| Cerebellar nucleus cell |
Cerebellar nucleus Cyclic burst firing Plateau potential generating Cell
|
spike max rise slope |
Two types of neurons in the rat cerebellar nuclei as distinguished by membrane potentials and intracellular fillings.
(NeuroElectro data)
(PubMed)
|
209.0
± 72.0
(52)
|
209.0 (mV/ms)
|
Data Table |
| Cerebellar nucleus cell |
Cerebellar nucleus Cyclic burst lacking Plateau potential lacking Cell
|
spike max rise slope |
Two types of neurons in the rat cerebellar nuclei as distinguished by membrane potentials and intracellular fillings.
(NeuroElectro data)
(PubMed)
|
200.0
± 93.0
(7)
|
200.0 (mV/ms)
|
Data Table |
| Cerebellum granule cell |
|
spike max rise slope |
Ionic mechanism of electroresponsiveness in cerebellar granule cells implicates the action of a persistent sodium current.
(NeuroElectro data)
(PubMed)
|
155.3
± 27.9
(8)
|
155.3 (mV/ms)
|
Data Table |
| Cerebellum granule cell |
|
spike max rise slope |
Ionic mechanism of electroresponsiveness in cerebellar granule cells implicates the action of a persistent sodium current.
(NeuroElectro data)
(PubMed)
|
151.1
± 54.6
(10)
|
151.1 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
|
spike max rise slope |
Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1.
(NeuroElectro data)
(PubMed)
|
368.52
(18)
|
368.52 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
|
spike max rise slope |
The leaner P/Q-type calcium channel mutation renders cerebellar Purkinje neurons hyper-excitable and eliminates Ca2+-Na+ spike bursts.
(NeuroElectro data)
(PubMed)
|
288.0
± 12.1
(17)
|
288.0 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
cerebellar vermis lobule III - V tonic firing purkinje cell
|
spike max rise slope |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
405.9
± 12.5
(25)
|
405.9 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
cerebellar vermis lobule III - V complex bursting purkinje cell
|
spike max rise slope |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
392.6
± 17.4
(12)
|
392.6 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
cerebellar vermis lobule X tonic firing purkinje cell
|
spike max rise slope |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
314.1
± 14.3
(13)
|
314.1 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
cerebellar vermis lobule X complex bursting purkinje cell
|
spike max rise slope |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
245.0
± 9.0
(11)
|
245.0 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
cerebellar vermis lobule X initial bursting purkinje cell
|
spike max rise slope |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
283.2
± 13.5
(10)
|
283.2 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
cerebellar vermis lobule X gap firing purkinje cell
|
spike max rise slope |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
114.4
± 16.5
(15)
|
114.4 (mV/ms)
|
Data Table |
| Cerebellum Purkinje cell |
|
spike max rise slope |
Calcium dynamics and electrophysiological properties of cerebellar Purkinje cells in SCA1 transgenic mice.
(NeuroElectro data)
(PubMed)
|
364.0
± 81.0
(28)
|
364.0 (mV/ms)
|
Data Table |
| Cochlear nucleus (ventral) bushy cell |
anterior ventral cochlear nucleus dorsal third high frequency region neuron
|
spike max rise slope |
Synaptic transmission at the cochlear nucleus endbulb synapse during age-related hearing loss in mice.
(NeuroElectro data)
(PubMed)
|
77.0
(10)
|
77.0 (mV/ms)
|
Data Table |
| Cochlear nucleus (ventral) bushy cell |
anterior ventral cochlear nucleus dorsal third high frequency region neuron
|
spike max rise slope |
Synaptic transmission at the cochlear nucleus endbulb synapse during age-related hearing loss in mice.
(NeuroElectro data)
(PubMed)
|
83.1
(8)
|
83.1 (mV/ms)
|
Data Table |
| Cochlear nucleus (ventral) bushy cell |
anterior ventral cochlear nucleus rostroventral third low frequency region neuron
|
spike max rise slope |
Synaptic transmission at the cochlear nucleus endbulb synapse during age-related hearing loss in mice.
(NeuroElectro data)
(PubMed)
|
87.7
(7)
|
87.7 (mV/ms)
|
Data Table |
| Cochlear nucleus (ventral) bushy cell |
anterior ventral cochlear nucleus dorsal third high frequency region neuron
|
spike max rise slope |
Synaptic transmission at the cochlear nucleus endbulb synapse during age-related hearing loss in mice.
(NeuroElectro data)
(PubMed)
|
88.3
(14)
|
88.3 (mV/ms)
|
Data Table |
| Cochlear nucleus (ventral) bushy cell |
anterior ventral cochlear nucleus dorsal third high frequency region neuron
|
spike max rise slope |
Synaptic transmission at the cochlear nucleus endbulb synapse during age-related hearing loss in mice.
(NeuroElectro data)
(PubMed)
|
74.9
(21)
|
74.9 (mV/ms)
|
Data Table |
| Dentate gyrus granule cell |
|
spike max rise slope |
Granule-like neurons at the hilar/CA3 border after status epilepticus and their synchrony with area CA3 pyramidal cells: functional implications of seizure-induced neurogenesis.
(NeuroElectro data)
(PubMed)
|
420.0
(5)
|
--
|
Data Table |
| Dentate gyrus granule cell |
Granule cells located 50 - 100 um from granule cell layer/hilar border
|
spike max rise slope |
Granule-like neurons at the hilar/CA3 border after status epilepticus and their synchrony with area CA3 pyramidal cells: functional implications of seizure-induced neurogenesis.
(NeuroElectro data)
(PubMed)
|
433.0
|
--
|
Data Table |
| Dentate gyrus granule cell |
|
spike max rise slope |
Preventing effect of L-type calcium channel blockade on electrophysiological alterations in dentate gyrus granule cells induced by entorhinal amyloid pathology.
(NeuroElectro data)
(PubMed)
|
73.56
± 6.306
(16)
|
73.56 (mV/ms)
|
Data Table |
| Dentate gyrus granule cell |
|
spike max rise slope |
Intrinsic membrane properties determine hippocampal differential firing pattern in vivo in anesthetized rats.
(NeuroElectro data)
(PubMed)
|
378.0
± 29.0
(18)
|
378.0 (mV/ms)
|
Data Table |
| Dentate gyrus granule cell |
|
spike max rise slope |
Interneurons of the dentate-hilus border of the rat dentate gyrus: morphological and electrophysiological heterogeneity.
(NeuroElectro data)
(PubMed)
|
1876.3
± 168.64
(16)
|
--
|
Data Table |
| Dentate gyrus hilar cell |
Dentate Gyrus nonadapting hilar interneuron
|
spike max rise slope |
Interneurons of the dentate-hilus border of the rat dentate gyrus: morphological and electrophysiological heterogeneity.
(NeuroElectro data)
(PubMed)
|
887.3
± 198.0
(6)
|
--
|
Data Table |
| Dentate gyrus hilar cell |
Dentate Gyrus strongly adapting hilar interneuron
|
spike max rise slope |
Interneurons of the dentate-hilus border of the rat dentate gyrus: morphological and electrophysiological heterogeneity.
(NeuroElectro data)
(PubMed)
|
751.0
± 146.8
(4)
|
--
|
Data Table |
| Dentate gyrus hilar cell |
Dentate Gyrus normally adapting hilar interneuron
|
spike max rise slope |
Interneurons of the dentate-hilus border of the rat dentate gyrus: morphological and electrophysiological heterogeneity.
(NeuroElectro data)
(PubMed)
|
743.7
± 63.8
(16)
|
--
|
Data Table |
| Dentate gyrus mossy cell |
|
spike max rise slope |
Survival of dentate hilar mossy cells after pilocarpine-induced seizures and their synchronized burst discharges with area CA3 pyramidal cells.
(NeuroElectro data)
(PubMed)
|
174.9
|
--
|
Data Table |
| Dentate gyrus mossy cell |
|
spike max rise slope |
Survival of dentate hilar mossy cells after pilocarpine-induced seizures and their synchronized burst discharges with area CA3 pyramidal cells.
(NeuroElectro data)
(PubMed)
|
177.4
|
--
|
Data Table |
| Dentate gyrus mossy cell |
|
spike max rise slope |
Proper layering is important for precisely timed activation of hippocampal mossy cells.
(NeuroElectro data)
(PubMed)
|
401.0
± 16.0
(18)
|
401.0 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
lumbar 4 and lumbar 5 dorsal root ganglion large cell
|
spike max rise slope |
Hyperexcitability of axotomized and neighboring unaxotomized sensory neurons is reduced days after perineural clonidine at the site of injury.
(NeuroElectro data)
(PubMed)
|
326.7
± 14.59
(36)
|
326.7 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
Nerve–dorsal root ganglion
|
spike max rise slope |
Axotomy increases the excitability of dorsal root ganglion cells with unmyelinated axons.
