Cited by 131Neurotransmitter Receptor Influence on BehaviorStress Responses and CortisolNeuroscience and Neuropharmacology Research

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Different stressors produce excitation or inhibition of mesolimbic dopamine neuron activity: response alteration by stress pre‐exposure

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Valenti, Ornella, Gill, Kathryn M., Grace, Anthony A.·2012·European Journal of Neuroscience

DOI 10.1111/j.1460-9568.2012.08038.xPMC PMC3335739

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Abstract

Stressors can exert a wide variety of responses, ranging from adaptive responses to pathological changes; moreover, recent studies suggest that mild stressors can attenuate the response of a system to major stressful events. We have previously shown that 2‐week exposure to cold, a comparatively mild inescapable stressor, induced a pronounced reduction in ventral tegmental area (VTA) dopamine (DA) neuron activity, whereas restraint stress increases DA neuron activity. However, it is not known if these stressors differentially impact the VTA in a region‐specific manner, if they differentially impact behavioral responses, or whether the effects of such different stressors are additive or antagonistic with regard to their impact on DA neuron firing. To address these questions, single‐unit extracellular recordings were performed in anesthetized control rats and rats exposed to chronic cold, and tested after delivery of a 2‐h restraint session. Chronic cold stress strongly attenuated the number of DA neurons firing in the VTA, and this effect occurred primarily in the medial and central VTA regions that preferentially project to reward‐related ventral striatal regions. Chronic cold exposure also prevented the pronounced increase in DA neuron population activity without affecting the behavioral sensitization to amphetamine produced by restraint stress. Taken together, these data show that a prolonged inescapable mild stressor can induce plastic changes that attenuate the DA system response to acute stress.

