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  1. Article ; Online: Reply to Piochon et al.: NMDARs in Purkinje cells are not involved in parallel fiber-Purkinje cell synaptic plasticity or motor learning.

    Schonewille, Martijn / Girasole, Allison E / De Zeeuw, Chris I / Bouvier, Guy

    Proceedings of the National Academy of Sciences of the United States of America

    2022  Volume 119, Issue 8

    MeSH term(s) Neuronal Plasticity ; Purkinje Cells/metabolism ; Receptors, N-Methyl-D-Aspartate/metabolism
    Chemical Substances Receptors, N-Methyl-D-Aspartate
    Language English
    Publishing date 2022-02-22
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2120480119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Striatal Indirect Pathway Dysfunction Underlies Motor Deficits in a Mouse Model of Paroxysmal Dyskinesia.

    Nelson, Alexandra B / Girasole, Allison E / Lee, Hsien-Yang / Ptáček, Louis J / Kreitzer, Anatol C

    The Journal of neuroscience : the official journal of the Society for Neuroscience

    2022  Volume 42, Issue 13, Page(s) 2835–2848

    Abstract: Abnormal involuntary movements, or dyskinesias, are seen in many neurologic diseases, including disorders where the brain appears grossly normal. This observation suggests that alterations in neural activity or connectivity may underlie dyskinesias. One ... ...

    Abstract Abnormal involuntary movements, or dyskinesias, are seen in many neurologic diseases, including disorders where the brain appears grossly normal. This observation suggests that alterations in neural activity or connectivity may underlie dyskinesias. One influential model proposes that involuntary movements are driven by an imbalance in the activity of striatal direct and indirect pathway neurons (dMSNs and iMSNs, respectively). Indeed, in some animal models, there is evidence that dMSN hyperactivity contributes to dyskinesia. Given the many diseases associated with dyskinesia, it is unclear whether these findings generalize to all forms. Here, we used male and female mice in a mouse model of paroxysmal nonkinesigenic dyskinesia (PNKD) to assess whether involuntary movements are related to aberrant activity in the striatal direct and indirect pathways. In this model, as in the human disorder PNKD, animals experience dyskinetic attacks in response to caffeine or alcohol. Using optically identified striatal single-unit recordings in freely moving PNKD mice, we found a loss of iMSN firing during dyskinesia bouts. Further, chemogenetic inhibition of iMSNs triggered dyskinetic episodes in PNKD mice. Finally, we found that these decreases in iMSN firing are likely because of aberrant endocannabinoid-mediated suppression of glutamatergic inputs. These data show that striatal iMSN dysfunction contributes to the etiology of dyskinesia in PNKD, and suggest that indirect pathway hypoactivity may be a key mechanism for the generation of involuntary movements in other disorders.
    MeSH term(s) Animals ; Chorea/chemically induced ; Corpus Striatum ; Disease Models, Animal ; Dyskinesias/etiology ; Female ; Levodopa/adverse effects ; Male ; Mice ; Neurons
    Chemical Substances Levodopa (46627O600J)
    Language English
    Publishing date 2022-02-14
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 604637-x
    ISSN 1529-2401 ; 0270-6474
    ISSN (online) 1529-2401
    ISSN 0270-6474
    DOI 10.1523/JNEUROSCI.1614-20.2022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Bridging the Gap: Muscarinic M4 Receptors Promote Striatal Plasticity in Health and Disease.

    Girasole, Allison E / Nelson, Alexandra B

    Neuron

    2015  Volume 88, Issue 4, Page(s) 621–623

    Abstract: In this issue of Neuron, Shen et al. (2015) demonstrate that the M4 muscarinic receptor regulates striatal plasticity. The authors use an M4-positive allosteric modulator, which facilitates long-term depression in direct pathway neurons and reverses ... ...

