Corticosteroid Responses to Limbic Stimulation in Man: Localization of Stimulus Sites

THE DETERMINATION OF 17, 21-DIHYDROXY-20-KETOSTEROIDS IN URINE AND PLASMA

SILBER, R. H., & Porter, C. C. (1954) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)65419-5 · Cited by 779

Clinical Applications of Studies on Stereotactically Implanted Electrodes in Temporal-Lobe Epilepsy

Crandall, P. H., WALTER, R. D., & Rand, R. W. (1963) · Journal of neurosurgery · doi:10.3171/jns.1963.20.10.0827 · Cited by 221

Plasma Corticosteroids: Changes in Concentration after Stimulation of Hippocampus and Amygdala

Mandell, A. J., Chapman, L. F., Rand, R. W., & WALTER, R. D. (1963) · Science · doi:10.1126/science.139.3560.1212 · Cited by 95

EFFECT OF LIMBIC STIMULATION ON RELEASE OF CORTICOSTEROIDS INTO THE ADRENAL VENOUS EFFLUENT OF THE CAT1

Slusher, M. A., & Hyde, J. E. (1961) · Endocrinology · doi:10.1210/endo-69-6-1080 · Cited by 57

Neural regulation of endocrine and autonomic stress responses

Ulrich-Lai, Y. M., & Herman, J. P. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2647 · Cited by 3,318

The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress

Smith, S. M., & Vale, W. W. (2006) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2006.8.4/ssmith · Cited by 1,948

Central mechanisms of stress integration: hierarchical circuitry controlling hypothalamo–pituitary–adrenocortical responsiveness

Herman, J. P., Figueiredo, H., Mueller, N. K., Ulrich-Lai, Y., Ostrander, M. M., Choi, D. C., & Cullinan, W. E. (2003) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2003.07.001 · Cited by 1,586

Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis

Herman, J. P., Ostrander, M. M., Mueller, N. K., & Figueiredo, H. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.006 · Cited by 1,322

Neuroimaging and neuropathological studies of depression: implications for the cognitive-emotional features of mood disorders

Drevets, W. C. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00203-8 · Cited by 1,146

Neuroendocrine pharmacology of stress

Carrasco, G. A., & Van de Kar, L. D. (2003) · European Journal of Pharmacology · doi:10.1016/s0014-2999(03)01285-8 · Cited by 914

INTENSIFICATION OF THE CENTRAL SEROTONINERGIC PROCESSES AS A POSSIBLE DETERMINANT OF THE THYMOLEPTIC EFFECT

Lapin, I. P., & Oxenkrug, G. F. (1969) · The Lancet · doi:10.1016/s0140-6736(69)91140-4 · Cited by 710

Chronic stress, cognitive functioning and mental health

Marin, M.-F., Lord, C., Andrews, J., Juster, R.-P., Sindi, S., Arsenault-Lapierre, G., Fiocco, A. J., & Lupien, S. J. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.02.016 · Cited by 654

Functional anatomical abnormalities in limbic and prefrontal cortical structures in major depression

Drevets, W. C. (2000) · Progress in Brain Research · doi:10.1016/s0079-6123(00)26027-5 · Cited by 659

Functional anatomical correlates of antidepressant drug treatment assessed using PET measures of regional glucose metabolism

Drevets, W. (2002) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(02)00102-5 · Cited by 581

Prefrontal cortical-amygdalar metabolism in major depression.

DREVETS, W. C. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09292.x · Cited by 557

Neuroimaging Abnormalities in the Amygdala in Mood Disorders

DREVETS, W. C. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07098.x · Cited by 544

Ventral subicular interaction with the hypothalamic paraventricular nucleus: Evidence for a relay in the bed nucleus of the stria terminalis

Cullinan, W. E., Herman, J. P., & Watson, S. J. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903320102 · Cited by 541

Antidepressants recruit new neurons to improve stress response regulation

Surget, A., Tanti, A., Leonardo, E. D., Laugeray, A., Rainer, Q., Touma, C., Palme, R., Griebel, G., Ibarguen-Vargas, Y., Hen, R., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.48 · Cited by 471

Glucose metabolism in the amygdala in depression: relationship to diagnostic subtype and plasma cortisol levels

Drevets, W. C., Price, J. L., Bardgett, M. E., Reich, T., Todd, R. D., & Raichle, M. E. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00687-6 · Cited by 457

Glucocorticoid regulation of diverse cognitive functions in normal and pathological emotional states

