Regulation of the HPA axis by cytokines.

Importance of exercise immunology in health promotion

Rosa, J. C., Lira, F., de Mello, M. D., & Santos, R. T. (2011) · Amino Acids · doi:10.1007/s00726-010-0786-x · Cited by 44

Inflammatory cytokine network in schizophrenia

Zakharyan, R., & Boyajyan, A. S. (2013) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2013.830774 · Cited by 45

Endotoxin Decreases Corticotropin-Releasing Factor Receptor 1 Messenger Ribonucleic Acid Levels in the Rat Pituitary

Aubry, J.-M., Turnbull, A. V., Pozzoli, G., RIVIER, C. L., & Vale, W. W. (1997) · Endocrinology · doi:10.1210/endo.138.4.5050 · Cited by 46

Short- and long-term effects of lipopolysaccharide-induced inflammation on rabbit sperm quality

Brecchia, G., Cardinali, R., Mourvaki, E., Collodel, G., Moretti, E., Bosco, A. D., & Castellini, C. (2009) · Animal Reproduction Science · doi:10.1016/j.anireprosci.2009.06.016 · Cited by 44

Role of Endogenous Glucocorticoids in Immune System Function: Regulation and Counterregulation

Spencer, R. L., Kalman, B. A., & Dhabhar, F. S. (2001) · Comprehensive physiology · doi:10.1002/cphy.cp070418 · Cited by 43

Serum interleukin-6 predicts cortisol release in acute stroke patients

Szczudlik, A., Dziedzic, T., Bartuś, S., Słowik, A., & Kiełtyka, A. (2004) · Journal of Endocrinological Investigation · doi:10.1007/bf03350908 · Cited by 42

Enhancement of the hypothalamic–pituitary–adrenal axis but not cytokine responses to stress challenges imposed during withdrawal from acute alcohol exposure in Sprague–Dawley rats

Buck, H. M., Hueston, C. M., Bishop, C., & Terrence Deak, B. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2388-z · Cited by 41

Selective increases in the cytokine, TNFα, in the prefrontal cortex of PCP-treated rats and human schizophrenic subjects: influence of antipsychotic drugs

Paterson, G., Ohashi, Y., Reynolds, G. P., Pratt, J. A., & MORRIS, B. J. (2006) · Journal of Psychopharmacology · doi:10.1177/0269881106062025 · Cited by 41

A novel isoquinoline compound abolishes chronic unpredictable mild stress-induced depressive-like behavior in mice

Pesarico, A. P., Sartori, G., Brüning, C. A., Mantovani, A. C., Duarte, T., Zeni, G. R., & Nogueira, C. W. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.03.049 · Cited by 42

The Restraint Stress-Induced Elevation in Plasma Interleukin-6 Negatively Regulates the Plasma TNF-α Level

Nukina, H., Sudo, N., Komaki, G., Yu, X.-N., Mine, K., & Kubo, C. (1998) · NeuroImmunoModulation · doi:10.1159/000026352 · Cited by 40

Inhibitory Effects of Endotoxin on LH Secretion in the Ovariectomized Monkey Are Prevented by Naloxone but Not by an Interleukin-1 Receptor Antagonist

Xiao, E., Xia‐Zhang, L., & Ferin, M. (1999) · NeuroImmunoModulation · doi:10.1159/000026415 · Cited by 40

Capacity to Produce Cytokines During Weight Restoration in Patients With Anorexia Nervosa

Nagata, T., Tobitani, W., Kiriike, N., Iketani, T., & Yamagami, S. (1999) · Psychosomatic Medicine · doi:10.1097/00006842-199905000-00018 · Cited by 40

Gut Microbial Dysbiosis and Cognitive Impairment in Bipolar Disorder: Current Evidence

Dai, W., Liu, J., Yan, Q., Teng, Z., Li, S., Yuan, H., Huang, J., Xiang, H., Tang, H., Wang, B., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.893567 · Cited by 42

Effects of Sleep Deprivation on Nocturnal Cytokine Concentrations in Depressed Patients and Healthy Control Subjects

Voderholzer, U., Fiebich, B. L., Dersch, R. S., Feige, B., Piosczyk, H., Kopasz, M., Riemann, D. W., & Lieb, K. (2012) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.11060142 · Cited by 37