    Abstract In this issue of Neuron, Shen et al. (2015) demonstrate that the M4 muscarinic receptor regulates striatal plasticity. The authors use an M4-positive allosteric modulator, which facilitates long-term depression in direct pathway neurons and reverses aberrant plasticity in levodopa-induced dyskinesia.
    MeSH term(s) Animals ; Dopamine Agents/toxicity ; Dyskinesia, Drug-Induced/metabolism ; Levodopa/toxicity ; Neostriatum/drug effects ; Neuronal Plasticity/drug effects ; Parkinsonian Disorders/drug therapy ; RGS Proteins/metabolism ; Receptor, Muscarinic M4/metabolism
    Chemical Substances Dopamine Agents ; RGS Proteins ; Receptor, Muscarinic M4 ; Levodopa (46627O600J)
    Language English
    Publishing date 2015-11-18
    Publishing country United States
    Document type Comment ; Journal Article
    ZDB-ID 808167-0
    ISSN 1097-4199 ; 0896-6273
    ISSN (online) 1097-4199
    ISSN 0896-6273
    DOI 10.1016/j.neuron.2015.11.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Probing striatal microcircuitry to understand the functional role of cholinergic interneurons.

    Girasole, Allison E / Nelson, Alexandra B

    Movement disorders : official journal of the Movement Disorder Society

    2015  Volume 30, Issue 10, Page(s) 1306–1318

    MeSH term(s) Animals ; Cholinergic Neurons/physiology ; Humans ; Interneurons/physiology ; Neostriatum/metabolism ; Neostriatum/physiology ; Neostriatum/physiopathology ; Signal Transduction/physiology
    Language English
    Publishing date 2015-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S. ; Review
    ZDB-ID 607633-6
    ISSN 1531-8257 ; 0885-3185
    ISSN (online) 1531-8257
    ISSN 0885-3185
    DOI 10.1002/mds.26340
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Functionally Distinct Connectivity of Developmentally Targeted Striosome Neurons.

    McGregor, Matthew M / McKinsey, Gabriel L / Girasole, Allison E / Bair-Marshall, Chloe J / Rubenstein, John L R / Nelson, Alexandra B

    Cell reports

    2020  Volume 29, Issue 6, Page(s) 1419–1428.e5

    Abstract: One long-standing model of striatal function divides the striatum into compartments called striosome and matrix. While some anatomical evidence suggests that these populations represent distinct striatal pathways with differing inputs and outputs, ... ...

    Abstract One long-standing model of striatal function divides the striatum into compartments called striosome and matrix. While some anatomical evidence suggests that these populations represent distinct striatal pathways with differing inputs and outputs, functional investigation has been limited by the methods for identifying and manipulating these populations. Here, we utilize hs599
    MeSH term(s) Animals ; Corpus Striatum/embryology ; Corpus Striatum/metabolism ; Corpus Striatum/physiology ; Dopaminergic Neurons/cytology ; Dopaminergic Neurons/drug effects ; Dopaminergic Neurons/metabolism ; Dopaminergic Neurons/physiology ; Mice ; Mice, Transgenic ; Motor Cortex/cytology ; Motor Cortex/metabolism ; Motor Cortex/physiology ; Neural Pathways/physiology ; Neurogenesis/drug effects ; Prefrontal Cortex/cytology ; Prefrontal Cortex/metabolism ; Prefrontal Cortex/physiology ; Substantia Nigra/cytology ; Substantia Nigra/metabolism ; Substantia Nigra/physiology
    Language English
    Publishing date 2020-02-28
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2019.09.076
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: NMDARs in granule cells contribute to parallel fiber-Purkinje cell synaptic plasticity and motor learning.

    Schonewille, Martijn / Girasole, Allison E / Rostaing, Philippe / Mailhes-Hamon, Caroline / Ayon, Annick / Nelson, Alexandra B / Triller, Antoine / Casado, Mariano / De Zeeuw, Chris I / Bouvier, Guy

    Proceedings of the National Academy of Sciences of the United States of America

    2021  Volume 118, Issue 37

    Abstract: Long-term synaptic plasticity is believed to be the cellular substrate of learning and memory. Synaptic plasticity rules are defined by the specific complement of receptors at the synapse and the associated downstream signaling mechanisms. In young ... ...

