Odours stimulate neuronal activity in the dorsolateral area of the hippocampal formation during path integration

The dorsolateral area of the hippocampal formation of birds is commonly assumed to play a central role in processing information needed for geographical positioning and homing. Previous work has interpreted odour-induced activity in this region as evidence for an ‘olfactory map’. Here, we show, using c-Fos expression as a marker, that neuronal activation in the dorsolateral area of the hippocampal formation of pigeons is primarily a response to odour novelty, not to the spatial distribution of odour sources that would be necessary for an olfactory map. Pigeons exposed to odours had significantly more neurons activated in this area of the brain than pigeons exposed to filtered air with odours removed. This increased activity was observed only in response to unfamiliar odours. No change in activity was observed when pigeons were exposed to home odours. These findings are consistent with non-home odours activating non-olfactory components of the pigeon''s navigation system. The pattern of neuronal activation in the triangular and dorsomedial areas of the hippocampal formation was, by contrast, consistent with the possibility that odours play a role in providing spatial information.     

A model for evoked activity of hippocampal neuronal population

A system of equations governing the activity of hippocampal neuron populations is proposed. This continual firing-rate model is aimed to simulate evoked potentials and synchronous wave activity of the neural tissue. The populations of excitatory and inhibitory neurons and the types of synaptic receptors are distinguished. The model is based on the idea of control and averaging of Hodgkin-Huxley equations, a simple model of a threshold elicitation of population action potential bursts, approximations of synaptic currents by the second-order differential equations, and hyperbolic partial derivative equation of axonal excitation propagation. The model was fitted to intracellular cordings of postsynaptic potentials and postsynaptic currents in CA1 of rat hippocampal slices.     

Field potentials evoked in the subiculum following postsynaptic discharge of hippocampal pyramidal neurons

Evoked potentials, represented by population spikes and slow waves, have been recorded from the subiculum, along its whole dorso-ventral extent, following postsynaptic activation and discharge of hippocampal pyramidal neurons. These potentials can be associated with synaptic excitatory effects generated on radially oriented neurons by hippocampal impulses reaching the subiculum at any dorso-ventral level, according to a segmental organization.     

Pannexin 1 activity in astroglia sets hippocampal neuronal network patterns

Astroglial release of molecules is thought to actively modulate neuronal activity, but the nature, release pathway, and cellular targets of these neuroactive molecules are still unclear. Pannexin 1, expressed by neurons and astrocytes, form nonselective large pore channels that mediate extracellular exchange of molecules. The functional relevance of these channels has been mostly studied in brain tissues, without considering their specific role in different cell types, or in neurons. Thus, our knowledge of astroglial pannexin 1 regulation and its control of neuronal activity remains very limited, largely due to the lack of tools targeting these channels in a cell-specific way. We here show that astroglial pannexin 1 expression in mice is developmentally regulated and that its activation is activity-dependent. Using astrocyte-specific molecular tools, we found that astroglial-specific pannexin 1 channel activation, in contrast to pannexin 1 activation in all cell types, selectively and negatively regulates hippocampal networks, with their disruption inducing a drastic switch from bursts to paroxysmal activity. This decrease in neuronal excitability occurs via an unconventional astroglial mechanism whereby pannexin 1 channel activity drives purinergic signaling-mediated regulation of hyperpolarisation-activated cyclic nucleotide (HCN)-gated channels. Our findings suggest that astroglial pannexin 1 channel activation serves as a negative feedback mechanism crucial for the inhibition of hippocampal neuronal networks.

Astrocytes have mostly been shown to boost neuronal activity. This study reveals that activity-dependent activation of astroglial pannexin 1 channels inhibits hippocampal neuronal networks by decreasing neuronal excitability via purinergic signaling, uncovering a novel astroglial negative feedback loop mechanism.     

