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1. Inhibition of monoamine oxidase activity by antidepressants and mood stabilizers
by Fišar, Zdeněk and Hroudová, Jana and Raboch, Jiří
Neuro-endocrinology letters, ISSN 0172-780X, 2010, Volume 31, Issue 5, pp. 645 - 656
Mood stabilizers | Monoamine oxidase inhibitors | Antidepressive agents | Endocrinology & Metabolism | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Mitochondria - enzymology | Citalopram - pharmacology | Clorgyline - pharmacology | Monoamine Oxidase - drug effects | Cerebral Cortex - cytology | Valproic Acid - pharmacology | Mianserin - analogs & derivatives | Mianserin - pharmacology | Desipramine - pharmacology | Swine | Antidepressive Agents - pharmacology | Cyclohexanols - pharmacology | Moclobemide - pharmacology | Fluoxetine - pharmacology | Monoamine Oxidase Inhibitors - pharmacology | Affect - drug effects | Benzodiazepines - pharmacology | Antimanic Agents - pharmacology | Lithium - pharmacology | Morpholines - pharmacology | Thiazepines - pharmacology | Mitochondria - drug effects | Iproniazid - pharmacology | Venlafaxine Hydrochloride | Cocaine - pharmacology | Animals | Pargyline - pharmacology | Amitriptyline - pharmacology | Imipramine - pharmacology | In Vitro Techniques | Monoamine Oxidase - metabolism
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2. Full Text Enhancement of the anti-immobility action of antidepressants by a selective 5-HT7 receptor antagonist in the forced swimming test in mice
by Wesołowska, Anna and Tatarczyńska, Ewa and Nikiforuk, Agnieszka and Chojnacka-Wójcik, Ewa
European journal of pharmacology, ISSN 0014-2999, 01/2007, Volume 555, Issue 1, pp. 43 - 47
Imipramine | Desipramine | Forced swimming test in mice | 5-HT | receptor antagonist | Moclobemide | Citalopram | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Biological and medical sciences | Pharmacology. Drug treatments | Medical sciences | Monoamine Oxidase Inhibitors - pharmacology | Citalopram - pharmacology | Motor Activity - drug effects | Male | Serotonin Antagonists - pharmacology | Sulfonamides - pharmacology | Receptors, Serotonin - metabolism | Desipramine - pharmacology | Animals | Drug Interactions | Adrenergic Uptake Inhibitors - pharmacology | Antidepressive Agents - pharmacology | Mice | Swimming | Moclobemide - pharmacology | Imipramine - pharmacology | Serotonin Uptake Inhibitors - pharmacology | Phenols - pharmacology | Index Medicus
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3. Full Text Antidepressants inhibit DNA methyltransferase 1 through reducing G9a levels
by Zimmermann, Nicole and Zschocke, Jürgen and Perisic, Tatjana and Yu, Shuang and Holsboer, Florian and Rein, Theo
Biochemical journal, ISSN 0264-6021, 11/2012, Volume 448, Issue 1, pp. 93 - 102
Antidepressant | Epigenetics | Histone methyltransferase | DNA methyltransferase 1 (DNMT1) | Astrocyte | Mood stabilizer | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Citalopram - pharmacology | Maleimides - pharmacology | Astrocytes - enzymology | DNA (Cytosine-5-)-Methyltransferases - antagonists & inhibitors | Cerebral Cortex - cytology | DNA (Cytosine-5-)-Methyltransferases - metabolism | Histone-Lysine N-Methyltransferase - antagonists & inhibitors | Neurons - physiology | Indoles - pharmacology | Antidepressive Agents - pharmacology | Cyclohexanols - pharmacology | Neurons - drug effects | Astrocytes - drug effects | Carbamazepine - pharmacology | Nerve Tissue Proteins - antagonists & inhibitors | Cells, Cultured - drug effects | Histone-Lysine N-Methyltransferase - pharmacology | DNA (Cytosine-5-)-Methyltransferase 1 | Enzyme Inhibitors - pharmacology | Glycolipids - pharmacology | Neural Stem Cells - drug effects | Cells, Cultured - physiology | Neural Stem Cells - physiology | Rats | Recombinant Proteins - pharmacology | Neural Stem Cells - enzymology | Rats, Sprague-Dawley | Cells, Cultured - enzymology | Protein Interaction Mapping | Nerve Tissue Proteins - metabolism | Venlafaxine Hydrochloride | Astrocytes - physiology | Animals | Cerebral Cortex - embryology | Histone-Lysine N-Methyltransferase - metabolism | Neurons - enzymology | Mice | Imipramine - pharmacology | Paroxetine - pharmacology | DNA Methylation - drug effects | Index Medicus
