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Reduction in endocannabinoid tone is a homeostatic mechanism for specific inhibitory synapses

  • Jimok Kim
    ,
  • Bradley E. Alger
  • University of Maryland, Baltimore
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

When chronic alterations in neuronal activity occur, network gain is maintained by global homeostatic scaling of synaptic strength, but the stability of microcircuits can be controlled by unique adaptations that differ from the global changes. It is not understood how specificity of synaptic tuning is achieved. We found that, although a large population of inhibitory synapses was homeostatically scaled down after chronic inactivity, decreased endocannabinoid tone specifically strengthened a subset of GABAergic synapses that express cannabinoid receptors. In rat hippocampal slice cultures, a 3-5-d blockade of neuronal firing facilitated uptake and degradation of anandamide. The consequent reduction in basal stimulation of cannabinoid receptors augmented GABA release probability, fostering rapid depression of synaptic inhibition and on-demand disinhibition. This regulatory mechanism, mediated by activity-dependent changes in tonic endocannabinoid level, permits selective local tuning of inhibitory synapses in hippocampal networks.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 592-600 (9 pages)

Journal (Volume, Issue Number)

Nature Neuroscience (Volume 13, Issue 5)

Publication milestones

  • Published - 05/2010

Publication status

Published - 05/2010

ISSN

1097-6256

Publication IDs

  • Scopus: 77951665718
  • PubMed: 20348918

Publication metrics

Metrics

SciVal
FWCI
3.39
SciVal
Author count
2
SciVal
citations
110
SciVal
Paper percentile
97
SciVal
Top percentile
5
Scopus
citations
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1

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Social media
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Funding Details

We thank T. Abrams and the members of the Alger laboratory for helpful comments and suggestions on this work. We thank T. Gover for expert assistance with the calcium-imaging experiments. This research was supported by US Institutes of Health grants R01 DA014625 and R01 MH077277 to B.E.A.
FundersFunding numbers
US National Institutes of Health
R01 MH077277, R01 DA014625
NIMH
R01MH077277
NIDA
R01DA014625