(NeuroElectro data)
(PubMed)
|
108.6
± 15.9
(12)
|
--
|
Data Table |
| Dorsal root ganglion cell |
Large dorsal root ganglion cell
|
spike max rise slope |
Long-term IL-1β exposure causes subpopulation-dependent alterations in rat dorsal root ganglion neuron excitability.
(NeuroElectro data)
(PubMed)
|
124.5
± 17.2
(12)
|
124.5 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
Small isolectin B4 negative dorsal root ganglion cell
|
spike max rise slope |
Long-term IL-1β exposure causes subpopulation-dependent alterations in rat dorsal root ganglion neuron excitability.
(NeuroElectro data)
(PubMed)
|
107.9
± 9.7
(23)
|
107.9 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
|
spike max rise slope |
Similar electrophysiological changes in axotomized and neighboring intact dorsal root ganglion neurons.
(NeuroElectro data)
(PubMed)
|
170.0
± 15.8
(24)
|
170.0 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
Medium dorsal root ganglion cell
|
spike max rise slope |
Long-term IL-1β exposure causes subpopulation-dependent alterations in rat dorsal root ganglion neuron excitability.
(NeuroElectro data)
(PubMed)
|
95.5
± 5.8
(36)
|
95.5 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
|
spike max rise slope |
Similar electrophysiological changes in axotomized and neighboring intact dorsal root ganglion neurons.
(NeuroElectro data)
(PubMed)
|
198.0
± 20.6
(18)
|
198.0 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
Small isolectin B4 positive dorsal root ganglion cell
|
spike max rise slope |
Long-term IL-1β exposure causes subpopulation-dependent alterations in rat dorsal root ganglion neuron excitability.
(NeuroElectro data)
(PubMed)
|
110.0
± 7.4
(20)
|
110.0 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
|
spike max rise slope |
Similar electrophysiological changes in axotomized and neighboring intact dorsal root ganglion neurons.
(NeuroElectro data)
(PubMed)
|
155.0
± 16.5
(13)
|
155.0 (mV/ms)
|
Data Table |
| Dorsal root ganglion cell |
|
spike max rise slope |
Distinctive neurophysiological properties of embryonic trigeminal and geniculate neurons in culture.
(NeuroElectro data)
(PubMed)
|
127.0
± 34.0
(173)
|
127.0 (mV/ms)
|
Data Table |
| Globus pallidus, external segment neuron |
External globus pallidus Npas1-expressing neurons projecting to striatum
|
spike max rise slope |
Parvalbumin+ Neurons and Npas1+ Neurons Are Distinct Neuron Classes in the Mouse External Globus Pallidus.
(NeuroElectro data)
(PubMed)
|
284.0
± 27.0
(8)
|
284.0 (mV/ms)
|
Data Table |
| Globus pallidus, external segment neuron |
External globus pallidus Lhx6 expressing neurons
|
spike max rise slope |
Parvalbumin+ Neurons and Npas1+ Neurons Are Distinct Neuron Classes in the Mouse External Globus Pallidus.
(NeuroElectro data)
(PubMed)
|
256.0
± 45.0
(15)
|
256.0 (mV/ms)
|
Data Table |
| Globus pallidus, external segment neuron |
External globus pallidus choline acetyltransferase expressing neurons
|
spike max rise slope |
Parvalbumin+ Neurons and Npas1+ Neurons Are Distinct Neuron Classes in the Mouse External Globus Pallidus.
(NeuroElectro data)
(PubMed)
|
193.0
± 14.0
(13)
|
193.0 (mV/ms)
|
Data Table |
| Globus pallidus, external segment neuron |
external globus pallidus parvalbumin-expressing neurons projecting to subthalamic nucleus
|
spike max rise slope |
Parvalbumin+ Neurons and Npas1+ Neurons Are Distinct Neuron Classes in the Mouse External Globus Pallidus.
(NeuroElectro data)
(PubMed)
|
453.0
± 41.0
(20)
|
453.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 oriens lacunosum moleculare neuron |
Hippocampus CA1 and CA2 non-fast spiking stramum oriens neuron
|
spike max rise slope |
Morphological and electrophysiological properties of pyramidal-like neurons in the stratum oriens of Cornu ammonis 1 and Cornu ammonis 2 area of Proechimys.
(NeuroElectro data)
(PubMed)
|
127.7
± 30.3
(15)
|
127.7 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Reduced seizure threshold and altered network oscillatory properties in a mouse model of Rett syndrome.
(NeuroElectro data)
(PubMed)
|
582.0
± 41.0
(14)
|
582.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Intrinsic membrane properties determine hippocampal differential firing pattern in vivo in anesthetized rats.
(NeuroElectro data)
(PubMed)
|
500.0
± 44.0
(13)
|
500.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Dorsal Hippocampus CA1 pyramidal cell
|
spike max rise slope |
Spatial Gene-Expression Gradients Underlie Prominent Heterogeneity of CA1 Pyramidal Neurons.
(NeuroElectro data)
(PubMed)
|
662.0
± 12.0
(46)
|
662.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
483.0
± 10.6
(9)
|
483.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Alpha5GABAA receptors regulate the intrinsic excitability of mouse hippocampal pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
201.9
± 20.6
(10)
|
201.9 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Action potential threshold of hippocampal pyramidal cells in vivo is increased by recent spiking activity.
(NeuroElectro data)
(PubMed)
|
354.3
± 76.9
(22)
|
354.3 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Neurophysiological modification of CA1 pyramidal neurons in a transgenic mouse expressing a truncated form of disrupted-in-schizophrenia 1.
(NeuroElectro data)
(PubMed)
|
452.0
± 19.0
(23)
|
452.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Hippocampus CA1 non-fast spiking stratum oriens pyramidal-like cell
|
spike max rise slope |
Morphological and electrophysiological properties of pyramidal-like neurons in the stratum oriens of Cornu ammonis 1 and Cornu ammonis 2 area of Proechimys.
(NeuroElectro data)
(PubMed)
|
141.3
± 24.5
(8)
|
141.3 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
cAMP response element-binding protein-mediated gene expression increases the intrinsic excitability of CA1 pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
321.0
± 8.4
(19)
|
321.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
BACE1 deficiency causes altered neuronal activity and neurodegeneration.
(NeuroElectro data)
(PubMed)
|
86.3
± 2.3
(11)
|
86.3 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Neurophysiological modification of CA1 pyramidal neurons in a transgenic mouse expressing a truncated form of disrupted-in-schizophrenia 1.
(NeuroElectro data)
(PubMed)
|
443.0
± 17.0
(19)
|
443.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Enhanced intrinsic excitability and EPSP-spike coupling accompany enriched environment-induced facilitation of LTP in hippocampal CA1 pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
0.42
± 0.001
(16)
|
0.42 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Downregulation of Spermine Augments Dendritic Persistent Sodium Currents and Synaptic Integration after Status Epilepticus.
(NeuroElectro data)
(PubMed)
|
322.0
± 15.0
(9)
|
322.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Hippocampus CA1 non-fast spiking pyramidal neuron
|
spike max rise slope |
Morphological and electrophysiological properties of pyramidal-like neurons in the stratum oriens of Cornu ammonis 1 and Cornu ammonis 2 area of Proechimys.
(NeuroElectro data)
(PubMed)
|
101.6
± 29.1
(7)
|
101.6 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Reduced Hyperpolarization-Activated Current Contributes to Enhanced Intrinsic Excitability in Cultured Hippocampal Neurons from PrP(-/-) Mice.
(NeuroElectro data)
(PubMed)
|
132.0
± 23.5
(5)
|
132.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
468.0
± 12.2
(9)
|
468.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Hippocampus CA1 and subiculum regular spiking pyramidal neurons
|
spike max rise slope |
Hippocampal pyramidal neurons comprise two distinct cell types that are countermodulated by metabotropic receptors.
(NeuroElectro data)
(PubMed)
|
460.0
± 21.0
(268)
|
--
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Dorsal Hippocampus CA1 pyramidal cell
|
spike max rise slope |
Mapping the electrophysiological and morphological properties of CA1 pyramidal neurons along the longitudinal hippocampal axis.
(NeuroElectro data)
(PubMed)
|
346.1
(26)
|
346.1 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
502.0
± 11.3
(8)
|
502.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Hippocampus CA1 and subiculum bursting pyramidal neurons
|
spike max rise slope |
Hippocampal pyramidal neurons comprise two distinct cell types that are countermodulated by metabotropic receptors.
(NeuroElectro data)
(PubMed)
|
488.0
± 21.0
(268)
|
--
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Doral End fo Intermediate Hippocampus CA1 pyramidal cell
|
spike max rise slope |
Mapping the electrophysiological and morphological properties of CA1 pyramidal neurons along the longitudinal hippocampal axis.
