|
Input Receptors |
Intrinsic Currents |
Output Transmitters |
Distal equivalent dendrite
|
Perforant path terminals
|
NMDA
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Perforant path terminals
|
AMPA
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Perforant path terminals
|
mGluR
|
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Hilar spiny interneuron terminals
|
GabaA
|
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Hilar spiny interneuron terminals
|
GabaB
|
|
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|
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Middle equivalent dendrite
|
Perforant path terminals
|
AMPA
|
|
Perforant path terminals
|
mGluR
|
|
Hilar spiny and aspiny interneuron terminals
|
GabaA
|
|
Perforant path terminals
|
NMDA
|
|
Hilar spiny and aspiny interneuron terminals
|
GabaB
|
|
|
I L high threshold
|
|
I Na,p
|
low density |
I Na,t
|
Indirect experimental evidence for dendritic Na channels was suggested by laminar filed potential studies (Jefferys JG, 197910 ). |
|
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Proximal equivalent dendrite
|
Hilar mossy cell collaterals and commissural cell terminals
|
NMDA
|
|
Hilar aspiny interneuron terminals
|
GabaB
|
|
Hilar mossy cell collaterals and commissural cell terminals
|
mGluR
|
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Hilar mossy cell collaterals and commissural cell terminals
|
AMPA
|
|
Hilar aspiny interneuron terminals
|
GabaA
|
|
|
I L high threshold
|
|
I Na,p
|
|
I Na,t
|
Indirect experimental evidence for dendritic Na channels was suggested by laminar filed potential studies (Jefferys JG, 197910 ). |
|
|
Soma
|
Basket cell terminals
|
GabaB
|
|
Basket cell terminals
|
GabaA
|
Whole cell and perforated patch recordings in slices showed bicuculline-dependent and ?independent GABA currents from juvenile rats, suggesting two types of GABAergic inputs. The bicuculline-independent component was present only at the earliest stages of maturation, had a later peak, slower time course of decay, and marked outward rectification. A trophic or signaling role rather than primarily inhibitory was suggested for this current (Liu YB et al, 1998 [rat]1 ). |
|
AMPA
|
NMDA and AMPA conductances properties were studied using patch-clamp recordings in morphologically identified cells in slices prepared from surgically removed medial temporal lobe specimens of epileptic patients (14 specimens from 14 patients (Isokawa M et al, 1997 [human]2 ). |
|
NMDA
|
NMDA and AMPA conductances properties were studied using patch-clamp recordings in morphologically identified cells in slices prepared from surgically removed medial temporal lobe specimens of epileptic patients (14 specimens from 14 patients). The wide range of changes in the slope conductance of the NMDA EPSCs suggests that the NMDA-receptor-mediated conductance could be altered in human epileptic DGCs (Isokawa M et al, 1997 [human]2 ). |
|
Nicotinic
|
|
|
I K,Ca
|
Voltage-clamp analysis suggested that IAHP in DG neurones is generated by about 1200 channels, and that about 60% are open at the peak of a maximal IAHP (Valiante TA et al, 1997 [rat]4 ). |
I L high threshold
|
Cells acutely dissociated from slices obtained from chronic temporal lobe epilepsy patients displayed a high-voltage activated Ca2+ conductance with a pronounced Ca2+-dependent inactivation (Nagerl UV and Mody I, 1998 [human]5 ). Patch-clamp recordings from human cells showed N-type, L-type and T-type currents that had similar pharmacological and kinetic characteristics as in control rats. The current density was significantly larger in human and in the kainate model compared to cells isolated from adult control rats (Beck H et al, 1998 [human]6 ). |
I N
|
Patch-clamp recordings from human cells showed N-type, L-type and T-type currents that had similar pharmacological and kinetic characteristics as in control rats. The current density was significantly larger in human and in the kainate model compared to cells isolated from adult control rats (Beck H et al, 1998 [human]6 ). |
I T low threshold
|
Patch-clamp recordings from human cells showed N-type, L-type and T-type currents that had similar pharmacological and kinetic characteristics as in control rats. The current density was significantly larger in human and in the kainate model compared to cells isolated from adult control rats (Beck H et al, 1998 [human]6 ). |
I A
|
Properties of potassium outward currents were investigated from 11 specimens obtained from patients with temporal lobe epilepsy. An IK but not IA or inwardly rectifying potassium currents, were observed in all cells (Beck H et al, 1996 [human]7 ). The properties of outward currents were investigated with patch-clamp in acutely isolated cells at various postnatal ages and at adulthood (2-3 mo). Kinetic analysis and pharmacological properties showed that IK and IA were present in these cells. IA and IK remained stable with respect to kinetic properties during ontogenesis, but the relative contribution and pharmacological properties varied with age. IA dominated in P5-7 cells whereas IK was prominent in most older cells (Beck H et al, 1992 [rat]8 ). |
I h
|
Patch-pipette recordings found no evidence for a ?sag? in hyperpolarizing responses, suggesting that this current is not present in these neurons (Lübke J et al, 19989 ). |
I Na,t
|
With whole-cell recordings the properties of a voltage-dependent Na+ currents were investigated in 42 DGC acutely isolated from the resected hippocampus of 20 patients with therapy-refractory temporal lobe epilepsy (TLE) using the whole-cell patch-clamp technique.The kinetic properties contributed to a reduction of the Na+ currents during repetitive stimulation that was more pronounced with higher stimulation frequencies and also showed a dependence on the holding potential (Reckziegel G et al, 1998 [human]11 ). The kinetic properties of this current were studied using the whole-cell voltage-clamp method in acutely isolated cells. No significant differences were found after induction of status epilepticus (Ketelaars SO et al, 200112 ). |
I K
|
Properties of K+ outward currents were investigated in human DG cells from 11 specimens obtained from patients with temporal lobe epilepsy. An IK was observed in all cells. The average current density, the time-dependent decay, and the resting membrane characteristics were not significantly different between patients with and without Ammon Horn Sclerosis. The V1/2(inact) was shifted in a hyperpolarizing direction in AHS (-67.7mV) compared with that in hippocampi not showing AHS (-47.7mV) (Beck H et al, 1996 [human]7 ). The properties of outward currents were investigated with patch-clamp in acutely isolated rat DGCs at various postnatal ages and at adulthood (2-3 mo). Kinetic analysis and pharmacological properties showed that IK and IA were present in these cells. IA and IK remained stable with respect to kinetic properties during ontogenesis, but the relative contribution and pharmacological properties varied with age. IA dominated in P5-7 cells whereas IK was prominent in most older cells (Beck H et al, 1992 [rat]8 ). |
|
|
Axon hillock
|
Chandelier cell terminals
|
GabaA
|
|
Chandelier cell terminals
|
GabaB
|
|
|
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Axon fiber
|
|
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Glutamate
|
To presynaptic kainate receptors in the CA3 region of the hippocampus
| Glutamate - kainate receptor (glur6)In mouse hippocampal slices, bath application of kainate caused presynaptic reduction in epscs at mossy fiber synapses on CA3 pyramidal cells in glur6 knockouts but not in glur5 knockouts.(Rockett R, 2010 [mice]14 ). |
|
Axon terminal
|
|
Kainate
|
It has been shown that activation of these receptors could facilitate transmitter release. Their activation is very fast (<10 ms) and lasts for seconds, and could contribute to the short-term plasticity characteristics of mossy fiber synapses (Schmitz D et al, 20013 ). |
|
I N
|
|
I L high threshold
|
Transients and kinetics for these channels were studied using whole-cell patch clamp recordings (Bischofberger J et al, 200213 ). |
|
Zn2+
|
CA3 pyramidal neuron proximal dendrites, mossy cell proximal dendrites, and basket cell basal dendrites
| |
Glutamate
|
CA3 pyramidal neuron proximal dendrites, mossy cell proximal dendrites, and basket cell basal dendrites
| |
Dynorphin
|
CA3 pyramidal neuron proximal dendrites, mossy cell proximal dendrites, and basket cell basal dendrites
| |
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