Dorsal striatal dopamine induces fronto-cortical hypoactivity and attenuates anxiety and compulsive behaviors in rats.


Journal

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
ISSN: 1740-634X
Titre abrégé: Neuropsychopharmacology
Pays: England
ID NLM: 8904907

Informations de publication

Date de publication:
01 2022
Historique:
received: 07 06 2021
accepted: 05 10 2021
revised: 27 09 2021
pubmed: 3 11 2021
medline: 3 3 2022
entrez: 2 11 2021
Statut: ppublish

Résumé

Dorsal striatal dopamine transmission engages the cortico-striato-thalamo-cortical (CSTC) circuit, which is implicated in many neuropsychiatric diseases, including obsessive-compulsive disorder (OCD). Yet it is unknown if dorsal striatal dopamine hyperactivity is the cause or consequence of changes elsewhere in the CSTC circuit. Classical pharmacological and neurotoxic manipulations of the CSTC and other brain circuits suffer from various drawbacks related to off-target effects and adaptive changes. Chemogenetics, on the other hand, enables a highly selective targeting of specific neuronal populations within a given circuit. In this study, we developed a chemogenetic method for selective activation of dopamine neurons in the substantia nigra, which innervates the dorsal striatum in the rat. We used this model to investigate effects of targeted dopamine activation on CSTC circuit function, especially in fronto-cortical regions. We found that chemogenetic activation of these neurons increased movement (as expected with increased dopamine release), rearings and time spent in center, while also lower self-grooming. Furthermore, this activation increased prepulse inhibition of the startle response in females. Remarkably, we observed reduced [

Identifiants

pubmed: 34725486
doi: 10.1038/s41386-021-01207-y
pii: 10.1038/s41386-021-01207-y
pmc: PMC8559920
doi:

Substances chimiques

Glutamic Acid 3KX376GY7L
Dopamine VTD58H1Z2X

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

454-464

Informations de copyright

© 2021. The Author(s), under exclusive licence to American College of Neuropsychopharmacology.

