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1. Full Text Environmental Novelty Activates β2-Adrenergic Signaling to Prevent the Impairment of Hippocampal LTP by Aβ Oligomers
by Li, Shaomin and Jin, Ming and Zhang, Dainan and Yang, Ting and Koeglsperger, Thomas and Fu, Hongjun and Selkoe, Dennis J
Neuron, ISSN 0896-6273, 03/2013, Volume 77, Issue 5, pp. 929 - 941
A central question about human brain aging is whether cognitive enrichment slows the development of Alzheimer changes. Here, we show that prolonged exposure to... 
Immunohistochemistry | Synaptosomes - drug effects | Receptors, Adrenergic, beta-2 - physiology | Amyloid beta-Peptides - pharmacology | Humans | Hippocampus - drug effects | Receptors, Adrenergic, beta-2 - drug effects | Excitatory Postsynaptic Potentials - drug effects | Adrenergic beta-2 Receptor Agonists - pharmacology | Long-Term Potentiation - drug effects | Dendritic Spines - drug effects | Receptors, AMPA - genetics | Physical Conditioning, Animal | Receptors, AMPA - physiology | Synaptosomes - physiology | Mice, Inbred C57BL | Blotting, Western | Microscopy, Confocal | Amyloid beta-Peptides - antagonists & inhibitors | Patch-Clamp Techniques | Animals | Signal Transduction - drug effects | Cytosol - metabolism | Environment | Mice | Amyloid beta-Peptides - chemistry | In Vitro Techniques | Electrophysiological Phenomena - drug effects
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2. Full Text Ethanol-mediated facilitation of AMPA receptor function in the Dorsomedial striatum: Implications for alcohol drinking behavior
by Wang, Jun and Hamida, Sami Ben and Darcq, Emmanuel and Zhu, Wenheng and Gibb, Stuart L and Lanfranco, Maria Fe and Carnicella, Sebastien and Ron, Dorit
Journal of Neuroscience, ISSN 0270-6474, 10/2012, Volume 32, Issue 43, pp. 15124 - 15132
We found previously that acute ex vivo as well as repeated cycles of in vivo ethanol exposure and withdrawal, including excessive voluntary consumption of... 
DOPAMINE NEURONS | NR2B-CONTAINING NMDA RECEPTORS | LASTING ADAPTATIONS | BASAL GANGLIA | D-ASPARTATE RECEPTORS | DORSAL STRIATUM | LONG-TERM POTENTIATION | MEDIUM SPINY NEURONS | SYNAPTIC PLASTICITY | NEUROSCIENCES | PROTEIN-KINASE-II | Synaptosomes - drug effects | Sulpiride - pharmacology | Electric Stimulation | Rats, Long-Evans | Male | Synaptosomes - metabolism | Corpus Striatum - cytology | Excitatory Postsynaptic Potentials - drug effects | N-Methylaspartate - pharmacology | Central Nervous System Depressants - pharmacology | Quinoxalines - pharmacology | Self Administration | Conditioning, Operant - drug effects | Long-Term Potentiation - drug effects | Neurons - drug effects | Receptors, AMPA - metabolism | Animals, Newborn | Sucrose - administration & dosage | Choice Behavior - drug effects | Food Preferences - drug effects | Rats | Excitatory Amino Acid Agonists - pharmacology | Excitatory Amino Acid Antagonists - pharmacology | Rats, Sprague-Dawley | GABA Antagonists - pharmacology | Evoked Potentials - drug effects | Up-Regulation - drug effects | Ethanol - pharmacology | Patch-Clamp Techniques | Animals | Analysis of Variance | Dopamine Antagonists - pharmacology | alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology | Corpus Striatum - drug effects | Picrotoxin - pharmacology | In Vitro Techniques | Sweetening Agents - administration & dosage
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3. Full Text Pharmacology of novel synthetic stimulants structurally related to the "bath salts" constituent 3,4-methylenedioxypyrovalerone (MDPV)
by Marusich, Julie A and Antonazzo, Kateland R and Wiley, Jenny L and Blough, Bruce E and Partilla, John S and Baumann, Michael H
Neuropharmacology, ISSN 0028-3908, 2014, Volume 87, pp. 206 - 213
There has been a dramatic rise in the abuse of synthetic cathinones known as "bath salts," including 3,4-methylenedioxypyrovalerone (MDPV), an analog linked to... 