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A neural substrate of prediction and reward
Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501
Dopamine transmission in the initiation and expression of drug- and stress-induced sensitization of motor activity.
Kalivas, P., & Stewart, J. (1991) · Brain research. Brain research reviews · doi:10.1016/0165-0173(91)90007-u · Cited by 2,087
The Nature of the Arrestin·Receptor Complex Determines the Ultimate Fate of the Internalized Receptor
Pan, L., Gurevich, E. V., & Gurevich, V. V. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209532200 · Cited by 1,758
Chronic Mild Stress (CMS) Revisited: Consistency and Behavioural-Neurobiological Concordance in the Effects of CMS
Willner, P. (2005) · Neuropsychobiology · doi:10.1159/000087097 · Cited by 1,605
The stressed hippocampus, synaptic plasticity and lost memories
Kim, J. J., & Diamond, D. M. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn849 · Cited by 1,543
Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex
Ikemoto, S. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.004 · Cited by 1,477
Intrinsic firing patterns of diverse neocortical neurons
Connors, B. W., & Gutnick, M. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90185-d · Cited by 1,440
Afferent modulation of dopamine neuron firing differentially regulates tonic and phasic dopamine transmission
Floresco, S. B., West, A. R., Ash, B., Moore, H., & Grace, A. A. (2003) · Nature Neuroscience · doi:10.1038/nn1103 · Cited by 1,106
Self-citation
Differential effect of stress on in vivo dopamine release in striatum, nucleus accumbens, and medial frontal cortex
Abercrombie, E. D., Keefe, K. A., DiFrischia, D. S., & Zigmond, M. J. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb09224.x · Cited by 1,106
Regulation of firing of dopaminergic neurons and control of goal-directed behaviors
Grace, A. A., Floresco, S. B., Goto, Y., & Lodge, D. J. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.003 · Cited by 1,034
Self-citation
Intracellular and extracellular electrophysiology of nigral dopaminergic neurons—1. Identification and characterization
Grace, A. A., & Bunney, B. S. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90135-5 · Cited by 937
Self-citation
Stressor specificity of central neuroendocrine responses: implications for stress-related disorders
Pacák, K., & Palkovits, M. (2001) · Endocrine Reviews · doi:10.1210/edrv.22.4.0436 · Cited by 926
Characterization of Neocortical Principal Cells and Interneurons by Network Interactions and Extracellular Features
Barthó, P., Hirase, H., Monconduit, L., Zugaro, M., Harris, K. D., & Buzsáki, G. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01170.2003 · Cited by 912
The control of firing pattern in nigral dopamine neurons: single spike firing
Grace, A., & Bunney, B. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-11-02866.1984 · Cited by 862
Self-citation
Psychopharmacology: The Fourth Generation of Progress
Kramlinger, K. G. (1995) · Mayo Clinic Proceedings · doi:10.4065/70.10.1021-a · Cited by 779
Projection-specific modulation of dopamine neuron synapses by aversive and rewarding stimuli
Lammel, S., Ion, D. I., Roeper, J., & Malenka, R. C. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.025 · Cited by 766
The role of stress in drug self-administration
Piazza, P. V., & Moal, M. L. (1998) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(97)01115-2 · Cited by 674
Regulation of ACTH Secretion: Variations on a Theme of B
DALLMAN, M. F., AKANA, S. F., CASCIO, C. S., DARLINGTON, D. N., JACOBSON, L., & LEVIN, N. (1987) · Proceedings of the 1986 Laurentian Hormone Conference · doi:10.1016/b978-0-12-571143-2.50010-1 · Cited by 655
Corticosteroids in relation to fear, anxiety and psychopathology
Korte, S. M. (2001) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00002-1 · Cited by 607
Role of brain norepinephrine in the behavioral response to stress
Morilak, D. A., Barrera, G., Echevarria, D. J., Garcia, A. S., Hernandez, A., Ma, S., & Petre, C. O. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.007 · Cited by 570
Interchangeability of Stress and Amphetamine in Sensitization
Antelman, S. M., Eichler, A. J., Black, C. A., & Kocan, D. J. (1980) · Science · doi:10.1126/science.7188649 · Cited by 562
Glutamatergic Afferents from the Hippocampus to the Nucleus Accumbens Regulate Activity of Ventral Tegmental Area Dopamine Neurons
Floresco, S., Todd, C. L., & Grace, A. A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-13-04915.2001 · Cited by 556
Self-citation