Effect of Acute Alcohol Treatment on the Release of ACTH, Corticosterone, and Pro‐Inflammatory Cytokines in Response to Endotoxin

RIVIER, C. L. (1999) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.1999.tb04169.x · Cited by 37

Balancing the mind: Toward a complete picture of the interplay between gut microbiota, inflammation and major depressive disorder

Dabboussi, N., Debs, E., Bouji, M., Rafei, R., & Farès, N. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.111056 · Cited by 38

Haplotype structure of inflammatory cytokines genes (IL1B, IL6 and TNF/LTA) in US Caucasians and African Americans

Belfer, I., Buzás, B., Hipp, H. S., Dean, M. C., Evans, C., Lorincz, I. S., Max, M. B., & Goldman, D. A. (2004) · Genes and Immunity · doi:10.1038/sj.gene.6364118 · Cited by 36

The comparison of sex differences in depression-like behaviors and neuroinflammatory changes in a rat model of depression induced by chronic stress

Xia, J., Wang, H., Zhang, C., Liu, B., Li, Y., Li, K., Li, P., & Song, C. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1059594 · Cited by 38

Social interactions alter proinflammatory cytokine gene expression and behavior following endotoxin administration

Weil, Z. M., Bowers, S., Pyter, L. M., & Nelson, R. J. (2005) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2005.05.001 · Cited by 35

Physical Illnesses Before Diagnosed as Schizophrenia: A Nationwide Case-Control Study

Chen, Y., Pan, C., Chang, C.-K., Chen, P., Chang, H., Tai, M.-H., Su, S., Tsai, S., Chen, C., & Kuo, C. (2020) · Schizophrenia Bulletin · doi:10.1093/schbul/sbaa009 · Cited by 34

Lipopolysaccharide-induced hypoactivity and behavioral tolerance development are modulated by the light-dark cycle in male and female rats

Franklin, A. E., Engeland, C. G., Kavaliers, M., & Ossenkopp, K. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1554-3 · Cited by 34

Individual Variation in Hypothalamus‐Pituitary‐Adrenal Responsiveness of Rats to Endotoxin and Interleukin‐1β

Lenczowski, M. J. P., Schmidt, E. D., van Dam, A., Gaykema, R. P. A., & Tilders, F. J. H. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb08322.x · Cited by 32

Leukemia inhibitory factor (LIF) induces acute adrenocorticotrophic hormone (ACTH) secretion in fetal rhesus macaque primates: a novel dynamic test of pituitary function

Akita, S., Conn, P. M., & Melmed, S. K. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.81.11.8923879 · Cited by 32

Effects of Social Conflict on Immune Responses and E. coli Growth Within Closed Chambers in Mice

Dréau, D., Sonnenfeld, G., Fowler, N., Morton, D. S., & Lyte, M. (1999) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00072-4 · Cited by 32

Effect of Lipopolysaccharide on Tumor Necrosis Factor and Prolactin Release from Rat Anterior Pituitary Cells

Theas, M. S., Laurentiis, A. D., Lasaga, M., Pisera, D. A., Duvilanski, B. H., & Seilicovich, A. (1998) · Endocrine · doi:10.1385/endo:8:3:241 · Cited by 32

Rheumatoid Arthritis and Risk of Depression in South Korea

Jeon, K. H., Han, K., Jung, J., Park, C. I., Eun, Y., Shin, D. W., & Kim, H. (2024) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.1139 · Cited by 32

Different roles attributed to Cav1 channel subtypes in spontaneous action potential firing and fine tuning of exocytosis in mouse chromaffin cells

Perez-Alvarez, A., Hernández-Vivanco, A., Caba-González, J. C., & Albillos, A. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07089.x · Cited by 30

Interleukin-1β differentially affects interleukin-6 and soluble interleukin-6 receptor in the blood and central nervous system of the monkey

Reyes, T. M., & Coe, C. L. (1996) · Journal of Neuroimmunology · doi:10.1016/0165-5728(96)00038-0 · Cited by 31

IL-1 is a mediator of increases in slow-wave sleep induced by CRH receptor blockade

Chang, F., & Opp, M. R. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.3.r793 · Cited by 31

Effects of granulocyte colony-stimulating factor on night sleep in humans

Schuld, A., Mullington, J., Hermann, D., Hinze-Selch, D., Fenzel, T., Holsboer, F., & Pollmächer, T. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.276.4.r1149 · Cited by 30