Characteristics of the hippocampal formation functioning during wakefulness and paradoxical sleep

In view of the available published data concerning various concentration of neuromodulators in the brain during paradoxical sleep and wakefulness and the evidence for the influences of neuromodulators on efficiency of synaptic inputs to hippocampal neurons it is concluded that during paradoxical sleep, increase in concentrations of acetylcholine, cortisol, and dopamine and simultaneous decrease in serotonin and noradrenaline levels could synergistically lead to essential depression of efficacy of synaptic transmission in the polysynaptic pathway through the hippocampus (i.e. in the perforant path to dentate gyrus, from the dentate gyrus to CA3 area, from CA3 to CA1 area and from CA1 to the subiculum) but potentiation of the efficacy of the perforant input to pyramids of CA1 and CA3 areas and increase in efficacy of associative connections between CA3 neurones. The specified changes in functioning of the hippocampal loop can underlie differences in storing and extraction of information from memory during paradoxical sleep as compared to wakefulness.     

Effect of stimulation of neocortical regions and the subiculum on hippocampal neurons in rabbits

In chronic experiments on rabbits using extracellular recording of unit activity in hippocampal area CA₁ the effects of stimulation of the subiculum, posterior cingulate cortex, and anterior and posterior nonprimary areas of the neocortex were investigated. The effects of such stimulation were compared in the intact and chronically isolated hippocampus. It is concluded from the results that direct two-way connections exist between CA₁ and the subiculum. Polysynaptic influences of the subiculum on CA₁ are realized through the entorhinal cortex, for they are not present in the isolated hippocampus. Influences of the neocortical areas studied on CA₁ are transmitted to some extent through a relay in the subiculum. The entorhinal cortex plays no part in the realization of polysynaptic effects. The effectiveness of these influences increases with removal of the principal hippocampal afferent systems.Institute of Biological Physics, Academy of Sciences of the USSR, Pushchino-on-Oka. Translated from Neirofiziologiya, Vol. 14, No. 3, pp. 315–323, May–June, 1982.     

Temperature dependence of neuronal activity in Guinea pig hypothalamic and hippocampal slices

Neuronal activity was recorded in surviving hippocampal and medial preoptic thalamic slices from guinea pigs using extracellular techniques during thermal changes. Rate of generating action potentials changed in seven of the 19 hypothalamic cells tested once a threshold temperature of 36–38°C had been reached. Above this range, activity in these neurons was temperature dependent. It is suggested that these neurons form a sensory element in the system controlling brain temperature over a narrow (1–2°C) range. In the hippocampus (the control structure), pyramidal layer cells were insensitive to temperatures in the 32–40°C range.Institute of Physiology, Academy of Sciences of the Byelorussian SSR, Minsk. Translated from Neirofiziologiya, Vol. 21, No. 3, pp. 358–365, May–June, 1989.     

Uncovering the synchronization dynamics from correlated neuronal activity quantifies assembly formation

 Synchronous network excitation is believed to play an outstanding role in neuronal information processing. Due to the stochastic nature of the contributing neurons, however, those synchronized states are difficult to detect in electrode recordings. We present a framework and a model for the identification of such network states and of their dynamics in a specific experimental situation. Our approach operationalizes the notion of neuronal groups forming assemblies via synchronization based on experimentally obtained spike trains. The dynamics of such groups is reflected in the sequence of synchronized states, which we describe as a renewal dynamics. We furthermore introduce a rate function which is dependent on the internal network phase that quantifies the activity of neurons contributing to the observed spike train. This constitutes a hidden state model which is formally equivalent to a hidden Markov model, and all its parameters can be accurately determined from the experimental time series using the Baum-Welch algorithm. We apply our method to recordings from the cat visual cortex which exhibit oscillations and synchronizations. The parameters obtained for the hidden state model uncover characteristic properties of the system including synchronization, oscillation, switching, background activity and correlations. In applications involving multielectrode recordings, the extracted models quantify the extent of assembly formation and can be used for a temporally precise localization of system states underlying a specific spike train. Received: 30 March 1993/Accepted in revised form: 16 April 1994     

Activity-dependent wiring of the developing hippocampal neuronal circuit

In the developing hippocampus, functional excitatory synaptic connections seem to be recruited from a preformed, initially silent synaptic network. This functional synapse induction requires presynaptic action potentials paired with postsynaptic depolarization, thus obeying Hebb's rule of association. During early postnatal development the hippocampus exhibits an endogenous form of patterned neuronal activity that is driven by GABAergic depolarization. We propose that this recurrent activity promotes the input-specific induction of functional synapses in the CA1 region. Thus, activity-dependent synaptic reorganization in the developing hippocampus appears to be dominated by an active recruitment of new synapses rather than an active elimination of redundant connections.     

