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1.
Brain Struct Funct ; 221(3): 1607-21, 2016 Apr.
Article in English | MEDLINE | ID: mdl-25618022

ABSTRACT

Graph theory was used to analyze the anatomical network of the rat hippocampal formation and the parahippocampal region (van Strien et al., Nat Rev Neurosci 10(4):272-282, 2009). For this analysis, the full network was decomposed along the three anatomical axes, resulting in three networks that describe the connectivity within the rostrocaudal, dorsoventral and laminar dimensions. The rostrocaudal network had a connection density of 12% and a path length of 2.4. The dorsoventral network had a high cluster coefficient (0.53), a relatively high path length (1.62) and a rich club was identified. The modularity analysis revealed three modules in the dorsoventral network. The laminar network contained most information. The laminar dimension revealed a network with high clustering coefficient (0.47), a relatively high path length (2.11) and four significantly increased characteristic network building blocks (structural motifs). Thirteen rich club nodes were identified, almost all of them situated in the parahippocampal region. Six connector hubs were detected and all of them were located in the entorhinal cortex. Three large modules were revealed, indicating a close relationship between the perirhinal and postrhinal cortex as well as between the lateral and medial entorhinal cortex. These results confirmed the central position of the entorhinal cortex in the (para)hippocampal network and this possibly explains why pathology in this region has such profound impact on cognitive function, as seen in several brain diseases. The results also have implications for the idea of strict separation of the "spatial" and the "non-spatial" information stream into the hippocampus. This two-stream memory model suggests that the information influx from, respectively, the postrhinal-medial entorhinal cortex and the perirhinal-lateral entorhinal cortex is separate, but the current analysis shows that this apparent separation is not determined by anatomical constraints.


Subject(s)
Hippocampus/anatomy & histology , Models, Neurological , Parahippocampal Gyrus/anatomy & histology , Animals , Female , Image Processing, Computer-Assisted , Male , Neural Pathways/anatomy & histology , Neurons , Rats
2.
Neurosci Res ; 87: 26-32, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25011063

ABSTRACT

Peripheral nerve injury leads to Wallerian degeneration, followed by regeneration, in which functionality and morphology of the nerve are restored. We previously described that deficiency for complement component C6, which prevents formation of the membrane attack complex, slows down degeneration and results in an earlier recovery of sensory function after sciatic nerve injury compared to WT animals. In this study, we determine whether C6(-/-) rats have an intrinsic trait that affects sciatic nerve regeneration after injury. To study the contribution of complement activation on degeneration and regeneration with only minimal effect of complement activation, a crush injury model with only modest complement deposition was used. We compared the morphological and functional aspects of crushed nerves during degeneration and regeneration in C6(-/-) and WT animals. Morphological changes of myelin and axons showed similar degeneration and regeneration patterns in WT and C6(-/-) injured nerves. Functional degeneration and regeneration, recorded by ex vivo electrophysiology and in vivo foot flick test, showed that the timeline of the restoration of nerve conduction and sensory recovery also followed similar patterns in WT and C6(-/-) animals. Our findings suggest that C6 deficiency by itself does not alter the regrowth capacity of the peripheral nerve after crush injury.


Subject(s)
Complement C6/deficiency , Nerve Regeneration , Peripheral Nerve Injuries/physiopathology , Sciatic Nerve/injuries , Sciatic Nerve/physiology , Animals , Axons/physiology , Complement C6/physiology , Male , Myelin Sheath/physiology , Rats , Wallerian Degeneration/physiopathology
3.
J Neurosci Methods ; 222: 189-98, 2014 Jan 30.
Article in English | MEDLINE | ID: mdl-24286698

ABSTRACT

BACKGROUND: Peripheral nerve damage induces a sequence of degeneration and regeneration events with a specific time course that leads to (partial) functional recovery. Quantitative electrophysiological analysis of degeneration and recovery over time is essential to understand the process. NEW METHOD: The presented ex vivo neurophysiological method evaluates functional recovery of the propagation of the compound action potential after crush injury of the rat sciatic nerve. A 32 channel electrode array was used to monitor compound action potential propagation at time points between 1h and 35 days after semi-quantitative crush injury of the rat sciatic nerve. RESULTS: The compound action potential was characterized by four measures: the latency, the duration, the amplitude and a measure that combined time and location. These four parameters reflected the subsequent steps in early axonal degradation, the transition to rapid degeneration followed by sprouting and the long period of remyelination that accompanied regeneration. COMPARISON WITH EXISTING METHODS: The neurophysiology measures of the compound action potential were compared with the morphology of the nerve at representative time points and analysis of functional recovery of action potential propagation was compared with a behavioral test: the foot flick test. CONCLUSIONS: Our data suggests that the ex vivo electrophysiological method is complementary to the classical behavioral foot flick test in that it allows a detailed time analysis of the degeneration and early regeneration phases at a high spatial and temporal sensitivity. The results were well-matched with observations made with immunohistochemical and morphological methods.


