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State-dependent changes in astrocyte regulation of extrasynaptic NMDA receptor signalling in neurosecretory neurons

  • Tiffany M. Fleming
    ,
  • Victoria Scott
    ,
  • Krishna Naskar
    ,
  • Natalie Joe
    ,
  • Colin H. Brown
    ,
  • Javier E. Stern(corresponding author)
*Corresponding author for this work
  • Medical College of Georgia
    ,
  • University of Otago
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Despite the long-established presence of glutamate NMDA receptors at extrasynaptic sites (eNMDARs), their functional roles remain poorly understood. Factors influencing the concentration and time course of glutamate in the extrasynaptic space, such as the topography of the neuronal-glial microenvironment, as well as glial glutamate transporters, are expected to affect eNMDAR-mediated signalling strength. In this study, we used in vitro and in vivo electrophysiological recordings to assess the properties, functional relevance and modulation of a persistent excitatory current mediated by activation of eNMDARs in hypothalamic supraoptic nucleus (SON) neurons. We found that ambient glutamate of a non-synaptic origin activates eNMDARs to mediate a persistent excitatory current (termed tonic I NMDA), which tonically stimulates neuronal activity. Pharmacological blockade of GLT1 astrocyte glutamate transporters, as well as the gliotoxin α-aminodadipic acid, enhanced tonic I NMDA and neuronal activity, supporting an astrocyte regulation of tonic I NMDA strength. Dehydration, a physiological challenge known to increase SON firing activity and to induce neuroglial remodelling, including reduced neuronal ensheathment by astrocyte processes, resulted in blunted GLT1 efficacy, enhanced tonic I NMDA strength, and increased neuronal activity. Taken together, our studies support the view that glial modulation of tonic I NMDA activation contributes to regulation of SON neuronal activity, contributing in turn to neuronal homeostatic responses during a physiological challenge.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 3929-3941 (13 pages)

Journal (Volume, Issue Number)

Journal of Physiology (Volume 589, Issue 16)

Publication milestones

  • Published - 08/2011

Publication status

Published - 08/2011

ISSN

0022-3751

Publication IDs

  • Scopus: 80051661227
  • PubMed: 21690192

Publication metrics

Metrics

SciVal
FWCI
1.75
SciVal
Author count
6
SciVal
citations
51
SciVal
Paper percentile
91
SciVal
Top percentile
10
Scopus
citations
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1

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Citation count
60
Captures
67