Neuroanatomical basis for facilitation of hypothalamic-pituitary-adrenal responses to a novel stressor after chronic stress
Bhatnagar, S., & Dallman, M. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00577-0 · Cited by 511
Firing modes of midbrain dopamine cells in the freely moving rat
Hyland, B. I., Reynolds, J. N. J., HAY, J. G., Perk, C. G., & Miller, R. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00267-1 · Cited by 487
Chronic Stress Induces Impairment of Spatial Working Memory Because of Prefrontal Dopaminergic Dysfunction
Mizoguchi, K., Yuzurihara, M., Ishige, A., Sasaki, H., Chui, D.-H., & Tabira, T. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-04-01568.2000 · Cited by 481
Increased dopamine and norepinephrine release in medial prefrontal cortex induced by acute and chronic stress: effects of diazepam
Finlay, J. M., Zigmond, M. J., & Abercrombie, E. D. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00331-x · Cited by 434
Chapter 19 The determinants of stress-induced activation of the prefrontal cortical dopamine system
(1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62691-6 · Cited by 364
What is stress?
Selye, H. (1956) · PubMed · Cited by 341
The mesoaccumbens dopamine in coping with stress
Cabib, S., & Puglisi-Allegra, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.04.012 · Cited by 329
Elevation of Adrenal Tyrosine Hydroxylase and Phenylethanolamine-N-Methyl Transferase by Repeated Immobilization of Rats
Květňanský, R., Weise, V. K., & Kopin, I. J. (1970) · Endocrinology · doi:10.1210/endo-87-4-744 · Cited by 317
Comparative analysis of ACTH and corticosterone sampling methods in rats
Vahl, T. P., Ulrich-Lai, Y. M., Ostrander, M. M., Dolgas, C. M., Elfers, E. E., Seeley, R. J., D'Alessio, D. A., & Herman, J. P. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00122.2005 · Cited by 304 · cited 2×
“Indeed, restraint stress has been used as a model of anxiety disorder (Padovan & Guimaraes, 2000; Vahl et al., 2005), whereas chronic mild, inescapable stressors have been used as a model of depression (Willner, 2005).”
BackgroundMethod
Prefrontal cortical dopamine depletion enhances the responsiveness of mesolimbic dopamine neurons to stress
Deutch, A. Y., Clark, W. A., & Roth, R. H. (1990) · Brain Research · doi:10.1016/0006-8993(90)91557-w · Cited by 302
Criteria for rationally evaluating animal models of postraumatic stress disorder
Yehuda, R., & Antelman, S. M. (1993) · Biological Psychiatry · doi:10.1016/0006-3223(93)90001-t · Cited by 301
The Hippocampus Modulates Dopamine Neuron Responsivity by Regulating the Intensity of Phasic Neuron Activation
Lodge, D. J., & Grace, A. A. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300963 · Cited by 280
Self-citation
Electrophysiological effects of cocaine in the mesoaccumbens dopamine system: repeated administration.
Henry, D. J., Greene, M. A., & White, F. (1989) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21086-2 · Cited by 268
Modulation of Hippocampal and Amygdalar-Evoked Activity of Nucleus Accumbens Neurons by Dopamine: Cellular Mechanisms of Input Selection
Floresco, S., Blaha, C. D., Yang, C. R., & Phillips, A. G. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02851.2001 · Cited by 242
A Subpopulation of Neurons in the Medial Prefrontal Cortex Encodes Emotional Learning with Burst and Frequency Codes through a Dopamine D4Receptor-Dependent Basolateral Amygdala Input
Laviolette, S. R., Lipski, W. J., & Grace, A. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1168-05.2005 · Cited by 235
Self-citation
Fast Spiking and Regular Spiking Neural Correlates of Fear Conditioning in the Medial Prefrontal Cortex of the Rat
Baeg, E. H. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.5.441 · Cited by 216
Acute stress induces time-dependent responses in dopamine mesolimbic system
Puglisi‐Allegra, S., Impérato, A., Angelucci, L., & Cabib, S. (1991) · Brain Research · doi:10.1016/0006-8993(91)90192-x · Cited by 213
Electrophysiological evidence for A10 dopamine autoreceptor subsensitivity following chronicd-amphetamine treatment
White, F. J., & Wang, R. Y. (1984) · Brain Research · doi:10.1016/0006-8993(84)90594-8 · Cited by 190
CRF receptor regulation and sensitization of ACTH responses to acute ether stress during chronic intermittent immobilization stress
Hauger, R. L., Lorang, M. T., Irwin, M. R., & Aguilera, G. (1990) · Brain Research · doi:10.1016/0006-8993(90)91738-3 · Cited by 189
Stress‐Induced Sensitization of Dopamine and Norepinephrine Efflux in Medial Prefrontal Cortex of the Rat
