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adaptation percent (1 – first/last ISI)

Common definition: 1 minus ratio of durations between early and late AP inter-spike intervals in an AP train, normalized to a percent

Electrophysiological values of adaptation percent (1 – first/last ISI) across neuron types from literature:

    Normalization criteria:
  • Values are unchanged from those reported. Refer to individual articles for definition and calculation methodology.

Neuron electrophysiology data values (Table form)

Neuron Type Neuron Description Ephys Prop Article Extracted Value Standardized Value Content Source
Hippocampus CA1 basket cell Hippocampus CA1 fast spiking basket cell adaptation percent (1 – first/last ISI) Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation. (NeuroElectro data) (PubMed) 20.0 ± 2.0 (20) 20.0 (ratio) Data Table
Hippocampus CA1 oriens lacunosum moleculare neuron Hippocampus CA1 oriens lacunosum moleculare non-fast-spiking neuron adaptation percent (1 – first/last ISI) Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation. (NeuroElectro data) (PubMed) 26.0 ± 3.0 (66) 26.0 (ratio) Data Table
Hippocampus CA1 pyramidal cell adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 49.0 ± 15.0 (6) 49.0 (ratio) Data Table
Hippocampus CA1 pyramidal cell adaptation percent (1 – first/last ISI) Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation. (NeuroElectro data) (PubMed) 40.0 ± 5.0 (53) 40.0 (ratio) Data Table
Neocortex basket cell Neocortex medial ganglionic eminence fast spiking interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 17.6 (71) 17.6 (ratio) Data Table
Neocortex basket cell Neocortex Layer 2-3 Fast-Spiking Interneuron adaptation percent (1 – first/last ISI) Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs. (NeuroElectro data) (PubMed) 11.0 ± 2.4 (9) 11.0 (ratio) Data Table
Neocortex basket cell Layer 5 somatosensory cortex Fast Spiking parvalbumin positive interneurons adaptation percent (1 – first/last ISI) Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons. (NeuroElectro data) (PubMed) 9.1 ± 5.9 (8) 9.1 (ratio) Data Table
Neocortex basket cell sensorimotor cortex fast spiking cell adaptation percent (1 – first/last ISI) Molecular and physiological diversity of cortical nonpyramidal cells. (NeuroElectro data) (PubMed) 15.3 ± 15.0 (34) 15.3 (ratio) Data Table
Neocortex bipolar neuron neocortex layer 2-3 cholinergic interneurons adaptation percent (1 – first/last ISI) Functional characterization of intrinsic cholinergic interneurons in the cortex. (NeuroElectro data) (PubMed) 60.4 ± 16.9 60.4 (ratio) Data Table
Neocortex layer 4 stellate cell Layer 4 sensorimotor cortex spiny stellate neurons adaptation percent (1 – first/last ISI) Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons. (NeuroElectro data) (PubMed) 65.8 ± 18.3 (10) 65.8 (ratio) Data Table
Neocortex pyramidal cell layer 2-3 Layer 2/3 sensorimotor cortex pyramidal neurons adaptation percent (1 – first/last ISI) Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons. (NeuroElectro data) (PubMed) 57.6 ± 10.0 (28) 57.6 (ratio) Data Table
Neocortex pyramidal cell layer 2-3 adaptation percent (1 – first/last ISI) Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs. (NeuroElectro data) (PubMed) 68.0 ± 2.7 (13) 68.0 (ratio) Data Table
Neocortex pyramidal cell layer 2-3 Somatosensory cortex layer 2/3 pyramidal neurons adaptation percent (1 – first/last ISI) Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine. (NeuroElectro data) (PubMed) 52.0 ± 4.0 (15) 52.0 (ratio) Data Table
Neocortex pyramidal cell layer 2-3 somatosensory cortex layer 2/3 regular-spiking pyramidal neuron adaptation percent (1 – first/last ISI) Threshold firing frequency-current relationships of neurons in rat somatosensory cortex: type 1 and type 2 dynamics. (NeuroElectro data) (PubMed) 71.4 ± 4.2 (20) 71.4 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Layer 6 sensorimotor cortex nonpyramidal VGluT1 expressing neurons adaptation percent (1 – first/last ISI) Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons. (NeuroElectro data) (PubMed) 48.7 ± 12.6 (71) 48.7 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Layer 5 somatosensory cortex small amplitude pyramidal cells adaptation percent (1 – first/last ISI) Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons. (NeuroElectro data) (PubMed) 20.3 ± 4.8 (10) 20.3 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 sensorimotor cortex pyramidal cell adaptation percent (1 – first/last ISI) Molecular and physiological diversity of cortical nonpyramidal cells. (NeuroElectro data) (PubMed) 66.2 ± 7.1 (29) 66.2 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 visual cortex layer 5 corticocortical pyramidal cell adaptation percent (1 – first/last ISI) Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics. (NeuroElectro data) (PubMed) 40.2 ± 3.9 (8) 40.2 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Layer 5 sensorimotor cortex pyramidal neurons adaptation percent (1 – first/last