Références

Graybiel AM. The basal ganglia. Curr Biol. 2000;10:R509–11. https://doi.org/10.1016/s0960-9822(00)00593-5 .
Ahmari SE, Dougherty DD. Dissecting OCD circuits: from animal models to targeted treatments. Depress Anxiety. 2015;32:550–62.
pubmed: 25952989 pmcid: 4515165 doi: 10.1002/da.22367
Peters SK, Dunlop K, Downar J. Cortico-striatal-thalamic loop circuits of the salience network: a central pathway in psychiatric disease and treatment. Front Syst Neurosci. 2016;10:1–23.
doi: 10.3389/fnsys.2016.00104
Simpson EH, Kellendonk C. Insights About Striatal Circuit Function and Schizophrenia From a Mouse Model of Dopamine D2 Receptor Upregulation. Biol Psychiatry. 2017;81:21–30.
pubmed: 27720388 doi: 10.1016/j.biopsych.2016.07.004
Howes OD, Kapur S. The Dopamine Hypothesis of Schizophrenia: Version III—The Final Common Pathway. Schizophr Bull. 2009;35:549–62.
pubmed: 19325164 pmcid: 2669582 doi: 10.1093/schbul/sbp006
Denys D, de Vries F, Cath D, Figee M, Vulink N, Veltman DJ, et al. Dopaminergic activity in Tourette syndrome and obsessive-compulsive disorder. Eur Neuropsychopharmacol. 2013;23:1423–31.
pubmed: 23876376 doi: 10.1016/j.euroneuro.2013.05.012
Zuo C, Ma Y, Sun B, Peng S, Zhang H, Eidelberg D, et al. Metabolic Imaging of Bilateral Anterior Capsulotomy in Refractory Obsessive Compulsive Disorder: an FDG PET Study. J Cereb Blood Flow Metab. 2013;33:880–7.
pubmed: 23443174 pmcid: 3677106 doi: 10.1038/jcbfm.2013.23
Horwitz B, Swedo SE, Grady CL, Pietrini P, Schapiro MB, Rapoport JL, et al. Cerebral metabolic pattern in obsessive-compulsive disorder: Altered intercorrelations between regional rates of glucose utilization. Psychiatry Res Neuroimaging. 1991;40:221–37.
doi: 10.1016/0925-4927(91)90014-H
Menzies L, Chamberlain SR, Laird AR, Thelen SM, Sahakian BJ, Bullmore ET. Integrating evidence from neuroimaging and neuropsychological studies of obsessive-compulsive disorder: The orbitofronto-striatal model revisited. Neurosci Biobehav Rev. 2008;32:525–49.
pubmed: 18061263 doi: 10.1016/j.neubiorev.2007.09.005
Whiteside SP, Port JD, Abramowitz JS. A meta–analysis of functional neuroimaging in obsessive–compulsive disorder. Psychiatry Res Neuroimaging. 2004;132:69–79.
doi: 10.1016/j.pscychresns.2004.07.001
Haber SN. Corticostriatal circuitry. Dialogues Clin Neurosci. 2016;18:7–21.
pubmed: 27069376 pmcid: 4826773 doi: 10.31887/DCNS.2016.18.1/shaber
Aoki Y, Aoki A, Suwa H. Reduction of N-acetylaspartate in the medial prefrontal cortex correlated with symptom severity in obsessive-compulsive disorder: Meta-analyses of 1 H-MRS studies. Transl Psychiatry. 2012;2:e153–10.
pubmed: 22892718 pmcid: 3432192 doi: 10.1038/tp.2012.78
Rosenberg DR, Macmaster FP, Keshavan MS, Fitzgerald KD, Stewart CM, Moore GJ. Decrease in caudate glutamatergic concentrations in pediatric obsessive-compulsive disorder patients taking paroxetine. J Am Acad Child Adolesc Psychiatry. 2000;39:1096–103.
pubmed: 10986805 doi: 10.1097/00004583-200009000-00008
Rosenberg DR, Mirza Y, Russell A, Tang J, Smith JM, Banerjee SP, et al. Reduced anterior cingulate glutamatergic concentrations in childhood OCD and major depression versus healthy controls. J Am Acad Child Adolesc Psychiatry. 2004;43:1146–53.
pubmed: 15322418 doi: 10.1097/01.chi.0000132812.44664.2d
Palner M, Kjaerby C, Knudsen GM, Cumming P. Effects of unilateral 6-OHDA lesions on [3H]-N- propylnorapomorphine binding in striatum ex vivo and vulnerability to amphetamine-evoked dopamine release in rat. Neurochem Int. 2011;58:243–7.
pubmed: 21163313 doi: 10.1016/j.neuint.2010.12.007
Casteels C, Lauwers E, Bormans G, Baekelandt V, Van Laere K. Metabolic-dopaminergic mapping of the 6-hydroxydopamine rat model for Parkinson’s disease. Eur J Nucl Med Mol Imaging. 2008;35:124–34.
pubmed: 17906859 doi: 10.1007/s00259-007-0558-3
Sala-Bayo J, Fiddian L, Nilsson SRO, Hervig ME, McKenzie C, Mareschi A, et al. Dorsal and ventral striatal dopamine D1 and D2 receptors differentially modulate distinct phases of serial visual reversal learning. Neuropsychopharmacology. 2020;45:736–44.
pubmed: 31940660 pmcid: 7075980 doi: 10.1038/s41386-020-0612-4
Witten IB, Steinberg EE, Lee SY, Davidson TJ, Zalocusky KA, Brodsky M, et al. Recombinase-Driver Rat Lines: Tools, Techniques, and Optogenetic Application to Dopamine-Mediated Reinforcement. Neuron. 2011;72:721–33.
pubmed: 22153370 pmcid: 3282061 doi: 10.1016/j.neuron.2011.10.028
Roughan JV, Flecknell PA. Behavioural effects of laparotomy and analgesic effects of ketoprofen and carprofen in rats. Pain. 2001;90:65–74.
pubmed: 11166971 doi: 10.1016/S0304-3959(00)00387-0
Keller SH, L’Estrade EN, Dall B, Palner M, Herth M. Quantification accuracy of a new HRRT high throughput rat hotel using transmission-based attenuation correction: A phantom study. 2016 IEEE Nuclear Science Symposium, Medical Imaging Conference and Room-Temperature Semiconductor Detector Workshop (NSS/MIC/RTSD). 2016, pp. 1–3. https://doi.org/10.1109/NSSMIC.2016.8069467 .
Baerentzen S, Casado-Sainz A, Lange D, Shalgunov V, Tejada IM, Xiong M, et al. The chemogenetic receptor ligand Clozapine N-oxide induces in vivo neuroreceptor occupancy and reduces striatal glutamate levels. Front Neurosci. 2019;13:187.
pubmed: 31001069 pmcid: 6456655 doi: 10.3389/fnins.2019.00187
Hoenig K, Hochrein A, Quednow BB, Maier W, Wagner M. Impaired prepulse inhibition of acoustic startle in obsessive-compulsive disorder. Biol Psychiatry. 2005;57:1153–8.
pubmed: 15866555 doi: 10.1016/j.biopsych.2005.01.040
Ahmari SE, Risbrough VB, Geyer MA, Simpson HB. Impaired sensorimotor gating in unmedicated adults with obsessive-compulsive disorder. Neuropsychopharmacology. 2012;37:1216–23.
pubmed: 22218093 pmcid: 3306882 doi: 10.1038/npp.2011.308
Manning EE, Wang AY, Saikali LM, Winner AS, Ahmari SE. Disruption of prepulse inhibition is associated with compulsive behavior severity and nucleus accumbens dopamine receptor changes in Sapap3 knockout mice. Sci Rep. 2021;11:9442.
pubmed: 33941812 pmcid: 8093235 doi: 10.1038/s41598-021-88769-5
Armbruster BN, Li X, Pausch MH, Herlitze S, Roth BL. Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand. Proc Natl Acad Sci USA. 2007;104:5163–8.
pubmed: 17360345 pmcid: 1829280 doi: 10.1073/pnas.0700293104
Salegio EA, Samaranch L, Kells AP, Mittermeyer G, San Sebastian W, Zhou S, et al. Axonal transport of adeno-associated viral vectors is serotype-dependent. Gene Ther. 2013;20:348–52.
pubmed: 22418061 doi: 10.1038/gt.2012.27
Aschauer DF, Kreuz S, Rumpel S. Analysis of Transduction Efficiency, Tropism and Axonal Transport of AAV Serotypes 1, 2, 5, 6, 8 and 9 in the Mouse Brain. PLoS One. 2013;8:e76310.
pubmed: 24086725 pmcid: 3785459 doi: 10.1371/journal.pone.0076310
San Sebastian W, Samaranch L, Heller G, Kells AP, Bringas J, Pivirotto P, et al. Adeno-associated virus type 6 is retrogradely transported in the non-human primate brain. Gene Ther. 2013;20:1178–83.
pubmed: 24067867 doi: 10.1038/gt.2013.48
Szablowski JO, Lee-gosselin A, Lue B, Malounda D, Shapiro MG. Non-invasive control of neural circuits. Nat Biomed Eng. 2018;2:1–11.
doi: 10.1038/s41551-018-0258-2
Mahler SV, Brodnik ZD, Cox BM, Buchta WC, Bentzley BS, Cope ZA, et al. Chemogenetic manipulations of ventral tegmental area dopamine neurons reveal multifaceted roles in cocaine abuse. BioRxiv. 2018;39:503–18.
Cho J, Ryu S, Lee S, Kim J, Kim HI. Optimizing clozapine for chemogenetic neuromodulation of somatosensory cortex. Sci Rep. 2020;10:1–11.
Mimura K, Nagai Y, Inoue KI, Matsumoto J, Hori Y, Sato C, et al. Chemogenetic activation of nigrostriatal dopamine neurons in freely moving common marmosets. iScience. 2021;24:103066. https://doi.org/10.1016/j.isci.2021.103066 .
Sciolino NR, Plummer NW, Chen Y-W, Alexander GM, Robertson SD, Dudek SM, et al. Recombinase-Dependent Mouse Lines for Chemogenetic Activation of Genetically Defined Cell Types. Cell Rep. 2016;15:2563–73.
pubmed: 27264177 pmcid: 4915594 doi: 10.1016/j.celrep.2016.05.034
Dell’Anno MT, Caiazzo M, Leo D, Dvoretskova E, Medrihan L, Colasante G, et al. Remote control of induced dopaminergic neurons in parkinsonian rats. J Clin Investig. 2014;124:3215–29.