(NeuroElectro data)
(PubMed)
|
386.8
(34)
|
386.8 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
499.0
± 11.1
(7)
|
499.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Depression of synaptic transmission by vascular endothelial growth factor in adult rat hippocampus and evidence for increased efficacy after chronic seizures.
(NeuroElectro data)
(PubMed)
|
362.5
± 39.3
(8)
|
362.5 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Altered intrinsic excitability of hippocampal CA1 pyramidal neurons in aged PDAPP mice.
(NeuroElectro data)
(PubMed)
|
371.43
(27)
|
371.43 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Normal electrical properties of hippocampal neurons modelling early Huntington disease pathogenesis.
(NeuroElectro data)
(PubMed)
|
109.0
(15)
|
109.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Ventral End fo Intermediate Hippocampus CA1 pyramidal cell
|
spike max rise slope |
Mapping the electrophysiological and morphological properties of CA1 pyramidal neurons along the longitudinal hippocampal axis.
(NeuroElectro data)
(PubMed)
|
410.6
(23)
|
410.6 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
498.0
± 11.8
(7)
|
498.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Tetanus toxin induces long-term changes in excitation and inhibition in the rat hippocampal CA1 area.
(NeuroElectro data)
(PubMed)
|
330.0
± 28.0
(25)
|
330.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Slowly inactivating component of Na+ current in peri-somatic region of hippocampal CA1 pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
259.8
± 19.5
|
259.8 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Normal electrical properties of hippocampal neurons modelling early Huntington disease pathogenesis.
(NeuroElectro data)
(PubMed)
|
100.7
(7)
|
100.7 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Ventral Hippocampus CA1 pyramidal cell
|
spike max rise slope |
Mapping the electrophysiological and morphological properties of CA1 pyramidal neurons along the longitudinal hippocampal axis.
(NeuroElectro data)
(PubMed)
|
390.2
(26)
|
390.2 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Delayed effects of corticosterone on slow after-hyperpolarization potentials in mouse hippocampal versus prefrontal cortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
423.9
± 19.0
(20)
|
423.9 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
494.0
± 11.8
(9)
|
494.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Resting and active properties of pyramidal neurons in subiculum and CA1 of rat hippocampus.
(NeuroElectro data)
(PubMed)
|
381.0
± 18.0
|
--
|
Data Table |
| Hippocampus CA1 pyramidal cell |
Ventral Hippocampus CA1 pyramidal cell
|
spike max rise slope |
Spatial Gene-Expression Gradients Underlie Prominent Heterogeneity of CA1 Pyramidal Neurons.
(NeuroElectro data)
(PubMed)
|
656.0
± 17.0
(31)
|
656.0 (mV/ms)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
spike max rise slope |
Modulation of hippocampal synaptic transmission by low concentrations of cell-permeant Ca2+ chelators: effects of Ca2+ affinity, chelator structure and binding kinetics.
(NeuroElectro data)
(PubMed)
|
480.0
± 20.0
(7)
|
480.0 (mV/ms)
|
Data Table |
| Hippocampus CA2 pyramidal neuron |
Hippocampus CA2 non-fast spiking pyramidal-like neuron
|
spike max rise slope |
Morphological and electrophysiological properties of pyramidal-like neurons in the stratum oriens of Cornu ammonis 1 and Cornu ammonis 2 area of Proechimys.
(NeuroElectro data)
(PubMed)
|
108.5
± 15.5
(7)
|
108.5 (mV/ms)
|
Data Table |
| Hippocampus CA2 pyramidal neuron |
Hippocampus CA2 non-fasting spiking pyramidal neuron
|
spike max rise slope |
Morphological and electrophysiological properties of pyramidal-like neurons in the stratum oriens of Cornu ammonis 1 and Cornu ammonis 2 area of Proechimys.
(NeuroElectro data)
(PubMed)
|
104.2
± 33.2
(11)
|
104.2 (mV/ms)
|
Data Table |
| Hippocampus CA3 pyramidal cell |
|
spike max rise slope |
Seizure, neuron loss, and mossy fiber sprouting in herpes simplex virus type 1-infected organotypic hippocampal cultures.
(NeuroElectro data)
(PubMed)
|
236.4
± 14.7
(17)
|
236.4 (mV/ms)
|
Data Table |
| Hippocampus CA3 pyramidal cell |
|
spike max rise slope |
Herpes simplex virus type 1 inoculation enhances hippocampal excitability and seizure susceptibility in mice.
(NeuroElectro data)
(PubMed)
|
225.0
± 13.0
(16)
|
225.0 (mV/ms)
|
Data Table |
| Hippocampus CA3 pyramidal cell |
|
spike max rise slope |
Intrinsic membrane properties determine hippocampal differential firing pattern in vivo in anesthetized rats.
(NeuroElectro data)
(PubMed)
|
287.0
± 11.0
(41)
|
287.0 (mV/ms)
|
Data Table |
| Hippocampus CA3 pyramidal cell |
|
spike max rise slope |
Local circuit abnormalities in chronically epileptic rats after intrahippocampal tetanus toxin injection in infancy.
(NeuroElectro data)
(PubMed)
|
269.1
± 46.4
(10)
|
269.1 (mV/ms)
|
Data Table |
| Medial entorhinal cortex layer II stellate cell |
|
spike max rise slope |
Temporal lobe epilepsy induces intrinsic alterations in Na channel gating in layer II medial entorhinal cortex neurons.
(NeuroElectro data)
(PubMed)
|
248.9
± 11.0
(18)
|
248.9 (mV/ms)
|
Data Table |
| Medial entorhinal cortex layer II stellate cell |
|
spike max rise slope |
Enhanced actions of adenosine in medial entorhinal cortex layer II stellate neurons in temporal lobe epilepsy are mediated via A(1)-receptor activation.
(NeuroElectro data)
(PubMed)
|
223.1
± 6.3
(19)
|
223.1 (mV/ms)
|
Data Table |
| Medial Nucleus of Trapezoid Body neuron |
|
spike max rise slope |
Kv1.1-containing channels are critical for temporal precision during spike initiation.
(NeuroElectro data)
(PubMed)
|
264.0
± 35.0
|
264.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus gabaergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
345.0
± 84.0
(59)
|
345.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
Medial vestibular nucleus non-GABAergic neurons expressing Thy1
|
spike max rise slope |
Firing properties of GABAergic versus non-GABAergic vestibular nucleus neurons conferred by a differential balance of potassium currents.
(NeuroElectro data)
(PubMed)
|
263.0
± 66.0
(39)
|
263.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus glutamatergic or glycinergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
521.0
± 102.0
(49)
|
521.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
Medial vestibular nucleus GABAergic neurons
|
spike max rise slope |
Firing properties of GABAergic versus non-GABAergic vestibular nucleus neurons conferred by a differential balance of potassium currents.
(NeuroElectro data)
(PubMed)
|
218.0
± 63.0
(35)
|
218.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus glutamatergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
536.0
± 117.0
(9)
|
536.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus glycinergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
494.0
± 132.0
(9)
|
494.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus non-glycinergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
341.0
± 70.0
(14)
|
341.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus glycinergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
340.0
± 93.0
(14)
|
340.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus gabaergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
328.0
± 76.0
(37)
|
328.0 (mV/ms)
|
Data Table |
| Medial vestibular nucleus neuron |
medial vestibular nucleus glutamatergic or glycinergic neuron
|
spike max rise slope |
Transgenic mouse lines subdivide medial vestibular nucleus neurons into discrete, neurochemically distinct populations.
(NeuroElectro data)
(PubMed)
|
450.0
± 101.0
(26)
|
450.0 (mV/ms)
|
Data Table |
| Neocortex basket cell |
Somatosensory cortex layer 2-3 nonpyramidal multipolar fast-spiking inhibitory interneuron
|
spike max rise slope |
Integration of broadband conductance input in rat somatosensory cortical inhibitory interneurons: an inhibition-controlled switch between intrinsic and input-driven spiking in fast-spiking cells.
(NeuroElectro data)
(PubMed)
|
292.0
± 48.0
(10)
|
0.292 (mV/ms)
|
Data Table |
| Neocortex basket cell |
Somatosensory cortex layer 5 multipolar fast-spiking parvalbumin positive interneuron
|
spike max rise slope |
Altered intrinsic properties of neuronal subtypes in malformed epileptogenic cortex.
(NeuroElectro data)
(PubMed)
|
256.0
± 12.0
(34)
|
256.0 (mV/ms)
|
Data Table |
| Neocortex basket cell |
Neocortex layer 1-4 fast-spiking GABAergic interneuron
|
spike max rise slope |
Impaired fast-spiking, suppressed cortical inhibition, and increased susceptibility to seizures in mice lacking Kv3.2 K+ channel proteins.
