Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS

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Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS. / Nieto-Gonzalez, Jose Luis; Moser, Jakob; Lauritzen, Martin; Schmitt-John, Thomas; Jensen, Kimmo.

In: Cerebral Cortex, Vol. 21, No. 3, 01.03.2011, p. 625-35.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Nieto-Gonzalez, JL, Moser, J, Lauritzen, M, Schmitt-John, T & Jensen, K 2011, 'Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS', Cerebral Cortex, vol. 21, no. 3, pp. 625-35. https://doi.org/10.1093/cercor/bhq134, https://doi.org/10.1093/cercor/bhq134

APA

Nieto-Gonzalez, J. L., Moser, J., Lauritzen, M., Schmitt-John, T., & Jensen, K. (2011). Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS. Cerebral Cortex, 21(3), 625-35. https://doi.org/10.1093/cercor/bhq134, https://doi.org/10.1093/cercor/bhq134

Vancouver

Nieto-Gonzalez JL, Moser J, Lauritzen M, Schmitt-John T, Jensen K. Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS. Cerebral Cortex. 2011 Mar 1;21(3):625-35. https://doi.org/10.1093/cercor/bhq134, https://doi.org/10.1093/cercor/bhq134

Author

Nieto-Gonzalez, Jose Luis ; Moser, Jakob ; Lauritzen, Martin ; Schmitt-John, Thomas ; Jensen, Kimmo. / Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS. In: Cerebral Cortex. 2011 ; Vol. 21, No. 3. pp. 625-35.

Bibtex

@article{e456d2c0fabc4f1bb65c24e7dbf59e90,
title = "Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS",
abstract = "Amyotrophic lateral sclerosis (ALS) is a progressive degenerative disease of the central nervous system. Symptomatic and presymptomatic ALS patients demonstrate cortical hyperexcitability, which raises the possibility that alterations in inhibitory gamma-aminobutyric acid (GABA)ergic system could underlie this dysfunction. Here, we studied the GABAergic system in cortex using patch-clamp recordings in the wobbler mouse, a model of ALS. In layer 5 pyramidal neurons of motor cortex, the frequency of GABA(A) receptor-mediated spontaneous inhibitory postsynaptic currents was reduced by 72% in wobbler mice. Also, miniature inhibitory postsynaptic currents recorded under blockade of action potentials were decreased by 64%. Tonic inhibition mediated by extrasynaptic GABA(A) receptors was reduced by 87%. In agreement, we found a decreased density of parvalbumin- and somatostatin-positive inhibitory interneurons and reduced vesicular GABA transporter immunoreactivity in the neuropil. Finally, we observed an increased input resistance and excitability of wobbler excitatory neurons, which could be explained by lack of GABA(A) receptor-mediated influences. In conclusion, we demonstrate decreases in GABAergic inhibition, which might explain the cortical hyperexcitability in wobbler mice.",
author = "Nieto-Gonzalez, {Jose Luis} and Jakob Moser and Martin Lauritzen and Thomas Schmitt-John and Kimmo Jensen",
year = "2011",
month = mar,
day = "1",
doi = "10.1093/cercor/bhq134",
language = "English",
volume = "21",
pages = "625--35",
journal = "Cerebral Cortex",
issn = "1047-3211",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS

AU - Nieto-Gonzalez, Jose Luis

AU - Moser, Jakob

AU - Lauritzen, Martin

AU - Schmitt-John, Thomas

AU - Jensen, Kimmo

PY - 2011/3/1

Y1 - 2011/3/1

N2 - Amyotrophic lateral sclerosis (ALS) is a progressive degenerative disease of the central nervous system. Symptomatic and presymptomatic ALS patients demonstrate cortical hyperexcitability, which raises the possibility that alterations in inhibitory gamma-aminobutyric acid (GABA)ergic system could underlie this dysfunction. Here, we studied the GABAergic system in cortex using patch-clamp recordings in the wobbler mouse, a model of ALS. In layer 5 pyramidal neurons of motor cortex, the frequency of GABA(A) receptor-mediated spontaneous inhibitory postsynaptic currents was reduced by 72% in wobbler mice. Also, miniature inhibitory postsynaptic currents recorded under blockade of action potentials were decreased by 64%. Tonic inhibition mediated by extrasynaptic GABA(A) receptors was reduced by 87%. In agreement, we found a decreased density of parvalbumin- and somatostatin-positive inhibitory interneurons and reduced vesicular GABA transporter immunoreactivity in the neuropil. Finally, we observed an increased input resistance and excitability of wobbler excitatory neurons, which could be explained by lack of GABA(A) receptor-mediated influences. In conclusion, we demonstrate decreases in GABAergic inhibition, which might explain the cortical hyperexcitability in wobbler mice.

AB - Amyotrophic lateral sclerosis (ALS) is a progressive degenerative disease of the central nervous system. Symptomatic and presymptomatic ALS patients demonstrate cortical hyperexcitability, which raises the possibility that alterations in inhibitory gamma-aminobutyric acid (GABA)ergic system could underlie this dysfunction. Here, we studied the GABAergic system in cortex using patch-clamp recordings in the wobbler mouse, a model of ALS. In layer 5 pyramidal neurons of motor cortex, the frequency of GABA(A) receptor-mediated spontaneous inhibitory postsynaptic currents was reduced by 72% in wobbler mice. Also, miniature inhibitory postsynaptic currents recorded under blockade of action potentials were decreased by 64%. Tonic inhibition mediated by extrasynaptic GABA(A) receptors was reduced by 87%. In agreement, we found a decreased density of parvalbumin- and somatostatin-positive inhibitory interneurons and reduced vesicular GABA transporter immunoreactivity in the neuropil. Finally, we observed an increased input resistance and excitability of wobbler excitatory neurons, which could be explained by lack of GABA(A) receptor-mediated influences. In conclusion, we demonstrate decreases in GABAergic inhibition, which might explain the cortical hyperexcitability in wobbler mice.

U2 - 10.1093/cercor/bhq134

DO - 10.1093/cercor/bhq134

M3 - Journal article

C2 - 20643756

VL - 21

SP - 625

EP - 635

JO - Cerebral Cortex

JF - Cerebral Cortex

SN - 1047-3211

IS - 3

ER -

ID: 34181837