3,4-Methylenedioxypyrovalerone | Synthetic cathinones | α-PVP | Locomotor activity | Functional observational battery | Monoamine transporter | ANALOGS | RATS | LOCOMOTOR-ACTIVITY | MEPHEDRONE | CATHINONE DERIVATIVES | MONOAMINE TRANSPORTERS | NEUROSCIENCES | INTOXICATION | alpha-PVP | IN-VITRO | DOPAMINE | PHARMACOLOGY & PHARMACY | 2ND-GENERATION LEGAL HIGHS | Dopamine Plasma Membrane Transport Proteins - metabolism | Synaptosomes - drug effects | Central Nervous System Stimulants - pharmacology | Motor Activity - drug effects | Male | Synaptosomes - metabolism | Pyrrolidines - pharmacology | Dose-Response Relationship, Drug | Benzodioxoles - chemistry | Locomotion - drug effects | Designer Drugs - pharmacology | Catecholamine Plasma Membrane Transport Proteins - metabolism | Brain - physiopathology | Catecholamine Plasma Membrane Transport Proteins - antagonists & inhibitors | Benzazepines - pharmacology | Random Allocation | Pyrrolidines - chemistry | Rats, Sprague-Dawley | Mice, Inbred ICR | Brain - drug effects | Designer Drugs - chemistry | Animals | Dopamine Antagonists - pharmacology | Central Nervous System Stimulants - chemistry | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Street Drugs - pharmacology | Benzodioxoles - pharmacology | RNA-Binding Proteins - metabolism | Street Drugs - chemistry | Bath products | Resveratrol
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4. Full Text Dual control of dopamine synthesis and release by presynaptic and postsynaptic dopamine D2 receptors
by Anzalone, Andrea and Lizardi-Ortiz, José E and Ramos, Maria and De Mei, Claudia and Hopf, F. Woodward and Iaccarino, Ciro and Halbout, Briac and Jacobsen, Jacob and Kinoshita, Chisato and Welter, Marc and Caron, Marc G and Bonci, Antonello and Sulzer, David and Borrelli, Emiliana
Journal of Neuroscience, ISSN 0270-6474, 06/2012, Volume 32, Issue 26, pp. 9023 - 9024
Dysfunctions of dopaminergic homeostasis leading to either low or high dopamine (DA) levels are causally linked to Parkinson's disease, schizophrenia, and... 