(NeuroElectro data)
(PubMed)
|
151.65
± 6.33
(10)
|
151.65 (mV/ms)
|
Data Table |
| Neocortex basket cell |
Neocortex layer 5-6 fast-spiking GABAergic interneuron
|
spike max rise slope |
Impaired fast-spiking, suppressed cortical inhibition, and increased susceptibility to seizures in mice lacking Kv3.2 K+ channel proteins.
(NeuroElectro data)
(PubMed)
|
155.54
± 2.9
(20)
|
155.54 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
posterior piriform cortex GABAergic irregular-spiking inhibitory interneuron
|
spike max rise slope |
GABAergic inhibitory interneurons in the posterior piriform cortex of the GAD67-GFP mouse.
(NeuroElectro data)
(PubMed)
|
74.6
± 6.45
(19)
|
74.6 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
posterior piriform cortex GABAergic late-spiking inhibitory interneuron
|
spike max rise slope |
GABAergic inhibitory interneurons in the posterior piriform cortex of the GAD67-GFP mouse.
(NeuroElectro data)
(PubMed)
|
68.2
± 3.76
(24)
|
68.2 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
Presubiculum somatostatin-expressing interneuron
|
spike max rise slope |
Diversity and overlap of parvalbumin and somatostatin expressing interneurons in mouse presubiculum.
(NeuroElectro data)
(PubMed)
|
598.0
(35)
|
598.0 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
posterior piriform cortex GABAergic regular-spiking non-pyramidal inhibitory interneuron
|
spike max rise slope |
GABAergic inhibitory interneurons in the posterior piriform cortex of the GAD67-GFP mouse.
(NeuroElectro data)
(PubMed)
|
85.7
± 4.62
(51)
|
85.7 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
Presubiculum parvalbumin interneuron
|
spike max rise slope |
Diversity and overlap of parvalbumin and somatostatin expressing interneurons in mouse presubiculum.
(NeuroElectro data)
(PubMed)
|
637.0
(46)
|
637.0 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
Presubiculum somatostatin-expressing interneuron
|
spike max rise slope |
Diversity and overlap of parvalbumin and somatostatin expressing interneurons in mouse presubiculum.
(NeuroElectro data)
(PubMed)
|
571.0
(61)
|
571.0 (mV/ms)
|
Data Table |
| Neocortex interneuron deep |
barrel cortex layer 6a GABAergic inhibitory interneuron
|
spike max rise slope |
Inter- and intralaminar subcircuits of excitatory and inhibitory neurons in layer 6a of the rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
76.9
± 21.9
(32)
|
76.9 (mV/ms)
|
Data Table |
| Neocortex Martinotti cell |
Barrel Cortex GAD67 expressing, somatostatin-containing Gabaergic interneurons
|
spike max rise slope |
Distinct subtypes of somatostatin-containing neocortical interneurons revealed in transgenic mice.
(NeuroElectro data)
(PubMed)
|
232.0
(33)
|
232.0 (mV/ms)
|
Data Table |
| Neocortex Martinotti cell |
Barrel Cortex GAD67 expressing, somatostatin-containing Gabaergic interneurons
|
spike max rise slope |
Distinct subtypes of somatostatin-containing neocortical interneurons revealed in transgenic mice.
(NeuroElectro data)
(PubMed)
|
191.0
(59)
|
191.0 (mV/ms)
|
Data Table |
| Neocortex Martinotti cell |
somatosensory cortex layer 6 martinotti cell
|
spike max rise slope |
Anatomical, physiological and molecular properties of Martinotti cells in the somatosensory cortex of the juvenile rat.
(NeuroElectro data)
(PubMed)
|
48.69
± 12.16
(7)
|
48.69 (mV/ms)
|
Data Table |
| Neocortex Martinotti cell |
Barrel Cortex GAD67 expressing, somatostatin-containing Gabaergic interneurons
|
spike max rise slope |
Distinct subtypes of somatostatin-containing neocortical interneurons revealed in transgenic mice.
(NeuroElectro data)
(PubMed)
|
261.0
(58)
|
261.0 (mV/ms)
|
Data Table |
| Neocortex Martinotti cell |
somatosensory cortex layer 5 martinotti cell
|
spike max rise slope |
Anatomical, physiological and molecular properties of Martinotti cells in the somatosensory cortex of the juvenile rat.
(NeuroElectro data)
(PubMed)
|
47.2
± 11.11
(25)
|
47.2 (mV/ms)
|
Data Table |
| Neocortex Martinotti cell |
Somatosensory cortex layer 5 low threshold-spiking interneuron
|
spike max rise slope |
Altered intrinsic properties of neuronal subtypes in malformed epileptogenic cortex.
(NeuroElectro data)
(PubMed)
|
244.0
± 13.0
(33)
|
244.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Prelimbic cortex layer 2-3 pyramidal cell
|
spike max rise slope |
Delayed effects of corticosterone on slow after-hyperpolarization potentials in mouse hippocampal versus prefrontal cortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
313.3
± 18.0
(20)
|
313.3 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Somatosensory and motor cortex layer 2-3 regular spiking pyramidal neurons
|
spike max rise slope |
Effects of temperature on calcium transients and Ca2+-dependent afterhyperpolarizations in neocortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
100.0
± 30.0
(20)
|
100.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
infralimbic cortex layer 2-3 pyramidal cell
|
spike max rise slope |
Delayed effects of corticosterone on slow after-hyperpolarization potentials in mouse hippocampal versus prefrontal cortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
290.0
± 14.0
(21)
|
290.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Somatosensory and motor cortex layer 2-3 regular spiking pyramidal neurons
|
spike max rise slope |
Effects of temperature on calcium transients and Ca2+-dependent afterhyperpolarizations in neocortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
149.0
± 37.0
(20)
|
149.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
somatosensory cortex layer 2/3 pyramidal neurons
|
spike max rise slope |
Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine.
(NeuroElectro data)
(PubMed)
|
331.0
± 13.0
(23)
|
331.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Layer 2/3 somatosensory cortex pyramidal neurons
|
spike max rise slope |
Neuromodulation by a cytokine: interferon-beta differentially augments neocortical neuronal activity and excitability.
(NeuroElectro data)
(PubMed)
|
162.0
± 7.5
(39)
|
162.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
|
spike max rise slope |
Functional roles of Kv1 channels in neocortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
159.0
± 64.0
|
159.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Dysplastic Cortex Regular Spiking Neuron
|
spike max rise slope |
Characterization of neuronal migration disorders in neocortical structures. II. Intracellular in vitro recordings.
(NeuroElectro data)
(PubMed)
|
276.0
± 8.8
(51)
|
276.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Orbital frontal cortex layer 2-3 pyramidal cell
|
spike max rise slope |
Delayed effects of corticosterone on slow after-hyperpolarization potentials in mouse hippocampal versus prefrontal cortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
355.1
± 14.0
(21)
|
355.1 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 6a barrel cortex pyramidal corticothalamic neuron with large terminal arbors
|
spike max rise slope |
Inter- and intralaminar subcircuits of excitatory and inhibitory neurons in layer 6a of the rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
99.3
± 18.5
(34)
|
99.3 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
somatosensory cortex layer 5a corticostriatal Etv1-expressing slender-tufted pyramidal neurons
|
spike max rise slope |
Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine.
(NeuroElectro data)
(PubMed)
|
310.0
± 10.0
(71)
|
310.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
barrel cortex layer 6a corticocortical pyramidal neuron with infragranular arborization axons
|
spike max rise slope |
Inter- and intralaminar subcircuits of excitatory and inhibitory neurons in layer 6a of the rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
105.1
± 22.6
(38)
|
105.1 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
|
spike max rise slope |
Protein-kinase C-dependent phosphorylation inhibits the effect of the antiepileptic drug topiramate on the persistent fraction of sodium currents.
(NeuroElectro data)
(PubMed)
|
322.1
± 23.0
(5)
|
322.1 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Somatosensory cortex layer 5b Glt25d2-expressing thick-tufted pyramidal neurons
|
spike max rise slope |
Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine.
(NeuroElectro data)
(PubMed)
|
352.0
± 12.0
(57)
|
352.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 5 somatosensory pyramidal neurons
|
spike max rise slope |
Neuromodulation by a cytokine: interferon-beta differentially augments neocortical neuronal activity and excitability.
(NeuroElectro data)
(PubMed)
|
182.3
± 13.2
(24)
|
182.3 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Secondary somatosensory cortex layer 5b corticospinal thick-tufted large pyramidal neuron
|
spike max rise slope |
Intrinsic electrophysiology of mouse corticospinal neurons: a class-specific triad of spike-related properties.