The role of Neurochemicals, Stress Hormones and Immune System in the Positive Feedback Loops between Diabetes, Obesity and Depression

Wilson, J. B., Epstein, M., Lopez, B., Brown, A. K., Lutfy, K., & Friedman, T. C. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1224612 · Cited by 35

Immuno-inflammatory changes across phases of early psychosis: The impact of antipsychotic medication and stage of illness

Kelsven, S., de la Fuente‐Sandoval, C., Achim, C. L., Reyes-Madrigal, F., Mirzakhanian, H., Domingues, I., & Cadenhead, K. S. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.01.003 · Cited by 29

A Low‐Protein, High‐Carbohydrate Diet Increases Fatty Acid Uptake and Reduces Norepinephrine‐Induced Lipolysis in Rat Retroperitoneal White Adipose Tissue

dos Santos, M. P., de França, S. A., dos Santos, J. T. F., Buzelle, S. L., Bertolini, G. L., Garófalo, M. A. R., Kettelhut, Í. D. C., Frasson, D., Chaves, V. E., & Kawashita, N. H. (2012) · Lipids · doi:10.1007/s11745-011-3648-8 · Cited by 28

Reduced Aggressiveness and Low Testosterone Levels in Autoimmune MRL-lpr Males

Šakić, B., Gurunlian, L., & Denburg, S. D. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(97)00422-8 · Cited by 29

Influence of corticotrophin releasing factor on neuronal cell death in vitro and in vivo

Craighead, M. W., Boutin, H., Middlehurst, K. M. L., Allan, S. M., Brooks, N. A. N., Kimber, I., & Rothwell, N. J. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02759-1 · Cited by 28

The overlooked mental health burden of polycystic ovary syndrome: neurobiological insights into PCOS-related depression

Dubé‐Zinatelli, E., Anderson, F., & Ismail, N. (2025) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2025.101203 · Cited by 29

Mouse Testing Methods in Psychoneuroimmunology: An Overview of How to Measure Sickness, Depressive/Anxietal, Cognitive, and Physical Activity Behaviors

York, J. M., Blevins, N. A., Baynard, T., & Freund, G. G. (2012) · Methods in molecular biology · doi:10.1007/978-1-62703-071-7_13 · Cited by 27

Maternal aggression persists following lipopolysaccharide-induced activation of the immune system

Weil, Z. M., Bowers, S., Dow, E. R., & Nelson, R. J. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.01.005 · Cited by 27

Changes in the immune and endocrine responses of patients with pulmonary tuberculosis undergoing specific treatment

Bongiovanni, B., Díaz, A., D’Attilio, L., Santucci, N. E., Dídoli, G., Lioi, S., Nannini, L. J., Gardeñez, W., Bogué, C., Besedovsky, H. O., et al. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06643.x · Cited by 27

Intracerebroventricular Passive Immunization. I. The Effect of Intracerebroventricular Administration of an Antiserum to Tumor Necrosis Factor-α on the Plasma Adrenocorticotropin Response to Lipopolysaccharide in Rats 1

Turnbull, A. V., & RIVIER, C. L. (1998) · Endocrinology · doi:10.1210/endo.139.1.5642 · Cited by 27

Lithium, Inflammation and Neuroinflammation with Emphasis on Bipolar Disorder—A Narrative Review

Damri, O., & Agam, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413277 · Cited by 26

A Unifying Theory for Autism: The Pathogenetic Triad as a Theoretical Framework

Sarovic, D. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.767075 · Cited by 30

α-MSH and γ-MSH inhibit IL-1β induced activation of the hypothalamic–pituitary–adrenal axis through central melanocortin receptors

Cragnolini, A. B., Perelló, M., Schiöth, H. B., & Scimonelli, T. N. (2004) · Regulatory Peptides · doi:10.1016/j.regpep.2004.06.011 · Cited by 26

Abnormal immune system development and function in schizophrenia helps reconcile diverse findings and suggests new treatment and prevention strategies

Anders, S. L., & Kinney, D. K. (2015) · Brain Research · doi:10.1016/j.brainres.2015.02.043 · Cited by 26

Ischemia-induced hyperglycemia: Consequences, neuroendocrine regulation, and a role for RAGE

Weil, Z. M. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.04.001 · Cited by 23

