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Pharmacological Reviews, ISSN 0031-6997, 09/2011, Volume 63, Issue 3, pp. 585 - 640
The neurotransmitter transporters (NTTs) belonging to the solute carrier 6 (SLC6) gene family (also referred to as the neurotransmitter-sodium-symporter family... 
BIOGENIC-AMINE TRANSPORTERS | TRANSMEMBRANE DOMAIN-I | PROTEIN-KINASE-C | CYSTEINE-SCANNING MUTAGENESIS | HUMAN DOPAMINE TRANSPORTER | PHARMACOLOGY & PHARMACY | GAMMA-AMINOBUTYRIC-ACID | MAJOR DEPRESSIVE DISORDER | HUMAN NOREPINEPHRINE TRANSPORTER | GABA UPTAKE INHIBITORS | HUMAN SEROTONIN TRANSPORTER | Amino Acid Transport Systems, Neutral - chemistry | Membrane Microdomains - metabolism | Humans | Plasma Membrane Neurotransmitter Transport Proteins - antagonists & inhibitors | Molecular Targeted Therapy | Nerve Tissue Proteins - chemistry | Protein Isoforms - metabolism | Protein Isoforms - agonists | Protein Isoforms - chemistry | Synaptic Transmission - drug effects | Neurons - metabolism | Neurons - drug effects | Nerve Tissue Proteins - antagonists & inhibitors | Amino Acid Transport Systems, Neutral - agonists | Nerve Tissue Proteins - agonists | Plasma Membrane Neurotransmitter Transport Proteins - agonists | Amino Acid Transport Systems, Neutral - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - metabolism | Organ Specificity | Protein Transport | Nerve Tissue Proteins - metabolism | Animals | Ligands | Plasma Membrane Neurotransmitter Transport Proteins - chemistry | Protein Processing, Post-Translational | Protein Isoforms - antagonists & inhibitors | Amino Acid Transport Systems, Neutral - antagonists & inhibitors
Journal Article
Science, ISSN 0036-8075, 9/2007, Volume 317, Issue 5843, pp. 1390 - 1393
Tricyclic antidepressants exert their pharmacological effect--inhibiting the reuptake of serotonin, norepinephrine, and dopamine--by directly blocking... 
Molecules | Salts | Neurotransmitters | Antidepressants | Reuptake | Serotonin plasma membrane transport proteins | Neurotransmitter transport proteins | Reports | Pharmacology | Inhibitory concentration 50 | Crystal structure | SENSITIVE DOPAMINE TRANSPORTER | NOREPINEPHRINE TRANSPORTERS | MULTIDISCIPLINARY SCIENCES | ION-BINDING | MONOAMINE TRANSPORTERS | SEROTONIN | INHIBITORS | Dopamine - chemistry | Antidepressive Agents, Tricyclic - metabolism | Caenorhabditis elegans Proteins - chemistry | Humans | Bacterial Proteins - chemistry | Caenorhabditis elegans Proteins - metabolism | Molecular Sequence Data | Crystallography, X-Ray | Serotonin - chemistry | Dopamine Uptake Inhibitors - metabolism | Drosophila Proteins - metabolism | Antidepressive Agents, Tricyclic - chemistry | Neurotransmitter Uptake Inhibitors - metabolism | Desipramine - metabolism | Conserved Sequence | Binding Sites | Dopamine - metabolism | Serotonin Uptake Inhibitors - metabolism | Amino Acid Sequence | Cell Line | Leucine - metabolism | Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors | Models, Molecular | Serotonin Uptake Inhibitors - chemistry | Drosophila Proteins - chemistry | Plasma Membrane Neurotransmitter Transport Proteins - metabolism | Leucine - chemistry | Sequence Homology, Amino Acid | Animals | Norepinephrine - metabolism | Desipramine - chemistry | Neurotransmitter Uptake Inhibitors - chemistry | Norepinephrine - chemistry | Serotonin - metabolism | Dopamine Uptake Inhibitors - chemistry | Protein Binding | Bacterial Proteins - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - chemistry | Protein Conformation | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Norepinephrine Plasma Membrane Transport Proteins - chemistry | Leucine | Structure | Desipramine | Health aspects | Antidepressants, Tricyclic | Inhibitor drugs | Psychiatry | Binding sites
Journal Article
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
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 2014, Volume 19, Issue 6, pp. 688 - 698
Pharmacologic blockade of monoamine oxidase A (MAOA) or serotonin transporter (5-HTT) has antidepressant and anxiolytic efficacy in adulthood. Yet, genetically... 