Separable actions of acetylcholine and noradrenaline on neuronal ensemble formation in hippocampal CA3 circuits

In the hippocampus, episodic memories are thought to be encoded by the formation of ensembles of synaptically coupled CA3 pyramidal cells driven by sparse but powerful mossy fiber inputs from dentate gyrus granule cells. The neuromodulators acetylcholine and noradrenaline are separately proposed as saliency signals that dictate memory encoding but it is not known if they represent distinct signals with separate mechanisms. Here, we show experimentally that acetylcholine, and to a lesser extent noradrenaline, suppress feed-forward inhibition and enhance Excitatory–Inhibitory ratio in the mossy fiber pathway but CA3 recurrent network properties are only altered by acetylcholine. We explore the implications of these findings on CA3 ensemble formation using a hierarchy of models. In reconstructions of CA3 pyramidal cells, mossy fiber pathway disinhibition facilitates postsynaptic dendritic depolarization known to be required for synaptic plasticity at CA3-CA3 recurrent synapses. We further show in a spiking neural network model of CA3 how acetylcholine-specific network alterations can drive rapid overlapping ensemble formation. Thus, through these distinct sets of mechanisms, acetylcholine and noradrenaline facilitate the formation of neuronal ensembles in CA3 that encode salient episodic memories in the hippocampus but acetylcholine selectively enhances the density of memory storage.     

Gene profiling of hippocampal neuronal culture

We performed mRNA expression profiling of mouse primary hippocampal neurones undergoing differentiation in vitro. We show that 2314 genes significantly changed expression during neuronal differentiation. The temporal resolution of our experiment (six time points) permits us to distinguish between gene expression patterns characteristic for the axonal and for the dendritic stages of neurite outgrowth. Cluster analysis reveals that, in the process of in vitro neuronal differentiation, a high level of expression of genes involved in the synthesis of DNA and proteins precedes the up regulation of genes involved in protein transport, energy generation and synaptic functions. We report in detail changes in gene expression for genes involved in the synaptic vesicle cycle. Data for other genes can be accessed at our website. We directly compare expression of 475 genes in the differentiating neurones and the developing mouse hippocampus. We demonstrate that the program of gene expression is accelerated in vitro as compared to the situation in vivo. When this factor is accounted for, the gene expression profiles in vitro and in vivo become very similar (median gene-wise correlation 0.787). Apparently once the cells have taken a neuronal fate, the further program of gene expression is largely independent of histological or anatomical context. Our results also demonstrate that a comparison across the two experimental platforms (cDNA microarrays and oligonucleotide chips) and across different biological paradigms is feasible.     

L-trans-PDC enhances hippocampal neuronal activity by stimulating glial glutamate release independently of blocking transporters

The glutamate transporter inhibitor, L-trans-pyrrolidine-2,4-dicarboxylic acid (PDC) reversibly enhanced hippocampal neuronal activity in the rat and mouse dentate gyrus. The PDC action was still found in mice lacking the glial glutamate transporter GLT-1. PDC did not influence the rate of spontaneous miniature excitatory postsynaptic currents and spontaneous inhibitory postsynaptic currents, ionotropic glutamate receptor currents, or GABA-evoked currents in cultured rat hippocampal neurons. PDC increased glutamate released from cultured hippocampal astrocytes from normal rats, normal mice, and GLT-1 knock-out mice, that is not inhibited by deleting extracellular Na(+), while the drug had no effect on the release from cultured rat hippocampal neurons. The results of the present study thus suggest that PDC stimulates glial glutamate release by a mechanism independent of inhibiting glutamate transporters, which perhaps causes an increase in synaptic glutamate concentrations, in part responsible for the enhancement in hippocampal neuronal activity.