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4. Full Text Antidepressant-like effect of nitric oxide synthase inhibitors and sildenafil against lipopolysaccharide-induced depressive-like behavior in mice
by Tomaz, V.S and Cordeiro, R.C and Costa, A.M.N and de Lucena, D.F and Nobre Júnior, H.V and de Sousa, F.C.F and Vasconcelos, S.M.M and Vale, M.L and Quevedo, J and Macêdo, D
Neuroscience, ISSN 0306-4522, 2014, Volume 268, pp. 236 - 246
Neurology | nitric oxide | depressive-like behavior | neuroinflammation | BDNF | LPS | oxidative stress | Depressive-like behavior | Oxidative stress | Neuroinflammation | Nitric oxide | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Vertebrates: nervous system and sense organs | Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer | Psychology. Psychoanalysis. Psychiatry | Psychopharmacology | Pharmacology. Drug treatments | Biological and medical sciences | Medical sciences | Neuropharmacology | Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) | Oxidative Stress - physiology | Nitric Oxide Synthase - antagonists & inhibitors | Depressive Disorder - drug therapy | Guanidines - pharmacology | Male | Sulfones - pharmacology | Lipopolysaccharides | Brain - metabolism | Sildenafil Citrate | Interleukin-1beta - metabolism | Behavior, Animal - drug effects | Antidepressive Agents - pharmacology | Brain-Derived Neurotrophic Factor - metabolism | Disease Models, Animal | NG-Nitroarginine Methyl Ester - pharmacology | Purines - pharmacology | Enzyme Inhibitors - pharmacology | Behavior, Animal - physiology | Depressive Disorder - metabolism | Piperazines - pharmacology | Brain - drug effects | Animals | Cyclic GMP - metabolism | Signal Transduction - drug effects | Arginine - pharmacology | Depressive Disorder - prevention & control | Signal Transduction - physiology | Mice | Nitric Oxide Synthase - metabolism | Oxidative Stress - drug effects | Imipramine - pharmacology | Nitric Oxide - metabolism | Antidepressants | Mitogens | Depression, Mental | Index Medicus
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5. Full Text Linalool and β-pinene exert their antidepressant-like activity through the monoaminergic pathway
by Guzmán-Gutiérrez, Silvia Laura and Bonilla-Jaime, Herlinda and Gómez-Cansino, Rocío and Reyes-Chilpa, Ricardo
Life sciences (1973), ISSN 0024-3205, 05/2015, Volume 128, pp. 24 - 29
Antidepressant | Monoterpenes | Aromatic compounds | β-Pinene | Linalool | Pharmacology & Pharmacy | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Serotonergic Neurons - physiology | Bridged Bicyclo Compounds - pharmacology | Serotonergic Neurons - drug effects | Male | Benzazepines - pharmacology | Serotonin Antagonists - pharmacology | Piperazines - pharmacology | Mice, Inbred ICR | Monoterpenes - pharmacology | Animals | Dopaminergic Neurons - drug effects | Antidepressive Agents - pharmacology | Pyridines - pharmacology | Adrenergic Neurons - drug effects | Imipramine - pharmacology | Index Medicus
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6. Full Text Discriminative stimulus properties of the atypical antipsychotic amisulpride: comparison to its isomers and to other benzamide derivatives, antipsychotic, antidepressant, and antianxiety drugs in C57BL/6 mice
by Donahue, Timothy J and Hillhouse, Todd M and Webster, Kevin A and Young, Richard and De Oliveira, Eliseu O and Porter, Joseph H