ISI) Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons. (NeuroElectro data) (PubMed) 59.5 ± 9.4 (33) 59.5 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 visual cortex layer 5 thick tufted pyramidal cell projecting to superior colliculus adaptation percent (1 – first/last ISI) Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics. (NeuroElectro data) (PubMed) 32.8 ± 4.1 (8) 32.8 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 visual cortex layer 5 corticocortical pyramidal cell adaptation percent (1 – first/last ISI) Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics. (NeuroElectro data) (PubMed) 77.3 ± 2.2 (7) 77.3 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Layer 5 somatosensory barrel cortex pyramidal neurons adaptation percent (1 – first/last ISI) Effect of common anesthetics on dendritic properties in layer 5 neocortical pyramidal neurons. (NeuroElectro data) (PubMed) 24.2 ± 5.6 (27) 24.2 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 visual cortex layer 5 thick tufted pyramidal cell projecting to superior colliculus adaptation percent (1 – first/last ISI) Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics. (NeuroElectro data) (PubMed) 76.7 ± 1.6 (8) 76.7 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 somatosensory cortex layer 5a corticostriatal Etv1-expressing slender-tufted pyramidal neurons adaptation percent (1 – first/last ISI) Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine. (NeuroElectro data) (PubMed) 76.0 ± 2.0 (21) 76.0 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Somatosensory cortex layer 5b Glt25d2-expressing thick-tufted pyramidal neurons adaptation percent (1 – first/last ISI) Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine. (NeuroElectro data) (PubMed) 17.0 ± 2.0 (27) 17.0 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Motor cortex layer 5 glutamatergic excitatory pyramidal neurons synapsing onto motor cortex layer 5 fast-spiking interneurons adaptation percent (1 – first/last ISI) Developmental synaptic changes increase the range of integrative capabilities of an identified excitatory neocortical connection. (NeuroElectro data) (PubMed) 15.0 ± 15.0 (36) 15.0 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Layer 5 somatosensory cortex large amplitude pyramidal cells adaptation percent (1 – first/last ISI) Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons. (NeuroElectro data) (PubMed) 18.5 ± 3.1 (9) 18.5 (ratio) Data Table
Neocortex pyramidal cell layer 5-6 Motor cortex layer 5 glutamatergic excitatory pyramidal neurons synapsing onto motor cortex layer 5 fast-spiking interneurons adaptation percent (1 – first/last ISI) Developmental synaptic changes increase the range of integrative capabilities of an identified excitatory neocortical connection. (NeuroElectro data) (PubMed) 12.0 ± 13.0 (20) 12.0 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 45.4 ± 11.2 (3) 45.4 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived late spiking 1 interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 46.8 ± 19.8 (26) 46.8 (ratio) Data Table
Neocortex uncharacterized cell neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron adaptation percent (1 – first/last ISI) The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors. (NeuroElectro data) (PubMed) 51.3 ± 14.5 (45) 51.3 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived late spiking 2 interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 58.0 ± 15.7 (19) 58.0 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived burst non-adapting 2 interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 58.9 ± 20.5 (5) 58.9 (ratio) Data Table
Neocortex uncharacterized cell neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron adaptation percent (1 – first/last ISI) The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors. (NeuroElectro data) (PubMed) 36.3 ± 9.8 (3) 36.3 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived irregular spiking interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 39.5 ± 11.6 (6) 39.5 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 31.8 ± 7.7 (5) 31.8 (ratio) Data Table
Neocortex uncharacterized cell sensorimotor cortex regular spiking non-pyramidal cell adaptation percent (1 – first/last ISI) Molecular and physiological diversity of cortical nonpyramidal cells. (NeuroElectro data) (PubMed) 46.6 ± 13.6 (48) 46.6 (ratio) Data Table
Neocortex uncharacterized cell somatosensory cortex CGE-derived delayed intrinsic bursting interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 41.9 ± 17.2 (5) 41.9 (ratio) Data Table
Nucleus of the solitary tract principal cell Ventrolateral Nucleus Tractus Solitarii 4-AP-/TEA-responsive cell adaptation percent (1 – first/last ISI) Localization and function of the Kv3.1b subunit in the rat medulla oblongata: focus on the nucleus tractus solitarii. (NeuroElectro data) (PubMed) 32.4 ± 3.3 (81) 32.4 (ratio) Data Table
