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Weixing Shen, Marc Flajolet, Paul Greengard, and D. J Surmeier (2008)

Dichotomous dopaminergic control of striatal synaptic plasticity.

Science, 321(5890):848–851.

At synapses between cortical pyramidal neurons and principal striatal medium spiny neurons (MSNs), postsynaptic D1 and D2 dopamine (DA) receptors are postulated to be necessary for the induction of long-term potentiation and depression, respectively-forms of plasticity thought to underlie associative learning. Because these receptors are restricted to two distinct MSN populations, this postulate demands that synaptic plasticity be unidirectional in each cell type. Using brain slices from DA receptor transgenic mice, we show that this is not the case. Rather, DA plays complementary roles in these two types of MSN to ensure that synaptic plasticity is bidirectional and Hebbian. In models of Parkinson's disease, this system is thrown out of balance, leading to unidirectional changes in plasticity that could underlie network pathology and symptoms.
Animals; Corpus Striatum; Dopamine; Glutamic Acid; Long-Term Potentiation; Long-Term Synaptic Depression; Mice; Mice, Transgenic; Neurons; Parkinsonian Disorders; Receptors, Dopamine D1; Receptors, Dopamine D2; Signal Transduction; Synapses
Relevant for: WP5 intrinsic/extrinsic motivations. An important paper that provides the last word (?) on the modulation of spike-timing-dependent plasticity in the striatum (the input nucleus of the basal ganglia which we think are critically involved in action selection, development and reinforcement learning).