Abstract
We have investigated the fundamental properties of central auditory glycinergic synapses in early postnatal development in normal and congenitally deaf (dn/dn) mice. Glycinergic miniature inhibitory postsynaptic currents (mIPSCs) were recorded using patch-clamp methods in neurons from a brain slice preparation of the medial nucleus of the trapezoid body (MNTB), at 12-14 days postnatal age. Our results show a number of significant differences between normal and deaf mice. The frequency of mIPSCs is greater (50%) in deaf versus normal mice. Mean mIPSC amplitude is smaller in deaf mice than in normal mice (mean mIPSC amplitude: deaf, 64 pA; normal, 106 pA). Peak-scaled fluctuation analysis of mIPSCs showed that mean single channel conductance is greater in the deaf mice (deaf, 64 pS; normal, 45 pS). The mean decay time course of mIPSCs is slower in MNTB neurons from deaf mice (mean half-width: deaf, 2.9 ms; normal, 2.3 ms). Light- and electron-microscopic immunolabeling results showed that MNTB neurons from deaf mice have more (30%) inhibitory synaptic sites (postsynaptic gephyrin clusters) than MNTB neurons in normal mice. Our results demonstrate substantial differences in glycinergic transmission in normal and congenitally deaf mice, supporting a role for activity during development in regulating both synaptic structure (connectivity) and the fundamental (quantal) properties of mIPSCs at central glycinergic synapses.
Original language | English |
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Pages (from-to) | 1006-1012 |
Number of pages | 7 |
Journal | Journal of Neurophysiology |
Volume | 91 |
Issue number | 2 |
DOIs | |
State | Published - Feb 2004 |
ASJC Scopus Subject Areas
- General Neuroscience
- Physiology
Keywords
- Comparative Study
- Research Support, US. Gov't, P.H.S
- Animals
- Animals, Newborn
- Brain Stem / physiology*
- Brain Stem / ultrastructure
- Deafness / congenital*
- Deafness / physiopathology*
- Glycine / physiology*
- Immunohistochemistry
- In Vitro Techniques
- Mice
- Mice, Inbred CBA
- Microscopy, Immunoelectron
- Neural Inhibition / physiology*
- Synapses / physiology
- Synapses / ultrastructure
- Synaptic Transmission / physiology*
- Glycine
Disciplines
- Medical Cell Biology
- Medical Neurobiology
- Medical Physiology
- Neurosciences
- Physiological Processes