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      Thinking Outside the Box (and Arrow): Current Themes in Striatal Dysfunction in Movement Disorders

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          Abstract

          The basal ganglia are an intricately connected assembly of subcortical nuclei, forming the core of an adaptive network connecting cortical and thalamic circuits. For nearly three decades, researchers and medical practitioners have conceptualized how the basal ganglia circuit works, and how its pathology underlies motor disorders such as Parkinson’s and Huntington’s diseases, using what is often referred to as the “box-and-arrow model”: a circuit diagram showing the broad strokes of basal ganglia connectivity and the pathological increases and decreases in the weights of specific connections that occur in disease. While this model still has great utility and has led to groundbreaking strategies to treat motor disorders, our evolving knowledge of basal ganglia function has made it clear that this classic model has several shortcomings that severely limit its predictive and descriptive abilities. In this review, we will focus on the striatum, the main input nucleus of the basal ganglia. We describe recent advances in our understanding of the rich microcircuitry and plastic capabilities of the striatum, factors not captured by the original box-and-arrow model, and provide examples of how such advances inform our current understanding of the circuit pathologies underlying motor disorders.

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          Most cited references170

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          Modulation of striatal projection systems by dopamine.

          The basal ganglia are a chain of subcortical nuclei that facilitate action selection. Two striatal projection systems--so-called direct and indirect pathways--form the functional backbone of the basal ganglia circuit. Twenty years ago, investigators proposed that the striatum's ability to use dopamine (DA) rise and fall to control action selection was due to the segregation of D(1) and D(2) DA receptors in direct- and indirect-pathway spiny projection neurons. Although this hypothesis sparked a debate, the evidence that has accumulated since then clearly supports this model. Recent advances in the means of marking neural circuits with optical or molecular reporters have revealed a clear-cut dichotomy between these two cell types at the molecular, anatomical, and physiological levels. The contrast provided by these studies has provided new insights into how the striatum responds to fluctuations in DA signaling and how diseases that alter this signaling change striatal function.
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            A critical time window for dopamine actions on the structural plasticity of dendritic spines.

            Animal behaviors are reinforced by subsequent rewards following within a narrow time window. Such reward signals are primarily coded by dopamine, which modulates the synaptic connections of medium spiny neurons in the striatum. The mechanisms of the narrow timing detection, however, remain unknown. Here, we optically stimulated dopaminergic and glutamatergic inputs separately and found that dopamine promoted spine enlargement only during a narrow time window (0.3 to 2 seconds) after the glutamatergic inputs. The temporal contingency was detected by rapid regulation of adenosine 3',5'-cyclic monophosphate in thin distal dendrites, in which protein-kinase A was activated only within the time window because of a high phosphodiesterase activity. Thus, we describe a molecular basis of reinforcement plasticity at the level of single dendritic spines.
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              Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop.

              This paper reviews some of the recent findings on different aspects of the anatomical organization of the basal ganglia. Attempts have been made to delineate the anatomical substrate of information processing along the cortico-basal ganglia-thalamo-cortical loop. Emphasis has been placed on data obtained with highly sensitive anterograde tract-tracing methods applied to the study of the main axis of the loop, which is composed of the striatum, the pallidum, and the substantia nigra. These findings have highlighted the complexities of the organization of the intrinsic basal ganglia circuitry, which comprises multiple modular units that are distributed according to highly ordered and repetitive patterns. Such an arrangement is well suited to convey cortical information in a highly specific manner throughout the basal ganglia. The basal ganglia circuitry is also designed so as to modulate in a precise manner the neuronal activity of several brain functional systems, which are involved in the direct control of different aspects of psychomotor behavior. Of utmost importance is the action of the basal ganglia on thalamocortical premotor neurons. It is through these neurons, which can be considered as a sort of final common pathway, that the basal ganglia ultimately influence the complex neuronal computation that goes on at cortical level.
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                Author and article information

                Journal
                Neuroscientist
                Neuroscientist
                NRO
                spnro
                The Neuroscientist
                SAGE Publications (Sage CA: Los Angeles, CA )
                1073-8584
                1089-4098
                31 October 2018
                August 2019
                : 25
                : 4
                : 359-379
                Affiliations
                [1 ]Department of Neurobiology and Behavior, Stony Brook University School of Medicine, Stony Brook, NY, USA
                [2 ]Department of Medical Neurobiology, The Hebrew University of Jerusalem, Jerusalem, Israel
                Author notes
                [*]Joshua L. Plotkin, Department of Neurobiology and Behavior, Stony Brook University School of Medicine, CMM Room 536, Stony Brook, NY 11794, USA. Email: joshua.plotkin@ 123456stonybrook.edu
                [*]Joshua A. Goldberg, Department of Medical Neurobiology, Institute of Medical Research Israel-Canada, The Faculty of Medicine, The Hebrew University of Jerusalem, Ein Kerem Campus, POB 12272, Jerusalem, 9112102, Israel. Email: joshg@ 123456ekmd.huji.ac.il
                Author information
                https://orcid.org/0000-0001-6232-7613
                https://orcid.org/0000-0002-5740-4087
                Article
                10.1177_1073858418807887
                10.1177/1073858418807887
                6529282
                30379121
                e90f4976-326a-4b63-9c6e-0a194437ee5a
                © The Author(s) 2018

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                Funding
                Funded by: United States-Israel Binational Science Foundation, FundRef https://doi.org/10.13039/501100001742;
                Award ID: 2015255
                Funded by: National Institute of Neurological Disorders and Stroke, FundRef https://doi.org/10.13039/100000065;
                Award ID: R01NS104089
                Funded by: H2020 European Research Council, FundRef https://doi.org/10.13039/100010663;
                Award ID: 646880-SynChI
                Categories
                Reviews

                neurodegenerative diseases,synaptic plasticity,striatal interneurons,direct and indirect pathway,dopamine acetylcholine balance,striatal projection neurons,synchronous oscillations

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