Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac

Striatal cholinergic interneurons provide modulation to striatal circuits involved in voluntary motor control and goal-directed behaviors through their autonomous tonic discharge and their firing “pause” responses to novel and rewarding environmental events. Striatal cholinergic interneuron hyperact...

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Publicado: 2018
Materias:
Kv7
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00283908_v137_n_p309_Paz
http://hdl.handle.net/20.500.12110/paper_00283908_v137_n_p309_Paz
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spelling paper:paper_00283908_v137_n_p309_Paz2023-06-08T14:55:08Z Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac Diclofenac Excitability Kv7 Retigabine Striatal cholinergic interneurons Synaptic integration diclofenac meclofenamic acid potassium channel potassium channel Kv7 retigabine unclassified drug acetylcholine agents affecting water, molecule or ion transport carbamic acid derivative diclofenac nonsteroid antiinflammatory agent phenylenediamine derivative potassium channel potassium channel blocking agent retigabine animal tissue Article excitatory postsynaptic potential summation interneuron male mouse negative feedback nerve cell excitability nerve cell inhibition nerve cell stimulation neuromodulation neurotransmission nonhuman priority journal striatal cholinergic interneuron animal corpus striatum drug effect excitatory postsynaptic potential interneuron metabolism physiology tissue culture technique transgenic mouse Acetylcholine Animals Anti-Inflammatory Agents, Non-Steroidal Carbamates Corpus Striatum Diclofenac Excitatory Postsynaptic Potentials Interneurons Male Membrane Transport Modulators Mice, Transgenic Phenylenediamines Potassium Channel Blockers Potassium Channels Tissue Culture Techniques Striatal cholinergic interneurons provide modulation to striatal circuits involved in voluntary motor control and goal-directed behaviors through their autonomous tonic discharge and their firing “pause” responses to novel and rewarding environmental events. Striatal cholinergic interneuron hyperactivity was linked to the motor deficits associated with Parkinson's disease and the adverse effects of chronic antiparkinsonian therapy like L-DOPA-induced dyskinesia. Here we addressed whether Kv7 channels, which provide negative feedback to excitation in other neuron types, are involved in the control of striatal cholinergic interneuron tonic activity and response to excitatory inputs. We found that autonomous firing of striatal cholinergic interneurons is not regulated by Kv7 channels. In contrast, Kv7 channels limit the summation of excitatory postsynaptic potentials in cholinergic interneurons through a postsynaptic mechanism. Striatal cholinergic interneurons have a high reserve of Kv7 channels, as their opening using pharmacological tools completely silenced the tonic firing and markedly reduced their intrinsic excitability. A strong inhibition of striatal cholinergic interneurons was also observed in response to the anti-inflammatory drugs diclofenac and meclofenamic acid, however, this effect was independent of Kv7 channels. These data bring attention to new potential molecular targets and pharmacological tools to control striatal cholinergic interneuron activity in pathological conditions where they are believed to be hyperactive, including Parkinson's disease. © 2018 Elsevier Ltd 2018 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00283908_v137_n_p309_Paz http://hdl.handle.net/20.500.12110/paper_00283908_v137_n_p309_Paz
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Diclofenac
Excitability
Kv7
Retigabine
Striatal cholinergic interneurons
Synaptic integration
diclofenac
meclofenamic acid
potassium channel
potassium channel Kv7
retigabine
unclassified drug
acetylcholine
agents affecting water, molecule or ion transport
carbamic acid derivative
diclofenac
nonsteroid antiinflammatory agent
phenylenediamine derivative
potassium channel
potassium channel blocking agent
retigabine
animal tissue
Article
excitatory postsynaptic potential summation
interneuron
male
mouse
negative feedback
nerve cell excitability
nerve cell inhibition
nerve cell stimulation
neuromodulation
neurotransmission
nonhuman
priority journal
striatal cholinergic interneuron
animal
corpus striatum
drug effect
excitatory postsynaptic potential
interneuron
metabolism
physiology
tissue culture technique
transgenic mouse
Acetylcholine
Animals
Anti-Inflammatory Agents, Non-Steroidal
Carbamates
Corpus Striatum
Diclofenac
Excitatory Postsynaptic Potentials
Interneurons
Male
Membrane Transport Modulators
