Central Catecholamine Neuron Systems: Anatomy and Physiology of the Norepinephrine and Epinephrine Systems

An integrative theory of locus coeruleus-norepinephrine function: adaptive gain and optimal performance

Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472

Large-scale neurocognitive networks and distributed processing for attention, language, and memory

Mesulam, M. (1990) · Annals of Neurology · doi:10.1002/ana.410280502 · Cited by 2,684

The locus coeruleus–noradrenergic system: modulation of behavioral state and state-dependent cognitive processes

Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529

Nucleus locus ceruleus: new evidence of anatomical and physiological specificity

Foote, S. L., Bloom, F. E., & Aston-Jones, G. (1983) · Physiological Reviews · doi:10.1152/physrev.1983.63.3.844 · Cited by 1,901

The locus coeruleus and noradrenergic modulation of cognition

Sara, S. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2573 · Cited by 1,848

Neurobiology of relapse to heroin and cocaine seeking: a review

Shalev, U., Grimm, J. W., & Shaham, Y. (2002) · Pharmacological Reviews · doi:10.1124/pr.54.1.1 · Cited by 880

Pathways of sexual desire

Pfaus, J. G. (2009) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2009.01309.x · Cited by 678

Noradrenergic Function in Panic Anxiety: Effects of Yohimbine in Healthy Subjects and Patients With Agoraphobia and Panic Disorder

Charney, D. S. (1984) · Archives of General Psychiatry · doi:10.1001/archpsyc.1984.01790190025003 · Cited by 599

Regulation of the hypothalamic corticotropin-releasing hormone neurosecretory system

Whitnall, M. H. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90035-q · Cited by 582

Effects of sleep and arousal on the processing of visual information in the cat

Livingstone, M. S., & Hubel, D. H. (1981) · Nature · doi:10.1038/291554a0 · Cited by 583

A genetically encoded fluorescent sensor for rapid and specific in vivo detection of norepinephrine

Feng, J., Zhang, C., Lischinsky, J. E., Jing, M., Zhou, J., Wang, H., Zhang, Y., Dong, A., Wu, Z., Wu, H., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.037 · Cited by 545

Consciousness and the brainstem

Parvizi, J. (2001) · Cognition · doi:10.1016/s0010-0277(00)00127-x · Cited by 503

Distribution of GLP‐1 Binding Sites in the Rat Brain: Evidence that Exendin‐4 is a Ligand of Brain GLP‐1 Binding Sites

Göke, R., Larsen, P. J., Mikkelsen, J. D., & Sheikh, S. P. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00650.x · Cited by 474

Stress-induced reinstatement of drug seeking: 20 years of progress

Mantsch, J. R., Baker, D. A., Funk, D., Lê, A. D., & Shaham, Y. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.142 · Cited by 438

Homeostasis, Stress, Trauma, and Adaptation

Perry, B. D., & Pollard, R. (1998) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/s1056-4993(18)30258-x · Cited by 440

Effect of the nigrostriatal dopamine system on acquired neural responses in the striatum of behaving monkeys

Aosaki, T., Graybiel, A. M., & Kimura, M. (1994) · Science · doi:10.1126/science.8023166 · Cited by 427

The pedunculopontine nucleus

GARCIARILL, E. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90016-t · Cited by 413

Neuroanatomical correlates of brainstem coma

Parvizi, J. (2003) · Brain · doi:10.1093/brain/awg166 · Cited by 400

Actions of noradrenaline recorded intracellularly in rat hippocampal CA1 pyramidal neurones, in vitro.

Madison, D. V., & Nicoll, R. A. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp016006 · Cited by 391

Is Heterosynaptic modulation essential for stabilizing hebbian plasiticity and memory

Bailey, C. H., Giustetto, M., Huang, Y.-Y., Hawkins, R. D., & Kandel, E. R. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036191 · Cited by 382

New evidence for neurotransmitter influences on brain development

Levitt, P., Harvey, J. A., Friedman, E., Simansky, K., & Murphy, E. H. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)01028-4 · Cited by 362

Comprehensive catecholaminergic projectome analysis reveals single-neuron integration of zebrafish ascending and descending dopaminergic systems

Tay, T. L., Ronneberger, O., Ryu, S., Nitschke, R., & Driever, W. (2011) · Nature Communications · doi:10.1038/ncomms1171 · Cited by 307

Neurochemical correlates of autistic disorder: a review of the literature

Lam, K. S. L., Aman, M. G., & Arnold, L. E. (2006) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2005.03.003 · Cited by 318

Alpha-2 Adrenergic Receptor Agonists Block Stress-Induced Reinstatement of Cocaine Seeking

Erb, S. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00158-x · Cited by 270

The neural representation of unexpected uncertainty during value-based decision making

Payzan-LeNestour, E., Dunne, S., Bossaerts, P., & O’Doherty, J. P. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.037 · Cited by 257

Tau pathology spread in PS19 tau transgenic mice following locus coeruleus (LC) injections of synthetic tau fibrils is determined by the LC's afferent and efferent connections

Iba, M., McBride, J. D., Guo, J. L., Zhang, B., Trojanowski, J. Q., & Lee, V. M.-Y. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1458-4 · Cited by 223

Modulators in concert for cognition: Modulator interactions in the prefrontal cortex

Briand, L. A., Gritton, H., Howe, W. M., Young, D. A., & Sarter, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.06.007 · Cited by 216

Participation of noradrenergic pathways in the expression of opiate withdrawal: biochemical and pharmacological evidence

MALDONADO, R. (1997) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00061-5 · Cited by 213

Evidence for a neurotrophic role of noradrenaline neurons in the postnatal development of rat cerebral cortex

Felten, D. L., Hallman, H., & Jonsson, G. (1982) · Journal of Neurocytology · doi:10.1007/bf01258008 · Cited by 211

Clonidine blocks stress-induced reinstatement of heroin seeking in rats: an effect independent of locus coeruleus noradrenergic neurons

Shaham, Y., Highfield, D., Delfs, J., Leung, S., & Stewart, J. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00899.x · Cited by 201

Modulation of Both the Early and the Late Phase of Mossy Fiber LTP by the Activation of β-Adrenergic Receptors

Huang, Y.-Y., & Kandel, E. R. (1996) · Neuron · doi:10.1016/s0896-6273(00)80080-x · Cited by 199

Role for insulin signaling in catecholaminergic neurons in control of energy homeostasis

Könner, A. C., Hess, S., Tovar, S., Mesaros, A., Sánchez-Lasheras, C., Evers, N., Verhagen, L. A. W., Brönneke, H. S., Kleinridders, A., Hampel, B., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.03.021 · Cited by 194

Effects of locus coeruleus lesions on auditory, long-latency, event-related potentials in monkey

Pineda, J., Foote, S., & Neville, H. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-01-00081.1989 · Cited by 184

Neuropeptide and small transmitter coexistence: Fundamental studies and relevance to mental illness

Hökfelt, T., Barde, S., Xu, Z.-Q. D., Kuteeva, E., Rüegg, J., Le Maitre, E., Risling, M., Kehr, J., Ihnatko, R., Theodorsson, E., et al. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00106 · Cited by 139

Actions of noradrenaline on neocortical neurons in vitro

Dodt, H.-U., Pawelzik, H., & Zieglga¨nsberger, W. (1991) · Brain Research · doi:10.1016/0006-8993(91)91303-i · Cited by 104

Untitled work

Kret (2014) · doi:10.1371/journal.pone.0104886 · Cited by 98

Stress-induced Relapse to Drug Seeking in the Rat; Role of the Bed Nucleus of the Stria Terminalis and Amygdala

Erb, S., Shaham, Y., & Stewart, J. (2001) · Stress · doi:10.3109/10253890109014753 · Cited by 73

Involvement of noradrenergic system within the central nucleus of the amygdala in naloxone-precipitated morphine withdrawal-induced conditioned place aversion in rats

Watanabe, T., Nakagawa, T., Yamamoto, R., Maeda, A., Minami, M., & Satoh, M. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1504-0 · Cited by 71

Methylphenidate and Atomoxetine Inhibit Social Play Behavior through Prefrontal and Subcortical Limbic Mechanisms in Rats

Achterberg, E. J. M., van Kerkhof, L. W. M., Damsteegt, R., Trezza, V., & Vanderschuren, L. J. M. J. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2945-14.2015 · Cited by 58

Fluxes of lactate into, from, and among gap junction-coupled astrocytes and their interaction with noradrenaline

Hertz, L., Gibbs, M. E., & Dienel, G. A. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00261 · Cited by 58

The neurobiology of social play behaviour: Past, present and future

Achterberg, E. J. M., & Vanderschuren, L. J. M. J. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105319 · Cited by 56

Dopamine and norepinephrine receptors participate in methylphenidate enhancement of in vivo hippocampal synaptic plasticity

Jenson, D., Yang, K., Acevedo-Rodriguez, A., Levine, A., Broussard, J. I., Tang, J., & Dani, J. A. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.029 · Cited by 52

Evidence of VTA and LC control of protein synthesis required for the behavioral tagging process

Moncada, D. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.003 · Cited by 50

Perspective: causes and functional significance of temporal variations in attention control

Lenartowicz, A., Simpson, G. V., & Cohen, M. S. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00381 · Cited by 38

Psychophysiological and biochemical changes in patients with panic attacks in a defined situational arousal

Braune, S., Albus, M., Fröhler, M., Höhn, T., & Scheibe, G. (1994) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf02193524 · Cited by 33

Development of dopamine‐beta hydroxylase—positive fiber innervation of the rat hippocampus

Moudy, A. M., Kunkel, D. D., & Schwartzkroin, P. A. (1993) · Synapse · doi:10.1002/syn.890150407 · Cited by 32

Interactions between inhibitory interneurons and excitatory associational circuitry in determining Spatio-Temporal dynamics of hippocampal dentate granule cells: A Large-Scale computational study

Hendrickson, P. J., Yu, G. J., Song, D., & Berger, T. W. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00155 · Cited by 18

Dopaminergic influence over hippocampal synaptic plasticity and function

I Broussard, J. (2012) · Clinical and Experimental Pharmacology · doi:10.4172/2161-1459.1000e108 · Cited by 15