pubmed: 24937431 pmcid: 4071410 doi: 10.1172/JCI74664
Bonaventura J, Eldridge MAG, Hu F, Gomez JL, Sanchez-Soto M, Abramyan AM, et al. High-potency ligands for DREADD imaging and activation in rodents and monkeys. Nat Commun. 2019;10:4627. https://doi.org/10.1038/s41467-019-12236-z .
Runegaard AH, Fitzpatrick CM, Woldbye DPD, Andreasen JT, Sørensen AT, Gether U. Modulating dopamine signaling and behavior with chemogenetics: concepts, progress, and challenges. Pharm Rev. 2019;71:123–56.
pubmed: 30814274 doi: 10.1124/pr.117.013995
Jackson BP, Dietz SM, Wightman RM. Fast-scan cyclic voltammetry of 5-hydroxytryptamine. Anal Chem 1995;67:1115–20.
pubmed: 7717525 doi: 10.1021/ac00102a015
Wang S, Tan Y, Zhang JE, Luo M. Pharmacogenetic activation of midbrain dopaminergic neurons induces hyperactivity. Neurosci Bull. 2013;29:517–24.
pubmed: 23516143 pmcid: 5561950 doi: 10.1007/s12264-013-1327-x
Boender AJ, de Jong JW, Boekhoudt L, Luijendijk MCM, van der Plasse G, Adan RAH. Combined use of the canine adenovirus-2 and DREADD-technology to activate specific neural pathways in vivo. PLoS One. 2014;9:e95392.
pubmed: 24736748 pmcid: 3988196 doi: 10.1371/journal.pone.0095392
Prut L, Belzung C. The open field as a paradigm to measure the effects of drugs on anxiety-like behaviors: a review. Eur J Pharmacol. 2003;463:3–33.
pubmed: 12600700 doi: 10.1016/S0014-2999(03)01272-X
Carli M, Prontera C, Samanin R. Effect of 5-HT1A agonists on stress-induced deficit in open field locomotor activity of rats: Evidence that this model identifies anxiolytic-like activity. Neuropharmacology. 1989;28:471–6.
pubmed: 2566948 doi: 10.1016/0028-3908(89)90081-6
Sturman O, Germain PL, Bohacek J. Exploratory rearing: a context- and stress-sensitive behavior recorded in the open-field test. Stress. 2018;21:443–52.
pubmed: 29451062 doi: 10.1080/10253890.2018.1438405
Berridge KC, Aldridge JW. Super-stereotypy I: Enhancement of a complex movement sequence by systemic dopamine D1 agonists. Synapse. 2000;37:194–204.
pubmed: 10881041 doi: 10.1002/1098-2396(20000901)37:3<194::AID-SYN3>3.0.CO;2-A
Kalueff AV, Stewart AM, Song C, Berridge KC, Graybiel AM, Fentress JC. Neurobiology of rodent self-grooming and its value for translational neuroscience. Nat Rev Neurosci. 2016;17:45–59.
pubmed: 26675822 doi: 10.1038/nrn.2015.8
Ahmari SE, Spellman T, Douglass NL, Kheirbek MA, Simpson HB, Deisseroth K, et al. Repeated cortico-striatal stimulation generates persistent OCD-like behavior. Science. 2013;340:1234–9.
pubmed: 23744948 pmcid: 3954809 doi: 10.1126/science.1234733
Ramírez-Armenta KI, Alatriste-León H, Verma-Rodríguez AK, Llanos-Moreno A, Ramírez-Jarquín JO, Tecuapetla F. Optogenetic inhibition of indirect pathway neurons in the dorsomedial striatum reduces excessive grooming in Sapap3-knockout mice. Neuropsychopharmacology. 2021. https://doi.org/10.1038/s41386-021-01161-9 .
Lu J, Cheng Y, Xie X, Woodson K, Bonifacio J, Disney E, et al. Whole-Brain Mapping of Direct Inputs to Dopamine D1 and D2 Receptor-Expressing Medium Spiny Neurons in the Posterior Dorsomedial Striatum. Eneuro. 2020. https://doi.org/10.1523/ENEURO.0348-20.2020 .
Bubser M, Koch M. Prepulse inhibition of the acoustic startle response of rats is reduced by 6-hydroxydopamine lesions of the medial prefrontal cortex. Psychopharmacology. 1994;113:487–92.
pubmed: 7862864 doi: 10.1007/BF02245228
Zavitsanou K. Dopamine antagonists in the orbital prefrontal cortex reduce prepulse inhibition of the acoustic startle reflex in the rat. Pharm Biochem Behav. 1999;63:55–61.
doi: 10.1016/S0091-3057(98)00234-2
Bikovsky L, Hadar R, Soto-Montenegro ML, Klein J, Weiner I, Desco M, et al. Deep brain stimulation improves behavior and modulates neural circuits in a rodent model of schizophrenia. Exp Neurol. 2016;283:142–50.
pubmed: 27302677 pmcid: 5319857 doi: 10.1016/j.expneurol.2016.06.012
Rohleder C, Wiedermann D, Neumaier B, Drzezga A, Timmermann L, Graf R, et al. The Functional Networks of Prepulse Inhibition: Neuronal Connectivity Analysis Based on FDG-PET in Awake and Unrestrained Rats. Front Behav Neurosci. 2016;10:148.
pubmed: 27493627 pmcid: 4954847 doi: 10.3389/fnbeh.2016.00148
Swerdlow NR, Geyer MA, Braff DL. Neural circuit regulation of prepulse inhibition of startle in the rat: Current knowledge and future challenges. Psychopharmacology. 2001;156:194–215.
pubmed: 11549223 doi: 10.1007/s002130100799
Koch M, Fendt M, Kretschmer BD. Role of the substantia nigra pars reticulata in sensorimotor gating, measured by prepulse inhibition of startle in rats. Behav Brain Res. 2000;117:153–62.
pubmed: 11099769 doi: 10.1016/S0166-4328(00)00299-0
Ahmari SE, Risbrough VB, Geyer MA, Simpson HB. Prepulse inhibition deficits in obsessive-compulsive disorder are more pronounced in females. Neuropsychopharmacology. 2016;41:2963–4.
pubmed: 27818517 pmcid: 5101545 doi: 10.1038/npp.2015.363
Rodrigues S, Salum C, Ferreira TL. Dorsal striatum D1-expressing neurons are involved with sensorimotor gating on prepulse inhibition test. J Psychopharmacol. 2017. https://doi.org/10.1177/0269881116686879 .
Bortolato M, Aru GN, Fà M, Frau R, Orrù M, Salis P, et al. Activation of D1, but not D2 receptors potentiates dizocilpine-mediated disruption of prepulse inhibition of the startle. Neuropsychopharmacology. 2005;30:561–74.
pubmed: 15328529 doi: 10.1038/sj.npp.1300547
Geyer MA, Krebs-Thomson K, Braff DL, Swerdlow NR. Pharmacological studies of prepulse inhibition models of sensorimotor gating deficits in schizophrenia: a decade in review. Psychopharmacology (Berl). 2001;156:117–54. https://doi.org/10.1007/s002130100811 .
Weber M, Chang W-L, Breier MR, Yang A, Millan MJ, Swerdlow NR. The effects of the dopamine D2 agonist sumanirole on prepulse inhibition in rats. Eur Neuropsychopharmacol. 2010;20:421–5.
pubmed: 20346635 pmcid: 2864324 doi: 10.1016/j.euroneuro.2010.02.011
Plappert CF, Pilz PKD, Schnitzler H-U. Factors governing prepulse inhibition and prepulse facilitation of the acoustic startle response in mice. Behav Brain Res. 2004;152:403–12.
pubmed: 15196809 doi: 10.1016/j.bbr.2003.10.025
Swerdlow N. Discrepant findings of clozapine effects on prepulse inhibition of startle: is it the route or the rat? Neuropsychopharmacology. 1998;18:50–56.
pubmed: 9408918 doi: 10.1016/S0893-133X(97)00110-3
Faraday MM. Rat sex and strain differences in responses to stress. Physiol Behav. 2002;75:507–22.
pubmed: 12062315 doi: 10.1016/S0031-9384(02)00645-5
Lehmann J, Pryce CR, Feldon J. Sex differences in the acoustic startle response and prepulse inhibition in Wistar rats. Behav Brain Res. 1999;104:113–7.
pubmed: 11125729 doi: 10.1016/S0166-4328(99)00058-3
Tylš F, Páleníček T, Kadeřábek L, Lipski M, Kubešová A, Horáček J. Sex differences and serotonergic mechanisms in the behavioural effects of psilocin. Behav Pharmacol. 2016;27:309–20.
pubmed: 26461483 doi: 10.1097/FBP.0000000000000198
Baldan Ramsey LC, Xu M, Wood N, Pittenger C. Lesions of the dorsomedial striatum disrupt prepulse inhibition. Neuroscience. 2011;180:222–8.
pubmed: 21315809 doi: 10.1016/j.neuroscience.2011.01.041
Ilg AK, Enkel T, Bartsch D, Bähner F. Behavioral Effects of Acute Systemic Low-Dose Clozapine in Wild-Type Rats: Implications for the Use of DREADDs in Behavioral Neuroscience. Front Behav Neurosci. 2018;12:173. https://doi.org/10.3389/fnbeh.2018.00173 .
MacLaren DAA, Browne RW, Shaw JK, Krishnan Radhakrishnan S, Khare P, Espana RA, et al. Clozapine N-Oxide Administration Produces Behavioral Effects in Long-Evans Rats: Implications for Designing DREADD Experiments. ENeuro. 2016;3:219–16.
doi: 10.1523/ENEURO.0219-16.2016
Gomez JL, Bonaventura J, Lesniak W, Mathews WB, Sysa-shah P, Rodriguez LA, et al. Chemogenetics revealed: dreadd occupancy and activation via converted clozapine. Science. 2017;357:503–7.
pubmed: 28774929 pmcid: 7309169 doi: 10.1126/science.aan2475
De Carolis L, Stasi MA, Serlupi-Crescenzi O, Borsini F, Nencini P. The effects of clozapine on quinpirole-induced non-regulatory drinking and prepulse inhibition disruption in rats. Psychopharmacology. 2010;212:105–15.