(NeuroElectro data)
(PubMed)
|
488.0
± 45.0
(7)
|
488.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
barrel cortex layer 5 pyramidal neuron
|
spike max rise slope |
Loss of sensory input increases the intrinsic excitability of layer 5 pyramidal neurons in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
616.0
± 17.5
(51)
|
616.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Primary motor cortex layer 5b corticostriatal pyramidal neuron
|
spike max rise slope |
Intrinsic electrophysiology of mouse corticospinal neurons: a class-specific triad of spike-related properties.
(NeuroElectro data)
(PubMed)
|
250.0
± 68.0
(10)
|
250.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Neocortex layer 5 Kv3.1 non-expressing pyramidal cell
|
spike max rise slope |
Transgenic mice expressing a fluorescent in vivo label in a distinct subpopulation of neocortical layer 5 pyramidal cells.
(NeuroElectro data)
(PubMed)
|
441.0
± 29.0
|
441.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Visual Cortex Layer 5 large thick-tufted Pyramidal Neurons
|
spike max rise slope |
Postnatal development of intrinsic and synaptic properties transforms signaling in the layer 5 excitatory neural network of the visual cortex.
(NeuroElectro data)
(PubMed)
|
314.0
± 29.0
(5)
|
314.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Primary motor cortex layer 5b corticospinal thick-tufted large pyramidal neuron
|
spike max rise slope |
Intrinsic electrophysiology of mouse corticospinal neurons: a class-specific triad of spike-related properties.
(NeuroElectro data)
(PubMed)
|
400.0
± 91.0
(23)
|
400.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Neocortex layer 5 Kv3.1 expressing pyramidal cell
|
spike max rise slope |
Transgenic mice expressing a fluorescent in vivo label in a distinct subpopulation of neocortical layer 5 pyramidal cells.
(NeuroElectro data)
(PubMed)
|
426.0
± 21.0
|
426.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Visual Cortex Layer 5 large thick-tufted Pyramidal Neurons
|
spike max rise slope |
Postnatal development of intrinsic and synaptic properties transforms signaling in the layer 5 excitatory neural network of the visual cortex.
(NeuroElectro data)
(PubMed)
|
419.0
± 27.0
(9)
|
419.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Somatosensory cortex layer 5 apical pyramidal cell
|
spike max rise slope |
Altered intrinsic properties of neuronal subtypes in malformed epileptogenic cortex.
(NeuroElectro data)
(PubMed)
|
287.0
± 11.0
(28)
|
287.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Primary motor cortex layer 5b corticospinal thick-tufted large pyramidal neuron
|
spike max rise slope |
Intrinsic electrophysiology of mouse corticospinal neurons: a class-specific triad of spike-related properties.
(NeuroElectro data)
(PubMed)
|
492.0
± 95.0
(9)
|
492.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Visual Cortex Layer 5 large thick-tufted Pyramidal Neurons
|
spike max rise slope |
Postnatal development of intrinsic and synaptic properties transforms signaling in the layer 5 excitatory neural network of the visual cortex.
(NeuroElectro data)
(PubMed)
|
475.0
± 17.0
(21)
|
475.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Primary motor cortex layer 5b corticospinal thick-tufted large pyramidal neuron
|
spike max rise slope |
Intrinsic electrophysiology of mouse corticospinal neurons: a class-specific triad of spike-related properties.
(NeuroElectro data)
(PubMed)
|
498.0
± 55.0
(10)
|
498.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Somatosensory Cortex Layer V Barrel Intrinsic Burst Cortical Neuron
|
spike max rise slope |
Differential modulatory effects of norepinephrine on synaptically driven responses of layer V barrel field cortical neurons.
(NeuroElectro data)
(PubMed)
|
358.0
± 103.0
(9)
|
358.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Sensorimotor Neocortex Layer 5 Regular Spiking Pyramidal Neuron
|
spike max rise slope |
Potentially epileptogenic dysfunction of cortical NMDA- and GABA-mediated neurotransmission in Otx1-/- mice.
(NeuroElectro data)
(PubMed)
|
198.7
± 13.2
(16)
|
198.7 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Somatosensory Cortex Layer V Barrel Mixed Burst/Spike Cortical Neuron
|
spike max rise slope |
Differential modulatory effects of norepinephrine on synaptically driven responses of layer V barrel field cortical neurons.
(NeuroElectro data)
(PubMed)
|
361.0
± 94.0
(62)
|
361.0 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Sensorimotor Neocortex Layer 5 Intrinsically Bursting Pyramidal Neuron
|
spike max rise slope |
Potentially epileptogenic dysfunction of cortical NMDA- and GABA-mediated neurotransmission in Otx1-/- mice.
(NeuroElectro data)
(PubMed)
|
223.1
± 12.1
(9)
|
223.1 (mV/ms)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
neocortex layer 5 large pyramidal cell
|
spike max rise slope |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
261.3
± 19.8
(20)
|
261.3 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
112.6
± 35.9
(11)
|
112.6 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spike max rise slope |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
0.49
± 0.46
(45)
|
0.49 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike max rise slope |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
184.0
± 45.0
(30)
|
184.0 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
spike max rise slope |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
175.4
(47)
|
175.4 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike max rise slope |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
180.0
± 25.0
(19)
|
180.0 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
92.1
(1)
|
92.1 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
spike max rise slope |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
217.4
(42)
|
217.4 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
116.5
± 28.2
(7)
|
116.5 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
124.8
± 34.5
(34)
|
124.8 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
119.5
± 25.0
(7)
|
119.5 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
124.5
± 31.8
(9)
|
124.5 (mV/ms)
|
Data Table |
| Neostriatum cholinergic cell |
Dorsolateral striatum cholinergic motor interneuron
|
spike max rise slope |
Reduction of an afterhyperpolarization current increases excitability in striatal cholinergic interneurons in rat parkinsonism.
(NeuroElectro data)
(PubMed)
|
218.0
± 13.8
(63)
|
218.0 (mV/ms)
|
Data Table |
| Neostriatum gabaergic interneuron |
Ventral striatum fast spiking gabaergic interneuron
|
spike max rise slope |
Membrane properties and synaptic connectivity of fast-spiking interneurons in rat ventral striatum.
(NeuroElectro data)
(PubMed)
|
93.0
± 9.0
(15)
|
93.0 (mV/ms)
|
Data Table |
| Neostriatum gabaergic interneuron |
Neostriatum fast spiking gabaergic interneuron
|
spike max rise slope |
Up and down states in striatal medium spiny neurons simultaneously recorded with spontaneous activity in fast-spiking interneurons studied in cortex-striatum-substantia nigra organotypic cultures.
(NeuroElectro data)
(PubMed)
|
95.0
± 13.0
(12)
|
95.0 (mV/ms)
|
Data Table |
| Neostriatum gabaergic interneuron |
Neostriatum fast-spiking interneuron
|
spike max rise slope |
Heterogeneity of spike frequency adaptation among medium spiny neurones from the rat striatum.
(NeuroElectro data)
(PubMed)
|
123.6
± 4.7
(7)
|
123.6 (mV/ms)
|
Data Table |
| Neostriatum medium spiny neuron |
|
spike max rise slope |
Up and down states in striatal medium spiny neurons simultaneously recorded with spontaneous activity in fast-spiking interneurons studied in cortex-striatum-substantia nigra organotypic cultures.
(NeuroElectro data)
(PubMed)
|
104.0
± 12.0
(14)
|
104.0 (mV/ms)
|
Data Table |
| Neostriatum medium spiny neuron |
|
spike max rise slope |
Electrophysiological and morphological changes in striatal spiny neurons in R6/2 Huntington's disease transgenic mice.
(NeuroElectro data)
(PubMed)
|
228.5
± 12.9
(13)
|
228.5 (mV/ms)
|
Data Table |
| Neostriatum medium spiny neuron |
|
spike max rise slope |
Electrophysiological and morphological changes in striatal spiny neurons in R6/2 Huntington's disease transgenic mice.
(NeuroElectro data)
(PubMed)
|
248.9
± 19.7
(8)
|
248.9 (mV/ms)
|
Data Table |
| Neostriatum medium spiny neuron |
|
spike max rise slope |
Regulation of action-potential firing in spiny neurons of the rat neostriatum in vivo.
(NeuroElectro data)
(PubMed)
|
0.86
± 0.21
(6)
|
0.86 (mV/ms)
|
Data Table |
| Neostriatum medium spiny neuron |
|
spike max rise slope |
Heterogeneity of spike frequency adaptation among medium spiny neurones from the rat striatum.
(NeuroElectro data)
(PubMed)
|
52.9
± 2.1
(139)
|
52.9 (mV/ms)
|
Data Table |
| Neostriatum medium spiny neuron |
|
spike max rise slope |
P2Y1 receptor modulation of Ca2+-activated K+ currents in medium-sized neurons from neonatal rat striatal slices.