MICE LACKING DOPAMINE-D-2 | TYROSINE-HYDROXYLASE ACTIVITY | KNOCK-OUT MICE | STRIATAL SYNAPTOSOMES | BASAL GANGLIA | IN-VIVO | CORTICOSTRIATAL TERMINALS | INHIBITORY CONTROL | DEFICIENT MICE | NEUROSCIENCES | NUCLEUS-ACCUMBENS | Tyrosine 3-Monooxygenase - metabolism | Chromatography, High Pressure Liquid - methods | Male | Neurons - cytology | Ventral Tegmental Area - cytology | RNA, Messenger - metabolism | Receptors, Dopamine D2 - metabolism | Excitatory Postsynaptic Potentials - drug effects | Substantia Nigra - cytology | Dose-Response Relationship, Drug | Phosphorylation - genetics | Synapses - metabolism | Dopamine Agents - pharmacology | Neurons - physiology | Phosphorylation - drug effects | Neurons - drug effects | Electric Stimulation - methods | Dopamine - metabolism | Excitatory Postsynaptic Potentials - genetics | Synapses - drug effects | Ventral Tegmental Area - drug effects | 3,4-Dihydroxyphenylacetic Acid - metabolism | Electrochemical Techniques | Presynaptic Terminals - drug effects | Mice, Inbred C57BL | Mice, Transgenic | Biophysics | Reaction Time - genetics | Mutation - genetics | Receptors, Dopamine D2 - genetics | Motor Activity - genetics | Patch-Clamp Techniques | Substantia Nigra - drug effects | Animals | Homovanillic Acid - metabolism | Analysis of Variance | Presynaptic Terminals - metabolism | Mice | Quinpirole - pharmacology | In Vitro Techniques
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5. Full Text The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain
by Nagai, Fumiko and Nonaka, Ryouichi and Satoh Hisashi Kamimura, Kanako
European Journal of Pharmacology, ISSN 0014-2999, 2007, Volume 559, Issue 2, pp. 132 - 137
We developed a reproducible, simple, and small-scale method for determining the re-uptake and release of monoamines (dopamine, serotonin (5-HT) and... 
Tryptamine | 5-MeO-DIPT | Piperazine | Methylone | 5-MeO-MIPT | MBDB | Psychoactive drug | AMT | Phenethylamine | Monoamines | 5-MeO-AMT | MECHANISM | NOREPINEPHRINE | TRANSPORTERS | piperazine | methylone | SEROTONIN RELEASE | COCAINE | psychoactive drug | NEUROTOXICITY | tryptamine | phenethylamine | ECSTASY | 3,4-METHYLENEDIOXYMETHAMPHETAMINE MDMA | DOPAMINE | PHARMACOLOGY & PHARMACY | STIMULANTS | monoamines | Synaptosomes - drug effects | Designer Drugs - pharmacology | Reproducibility of Results | Dopamine Uptake Inhibitors - pharmacology | Rats | Male | Biological Assay - methods | Synaptosomes - metabolism | Rats, Sprague-Dawley | Brain - drug effects | Brain - metabolism | Dose-Response Relationship, Drug | Animals | Norepinephrine - metabolism | Psychotropic Drugs - pharmacology | Serotonin - metabolism | Adrenergic Uptake Inhibitors - pharmacology | Synaptic Transmission - drug effects | Biogenic Monoamines - metabolism | In Vitro Techniques | Serotonin Uptake Inhibitors - pharmacology | Dopamine - metabolism | Psychotropic drugs | Drugs
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6. Full Text Pyridazine-derivatives Enhance Structural and Functional Plasticity of Tripartite Synapse Via Activation of Local Translation in Astrocytic Processes
by Foster, Joshua B and Zhao, Fangli and Wang, Xueqin and Xu, Zan and Lin, Chien-liang Glenn and Lin, Kuanhung and Askwith, Candice C and Hodgetts, Kevin J
Neuroscience, ISSN 0306-4522, 09/2018, Volume 388, pp. 224 - 238
Excitatory amino acid transporter 2 (EAAT2) is primarily located in perisynaptic astrocytic processes (PAP) where it plays a critical role in synaptic... 