Erickson, K., Drevets, W. C., & Schulkin, J. A. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00033-2 · Cited by 422

Stimulation and Regional Ablation of the Amygdaloid Complex with Reference to Functional Representations

Kaada, B. R. (1972) · Advances in behavioral biology · doi:10.1007/978-1-4615-8987-7_8 · Cited by 405

Pathoetiological Model of Delirium: a Comprehensive Understanding of the Neurobiology of Delirium and an Evidence-Based Approach to Prevention and Treatment

Maldonado, J. R. (2008) · Critical Care Clinics · doi:10.1016/j.ccc.2008.06.004 · Cited by 345

Hippocampal Remodeling and Damage by Corticosteroids Implications for Mood Disorders

Brown, E. S. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00054-8 · Cited by 344

The descending afferent connections of the paraventricular nucleus of the hypothalamus (PVN)

Silverman, A., Hoffman, D. L., & Zimmerman, E. A. (1981) · Brain Research Bulletin · doi:10.1016/s0361-9230(81)80068-8 · Cited by 326

Enlargement of the Amygdala in Patients with a First Episode of Major Depression

Frodl, T., Meisenzahl, E., Zetzsche, T., Bottlender, R., Born, C., Groll, C., Jäger, M., Leinsinger, G., Hahn, K., & Möller, H.-J. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01359-2 · Cited by 316

Adult Neurogenesis: Beyond Learning and Memory

Cameron, H. A., & Glover, L. R. (2014) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015006 · Cited by 322

Neighborhood matters: divergent patterns of stress-induced plasticity across the brain

Chattarji, S., Tomar, A., Suvrathan, A., Ghosh, S., & Rahman, M. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4115 · Cited by 248

Role of the ventral subiculum in stress integration

Herman, J. P., & Mueller, N. K. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.05.035 · Cited by 235

HPA axis activity in patients with panic disorder: review and synthesis of four studies

Abelson, J. L., Khan, S. A., Liberzon, I., & Young, E. A. (2006) · Depression and Anxiety · doi:10.1002/da.20220 · Cited by 224

Metabolic syndrome, age‐associated neuroendocrine disorders, and dysregulation of tryptophan—kynurenine metabolism

Oxenkrug, G. F. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05356.x · Cited by 223

Tryptophan kynurenine metabolism as a common mediator of genetic and environmental impacts in major depressive disorder: the serotonin hypothesis revisited 40 years later.

Oxenkrug, G. F. (2010) · PubMed · Cited by 212

Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala

Murray, E. A., Wise, S. P., & Drevets, W. C. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.041 · Cited by 208

Delaying aging and the aging-associated decline in protein homeostasis by inhibition of tryptophan degradation

van der Goot, A. T., Zhu, W., Vázquez‐Manrique, R. P., Seinstra, R. I., Dettmer, K., Michels, H., Farina, F., Krijnen, J., Melki, R., Buijsman, R. C., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203083109 · Cited by 199

Ventral subiculum regulates hypothalamo–pituitary–adrenocortical and behavioural responses to cognitive stressors

Herman, J. P., Dolgas, C. M., & Carlson, S. L. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00055-4 · Cited by 193

Adult neurogenesis in the mammalian dentate gyrus

Abbott, L. C., & Nigussie, F. (2019) · Anatomia Histologia Embryologia · doi:10.1111/ahe.12496 · Cited by 183

Stress, seizures, and hypothalamic–pituitary–adrenal axis targets for the treatment of epilepsy

Maguire, J. L., & Salpekar, J. A. (2012) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2012.09.040 · Cited by 173

Can architectural design alter the physiological reaction to psychosocial stress? A virtual TSST experiment

Fich, L. B., Jönsson, P., Kirkegaard, P. H., Wallergård, M., Garde, A. H., & Hansen, Å. M. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.05.034 · Cited by 150

Adrenal Cortical Activity in Pathological Emotional States : A Review

Rubín, R. T., & Mandell, A. J. (1966) · American Journal of Psychiatry · doi:10.1176/ajp.123.4.387 · Cited by 126

Neuroinflammation as an etiological trigger for depression comorbid with inflammatory bowel disease

Craig, C. F., Filippone, R. T., Stavely, R., Bornstein, J. C., Apostolopoulos, V., & Nurgali, K. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02354-1 · Cited by 124

Serotonin Now: Clinical Implications of Inhibiting Its Synthesis with Para-Chlorophenylalanine

