
Artificial Synaptic Devices Based on Natural Chicken Albumen Coupled Electric-Double-Layer Transistors.Sci Rep. 2016 Mar 24;6:23578. doi: 10.1038/srep23578. Sci Rep. 2016. PMID: 27008981 Free PMC article.
-
Precise excitation-inhibition balance controls gain and timing in the hippocampus.Elife. 2019 Apr 25;8:e43415. doi: 10.7554/eLife.43415. Elife. 2019. PMID: 31021319 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous
