Amygdala basolateral nucleus pyramidal neuron |
|
sag amplitude |
Increased Basolateral Amygdala Pyramidal Cell Excitability May Contribute to the Anxiogenic Phenotype Induced by Chronic Early-Life Stress.
(NeuroElectro data)
(PubMed)
|
-4.98
± 0.92
(16)
|
-4.98 (mV)
|
Data Table |
Basalis nucleus cholinergic neuron |
Magnocellular preoptic nucleus/substantia innominata cholinergic neurons
|
sag amplitude |
Adenosine inhibits basal forebrain cholinergic and noncholinergic neurons in vitro.
(NeuroElectro data)
(PubMed)
|
0.96
± 0.28
(40)
|
0.96 (mV)
|
Data Table |
Cerebellum Golgi cell |
Small cerebellum golgi cell
|
sag amplitude |
Cerebellar globular cells receive monoaminergic excitation and monosynaptic inhibition from Purkinje cells.
(NeuroElectro data)
(PubMed)
|
6.5
± 0.8
(13)
|
6.5 (mV)
|
Data Table |
Cerebellum Lugaro cell |
small fusiform Lugaro cell
|
sag amplitude |
Cerebellar globular cells receive monoaminergic excitation and monosynaptic inhibition from Purkinje cells.
(NeuroElectro data)
(PubMed)
|
6.7
± 0.9
(8)
|
6.7 (mV)
|
Data Table |
Cerebellum Purkinje cell |
|
sag amplitude |
Excitability and synaptic alterations in the cerebellum of APP/PS1 mice.
(NeuroElectro data)
(PubMed)
|
47.6
± 3.0
(8)
|
47.6 (mV)
|
Data Table |
Cerebellum Purkinje cell |
cerebellar vermis lobule X tonic firing purkinje cell
|
sag amplitude |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
21.0
± 1.3
(13)
|
21.0 (mV)
|
Data Table |
Cerebellum Purkinje cell |
cerebellar vermis lobule III - V complex bursting purkinje cell
|
sag amplitude |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
18.4
± 1.5
(12)
|
18.4 (mV)
|
Data Table |
Cerebellum Purkinje cell |
cerebellar vermis lobule III - V tonic firing purkinje cell
|
sag amplitude |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
16.4
± 0.8
(25)
|
16.4 (mV)
|
Data Table |
Cerebellum Purkinje cell |
cerebellar vermis lobule X gap firing purkinje cell
|
sag amplitude |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
23.2
± 1.3
(15)
|
23.2 (mV)
|
Data Table |
Cerebellum Purkinje cell |
cerebellar vermis lobule X initial bursting purkinje cell
|
sag amplitude |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
24.1
± 1.9
(10)
|
24.1 (mV)
|
Data Table |
Cerebellum Purkinje cell |
|
sag amplitude |
Excitability and synaptic alterations in the cerebellum of APP/PS1 mice.
(NeuroElectro data)
(PubMed)
|
41.3
± 2.5
(14)
|
41.3 (mV)
|
Data Table |
Cerebellum Purkinje cell |
cerebellar vermis lobule X complex bursting purkinje cell
|
sag amplitude |
Lobule-specific membrane excitability of cerebellar Purkinje cells.
(NeuroElectro data)
(PubMed)
|
21.8
± 0.7
(11)
|
21.8 (mV)
|
Data Table |
Globus pallidus intrinsic cell |
Medial Globus pallidus Lhx6- expressing neurons
|
sag amplitude |
Transgenic mouse lines subdivide external segment of the globus pallidus (GPe) neurons and reveal distinct GPe output pathways.
(NeuroElectro data)
(PubMed)
|
16.1
± 7.0
(40)
|
16.1 (mV)
|
Data Table |
Globus pallidus intrinsic cell |
Lateral globus pallidus parvalbumin-expressing neurons
|
sag amplitude |
Transgenic mouse lines subdivide external segment of the globus pallidus (GPe) neurons and reveal distinct GPe output pathways.
(NeuroElectro data)
(PubMed)
|
13.8
± 5.5
(30)
|
13.8 (mV)
|
Data Table |
Globus pallidus intrinsic cell |
dorsal globus pallidus GABAergic neuron
|
sag amplitude |
Supersensitive presynaptic dopamine D2 receptor inhibition of the striatopallidal projection in nigrostriatal dopamine-deficient mice.
(NeuroElectro data)
(PubMed)
|
4.8
± 0.6
(26)
|
4.8 (mV)
|
Data Table |
Globus pallidus intrinsic cell |
dorsal globus pallidus GABAergic neuron
|
sag amplitude |
Supersensitive presynaptic dopamine D2 receptor inhibition of the striatopallidal projection in nigrostriatal dopamine-deficient mice.
(NeuroElectro data)
(PubMed)
|
8.9
± 0.7
(37)
|
8.9 (mV)
|
Data Table |
Globus pallidus, external segment neuron |
Globus Pallidus high frequency firing external segment neuron
|
sag amplitude |
Electrophysiological characteristics of globus pallidus neurons.
(NeuroElectro data)
(PubMed)
|
18.0
± 7.0
(24)
|
18.0 (mV)
|
Data Table |
Globus pallidus, external segment neuron |
Globus Pallidus slow frequency firing external segment neuron
|
sag amplitude |
Electrophysiological characteristics of globus pallidus neurons.
(NeuroElectro data)
(PubMed)
|
23.0
± 12.0
(38)
|
23.0 (mV)
|
Data Table |
Globus pallidus, external segment neuron |
Globus Pallidus burst firing external segment neuron
|
sag amplitude |
Electrophysiological characteristics of globus pallidus neurons.
(NeuroElectro data)
(PubMed)
|
42.0
± 8.0
(14)
|
42.0 (mV)
|
Data Table |
Hippocampus CA1 basket cell |
|
sag amplitude |
Characterization of neurons in the CA2 subfield of the adult rat hippocampus.
(NeuroElectro data)
(PubMed)
|
0.1
± 0.2
(10)
|
0.1 (mV)
|
Data Table |
Hippocampus CA1 basket cell |
Hippocampus CA1 parvalbumin-expressing basket cell
|
sag amplitude |
Local circuitry involving parvalbumin-positive basket cells in the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
0.1
± 0.1
(16)
|
0.1 (mV)
|
Data Table |
Hippocampus CA1 oriens lacunosum moleculare neuron |
Hippocampus CA1 and CA2 non-fast spiking stramum oriens neuron
|
sag amplitude |
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)
|
2.8
± 1.1
(15)
|
2.8 (mV)
|
Data Table |
Hippocampus CA1 oriens lacunosum moleculare neuron |
Hippocampal CA1 somatostatin-positive inhibitory interneuron
|
sag amplitude |
Learning increases intrinsic excitability of hippocampal interneurons.
(NeuroElectro data)
(PubMed)
|
2.79
± 0.16
(25)
|
2.79 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
Hippocampus CA1 non-fast spiking stratum oriens pyramidal-like cell
|
sag amplitude |
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)
|
4.9
± 1.4
(8)
|
4.9 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
Hippocampal CA1 Dorsal Pyramidal Neuron
|
sag amplitude |
Learning-dependent plasticity of hippocampal CA1 pyramidal neuron postburst afterhyperpolarizations and increased excitability after inhibitory avoidance learning depend upon basolateral amygdala inputs.
(NeuroElectro data)
(PubMed)
|
8.3
± 0.5
(12)
|
8.3 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Strong CA2 pyramidal neuron synapses define a powerful disynaptic cortico-hippocampal loop.
(NeuroElectro data)
(PubMed)
|
8.4
± 0.3
(8)
|
8.4 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Frequency dependence of CA3 spike phase response arising from h-current properties.
(NeuroElectro data)
(PubMed)
|
0.3
± 0.02
(21)
|
0.3 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
Hippocampal CA1 Ventral Pyramidal Neuron
|
sag amplitude |
Learning-dependent plasticity of hippocampal CA1 pyramidal neuron postburst afterhyperpolarizations and increased excitability after inhibitory avoidance learning depend upon basolateral amygdala inputs.
(NeuroElectro data)
(PubMed)
|
6.2
± 0.4
(29)
|
6.2 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
Hippocampus CA1 non-fast spiking pyramidal neuron
|
sag amplitude |
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)
|
10.3
± 3.1
(7)
|
10.3 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Modulation of BK channels contributes to activity-dependent increase of excitability through MTORC1 activity in CA1 pyramidal cells of mouse hippocampus.
(NeuroElectro data)
(PubMed)
|
2.1
± 0.6
(5)
|
2.1 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Modulation of BK channels contributes to activity-dependent increase of excitability through MTORC1 activity in CA1 pyramidal cells of mouse hippocampus.
(NeuroElectro data)
(PubMed)
|
1.5
± 0.2
(13)
|
1.5 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
1.3
± 0.7
(6)
|
1.3 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
Dorsal Hippocampus CA1 pyramidal cell
|
sag amplitude |
Watermaze learning enhances excitability of CA1 pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
6.9
± 0.2
(40)
|
6.9 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Modulation of BK channels contributes to activity-dependent increase of excitability through MTORC1 activity in CA1 pyramidal cells of mouse hippocampus.
(NeuroElectro data)
(PubMed)
|
2.4
± 0.2
(6)
|
2.4 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
Ventral Hippocampus CA1 pyramidal cell
|
sag amplitude |
Watermaze learning enhances excitability of CA1 pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
7.2
± 0.3
(40)
|
7.2 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Modulation of BK channels contributes to activity-dependent increase of excitability through MTORC1 activity in CA1 pyramidal cells of mouse hippocampus.
(NeuroElectro data)
(PubMed)
|
1.9
± 0.2
(18)
|
1.9 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Effects of prenatal cocaine exposure on the developing hippocampus: intrinsic and synaptic physiology.
(NeuroElectro data)
(PubMed)
|
6.2
± 1.3
(10)
|
6.2 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Enhanced intrinsic excitability and EPSP-spike coupling accompany enriched environment-induced facilitation of LTP in hippocampal CA1 pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
13.3
± 0.3
(16)
|
13.3 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Effects of prenatal cocaine exposure on the developing hippocampus: intrinsic and synaptic physiology.
(NeuroElectro data)
(PubMed)
|
4.7
± 0.6
(18)
|
4.7 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Learning increases intrinsic excitability of hippocampal interneurons.
(NeuroElectro data)
(PubMed)
|
3.82
± 0.43
(32)
|
3.82 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Intrinsic neuronal excitability is reversibly altered by a single experience in fear conditioning.
(NeuroElectro data)
(PubMed)
|
-3.8
± 0.2
(19)
|
-3.8 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
hippocampus CA1 pyramidal GABAergic cell
|
sag amplitude |
Anti-GAD65 Containing Cerebrospinal Fluid Does not Alter GABAergic Transmission.
(NeuroElectro data)
(PubMed)
|
-5.1
± 0.9
(9)
|
-5.1 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Effects of prenatal cocaine exposure on the developing hippocampus: intrinsic and synaptic physiology.
(NeuroElectro data)
(PubMed)
|
5.0
± 0.7
(19)
|
5.0 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Increasing SK2 Channel Activity Impairs Associative Learning.
(NeuroElectro data)
(PubMed)
|
3.22
± 0.29
(9)
|
3.22 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Hippocampal heterotopia with molecular and electrophysiological properties of neocortical neurons.
(NeuroElectro data)
(PubMed)
|
4.9
± 0.4
|
4.9 (mV)
|
Data Table |
Hippocampus CA1 pyramidal cell |
|
sag amplitude |
Trace fear conditioning enhances synaptic and intrinsic plasticity in rat hippocampus.
(NeuroElectro data)
(PubMed)
|
5.9
± 0.5
(18)
|
5.9 (mV)
|
Data Table |
Hippocampus CA2 basket cell broad |
Hippocampus CA2 dendritic wide arbor basket parvalbumin-expressing cell
|
sag amplitude |
Local circuitry involving parvalbumin-positive basket cells in the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
12.9
± 10.2
(18)
|
12.9 (mV)
|
Data Table |
Hippocampus CA2 basket cell broad |
HIppocampus CA2 wide arbor basket cell
|
sag amplitude |
Characterization of neurons in the CA2 subfield of the adult rat hippocampus.
(NeuroElectro data)
(PubMed)
|
20.2
± 9.4
(10)
|
0.202 (mV)
|
Data Table |
Hippocampus CA2 pyramidal neuron |
Hippocampus CA2 non-fast spiking pyramidal-like neuron
|
sag amplitude |
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)
|
3.7
± 2.5
(7)
|
3.7 (mV)
|
Data Table |
Hippocampus CA2 pyramidal neuron |
Hippocampus CA2 non-fasting spiking pyramidal neuron
|
sag amplitude |
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)
|
10.0
± 3.8
(11)
|
10.0 (mV)
|
Data Table |
Hippocampus CA2 pyramidal neuron |
|
sag amplitude |
Strong CA2 pyramidal neuron synapses define a powerful disynaptic cortico-hippocampal loop.
(NeuroElectro data)
(PubMed)
|
4.1
± 0.2
(8)
|
4.1 (mV)
|
Data Table |
Hippocampus CA3 basket cell |
Hippocampus CA3 basket CB1-expressing cell
|
sag amplitude |
Anatomically heterogeneous populations of CB1 cannabinoid receptor-expressing interneurons in the CA3 region of the hippocampus show homogeneous input-output characteristics.
(NeuroElectro data)
(PubMed)
|
0.43
(14)
|
0.43 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Strong CA2 pyramidal neuron synapses define a powerful disynaptic cortico-hippocampal loop.
(NeuroElectro data)
(PubMed)
|
4.3
± 0.4
(6)
|
4.3 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Effects of prenatal cocaine exposure on the developing hippocampus: intrinsic and synaptic physiology.
(NeuroElectro data)
(PubMed)
|
4.8
± 1.8
(12)
|
4.8 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Frequency dependence of CA3 spike phase response arising from h-current properties.
(NeuroElectro data)
(PubMed)
|
0.16
± 0.01
(40)
|
0.16 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Aging-Related Hyperexcitability in CA3 Pyramidal Neurons Is Mediated by Enhanced A-Type K+ Channel Function and Expression.
(NeuroElectro data)
(PubMed)
|
-2.32
± 0.17
(44)
|
-2.32 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Effects of prenatal cocaine exposure on the developing hippocampus: intrinsic and synaptic physiology.
(NeuroElectro data)
(PubMed)
|
3.4
± 1.0
(15)
|
3.4 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Aging-Related Hyperexcitability in CA3 Pyramidal Neurons Is Mediated by Enhanced A-Type K+ Channel Function and Expression.
(NeuroElectro data)
(PubMed)
|
-2.28
± 0.13
(52)
|
-2.28 (mV)
|
Data Table |
Hippocampus CA3 pyramidal cell |
|
sag amplitude |
Effects of prenatal cocaine exposure on the developing hippocampus: intrinsic and synaptic physiology.
(NeuroElectro data)
(PubMed)
|
3.0
± 1.0
(14)
|
3.0 (mV)
|
Data Table |
Inferior colliculus neuron |
inferior colliculus hyperpolarization-activated mixed cation current neuron
|
sag amplitude |
In vivo dynamic clamp study of I(h) in the mouse inferior colliculus.
(NeuroElectro data)
(PubMed)
|
-4.2
± 0.09
(19)
|
-4.2 (mV)
|
Data Table |
Medial entorhinal cortex layer III pyramidal cell |
|
sag amplitude |
Selective activation of parvalbumin- or somatostatin-expressing interneurons triggers epileptic seizurelike activity in mouse medial entorhinal cortex.
(NeuroElectro data)
(PubMed)
|
2.0
± 0.2
(30)
|
2.0 (mV)
|
Data Table |
Neocortex basket cell |
Auditory cortex layer 2-3 fast-spiking interneuron
|
sag amplitude |
Development of inhibitory timescales in auditory cortex.
(NeuroElectro data)
(PubMed)
|
0.2
± 0.2
(50)
|
0.2 (mV)
|
Data Table |
Neocortex basket cell |
Neocortex medial ganglionic eminence fast spiking interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
2.9
(71)
|
2.9 (mV)
|
Data Table |
Neocortex basket cell |
frontal cortex fast spiking neuron
|
sag amplitude |
Neuregulin-1 signals from the periphery regulate AMPA receptor sensitivity and expression in GABAergic interneurons in developing neocortex.
(NeuroElectro data)
(PubMed)
|
-8.7
± 1.8
(20)
|
-8.7 (mV)
|
Data Table |
Neocortex basket cell |
Neocortex Layer 2-3 Fast-Spiking Interneuron
|
sag amplitude |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
3.8
± 0.3
(9)
|
3.8 (mV)
|
Data Table |
Neocortex basket cell |
primary somatosensory cortex barrel field layer 4 parvalbumin expressing early onset firing fast spiking interneuron
|
sag amplitude |
Two functional inhibitory circuits are comprised of a heterogeneous population of fast-spiking cortical interneurons.
(NeuroElectro data)
(PubMed)
|
4.82
± 0.39
(88)
|
4.82 (mV)
|
Data Table |
Neocortex basket cell |
primary somatosensory cortex barrel field layer 4 parvalbumin expressing delayed firing fast spiking interneuron
|
sag amplitude |
Two functional inhibitory circuits are comprised of a heterogeneous population of fast-spiking cortical interneurons.
(NeuroElectro data)
(PubMed)
|
5.61
± 0.37
(83)
|
5.61 (mV)
|
Data Table |
Neocortex basket cell |
Auditory cortex layer 2-3 fast-spiking interneuron
|
sag amplitude |
Development of inhibitory timescales in auditory cortex.
(NeuroElectro data)
(PubMed)
|
1.6
± 1.3
(36)
|
1.6 (mV)
|
Data Table |
Neocortex basket cell |
Layer 5 somatosensory cortex Fast Spiking parvalbumin positive interneurons
|
sag amplitude |
Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons.
(NeuroElectro data)
(PubMed)
|
1.17
± 0.3
(8)
|
1.17 (mV)
|
Data Table |
Neocortex basket cell |
Auditory cortex layer 2-3 fast-spiking interneuron
|
sag amplitude |
Development of inhibitory timescales in auditory cortex.
(NeuroElectro data)
(PubMed)
|
0.3
± 0.2
(59)
|
0.3 (mV)
|
Data Table |
Neocortex Martinotti cell |
somatosensory cortex layer 5 martinotti cell
|
sag amplitude |
Anatomical, physiological and molecular properties of Martinotti cells in the somatosensory cortex of the juvenile rat.
(NeuroElectro data)
(PubMed)
|
4.44
± 4.17
(25)
|
4.44 (mV)
|
Data Table |
Neocortex Martinotti cell |
somatosensory cortex layer 6 martinotti cell
|
sag amplitude |
Anatomical, physiological and molecular properties of Martinotti cells in the somatosensory cortex of the juvenile rat.
(NeuroElectro data)
(PubMed)
|
5.37
± 2.78
(7)
|
5.37 (mV)
|
Data Table |
Neocortex Martinotti cell |
Somatosensory cortex layer 2-3 somatostatin-expressing inhibitory neuron
|
sag amplitude |
Postnatal maturation of somatostatin-expressing inhibitory cells in the somatosensory cortex of GIN mice.
(NeuroElectro data)
(PubMed)
|
3.0
± 0.6
(16)
|
3.0 (mV)
|
Data Table |
Neocortex Martinotti cell |
Somatosensory cortex layer 2-3 somatostatin-expressing inhibitory neuron
|
sag amplitude |
Postnatal maturation of somatostatin-expressing inhibitory cells in the somatosensory cortex of GIN mice.
(NeuroElectro data)
(PubMed)
|
5.6
± 0.5
(22)
|
5.6 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
medial prefrontal cortex prelimbic area layers 2-3 pyramidal neuron
|
sag amplitude |
Strychnine-sensitive glycine receptors on pyramidal neurons in layers II/III of the mouse prefrontal cortex are tonically activated.
(NeuroElectro data)
(PubMed)
|
2.7
± 0.4
(30)
|
2.7 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
Somatosensory cortex layer 2-3 regular-spiking pyramidal cell
|
sag amplitude |
Postnatal maturation of somatostatin-expressing inhibitory cells in the somatosensory cortex of GIN mice.
(NeuroElectro data)
(PubMed)
|
1.02
± 0.3
(13)
|
1.02 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
|
sag amplitude |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
3.0
± 0.4
(13)
|
3.0 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
Auditory Cortex layer 2-3 pyramidal cell
|
sag amplitude |
Transient Hearing Loss Within a Critical Period Causes Persistent Changes to Cellular Properties in Adult Auditory Cortex.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.1
(24)
|
1.4 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
Somatosensory cortex layer 2-3 regular-spiking pyramidal cell
|
sag amplitude |
Postnatal maturation of somatostatin-expressing inhibitory cells in the somatosensory cortex of GIN mice.
(NeuroElectro data)
(PubMed)
|
2.7
± 0.6
(11)
|
2.7 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
Auditory Cortex layer 2-3 pyramidal cell
|
sag amplitude |
Transient Hearing Loss Within a Critical Period Causes Persistent Changes to Cellular Properties in Adult Auditory Cortex.
(NeuroElectro data)
(PubMed)
|
1.3
± 0.1
(24)
|
1.3 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
dorsal frontal cortex layer 2/3 Tbr2 expressing pyramidal cell
|
sag amplitude |
Neural precursor lineages specify distinct neocortical pyramidal neuron types.
(NeuroElectro data)
(PubMed)
|
2.5
|
2.5 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
|
sag amplitude |
Hippocampal heterotopia with molecular and electrophysiological properties of neocortical neurons.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.5
|
1.4 (mV)
|
Data Table |
Neocortex pyramidal cell layer 2-3 |
dorsal frontal cortex layer 2/3 non-Tbr2 expressing pyramidal cell
|
sag amplitude |
Neural precursor lineages specify distinct neocortical pyramidal neuron types.
(NeuroElectro data)
(PubMed)
|
1.2
|
1.2 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
visual cortex layer 5 Efr3a-expressing corticocortical cortico-nonstriatal projecting regular spiking slender-tufted pyramidal neuron
|
sag amplitude |
Three Types of Cortical Layer 5 Neurons That Differ in Brain-wide Connectivity and Function.
(NeuroElectro data)
(PubMed)
|
11.6
± 1.07
(9)
|
11.6 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Layer 5 somatosensory cortex small amplitude pyramidal cells
|
sag amplitude |
Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons.
(NeuroElectro data)
(PubMed)
|
4.35
± 0.8
(10)
|
4.35 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
visual cortex layer 5 Glt25d2-expressing corticopontine intrinsically bursting thick-tufted pyramidal neuron
|
sag amplitude |
Three Types of Cortical Layer 5 Neurons That Differ in Brain-wide Connectivity and Function.
(NeuroElectro data)
(PubMed)
|
10.99
± 1.57
(9)
|
10.99 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Visual cortex layer 5 Tlx3-expressing corticocortical regular spiking slender-tufted pyramidal neuron
|
sag amplitude |
Three Types of Cortical Layer 5 Neurons That Differ in Brain-wide Connectivity and Function.
(NeuroElectro data)
(PubMed)
|
2.46
± 0.37
(16)
|
2.46 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
primary somatosensory cortex layer 5 pyramidal neurons
|
sag amplitude |
Early postnatal plasticity in neocortex of Fmr1 knockout mice.
(NeuroElectro data)
(PubMed)
|
2.5
± 0.3
|
2.5 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
medial prefrontal cortex prelimbic area layers 5-6 pyramidal neuron
|
sag amplitude |
Strychnine-sensitive glycine receptors on pyramidal neurons in layers II/III of the mouse prefrontal cortex are tonically activated.
(NeuroElectro data)
(PubMed)
|
4.0
± 0.5
(30)
|
4.0 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Temporoparietal Cortex Layer 5 Pyramidal Cell
|
sag amplitude |
Increased excitability and inward rectification in layer V cortical pyramidal neurons in the epileptic mutant mouse Stargazer.
(NeuroElectro data)
(PubMed)
|
1.6
± 0.6
(5)
|
--
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Somatosensory cortex layer V Satb2 expressing Ctip2 expressing double-firing thick-tufted pyramidal neuron
|
sag amplitude |
Area-specific development of distinct projection neuron subclasses is regulated by postnatal epigenetic modifications.
(NeuroElectro data)
(PubMed)
|
1.2
± 0.2
(9)
|
1.2 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
somatosensory cortex layer V corticocallosal projecting pyramidal cell
|
sag amplitude |
Morphological, electrophysiological, and synaptic properties of corticocallosal pyramidal cells in the neonatal rat neocortex.
(NeuroElectro data)
(PubMed)
|
6.6
± 3.9
(22)
|
6.6 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Somatosensory cortex layer V Ctip2 expressing Satb2 expressing single-firing thick-tufted pyramidal neuron
|
sag amplitude |
Area-specific development of distinct projection neuron subclasses is regulated by postnatal epigenetic modifications.
(NeuroElectro data)
(PubMed)
|
3.1
± 0.5
(9)
|
3.1 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
somatosensory cortex layer V thick tufted pyramidal cell
|
sag amplitude |
Morphological, electrophysiological, and synaptic properties of corticocallosal pyramidal cells in the neonatal rat neocortex.
(NeuroElectro data)
(PubMed)
|
5.8
± 3.4
(35)
|
5.8 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Somatosensory cortex layer V Ctip2 expressing single-firing thick-tufted pyramidal neuron
|
sag amplitude |
Area-specific development of distinct projection neuron subclasses is regulated by postnatal epigenetic modifications.
(NeuroElectro data)
(PubMed)
|
4.8
± 1.5
(7)
|
4.8 (mV)
|
Data Table |
Neocortex pyramidal cell layer 5-6 |
Layer 5 somatosensory cortex large amplitude pyramidal cells
|
sag amplitude |
Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons.
(NeuroElectro data)
(PubMed)
|
4.3
± 0.8
(9)
|
4.3 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
2.3
± 1.8
(19)
|
2.3 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
2.1
± 1.5
(26)
|
2.1 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
2.7
± 1.5
(3)
|
2.7 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.3
± 1.5
(5)
|
1.3 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
3.8
± 3.8
(5)
|
3.8 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
0.7
± 0.9
(5)
|
0.7 (mV)
|
Data Table |
Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
sag amplitude |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
1.17
± 0.12
(31)
|
1.17 (mV)
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
4.4
± 3.6
(6)
|
4.4 (mV)
|
Data Table |
Neocortex uncharacterized cell |
|
sag amplitude |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
13.8
± 5.6
|
--
|
Data Table |
Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
6.8
± 3.8
(18)
|
6.8 (mV)
|
Data Table |
Neostriatum gabaergic interneuron |
Neostriatum somatostatin/neuropeptide-Y/neuronal nitric oxide synthase-negative Htr3a-expressing low-threshold spiking gabaergic interneurons
|
sag amplitude |
Novel Striatal GABAergic Interneuron Populations Labeled in the 5HT3aEGFP Mouse.
(NeuroElectro data)
(PubMed)
|
2.97
± 0.39
(68)
|
2.97 (mV)
|
Data Table |
Neostriatum gabaergic interneuron |
Neostriatum neuropeptide-Y-negative Htr3a-expressing late-spiking neurogliaform gabaergic interneuron
|
sag amplitude |
Novel Striatal GABAergic Interneuron Populations Labeled in the 5HT3aEGFP Mouse.
(NeuroElectro data)
(PubMed)
|
0.53
± 0.09
(20)
|
0.53 (mV)
|
Data Table |
Neostriatum gabaergic interneuron |
Neostriatum parvalbumin-expressing Htr3a-expressing fast-spiking gabaergic interneurons
|
sag amplitude |
Novel Striatal GABAergic Interneuron Populations Labeled in the 5HT3aEGFP Mouse.
(NeuroElectro data)
(PubMed)
|
0.92
± 0.33
(41)
|
0.92 (mV)
|
Data Table |
Nucleus accumbens medium spiny neuron |
nucleus accumbens core medium spiny neuron
|
sag amplitude |
Presynaptic homeostatic plasticity rescues long-term depression after chronic Delta 9-tetrahydrocannabinol exposure.
(NeuroElectro data)
(PubMed)
|
1.22
(8)
|
1.22 (mV)
|
Data Table |
Olfactory bulb (main) mitral cell |
|
sag amplitude |
Postnatal development attunes olfactory bulb mitral cells to high-frequency signaling.
(NeuroElectro data)
(PubMed)
|
3.8
± 4.1
(45)
|
3.8 (mV)
|
Data Table |
Olfactory bulb (main) mitral cell |
|
sag amplitude |
Greater excitability and firing irregularity of tufted cells underlies distinct afferent-evoked activity of olfactory bulb mitral and tufted cells.
(NeuroElectro data)
(PubMed)
|
2.0
± 2.6
(35)
|
2.0 (mV)
|
Data Table |
Olfactory bulb (main) tufted cell (middle) |
|
sag amplitude |
Greater excitability and firing irregularity of tufted cells underlies distinct afferent-evoked activity of olfactory bulb mitral and tufted cells.
(NeuroElectro data)
(PubMed)
|
4.4
± 6.1
(28)
|
4.4 (mV)
|
Data Table |
Olfactory tubercle Islets of Calleja spiny granule neuron |
Olfactory tubercle intermittent firing multipolar sparsely spiny neurons
|
sag amplitude |
Diversity of neural signals mediated by multiple, burst-firing mechanisms in rat olfactory tubercle neurons.
(NeuroElectro data)
(PubMed)
|
38.9
(32)
|
38.9 (mV)
|
Data Table |
Olfactory tubercle Islets of Calleja spiny granule neuron |
Olfactory tubercle regenerative bursting neurons
|
sag amplitude |
Diversity of neural signals mediated by multiple, burst-firing mechanisms in rat olfactory tubercle neurons.
(NeuroElectro data)
(PubMed)
|
71.4
(21)
|
71.4 (mV)
|
Data Table |
Olfactory tubercle Islets of Calleja spiny granule neuron |
Olfactory tubercle non-regenerative bursting neurons
|
sag amplitude |
Diversity of neural signals mediated by multiple, burst-firing mechanisms in rat olfactory tubercle neurons.
(NeuroElectro data)
(PubMed)
|
84.2
(77)
|
84.2 (mV)
|
Data Table |
Olfactory tubercle Islets of Calleja spiny granule neuron |
Olfactory tubercle regular spiking spiny-dense pyramidal-shaped neurons
|
sag amplitude |
Diversity of neural signals mediated by multiple, burst-firing mechanisms in rat olfactory tubercle neurons.
(NeuroElectro data)
(PubMed)
|
42.9
(36)
|
42.9 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence deep and superficial layer regular intrinsic bursting Interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
3.8
(17)
|
3.8 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex ChAt-positive GAD67-positive burst-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
10.6
± 1.5
(10)
|
10.6 (mV)
|
Data Table |
Other |
Prefrontal cortex layer 1 non-late-spiking GABAergic interneurons
|
sag amplitude |
Thalamic control of layer 1 circuits in prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
5.9
± 0.9
(11)
|
5.9 (mV)
|
Data Table |
Other |
Hippocampus GluN2D-EGFP-positive interneuron
|
sag amplitude |
GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice.
(NeuroElectro data)
(PubMed)
|
2.0
± 2.7
(25)
|
2.0 (mV)
|
Data Table |
Other |
Stratum radiatum non-pyramidal regular-spiking rebounding cells
|
sag amplitude |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
2.9
± 2.5
|
2.9 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence superficial layer delayed-fast spiking Interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
2.6
(25)
|
2.6 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex ChAt-negative GAD67-negative PAG-expressing VGLUT-positive slow/cluster-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
2.76
± 0.2
(21)
|
2.76 (mV)
|
Data Table |
Other |
Prefrontal cortex layer 1 late-spiking GABAergic interneurons
|
sag amplitude |
Thalamic control of layer 1 circuits in prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
2.9
± 0.4
(14)
|
2.9 (mV)
|
Data Table |
Other |
Cerebellum Globular cell
|
sag amplitude |
Cerebellar globular cells receive monoaminergic excitation and monosynaptic inhibition from Purkinje cells.
(NeuroElectro data)
(PubMed)
|
12.8
± 2.4
(10)
|
12.8 (mV)
|
Data Table |
Other |
Hippocampus GluN2D-EGFP-positive interneuron
|
sag amplitude |
GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice.
(NeuroElectro data)
(PubMed)
|
3.4
± 2.4
|
3.4 (mV)
|
Data Table |
Other |
Stratum radiatum fast-spiking interneurons
|
sag amplitude |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
7.5
± 4.8
(5)
|
7.5 (mV)
|
Data Table |
Other |
Prefrontal cortex layer 1 GABAergic uncharacterized interneurons
|
sag amplitude |
Thalamic control of layer 1 circuits in prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
2.3
± 0.4
(9)
|
2.3 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex ChAt-positive GAD67-positive fast-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
6.11
± 0.4
(6)
|
6.11 (mV)
|
Data Table |
Other |
Substantia pars nigra reticulata GABAergic neurons
|
sag amplitude |
Morphological and physiological properties of parvalbumin- and calretinin-containing gamma-aminobutyric acidergic neurons in the substantia nigra.
(NeuroElectro data)
(PubMed)
|
5.57
± 0.89
(13)
|
5.57 (mV)
|
Data Table |
Other |
Stratum radiatum non-pyramidal regular-spiking rapidly adapting cells
|
sag amplitude |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
1.3
± 2.0
|
1.3 (mV)
|
Data Table |
Other |
Hippocampus CA2 narrow arbor basket cell
|
sag amplitude |
Characterization of neurons in the CA2 subfield of the adult rat hippocampus.
(NeuroElectro data)
(PubMed)
|
0.1
± 0.1
(6)
|
0.1 (mV)
|
Data Table |
Other |
Medullary reticular formation pre-oromotor multipolar neuron
|
sag amplitude |
Intrinsic membrane properties of pre-oromotor neurons in the intermediate zone of the medullary reticular formation.
(NeuroElectro data)
(PubMed)
|
6.53
± 1.83
(18)
|
6.53 (mV)
|
Data Table |
Other |
Hippocampus CA3 mossy fiber associated CB1-expressing interneurons
|
sag amplitude |
Anatomically heterogeneous populations of CB1 cannabinoid receptor-expressing interneurons in the CA3 region of the hippocampus show homogeneous input-output characteristics.
(NeuroElectro data)
(PubMed)
|
0.23
(16)
|
0.23 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence deep and superficial layer irregular intrinsic bursting interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
2.5
(9)
|
2.5 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex ChAt-positive GAD67-positive slow-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
4.5
± 1.8
(3)
|
4.5 (mV)
|
Data Table |
Other |
Substantia pars nigra reticulata GABAergic parvalbumin-positive calretinin-positive neurons
|
sag amplitude |
Morphological and physiological properties of parvalbumin- and calretinin-containing gamma-aminobutyric acidergic neurons in the substantia nigra.
(NeuroElectro data)
(PubMed)
|
2.44
(1)
|
2.44 (mV)
|
Data Table |
Other |
Hippocampus CA2 wide arbor stratum oriens and striatum radiatum innervating bistratified cells
|
sag amplitude |
Characterization of neurons in the CA2 subfield of the adult rat hippocampus.
(NeuroElectro data)
(PubMed)
|
5.0
(2)
|
0.05 (mV)
|
Data Table |
Other |
Hippocampus CA2 narrow dendritic arbor basket parvalbumin-expressing cell
|
sag amplitude |
Local circuitry involving parvalbumin-positive basket cells in the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
0.6
± 0.1
(14)
|
0.6 (mV)
|
Data Table |
Other |
Medullary reticular formation pre-oromotor pyramidal neuron
|
sag amplitude |
Intrinsic membrane properties of pre-oromotor neurons in the intermediate zone of the medullary reticular formation.
(NeuroElectro data)
(PubMed)
|
11.0
± 4.02
(6)
|
11.0 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence delayed non-fast spiking 1 interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
5.0
(11)
|
5.0 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex GABAergic GAD67-positive burst-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
11.2
± 1.2
(12)
|
11.2 (mV)
|
Data Table |
Other |
Hippocampus CA2 narrow arbor stratum oriens and striatum radiatum innervating bistratified cells
|
sag amplitude |
Characterization of neurons in the CA2 subfield of the adult rat hippocampus.
(NeuroElectro data)
(PubMed)
|
0.1
± 0.1
(3)
|
0.1 (mV)
|
Data Table |
Other |
Substantia pars nigra reticulata GABAergic calretinin-positive neurons
|
sag amplitude |
Morphological and physiological properties of parvalbumin- and calretinin-containing gamma-aminobutyric acidergic neurons in the substantia nigra.
(NeuroElectro data)
(PubMed)
|
7.16
± 0.94
(16)
|
7.16 (mV)
|
Data Table |
Other |
Medial Septum Diagonal Band Area Gabaergic hippocampus inervated slow firing neurons
|
sag amplitude |
The hippocamposeptal pathway generates rhythmic firing of GABAergic neurons in the medial septum and diagonal bands: an investigation using a complete septohippocampal preparation in vitro.
(NeuroElectro data)
(PubMed)
|
1.5
± 0.5
(20)
|
1.5 (mV)
|
Data Table |
Other |
Medullary reticular formation pre-oromotor fusiform neuron
|
sag amplitude |
Intrinsic membrane properties of pre-oromotor neurons in the intermediate zone of the medullary reticular formation.