pyridazine derivatives | tripartite synapse | synaptic plasticity | local translation | glutamate transporter EAAT2 | perisynaptic astrocytic processes | PERIPHERAL PROCESSES | C57BL/6J MICE | INCREASED EXPRESSION | ALZHEIMERS-DISEASE | GLIAL PLASMALEMMAL VESICLES | ACTIN-BINDING | AMYOTROPHIC-LATERAL-SCLEROSIS | NEUROSCIENCES | UP-REGULATION | GLT-1 | Synaptosomes - drug effects | Membrane Microdomains - metabolism | Neuronal Plasticity - drug effects | Proteome - drug effects | Neurons - cytology | Pyridazines - pharmacology | Synaptosomes - metabolism | RNA, Messenger - metabolism | Prosencephalon - drug effects | Neuronal Plasticity - physiology | Synapses - metabolism | Neurons - metabolism | Prosencephalon - metabolism | Neurons - drug effects | Astrocytes - cytology | Astrocytes - drug effects | Synapses - drug effects | Tissue Culture Techniques | Excitatory Amino Acid Transporter 2 - metabolism | Animals | Membrane Microdomains - drug effects | Prosencephalon - cytology | Central Nervous System Agents - pharmacology | Protein Biosynthesis - drug effects | Mice | Astrocytes - metabolism
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7. Full Text The P2X7 receptor antagonist Brilliant Blue G attenuates contralateral rotations in a rat model of Parkinsonism through a combined control of synaptotoxicity, neurotoxicity and gliosis
by Carmo, Marta R.S and Menezes, Ana Paula F and Nunes, Ana Carla L and Pliássova, Anna and Rolo, Anabela P and Palmeira, Carlos M and Cunha, Rodrigo A and Canas, Paula M and Andrade, Geanne M
Neuropharmacology, ISSN 0028-3908, 06/2014, Volume 81, pp. 142 - 152
Parkinson's disease (PD) involves an initial loss of striatal dopaminergic terminals evolving into a degeneration of dopaminergic neurons in the substantia... 
Neuroprotection | Parkinson's disease | Dopamine | Synaptotoxicity | Astrocytes | ATP | P2X7 receptor | Microglia | CEREBELLAR GRANULE NEURONS | EXTRACELLULAR ATP | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | ALZHEIMERS-DISEASE | PREVENTS ATP EXCITOTOXICITY | BRAIN SYNAPTOSOMES | NEUROSCIENCES | CEREBROCORTICAL NERVE-TERMINALS | ADENOSINE A(2A) RECEPTORS | PURINERGIC P2X RECEPTOR | IN-VIVO | PHARMACOLOGY & PHARMACY | Rats, Wistar | Rosaniline Dyes - therapeutic use | Motor Activity - drug effects | Male | Purinergic P2X Receptor Antagonists - pharmacology | Neurotoxicity Syndromes - drug therapy | Brain - metabolism | Parkinsonian Disorders - drug therapy | Reaction Time - drug effects | Exploratory Behavior - drug effects | Functional Laterality - drug effects | Purinergic P2X Receptor Antagonists - therapeutic use | Disease Models, Animal | Parkinsonian Disorders - physiopathology | Rats | Rosaniline Dyes - pharmacology | Parkinsonian Disorders - chemically induced | Maze Learning - drug effects | Brain - drug effects | Neurotoxicity Syndromes - etiology | Oxidopamine - toxicity | Animals | Memory Disorders - drug therapy | Memory Disorders - etiology | Cell Line, Tumor | Avoidance Learning - drug effects | Gliosis - drug therapy | Neurosciences | Hydroxylases | Cells | Index Medicus
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8. Evidence for the involvement of dopamine transporters in behavioral stimulant effects of modafinil
by Zolkowska, Dorota and Jain, Raka and Rothman, Richard B and Partilla, John S and Roth, Bryan L and Setola, Vincent and Prisinzano, Thomas E and Baumann, Michael H
Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 05/2009, Volume 329, Issue 2, pp. 738 - 746
Modafinil is prescribed for numerous medical conditions, but the drug's mechanism of action is unclear. Here, we examined the interaction of modafinil with... 