Sjoerdsma, A., LOVENBERG, W., ENGELMAN, K., CARPENTER, W. T., WYATT, R. J., & GESSA, G. L. (1970) · Annals of Internal Medicine · doi:10.7326/0003-4819-73-4-607 · Cited by 110

Developmental pathology, dopamine, stress and schizophrenia

Lodge, D. J., & Grace, A. A. (2011) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2010.08.002 · Cited by 109

A metabolic function of the hippocampal sharp wave-ripple

Tingley, D., McClain, K., Kaya, E., Carpenter, J., & Buzsáki, G. (2021) · Nature · doi:10.1038/s41586-021-03811-w · Cited by 108

Serotonin and the Neuroendocrine Regulation of the Hypothalamic–Pituitary–Adrenal Axis in Health and Disease

Sullivan, N. R., & de Kar, L. D. V. (2003) · Vitamins and hormones · doi:10.1016/s0083-6729(03)01006-9 · Cited by 108

Corticolimbic dysregulation and chronic methamphetamine abuse

Baicy, K., & London, E. D. (2007) · Addiction · doi:10.1111/j.1360-0443.2006.01777.x · Cited by 105

Toward a Psychobiology of Transcendence: God in the Brain

Mandell, A. J. (1980) · Springer eBooks · doi:10.1007/978-1-4684-3456-9_14 · Cited by 102

Mourning and melancholia revisited: correspondences between principles of Freudian metapsychology and empirical findings in neuropsychiatry

Carhart-Harris, R. L., Mayberg, H. S., Malizia, A. L., & Nutt, D. (2008) · Annals of General Psychiatry · doi:10.1186/1744-859x-7-9 · Cited by 113

Effects of increasing tryptophan intake on growth and physiological changes in nursery pigs1

Shen, Y. B., Voilqué, G., Kim, J. D., Odle, J., & Kim, S. W. (2012) · Journal of Animal Science · doi:10.2527/jas.2011-4203 · Cited by 97

Differential fornix ablations and the circadian rhythmicity of adrenal corticosteroid secretion

Fischette, C. T., Komisaruk, B. R., Edinger, H. M., Feder, H. H., & Siegel, A. (1980) · Brain Research · doi:10.1016/0006-8993(80)90073-6 · Cited by 89

Neural Correlates of Protection Motivation for Secure IT Behaviors: An fMRI Examination

Warkentin, M. E., Walden, E. A., Johnston, A. C., & Straub, D. W. (2016) · Journal of the Association for Information Systems · doi:10.17705/1jais.00424 · Cited by 90

Effects of amygdaloid stimulation on pituitary-adrenal activity in conscious cats

Matheson, G. K., Branch, B. J., & Taylor, A. N. (1971) · Brain Research · doi:10.1016/0006-8993(71)90160-0 · Cited by 77

Effects of Lesions and Electrical Stimulation of the Amygdala on Hypothalamic-Hypophyseal-Regulation

Zolovick, A. J. (1972) · Advances in behavioral biology · doi:10.1007/978-1-4615-8987-7_25 · Cited by 75

Neuroplasticity in mood disorders

Drevets, W. C. (2004) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2004.6.2/wdrevets · Cited by 75

Implications of altered limbic‐hypothalamicpituitary‐adrenocortical (LHPA)‐function for neurobiology of depression

Holsboer, F. (1988) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1988.tb08556.x · Cited by 73

A combined electron microscopic HRP and immunocytochemical study of the limbic projections to rat hypothalamic nuclei containing vasopressin and oxytocin neurons

Oldfield, B. J., Hou-Yu, A., & Silverman, A. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902310209 · Cited by 69

The Hippocampus and the Pituitary-Adrenal System Hormones

Bohus, B. (1975) · Springer eBooks · doi:10.1007/978-1-4684-2976-3_13 · Cited by 70

Cellular and Extracellular Regulatory Mechanisms of Hypothalamic Corticotropin-Releasing Hormone Neurons.

