D2Dopamine Receptors in Striatal Medium Spiny Neurons Reduce L-Type Ca2+Currents and Excitability via a Novel PLCβ1–IP3–Calcineurin-Signaling Cascade

The functional anatomy of basal ganglia disorders

Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353

Molecular and Cellular Basis of Addiction

Nestler, E. J., & Aghajanian, G. K. (1997) · Science · doi:10.1126/science.278.5335.58 · Cited by 1,295

Regulation of Gene Expression in Hippocampal Neurons by Distinct Calcium Signaling Pathways

Bading, H., Ginty, D. D., & Greenberg, M. E. (1993) · Science · doi:10.1126/science.8097060 · Cited by 1,157

The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia

Gerfen, C. R. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.001441 · Cited by 1,004

Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens

Nicola, S. M., Surmeier, D. J., & Malenka, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.185 · Cited by 931

The Dopamine Hypothesis of Schizophrenia: A Review*

Meltzer, H. Y., & Stahl, S. M. (1976) · Schizophrenia Bulletin · doi:10.1093/schbul/2.1.19 · Cited by 883

Regulation of Phosphoinositide-specific Phospholipase C Isozymes

Rhee, S. G., & Bae, Y. S. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.24.15045 · Cited by 876

Calmodulin Is the Ca2+ Sensor for Ca2+-Dependent Inactivation of L-Type Calcium Channels

Peterson, B. Z., DeMaria, C. D., & Yue, D. T. (1999) · Neuron · doi:10.1016/s0896-6273(00)80709-6 · Cited by 856

The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons

Wilson, C. J., & Kawaguchi, Y. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-07-02397.1996 · Cited by 798

Coordinated Expression of Dopamine Receptors in Neostriatal Medium Spiny Neurons

Surmeier, D. J., Song, W., & Yan, Z. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06579.1996 · Cited by 762

Altered profile and D2-dopamine receptor modulation of high voltage-activated calcium current in striatal medium spiny neurons from animal models of Parkinson's disease

Martella, G., Madeo, G., Schirinzi, T., Tassone, A., Sciamanna, G., Spadoni, F., Stefani, A., Shen, J., Pisani, A., & Bonsi, P. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2010.12.057 · Cited by 16

Canadian Association of Neurosciences Review: The Role of Dopamine Receptor Function in Neurodegenerative Diseases

Lebel, M., Robinson, P., & Cyr, M. (2007) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100005746 · Cited by 16

The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R- and D2R-Like Dopamine Receptors

Ponce, G., Quiñones‐Lombraña, A., Martín-Palanco, N. G., Solsona, E. R., Jiménez‐Arriero, M. Á., Palomo, T., & Hoenicka, J. (2015) · Neurotoxicity Research · doi:10.1007/s12640-015-9545-9 · Cited by 16

Mechanism of dopamine D2 receptor-induced Ca2+ release in PC-12 cells

Frégeau, M., Carrier, M., & Guillemette, G. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.08.021 · Cited by 16

Voltage-Gated Ca2+ Channel Mediated Ca2+ Influx in Epileptogenesis

Siwek, M. S., Henseler, C., Broich, K., Papazoglou, A., & Weiergräber, M. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-2888-2_55 · Cited by 15

Dopamine D2 Receptor-Mediated Modulation of Rat Retinal Ganglion Cell Excitability

Yin, N., Yang, Y., Cheng, S., Wang, H., Hu, X. T., Miao, Y., Li, F., & Wang, Z. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00431-3 · Cited by 15

Section II. The Dopamine System

Smythies, J. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)64002-0 · Cited by 15

Opioid‐mediated modulation of calcium currents in striatal and pallidal neurons following reserpine treatment: Focus on kappa response

Spadoni, F., Martella, G., Martorana, A., Lavaroni, F., D’Angelo, V., Bernardi, G., & Stefani, A. (2003) · Synapse · doi:10.1002/syn.10294 · Cited by 15

Peripheral Antinociception Induced by Aripiprazole Is Mediated by the Opioid System

Ferreira, R. C. M., Almeida-Santos, A. F., Duarte, I. D. G., de Aguiar, D. C., Moreira, F. A., & Romero, T. R. L. (2017) · BioMed Research International · doi:10.1155/2017/8109205 · Cited by 14

Calcium currents in striatal fast-spiking interneurons: dopaminergic modulation of CaV1 channels

Rendón-Ochoa, E. A., Hernández-Flores, T., Avilés-Rosas, V. H., Cáceres-Chávez, V. A., Duhne, M., Laville, A., Tapia, D., Galarraga, E., & Bargas, J. (2018) · BMC Neuroscience · doi:10.1186/s12868-018-0441-0 · Cited by 13

A single spiking neuron that can represent interval timing: analysis, plasticity and multi-stability

Shouval, H. Z., & Gavornik, J. P. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0273-0 · Cited by 15

Activation of Phosphatidylinositol-Linked Novel D1 Dopamine Receptors Inhibits High-Voltage-Activated Ca2+ Currents in Primary Cultured Striatal Neurons

Ma, L.-Q., Liu, C., Wang, F., Xie, N., Gu, J. F., Fu, H. Q., Wang, J., Cai, F., Liu, J., & Chen, J. (2009) · Journal of Neurophysiology · doi:10.1152/jn.90345.2008 · Cited by 12

Effects of feedback delay on learning from positive and negative feedback in patients with Parkinson's disease off medication

Weismüller, B., Ghio, M., Logmin, K., Hartmann, C. J., Schnitzler, A., Pollok, B., Südmeyer, M., & Bellebaum, C. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.05.010 · Cited by 14

Activation of protein kinase C and inositol 1,4,5-triphosphate receptors antagonistically modulate voltage-gated sodium channels in striatal neurons

Hourez, R., Azdad, K., Vanwalleghem, G. C., Roussel, C., Gall, D., & Schiffmann, S. N. (2005) · Brain Research · doi:10.1016/j.brainres.2005.08.031 · Cited by 14

Acute nigro-striatal blockade alters cortico-striatal encoding: An in vivo electrophysiological study

Prosperetti, C., Giovanni, G. D., Stefani, A., Möller, J. C., & Galati, S. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.03.018 · Cited by 13

Aberrant learning in Parkinson's disease: A neurocomputational study on bradykinesia

Ursino, M., & Baston, C. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13960 · Cited by 13

L-type Ca2+ channel activity determines modulation of GABA release by dopamine in the substantia nigra reticulata and the globus pallidus of the rat

Recillas‐Morales, S., Sanchez‐Vega, L., Ochoa-Sánchez, N., Caballero-Florán, I. H., Paz‐Bermúdez, F. J., da Silva, I. J. S., Aceves, J., Erlij, D., & Florán, B. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.037 · Cited by 13

Characterising the developmental profile of human embryonic stem cell-derived medium spiny neuron progenitors and assessing mature neuron function using a CRISPR-generated human DARPP-32 WT/eGFP-AMP reporter line

Hunt, C. P. J., Pouton, C. W., & Haynes, J. M. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.01.003 · Cited by 13

Selective inhibition of phosphodiesterase 10A impairs appetitive and aversive conditioning and incentive salience attribution

Piccart, E., Langlois, X., Vanhoof, G., & D’Hooge, R. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.08.006 · Cited by 12

BK channels mediate dopamine inhibition of firing in a subpopulation of core nucleus accumbens medium spiny neurons

Ji, X., & Martin, G. E. (2014) · Brain Research · doi:10.1016/j.brainres.2014.09.015 · Cited by 12

Effects of local activation and blockade of dopamine D4 receptors in the spiking activity of the reticular thalamic nucleus in normal and in ipsilateral dopamine-depleted rats

Barrientos, R., Alatorre, A., Martínez-Escudero, J. R., Garcı́a-Ramı́rez, M., Oviedo-Chávez, A., Delgado, A., & Querejeta, E. (2019) · Brain Research · doi:10.1016/j.brainres.2019.01.042 · Cited by 12

Endogenous neurotensin attenuates dopamine-dependent locomotion and stereotypy

Chartoff, E. H., Szczypka, M. S., Palmiter, R. D., & Dorsa, D. M. (2004) · Brain Research · doi:10.1016/j.brainres.2004.06.061 · Cited by 12

The Role of Striatal Cav1.3 Calcium Channels in Therapeutics for Parkinson’s Disease

Caulfield, M. E., Manfredsson, F. P., & Steece‐Collier, K. (2023) · Handbook of experimental pharmacology · doi:10.1007/164_2022_629 · Cited by 13