Nucleus of the solitary tract principal cell Comissural Nucleus Tractus Solitarii 4-AP-/TEA-unresponsive commissural cell adaptation percent (1 – first/last ISI) Localization and function of the Kv3.1b subunit in the rat medulla oblongata: focus on the nucleus tractus solitarii. (NeuroElectro data) (PubMed) 39.0 ± 5.3 (16) 39.0 (ratio) Data Table
Other Neocortex medial ganglionic eminence superficial layer late spiking interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 33.4 (17) 33.4 (ratio) Data Table
Other lateral habenular nucleus tonic regular-spiking cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 24.4 ± 3.3 (32) 24.4 (ratio) Data Table
Other medial septal/diagonal band complex regular spiking neurons projecting to fornix adaptation percent (1 – first/last ISI) Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex. (NeuroElectro data) (PubMed) 68.9 ± 18.42 (24) 68.9 (ratio) Data Table
Other Corpus callosum white matter interstitial non-adapting interneurons projecting to lower subcortical layers adaptation percent (1 – first/last ISI) 5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks. (NeuroElectro data) (PubMed) 30.0 ± 7.0 (7) 30.0 (ratio) Data Table
Other lateral habenular nucleus large round-ovoid polymorphic cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 15.4 ± 4.4 (7) 15.4 (ratio) Data Table
Other medial septal/diagonal band complex type I burst-firing neurons adaptation percent (1 – first/last ISI) Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex. (NeuroElectro data) (PubMed) 54.8 ± 39.1 (7) 54.8 (ratio) Data Table
Other corpus callosum white matter interstitial non-adapting bursting interneuron projecting to lower subcortical layers adaptation percent (1 – first/last ISI) 5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks. (NeuroElectro data) (PubMed) 70.0 ± 11.0 (18) 70.0 (ratio) Data Table
Other Neocortex medial ganglionic eminence deep and superficial layer irregular intrinsic bursting interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 41.7 (9) 41.7 (ratio) Data Table
Other lateral habenular nucleus silent cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 22.9 ± 4.3 (31) 22.9 (ratio) Data Table
Other medial septal/diagonal band complex fast spiking GABAergic neurons projecting to fornix adaptation percent (1 – first/last ISI) Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex. (NeuroElectro data) (PubMed) 52.3 ± 20.4 (20) 52.3 (ratio) Data Table
Other Corpus callosum white matter interstitial adapting interneurons projecting to lower subcortical layers adaptation percent (1 – first/last ISI) 5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks. (NeuroElectro data) (PubMed) 47.0 ± 5.0 (4) 47.0 (ratio) Data Table
Other Stratum radiatum fast-spiking interneurons adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 26.0 ± 10.0 (5) 26.0 (ratio) Data Table
Other Neocortex medial ganglionic eminence non-fast spiking 1 interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 36.2 (16) 36.2 (ratio) Data Table
Other neocortex layer 2/3 GABAergic late-spiking subtype 2 Htr3a-expressing interneuron adaptation percent (1 – first/last ISI) The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors. (NeuroElectro data) (PubMed) 53.9 ± 16.3 (15) 53.9 (ratio) Data Table
Other somatosensory cortex CGE-derived burst non-adapting 1 interneuron adaptation percent (1 – first/last ISI) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. (NeuroElectro data) (PubMed) 72.2 ± 10.6 (6) 72.2 (ratio) Data Table
Other lateral habenular nucleus thick spiny bipolar vertical cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 21.5 ± 3.3 (7) 21.5 (ratio) Data Table
Other medial septal/diagonal band complex type II burst-firing neurons projecting to fornix adaptation percent (1 – first/last ISI) Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex. (NeuroElectro data) (PubMed) 66.1 ± 16.2 (8) 66.1 (ratio) Data Table
Other Stratum radiatum non-pyramidal regular-spiking non-rebounding cells adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 41.0 ± 11.0 41.0 (ratio) Data Table
Other neocortex layer 2/3 GABAergic burst non-adapting subtype 1 Htr3a-expressing interneuron adaptation percent (1 – first/last ISI) The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors. (NeuroElectro data) (PubMed) 63.7 ± 18.2 (18) 63.7 (ratio) Data Table
Other Neocortex medial ganglionic eminence superficial layer delayed-fast spiking Interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 15.5 (25) 15.5 (ratio) Data Table
Other Stratum radiatum non-pyramidal regular-spiking rapidly adapting cells adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 71.0 ± 13.0 71.0 (ratio) Data Table
Other lateral habenular nucleus dense arbor neurogliaform cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 21.8 ± 8.1 (3) 21.8 (ratio) Data Table
Other medial septum diagonal band of Broca fast firing large sag VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells adaptation percent (1 – first/last ISI) 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) 15.4 ± 6.2 (12) 15.4 (ratio) Data Table