    Abstract Long-term synaptic plasticity is believed to be the cellular substrate of learning and memory. Synaptic plasticity rules are defined by the specific complement of receptors at the synapse and the associated downstream signaling mechanisms. In young rodents, at the cerebellar synapse between granule cells (GC) and Purkinje cells (PC), bidirectional plasticity is shaped by the balance between transcellular nitric oxide (NO) driven by presynaptic
    MeSH term(s) Animals ; Brain/physiology ; Cerebellum/physiology ; Excitatory Postsynaptic Potentials/physiology ; Female ; Humans ; Learning/physiology ; Long-Term Potentiation/physiology ; Long-Term Synaptic Depression/physiology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Motor Activity/physiology ; Neuronal Plasticity/physiology ; Neurons/metabolism ; Presynaptic Terminals/physiology ; Purkinje Cells/metabolism ; Receptors, N-Methyl-D-Aspartate/metabolism ; Synapses/metabolism
    Chemical Substances Receptors, N-Methyl-D-Aspartate
    Language English
    Publishing date 2021-06-29
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2102635118
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: A Subpopulation of Striatal Neurons Mediates Levodopa-Induced Dyskinesia.

    Girasole, Allison E / Lum, Matthew Y / Nathaniel, Diane / Bair-Marshall, Chloe J / Guenthner, Casey J / Luo, Liqun / Kreitzer, Anatol C / Nelson, Alexandra B

    Neuron

    2018  Volume 97, Issue 4, Page(s) 787–795.e6

    Abstract: Parkinson's disease is characterized by the progressive loss of midbrain dopamine neurons. Dopamine replacement therapy with levodopa alleviates parkinsonian motor symptoms but is complicated by the development of involuntary movements, termed levodopa- ... ...

    Abstract Parkinson's disease is characterized by the progressive loss of midbrain dopamine neurons. Dopamine replacement therapy with levodopa alleviates parkinsonian motor symptoms but is complicated by the development of involuntary movements, termed levodopa-induced dyskinesia (LID). Aberrant activity in the striatum has been hypothesized to cause LID. Here, to establish a direct link between striatal activity and dyskinesia, we combine optogenetics and a method to manipulate dyskinesia-associated neurons, targeted recombination in active populations (TRAP). We find that TRAPed cells are a stable subset of sensorimotor striatal neurons, predominantly from the direct pathway, and that reactivation of TRAPed striatal neurons causes dyskinesia in the absence of levodopa. Inhibition of TRAPed cells, but not a nonspecific subset of direct pathway neurons, ameliorates LID. These results establish that a distinct subset of striatal neurons is causally involved in LID and indicate that successful therapeutic strategies for treating LID may require targeting functionally selective neuronal subtypes.
    MeSH term(s) Animals ; Antiparkinson Agents/administration & dosage ; Corpus Striatum/drug effects ; Corpus Striatum/physiopathology ; Disease Models, Animal ; Dyskinesia, Drug-Induced/physiopathology ; Female ; Levodopa/administration & dosage ; Male ; Mice, Inbred C57BL ; Mice, Transgenic ; Motor Cortex/drug effects ; Motor Cortex/physiopathology ; Neural Pathways/drug effects ; Neural Pathways/physiopathology ; Neurons/drug effects ; Neurons/physiology ; Optogenetics ; Parkinson Disease/physiopathology
    Chemical Substances Antiparkinson Agents ; Levodopa (46627O600J)
    Language English
    Publishing date 2018-02-01
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 808167-0
    ISSN 1097-4199 ; 0896-6273
    ISSN (online) 1097-4199
    ISSN 0896-6273
    DOI 10.1016/j.neuron.2018.01.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Thyroid hormone rewires cortical circuits to coordinate body-wide metabolism and exploratory drive.

    Hochbaum, Daniel R / Dubinsky, Alexandra C / Farnsworth, Hannah C / Hulshof, Lauren / Kleinberg, Giona / Urke, Amanda / Wang, Wengang / Hakim, Richard / Robertson, Keira / Park, Canaria / Solberg, Alyssa / Yang, Yechan / Baynard, Caroline / Nadaf, Naeem M / Beron, Celia C / Girasole, Allison E / Chantranupong, Lynne / Cortopassi, Marissa / Prouty, Shannon /
    Geistlinger, Ludwig / Banks, Alexander / Scanlan, Thomas / Greenberg, Michael E / Boulting, Gabriella L / Macosko, Evan Z / Sabatini, Bernardo L

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Animals adapt to varying environmental conditions by modifying the function of their internal organs, including the brain. To be adaptive, alterations in behavior must be coordinated with the functional state of organs throughout the body. Here we find ... ...