Differential Effects of One and Repeated Endotoxin Treatment on Pituitary- Adrenocortical Hormones in the Mouse: Role of Interleukin-1 and Tumor Necrosis Factor-α

Nagano, I., Takao, T., Nanamiya, W., Takemura, T., Nishiyama, M., Asaba, K., Makino, S., Souza, E. B. D., & Hashimoto, K. (1999) · NeuroImmunoModulation · doi:10.1159/000026386 · Cited by 23

The Cochlear CRF Signaling Systems and their Mechanisms of Action in Modulating Cochlear Sensitivity and Protection Against Trauma

Graham, C. E., Basappa, J., Turcan, Ş., & Vetter, D. E. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8203-3 · Cited by 22

Interactions among immune, endocrine, and behavioural response to infection

Weil, Z. M., Martin, L. B., & Nelson, R. J. (2006) · Springer eBooks · doi:10.1007/978-4-431-36025-4_21 · Cited by 22

Ubiquitin-Specific Protease 2 Modulates the Lipopolysaccharide-Elicited Expression of Proinflammatory Cytokines in Macrophage-like HL-60 Cells

Kitamura, H., Ishino, T., Shimamoto, Y., Okabe, J., Miyamoto, T., Takahashi, E., & Miyoshi, I. (2017) · Mediators of Inflammation · doi:10.1155/2017/6909415 · Cited by 23

Projections from subfornical organ to bed nucleus of the stria terminalis modulate inflammation-induced anxiety-like behaviors in mice

Zhang, J., Xie, C., Xu, P., Tong, Q., Xiao, L., & Zhong, J. (2024) · Science Advances · doi:10.1126/sciadv.adp9413 · Cited by 21

Estradiol Increases the Expression of TNF-α and TNF Receptor 1 in Lactotropes

Zaldivar, V., Magri, M. L., Zárate, S., Jaita, G., Eijo, G., Radl, D. B., Ferraris, J., Pisera, D. A., & Seilicovich, A. (2011) · Neuroendocrinology · doi:10.1159/000323760 · Cited by 21

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Luthra, N. S., Clow, A., & Corcos, D. M. (2022) · Brain Sciences · doi:10.3390/brainsci12121695 · Cited by 20

Heat Stress Modulates Brain Monoamines and Their Metabolites Production in Broiler Chickens Co-Infected with Clostridium perfringens Type A and Eimeria spp.

Calefi, A. S., Fonseca, J. G. D. S., Nunes, C. A. D. Q., Lima, A. P., Quinteiro-Filho, W. M., Flório, J. C., Zager, A., Ferreira, A. J. P., & Palermo‐Neto, J. (2019) · Veterinary Sciences · doi:10.3390/vetsci6010004 · Cited by 20

Understanding Cytokines Part II: Implications for Nursing Research and Practice

Corwin, E. J. (2000) · Biological Research For Nursing · doi:10.1177/109980040000200105 · Cited by 20

Activation of the Hypothalamic- Pituitary-Adrenal Axis in IL-1β-Converting Enzyme-Deficient Mice

Liège, S., Moze, E., Kelley, K. W., Parnet, P., & Neveu, P. J. (2000) · NeuroImmunoModulation · doi:10.1159/000026438 · Cited by 20

Integrative aspects of a human model of endotoxemia

Ottaway, C. A., Fong, I. W., da Silva, B., Singer, W., & Karrass, L. (1998) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y98-041 · Cited by 20

Evidence for Paracrine Signaling Between Macrophages and Bovine Adrenal Chromaffin Cell Ca2+Channels

Currie, K., Zhou, Z., & Fox, A. P. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.1.280 · Cited by 20

Role of neurotransmitters in the regulation of cutaneous wound healing

Gupta, D., Kaushik, D., & Mohan, V. (2022) · Experimental Brain Research · doi:10.1007/s00221-022-06372-0 · Cited by 20

Early-Life Maternal Deprivation Predicts Stronger Sickness Behaviour and Reduced Immune Responses to Acute Endotoxaemia in a Pig Model

Brückmann, R., Tuchscherer, M., Tuchscherer, A., Gimsa, U., & Kanitz, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155212 · Cited by 20

Neuroimmune Pharmacology of Neurodegenerative and Mental Diseases

Shie, F., Chen, Y., Chen, C., & Ho, I.-K. (2010) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-010-9241-8 · Cited by 19