Gresch, P. J., Sved, A. F., Zigmond, M. J., & Finlay, J. M. (1994) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1994.63020575.x · Cited by 179
The Effects of Stress on Central Dopaminergic Neurons: Possible Clinical Implications
Finlay, J. M., & Zigmond, M. J. (1997) · Neurochemical Research · doi:10.1023/a:1022075324164 · Cited by 177
Corticotropin-Releasing Hormone Directly Activates Noradrenergic Neurons of the Locus Ceruleus RecordedIn Vitro
Jedema, H. P., & Grace, A. A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2830-04.2004 · Cited by 176
Self-citation
Biochemical Adaptations in the Mesolimbic Dopamine System in Response to Repeated Stress
Ortiz, J. (1996) · Neuropsychopharmacology · doi:10.1016/0893-133x(95)00152-4 · Cited by 174
Aversive stimuli alter ventral tegmental area dopamine neuron activity via a common action in the ventral hippocampus
Valenti, O., Lodge, D. J., & Grace, A. A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5310-10.2011 · Cited by 173
Self-citation
Noradrenergic Modulation of Basolateral Amygdala Neuronal Activity: Opposing Influences of α-2 and β Receptor Activation
Buffalari, D., & Grace, A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2007-07.2007 · Cited by 157
Self-citation
Activation of the ventral medial prefrontal cortex during an uncontrollable stressor reproduces both the immediate and long-term protective effects of behavioral control
Amat, J., Paul, E., Watkins, L. R., & Maier, S. F. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.005 · Cited by 153
Response of anterior pituitary hormones to chronic stress. The specificity of adaptation
Armario, A., López‐Calderón, A., Jolín, T., & Balasch, J. (1986) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(86)90011-4 · Cited by 150
Textbook of environmental physiology
Folk, G. E. (1974) · Cited by 144
Prevention of denervation atrophy in muscle: Mammalian neurotrophic factor is not transferrin
Davis, H. L., & Heinicke, E. (1984) · Brain Research · doi:10.1016/0006-8993(84)90595-x · Cited by 144
Immobilization and cold stress affect sympatho–adrenomedullary system and pituitary–adrenocortical axis of rats exposed to long-term isolation and crowding
DRONJAK, S., GAVRILOVI, L., FILIPOVI, D., & RADOJI, M. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.01.011 · Cited by 142
Chronic mild stress generates clear depressive but ambiguous anxiety-like behaviour in rats
Kompagne, H., Bárdos, G., Szénási, G., Gacsályi, I., Hársing, L. G., & Lévay, G. I. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.06.008 · Cited by 139
Restraint-induced hypoactivity in an elevated plus-maze
Padovan, C. M., & Guimarães, F. S. (2000) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2000000100011 · Cited by 133
Chronic Cold Stress Reduces the Spontaneous Activity of Ventral Tegmental Dopamine Neurons
Moore, H. M. (2001) · Neuropsychopharmacology · doi:10.1016/s0893-133x(00)00188-3 · Cited by 129
Amphetamine Activation of Hippocampal Drive of Mesolimbic Dopamine Neurons: A Mechanism of Behavioral Sensitization
Lodge, D. J., & Grace, A. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1582-08.2008 · Cited by 127
Self-citation
Norepinephrine Release in Medial Amygdala Facilitates Activation of the Hypothalamic‐Pituitary‐Adrenal Axis in Response to Acute Immobilisation Stress
Ma, S., & Morilak, D. A. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01279.x · Cited by 111
Transituational immunization and therapy of learned helplessness in the rat.
Williams, J. L., & Maier, S. F. (1977) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.3.3.240 · Cited by 101
Chronic cold stress sensitizes brain noradrenergic reactivity and noradrenergic facilitation of the HPA stress response in Wistar Kyoto rats
Pardon, M., Ma, S., & Morilak, D. A. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02355-2 · Cited by 97
Chronic Intermittent Cold Stress Sensitises the Hypothalamic‐Pituitary‐Adrenal Response to a Novel Acute Stress by Enhancing Noradrenergic Influence in the Rat Paraventricular Nucleus
Ma, S., & Morilak, D. A. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01372.x · Cited by 94
Regulation of Tyrosine Hydroxylase and Dopamine β‐Hydroxylase mRNA Levels in Rat Adrenals by a Single and Repeated Immobilization Stress
McMahon, A., Kvetňansk, R., Fukuhara, K., Weise, V. K., Kopin, I. J., & Sabban, E. L. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb10954.x · Cited by 90
A single exposure to immobilization causes long-lasting pituitary-adrenal and behavioral sensitization to mild stressors