(NeuroElectro data)
(PubMed)
|
9.4
± 1.62
(12)
|
9.4 (mV)
|
Data Table |
Other |
Hippocampus CA3 dendritic layer-innervating CB1-expressing interneurons
|
sag amplitude |
Anatomically heterogeneous populations of CB1 cannabinoid receptor-expressing interneurons in the CA3 region of the hippocampus show homogeneous input-output characteristics.
(NeuroElectro data)
(PubMed)
|
0.19
(26)
|
0.19 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence non-fast spiking 2 interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
3.5
(6)
|
3.5 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex cholinergic ChAT-positive slow-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
3.0
± 0.6
(14)
|
3.0 (mV)
|
Data Table |
Other |
Medial Septum Diagonal Band Area Gabaergic hippocampus inervated fast firing neurons
|
sag amplitude |
The hippocamposeptal pathway generates rhythmic firing of GABAergic neurons in the medial septum and diagonal bands: an investigation using a complete septohippocampal preparation in vitro.
(NeuroElectro data)
(PubMed)
|
7.0
± 0.8
(9)
|
7.0 (mV)
|
Data Table |
Other |
Substantia pars nigra reticulata GABAergic parvalbumin-positive neurons
|
sag amplitude |
Morphological and physiological properties of parvalbumin- and calretinin-containing gamma-aminobutyric acidergic neurons in the substantia nigra.
(NeuroElectro data)
(PubMed)
|
6.12
± 0.64
(25)
|
6.12 (mV)
|
Data Table |
Other |
medial septum diagonal band of Broca fast firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
sag amplitude |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
4.6
± 0.7
(19)
|
--
|
Data Table |
Other |
Hippocampus CA3 perforant-path associated CB1-expressing interneurons
|
sag amplitude |
Anatomically heterogeneous populations of CB1 cannabinoid receptor-expressing interneurons in the CA3 region of the hippocampus show homogeneous input-output characteristics.
(NeuroElectro data)
(PubMed)
|
0.44
(11)
|
0.44 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence non-fast spiking 1 interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
5.0
(16)
|
5.0 (mV)
|
Data Table |
Other |
Medial Septum Diagonal Band Area Gabaergic hippocampus inervated burst firing neurons
|
sag amplitude |
The hippocamposeptal pathway generates rhythmic firing of GABAergic neurons in the medial septum and diagonal bands: an investigation using a complete septohippocampal preparation in vitro.
(NeuroElectro data)
(PubMed)
|
6.7
± 0.6
(31)
|
6.7 (mV)
|
Data Table |
Other |
Hippocampus CA1 stratum oriens and striatum radiatum innervating bistratified cells
|
sag amplitude |
Characterization of neurons in the CA2 subfield of the adult rat hippocampus.
(NeuroElectro data)
(PubMed)
|
0.2
± 0.1
(5)
|
0.2 (mV)
|
Data Table |
Other |
Neocortex Layer 2-3 Regular-Spiking Non-Pyramidal Interneuron
|
sag amplitude |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
11.5
± 1.2
(14)
|
11.5 (mV)
|
Data Table |
Other |
Auditory Cortex Layer 2/3 Pyramidal Cells
|
sag amplitude |
Transient Hearing Loss Within a Critical Period Causes Persistent Changes to Cellular Properties in Adult Auditory Cortex.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.1
(24)
|
1.4 (mV)
|
Data Table |
Other |
Magnocellular preoptic nucleus/substantia innominata adenosine inhibited noncholinergic neurons
|
sag amplitude |
Adenosine inhibits basal forebrain cholinergic and noncholinergic neurons in vitro.
(NeuroElectro data)
(PubMed)
|
11.1
± 0.7
(25)
|
11.1 (mV)
|
Data Table |
Other |
medial septum diagonal band of Broca cluster firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
sag amplitude |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
6.4
± 1.3
(13)
|
--
|
Data Table |
Other |
somatosensory cortex CGE-derived burst non-adapting 1 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.5
± 1.9
(6)
|
1.5 (mV)
|
Data Table |
Other |
Neocortex medial ganglionic eminence non-fast spiking 2 interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
4.3
(17)
|
4.3 (mV)
|
Data Table |
Other |
Medial Septum Diagonal Band Area Gabaergic hippocampus inervated cluster firing neurons
|
sag amplitude |
The hippocamposeptal pathway generates rhythmic firing of GABAergic neurons in the medial septum and diagonal bands: an investigation using a complete septohippocampal preparation in vitro.
(NeuroElectro data)
(PubMed)
|
4.6
± 0.7
(12)
|
4.6 (mV)
|
Data Table |
Other |
Hippocampus CA2 stratum pyramidal projecting to stratum radiatum interneuron
|
sag amplitude |
SP-SR interneurones: a novel class of neurones of the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
8.1
± 3.6
(8)
|
8.1 (mV)
|
Data Table |
Other |
Neocortex Layer 2-3 Irregular-Spiking Interneuron
|
sag amplitude |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
10.7
± 2.1
(17)
|
10.7 (mV)
|
Data Table |
Other |
Medial entorhinal cortex layer 3 somatostatin positive interneurons
|
sag amplitude |
Selective activation of parvalbumin- or somatostatin-expressing interneurons triggers epileptic seizurelike activity in mouse medial entorhinal cortex.
(NeuroElectro data)
(PubMed)
|
12.0
± 3.0
(12)
|
12.0 (mV)
|
Data Table |
Other |
Auditory Cortex Layer 2/3 Pyramidal Cells
|
sag amplitude |
Transient Hearing Loss Within a Critical Period Causes Persistent Changes to Cellular Properties in Adult Auditory Cortex.
(NeuroElectro data)
(PubMed)
|
1.3
± 0.1
(24)
|
1.3 (mV)
|
Data Table |
Other |
Magnocellular preoptic nucleus/substantia innominata adenosine non-inhibited noncholinergic neurons
|
sag amplitude |
Adenosine inhibits basal forebrain cholinergic and noncholinergic neurons in vitro.
(NeuroElectro data)
(PubMed)
|
3.6
± 0.4
(14)
|
3.6 (mV)
|
Data Table |
Other |
medial septum diagonal band of Broca burst firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
sag amplitude |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
3.2
± 1.1
(11)
|
--
|
Data Table |
Other |
Neocortex medial ganglionic eminence superficial layer late spiking interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
3.1
(17)
|
3.1 (mV)
|
Data Table |
Other |
Hippocampus CA1 bistratified cell
|
sag amplitude |
SP-SR interneurones: a novel class of neurones of the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
0.3
± 0.1
(8)
|
0.3 (mV)
|
Data Table |
Other |
Medial entorhinal cortex layer 3 parvalbumin positive interneuron
|
sag amplitude |
Selective activation of parvalbumin- or somatostatin-expressing interneurons triggers epileptic seizurelike activity in mouse medial entorhinal cortex.