anxiety | development | serotonin | aggression | depression | dopamine | BRAIN-SEROTONIN | RHESUS-MONKEYS | PSYCHIATRY | ENVIRONMENT INTERACTIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEFICIENT MICE | NEUROSCIENCES | GENE | SOMATOSENSORY CORTEX | MONOAMINE-OXIDASE-A | TRANSPORTER KNOCKOUT MICE | DORSAL RAPHE NUCLEUS | Aggression - physiology | Dopamine Plasma Membrane Transport Proteins - metabolism | Depression - physiopathology | Male | Brain - growth & development | Mice, 129 Strain | Brain - physiology | Dopaminergic Neurons - drug effects | Dopaminergic Neurons - physiology | Female | Dopamine - metabolism | Affect - drug effects | 3,4-Dihydroxyphenylacetic Acid - metabolism | Affect - physiology | Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors | Amphetamine - pharmacology | Anxiety - physiopathology | Brain - drug effects | Dopamine Plasma Membrane Transport Proteins - antagonists & inhibitors | Serotonin Plasma Membrane Transport Proteins - metabolism | Animals | Serotonin - metabolism | Central Nervous System Agents - pharmacology | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Aggression - drug effects | Monoamine Oxidase - metabolism | Passive-aggressive personality | Dopamine | Genetic susceptibility | Serotonin | Genetic research | Genetic aspects | Research | Properties | Mouse | Aggression | Development | Depression | Anxiety
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 503, Issue 7474, pp. 141 - 145
The biogenic amine transporters (BATs) regulate endogenous neurotransmitter concentrations and are targets for a broad range of therapeutic agents including... 
NEUROTRANSMITTER | HIGH-AFFINITY RECOGNITION | MECHANISM | DETERMINANTS | BACTERIAL HOMOLOG | MULTIDISCIPLINARY SCIENCES | BINDING-SITE | SELECTIVE RECOGNITION | LEUT | HUMAN SEROTONIN TRANSPORTER | CHLORIDE | Antidepressive Agents, Tricyclic - metabolism | Humans | Protein Conformation - drug effects | Bacterial Proteins - chemistry | Crystallography, X-Ray | Plasma Membrane Neurotransmitter Transport Proteins - antagonists & inhibitors | Structure-Activity Relationship | Sodium - metabolism | Recombinant Fusion Proteins - metabolism | Mazindol - pharmacology | Serotonin Plasma Membrane Transport Proteins - chemistry | Serotonin Plasma Membrane Transport Proteins - genetics | Chlorides - metabolism | Biogenic Amines - metabolism | Sertraline - metabolism | Serotonin Uptake Inhibitors - metabolism | Bacterial Proteins - antagonists & inhibitors | Reproducibility of Results | Sertraline - pharmacology | Bacterial Proteins - genetics | Models, Molecular | Antidepressive Agents, Second-Generation - pharmacology | Mazindol - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - metabolism | Recombinant Fusion Proteins - chemistry | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Binding, Competitive - drug effects | Serotonin Plasma Membrane Transport Proteins - metabolism | Norepinephrine - metabolism | Antidepressive Agents, Tricyclic - pharmacology | Recombinant Fusion Proteins - genetics | Bacterial Proteins - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - chemistry | Mutation | Antidepressive Agents, Second-Generation - metabolism | Serotonin Uptake Inhibitors - pharmacology | Neurotransmitters | Carrier proteins | Physiological aspects | Serotonin uptake inhibitors | Pharmacology | Research | Molecular biology | Biogenic amines | Health aspects | Antidepressants, Tricyclic | Competition | Dopamine | Binding sites
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2011, Volume 108, Issue 29, pp. 12137 - 12142
Inhibitors of the serotonin transporter (SERT) and norepinephrine transporter (NET) are widely used in the treatment of major depressive disorder. Although... 
