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Labile glutamate si...
Labile glutamate signaling onto CA1 pyramidal cells in the developing hippocampus depends mechanistically on input pathway
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- Ma, Rong (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
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- Xiao, Min-Yi, 1964 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
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- Gustafsson, Bengt, 1946 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
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(creator_code:org_t)
- Elsevier BV, 2016
- 2016
- Engelska.
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Ingår i: Neuroscience. - : Elsevier BV. - 0306-4522. ; 337, s. 27-36
- Relaterad länk:
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https://gup.ub.gu.se...
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visa fler...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- The apical dendrite of hippocampal CA1 pyramidal cells receives information from the entorhinal cortex via the dentate gyrus and CA3 (Schaffer-collateral (SC) input) proximally within the stratum radiatum (SR) and directly from the entorhinal cortex/thalamus distally within the stratum lacunosum–moleculare (SLM). During the early postnatal development, very low/low frequency (0.033–1Hz) activation of previously non-stimulated (naïve) SC synapses (SR-CA1 synapses) results in a stimulus-, but not frequency-, dependent depression which is explained by postsynaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) silencing. This lability of AMPA signaling has been suggested to play a role in the activity-dependent organization of the SR synaptic input. Compared with the SR region the SLM region is matured earlier and may become organized in a different manner. Here, using field recordings of synaptic activity in hippocampal slices from 2nd postnatal week rats, we found that SLM-CA1 synapses are also readily depressed by activity in the very low/low frequency range (0.033–1Hz). The depression was, however, quite distinct from that of SR-CA1 synapses, being frequency dependent and reversing faster following stimulus interruption. Bath application of an AMPA receptor agonist produced only a small (−8%) post-application (10min) depression of SLM-CA1 synapses in contrast to that of SR-CA1 synapses (−33%). The SLM-CA1 synapses did also exhibit less long-term depression than the SR-CA1 synapses. We conclude that in the developing hippocampus the labile glutamate signaling onto CA1 pyramidal cell depends mechanistically on input pathway. The labile AMPA signaling at SLM-CA1 synapses is most likely explained by a presynaptic mechanism with limited amount of postsynaptic AMPA silencing. © 2016 IBRO
Ämnesord
- NATURVETENSKAP -- Biologi -- Cellbiologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences -- Cell Biology (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Neurosciences (hsv//eng)
Nyckelord
- AMPA silencing
- development
- hippocampus
- synapse
- synaptic depression
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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