Neurotransmitters regulate β cells insulin secretion: A neglected factor

Kong, C.-C., Cheng, J., & Wang, W. (2023) · World Journal of Clinical Cases · doi:10.12998/wjcc.v11.i28.6670 · Cited by 13

Dopaminergic Modulation of Spiny Neurons in the Turtle Striatum

Barral, J. A., Galarraga, E., Tapia, D., Flores-Barrera, E., Reyes, A., & Bargas, J. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9499-7 · Cited by 11

Modulation of Ca2+-currents by sequential and simultaneous activation of adenosine A1 and A2A receptors in striatal projection neurons

Hernández-González, O., Hernández-Flores, T., Prieto, G. A., Pérez‐Burgos, A., Arias-García, M. A., Galarraga, E., & Bargas, J. (2013) · Purinergic Signalling · doi:10.1007/s11302-013-9386-z · Cited by 11

Valproate attenuates dextroamphetamine-induced subjective changes more than lithium

Willson, M. C., Bell, E. C., Dave, S., Asghar, S., McGrath, B. M., & Silverstone, P. H. (2005) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2005.04.015 · Cited by 11

Dopamine-mediated calcium channel regulation in synaptic suppression in L. stagnalis interneurons

Dong, N., Lee, D. W. K., Sun, H., & Feng, Z. (2018) · Channels · doi:10.1080/19336950.2018.1457897 · Cited by 11

Chick RGS2L demonstrates concentration‐dependent selectivity for pertussis toxin‐sensitive and ‐insensitive pathways that inhibit L‐type Ca2+ channels

Tosetti, P., Parente, V., Taglietti, V., Dunlap, K., & Toselli, M. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.034439 · Cited by 11

Investigating cell-specific effects of FMRP deficiency on spiny projection neurons in a mouse model of Fragile X syndrome

Giua, G., Lassalle, O., Makrini, L., Valjent, E., Chavis, P., & Manzoni, O. J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1146647 · Cited by 9

Role of Endocannabinoid System in the Peripheral Antinociceptive Action of Aripiprazole

Ferreira, R. C. M., Almeida-Santos, A. F., Duarte, I. D. G., de Aguiar, D. C., Moreira, F. A., & Romero, T. R. L. (2018) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000003723 · Cited by 10

Inhibition of striatal dopamine release by the L‐type calcium channel inhibitor isradipine co‐varies with risk factors for Parkinson's

Brimblecombe, K. R., Connor‐Robson, N., Bataille, C. J. R., Roberts, B. M., Gracie, C. J., O’Connor, B., Naudé, R. T. W., Karthik, G., Russell, A. J., Wade‐Martins, R., et al. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16180 · Cited by 13

Tacrolimus, a specific inhibitor of calcineurin, modifies the locomotor activity of quinpirole, but not that of SKF82958, in male rats

Sakanoue, M., Mori, N., Takei, N., Kawai, M., Tani, K., Suzuki, K., Iwata, Y., Sekine, Y., Ashby, C. R., & Minabe, Y. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)01260-8 · Cited by 10

The Subthalamic Nucleus

Charpier, S., Beurrier, C., & Paz, J. T. (2010) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-374767-9.00015-9 · Cited by 10

Amphetamine injections into the nucleus accumbens affect neither acquisition/expression of conditioned fear nor baseline startle response

Schwienbacher, I., Fendt, M., & Schnitzler, H. (2004) · Experimental Brain Research · doi:10.1007/s00221-004-2160-2 · Cited by 9

State-dependent modulation of spiny projection neurons controls levodopa-induced dyskinesia in a mouse model of Parkinson’s disease

Zhai, S., Cui, Q., Wokosin, D. L., Sun, L., Tkatch, T., Crittenden, J. R., Graybiel, A. M., & Surmeier, D. J. (2025) · Science Advances · doi:10.1126/sciadv.adv8224 · Cited by 11

Histamine H3 receptor activation stimulates calcium mobilization in a subpopulation of rat striatal neurons in primary culture, but not in synaptosomes

Rivera-Ramírez, N., Montejo-López, W., López-Méndez, M.-C., Guerrero-Hernández, A., Molina‐Hernández, A., García-Hernández, U., & Arias‐Montaño, J. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.10.005 · Cited by 9

Dopaminergic Modulation of Striatal Inhibitory Transmission and Long-Term Plasticity

Nieto-Mendoza, E., & Hernández, E. (2015) · Neural Plasticity · doi:10.1155/2015/789502 · Cited by 9

Changes in cytoskeletal gene expression linked to MPTP-treatment in Mice

Cuadrado‐Tejedor, M., Sesma, M. T., Giménez‐Amaya, J. M., & Ortíz, L. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2005.05.014 · Cited by 9

Subregional Differences in Medium Spiny Neuron Intrinsic Excitability Properties between Nucleus Accumbens Core and Shell in Male Rats

Maria-Rios, C. E., Murphy, G. G., & Morrow, J. D. (2023) · eNeuro · doi:10.1523/eneuro.0432-22.2023 · Cited by 8

Association of PPP1R1B polymorphisms with working memory in healthy Han Chinese adults

Ma, H., Qiu, R., Zhang, W., Chen, X., Zhang, L., & Wang, M. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.989046 · Cited by 8

Downregulation of the cAMP/PKA Pathway in PC12 Cells Overexpressing NCS-1

Souza, B. R., Torres, K., de Miranda, D. M., Motta, B. S., Caetano, F., Rosa, D. V., de Souza, R. P., Giovani, A., Carneiro, D. S., Guimarães, M. M., et al. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9562-4 · Cited by 7

Diversity of Up-State Voltage Transitions During Different Network States

Vautrelle, N., Carrillo‐Reid, L., & Bargas, J. (2008) · Humana Press eBooks · doi:10.1007/978-1-60327-252-0_5 · Cited by 8

Distinct expression patterns of inwardly rectifying potassium currents in developing cerebellar granule cells of the hemispheres and the vermis

Brandalise, F., Luján, R., Leone, R., Lodola, F., Cesaroni, V., Romano, C., Gerber, U. R., & Rossi, P. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13219 · Cited by 8

L-type calcium channel gating is modulated by bradykinin with a PKC-dependent mechanism in NG108-15 cells

Toselli, M., & Taglietti, V. (2004) · European Biophysics Journal · doi:10.1007/s00249-004-0444-x · Cited by 8

In vitro functional characteristics of dopamine D2 receptor partial agonists in second and third messenger-based assays of cloned human dopamine D2Long receptor signalling

Jordan, S., Regardie, K., Johnson, J. L., Chen, R., Kambayashi, J., McQuade, R. D., Kitagawa, H., Tadori, Y., & Kikuchi, T. (2006) · Journal of Psychopharmacology · doi:10.1177/0269881106072090 · Cited by 8

Dopamine D3 receptor modulates D2 receptor effects on cAMP and GABA release at striatopallidal terminals—Modulation by the Ca 2+ –Calmodulin–CaMKII system

Villalobos‐Escobedo, F. S., Jijón‐Lorenzo, R., Ávalos‐Fuentes, J. A., Paz‐Bermúdez, F. J., Recillas‐Morales, S., Rojas, I. C., Leyva‐Gómez, G., Cortés, H., & Florán, B. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16237 · Cited by 7

Dopamine D 2 and Adenosine A 2A Receptors Interaction on Ca 2+ Current Modulation in a Rodent Model of Parkinsonism

Rendón-Ochoa, E. A., Padilla‐Orozco, M., Calderón, V., Avilés-Rosas, V. H., Hernández‐González, O., Hernández-Flores, T., Perez-Ramirez, M. B., Palomero‐Rivero, M., Galarraga, E., & Bargas, J. (2022) · ASN NEURO · doi:10.1177/17590914221102075 · Cited by 7

Understanding decision-making deficits in neurological conditions: insights from models of natural action selection

Frank, M. J., Scheres, A., & Sherman, S. J. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511731525.019 · Cited by 8

Dopamine D4 receptor modulates inhibitory transmission in pallido‐pallidal terminals and regulates motor behavior

Rojas, I. C., Acosta‐García, J., Caballero-Florán, R. N., Jijón‐Lorenzo, R., Recillas‐Morales, S., Ávalos‐Fuentes, J. A., Paz‐Bermúdez, F. J., Leyva‐Gómez, G., Cortés, H., & Florán, B. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15020 · Cited by 7

Inhibitory Effect of Apomorphine on Focal and Nonfocal Plasticity in the Human Motor Cortex

Fresnoza, S. M., Batsikadze, G., Müller, L. E., Rost, C., Chamoun, M., Paulus, W., Kuo, M., & Nitsche, M. A. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13050718 · Cited by 7

Cell–cell communication by Endocannabinoids during Immune Surveillance of the Central Nervous System

Ullrich, O., Schneider‐Stock, R., & Zipp, F. (2006) · Springer eBooks · doi:10.1007/400_015 · Cited by 7

L-type calcium channel blockade on haloperidol-induced c-Fos expression in the striatum

Lee, J., Rushlow, W. J., & Rajakumar, N. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.08.013 · Cited by 7

Erasing “bad memories”: reversing aberrant synaptic plasticity as therapy for neurological and psychiatric disorders

Shi, Z., Wen, K., Sammudin, N. H., LoRocco, N. C., & Zhuang, X. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03013-0 · Cited by 7

In VitroEffect and Mechanism of Action of Ergot Alkaloid Dihydroergocristine in Chemoresistant Prostate Cancer Cells

BAI, L., Li, X., Ma, X., ZHAO, R., & Wu, D. (2020) · Anticancer Research · doi:10.21873/anticanres.14626 · Cited by 6

Investigating the ligand agonism and antagonism at the D2long receptor by dynamic mass redistribution

Forster, L., & Pockes, S. (2022) · Scientific Reports · doi:10.1038/s41598-022-14311-w · Cited by 6

Neuroprotection in late life attention-deficit/hyperactivity disorder: A review of pharmacotherapy and phenotype across the lifespan

Dutta, C. N., Christov‐Moore, L., Ombao, H., & Douglas, P. K. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.938501 · Cited by 8

D1 and D2 Dopamine Receptor Modulation of Glutamatergic Signaling in Striatal Medium Spiny Neurons

Surmeier, D. J., Day, M., Gertler, T. S., Chan, C. S., & Shen, W. (2010) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-374767-9.00006-8 · Cited by 6

Autoreceptor preference of dopamine D2 receptor agonists correlates with preferential coupling to cyclic AMP

Mercier, D. W., Falardeau, P., & vesque, D. L. (2001) · Neuroreport · doi:10.1097/00001756-200105250-00036 · Cited by 6

Harmaline toxicity on dorsal striatal neurons and its role in tremor

Zhan, X., Do, L. V., Zou, L. B., Zhan, R. S., Jones, M., Nawaz, S., & Manaye, K. F. (2023) · NeuroToxicology · doi:10.1016/j.neuro.2023.10.005 · Cited by 5

Action Potential Firing Patterns Regulate Dopamine Release via Voltage‐Sensitive Dopamine D2 Autoreceptors in Mouse Striatum In Vivo

Sun, X., Yin, L., Qiao, Z., Younus, M., Chen, G., Wu, X., Li, J., Kang, X., Xu, H., Zhou, L., et al. (2024) · Advanced Science · doi:10.1002/advs.202412229 · Cited by 5

Quantitative Systems Pharmacology Development and Application in Neuroscience

Geerts, H. (2025) · Handbook of experimental pharmacology · doi:10.1007/164_2024_739 · Cited by 6

Consecutive treatments of methamphetamine promote the development of cardiac pathological symptoms in zebrafish

Zhang, J., Nguyen, A. H., Jilani, D., Torres, R. S. T., Schmiess-Heine, L., Le, T., Xia, X., & Cao, H. (2023) · PLoS ONE · doi:10.1371/journal.pone.0294322 · Cited by 5

Reward expectation and receipt differentially modulate the spiking of accumbens D1+ and D2+ neurons

Faust, T. W., Mohebi, A., & Berke, J. D. (2025) · Current Biology · doi:10.1016/j.cub.2025.02.007 · Cited by 8

Brain stimulation reward is altered by affecting dopamine–glutamate interactions in the central extended amygdala

Waraczynski, M. A., Zwifelhofer, W., & Kuehn, L. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.019 · Cited by 5

The Striatal Skeleton

Plenz, D., & Wickens, J. R. (2010) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-374767-9.00005-6 · Cited by 5

Coupling of D2R Short but not D2R Long receptor isoform to the Rho/ROCK signaling pathway renders striatal neurons vulnerable to mutant huntingtin

Galan‐Rodriguez, B., Martin, E., Brouillet, E., Déglon, N., Betuing, S., & Caboche, J. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13415 · Cited by 5

Modulation of High Voltage-Activated Calcium Channels by G Protein-Coupled Receptors

Beedle, A. M., & Zamponi, G. W. (2004) · Springer eBooks · doi:10.1007/978-1-4419-9254-3_10 · Cited by 5

Lactate dynamics in Parkinson’s disease: striatal circuit vulnerability, biomarker potential, and therapeutic windows

Kong, J., Yang, Z., Wang, Y., Liu, L., Liu, Y., & Chen, W. (2026) · Molecular Medicine · doi:10.1186/s10020-026-01551-z · Cited by 4

Catecholaminergic innervation and D2-like dopamine receptor-mediated modulation of brainstem nucleus incertus neurons in the rat

Szlaga, A., Sambak, P., Guguła, A., Trenk, A., Gundlach, A. L., & Błasiak, A. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109216 · Cited by 4

Quinpirole inhibits levodopa-induced dyskinesias at structural and behavioral levels: Efficacy negated by co-administration of isradipine

Collier, T. J., Begg, L. R., Stancati, J. A., Mercado, N. M., Sellnow, R. C., Sandoval, I. M., Sortwell, C. E., & Steece‐Collier, K. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114522 · Cited by 4

Dopamine and Memory

LaLumiere, R. T. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-408139-0.00005-5 · Cited by 4

Adaptive Gene Regulation in the Striatum of RGS9-Deficient Mice

Busse, K., Strotmann, R., Strecker, K., Wegner, F., Devanathan, V., Gohla, A., Schöneberg, T., & Schwarz, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092605 · Cited by 5

Spontaneous behaviour is shaped by dopamine in two ways

Khatib, D., & Morris, G. (2023) · Nature · doi:10.1038/d41586-023-00004-5 · Cited by 4

Regulation of Striatal Signaling by Protein Phosphatases

Girault, J., Greengard, P., & Nairn, A. C. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00029-5 · Cited by 5

Modulation of CaV1.3b L-type calcium channels by M1 muscarinic receptors varies with CaVβ subunit expression

Roberts-Crowley, M. L., & Rittenhouse, A. R. (2018) · BMC Research Notes · doi:10.1186/s13104-018-3783-x · Cited by 4

Deep brain stimulation: Anatomical, physiological, and computational mechanisms

Moyer, J. T., Danish, S. F., & Finkel, L. H. (2011) · Network Computation in Neural Systems · doi:10.3109/0954898x.2011.638356 · Cited by 4

Peering into the Dendritic Machinery of Striatal Medium Spiny Neurons

Surmeier, D. J., & Spruston, N. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.021 · Cited by 4

Deprenyl enhances the striatal neuronal damage produced by quinolinic acid

de Pablos, R. M., Herrera, A. J., Tomás‐Camardiel, M., Machado, A., & Cano, J. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.08.007 · Cited by 4

Neural Processing of Immediate versus Delayed Feedback in Action–Feedback and Stimulus–Feedback Associations

Röhlinger, M., Albrecht, C., Ghio, M., & Bellebaum, C. (2025) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.a.49 · Cited by 4

Dopamine receptors D1, D2, and D4 modulate electrical synapses and excitability in the thalamic reticular nucleus

Vaughn, M. J., Yellamelli, N., Burger, R. M., & Haas, J. S. (2024) · Journal of Neurophysiology · doi:10.1152/jn.00260.2024 · Cited by 2

Dopamine and Serotonin Crosstalk Within the Dopaminergic and Serotonergic Systems

Zhou, F.-M., & Dani, J. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-09622-3_9 · Cited by 3

CaV 1.3 channel blockade in the extended amygdala has a delayed effect on the reward efficacy of medial forebrain bundle stimulation

Waraczynski, M. A., Abbott, S., & Schultz, A. V. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.10.022 · Cited by 3

NMDA and Dopamine

Jocoy, E. L., Cepeda, C., Levine, M. S., & André, V. M. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch3 · Cited by 3

Cardiotoxic effects of methamphetamine associated with electrophysiological and epigenetic aberrations in zebrafishPreprint

Zhang, J., Nguyen, A. H., Schmiess-Heine, L., Le, T., Xia, X., Lau, M., Lee, J., & Cao, H. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.16.460189 · Cited by 3

Reward expectation selectively boosts the firing of accumbens D1+ neurons during motivated approachPreprint

Faust, T. W., Mohebi, A., & Berke, J. D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.02.556060 · Cited by 3

Distinct modes of dopamine modulation on striatopallidal synaptic transmission

Lee, Y. L., Reva, M., Kim, K. J., Kim, H.-J., Kim, Y., Cho, E., Jeong, M., Kwak, Y., Myung, K., Li, Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-71426-8 · Cited by 2

D2-like receptor activation does not initiate a brain docosahexaenoic acid signal in unanesthetized rats

Taha, A. Y., Chang, L., Chen, M., Rapoport, S. I., & Ramadan, E. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-113 · Cited by 2

Bruxism in patients of moderate to severe traumatic brain injury: Management results suggesting an etiological mechanism

Chaudhuri, P. (2014) · Indian Journal of Neurotrauma · doi:10.1016/j.ijnt.2014.02.002 · Cited by 2

Magnesium ions prevent the development of hyperkinesia evoked by administration of picrotoxin into the rat neostriatum

Yakimovskii, А. F., & Varshavskaya, V. M. (2007) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-007-0087-3 · Cited by 2

Characterization of ST14A Cells for Studying Modulation of Voltage-Gated Calcium Channels

Roberts-Crowley, M. L., & Rittenhouse, A. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132469 · Cited by 2

Electrophysiology of the Corticostriatal Network in Vivo

Pidoux, M., Mahon, S., & Charpier, S. (2011) · Frontiers in neuroscience · doi:10.1201/b11284-8 · Cited by 2

Dopaminergic Modulation of Glutamatergic Signaling in Striatal Spiny Projection Neurons

Shen, W., Plokin, J. L., Zhai, S., & Surmeier, D. J. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00009-x · Cited by 2

Endocannabinoid-Dependent Synaptic Plasticity in the Striatum

Atwood, B. K., & Lovinger, D. M. (2017) · Springer eBooks · doi:10.1007/978-3-319-57371-7_5 · Cited by 2

Dopaminergic Modulation of Glutamatergic Signaling in Striatal Medium Spiny Neurons

Shen, W., & Surmeier, D. J. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-333-6_7 · Cited by 2

Mitochondrial Dysfunction: A Key Player in the Pathogenesis of Autism Spectrum Disorders and Alzheimer’s Disease

Farhana, A., & Khan, Y. S. (2021) · Springer eBooks · doi:10.1007/978-981-16-4558-7_2 · Cited by 2

Reward

Schultz, W. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00059-2 · Cited by 3

Modulation of VGCCs by G-Protein Coupled Receptors and Their Second Messengers

Mark, M. D., Schwitalla, J. C., & Herlitze, S. (2022) · Springer eBooks · doi:10.1007/978-3-031-08881-0_7 · Cited by 2

Endogenous cannabinoids − a local message in and between the nervous and immune system

Ullrich, O., & Schneider‐Stock, R. (2005) · Signal Transduction · doi:10.1002/sita.200400043 · Cited by 2

Cellular Actions of Dopamine

Surmeier, D. J., & Calabresi, P. (2002) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-56051-4_11 · Cited by 2

Persistent Blood-giving

Biske, E. M. (1942) · BMJ · doi:10.1136/bmj.2.4260.266-c

Presynaptic Dopamine D2 Receptors Modulate [ 3 H]GABA Release at StriatoPallidal Terminals via Activation of PLC → IP3 → Calcineurin and Inhibition of AC → cAMP → PKA Signaling Cascades

Jijón‐Lorenzo, R., Caballero-Florán, I. H., Recillas‐Morales, S., Cortés, H., Ávalos‐Fuentes, J. A., Paz‐Bermúdez, F. J., Erlij, D., & Florán, B. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.12.041 · Cited by 27

Dopamine Receptor-mediated Ca2+ Signaling in Striatal Medium Spiny Neurons

Tang, T.-S., & Борисович, Б. И. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407389200 · Cited by 72

Striatal D2 Receptors Regulate Dendritic Morphology of Medium Spiny Neurons via Kir2 Channels

Cazorla, M., Shegda, M., Ramesh, B., Harrison, N. L., & Kellendonk, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6056-11.2012 · Cited by 105

S.11.05 Pharmacotherapy of stress related anxiety disorders

Kasper, S. F. (2007) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(07)70223-7