Tricyclic antidepressive agents | Antidepressants | Norepinephrine plasma membrane transport proteins | Reuptake | Serotonin plasma membrane transport proteins | Norepinephrine | Enantiomers | Experimental procedures | Binding sites | Chemicals | Monoamine | Neurotransmitter | SLC6 transporter | HIGH-AFFINITY RECOGNITION | NEUROTRANSMITTER TRANSPORTERS | MULTIDISCIPLINARY SCIENCES | CITALOPRAM | MONOAMINE TRANSPORTERS | monoamine | BACTERIAL HOMOLOG | SUBSTRATE | DOPAMINE | BINDING-SITE | LEUT | neurotransmitter | STRUCTURAL DOMAINS | Humans | Cercopithecus aethiops | Molecular Sequence Data | Structure-Activity Relationship | Antidepressive Agents - metabolism | Citalopram - metabolism | Serotonin Plasma Membrane Transport Proteins - chemistry | Serotonin Plasma Membrane Transport Proteins - genetics | DNA Mutational Analysis | Norepinephrine Plasma Membrane Transport Proteins - genetics | Base Sequence | Radioligand Assay | Serotonin Uptake Inhibitors - metabolism | Amino Acid Sequence | Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors | Crystallization | Models, Molecular | Binding Sites - genetics | Genetic Vectors - genetics | Serotonin Plasma Membrane Transport Proteins - metabolism | Animals | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Propylamines - metabolism | COS Cells | Norepinephrine Plasma Membrane Transport Proteins - chemistry | Benzofurans - metabolism | Biological Sciences
Journal Article
Pharmacology, Biochemistry and Behavior, ISSN 0091-3057, 01/2012, Volume 100, Issue 3, pp. 431 - 439
Fructus Akebiae is a traditional Chinese herbal extract that has been used for the treatment of depressive disorders in China. Previous studies demonstrated... 
Antidepressant | Reuptake inhibitor | Fructus Akebiae | TREATMENT-RESISTANT DEPRESSION | TRANSPORTER | MAJOR DEPRESSION | NEUROSCIENCES | VENLAFAXINE | BANXIA-HOUPU DECOCTION | PROFILE | PLASMA | ANTIDEPRESSANT AGENTS | BEHAVIORAL SCIENCES | PHARMACOLOGY & PHARMACY | RAT-BRAIN | RECEPTOR-BINDING | Dopamine Plasma Membrane Transport Proteins - metabolism | Synaptosomes - drug effects | Frontal Lobe - metabolism | Humans | Oleanolic Acid - analogs & derivatives | Drugs, Chinese Herbal - pharmacology | Neurotransmitter Uptake Inhibitors - pharmacology | Oleanolic Acid - pharmacology | Male | Synaptosomes - metabolism | Dose-Response Relationship, Drug | Serotonin Plasma Membrane Transport Proteins - chemistry | Serotonin Plasma Membrane Transport Proteins - genetics | Norepinephrine Plasma Membrane Transport Proteins - genetics | HEK293 Cells | Neurons - drug effects | Recombinant Proteins - metabolism | Nerve Tissue Proteins - antagonists & inhibitors | Recombinant Proteins - antagonists & inhibitors | Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors | Rats | Recombinant Proteins - genetics | Dopamine Plasma Membrane Transport Proteins - genetics | Nerve Tissue Proteins - genetics | Rats, Sprague-Dawley | Oleanolic Acid - analysis | Brain - drug effects | Dopamine Plasma Membrane Transport Proteins - antagonists & inhibitors | Nerve Tissue Proteins - metabolism | Serotonin Plasma Membrane Transport Proteins - metabolism | Up-Regulation - drug effects | Animals | Drugs, Chinese Herbal - chemistry | Frontal Lobe - drug effects | Biogenic Monoamines - metabolism | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Phenols | Medicine, Herbal | Antidepressants | Animal behavior | Medicine, Botanic | Depression, Mental | Index Medicus
Journal Article
PHARMACOLOGICAL REPORTS, ISSN 1734-1140, 02/2018, Volume 70, Issue 1, pp. 146 - 155
Background: Clobenpropit, a potent antagonist/inverse agonist at the histamine H-3 receptor (H3R), reduced the cytotoxic action of 6-hydroxydopamine (6-OHDA)... 