Mice, Transgenic
Phenylenediamines
Potassium Channel Blockers
Potassium Channels
Tissue Culture Techniques
spellingShingle Diclofenac
Excitability
Kv7
Retigabine
Striatal cholinergic interneurons
Synaptic integration
diclofenac
meclofenamic acid
potassium channel
potassium channel Kv7
retigabine
unclassified drug
acetylcholine
agents affecting water, molecule or ion transport
carbamic acid derivative
diclofenac
nonsteroid antiinflammatory agent
phenylenediamine derivative
potassium channel
potassium channel blocking agent
retigabine
animal tissue
Article
excitatory postsynaptic potential summation
interneuron
male
mouse
negative feedback
nerve cell excitability
nerve cell inhibition
nerve cell stimulation
neuromodulation
neurotransmission
nonhuman
priority journal
striatal cholinergic interneuron
animal
corpus striatum
drug effect
excitatory postsynaptic potential
interneuron
metabolism
physiology
tissue culture technique
transgenic mouse
Acetylcholine
Animals
Anti-Inflammatory Agents, Non-Steroidal
Carbamates
Corpus Striatum
Diclofenac
Excitatory Postsynaptic Potentials
Interneurons
Male
Membrane Transport Modulators
Mice, Transgenic
Phenylenediamines
Potassium Channel Blockers
Potassium Channels
Tissue Culture Techniques
Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
topic_facet Diclofenac
Excitability
Kv7
Retigabine
Striatal cholinergic interneurons
Synaptic integration
diclofenac
meclofenamic acid
potassium channel
potassium channel Kv7
retigabine
unclassified drug
acetylcholine
agents affecting water, molecule or ion transport
carbamic acid derivative
diclofenac
nonsteroid antiinflammatory agent
phenylenediamine derivative
potassium channel
potassium channel blocking agent
retigabine
animal tissue
Article
excitatory postsynaptic potential summation
interneuron
male
mouse
negative feedback
nerve cell excitability
nerve cell inhibition
nerve cell stimulation
neuromodulation
neurotransmission
nonhuman
priority journal
striatal cholinergic interneuron
animal
corpus striatum
drug effect
excitatory postsynaptic potential
interneuron
metabolism
physiology
tissue culture technique
transgenic mouse
Acetylcholine
Animals
Anti-Inflammatory Agents, Non-Steroidal
Carbamates
Corpus Striatum
Diclofenac
Excitatory Postsynaptic Potentials
Interneurons
Male
Membrane Transport Modulators
Mice, Transgenic
Phenylenediamines
Potassium Channel Blockers
Potassium Channels
Tissue Culture Techniques
description Striatal cholinergic interneurons provide modulation to striatal circuits involved in voluntary motor control and goal-directed behaviors through their autonomous tonic discharge and their firing “pause” responses to novel and rewarding environmental events. Striatal cholinergic interneuron hyperactivity was linked to the motor deficits associated with Parkinson's disease and the adverse effects of chronic antiparkinsonian therapy like L-DOPA-induced dyskinesia. Here we addressed whether Kv7 channels, which provide negative feedback to excitation in other neuron types, are involved in the control of striatal cholinergic interneuron tonic activity and response to excitatory inputs. We found that autonomous firing of striatal cholinergic interneurons is not regulated by Kv7 channels. In contrast, Kv7 channels limit the summation of excitatory postsynaptic potentials in cholinergic interneurons through a postsynaptic mechanism. Striatal cholinergic interneurons have a high reserve of Kv7 channels, as their opening using pharmacological tools completely silenced the tonic firing and markedly reduced their intrinsic excitability. A strong inhibition of striatal cholinergic interneurons was also observed in response to the anti-inflammatory drugs diclofenac and meclofenamic acid, however, this effect was independent of Kv7 channels. These data bring attention to new potential molecular targets and pharmacological tools to control striatal cholinergic interneuron activity in pathological conditions where they are believed to be hyperactive, including Parkinson's disease. © 2018 Elsevier Ltd
title Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
title_short Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
title_full Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
title_fullStr Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
title_full_unstemmed Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
title_sort inhibition of striatal cholinergic interneuron activity by the kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac
publishDate 2018
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00283908_v137_n_p309_Paz
http://hdl.handle.net/20.500.12110/paper_00283908_v137_n_p309_Paz
_version_ 1768543644938141696