Other neocortex layer 2/3 GABAergic burst non-adapting subtype 2 Htr3a-expressing interneuron adaptation percent (1 – first/last ISI) The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors. (NeuroElectro data) (PubMed) 59.4 ± 21.4 (5) 59.4 (ratio) Data Table
Other Neocortex Layer 2-3 Regular-Spiking Non-Pyramidal Interneuron adaptation percent (1 – first/last ISI) Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs. (NeuroElectro data) (PubMed) 55.0 ± 5.8 (14) 55.0 (ratio) Data Table
Other Neocortex medial ganglionic eminence deep and superficial layer regular intrinsic bursting Interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 44.4 (17) 44.4 (ratio) Data Table
Other Stratum radiatum delayed spiking interneurons adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 34.0 ± 13.0 34.0 (ratio) Data Table
Other lateral habenular nucleus bursting cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 32.2 ± 4.3 (3) 32.2 (ratio) Data Table
Other medial septum diagonal band of Broca fast firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells adaptation percent (1 – first/last ISI) 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) 13.4 ± 3.8 (19) 13.4 (ratio) Data Table
Other neocortex layer 2/3 GABAergic irregular spiking bipolar Htr3a-expressing interneuron adaptation percent (1 – first/last ISI) The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors. (NeuroElectro data) (PubMed) 41.5 ± 11.6 (30) 41.5 (ratio) Data Table
Other Neocortex medial ganglionic eminence non-fast spiking 2 interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 33.1 (6) 33.1 (ratio) Data Table
Other Stratum radiatum non-pyramidal regular-spiking rebounding cells adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 41.0 ± 27.0 41.0 (ratio) Data Table
Other lateral habenular nucleus aspiny spherical cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 23.5 ± 4.9 (31) 23.5 (ratio) Data Table
Other medial septum diagonal band of Broca burst firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells adaptation percent (1 – first/last ISI) 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) 37.3 ± 9.1 (11) 37.3 (ratio) Data Table
Other Neocortex medial ganglionic eminence delayed non-fast spiking 1 interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 29.5 (11) 29.5 (ratio) Data Table
Other Stratum radiatum irregularly spiking interneurons adaptation percent (1 – first/last ISI) NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases. (NeuroElectro data) (PubMed) 80.0 80.0 (ratio) Data Table
Other lateral habenular nucleus aspiny spindle-shaped horizontal fusiform cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 30.4 ± 4.5 (17) 30.4 (ratio) Data Table
Other medial septum diagonal band of Broca cluster firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells adaptation percent (1 – first/last ISI) 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) 51.8 ± 10.4 (13) 51.8 (ratio) Data Table
Other Hippocampus CA1 trilaminar fast spiking interneuron adaptation percent (1 – first/last ISI) Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation. (NeuroElectro data) (PubMed) 18.0 ± 4.0 (21) 18.0 (ratio) Data Table
Other somatosensory cortex layer 2/3 fast-spiking inhibitory interneuron adaptation percent (1 – first/last ISI) Threshold firing frequency-current relationships of neurons in rat somatosensory cortex: type 1 and type 2 dynamics. (NeuroElectro data) (PubMed) 56.2 ± 6.7 (23) 56.2 (ratio) Data Table
Other Neocortex medial ganglionic eminence non-fast spiking 2 interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 32.1 (17) 32.1 (ratio) Data Table
Other lateral habenular nucleus tonic irregular-spiking adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 18.7 ± 4.1 (8) 18.7 (ratio) Data Table
Other medial septum diagonal band of Broca slow firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells adaptation percent (1 – first/last ISI) 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) 27.3 ± 12.4 (11) 27.3 (ratio) Data Table
Other Neocortex medial ganglionic eminence initial adapting interneuron adaptation percent (1 – first/last ISI) Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors. (NeuroElectro data) (PubMed) 45.1 (7) 45.1 (ratio) Data Table
Other lateral habenular nucleus aspiny spindle-shaped vertical fusiform cell adaptation percent (1 – first/last ISI) Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices. (NeuroElectro data) (PubMed) 24.7 ± 4.8 (9) 24.7 (ratio) Data Table
Other medial septal/diagonal band complex slow firing cholinergic neurons projecting to fornix adaptation percent (1 – first/last ISI) Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex. (NeuroElectro data) (PubMed) 64.2 ± 30.0 (10) 64.2 (ratio) Data Table
Other Corpus callosum white matter interstitial adapting bursting interneurons projecting to lower subcortical layers adaptation percent (1 – first/last ISI) 5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks. (NeuroElectro data) (PubMed) 77.0 ± 11.0 (5) 77.0 (ratio) Data Table