Belda, X., Fuentes, S., Nadal, R. A., & Armario, A. (2008) · Hormones and Behavior · doi:10.1016/j.yhbeh.2008.07.003 · Cited by 85
Different effects of repeated stressful experiences on mesocortical and mesolimbic dopamine metabolism
Cabib, S., & Puglisi‐Allegra, S. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00750-6 · Cited by 73
Effects of Handling or Immobilization on Plasma Levels of 3,4‐Dihydroxyphenylalanine, Catecholamines, and Metabolites in Rats
Kvetňansk, R., Goldstein, D. S., Weise, V. K., Holmes, C. S., Szemeredi, K., Bagdy, G., & Kopin, I. J. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb10977.x · Cited by 73
Fine Topography of Brain Areas Activated by Cold Stress
Baffi, J., & Palkovits, M. (2000) · Neuroendocrinology · doi:10.1159/000054577 · Cited by 67
Chronic cold stress alters the basal and evoked electrophysiological activity of rat locus coeruleus neurons
Mana, M. J., & Grace, A. A. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00225-x · Cited by 66
Self-citation
Sensitization of norepinephrine release in medial prefrontal cortex: effect of different chronic stress protocols
Jedema, H. P., Sved, A. F., Zigmond, M. J., & Finlay, J. M. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01369-4 · Cited by 65
Chronic Exposure to Cold Stress Alters Electrophysiological Properties of Locus Coeruleus Neurons Recorded In Vitro
Jedema, H., & Grace, A. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300020 · Cited by 61
Self-citation
The effects of prior chronic stress on cardiovascular responses to acute restraint and formalin injection
Bhatnagar, S., Dallman, M. F., Roderick, R. E., Basbaum, A. I., & Taylor, B. K. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00382-5 · Cited by 60
Effects of chronic intermittent cold stress on pituitary adrenocortical and sympathetic adrenomedullary functioning
Bhatnagar, S., Mitchell, J. B., Betito, K., Boksa, P., & Meaney, M. J. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(94)00161-8 · Cited by 59
Left and right 6-hydroxydopamine lesions of the medial prefrontal cortex differentially alter subcortical dopamine utilization and the behavioral response to stress
Carlson, J. N., Visker, K. E., Keller, R. W., & Glick, S. D. (1996) · Brain Research · doi:10.1016/0006-8993(95)01290-7 · Cited by 58
Tyrosine hydroxylase activity and catecholamine biosynthesis in the adrenal medulla of rats during stress.
Fluharty, S. J., Snyder, G. L., Zigmond, M. J., & Stricker, E. M. (1985) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21117-x · Cited by 58
Divergent activation of ventromedial and ventrolateral dopamine systems in animal models of amphetamine sensitization and schizophrenia
Lodge, D., & Grace, A. (2011) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711000113 · Cited by 52
Self-citation
The Significance of the Adrenals for Adaptation
Selye, H. (1937) · Science · doi:10.1126/science.85.2201.247 · Cited by 44
Antipsychotic drug-induced increases in ventral tegmental area dopamine neuron population activity via activation of the nucleus accumbens–ventral pallidum pathway
Valenti, O., & Grace, A. A. (2009) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145709990599 · Cited by 44
Self-citation
A Glutamate–Dopamine Interaction in the Persistent Enhanced Response to Amphetamine in Nucleus Accumbens Core but not Shell Following a Single Restraint Stress
Pacchioni, A. M., Cador, M., Bregonzio, C., & Cancela, L. M. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301080 · Cited by 41
Thermal homeostasis in rats after intrahypothalamic injections of 6-hyroxydopamine
Zoeren, J. V., & Stricker, E. (1976) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1976.230.4.932 · Cited by 39
Intrastriatal kainic acid: acute effects on electrophysiological and biochemical measures of nigrostriatal dopaminergic activity.
Braszko, J. J., Bannon, M. J., Bunney, B. S., & Roth, R. H. (1981) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)32416-x · Cited by 37
NORADRENALINE RELEASE IN RATS DURING PROLONGED COLD‐STRESS AND REPEATED SWIM‐STRESS
BENEDICT, C. R., Fillenz, M., & Stanford, S. C. (1979) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1979.tb13689.x · Cited by 34
Entorhinal Cortex Inhibits Medial Prefrontal Cortex and Modulates the Activity States of Electrophysiologically Characterized Pyramidal Neurons In Vivo
Valenti, O., & Grace, A. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn114 · Cited by 21
Self-citation
Stress and Catecholamines
Eliasson, K. (2009) · Acta Medica Scandinavica · doi:10.1111/j.0954-6820.1984.tb04994.x · Cited by 18