IN-VITRO | PROMOTING DRUG MODAFINIL | NOREPINEPHRINE TRANSPORTER | COCAINE DEPENDENCE | DOUBLE-BLIND | CONSCIOUS RAT | PHARMACOLOGY & PHARMACY | RELEASE | GBR12909 | AMPHETAMINE | NUCLEUS-ACCUMBENS | Methamphetamine - pharmacology | Dopamine Agonists - pharmacology | Dopamine Plasma Membrane Transport Proteins - metabolism | Synaptosomes - drug effects | Central Nervous System Stimulants - pharmacology | Nucleus Accumbens - metabolism | Motor Activity - drug effects | Rats | Male | Synaptosomes - metabolism | Rats, Sprague-Dawley | Dose-Response Relationship, Drug | Animals | Microdialysis | Amphetamine-Related Disorders - prevention & control | Protein Binding | Behavior, Animal - drug effects | Benzhydryl Compounds - pharmacology | Radioligand Assay | Nucleus Accumbens - drug effects | Binding Sites | Amphetamine-Related Disorders - metabolism | Index Medicus
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9. Full Text Calpain-2-mediated PTEN degradation contributes to BDNF-induced stimulation of dendritic protein synthesis
by Briz, Victor and Hsu, Yu-Tien and Li, Yi and Lee, Erin and Bi, Xiaoning and Baudry, Michel
Journal of Neuroscience, ISSN 0270-6474, 03/2013, Volume 33, Issue 10, pp. 4317 - 4328
Memory consolidation has been suggested to be protein synthesis dependent. Previous data indicate that BDNF-induced dendritic protein synthesis is a key event... 
HIPPOCAMPAL SLICES | MESSENGER-RNA TRANSLATION | ACTIVATION | CALPAIN | NEUROTROPHIC FACTOR | PHOSPHATIDYLINOSITOL 3-KINASE | KINASE | TUBEROUS SCLEROSIS | LONG-TERM POTENTIATION | SYNAPTIC PLASTICITY | NEUROSCIENCES | RNA, Small Interfering - genetics | Synaptosomes - drug effects | Calpain - metabolism | Nitriles - pharmacology | TOR Serine-Threonine Kinases - metabolism | Embryo, Mammalian | Male | Dendrites - ultrastructure | Green Fluorescent Proteins - genetics | Synaptosomes - metabolism | Calpain - genetics | Cerebral Cortex - cytology | Brain-Derived Neurotrophic Factor - pharmacology | Neurons - ultrastructure | Transfection | Phosphorylation - drug effects | Neurons - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Oxazines - pharmacology | Dendrites - drug effects | Dendrites - metabolism | Butadienes - pharmacology | Tumor Suppressor Proteins - metabolism | Dipeptides - pharmacology | Cells, Cultured | Enzyme Inhibitors - pharmacology | PTEN Phosphohydrolase - metabolism | Rats | Enzyme Activation - drug effects | Hippocampus - cytology | Rats, Sprague-Dawley | Animals | Tuberous Sclerosis Complex 2 Protein | Analysis of Variance | Signal Transduction - drug effects | Calcium-Calmodulin-Dependent Protein Kinase Kinase - metabolism | Protein Biosynthesis - drug effects | Tuberous Sclerosis Complex 1 Protein | Enzyme Activation - genetics | In Vitro Techniques | RNA, Small Interfering - metabolism
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10. Full Text The designer methcathinone analogs, mephedrone and methylone, are substrates for monoamine transporters in brain tissue
by Baumann, Michael H and Ayestas Jr, Mario A and Partilla, John S and Sink, Jacqueline R and Shulgin, Alexander T and Daley, Paul F and Brandt, Simon D and Rothman, Richard B and Ruoho, Arnold E and Cozzi, Nicholas V
Neuropsychopharmacology, ISSN 0893-133X, 04/2012, Volume 37, Issue 5, pp. 1192 - 1203
The nonmedical use of 'designer' cathinone analogs, such as 4-methylmethcathinone (mephedrone) and 3,4-methylenedioxymethcathinone (methylone), is increasing... 
