During postnatal development endogenous neurosteroids influence GABA-ergic neurotransmission of mouse cortical neurons
Autor: | Jeremy J. Lambert, Jerome D. Swinny, Dianne R. Peden, Delia Belelli, Scott J. Mitchell, Mohsen Seifi, Adam R. Brown, Murray B. Herd |
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Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Male Neuroactive steroid Mice Transgenic Pharmacy Neonatal development Neurotransmission Biology Miniature Postsynaptic Potentials Inhibitory postsynaptic potential Synaptic Transmission Article 03 medical and health sciences Cellular and Molecular Neuroscience Mice 0302 clinical medicine medicine Neurosteroid Animals Pharmacology Cerebral Cortex Neurotransmitter Agents GABAA receptor Pyramidal Cells RCUK Mice Inbred C57BL MRC 030104 developmental biology medicine.anatomical_structure nervous system Cerebral cortex Cortex GABAergic Developmental plasticity Female Neuroscience 030217 neurology & neurosurgery |
Zdroj: | Neuropharmacology Brown, A R, Mitchell, S J, Peden, D R, Herd, M B, Seifi, M, Swinny, J D, Belelli, D & Lambert, J J 2016, ' During postnatal development endogenous neurosteroids influence GABA-ergic neurotransmission of mouse cortical neurons ', Neuropharmacology, vol. 103, pp. 163-173 . https://doi.org/10.1016/j.neuropharm.2015.11.019 |
ISSN: | 1873-7064 |
DOI: | 10.1016/j.neuropharm.2015.11.019 |
Popis: | As neuronal development progresses, GABAergic synaptic transmission undergoes a defined program of reconfiguration. For example, GABAA receptor (GABAAR)-mediated synaptic currents, (miniature inhibitory postsynaptic currents; mIPSCs), which initially exhibit a relatively slow decay phase, become progressively reduced in duration, thereby supporting the temporal resolution required for mature network activity. Here we report that during postnatal development of cortical layer 2/3 pyramidal neurons, GABAAR-mediated phasic inhibition is influenced by a resident neurosteroid tone, which wanes in the second postnatal week, resulting in the brief phasic events characteristic of mature neuronal signalling. Treatment of cortical slices with the immediate precursor of 5α-pregnan-3α-ol-20-one (5α3α), the GABAAR-inactive 5α-dihydroprogesterone, (5α-DHP), greatly prolonged the mIPSCs of P20 pyramidal neurons, demonstrating these more mature neurons retain the capacity to synthesize GABAAR-active neurosteroids, but now lack the endogenous steroid substrate. Previously, such developmental plasticity of phasic inhibition was ascribed to the expression of synaptic GABAARs incorporating the α1 subunit. However, the duration of mIPSCs recorded from L2/3 cortical neurons derived from α1 subunit deleted mice, were similarly under the developmental influence of a neurosteroid tone. In addition to principal cells, synaptic GABAARs of L2/3 interneurons were modulated by native neurosteroids in a development-dependent manner. In summary, local neurosteroids influence synaptic transmission during a crucial period of cortical neurodevelopment, findings which may be of importance for establishing normal network connectivity. Highlights • Upon postnatal maturation GABAA receptor synaptic inhibition is reduced in duration. • Reduced synthesis of local neurosteroids contributes to this cortical plasticity. • The study reveals a potent mechanism to locally regulate cortical neuron activity. |
Databáze: | OpenAIRE |
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