Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons
Synapses in the cerebral cortex constantly change and this dynamic property regulated by the action of neuromodulators such as dopamine (DA), is essential for reward learning and memory. DA modulates spike-timing-dependent plasticity (STDP), a cellular model of learning and memory, in juvenile roden...
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doaj-200e8608f0374af2b970e2f3cfbe92752021-04-22T14:26:46ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022021-04-011510.3389/fncel.2021.668980668980Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical NeuronsEmma Louise Louth0Emma Louise Louth1Rasmus Langelund Jørgensen2Anders Rosendal Korshoej3Jens Christian Hedemann Sørensen4Marco Capogna5Marco Capogna6Marco Capogna7Department of Biomedicine, Aarhus University, Aarhus, DenmarkDANDRITE, The Danish Research Institute of Translational Neuroscience, Aarhus University, Aarhus, DenmarkDepartment of Neurosurgery, Aarhus University Hospital, Aarhus, DenmarkDepartment of Neurosurgery, Aarhus University Hospital, Aarhus, DenmarkDepartment of Neurosurgery, Aarhus University Hospital, Aarhus, DenmarkDepartment of Biomedicine, Aarhus University, Aarhus, DenmarkDANDRITE, The Danish Research Institute of Translational Neuroscience, Aarhus University, Aarhus, DenmarkCenter for Proteins in Memory–PROMEMO, Danish National Research Foundation, Aarhus University, Aarhus, DenmarkSynapses in the cerebral cortex constantly change and this dynamic property regulated by the action of neuromodulators such as dopamine (DA), is essential for reward learning and memory. DA modulates spike-timing-dependent plasticity (STDP), a cellular model of learning and memory, in juvenile rodent cortical neurons. However, it is unknown whether this neuromodulation also occurs at excitatory synapses of cortical neurons in mature adult mice or in humans. Cortical layer V pyramidal neurons were recorded with whole cell patch clamp electrophysiology and an extracellular stimulating electrode was used to induce STDP. DA was either bath-applied or optogenetically released in slices from mice. Classical STDP induction protocols triggered non-hebbian excitatory synaptic depression in the mouse or no plasticity at human cortical synapses. DA reverted long term synaptic depression to baseline in mouse via dopamine 2 type receptors or elicited long term synaptic potentiation in human cortical synapses. Furthermore, when DA was applied during an STDP protocol it depressed presynaptic inhibition in the mouse but not in the human cortex. Thus, DA modulates excitatory synaptic plasticity differently in human vs. mouse cortex. The data strengthens the importance of DA in gating cognition in humans, and may inform on therapeutic interventions to recover brain function from diseases.https://www.frontiersin.org/articles/10.3389/fncel.2021.668980/fulldopaminehuman cortical sliceslayer 5 pyramidal neuronsspike timing dependent plasticitysynaptic inhibition |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Emma Louise Louth Emma Louise Louth Rasmus Langelund Jørgensen Anders Rosendal Korshoej Jens Christian Hedemann Sørensen Marco Capogna Marco Capogna Marco Capogna |
spellingShingle |
Emma Louise Louth Emma Louise Louth Rasmus Langelund Jørgensen Anders Rosendal Korshoej Jens Christian Hedemann Sørensen Marco Capogna Marco Capogna Marco Capogna Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons Frontiers in Cellular Neuroscience dopamine human cortical slices layer 5 pyramidal neurons spike timing dependent plasticity synaptic inhibition |
author_facet |
Emma Louise Louth Emma Louise Louth Rasmus Langelund Jørgensen Anders Rosendal Korshoej Jens Christian Hedemann Sørensen Marco Capogna Marco Capogna Marco Capogna |
author_sort |
Emma Louise Louth |
title |
Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons |
title_short |
Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons |
title_full |
Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons |
title_fullStr |
Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons |
title_full_unstemmed |
Dopaminergic Neuromodulation of Spike Timing Dependent Plasticity in Mature Adult Rodent and Human Cortical Neurons |
title_sort |
dopaminergic neuromodulation of spike timing dependent plasticity in mature adult rodent and human cortical neurons |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cellular Neuroscience |
issn |
1662-5102 |
publishDate |
2021-04-01 |
description |
Synapses in the cerebral cortex constantly change and this dynamic property regulated by the action of neuromodulators such as dopamine (DA), is essential for reward learning and memory. DA modulates spike-timing-dependent plasticity (STDP), a cellular model of learning and memory, in juvenile rodent cortical neurons. However, it is unknown whether this neuromodulation also occurs at excitatory synapses of cortical neurons in mature adult mice or in humans. Cortical layer V pyramidal neurons were recorded with whole cell patch clamp electrophysiology and an extracellular stimulating electrode was used to induce STDP. DA was either bath-applied or optogenetically released in slices from mice. Classical STDP induction protocols triggered non-hebbian excitatory synaptic depression in the mouse or no plasticity at human cortical synapses. DA reverted long term synaptic depression to baseline in mouse via dopamine 2 type receptors or elicited long term synaptic potentiation in human cortical synapses. Furthermore, when DA was applied during an STDP protocol it depressed presynaptic inhibition in the mouse but not in the human cortex. Thus, DA modulates excitatory synaptic plasticity differently in human vs. mouse cortex. The data strengthens the importance of DA in gating cognition in humans, and may inform on therapeutic interventions to recover brain function from diseases. |
topic |
dopamine human cortical slices layer 5 pyramidal neurons spike timing dependent plasticity synaptic inhibition |
url |
https://www.frontiersin.org/articles/10.3389/fncel.2021.668980/full |
work_keys_str_mv |
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