    Abstract Animals adapt to varying environmental conditions by modifying the function of their internal organs, including the brain. To be adaptive, alterations in behavior must be coordinated with the functional state of organs throughout the body. Here we find that thyroid hormone- a prominent regulator of metabolism in many peripheral organs- activates cell-type specific transcriptional programs in anterior regions of cortex of adult mice via direct activation of thyroid hormone receptors. These programs are enriched for axon-guidance genes in glutamatergic projection neurons, synaptic regulators across both astrocytes and neurons, and pro-myelination factors in oligodendrocytes, suggesting widespread remodeling of cortical circuits. Indeed, whole-cell electrophysiology recordings revealed that thyroid hormone induces local transcriptional programs that rewire cortical neural circuits via pre-synaptic mechanisms, resulting in increased excitatory drive with a concomitant sensitization of recruited inhibition. We find that thyroid hormone bidirectionally regulates innate exploratory behaviors and that the transcriptionally mediated circuit changes in anterior cortex causally promote exploratory decision-making. Thus, thyroid hormone acts directly on adult cerebral cortex to coordinate exploratory behaviors with whole-body metabolic state.
    Language English
    Publishing date 2023-08-10
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.08.10.552874
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Remodeling of intrinsic cardiac neurons: effects of β-adrenergic receptor blockade in guinea pig models of chronic heart disease.

    Hardwick, Jean C / Southerland, E Marie / Girasole, Allison E / Ryan, Shannon E / Negrotto, Sara / Ardell, Jeffrey L

    American journal of physiology. Regulatory, integrative and comparative physiology

    2012  Volume 303, Issue 9, Page(s) R950–8

    Abstract: Chronic heart disease induces remodeling of cardiac tissue and associated neuronal components. Treatment of chronic heart disease often involves pharmacological blockade of adrenergic receptors. This study examined the specific changes in neuronal ... ...

    Abstract Chronic heart disease induces remodeling of cardiac tissue and associated neuronal components. Treatment of chronic heart disease often involves pharmacological blockade of adrenergic receptors. This study examined the specific changes in neuronal sensitivity of guinea pig intrinsic cardiac neurons to autonomic modulators in animals with chronic cardiac disease, in the presence or absence of adrenergic blockage. Myocardial infarction (MI) was produced by ligature of the coronary artery and associated vein on the dorsal surface of the heart. Pressure overload (PO) was induced by a banding of the descending dorsal aorta (∼20% constriction). Animals were allowed to recover for 2 wk and then implanted with an osmotic pump (Alzet) containing either timolol (2 mg·kg(-1)·day(-1)) or vehicle, for a total of 6-7 wk of drug treatment. At termination, intracellular recordings from individual neurons in whole mounts of the cardiac plexus were used to assess changes in physiological responses. Timolol treatment did not inhibit the increased sensitivity to norepinephrine seen in both MI and PO animals, but it did inhibit the stimulatory effects of angiotensin II on the norepinephrine-induced increases in neuronal excitability. Timolol treatment also inhibited the increase in synaptically evoked action potentials observed in PO animals with stimulation of fiber tract bundles. These results demonstrate that β-adrenergic blockade can inhibit specific aspects of remodeling within the intrinsic cardiac plexus. In addition, this effect was preferentially observed with active cardiac disease states, indicating that the β-receptors were more influential on remodeling during dynamic disease progression.
    MeSH term(s) Adrenergic Agonists/pharmacology ; Adrenergic beta-Antagonists/pharmacology ; Angiotensin II/pharmacology ; Animals ; Cholinergic Agents/pharmacology ; Chronic Disease ; Disease Models, Animal ; Evoked Potentials/drug effects ; Evoked Potentials/physiology ; Guinea Pigs ; Heart/innervation ; Heart Diseases/physiopathology ; Male ; Myocardial Infarction/physiopathology ; Neurons/drug effects ; Neurons/physiology ; Receptors, Adrenergic, beta/drug effects ; Receptors, Adrenergic, beta/physiology ; Timolol/pharmacology
    Chemical Substances Adrenergic Agonists ; Adrenergic beta-Antagonists ; Cholinergic Agents ; Receptors, Adrenergic, beta ; Angiotensin II (11128-99-7) ; Timolol (817W3C6175)
    Language English
    Publishing date 2012-08-29
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 603839-6
    ISSN 1522-1490 ; 0363-6119
    ISSN (online) 1522-1490
    ISSN 0363-6119
    DOI 10.1152/ajpregu.00223.2012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Angiotensin II potentiates adrenergic and muscarinic modulation of guinea pig intracardiac neurons.

