Literature DB >> 26220941

A new knock-in mouse model of l-DOPA-responsive dystonia.

Samuel J Rose1, Xin Y Yu1, Ann K Heinzer2, Porter Harrast1, Xueliang Fan1, Robert S Raike1, Valerie B Thompson1, Jean-Francois Pare3, David Weinshenker4, Yoland Smith5, Hyder A Jinnah6, Ellen J Hess7.   

Abstract

Abnormal dopamine neurotransmission is associated with many different genetic and acquired dystonic disorders. For instance, mutations in genes critical for the synthesis of dopamine, including GCH1 and TH cause l-DOPA-responsive dystonia. Despite evidence that implicates abnormal dopamine neurotransmission in dystonia, the precise nature of the pre- and postsynaptic defects that result in dystonia are not known. To better understand these defects, we generated a knock-in mouse model of l-DOPA-responsive dystonia (DRD) mice that recapitulates the human p.381Q>K TH mutation (c.1141C>A). Mice homozygous for this mutation displayed the core features of the human disorder, including reduced TH activity, dystonia that worsened throughout the course of the active phase, and improvement in the dystonia in response to both l-DOPA and trihexyphenidyl. Although the gross anatomy of the nigrostriatal dopaminergic neurons was normal in DRD mice, the microstructure of striatal synapses was affected whereby the ratio of axo-spinous to axo-dendritic corticostriatal synaptic contacts was reduced. Microinjection of l-DOPA directly into the striatum ameliorated the dystonic movements but cerebellar microinjections of l-DOPA had no effect. Surprisingly, the striatal dopamine concentration was reduced to ∼1% of normal, a concentration more typically associated with akinesia, suggesting that (mal)adaptive postsynaptic responses may also play a role in the development of dystonia. Administration of D1- or D2-like dopamine receptor agonists to enhance dopamine signalling reduced the dystonic movements, whereas administration of D1- or D2-like dopamine receptor antagonists to further reduce dopamine signalling worsened the dystonia, suggesting that both receptors mediate the abnormal movements. Further, D1-dopamine receptors were supersensitive; adenylate cyclase activity, locomotor activity and stereotypy were exaggerated in DRD mice in response to the D1-dopamine receptor agonist SKF 81297. D2-dopamine receptors exhibited a change in the valence in DRD mice with an increase in adenylate cyclase activity and blunted behavioural responses after challenge with the D2-dopamine receptor agonist quinpirole. Together, our findings suggest that the development of dystonia may depend on a reduction in dopamine in combination with specific abnormal receptor responses.
© The Author (2015). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  corticostriatal; dopamine; striatum; trihexyphenidyl; tyrosine hydroxylase

Mesh:

Substances:

Year:  2015        PMID: 26220941      PMCID: PMC4627353          DOI: 10.1093/brain/awv212

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  74 in total

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2.  Targeted disruption of the tyrosine hydroxylase locus results in severe catecholamine depletion and perinatal lethality in mice.

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Authors:  B Lüdecke; P M Knappskog; P T Clayton; R A Surtees; J D Clelland; S J Heales; M P Brand; K Bartholomé; T Flatmark
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4.  Noradrenaline is essential for mouse fetal development.

Authors:  S A Thomas; A M Matsumoto; R D Palmiter
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Review 5.  Differential striatal spine pathology in Parkinson's disease and cocaine addiction: a key role of dopamine?

Authors:  R M Villalba; Y Smith
Journal:  Neuroscience       Date:  2013-07-16       Impact factor: 3.590

6.  Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene.

Authors:  P M Knappskog; T Flatmark; J Mallet; B Lüdecke; K Bartholomé
Journal:  Hum Mol Genet       Date:  1995-07       Impact factor: 6.150

7.  Dopamine-deficient mice are severely hypoactive, adipsic, and aphagic.

Authors:  Q Y Zhou; R D Palmiter
Journal:  Cell       Date:  1995-12-29       Impact factor: 41.582

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Authors:  Rajiv Devanagondi; Kiyoshi Egami; Mark S LeDoux; Ellen J Hess; H A Jinnah
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9.  Spatiotemporal pattern of striatal ERK1/2 phosphorylation in a rat model of L-DOPA-induced dyskinesia and the role of dopamine D1 receptors.

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Journal:  Biol Psychiatry       Date:  2007-07-26       Impact factor: 13.382

10.  Functional studies of tyrosine hydroxylase missense variants reveal distinct patterns of molecular defects in Dopa-responsive dystonia.

Authors:  Agnete Fossbakk; Rune Kleppe; Per M Knappskog; Aurora Martinez; Jan Haavik
Journal:  Hum Mutat       Date:  2014-06-03       Impact factor: 4.878

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2.  Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.

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3.  Parkinsonism without dopamine neuron degeneration in aged l-dopa-responsive dystonia knockin mice.

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Review 6.  The neurobiological basis for novel experimental therapeutics in dystonia.

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7.  Trihexyphenidyl rescues the deficit in dopamine neurotransmission in a mouse model of DYT1 dystonia.

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Review 8.  Defining research priorities in dystonia.

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10.  Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes.

Authors:  Natalie M Frederick; Parth V Shah; Alessandro Didonna; Monica R Langley; Anumantha G Kanthasamy; Puneet Opal
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