Cargando…

Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability

Short-term plasticity plays a key role in synaptic transmission and has been extensively investigated for excitatory synapses. Much less is known about inhibitory synapses. Here we analyze the performance of glycinergic connections between the medial nucleus of the trapezoid body (MNTB) and the late...

Descripción completa

Detalles Bibliográficos
Autores principales: Kramer, Florian, Griesemer, Désirée, Bakker, Dennis, Brill, Sina, Franke, Jürgen, Frotscher, Erik, Friauf, Eckhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948056/
https://www.ncbi.nlm.nih.gov/pubmed/24653676
http://dx.doi.org/10.3389/fncir.2014.00014
_version_ 1782306745522061312
author Kramer, Florian
Griesemer, Désirée
Bakker, Dennis
Brill, Sina
Franke, Jürgen
Frotscher, Erik
Friauf, Eckhard
author_facet Kramer, Florian
Griesemer, Désirée
Bakker, Dennis
Brill, Sina
Franke, Jürgen
Frotscher, Erik
Friauf, Eckhard
author_sort Kramer, Florian
collection PubMed
description Short-term plasticity plays a key role in synaptic transmission and has been extensively investigated for excitatory synapses. Much less is known about inhibitory synapses. Here we analyze the performance of glycinergic connections between the medial nucleus of the trapezoid body (MNTB) and the lateral superior olive (LSO) in the auditory brainstem, where high spike rates as well as fast and precise neurotransmission are hallmarks. Analysis was performed in acute mouse slices shortly after hearing onset (postnatal day (P)11) and 8 days later (P19). Stimulation was done at 37°C with 1–400 Hz for 40 s. Moreover, in a novel approach named marathon experiments, a very prolonged stimulation protocol was employed, comprising 10 trials of 1-min challenge and 1-min recovery periods at 50 and 1 Hz, respectively, thus lasting up to 20 min and amounting to >30,000 stimulus pulses. IPSC peak amplitudes displayed short-term depression (STD) and synaptic attenuation in a frequency-dependent manner. No facilitation was observed. STD in the MNTB-LSO connections was less pronounced than reported in the upstream calyx of Held-MNTB connections. At P11, the STD level and the failure rate were slightly lower within the ms-to-s range than at P19. During prolonged stimulation periods lasting 40 s, P19 connections sustained virtually failure-free transmission up to frequencies of 100 Hz, whereas P11 connections did so only up to 50 Hz. In marathon experiments, P11 synapses recuperated reproducibly from synaptic attenuation during all recovery periods, demonstrating a robust synaptic machinery at hearing onset. At 26°C, transmission was severely impaired and comprised abnormally high amplitudes after minutes of silence, indicative of imprecisely regulated vesicle pools. Our study takes a fresh look at synaptic plasticity and stability by extending conventional stimulus periods in the ms-to-s range to minutes. It also provides a framework for future analyses of synaptic plasticity.
format Online
Article
Text
id pubmed-3948056
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-39480562014-03-20 Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability Kramer, Florian Griesemer, Désirée Bakker, Dennis Brill, Sina Franke, Jürgen Frotscher, Erik Friauf, Eckhard Front Neural Circuits Neuroscience Short-term plasticity plays a key role in synaptic transmission and has been extensively investigated for excitatory synapses. Much less is known about inhibitory synapses. Here we analyze the performance of glycinergic connections between the medial nucleus of the trapezoid body (MNTB) and the lateral superior olive (LSO) in the auditory brainstem, where high spike rates as well as fast and precise neurotransmission are hallmarks. Analysis was performed in acute mouse slices shortly after hearing onset (postnatal day (P)11) and 8 days later (P19). Stimulation was done at 37°C with 1–400 Hz for 40 s. Moreover, in a novel approach named marathon experiments, a very prolonged stimulation protocol was employed, comprising 10 trials of 1-min challenge and 1-min recovery periods at 50 and 1 Hz, respectively, thus lasting up to 20 min and amounting to >30,000 stimulus pulses. IPSC peak amplitudes displayed short-term depression (STD) and synaptic attenuation in a frequency-dependent manner. No facilitation was observed. STD in the MNTB-LSO connections was less pronounced than reported in the upstream calyx of Held-MNTB connections. At P11, the STD level and the failure rate were slightly lower within the ms-to-s range than at P19. During prolonged stimulation periods lasting 40 s, P19 connections sustained virtually failure-free transmission up to frequencies of 100 Hz, whereas P11 connections did so only up to 50 Hz. In marathon experiments, P11 synapses recuperated reproducibly from synaptic attenuation during all recovery periods, demonstrating a robust synaptic machinery at hearing onset. At 26°C, transmission was severely impaired and comprised abnormally high amplitudes after minutes of silence, indicative of imprecisely regulated vesicle pools. Our study takes a fresh look at synaptic plasticity and stability by extending conventional stimulus periods in the ms-to-s range to minutes. It also provides a framework for future analyses of synaptic plasticity. Frontiers Media S.A. 2014-03-10 /pmc/articles/PMC3948056/ /pubmed/24653676 http://dx.doi.org/10.3389/fncir.2014.00014 Text en Copyright © 2014 Kramer, Griesemer, Bakker, Brill, Franke, Frotscher and Friauf. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Kramer, Florian
Griesemer, Désirée
Bakker, Dennis
Brill, Sina
Franke, Jürgen
Frotscher, Erik
Friauf, Eckhard
Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
title Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
title_full Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
title_fullStr Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
title_full_unstemmed Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
title_short Inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
title_sort inhibitory glycinergic neurotransmission in the mammalian auditory brainstem upon prolonged stimulation: short-term plasticity and synaptic reliability
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948056/
https://www.ncbi.nlm.nih.gov/pubmed/24653676
http://dx.doi.org/10.3389/fncir.2014.00014
work_keys_str_mv AT kramerflorian inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability
AT griesemerdesiree inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability
AT bakkerdennis inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability
AT brillsina inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability
AT frankejurgen inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability
AT frotschererik inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability
AT friaufeckhard inhibitoryglycinergicneurotransmissioninthemammalianauditorybrainstemuponprolongedstimulationshorttermplasticityandsynapticreliability