Itoi, K., Seasholtz, A. F., & Watson, S. J. (1998) · Endocrine Journal · doi:10.1507/endocrj.45.13 · Cited by 62

Cognition from the Body-Brain Partnership: Exaptation of Memory

Buzsáki, G., & Tingley, D. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-101222-110632 · Cited by 66

Diurnal cortisol amplitude and fronto-limbic activity in response to stressful stimuli

Cunningham‐Bussel, A., Root, J. C., Butler, T., Tüscher, O., Pan, H., Epstein, J., Weisholtz, D. S., Pavony, M. T., Silverman, M. E., Goldstein, M. S., et al. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.11.011 · Cited by 57

Perinatal exposure to 50 ppb sodium arsenate induces hypothalamic-pituitary-adrenal axis dysregulation in male C57BL/6 mice

Goggin, S. L., Labrecque, M. T., & Allan, A. M. (2012) · NeuroToxicology · doi:10.1016/j.neuro.2012.08.010 · Cited by 53

Elevated CYP2C19 expression is associated with depressive symptoms and hippocampal homeostasis impairment

Jukić, M. M., Opel, N., Ström, J., Carrillo‐Roa, T., Miksys, S. L., Novalen, M., Renblom, A., Sim, S. C., Peñas‐Lledó, E., Courtet, P., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.204 · Cited by 53

A [14C]2-Deoxyglucose analysis of the functional neural pathways of the limbic forebrain in the rat. III. The hippocampal formation

Watson, R. E., Edinger, H. M., & Siegel, A. (1983) · Brain Research Reviews · doi:10.1016/0165-0173(83)90012-7 · Cited by 52

Resilience to adversity is associated with increased activity and connectivity in the VTA and hippocampus

Richter, A., Krämer, B., Diekhof, E. K., & Gruber, O. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101920 · Cited by 54

Association between Changes in Adrenal Secretion and Cerebral Morphometric Correlates in Normal Aging and Senile Dementia

Magri, F., Terenzi, F., Ricciardi, T., Fioravanti, M., Solerte, S. B., Stabile, M., Balza, G., Gandini, C., Villa, M., & Ferrari, E. (2000) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000017220 · Cited by 48

The cerebello-hypothalamic–pituitary–adrenal axis dysregulation hypothesis in depressive disorder

Schutter, D. J. L. G. (2012) · Medical Hypotheses · doi:10.1016/j.mehy.2012.08.027 · Cited by 47

Reduced anterior hippocampal formation volume in hyponatremic schizophrenic patients

Goldman, M. B., Torres, I. J., Keedy, S., Marlow-O’Connor, M., Beenken, B., & Pilla, R. S. (2007) · Hippocampus · doi:10.1002/hipo.20292 · Cited by 45

The intersections of stress, anxiety and epilepsy

Salpekar, J. A., Basu, T., Thangaraj, S., & Maguire, J. L. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.02.001 · Cited by 44

Tryptophan Metabolism Is Associated with BMI and Adipose Tissue Mass and Linked to Metabolic Disease in Pediatric Obesity

Lischka, J., Schanzer, A., Baumgartner-Kaut, M., de Gier, C., Greber‐Platzer, S., & Zeyda, M. (2022) · Nutrients · doi:10.3390/nu14020286 · Cited by 44

Hypothalamic-Pituitary-Adrenal Axis, Glucocorticoids, and Neurologic Disease

Herman, J. P., & Seroogy, K. B. (2006) · Neurologic Clinics · doi:10.1016/j.ncl.2006.03.006 · Cited by 42

Neuroendocrine Responses to a Cold Pressor Stimulus in Polydipsic Hyponatremic and in Matched Schizophrenic Patients

Goldman, M. B., Gnerlich, J. L., & Hussain, N. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301282 · Cited by 40

Chronic Non-Social Stress Affects Depressive Behaviors But Not Anxiety in Mice

Yoon, S. H., Kim, B., Ye, S., & Kim, M. (2014) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2014.18.3.263 · Cited by 40

Search and attention: Interactions of the hippocampal-septal axis, adrenocortical and gonadal hormones

Oades, R. D. (1979) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(79)90024-1 · Cited by 37

A match-mismatch theory of limbic system function

Cormier, S. M. (1981) · Physiological Psychology · doi:10.3758/bf03326955 · Cited by 36

Stimulus intensity-dependent modulations of hippocampal long-term potentiation by basolateral amygdala priming

Li, Z., & Richter‐Levin, G. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00021 · Cited by 35

Stress and the Reproductive System

Ferin, M. (2006) · Elsevier eBooks · doi:10.1016/b978-012515400-0/50053-1 · Cited by 35

Cushing's Disease as a Psychosomatic Disorder: A Selective Review of the Clinical and Experimental Literature and a Report of Ten Cases

Gifford, S. R., & Gunderson, J. G. (1970) · Perspectives in biology and medicine · doi:10.1353/pbm.1970.0019 · Cited by 35

Influence of cadmium chloride, mercuric chloride, and sodium vanadate on the glutathione‐conjugating enzyme system in liver, kidney, and brain of mice

Siegers, C. ‐., Schenke, M., & Younes, M. (1987) · Journal of Toxicology and Environmental Health · doi:10.1080/15287398709531058 · Cited by 35

Plasma ACTH and corticosterone responses to limbic kindling in the rat

SZAFARCZYK, A., Caracchini, M., Rondouin, G., IXART, G., Malaval, F., & ASSENMACHER, I. (1986) · Experimental Neurology · doi:10.1016/0014-4886(86)90300-6 · Cited by 34

The tuning of the nervous system: physiological foundations and implications for behavior

Gellhorn, E. (1967) · Perspectives in Biology and Medicine · doi:10.1353/pbm.1967.0021 · Cited by 33

Hippocampal influence on amygdala unit activity in awake squirrel monkeys

Morrison, F., & Poletti, C. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90889-6 · Cited by 32

Hippocampus-Anterior Hypothalamic Circuit Modulates Stress-Induced Endocrine and Behavioral Response

Bang, J. Y., Zhao, J., Rahman, M. F., St-Cyr, S., McGowan, P. O., & Kim, J. C. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.894722 · Cited by 32

Modulatory effects of acupuncture on murine depression-like behavior following chronic systemic inflammation

Kwon, S., Lee, B., Yeom, M., Sur, B., Kim, M., Kim, S.-T., Park, H., Lee, H., & Hahm, D. (2012) · Brain Research · doi:10.1016/j.brainres.2012.07.009 · Cited by 29

Neuroimaging and Neuropathological Studies of Mood Disorders

Drevets, W. C., & Price, J. L. (2005) · Biology of Depression · doi:10.1002/9783527619672.ch17 · Cited by 26

Long term effects of stress on hippocampal function: Emphasis on early life stress paradigms and potential involvement of neuropeptide Y

Alviña, K., Farshbaf, M. J., & Mondal, A. K. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24614 · Cited by 23

The Hippocampus and Regulation of the Hypothalamic-Hypophyseal-Adrenal Cortical Axis

Hartesveldt, C. V. (1975) · Springer eBooks · doi:10.1007/978-1-4684-2976-3_15 · Cited by 23

Can the neural–cortisol association be moderated by experience-induced changes in awareness?

Lau, W. K., Leung, M.-K., Chan, C. C. H., Wong, S. S. Y., & Lee, T. M. C. (2015) · Scientific Reports · doi:10.1038/srep16620 · Cited by 22

Neuroendocrine effects of limbic activation by electrical, spontaneous, and pharmacological modes: Relevance to the pathophysiology of affective dysregulation in psychiatric disorders

Kling, M. A., Kellner, C. H., Post, R. M., Cowdry, R. W., Gardner, D. L., Coppola, R., Putnam, F. W., & Gold, P. W. (1987) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(87)90016-9 · Cited by 22

Electrical activity generated in subicular and entorhinal cortices after electrical stimulation of the lateral and basolateral amygdala of the rat

Colino, A., & de Molina, A. F. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90282-4 · Cited by 20

The Limbic-Hypothalamic-Pituitary-Adrenal System and Human Behavior

Carpenter, W. T., & GRUEN, P. H. (1978) · Springer eBooks · doi:10.1007/978-1-4684-3189-6_2 · Cited by 20

Successful use of inhaled nitric oxide to decrease intracranial pressure in a patient with severe traumatic brain injury complicated by acute respiratory distress syndrome: a role for an anti-inflammatory mechanism?

Papadimos, T. J., Medhkour, A., & Yermal, S. (2009) · Scandinavian Journal of Trauma Resuscitation and Emergency Medicine · doi:10.1186/1757-7241-17-5 · Cited by 19

The Psychobiology of Trance: II: Physiological and Endocrine Correlates

Ervin, F. R., Palmour, R. M., Pearson Murphy, B. E., Prince, R., & Simons, R. C. (1988) · Transcultural Psychiatric Research Review · doi:10.1177/136346158802500402 · Cited by 19

Hormonal dissociation of limbic lesion effects on shuttle box avoidance in rats.

Lovely, R. H. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0076807 · Cited by 19

ORAL CONTRACEPTIVES AND DEPRESSION

Price, S., & Toseland, P. A. (1969) · The Lancet · doi:10.1016/s0140-6736(69)92466-0 · Cited by 18

Hypothalamo-Pituitary-Adrenocortical Axis, Glucocorticoids, and Neurologic Disease

Doczy, E. J., Seroogy, K. B., Harrison, C. R., & Herman, J. P. (2009) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2009.02.003 · Cited by 16

Idle Behaviors of the Hippocampus Reflect Endogenous Cortisol Levels in Youth

Thomason, M. E., Tocco, M. A., Quednau, K., Bedway, A. R., & Carré, J. M. (2013) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2013.04.004 · Cited by 18

The Amygdala and Anxiety

Linsambarth, S., Moraga‐Amaro, R., Quintana-Donoso, D., Rojas, S., & Stehberg, J. (2017) · InTech eBooks · doi:10.5772/intechopen.68618 · Cited by 17

Daily Rhythms of Steroid and Associated Pituitary Hormones in Man and their Relationship to Sleep

Daly, J. R., & EVANS, J. I. (1974) · Advances in Steroid Biochemistry and Pharmacology · doi:10.1016/b978-0-12-037504-2.50005-5 · Cited by 16

Stress Neurobiology and Developmental Psychopathology

Jacoby, N., Overfeld, J., Binder, E. B., & Heim, C. M. (2016) · Wiley eBooks · doi:10.1002/9781119125556.devpsy221 · Cited by 16

Sleep-Endocrinology Studies in Man

Rubín, R. T. (1975) · Progress in brain research · doi:10.1016/s0079-6123(08)63646-8 · Cited by 15

Aging-Related Adaptations in the Corticotropic Axis: Modulation by Gender

Veldhuis, J. D., Keenan, D. M., Roelfsema, F., & Iranmanesh, A. (2005) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2005.07.014 · Cited by 14

Hippocampal interneurons are direct targets for circulating glucocorticoids

Kraus, K. L., Chordia, A. P., Drake, A. W., Herman, J. P., & Danzer, S. C. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25322 · Cited by 14

The Role of Hippocampal NMDA Receptors in Long-Term Emotional Responses following Muscarinic Receptor Activation

Hoeller, A. A., Costa, A. P., Bicca, M. A., MATHEUS, F. C., Lach, G., Spiga, F., Lightman, S. L., Walz, R., Collingridge, G. L., Bortolotto, Z. A., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147293 · Cited by 12

Neural Regulation of Pituitary Function

Stuenkel, C. A. (1991) · Epilepsia · doi:10.1111/j.1528-1157.1991.tb05888.x · Cited by 10

The adrenocortical response to craniotomy for brain tumor

Shenkin, H. A., Gutterman, P., & Bouzarth, W. F. (1971) · Journal of neurosurgery · doi:10.3171/jns.1971.34.5.0657 · Cited by 9

Electroencephalography

Proler, M. L., Frost, J. D., Maulsby, R. L., & Crawley, J. W. (1967) · Elsevier eBooks · doi:10.1016/b978-1-4831-9662-6.50015-9 · Cited by 9

Plasma Corticosteroids: Changes in Concentration after Stimulation of Hippocampus and Amygdala

Mandell, A. J., Chapman, L. F., Rand, R. W., & WALTER, R. D. (1963) · Science · doi:10.1126/science.139.3560.1212 · Cited by 95

Plasma Corticosterone Responses to Electrical Stimulation of the Amygdaloid Complex: Cytoarchitectural Specificity

Dunn, J. D., & Whitener, J. (2008) · Neuroendocrinology · doi:10.1159/000124442 · Cited by 154

INCREASE OF PLASMA 17-HYDROXYCORTICOSTEROIDS BY CEREBRAL CORTICAL AND AMYGDALOID STIMULATION IN THE CAT

Setekleiv, J., Skaug, O. E., & Kaada, B. R. (1961) · Journal of Endocrinology · doi:10.1677/joe.0.0220119 · Cited by 38

Differential plasma corticosterone responses to hippocampal stimulation

Dunn, J. D., & Orr, S. E. (1984) · Experimental Brain Research · doi:10.1007/bf00235813 · Cited by 152

Plasma Growth Hormone and Cortisol Changes Following Limbic Stimulation in Conscious Monkeys

Ehle, A. L., Mason, J. W., & Pennington, L. L. (2008) · Neuroendocrinology · doi:10.1159/000122654 · Cited by 14