NISOXETINE | D-1 | Norepinephrine transporter | RELEASE | ACCURACY | Clobenpropit | MODELS | SH-SY5Y cells | Dopamine transporter | PHARMACOLOGY & PHARMACY | Histamine H-3 receptor | EXPRESSION | STRUCTURAL DOMAINS | Thiourea - metabolism | Dopamine Plasma Membrane Transport Proteins - metabolism | Synaptosomes - drug effects | Humans | Imidazoles - chemistry | Dopamine Plasma Membrane Transport Proteins - chemistry | Synaptosomes - metabolism | Thiourea - pharmacology | Dopamine Uptake Inhibitors - metabolism | Drosophila Proteins - metabolism | Brain - metabolism | Dose-Response Relationship, Drug | Receptors, Histamine H3 - metabolism | Binding Sites | Drosophila Proteins - antagonists & inhibitors | Dopamine - metabolism | Histamine H3 Antagonists - chemistry | Imidazoles - metabolism | Dopamine Uptake Inhibitors - pharmacology | Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors | Rats | Imidazoles - pharmacology | Thiourea - chemistry | Brain - drug effects | Dopamine Plasma Membrane Transport Proteins - antagonists & inhibitors | Histamine H3 Antagonists - pharmacology | Animals | Drug Inverse Agonism | Dopamine Uptake Inhibitors - chemistry | Receptors, Histamine H3 - drug effects | Cell Line, Tumor | Histamine H3 Antagonists - metabolism | Protein Binding | Protein Conformation | Molecular Docking Simulation | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Thiourea - analogs & derivatives
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 09/2010, Volume 114, Issue 6, pp. 1745 - 1755
J. Neurochem. (2010) 114, 1745–1755. Catechol‐O‐methyltransferase (COMT) plays an active role in the metabolism of dopamine (DA) in the prefrontal cortex... 
mouse | catechol‐O‐methyltransferase | microdialysis | dopamine | prefrontal cortex | uptake inhibition | catechol-O-methyltransferase | EXTRACELLULAR DOPAMINE | BIOCHEMISTRY & MOLECULAR BIOLOGY | (COMT)-DEFICIENT MICE | DISRUPTED MICE | NEUROSCIENCES | OBSESSIVE-COMPULSIVE DISORDER | NUCLEUS-ACCUMBENS | RAT FRONTAL-CORTEX | NOREPINEPHRINE TRANSPORTER | VAL(108/158) MET GENOTYPE | NORADRENALINE CARRIER | Monoamine Oxidase Inhibitors - pharmacology | Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors | Nucleus Accumbens - metabolism | Catechol O-Methyltransferase - physiology | Male | Catechol O-Methyltransferase - genetics | Corpus Striatum - metabolism | Mice, Knockout | Dopamine Plasma Membrane Transport Proteins - antagonists & inhibitors | Animals | Microdialysis | Prefrontal Cortex - drug effects | Prefrontal Cortex - metabolism | Female | Mice | Mutation | Norepinephrine Plasma Membrane Transport Proteins - metabolism | Dopamine - metabolism | Phenols | Cell research | Neurosciences | Universities and colleges | Neurons | Pharmacy | Neurochemistry | Brain | Dopamine | Metabolism | Rodents | Cortex (prefrontal) | Norepinephrine transporter | Glial cells | Amine oxidase (flavin-containing) | Nucleus accumbens | Gene disruption | Neostriatum | Dopamine transporter | Genotypes | monoamines
Journal Article