pubmed: 20623106 doi: 10.1007/s00213-010-1937-1
Apetz N, Kordys E, Simon M, Mang B, Aswendt M, Wiedermann D, et al. Effects of subthalamic deep brain stimulation on striatal metabolic connectivity in a rat hemiparkinsonian model. Dis Model Mech. 2019;12:dmm039065. https://doi.org/10.1242/dmm.039065 .
Urban DJ, Zhu H, Marcinkiewcz CA, Michaelides M, Oshibuchi H, Rhea D, et al. Elucidation of The Behavioral Program and Neuronal Network Encoded by Dorsal Raphe Serotonergic Neurons. Neuropsychopharmacology. 2016;41:1404–15. https://doi.org/10.1038/npp.2015.293 . Epub 2015 Sep 18.
Michaelides M, Anderson SAR, Ananth M, Smirnov D, Thanos PK, Neumaier JF, et al. Whole-brain circuit dissection in free-moving animals reveals cell-specific mesocorticolimbic networks. J Clin Investig. 2013;123:5342–50.
pubmed: 24231358 pmcid: 3859392 doi: 10.1172/JCI72117
Servaes S, Glorie D, Verhaeghe J, Wyffels L, Stroobants S, Staelens S. [18F]-FDG PET neuroimaging in rats with quinpirole-induced checking behavior as a model for obsessive compulsive disorder. Psychiatry Res Neuroimaging. 2016;257:31–38.
pubmed: 27771554 doi: 10.1016/j.pscychresns.2016.10.003
Borghammer P, Cumming P, Aanerud J, Gjedde A. Artefactual subcortical hyperperfusion in PET studies normalized to global mean: Lessons from Parkinson’s disease. Neuroimage. 2009;45:249–57.
pubmed: 18718541 doi: 10.1016/j.neuroimage.2008.07.042
Moffett JR, Namboodiri MAA, Neale JH. Enhanced carbodiimide fixation for immunohistochemistry: Application to the comparative distributions of N-acetylaspartylglutamate and N- acetylaspartate immunoreactivities in rat brain. J Histochem Cytochem. 1993;41:559–70.
pubmed: 8450195 doi: 10.1177/41.4.8450195
Bak LK, Schousboe A, Waagepetersen HS. The glutamate/GABA-glutamine cycle: aspects of transport, neurotransmitter homeostasis and ammonia transfer. J Neurochem. 2006;98:641–53.
pubmed: 16787421 doi: 10.1111/j.1471-4159.2006.03913.x
Agarwal N, Renshaw PF. Proton MR spectroscopy - Detectable major neurotransmitters of the brain: Biology and possible clinical applications. Am J Neuroradiol. 2012;33:595–602.
pubmed: 22207303 pmcid: 4627491 doi: 10.3174/ajnr.A2587
Zhao J, Ramadan E, Cappiello M, Wroblewska B, Bzdega T, Neale JH. NAAG inhibits KCl-induced [3H]-GABA release via mGluR3, cAMP, PKA and L-type calcium conductance. Eur J Neurosci. 2001;13:340–6.
pubmed: 11168538
Sulzer D, Joyce MP, Lin L, Geldwert D, Haber SN, Hattori T, et al. Dopamine neurons make glutamatergic synapses in vitro. J Neurosci. 1998;18:4588–602.
pubmed: 9614234 pmcid: 6792695 doi: 10.1523/JNEUROSCI.18-12-04588.1998
Trudeau LÉ. Glutamate co-transmission as an emerging concept in monoamine neuron function. J Psychiatry Neurosci. 2004;29:296–310.
pubmed: 15309046 pmcid: 446224
Joo YH, Kim YK, Choi IG, Kim HJ, Son YD, Kim HK, et al. In vivo glucose metabolism and glutamate levels in mGluR5 knockout mice: a multimodal neuroimaging study using [18F]FDG microPET and MRS. EJNMMI Res. 2020;10:116. https://doi.org/10.1186/s13550-020-00716-z .
Wang Z, Maia TV, Marsh R, Colibazzi T, Gerber A, Peterson BS. The neural circuits that generate tics in Tourette’s syndrome. Am J Psychiatry. 2011;168:1326–37.
pubmed: 21955933 pmcid: 4246702 doi: 10.1176/appi.ajp.2011.09111692
Figee M, Luigjes J, Smolders R, Valencia-Alfonso CE, Van Wingen G, De, et al. Deep brain stimulation restores frontostriatal network activity in obsessive-compulsive disorder. Nat Neurosci. 2013;16:386–7.
pubmed: 23434914 doi: 10.1038/nn.3344
Nordstrom EJ, Bittner KC, McGrath MJ, Parks CR, Burton FH. Hyperglutamatergic cortico-striato-thalamo-cortical circuit breaker drugs alleviate tics in a transgenic circuit model of Tourette’s syndrome. Brain Res. 2015;1629:38–53.
pubmed: 26453289 doi: 10.1016/j.brainres.2015.09.032
Ceccherini-Nelli A, Guazzelli M. Treatment of refractory OCD with the dopamine agonist bromocriptine. J Clin Psychiatry. 1994;55:415–6.
pubmed: 7929024