(NeuroElectro data)
(PubMed)
|
133.0
± 3.53
(7)
|
133.0 (mV/ms)
|
Data Table |
| Nucleus accumbens medium spiny neuron |
Ventral striatum neurons
|
spike max rise slope |
Tau-mediated NMDA receptor impairment underlies dysfunction of a selectively vulnerable network in a mouse model of frontotemporal dementia.
(NeuroElectro data)
(PubMed)
|
105.8
(9)
|
105.8 (mV/ms)
|
Data Table |
| Nucleus accumbens medium spiny neuron |
Ventral Striatum Medium spiny neuron
|
spike max rise slope |
Membrane properties and synaptic connectivity of fast-spiking interneurons in rat ventral striatum.
(NeuroElectro data)
(PubMed)
|
109.0
± 9.0
(15)
|
109.0 (mV/ms)
|
Data Table |
| Nucleus of the solitary tract intrinsic cell |
|
spike max rise slope |
H₂O₂ induces delayed hyperexcitability in nucleus tractus solitarii neurons.
(NeuroElectro data)
(PubMed)
|
195.39
± 11.47
(23)
|
195.39 (mV/ms)
|
Data Table |
| Nucleus of the solitary tract principal cell |
rostral nucleus of the solitary tract neuron
|
spike max rise slope |
Pre- and postnatal differences in membrane, action potential, and ion channel properties of rostral nucleus of the solitary tract neurons.
(NeuroElectro data)
(PubMed)
|
34.0
± 4.0
(25)
|
34.0 (mV/ms)
|
Data Table |
| Nucleus of the solitary tract principal cell |
rostral nucleus of the solitary tract neuron
|
spike max rise slope |
Pre- and postnatal differences in membrane, action potential, and ion channel properties of rostral nucleus of the solitary tract neurons.
(NeuroElectro data)
(PubMed)
|
44.0
± 5.0
(18)
|
44.0 (mV/ms)
|
Data Table |
| Nucleus of the solitary tract principal cell |
|
spike max rise slope |
Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice.
(NeuroElectro data)
(PubMed)
|
119.44
± 15.87
(13)
|
119.44 (mV/ms)
|
Data Table |
| Nucleus of the solitary tract principal cell |
rostral nucleus of the solitary tract neuron
|
spike max rise slope |
Pre- and postnatal differences in membrane, action potential, and ion channel properties of rostral nucleus of the solitary tract neurons.
(NeuroElectro data)
(PubMed)
|
82.0
± 4.0
(39)
|
82.0 (mV/ms)
|
Data Table |
| Olfactory bulb (main) Blanes cell |
Olfactory bulb deep short-axon cells
|
spike max rise slope |
Rapid Feedforward Inhibition and Asynchronous Excitation Regulate Granule Cell Activity in the Mammalian Main Olfactory Bulb.
(NeuroElectro data)
(PubMed)
|
272.3
± 83.3
(9)
|
272.3 (mV/ms)
|
Data Table |
| Olfactory bulb (main) granule cell |
|
spike max rise slope |
Rapid Feedforward Inhibition and Asynchronous Excitation Regulate Granule Cell Activity in the Mammalian Main Olfactory Bulb.
(NeuroElectro data)
(PubMed)
|
167.8
± 64.3
(31)
|
167.8 (mV/ms)
|
Data Table |
| Olfactory bulb (main) mitral cell |
|
spike max rise slope |
Postnatal development attunes olfactory bulb mitral cells to high-frequency signaling.
(NeuroElectro data)
(PubMed)
|
175.5
± 52.3
(48)
|
175.5 (mV/ms)
|
Data Table |
| Olfactory cortex large multipolar cell |
posterior piriform cortex round smooth GABAergic fast-spiking inhibitory interneuron
|
spike max rise slope |
GABAergic inhibitory interneurons in the posterior piriform cortex of the GAD67-GFP mouse.
(NeuroElectro data)
(PubMed)
|
109.0
± 16.7
(12)
|
109.0 (mV/ms)
|
Data Table |
| Other |
hypothalamic non-GnRH expressing neuron
|
spike max rise slope |
GABA- and glutamate-activated channels in green fluorescent protein-tagged gonadotropin-releasing hormone neurons in transgenic mice.
(NeuroElectro data)
(PubMed)
|
105.0
± 39.9
(26)
|
105.0 (mV/ms)
|
Data Table |
| Other |
Layer IV Excitatory Barrel Neurons
|
spike max rise slope |
Increased excitability of cortical neurons induced by associative learning: an ex vivo study.
(NeuroElectro data)
(PubMed)
|
405.0
± 15.0
(33)
|
405.0 (mV/ms)
|
Data Table |
| Other |
Dentate gyrus GABAergic neurons
|
spike max rise slope |
Multiple roles for mammalian target of rapamycin signaling in both glutamatergic and GABAergic synaptic transmission.
(NeuroElectro data)
(PubMed)
|
116.0
± 8.0
(23)
|
116.0 (mV/ms)
|
Data Table |
| Other |
medial septum/diagonal band of Broca complex septo-hippocampal parvalbumin-positive GABAergic neuron
|
spike max rise slope |
Synergy of direct and indirect cholinergic septo-hippocampal pathways coordinates firing in hippocampal networks.
(NeuroElectro data)
(PubMed)
|
318.5
± 110.3
(10)
|
318.5 (mV/ms)
|
Data Table |
| Other |
Olfactory Bulb dopaminergic biphasic interneuron
|
spike max rise slope |
A distinct subtype of dopaminergic interneuron displays inverted structural plasticity at the axon initial segment.
(NeuroElectro data)
(PubMed)
|
182.0
± 19.0
(17)
|
182.0 (mV/ms)
|
Data Table |
| Other |
lateral olivocochlear brainstem neuron
|
spike max rise slope |
Physiological characterization of vestibular efferent brainstem neurons using a transgenic mouse model.
(NeuroElectro data)
(PubMed)
|
160.2
± 16.3
(13)
|
160.2 (mV/ms)
|
Data Table |
| Other |
neocortex layer 1 classical stuttering GABAergic cells
|
spike max rise slope |
Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex.
(NeuroElectro data)
(PubMed)
|
65.93
(14)
|
65.93 (mV/ms)
|
Data Table |
| Other |
lamina terminalis- preoptic area-diagonal band of Broca GnRH expressing neurons
|
spike max rise slope |
GABA- and glutamate-activated channels in green fluorescent protein-tagged gonadotropin-releasing hormone neurons in transgenic mice.
(NeuroElectro data)
(PubMed)
|
88.9
± 33.1
(26)
|
88.9 (mV/ms)
|
Data Table |
| Other |
Lateral central amygdala late-spiking GABAergic neuron
|
spike max rise slope |
Wiring Specificity and Synaptic Diversity in the Mouse Lateral Central Amygdala.
(NeuroElectro data)
(PubMed)
|
232.0
± 10.0
(50)
|
232.0 (mV/ms)
|
Data Table |
| Other |
medial septum/diagonal band of Broca complex septo-hippocampal cholinergic neuron
|
spike max rise slope |
Synergy of direct and indirect cholinergic septo-hippocampal pathways coordinates firing in hippocampal networks.
(NeuroElectro data)
(PubMed)
|
133.8
± 63.3
(11)
|
133.8 (mV/ms)
|
Data Table |
| Other |
Olfactory Bulb dopaminergic monophasic interneuron
|
spike max rise slope |
A distinct subtype of dopaminergic interneuron displays inverted structural plasticity at the axon initial segment.
(NeuroElectro data)
(PubMed)
|
158.0
± 20.0
(21)
|
158.0 (mV/ms)
|
Data Table |
| Other |
dorsal brainstem ChAT-expressing vestibular efferent neuron
|
spike max rise slope |
Physiological characterization of vestibular efferent brainstem neurons using a transgenic mouse model.
(NeuroElectro data)
(PubMed)
|
104.4
± 11.4
(9)
|
104.4 (mV/ms)
|
Data Table |
| Other |
somatosensory cortex layer 1 classical non-accomodating GABAergic cells
|
spike max rise slope |
Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex.
(NeuroElectro data)
(PubMed)
|
63.02
(40)
|
63.02 (mV/ms)
|
Data Table |
| Other |
Lateral central amygdala early-spiking GABAergic neuron
|
spike max rise slope |
Wiring Specificity and Synaptic Diversity in the Mouse Lateral Central Amygdala.
(NeuroElectro data)
(PubMed)
|
223.0
± 12.0
(40)
|
223.0 (mV/ms)
|
Data Table |
| Other |
Olfactory Bulb dopaminergic biphasic interneuron
|
spike max rise slope |
A distinct subtype of dopaminergic interneuron displays inverted structural plasticity at the axon initial segment.