Subject(s)
Nerve Degeneration , Nerve Regeneration , Sciatic Nerve/injuries , Sciatic Neuropathy/pathology , Sciatic Neuropathy/physiopathology , Action Potentials , Animals , Axons/pathology , Axons/physiology , Electric Stimulation , Electrodes , Electrophysiology/methods , Fluorescent Antibody Technique , In Vitro Techniques , Male , Nerve Crush , Nerve Degeneration/pathology , Nerve Degeneration/physiopathology , Neural Conduction , Neurophysiology/methods , Rats , Recovery of Function , Sciatic Nerve/pathology , Sciatic Nerve/physiopathology , Sciatic Neuropathy/etiology , Sensation/physiology , Tibial Nerve/pathology , Tibial Nerve/physiopathology , Time Factors
4.
Hippocampus ; 19(11): 1065-77, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19338021

ABSTRACT

Theta oscillations (4-12 Hz) are associated with learning and memory and are found in the hippocampus and the entorhinal cortex (EC). The spatio-temporal organization of rhythmic activity in the hippocampal-EC complex was investigated in vitro. The voltage sensitive absorption dye NK3630 was used to record the changes in aggregated membrane voltage simultaneously from the neuronal networks involved. Oscillatory activity at 7.0 Hz (range, 5.8-8.2) was induced in the slice with the muscarinic agonist carbachol (75-100 microM) in the presence of bicuculline (5 microM). Time relations between all recording sites were analyzed using cross-correlation functions which revealed systematic phase shifts in the theta oscillation recorded from the different entorhinal and hippocampal subregions. These phase shifts could be interpreted as propagation delays. The oscillation propagates over the slice in a characteristic spatio-temporal sequence, where the entorhinal cortex leads, followed by the subiculum and then the dentate gyrus (DG), to finally reach the CA3 and the CA1 area. The delay from dentate gyrus to the CA3 area was 12.4 +/- 1.1 ms (mean +/- s.e.m.) and from the CA3 to the CA1 region it was 10.9 +/- 1.9 ms. The propagation delays between the hippocampal subregions resemble the latencies of electrically evoked responses in the same subregions. Removing the entorhinal cortex from the slice changed the spatiotemporal pattern into a more clustered pattern with higher local synchrony. We conclude that in the slice, carbachol-induced theta oscillations are initiated in the entorhinal cortex. The EC could serve to control the information flow through the neuronal network in the subregions of the hippocampus by synchronizing and/or entraining their responses to external inputs.


Subject(s)
Biological Clocks/physiology , Entorhinal Cortex/physiology , Evoked Potentials/physiology , Hippocampus/physiology , Nonlinear Dynamics , Animals , Bicuculline/pharmacology , Biological Clocks/drug effects , Brain Mapping , Carbachol/pharmacology , Cholinergic Agonists/pharmacology , Evoked Potentials/drug effects , GABA Agonists/pharmacology , GABA Antagonists/pharmacology , In Vitro Techniques , Male , Muscimol/pharmacology , Neural Pathways/physiology , Rats , Rats, Wistar , Spectrum Analysis , Time Factors , Voltage-Sensitive Dye Imaging/methods
5.
Nat Rev Neurosci ; 10(4): 272-82, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19300446

ABSTRACT

Converging evidence suggests that each parahippocampal and hippocampal subregion contributes uniquely to the encoding, consolidation and retrieval of declarative memories, but their precise roles remain elusive. Current functional thinking does not fully incorporate the intricately connected networks that link these subregions, owing to their organizational complexity; however, such detailed anatomical knowledge is of pivotal importance for comprehending the unique functional contribution of each subregion. We have therefore developed an interactive diagram with the aim to display all of the currently known anatomical connections of the rat parahippocampal-hippocampal network. In this Review, we integrate the existing anatomical knowledge into a concise description of this network and discuss the functional implications of some relatively underexposed connections.


Subject(s)
Cell Communication/physiology , Memory/physiology , Nerve Net/physiology , Animals , Cell Adhesion/physiology , Humans
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