| Literature DB >> 26549453 |
Massimo Trusel1, Anna Cavaccini1, Marta Gritti2, Barbara Greco1, Pierre-Philippe Saintot1, Cristiano Nazzaro1, Milica Cerovic3, Ilaria Morella4, Riccardo Brambilla3, Raffaella Tonini5.
Abstract
The basal ganglia play a critical role in shaping motor behavior. For this function, the activity of medium spiny neurons (MSNs) of the striatonigral and striatopallidal pathways must be integrated. It remains unclear whether the activity of the two pathways is primarily coordinated by synaptic plasticity mechanisms. Using a model of Parkinson's disease, we determined the circuit and behavioral effects of concurrently regulating cell-type-specific forms of corticostriatal long-term synaptic depression (LTD) by inhibiting small-conductance Ca(2+)-activated K(+) channels (SKs) of the dorsolateral striatum. At striatopallidal synapses, SK channel inhibition rescued the disease-linked deficits in endocannabinoid (eCB)-dependent LTD. At striatonigral cells, inhibition of these channels counteracted a form of adenosine-mediated LTD by activating the ERK cascade. Interfering with eCB-, adenosine-, and ERK signaling in vivo alleviated motor abnormalities, which supports that synaptic modulation of striatal pathways affects behavior. Thus, our results establish a central role of coordinated synaptic plasticity at MSN subpopulations in motor control.Entities:
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Year: 2015 PMID: 26549453 DOI: 10.1016/j.celrep.2015.10.009
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423