(NeuroElectro data)
(PubMed)
|
205.0
± 21.0
(18)
|
205.0 (mV/ms)
|
Data Table |
| Other |
Lateral hypothalamus GAD65-GFP fast spiking neurons
|
spike max rise slope |
Lateral hypothalamic GAD65 neurons are spontaneously firing and distinct from orexin- and melanin-concentrating hormone neurons.
(NeuroElectro data)
(PubMed)
|
334.2
± 18.1
(20)
|
334.2 (mV/ms)
|
Data Table |
| Other |
neocortex layer 1 classical irregular spiking GABAergic cells
|
spike max rise slope |
Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex.
(NeuroElectro data)
(PubMed)
|
70.75
(8)
|
70.75 (mV/ms)
|
Data Table |
| Other |
Tectum principal neuron
|
spike max rise slope |
Multisensory integration in mesencephalic trigeminal neurons in Xenopus tadpoles.
(NeuroElectro data)
(PubMed)
|
22.7
± 2.04
|
22.7 (mV/ms)
|
Data Table |
| Other |
Rostral ventromedial medulla neutral slow-spiking inhibitory neurons
|
spike max rise slope |
Intrinsic membrane characteristics distinguish two subsets of nociceptive modulatory neurons in rat RVM.
(NeuroElectro data)
(PubMed)
|
281.0
± 21.0
(5)
|
281.0 (mV/ms)
|
Data Table |
| Other |
Lateral hypothalamus GAD65-GFP late spiking neurons
|
spike max rise slope |
Lateral hypothalamic GAD65 neurons are spontaneously firing and distinct from orexin- and melanin-concentrating hormone neurons.
(NeuroElectro data)
(PubMed)
|
195.1
± 19.8
(15)
|
195.1 (mV/ms)
|
Data Table |
| Other |
somatosensory cortex layer 1 bursting non-accommodating GABAergic cells
|
spike max rise slope |
Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex.
(NeuroElectro data)
(PubMed)
|
61.43
|
61.43 (mV/ms)
|
Data Table |
| Other |
Medial entorhinal cortex layer 2 non-stellate cell
|
spike max rise slope |
Temporal lobe epilepsy induces intrinsic alterations in Na channel gating in layer II medial entorhinal cortex neurons.
(NeuroElectro data)
(PubMed)
|
255.7
± 13.0
(14)
|
255.7 (mV/ms)
|
Data Table |
| Other |
Rostral ventromedial medulla fast-spiking off-response neurons
|
spike max rise slope |
Intrinsic membrane characteristics distinguish two subsets of nociceptive modulatory neurons in rat RVM.
(NeuroElectro data)
(PubMed)
|
287.0
± 27.0
(5)
|
287.0 (mV/ms)
|
Data Table |
| Other |
left atrial appendage myocyte
|
spike max rise slope |
Free Fatty Acid Effects on the Atrial Myocardium: Membrane Ionic Currents Are Remodeled by the Disruption of T-Tubular Architecture.
(NeuroElectro data)
(PubMed)
|
192.5
± 18.3
(6)
|
--
|
Data Table |
| Other |
Lateral hypothalamus GAD65-GFP low-threshold spiking neurons
|
spike max rise slope |
Lateral hypothalamic GAD65 neurons are spontaneously firing and distinct from orexin- and melanin-concentrating hormone neurons.
(NeuroElectro data)
(PubMed)
|
226.9
± 16.9
(33)
|
226.9 (mV/ms)
|
Data Table |
| Other |
somatosensory cortex layer 1 classical adapting GABAergic cells
|
spike max rise slope |
Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex.
(NeuroElectro data)
(PubMed)
|
65.75
(11)
|
65.75 (mV/ms)
|
Data Table |
| Other |
Rostral ventromedial medulla fast-spiking on-response neurons
|
spike max rise slope |
Intrinsic membrane characteristics distinguish two subsets of nociceptive modulatory neurons in rat RVM.
(NeuroElectro data)
(PubMed)
|
280.0
± 16.0
(5)
|
280.0 (mV/ms)
|
Data Table |
| Other |
left atrial appendage myocyte
|
spike max rise slope |
Free Fatty Acid Effects on the Atrial Myocardium: Membrane Ionic Currents Are Remodeled by the Disruption of T-Tubular Architecture.
(NeuroElectro data)
(PubMed)
|
223.9
± 13.1
(22)
|
--
|
Data Table |
| Other |
Lateral hypothalamus GAD65-GFP regular spiking neurons
|
spike max rise slope |
Lateral hypothalamic GAD65 neurons are spontaneously firing and distinct from orexin- and melanin-concentrating hormone neurons.
(NeuroElectro data)
(PubMed)
|
220.4
± 11.3
(71)
|
220.4 (mV/ms)
|
Data Table |
| Other |
Basolateral amygdala cholecystokinin induced burst-spiking interneurons
|
spike max rise slope |
Cholecystokinin excites interneurons in rat basolateral amygdala.
(NeuroElectro data)
(PubMed)
|
181.0
± 14.0
|
181.0 (mV/ms)
|
Data Table |
| Other |
rostral ventromedial medulla slow-spiking off -response neurons
|
spike max rise slope |
Intrinsic membrane characteristics distinguish two subsets of nociceptive modulatory neurons in rat RVM.
(NeuroElectro data)
(PubMed)
|
344.0
± 24.0
(1)
|
344.0 (mV/ms)
|
Data Table |
| Other |
left atrial appendage myocyte
|
spike max rise slope |
Free Fatty Acid Effects on the Atrial Myocardium: Membrane Ionic Currents Are Remodeled by the Disruption of T-Tubular Architecture.
(NeuroElectro data)
(PubMed)
|
227.9
± 12.6
(9)
|
--
|
Data Table |
| Other |
CA3 projecting hippocampus Granule Cell
|
spike max rise slope |
Two electrophysiologically distinct types of granule cells in epileptic human hippocampus.
(NeuroElectro data)
(PubMed)
|
272.0
± 55.0
|
272.0 (mV/ms)
|
Data Table |
| Other |
presubiculum regular spiking pyramidal cells in layers II/III
|
spike max rise slope |
Cellular neuroanatomy of rat presubiculum.
(NeuroElectro data)
(PubMed)
|
506.0
(24)
|
506.0 (mV/ms)
|
Data Table |
| Other |
Basolateral amygdala cholecystokinin induced regular-firing interneurons
|
spike max rise slope |
Cholecystokinin excites interneurons in rat basolateral amygdala.
(NeuroElectro data)
(PubMed)
|
171.0
± 5.0
|
171.0 (mV/ms)
|
Data Table |
| Other |
Rostral ventromedial medulla slow-spiking on-response neurons
|
spike max rise slope |
Intrinsic membrane characteristics distinguish two subsets of nociceptive modulatory neurons in rat RVM.
(NeuroElectro data)
(PubMed)
|
275.0
± 20.0
(3)
|
275.0 (mV/ms)
|
Data Table |
| Other |
presubiculum intrinsically bursting cells in layers IV
|
spike max rise slope |
Cellular neuroanatomy of rat presubiculum.
(NeuroElectro data)
(PubMed)
|
359.0
(6)
|
359.0 (mV/ms)
|
Data Table |
| Other |
Medial Prefrontal Cortex pyramidal neuron
|
spike max rise slope |
Activation of Pyramidal Neurons in Mouse Medial Prefrontal Cortex Enhances Food-Seeking Behavior While Reducing Impulsivity in the Absence of an Effect on Food Intake.
(NeuroElectro data)
(PubMed)
|
155.4
± 3.6
(10)
|
155.4 (mV/ms)
|
Data Table |
| Other |
Basolateral amygdala cholecystokinin induced projection neurons
|
spike max rise slope |
Cholecystokinin excites interneurons in rat basolateral amygdala.
(NeuroElectro data)
(PubMed)
|
198.0
± 13.0
|
198.0 (mV/ms)
|
Data Table |
| Other |
presubiculum regular spiking pyramidal cells in layer V/VI
|
spike max rise slope |
Cellular neuroanatomy of rat presubiculum.
(NeuroElectro data)
(PubMed)
|
367.0
(17)
|
367.0 (mV/ms)
|
Data Table |
| Other |
Basolateral amygdala cholecystokinin induced fast spiking type 2 interneurons
|
spike max rise slope |
Cholecystokinin excites interneurons in rat basolateral amygdala.
(NeuroElectro data)
(PubMed)
|
171.0
± 8.0
|
171.0 (mV/ms)
|
Data Table |
| Other |
presubiculum regular spiking pyramidal cells in layer V/VI
|
spike max rise slope |
Cellular neuroanatomy of rat presubiculum.