Psychopharmacology, ISSN 0033-3158, 12/2017, Volume 234, Issue 23, pp. 3507 - 3520
Drug discrimination | Neurosciences | Amisulpride | Schizophrenia | Isomers | Anxiolytics | Discriminative stimulus | Antipsychotics | Biomedicine | Antidepressants | C57BL/6 mice | Benzamides | Pharmacology/Toxicology | Psychiatry | Pharmacology & Pharmacy | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Sulpiride - pharmacology | Conditioning, Operant - physiology | Male | Sulpiride - analogs & derivatives | Clozapine - pharmacology | Discrimination Learning - drug effects | Clozapine - chemistry | Conditioning, Operant - drug effects | Antidepressive Agents - chemistry | Anti-Anxiety Agents - chemistry | Antidepressive Agents - pharmacology | Benzamides - pharmacology | Quetiapine Fumarate - pharmacology | Benzamides - chemistry | Quetiapine Fumarate - chemistry | Mice, Inbred C57BL | Chlorpromazine - chemistry | Risperidone - pharmacology | Anti-Anxiety Agents - pharmacology | Chlorpromazine - pharmacology | Risperidone - chemistry | Discrimination Learning - physiology | Animals | Antipsychotic Agents - chemistry | Mice | Antipsychotic Agents - pharmacology | Sulpiride - chemistry | Dosage and administration | Antipsychotic drugs | Comparative analysis | Drug interactions | Antianxiety agents | Stereoisomers | Drugs | Neuroleptics | Olanzapine | Operant conditioning | Mental disorders | Aripiprazole | Benzamide | Metoclopramide | Chlorpromazine | Sulpiride | Serotonin S7 receptors | Psychotropic drugs | Imipramine | Receptors | Bupropion | Mianserin | Risperidone | Dopamine D2 receptors | Drug dosages | Quetiapine | Raclopride | Dopamine | Serotonin | Dopamine D3 receptors | Chlordiazepoxide | Pharmacology | Clozapine | Derivatives | Properties (attributes) | Serotonin receptors | Index Medicus
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7. Full Text Pharmacophore modeling for hERG channel facilitation
by Yamakawa, Yuko and Furutani, Kazuharu and Inanobe, Atsushi and Ohno, Yuko and Kurachi, Yoshihisa
Biochemical and biophysical research communications, ISSN 0006-291X, 02/2012, Volume 418, Issue 1, pp. 161 - 166
Facilitation | Pharmacology | hERG channel | Pharmacophore model | HERG channel | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Nortriptyline - chemistry | Metoprolol - pharmacology | Humans | Sotalol - chemistry | Imipramine - chemistry | ERG1 Potassium Channel | Nortriptyline - pharmacology | Propranolol - pharmacology | Chlorpheniramine - chemistry | Ether-A-Go-Go Potassium Channels - physiology | Metoprolol - chemistry | Haloperidol - pharmacology | Potassium Channel Blockers - pharmacology | Quantitative Structure-Activity Relationship | Atenolol - pharmacology | Terfenadine - pharmacology | Fluoxetine - pharmacology | Promethazine - chemistry | Xenopus laevis | Propranolol - chemistry | Fluoxetine - chemistry | Verapamil - pharmacology | Haloperidol - chemistry | Verapamil - chemistry | Ether-A-Go-Go Potassium Channels - antagonists & inhibitors | Animals | Sotalol - pharmacology | Atenolol - chemistry | Hydrophobic and Hydrophilic Interactions | Terfenadine - chemistry | Chlorpheniramine - pharmacology | Imipramine - pharmacology | Potassium Channel Blockers - chemistry | Promethazine - pharmacology | Analysis | Models | Universities and colleges | Index Medicus
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8. Full Text Antidepressant-like action of the hydromethanolic flower extract of Tagetes erecta L. in mice and its possible mechanism of action
by Khulbe, Aarti and Pandey, Savita and Sah, Sangeeta
Indian journal of pharmacology, ISSN 0253-7613, 07/2013, Volume 45, Issue 4, pp. 386 - 390