Auteurs

Agata Casado-Sainz (A)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Frederik Gudmundsen (F)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Simone L Baerentzen (SL)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Denise Lange (D)

Department of Sleep and Human Factors Research, Institute of Aerospace Medicine, German Aerospace Center (DLR), Cologne, Germany.

Annemette Ringsted (A)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Isabel Martinez-Tejada (I)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Siria Medina (S)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Hedok Lee (H)

Department of Anesthesiology and Pediatric Anesthesiology, Yale University, New Haven, CT, USA.

Claus Svarer (C)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Sune H Keller (SH)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Martin Schain (M)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Celia Kjaerby (C)

Center for Translational Neuromedicine, University of Copenhagen, Copenhagen, Denmark.

Patrick M Fisher (PM)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark.

Paul Cumming (P)

Department of Nuclear Medicine, Bern University Hospital, Bern, Switzerland.
School of Psychology and Counselling, Queensland University of Technology, Brisbane, QLD, Australia.

Mikael Palner (M)

Neurobiology Research Unit, Copenhagen University Hospital, Copenhagen, Denmark. mikael.palner@nru.dk.
Clinical Physiology and Nuclear Medicine, Department of Clinical Research, University of Southern Denmark, Odense, Denmark. mikael.palner@nru.dk.
Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark. mikael.palner@nru.dk.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH