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1. Full Text Pharmacological validation of behavioural measures of akinesia and dyskinesia in a rat model of Parkinson's disease
by Lundblad, M and Andersson, M and Winkler, C and Kirik, D and Wierup, N and Cenci, M. A
European Journal of Neuroscience, ISSN 0953-816X, 01/2002, Volume 15, Issue 1, pp. 120 - 132
In an attempt to define clinically relevant models of akinesia and dyskinesia in 6‐hydroxydopamine (6‐OHDA)‐lesioned rats, we have examined the effects of... 
movement disorders | preclinical | circling | turning | stereotypies | Turning | Stereotypies | Preclinical | Circling | Movement disorders | CLOZAPINE | stereotypes | RECEPTOR BLOCKADE | LEVODOPA-INDUCED DYSKINESIAS | 6-HYDROXYDOPAMINE-INDUCED DEGENERATION | NEUROTROPHIC FACTOR | DOPA-INDUCED DYSKINESIAS | MEDIATED GENE-TRANSFER | NEUROSCIENCES | INTRASTRIATAL 6-HYDROXYDOPAMINE | MESSENGER-RNA | MPTP MONKEYS | Levodopa - pharmacology | Antiparkinson Agents - pharmacology | Dyskinesia, Drug-Induced - psychology | Stereotyped Behavior - drug effects | Motor Activity - drug effects | Rats | Bromocriptine - pharmacology | Rats, Sprague-Dawley | Rotation | Anti-Dyskinesia Agents - pharmacology | Gait - drug effects | Animals | Oxidopamine - pharmacology | Dyskinesia, Drug-Induced - drug therapy | Parkinson Disease, Secondary - psychology | Sympatholytics - pharmacology | Behavior, Animal - drug effects | Female | Parkinson Disease, Secondary - chemically induced | Index Medicus
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2. Full Text Vesicular Dopamine Release Elicits an Inhibitory Postsynaptic Current in Midbrain Dopamine Neurons
by Beckstead, Michael J and Grandy, David K and Wickman, Kevin and Williams, John T
Neuron, ISSN 0896-6273, 2004, Volume 42, Issue 6, pp. 939 - 946
Synchronous activation of dopamine neurons, for instance upon presentation of an unexpected rewarding stimulus, results in the release of dopamine from both... 
SYNAPTIC INPUTS | SUBSTANTIA-NIGRA NEURONS | DENDRO-DENDRITIC SYNAPSES | POTASSIUM CHANNELS | QUANTAL SIZE | FIRING PATTERN | MEMBRANE-PROPERTIES | DEFICIENT MICE | NEUROSCIENCES | MEDIATED VOLUME TRANSMISSION | VENTRAL TEGMENTAL AREA | Sulpiride - pharmacology | G Protein-Coupled Inwardly-Rectifying Potassium Channels | Mesencephalon - cytology | Calcium - metabolism | Male | Dose-Response Relationship, Drug | Dopamine Agents - pharmacology | Neurons - physiology | Organophosphorus Compounds - pharmacology | Reserpine - pharmacology | Female | Tetrodotoxin - pharmacology | Neurons - drug effects | Electric Stimulation - methods | Action Potentials - drug effects | Dopamine - metabolism | Levodopa - pharmacology | Dopamine Uptake Inhibitors - pharmacology | Mice, Inbred C57BL | Potassium Channels, Inwardly Rectifying | Sodium Channel Blockers - pharmacology | Iontophoresis - methods | Calcium Channel Blockers - pharmacology | Receptors, Dopamine D2 - genetics | GABA Antagonists - pharmacology | Mice, Knockout | Potassium Channels - genetics | Cocaine - pharmacology | Animals | Analysis of Variance | Dopamine Antagonists - pharmacology | Receptors, Dopamine D3 | Adrenergic Uptake Inhibitors - pharmacology | Mice | In Vitro Techniques | Neurons - radiation effects | Dose-Response Relationship, Radiation | Neural Inhibition - drug effects | Dopamine | Neurons | Experiments | Variance analysis | Rodents | Parkinsons disease | Index Medicus
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3. L-DOPA and behavior
by Malitz, Sidney
1972, 144
Psychotherapy | Dopa
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4. Full Text Glutamate spillover drives endocannabinoid production and inhibits GABAergic transmission in the Substantia Nigra pars compacta
by Freestone, Peter S and Guatteo, Ezia and Piscitelli, Fabiana and di Marzo, Vincenzo and Lipski, Janusz and Mercuri, Nicola B
Neuropharmacology, ISSN 0028-3908, 04/2014, Volume 79, pp. 467 - 475
Endocannabinoids (eCBs) modulate synaptic transmission in the brain, but little is known of their regulatory role in nigral dopaminergic neurons, and whether... 
Electrophysiology | Cannabinoids | Parkinson's disease | Synaptic transmission | Dopaminergic | ENDOGENOUS CANNABINOIDS | RAT | SYNAPTIC-TRANSMISSION | ANANDAMIDE | METABOTROPIC GLUTAMATE | DOPAMINERGIC-NEURONS | SELF-INHIBITION | RELEASE | NEUROSCIENCES | PHARMACOLOGY & PHARMACY | DIACYLGLYCEROL LIPASE | RECEPTORS | Endocannabinoids - metabolism | Synaptic Transmission - physiology | Rats, Wistar | Calcium - metabolism | Benzofurans - pharmacology | Receptors, Metabotropic Glutamate - metabolism | Piperidines - pharmacology | Dopamine Agents - pharmacology | Neurons - physiology | Cannabinoid Receptor Antagonists - pharmacology | Dopaminergic Neurons - drug effects | Dopaminergic Neurons - physiology | Synaptic Transmission - drug effects | Neurons - drug effects | Dopamine - metabolism | Guanosine Diphosphate - pharmacology | Pyrazoles - pharmacology | Levodopa - pharmacology | Dopamine - pharmacology | Inhibitory Postsynaptic Potentials - physiology | Rats | Thionucleotides - pharmacology | Arachidonic Acids - pharmacology | Receptor, Cannabinoid, CB1 - metabolism | Substantia Nigra - drug effects | Animals | Dopamine - analogs & derivatives | Guanosine Diphosphate - analogs & derivatives | Central Nervous System Agents - pharmacology | Glutamic Acid - metabolism | Receptor, Cannabinoid, CB1 - antagonists & inhibitors | In Vitro Techniques | Substantia Nigra - physiology | Inhibitory Postsynaptic Potentials - drug effects | Receptors, Metabotropic Glutamate - antagonists & inhibitors | GABA | Glutamate | Gross domestic product | Dopamine receptors | Index Medicus
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5. Full Text Benzo( α)pyrene-induced up-regulation of CYP1A2 gene expression: Role of adrenoceptor-linked signaling pathways
by Konstandi, Maria and Kostakis, Dimitris and Harkitis, Panagiotis and Johnson, Elizabeth O and Marselos, Marios and Adamidis, Konstadinos and Lang, Matti A and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för farmaceutisk biovetenskap and Uppsala universitet and Farmaceutiska fakulteten
Life Sciences, ISSN 0024-3205, 2006, Volume 79, Issue 4, pp. 331 - 341
CYP1A2, a principal catalyst for metabolism of various therapeutic drugs and carcinogens, among others, is in part regulated by the stress response. This study... 
Benzo( α)pyrene | Catecholamines | Adrenoceptors | Rat | CYP1A2 | Benzo(α)pyrene | benzo(alpha)pyrene | MEDICINE, RESEARCH & EXPERIMENTAL | catecholamines | rat | BIOACTIVATION | METABOLIC-ACTIVATION | CYTOCHROMES P-450 | ENZYMES | LIVER | PHARMACOLOGY & PHARMACY | HYDROCARBON RECEPTOR | adrenoceptors | RAT-BRAIN | STRESS | NORADRENALINE | Gene Expression Regulation, Enzymologic - drug effects | Up-Regulation | Catecholamines - metabolism | Rats, Wistar | Male | Adrenergic alpha-Antagonists - pharmacology | RNA, Messenger - metabolism | Prazosin - pharmacology | Cytochrome P-450 CYP1A2 - genetics | Sympatholytics - pharmacology | Reserpine - pharmacology | Dexmedetomidine - pharmacology | Benzo(a)pyrene - pharmacology | Oxidoreductases - biosynthesis | Levodopa - pharmacology | Signal Transduction | Oxidoreductases - genetics | Receptors, Adrenergic - metabolism | Rats | Animals | Cytochrome P-450 Enzyme System - biosynthesis | Cytochrome P-450 Enzyme System - genetics | Adrenergic Uptake Inhibitors - pharmacology | Adrenergic alpha-Agonists - pharmacology | Cytochromes | Guanethidine - pharmacology | Epinephrine - pharmacology | Index Medicus | Comparative Study | Reserpine/pharmacology | Cytochrome P-450 Enzyme System/biosynthesis/genetics | Receptors; Adrenergic/metabolism | Dexmedetomidine/pharmacology | Oxidoreductases/biosynthesis/genetics | Research Support; Non-U.S. Gov't | Epinephrine/pharmacology | Guanethidine/pharmacology | Gene Expression Regulation; Enzymologic/drug effects | Cytochrome P-450 CYP1A2/genetics | Rats; Wistar | RNA; Messenger/metabolism | Adrenergic alpha-Agonists/pharmacology | Prazosin/pharmacology | Benzo(a)pyrene/pharmacology | Sympatholytics/pharmacology | Adrenergic Uptake Inhibitors/pharmacology | Catecholamines/metabolism | Adrenergic alpha-Antagonists/pharmacology | Levodopa/pharmacology
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6. Full Text Pro‐oxidant effects of Ecstasy and its metabolites in mouse brain synaptosomes
by Barbosa, Daniel José and Capela, João Paulo and Oliveira, Jorge MA and Silva, Renata and Ferreira, Luísa Maria and Siopa, Filipa and Branco, Paula Sério and Fernandes, Eduarda and Duarte, José Alberto and de Lourdes Bastos, Maria and Carvalho, Félix
British Journal of Pharmacology, ISSN 0007-1188, 02/2012, Volume 165, Issue 4b, pp. 1017 - 1033
BACKGROUND AND PURPOSE 3,4-Methylenedioxymethamphetamine (MDMA or Ecstasy) is a worldwide major drug of abuse known to elicit neurotoxic effects. The... 
neurotoxicity | mitochondria | synaptosomes | 3,4‐methylenedioxymethamphetamine (MDMA or ‘Ecstasy’) | MDMA metabolites | monoamine oxidase | oxidative stress | 3,4-methylenedioxymethamphetamine (MDMA or 'Ecstasy') | INDUCED DOPAMINERGIC NEUROTOXICITY | ALPHA-METHYLDOPAMINE | ISOLATED RAT HEPATOCYTES | 4-methylenedioxymethamphetamine (MDMA or Ecstasy') | SEROTONERGIC NEUROTOXICITY | METHYLENEDIOXYMETHAMPHETAMINE MDMA | IN-VITRO MODEL | MONOAMINE-OXIDASE-B | PHARMACOLOGY & PHARMACY | HYDROGEN-PEROXIDE | PARKINSONS-DISEASE | Levodopa - pharmacology | Synaptosomes - drug effects | 3,4-Dihydroxyphenylacetic Acid - pharmacology | Brain - cytology | Hallucinogens - pharmacology | Glutathione - analogs & derivatives | Glutathione - metabolism | Synaptosomes - physiology | 3,4-Methylenedioxyamphetamine - pharmacology | Dopamine - pharmacology | Male | Antioxidants - pharmacology | Membrane Potential, Mitochondrial - drug effects | Protein Carbonylation - drug effects | Serotonin - pharmacology | Hydrogen Peroxide - metabolism | Glutathione - pharmacology | Animals | Mice | Oxidative Stress - drug effects | Deoxyepinephrine - analogs & derivatives | Deoxyepinephrine - pharmacology | Ecstasy | Neurotoxicity | Dopamine | Metabolites | Index Medicus | Research Papers | 3,4-methylenedioxymethamphetamine (MDMA or ‘Ecstasy’)
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7. Full Text Pharmacological manipulation of cortical inhibition in the dorsolateral prefrontal cortex
by Salavati, Bahar and Rajji, Tarek K and Zomorrodi, Reza and Blumberger, Daniel M and Chen, Robert and Pollock, Bruce G and Daskalakis, Zafiris J
Neuropsychopharmacology, ISSN 0893-133X, 2018, Volume 43, Issue 2, pp. 354 - 361
Cortical inhibition (CI) occurs largely through GABA receptor-mediated inhibitory neurotransmission, which can be modulated by cholinergic, dopaminergic, and... 
TMS-EEG | PSYCHIATRY | SCHIZOPHRENIA | GABA(B) RECEPTORS | FAST-SPIKING INTERNEURONS | NEUROSCIENCES | HUMAN MOTOR CORTEX | DEXTROMETHORPHAN | TRANSCRANIAL MAGNETIC STIMULATION | EXCITABILITY | NEURONS | DOPAMINE | PHARMACOLOGY & PHARMACY | Humans | Male | GABA-B Receptor Agonists - administration & dosage | Young Adult | Prefrontal Cortex - drug effects | Levodopa - administration & dosage | Dopamine Agents - pharmacology | Rivastigmine | GABA-B Receptor Agonists - pharmacology | Adult | Female | Dopamine Agents - administration & dosage | Baclofen - pharmacology | Levodopa - pharmacology | Dextromethorphan - pharmacology | Double-Blind Method | Excitatory Amino Acid Antagonists - administration & dosage | Excitatory Amino Acid Antagonists - pharmacology | Transcranial Magnetic Stimulation - methods | Electroencephalography - methods | Cross-Over Studies | Cholinesterase Inhibitors - administration & dosage | Cholinesterase Inhibitors - pharmacology | Neural Inhibition - drug effects | Dextromethorphan - administration & dosage | γ-Aminobutyric acid B receptors | Drugs | Dihydroxyphenylalanine | Cortex (prefrontal) | Transcranial magnetic stimulation | EEG | Dextromethorphan | Pharmacology | Electroencephalography | Drug screening | γ-Aminobutyric acid | Neurotransmitters | Blindness | Baclofen | Glutamatergic transmission | Levodopa | Inhibition | Dopa | Magnetic fields | Neurotransmission | Dopamine receptors | Index Medicus | Original
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8. Full Text Pharmacological profile of opicapone, a third‐generation nitrocatechol catechol‐O‐methyl transferase inhibitor, in the rat
by Bonifácio, M J and Torrão, L and Loureiro, A I and Palma, P N and Wright, L C and Soares‐da‐Silva, P
British Journal of Pharmacology, ISSN 0007-1188, 04/2015, Volume 172, Issue 7, pp. 1739 - 1752
Background and PurposeCatechol-O-methyltransferase (COMT) is an important target in the levodopa treatment of Parkinson's disease; however, the inhibitors... 
ENTACAPONE | METHYLTRANSFERASE INHIBITOR | PHARMACOKINETICS | EFFICACY | SAFETY | FLUCTUATIONS | TOLERABILITY | PHARMACOLOGY & PHARMACY | PHARMACODYNAMICS | TOLCAPONE | LEVODOPA | Antiparkinson Agents - pharmacology | Nitriles - pharmacology | Rats, Wistar | Catechol O-Methyltransferase Inhibitors - pharmacology | Humans | Benzophenones - pharmacology | Levodopa - pharmacokinetics | Male | Hepatocytes - metabolism | Membrane Potential, Mitochondrial - drug effects | Brain - metabolism | Catechol O-Methyltransferase - metabolism | Nitrophenols - pharmacology | Oxadiazoles - pharmacology | Adenosine Triphosphate - metabolism | Catechols - pharmacology | Oxadiazoles - pharmacokinetics | Hepatocytes - drug effects | Cell Survival - drug effects | Cells, Cultured | Levodopa - blood | Brain - drug effects | Animals | Models, Biological | Oxadiazoles - blood | Dopa | Catechin | Transferases | Parkinsons disease | Index Medicus
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9. Full Text Differential involvement of D1 and D2 dopamine receptors in L-DOPA-induced angiogenic activity in a Rat model of parkinson's disease
by Lindgren, Hanna S and Ohlin, K. Elisabet and Cenci, M. Angela and Basala gangliernas patofysiologi and Lund University and Basal Ganglia Pathophysiology and Lunds universitet
Neuropsychopharmacology, ISSN 0893-133X, 11/2009, Volume 34, Issue 12, pp. 2477 - 2488
Angiogenesis occurs in the brains of Parkinson's disease patients, but the effects of dopamine replacement therapy on this process have not been examined.... 
Angiogenesis | 6-OHDA | Blood-brain barrier | L-DOPA | Dopamine receptors | Dyskinesia | blood-brain barrier | ROTATIONAL BEHAVIOR | PSYCHIATRY | angiogenesis | BASAL GANGLIA | CEREBRAL GLUCOSE-UTILIZATION | dyskinesia | SUBSTANTIA-NIGRA | NEUROSCIENCES | AUTORADIOGRAPHIC LOCALIZATION | dopamine receptors | ADULT-RAT | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | INDUCED DYSKINESIA | PARS RETICULATA | ENDOTHELIAL GROWTH-FACTOR | Antiparkinson Agents - pharmacology | Aminoacetonitrile - analogs & derivatives | Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors | Oxidopamine | Receptors, Dopamine D2 - metabolism | Receptors, Dopamine D1 - metabolism | Protease Inhibitors - pharmacology | Dopamine Agents - pharmacology | Parkinsonian Disorders - drug therapy | Receptors, Dopamine D1 - agonists | Female | Neovascularization, Pathologic - physiopathology | Disease Models, Animal | Receptors, Dopamine D1 - antagonists & inhibitors | Levodopa - pharmacology | Parkinsonian Disorders - physiopathology | Receptors, Dopamine D2 - agonists | Rats | Bromocriptine - pharmacology | Parkinsonian Disorders - chemically induced | Benzazepines - pharmacology | Neovascularization, Pathologic - chemically induced | Basal Ganglia - physiology | Rats, Sprague-Dawley | Animals | Neovascularization, Pathologic - drug therapy | Basal Ganglia - blood supply | 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - pharmacology | Aminoacetonitrile - pharmacology | Dopamine D2 Receptor Antagonists | Salicylamides - pharmacology | Basal Ganglia - drug effects | Index Medicus | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
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10. Full Text Opicapone as an adjunct to levodopa in patients with Parkinson's disease and end-of-dose motor fluctuations: a randomised, double-blind, controlled trial
by Ferreira, Joaquim J, Prof and Lees, Andrew, Prof and Rocha, José-Francisco, BSc and Poewe, Werner, Prof and Rascol, Olivier, Prof and Soares-da-Silva, Patrício, Prof and Bi-Pk 1 Investigators and Bi-Park 1 investigators
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 2, pp. 154 - 165
Summary Background Opicapone is a novel, once-daily, potent third-generation catechol-O-methyltransferase inhibitor. We aimed to assess the safety and efficacy... 
Neurology | METHYLTRANSFERASE INHIBITORS | SYMPTOMS | SCALE | PHARMACOKINETICS | CLINICAL NEUROLOGY | LIFE | Oxadiazoles - administration & dosage | Antiparkinson Agents - pharmacology | Catechol O-Methyltransferase Inhibitors - administration & dosage | Nitriles - pharmacology | Outcome Assessment (Health Care) | Catechol O-Methyltransferase Inhibitors - pharmacology | Humans | Middle Aged | Male | Dyskinesia, Drug-Induced - prevention & control | Parkinson Disease - drug therapy | Nitriles - administration & dosage | Levodopa - administration & dosage | Oxadiazoles - pharmacology | Aged, 80 and over | Catechols - pharmacology | Adult | Female | Drug Therapy, Combination | Dyskinesia, Drug-Induced - etiology | Levodopa - pharmacology | Double-Blind Method | Europe | Antiparkinson Agents - adverse effects | Levodopa - adverse effects | Aged | Antiparkinson Agents - administration & dosage | Catechols - administration & dosage | Clinical trials | Medical colleges | Neurosciences | Catechin | Dopa | Transferases | Drug dosages | Parkinsons disease | Clinical medicine | Index Medicus
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11. Full Text Synergy between l-DOPA and a novel positive allosteric modulator of metabotropic glutamate receptor 4: Implications for Parkinson's disease treatment and dyskinesia
by Bennouar, Khaled-Ezaheir and Uberti, Michelle A and Melon, Christophe and Bacolod, Maria D and Jimenez, Hermogenes N and Cajina, Manuel and Kerkerian-Le Goff, Lydia and Doller, Darío and Gubellini, Paolo
Neuropharmacology, ISSN 0028-3908, 03/2013, Volume 66, pp. 158 - 169
Group III metabotropic glutamate (mGlu) receptors are localized in presynaptic terminals within basal ganglia (BG) circuitry that become hyperactive due to... 
Striatum | Basal ganglia | Akinesia | Rat | Lu AF21934 | l-DOPA-induced dyskinesia | Electrophysiology | HIGH-FREQUENCY STIMULATION | NEUROLOGICAL DISEASES | NEUROSCIENCES | RAT MODEL | STRIATAL SYNAPTIC PLASTICITY | MEDIATED MODULATION | SUBTHALAMIC NUCLEUS | UNILATERAL 6-HYDROXYDOPAMINE LESIONS | PHARMACOLOGY & PHARMACY | DEEP BRAIN-STIMULATION | L-DOPA-induced dyskinesia | MOLECULAR-MECHANISMS | Anilides - therapeutic use | Catalepsy - drug therapy | Synaptic Transmission - physiology | Excitatory Amino Acid Agonists - therapeutic use | Receptors, Metabotropic Glutamate - physiology | Male | Aminobutyrates - pharmacology | Anilides - pharmacokinetics | Parkinson Disease - drug therapy | Oxidopamine | Aminobutyrates - therapeutic use | Excitatory Postsynaptic Potentials - drug effects | Dose-Response Relationship, Drug | Excitatory Postsynaptic Potentials - physiology | Haloperidol - antagonists & inhibitors | Allosteric Regulation - physiology | Dyskinesia, Drug-Induced - drug therapy | Catalepsy - chemically induced | Synaptic Transmission - drug effects | Haloperidol - pharmacology | Disease Models, Animal | Allosteric Regulation - drug effects | Aminobutyrates - agonists | Levodopa - pharmacology | Cyclohexanecarboxylic Acids - therapeutic use | Phosphinic Acids - agonists | Levodopa - therapeutic use | Phosphinic Acids - therapeutic use | Rats | Excitatory Amino Acid Agonists - pharmacology | Rats, Sprague-Dawley | Drug Synergism | Animals | Cyclohexanecarboxylic Acids - pharmacology | Levodopa - adverse effects | Phosphinic Acids - pharmacology | Anilides - pharmacology | Excitatory Amino Acid Agonists - pharmacokinetics | Cyclohexanecarboxylic Acids - pharmacokinetics | Receptors, Metabotropic Glutamate - agonists | Receptors, Metabotropic Glutamate - antagonists & inhibitors | Physiological aspects | Phenols | Amino acids | Parkinson's disease | Glutamate | Drug therapy | Index Medicus | 6-Hydroxydopamine | Phosphinic Acids | Excitatory Amino Acid Agonists | Allosteric Regulation | Catalepsy | Haloperidol | Aminobutyrates | Cellular Biology | Synaptic Transmission | Receptors, Metabotropic Glutamate | Parkinson Disease | Anilides | Life Sciences | Excitatory Postsynaptic Potentials | Cyclohexanecarboxylic Acids | Dyskinesia, Drug-Induced | Levodopa
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12. Full Text In 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-Treated Primates, the Selective 5-Hydroxytryptamine 1a Agonist (R)-(+)-8-OHDPAT Inhibits Levodopa-Induced Dyskinesia but Only with\ Increased Motor Disability
by Mahmoud M. Iravani and Kayhan Tayarani-Binazir and Wing B. Chu and Michael J. Jackson and Peter Jenner
Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 12/2006, Volume 319, Issue 3, pp. 1225 - 1234
5-Hydroxytryptamine 1a (5-HT 1a ) receptor agonists, such as sarizotan and tandospirone, are reported to reduce levodopa-induced dyskinesia in... 
SARIZOTAN | STRIATAL DOPAMINE RELEASE | RAT STRIATUM | IN-VIVO | PHARMACOLOGY & PHARMACY | 5-HT1A RECEPTOR AGONIST | ANTAGONISTS | EXPRESSION | 8-OH-DPAT | BRAIN | PARKINSONS-DISEASE | 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine - pharmacology | Dopamine Agonists - pharmacology | Data Interpretation, Statistical | Levodopa - antagonists & inhibitors | Benzothiazoles - pharmacology | Callithrix | Receptors, Dopamine D2 - agonists | Motor Activity - drug effects | Male | Dyskinesia, Drug-Induced - prevention & control | Levodopa - toxicity | 8-Hydroxy-2-(di-n-propylamino)tetralin - pharmacology | Serotonin Antagonists - pharmacology | Piperazines - pharmacology | Serotonin Receptor Agonists - pharmacology | Receptor, Serotonin, 5-HT1A - drug effects | Animals | Female | Dopamine Agents - toxicity | Pyridines - pharmacology | Index Medicus
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