Antidepressant | nitric oxide pathway | sigma receptors | serotonergic pathway | Tagetes erecta | forced swim test | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Plant Extracts - pharmacology | Motor Activity - drug effects | Nitric Oxide Synthase - antagonists & inhibitors | Male | Receptors, sigma - antagonists & inhibitors | Flowers | Sulfones - pharmacology | Sildenafil Citrate | Water - chemistry | Antidepressive Agents - pharmacology | Methanol - chemistry | Phosphodiesterase 5 Inhibitors - pharmacology | Progesterone - pharmacology | Fenclonine - pharmacology | NG-Nitroarginine Methyl Ester - pharmacology | Fluoxetine - pharmacology | Purines - pharmacology | Pentazocine - pharmacology | Receptors, sigma - agonists | Serotonin Antagonists - pharmacology | Piperazines - pharmacology | Animals | Arginine - pharmacology | Adrenergic Uptake Inhibitors - pharmacology | Mice | Tagetes | Imipramine - pharmacology | Serotonin Uptake Inhibitors - pharmacology | Care and treatment | Marigolds | Chemical properties | Health aspects | Depression, Mental | Pharmacology | Mental depression | Antidepressants | Natural products | Index Medicus
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9. Full Text Effects of antidepressant drugs on synaptic protein levels and dendritic outgrowth in hippocampal neuronal cultures
by Seo, Mi Kyoung and Lee, Chan Hong and Cho, Hye Yeon and Lee, Jung Goo and Lee, Bong Ju and Kim, Ji Eun and Seol, Wongi and Kim, Young Hoon and Park, Sung Woo
Neuropharmacology, ISSN 0028-3908, 04/2014, Volume 79, pp. 222 - 233
Signaling | Dendritic outgrowth | Hippocampal plasticity | Synaptic proteins | Antidepressant drugs | Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Dendrites - drug effects | Fluoxetine - pharmacology | Citalopram - pharmacology | Sertraline - pharmacology | Cells, Cultured | Rats | Antidepressive Agents, Second-Generation - pharmacology | Thiazepines - pharmacology | Hippocampus - drug effects | Nerve Tissue Proteins - drug effects | Rats, Sprague-Dawley | Animals | Cell Enlargement - drug effects | Antidepressive Agents, Tricyclic - pharmacology | Dendrites - physiology | Tranylcypromine - pharmacology | Neurons - physiology | Antidepressive Agents - pharmacology | Hippocampus - physiology | Imipramine - pharmacology | Neurons - drug effects | Paroxetine - pharmacology | Drugs | Proteins | Paroxetine | Imipramine | Medical colleges | Fluoxetine | Neurons | Analysis | Depression, Mental | Index Medicus
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10. Full Text Involvement of 5-HT2C and 5-HT1A receptors of the basolateral nucleus of the amygdala in the anxiolytic effect of chronic antidepressant treatment
by Vicente, Maria Adrielle and Zangrossi, Helio
Neuropharmacology, ISSN 0028-3908, 04/2014, Volume 79, pp. 127 - 135
Antidepressants and basolateral amygdala | Anxiety | Serotonin | 5-HT2C receptors | Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amygdala - drug effects | Rats, Wistar | Serotonin 5-HT1 Receptor Antagonists - pharmacology | Receptor, Serotonin, 5-HT2C - metabolism | Male | Serotonin 5-HT2 Receptor Agonists - pharmacology | Anxiety - drug therapy | Exploratory Behavior - physiology | Exploratory Behavior - drug effects | Receptor, Serotonin, 5-HT1A - metabolism | Fluoxetine - pharmacology | Panic - drug effects | Maze Learning - physiology | Anti-Anxiety Agents - pharmacology | Anxiety - physiopathology | Rats | Antidepressive Agents, Second-Generation - pharmacology | Avoidance Learning - physiology | Maze Learning - drug effects | Piperazines - pharmacology | Panic - physiology | Animals | Antidepressive Agents, Tricyclic - pharmacology | Avoidance Learning - drug effects | Pyridines - pharmacology | Imipramine - pharmacology | Pyrazines - pharmacology | Amygdala - physiology | Imipramine | Fluoxetine | Antianxiety agents | Index Medicus
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