serotonin (5-HT) | microdialysis | transporters | mesolimbic | dopamine | MDMA | NOREPINEPHRINE | PSYCHIATRY | CATHINONE | NEUROTOXICITY | NEUROSCIENCES | 4-METHYLMETHCATHINONE MEPHEDRONE | METABOLISM | DRUGS | 3,4-METHYLENEDIOXYMETHAMPHETAMINE | PHARMACOLOGY & PHARMACY | STIMULANT | Dopamine Plasma Membrane Transport Proteins - metabolism | Synaptosomes - drug effects | Microdialysis - methods | Nucleus Accumbens - metabolism | Male | Chromatography, High Pressure Liquid | Methamphetamine - chemistry | Dose-Response Relationship, Drug | N-Methyl-3,4-methylenedioxyamphetamine - pharmacology | Time Factors | Serotonin - pharmacokinetics | Methamphetamine - analogs & derivatives | Dopamine - metabolism | Locomotion - drug effects | Methamphetamine - pharmacology | Hallucinogens - pharmacology | 1-Methyl-4-phenylpyridinium - pharmacokinetics | Rats | Rats, Sprague-Dawley | Animals | Analysis of Variance | Membrane Transport Proteins | Serotonin - metabolism | Electrochemistry | Norepinephrine Plasma Membrane Transport Proteins - metabolism | In Vitro Techniques | Nucleus Accumbens - drug effects | Tritium - pharmacokinetics | mephedrone | release | methylone | serotonin | monoamine | Original | addiction and substance abuse
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11. Full Text Selective Activation of Cholinergic Interneurons Enhances Accumbal Phasic Dopamine Release: Setting the Tone for Reward Processing
by Cachope, Roger and Mateo, Yolanda and Mathur, Brian N and Irving, James and Wang, Hui-Ling and Morales, Marisela and Lovinger, David M and Cheer, Joseph F
Cell Reports, ISSN 2211-1247, 07/2012, Volume 2, Issue 1, pp. 33 - 41
Dopamine plays a critical role in motor control, addiction, and reward-seeking behaviors, and its release dynamics have traditionally been linked to changes in... 
H-3 DOPAMINE | PRESYNAPTIC NICOTINIC RECEPTORS | RAT STRIATUM | TONICALLY ACTIVE NEURONS | ACETYLCHOLINE | MIDBRAIN DOPAMINE | SYNAPTOSOMES | DIFFUSE TRANSMISSION | SUBUNIT COMPOSITION | CAUDATE | CELL BIOLOGY | Interneurons - physiology | Receptors, Nicotinic - metabolism | Cholinergic Neurons - metabolism | Nucleus Accumbens - metabolism | Interneurons - drug effects | Substrate Specificity | Male | Mice, Transgenic | Cholinergic Neurons - drug effects | Cholinergic Neurons - physiology | Up-Regulation - drug effects | Animals | Interneurons - metabolism | Receptors, Nicotinic - physiology | Models, Biological | Dopaminergic Neurons - metabolism | Mice | Reward | Nucleus Accumbens - drug effects | Receptors, Nicotinic - genetics | Dopamine - metabolism | Addiction
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12. Full Text Neuroadaptations in the cellular and postsynaptic group 1 metabotropic glutamate receptor mGluR5 and Homer proteins following extinction of cocaine self-administration
by Ghasemzadeh, M. Behnam and Vasudevan, Preethi and Mueller, Christopher and Seubert, Chad and Mantsch, John R
Neuroscience Letters, ISSN 0304-3940, 03/2009, Volume 452, Issue 2, pp. 167 - 171
This study examined the role of group1 metabotropic glutamate receptor mGluR5 and associated postsynaptic scaffolding protein Homer1b/c in behavioral... 
