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Tonic GABA<sub>A</sub>Receptor-Mediated Currents of Human Cortical GABAergic Interneurons Vary Amongst Cell Types

Abstract:
Persistent anion conductances through GABAA receptors (GABAARs) are important modulators of neuronal excitability. However, it is currently unknown how the amplitudes of these currents vary among different cell types in the human neocortex, particularly among diverse GABAergic interneurons. We have recorded 101 interneurons in and near layer 1 from cortical tissue surgically resected from both male and female patients, visualized 84 of them and measured tonic GABAAR currents in 48 cells with an intracellular [Cl-] of 65 mm and in the presence of 5 μm GABA. We compare these tonic currents among five groups of interneurons divided by firing properties and four types of interneuron defined by axonal distributions; rosehip, neurogliaform, stalked-bouton, layer 2-3 innervating and a pool of other cells. Interestingly, the rosehip cell, a type of interneuron only described thus far in human tissue, and layer 2-3 innervating cells exhibit larger tonic currents than other layer 1 interneurons, such as neurogliaform and stalked-bouton cells; the latter two groups showing no difference. The positive allosteric modulators of GABAARs allopregnanolone and DS2 also induced larger current shifts in the rosehip and layer 2-3 innervating cells, consistent with higher expression of the δ subunit of the GABAAR in these neurons. We have also examined how patient parameters, such as age, seizures, type of cancer and anticonvulsant treatment may alter tonic inhibitory currents in human neurons. The cell type-specific differences in tonic inhibitory currents could potentially be used to selectively modulate cortical circuitry.SIGNIFICANCE STATEMENT Tonic currents through GABAA receptors (GABAARs) are a potential therapeutic target for a number of neurologic and psychiatric conditions. Here, we show that these currents in human cerebral cortical GABAergic neurons display cell type-specific differences in their amplitudes which implies differential modulation of their excitability. Additionally, we examine whether the amplitudes of the tonic currents measured in our study show any differences between patient populations, finding some evidence that age, seizures, type of cancer, and anticonvulsant treatment may alter tonic inhibition in human tissue. These results advance our understanding of how pathology affects neuronal excitability and could potentially be used to selectively modulate cortical circuitry.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1523/jneurosci.0175-21.2021

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-8674-7997
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-0257-5441
More by this author
Institution:
University of Oxford
Role:
Author
More by this author
Institution:
University of Oxford
Role:
Author
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-3103-6359


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Funder identifier:
10.13039/501100000265
Grant:
MR/R011567/1
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Funder identifier:
10.13039/501100000781
Grant:
ERC-2015-AdG 694988


Publisher:
Society for Neuroscience
Journal:
The Journal of Neuroscience More from this journal
Volume:
41
Issue:
47
Pages:
9702-9719
Publication date:
2021-10-19
DOI:
EISSN:
1529-2401
ISSN:
0270-6474


Language:
English
Keywords:
Pubs id:
1205942
Local pid:
pubs:1205942
Source identifiers:
W3207086292
Deposit date:
2026-03-26
ARK identifier:
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