(NeuroElectro data)
(PubMed)
|
340.0
(11)
|
340.0 (mV/ms)
|
Data Table |
| Other |
Basolateral amygdala cholecystokinin induced fast spiking type 1 interneurons
|
spike max rise slope |
Cholecystokinin excites interneurons in rat basolateral amygdala.
(NeuroElectro data)
(PubMed)
|
189.0
± 4.0
|
189.0 (mV/ms)
|
Data Table |
| Other |
Dentate gyrus glutamergic neurons
|
spike max rise slope |
Multiple roles for mammalian target of rapamycin signaling in both glutamatergic and GABAergic synaptic transmission.
(NeuroElectro data)
(PubMed)
|
212.0
± 14.0
(21)
|
212.0 (mV/ms)
|
Data Table |
| Other |
Olfactory Bulb dopaminergic monophasic interneuron
|
spike max rise slope |
A distinct subtype of dopaminergic interneuron displays inverted structural plasticity at the axon initial segment.
(NeuroElectro data)
(PubMed)
|
172.0
± 21.0
(23)
|
172.0 (mV/ms)
|
Data Table |
| Other |
Neostriatum long-lasting afterhyperpolarization interneuron
|
spike max rise slope |
Heterogeneity of spike frequency adaptation among medium spiny neurones from the rat striatum.
(NeuroElectro data)
(PubMed)
|
75.4
± 6.3
(11)
|
75.4 (mV/ms)
|
Data Table |
| Spinal cord ventral horn motor neuron alpha |
|
spike max rise slope |
Motor neuron rescue in spinal muscular atrophy mice demonstrates that sensory-motor defects are a consequence, not a cause, of motor neuron dysfunction.
(NeuroElectro data)
(PubMed)
|
97.0
± 9.0
(12)
|
97.0 (mV/ms)
|
Data Table |
| Spinal cord ventral horn motor neuron alpha |
spinal cord lumbar motor neuron
|
spike max rise slope |
Early excitability changes in lumbar motoneurons of transgenic SOD1G85R and SOD1G(93A-Low) mice.
(NeuroElectro data)
(PubMed)
|
151.6
± 7.4
(33)
|
151.6 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum regular spiking pyramidal neuron
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
341.0
± 4.0
(218)
|
341.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
|
spike max rise slope |
Adenosine A1 receptors presynaptically modulate excitatory synaptic input onto subiculum neurons.
(NeuroElectro data)
(PubMed)
|
309.8
± 10.1
(8)
|
309.8 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to amygdala
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
331.0
± 7.0
(33)
|
331.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to lateral entorhinal cortex
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
345.0
± 16.0
(51)
|
345.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to orbitofrontal cortex
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
349.0
± 8.0
(50)
|
349.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to nucleus accumbens
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
327.0
± 13.0
(64)
|
327.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
Presubicular pyramidal cells
|
spike max rise slope |
Diversity and overlap of parvalbumin and somatostatin expressing interneurons in mouse presubiculum.
(NeuroElectro data)
(PubMed)
|
517.0
(17)
|
517.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to thalamic nucleus
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
359.0
± 4.0
(68)
|
359.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to presubiculum
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
354.0
± 8.0
(23)
|
354.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
Subiculum regular spiking pyramidal cell
|
spike max rise slope |
Resting and active properties of pyramidal neurons in subiculum and CA1 of rat hippocampus.
(NeuroElectro data)
(PubMed)
|
299.0
± 17.0
|
--
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to ventromedial hypothalamus
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
374.0
± 6.0
(46)
|
374.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
Subiculum weak bursting pyramidal cell
|
spike max rise slope |
Resting and active properties of pyramidal neurons in subiculum and CA1 of rat hippocampus.
(NeuroElectro data)
(PubMed)
|
264.0
± 18.0
|
--
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to medial entorhinal cortex
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
356.0
± 6.0
(28)
|
356.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
Subiculum strong bursting pyramidal cell
|
spike max rise slope |
Resting and active properties of pyramidal neurons in subiculum and CA1 of rat hippocampus.
(NeuroElectro data)
(PubMed)
|
297.0
± 22.0
|
--
|
Data Table |
| Subiculum pyramidal cell |
subiculum pyramidal neuron projecting to retrosplenial cortex
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
379.0
± 8.0
(43)
|
379.0 (mV/ms)
|
Data Table |
| Subiculum pyramidal cell |
subiculum bursting pyramidal neuron
|
spike max rise slope |
Target-specific output patterns are predicted by the distribution of regular-spiking and bursting pyramidal neurons in the subiculum.
(NeuroElectro data)
(PubMed)
|
367.0
± 3.0
(188)
|
367.0 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Regulation of action potential size and excitability in substantia nigra compacta neurons: sensitivity to 4-aminopyridine.
(NeuroElectro data)
(PubMed)
|
193.0
± 8.0
(35)
|
193.0 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
23.8
± 8.6
|
23.8 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
54.9
± 18.4
|
54.9 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Molecular and functional differences in voltage-activated sodium currents between GABA projection neurons and dopamine neurons in the substantia nigra.
(NeuroElectro data)
(PubMed)
|
71.8
± 8.8
(9)
|
71.8 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
61.5
± 21.0
|
61.5 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
50.6
± 15.6
|
50.6 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Pacemaker rate and depolarization block in nigral dopamine neurons: a somatic sodium channel balancing act.
(NeuroElectro data)
(PubMed)
|
125.7
± 9.0
(9)
|
125.7 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
25.1
± 19.2
|
25.1 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Differences in Na+ conductance density and Na+ channel functional properties between dopamine and GABA neurons of the rat substantia nigra.
(NeuroElectro data)
(PubMed)
|
103.7
± 7.2
|
103.7 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
24.5
± 10.8
|
24.5 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
54.2
± 14.5
|
54.2 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
47.6
± 21.7
|
47.6 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
59.3
± 21.2
|
59.3 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
36.3
± 21.2
|
36.3 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
54.3
± 21.1
|
54.3 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
56.2
± 18.3
|
56.2 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
58.2
± 16.2
|
58.2 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
32.8
± 14.8
|
32.8 (mV/ms)
|
Data Table |
| Substantia nigra pars compacta dopaminergic cell |
|
spike max rise slope |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
63.0
± 14.3
|
63.0 (mV/ms)
|
Data Table |
| Substantia nigra pars reticulata interneuron GABA |
|
spike max rise slope |
Molecular and functional differences in voltage-activated sodium currents between GABA projection neurons and dopamine neurons in the substantia nigra.
(NeuroElectro data)
(PubMed)
|
183.8
± 17.3
(12)
|
183.8 (mV/ms)
|
Data Table |
| Substantia nigra pars reticulata interneuron GABA |
|
spike max rise slope |
Differences in Na+ conductance density and Na+ channel functional properties between dopamine and GABA neurons of the rat substantia nigra.
(NeuroElectro data)
(PubMed)
|
320.5
± 28.3
|
320.5 (mV/ms)
|
Data Table |
| Superior colliculus superficial layer neuron |
stratum griseum superficiale of superior colliculus interneuron
|
spike max rise slope |
Neonatal neuronal circuitry shows hyperexcitable disturbance in a mouse model of the adult-onset neurodegenerative disease amyotrophic lateral sclerosis.
(NeuroElectro data)
(PubMed)
|
109.0
± 24.0
(8)
|
109.0 (mV/ms)
|
Data Table |
| Thalamic reticular nucleus cell |
Thalamic reticular nucleus fast-spiking GABAergic cell
|
spike max rise slope |
Resilient RTN fast spiking in Kv3.1 null mice suggests redundancy in the action potential repolarization mechanism.
(NeuroElectro data)
(PubMed)
|
515.4
± 25.8
(16)
|
515.4 (mV/ms)
|
Data Table |
| Thalamic reticular nucleus cell |
Thalamic reticular nucleus fast-spiking GABAergic cell
|
spike max rise slope |
Resilient RTN fast spiking in Kv3.1 null mice suggests redundancy in the action potential repolarization mechanism.
(NeuroElectro data)
(PubMed)
|
350.6
± 14.6
(16)
|
350.6 (mV/ms)
|
Data Table |
| Thalamus relay cell |
Lateral dorsal thalamic relay nucleus
|
spike max rise slope |
Differential regulation of action potential firing in adult murine thalamocortical neurons by Kv3.2, Kv1, and SK potassium and N-type calcium channels.
(NeuroElectro data)
(PubMed)
|
336.2
(82)
|
336.2 (mV/ms)
|
Data Table |
| Trigeminal nucleus principal cell |
Mesencephalic trigeminal unipolar neuron
|
spike max rise slope |
Multisensory integration in mesencephalic trigeminal neurons in Xenopus tadpoles.
(NeuroElectro data)
(PubMed)
|
95.33
± 3.01
|
95.33 (mV/ms)
|
Data Table |