Nucleus accumbens | Scaffolding protein | Receptor trafficking | PSD-95 | Actin | Dorsal striatum | MEMBRANE | RATS | NEUROSCIENCES | DENSITY | RELAPSE | AMPA RECEPTORS | REINSTATEMENT | SEEKING BEHAVIOR | ANTAGONIST MPEP | WITHDRAWAL | Brain Chemistry - drug effects | Disks Large Homolog 4 Protein | Receptors, Metabotropic Glutamate - drug effects | Synaptosomes - drug effects | Synaptic Transmission - physiology | Intracellular Signaling Peptides and Proteins - drug effects | Nucleus Accumbens - metabolism | Actins - metabolism | Adaptation, Physiological - drug effects | Extinction, Psychological - drug effects | Neuronal Plasticity - drug effects | Actins - drug effects | Intracellular Signaling Peptides and Proteins - metabolism | Receptors, Metabotropic Glutamate - metabolism | Cocaine-Related Disorders - physiopathology | Synaptosomes - metabolism | Carrier Proteins - drug effects | Corpus Striatum - metabolism | Brain - metabolism | Self Administration | Cocaine-Related Disorders - metabolism | Neuronal Plasticity - physiology | Homer Scaffolding Proteins | Receptor, Metabotropic Glutamate 5 | Synaptic Transmission - drug effects | Membrane Proteins - metabolism | Extinction, Psychological - physiology | Disease Models, Animal | Nucleus Accumbens - physiopathology | Corpus Striatum - physiopathology | Dopamine Uptake Inhibitors - pharmacology | Presynaptic Terminals - drug effects | Brain - physiopathology | Adaptation, Physiological - physiology | Rats | Brain Chemistry - physiology | Brain - drug effects | Cocaine - pharmacology | Animals | Carrier Proteins - metabolism | Corpus Striatum - drug effects | Membrane Proteins - drug effects | Presynaptic Terminals - metabolism | Glutamic Acid - metabolism | Nucleus Accumbens - drug effects | Glutamate | Muscle proteins | Index Medicus | actin | dorsal striatum | scaffolding protein | receptor trafficking
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13. Full Text Effects of diet and insulin on dopamine transporter activity and expression in rat caudate‐putamen, nucleus accumbens, and midbrain
by Jones, Kymry T and Woods, Catherine and Zhen, Juan and Antonio, Tamara and Carr, Kenneth D and Reith, Maarten E. A
Journal of Neurochemistry, ISSN 0022-3042, 03/2017, Volume 140, Issue 5, pp. 728 - 740
Food restriction (FR) and obesogenic (OB) diets are known to alter brain dopamine transmission and exert opposite modulatory effects on behavioral... 
CFT | food restriction | insulin | dopamine uptake | rotating disk electrode voltammetry | obesity | CHRONIC FOOD RESTRICTION | SURFACE LOCALIZATION | ELECTRODE VOLTAMMETRIC MEASUREMENTS | CONDITIONED PLACE PREFERENCE | HIGH-FAT DIET | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUBSTANTIA-NIGRA | NEUROSCIENCES | IN-VITRO | D2 RECEPTOR | DORSAL STRIATUM | MESOLIMBIC DOPAMINE | Brain Chemistry - drug effects | Dopamine Plasma Membrane Transport Proteins - metabolism | Synaptosomes - drug effects | Body Weight | Caloric Restriction | Mesencephalon - metabolism | Nucleus Accumbens - metabolism | Male | Synaptosomes - metabolism | Receptors, Dopamine D2 - metabolism | Mesencephalon - drug effects | Dopamine - metabolism | Insulin - pharmacology | Biotinylation | Dopamine Plasma Membrane Transport Proteins - biosynthesis | Rats | Dopamine Plasma Membrane Transport Proteins - genetics | Putamen - drug effects | Rats, Sprague-Dawley | Caudate Nucleus - metabolism | Hypoglycemic Agents - pharmacology | Obesity - metabolism | Animals | Diet | Caudate Nucleus - drug effects | Nucleus Accumbens - drug effects | Putamen - metabolism | Phenols | Insulin | Neurochemistry | Dopamine | Adaptations | Brain | Drug abuse | Mesencephalon | Rotating disks | Nuclei | Putamen | Nucleus accumbens | Sensitivity | Food availability | Rodents | Dopamine transporter | Sensitivity enhancement | Dopamine D2 receptors | Tropane | Transporter | Dopamine receptors
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