    Girasole, Allison E / Palmer, Christopher P / Corrado, Samantha L / Marie Southerland, E / Ardell, Jeffrey L / Hardwick, Jean C

    American journal of physiology. Regulatory, integrative and comparative physiology

    2011  Volume 301, Issue 5, Page(s) R1391–9

    Abstract: The intrinsic cardiac plexus represents a major peripheral integration site for neuronal, hormonal, and locally produced neuromodulators controlling efferent neuronal output to the heart. This study examined the interdependence of norepinephrine, ... ...

    Abstract The intrinsic cardiac plexus represents a major peripheral integration site for neuronal, hormonal, and locally produced neuromodulators controlling efferent neuronal output to the heart. This study examined the interdependence of norepinephrine, muscarinic agonists, and ANG II, to modulate intrinsic cardiac neuronal activity. Intracellular voltage recordings from whole-mount preparations of the guinea pig cardiac plexus were used to determine changes in active and passive electrical properties of individual intrinsic cardiac neurons. Application of either adrenergic or muscarinic agonists induced changes in neuronal resting membrane potentials, decreased afterhyperpolarization duration of single action potentials, and increased neuronal excitability. Adrenergic responses were inhibited by removal of extracellular calcium ions, while muscarinic responses were inhibited by application of TEA. The adrenergic responses were heterogeneous, responding to a variety of receptor-specific agonists (phenylephrine, clonidine, dobutamine, and terbutaline), although α-receptor agonists produced the most frequent responses. Application of ANG II alone produced a significant increase in excitability, while application of ANG II in combination with either adrenergic or muscarinic agonists produced a much larger potentiation of excitability. The ANG II-induced modulation of firing was blocked by the angiotensin type 2 (AT(2)) receptor inhibitor PD 123319 and was mimicked by the AT(2) receptor agonist CGP-42112A. AT(1) receptor blockade with telmasartin did not alter neuronal responses to ANG II. These data demonstrate that ANG II potentiates both muscarinically and adrenergically mediated activation of intrinsic cardiac neurons, doing so primarily via AT(2) receptor-dependent mechanisms. These neurohumoral interactions may be fundamental to regulation of neuronal excitability within the intrinsic cardiac nervous system.
    MeSH term(s) Adrenergic Agonists/pharmacology ; Angiotensin II/metabolism ; Angiotensin Receptor Antagonists/pharmacology ; Animals ; Calcium/metabolism ; Electric Stimulation ; Guinea Pigs ; Heart/innervation ; In Vitro Techniques ; Male ; Membrane Potentials ; Muscarinic Agonists/pharmacology ; Neurons/drug effects ; Neurons/metabolism ; Potassium/metabolism ; Potassium Channel Blockers/pharmacology ; Receptor, Angiotensin, Type 1/drug effects ; Receptor, Angiotensin, Type 1/metabolism ; Receptor, Angiotensin, Type 2/drug effects ; Receptor, Angiotensin, Type 2/metabolism ; Receptors, Adrenergic/drug effects ; Receptors, Adrenergic/metabolism ; Receptors, Muscarinic/drug effects ; Receptors, Muscarinic/metabolism ; Time Factors
    Chemical Substances Adrenergic Agonists ; Angiotensin Receptor Antagonists ; Muscarinic Agonists ; Potassium Channel Blockers ; Receptor, Angiotensin, Type 1 ; Receptor, Angiotensin, Type 2 ; Receptors, Adrenergic ; Receptors, Muscarinic ; Angiotensin II (11128-99-7) ; Potassium (RWP5GA015D) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2011-08-24
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 603839-6
    ISSN 1522-1490 ; 0363-6119
    ISSN (online) 1522-1490
    ISSN 0363-6119
    DOI 10.1152/ajpregu.00145.2011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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