(NeuroElectro data)
(PubMed)
|
2.0
± 0.5
(18)
|
2.0 (mV)
|
Data Table |
Other |
Auditory Cortex Layer 2/3 Pyramidal Cells
|
sag amplitude |
Transient Hearing Loss Within a Critical Period Causes Persistent Changes to Cellular Properties in Adult Auditory Cortex.
(NeuroElectro data)
(PubMed)
|
0.6
± 0.1
(22)
|
0.6 (mV)
|
Data Table |
Other |
medial septum diagonal band of Broca fast firing large sag VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
sag amplitude |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
16.1
± 1.4
(12)
|
--
|
Data Table |
Other |
Neocortex medial ganglionic eminence initial adapting interneuron
|
sag amplitude |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
0.9
(7)
|
0.9 (mV)
|
Data Table |
Other |
Stratum radiatum delayed spiking interneurons
|
sag amplitude |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
2.0
± 2.9
|
2.0 (mV)
|
Data Table |
Other |
Hippocampus CA2 bistratified wide arbor cell
|
sag amplitude |
SP-SR interneurones: a novel class of neurones of the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
22.7
± 17.6
(3)
|
22.7 (mV)
|
Data Table |
Other |
Medial septum-diagonal band complex GABAergic GAD67-positive fast-firing neurons
|
sag amplitude |
Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity.
(NeuroElectro data)
(PubMed)
|
6.6
± 1.3
(12)
|
6.6 (mV)
|
Data Table |
Other |
medial septum diagonal band of Broca slow firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
sag amplitude |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
4.9
± 1.4
(11)
|
--
|
Data Table |
Other |
Hippocampus GluN2D-EGFP-positive interneuron
|
sag amplitude |
GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice.
(NeuroElectro data)
(PubMed)
|
0.86
± 2.4
(8)
|
0.86 (mV)
|
Data Table |
Other |
Stratum radiatum irregularly spiking interneurons
|
sag amplitude |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
11.0
|
11.0 (mV)
|
Data Table |
Other |
Hippocampus CA2 bistratified narrow arbor cell
|
sag amplitude |
SP-SR interneurones: a novel class of neurones of the CA2 region of the hippocampus.
(NeuroElectro data)
(PubMed)
|
0.2
± 0.2
(9)
|
0.2 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
28.2
± 4.0
|
28.2 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
31.2
± 5.2
|
31.2 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
32.4
± 3.7
|
32.4 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
30.2
± 7.2
|
30.2 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
29.4
± 5.7
|
29.4 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
28.5
± 8.3
|
28.5 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
29.5
± 4.2
|
29.5 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
28.6
± 6.2
|
28.6 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
The mechanism of ethanol action on midbrain dopaminergic neuron firing: a dynamic-clamp study of the role of I(h) and GABAergic synaptic integration.
(NeuroElectro data)
(PubMed)
|
41.0
± 2.4
(36)
|
41.0 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
27.9
± 6.5
|
27.9 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
28.1
± 7.4
|
28.1 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
27.5
± 6.6
|
27.5 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
33.3
± 4.2
|
33.3 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
29.6
± 6.2
|
29.6 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
Substantia nigra pars compacta calbindin expressing dopaminergic cell
|
sag amplitude |
I(h) channels contribute to the different functional properties of identified dopaminergic subpopulations in the midbrain.
(NeuroElectro data)
(PubMed)
|
25.3
± 2.18
(14)
|
25.3 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
35.6
± 2.9
|
35.6 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
Substantia nigra pars compacta calbindin-negative dopaminergic cell
|
sag amplitude |
I(h) channels contribute to the different functional properties of identified dopaminergic subpopulations in the midbrain.
(NeuroElectro data)
(PubMed)
|
37.3
± 0.72
(69)
|
37.3 (mV)
|
Data Table |
Substantia nigra pars compacta dopaminergic cell |
|
sag amplitude |
Non-linear developmental trajectory of electrical phenotype in rat substantia nigra pars compacta dopaminergic neurons.
(NeuroElectro data)
(PubMed)
|
34.1
± 4.5
|
34.1 (mV)
|
Data Table |
Substantia nigra pars reticulata interneuron GABA |
|
sag amplitude |
The mechanism of ethanol action on midbrain dopaminergic neuron firing: a dynamic-clamp study of the role of I(h) and GABAergic synaptic integration.
(NeuroElectro data)
(PubMed)
|
15.1
± 1.0
(68)
|
15.1 (mV)
|
Data Table |
Subthalamic nucleus neuron |
|
sag amplitude |
Nicotinic receptor subtype-selective circuit patterns in the subthalamic nucleus.
(NeuroElectro data)
(PubMed)
|
10.4
± 1.6
(20)
|
10.4 (mV)
|
Data Table |
Ventral tegmental area dopamine neuron |
|
sag amplitude |
The mechanism of ethanol action on midbrain dopaminergic neuron firing: a dynamic-clamp study of the role of I(h) and GABAergic synaptic integration.
(NeuroElectro data)
(PubMed)
|
45.6
± 2.3
(42)
|
45.6 (mV)
|
Data Table |
Ventral tegmental area dopamine neuron |
Ventral tegmental area calbindin-negative dopaminergic cell
|
sag amplitude |
I(h) channels contribute to the different functional properties of identified dopaminergic subpopulations in the midbrain.
(NeuroElectro data)
(PubMed)
|
31.0
± 1.72
(21)
|
31.0 (mV)
|
Data Table |
Ventral tegmental area dopamine neuron |
Ventral tegmental area calbindin expressing dopaminergic neuron
|
sag amplitude |
I(h) channels contribute to the different functional properties of identified dopaminergic subpopulations in the midbrain.
(NeuroElectro data)
(PubMed)
|
11.9
± 1.06
(21)
|
11.9 (mV)
|
Data Table |
Ventral tegmental area dopamine neuron |
|
sag amplitude |
Cav1.2 and Cav1.3 L-type calcium channels regulate dopaminergic firing activity in the mouse ventral tegmental area.
(NeuroElectro data)
(PubMed)
|
20.98
± 1.17
|
20.98 (mV)
|
Data Table |