Flagged first, then by citations

1 of the 83 references couldn’t be matched to a known paper.

Research works printed but not linked: 2

Chang C.H., 2011, Beta noradrenergic receptors modulate acute restraint‐mediated down‐regulation of dopamine system activity, Soc. Neurosci.
Willner P., 1995, Psychopharmacology: The Fourth Generation of Progress, 921

Sorted by citations

The brain reward circuitry in mood disorders
Russo, S. J., & Nestler, E. J. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3381 · Cited by 1,870
Dysregulation of the dopamine system in the pathophysiology of schizophrenia and depression
Grace, A. A. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.57 · Cited by 1,166
Self-citation
Rapid regulation of depression-related behaviours by control of midbrain dopamine neurons
Chaudhury, D., Walsh, J. J., Friedman, A. K., Juarez, B., Ku, S. M., Koo, J. W., Ferguson, D., Tsai, H.-C., Pomeranz, L., Christoffel, D. J., et al. (2013) · Nature · doi:10.1038/nature11713 · Cited by 1,156
Dopamine neurons modulate neural encoding and expression of depression-related behaviour
Tye, K. M., Mirzabekov, J. J., Warden, M. R., Ferenczi, E. A., Tsai, H.-C., Finkelstein, J., Kim, S.-Y., Adhikari, A., Thompson, K. R., Andalman, A. S., et al. (2013) · Nature · doi:10.1038/nature11740 · Cited by 1,073
The Role of Genes, Stress, and Dopamine in the Development of Schizophrenia
Howes, O. D., McCutcheon, R. A., Owen, M. J., & Murray, R. M. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.07.014 · Cited by 640

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Authors: Valenti, O., Gill, K. M., & Grace, A. A.
Affiliations: University of Pittsburgh (US)
ORCID: Valenti, Ornella
Grace, Anthony A.
Venue: European Journal of Neuroscience
Publisher: Wiley
Published: 2012-04
Volume: 35
Issue: 8
Pages: 1312-1321
ISSN: 0953-816X (ISSN-L)
1460-9568
DOI: 10.1111/j.1460-9568.2012.08038.x
PMC: PMC3335739
OpenAlex: W2104293622
Cited by: 131
References: 83
Citations by year: 2026: 5 · 2025: 7 · 2024: 4 · 2023: 7 · 2022: 6 · 2021: 12 · 2020: 11 · 2019: 11 · 2018: 14 · 2017: 13 · 2016: 12 · 2015: 8 · 2014: 4 · 2013: 12 · 2012: 4
FWCI: 3.69
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 17 d)
Locations: European Journal of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute of Mental Health (R37MH057440)
National Institute on Drug Abuse (DA 15408, R56DA015408, R01DA015408)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: mesolimbic dopamine system, ventral tegmental area, chronic cold stress, restraint stress, stress adaptation, amphetamine sensitization, ventral striatum, single-unit recording, stressor specificity
MeSH terms: Action Potentials, Afferent Pathways, Amphetamine, Analysis of Variance, Animals, Cold Temperature, Disease Models, Animal, Male, Motor Activity, Neural Inhibition, Restraint, Physical, Stress, Psychological, Time Factors, Dopamine Agents, Rats, Sprague-Dawley, Prefrontal Cortex, Ventral Tegmental Area, Rats, Dopaminergic Neurons

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Different stressors produce excitation or inhibition of mesolimbic dopamine neuron activity: response alteration by stress pre‐exposure

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