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Moroni, L., Mazzetti, M., Ramirez, G. A., Farina, N., Bozzolo, E. P., Guerrieri, S., Moiola, L., Filippi, M., Mattei, V. E. D., & Dagna, L. (2021) · Current Rheumatology Reports · doi:10.1007/s11926-021-01019-5 · Cited by 17

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Smith, K. B., Murack, M., & Ismail, N. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.110701 · Cited by 17

SARS-CoV-2 infection and female reproductive health: A narrative review

Maher, M., & Owens, L. A. (2023) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2023.101760 · Cited by 17

Psychoneuroendocrine immunology: site of recognition, learning and memory in the immune system and the brain

Hiramoto, R. N., Rogers, C. F., Demissie, S., Hsueh, C., Hiramoto, N. S., Lorden, J. F., & Ghanta, V. K. (1997) · International Journal of Neuroscience · doi:10.3109/00207459708986405 · Cited by 17

Acute Cortisol Profile Associations With Cognitive Impairment After Severe Traumatic Brain Injury

Barton, D. J., Kumar, R. G., Schuster, A. A., Juengst, S. B., Oh, B., & Wagner, A. K. (2021) · Neurorehabilitation and neural repair · doi:10.1177/15459683211048771 · Cited by 16

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Cox, D., Chan, M., & Bahn, S. (2015) · Journal of Nervous and Mental Disease · doi:10.1097/nmd.0000000000000289 · Cited by 20

Persistent adaptation by chronic alcohol is facilitated by neuroimmune activation linked to stress and CRF

Breese, G. R., & Knapp, D. J. (2016) · Alcohol · doi:10.1016/j.alcohol.2016.01.005 · Cited by 16

Systemic blockade of complement C5a receptors reduces lipopolysacharride-induced responses in the paraventricular nucleus and the central amygdala

Crane, J. W., & Buller, K. M. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.07.012 · Cited by 17

Plasma Corticosterone and Immune Reactivity in Restrained Female C3H Mice

Li, K., Liège, S., Moze, E., & Neveu, P. J. (2000) · Stress · doi:10.3109/10253890009001134 · Cited by 16

Prediction of post-stroke depression with combined blood biomarkers IL-6, TNF-a, and fatty acid binding protein: A prospective study

Wang, L., Chunyou, C., Zhu, J., Bao, X.-J., & Tao, X. (2023) · Journal of Medical Biochemistry · doi:10.5937/jomb0-43904 · Cited by 15

Ankylosing spondylitis and psychiatric disorders in European population: a Mendelian randomization study

Zuo, H., & Li, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1277959 · Cited by 18

Differential Qualitative and Temporal Changes in the Response of the Hypothalamus-Pituitary-Adrenal Axis in Rats after Localized or Total-Body Irradiation

Lebaron-Jacobs, L., Wysocki, J., & Griffiths, N. M. (2004) · Radiation Research · doi:10.1667/rr3180 · Cited by 15

Responsiveness of hypothalamo-pituitary-adrenal axis to leptin is impaired in diet-induced obese rats

Shin, A. C., MohanKumar, S. M. J., Balasubramanian, P., Sirivelu, M. P., Linning, K. D., Woolcock, A., James, M., & MohanKumar, P. S. (2019) · Nutrition and Diabetes · doi:10.1038/s41387-019-0076-y · Cited by 15

Self-Stimulation from the Mesencephalon Following Intraventricular Interleukin-2 Administration

Hebb, A. L. O., Zacharko, R. M., & Anisman, H. (1998) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00447-4 · Cited by 15

The microbiota-gut-brain axis: a potential target in the small-molecule compounds and gene therapeutic strategies for Parkinson’s disease

Jiao, F., Zhou, L., & Wu, Z. (2024) · Neurological Sciences · doi:10.1007/s10072-024-07878-x · Cited by 13

The microbiota-gut-brain axis in Huntington's disease

Love, C. J., Masson, B. A., Gubert, C., & Hannan, A. J. (2022) · International review of neurobiology · doi:10.1016/bs.irn.2022.06.005 · Cited by 14

Mind-Body Interrelationship in DNA Methylation

Szyf, M. (2012) · Chemical immunology/Fortschritte der Allergielehre/Progress in allergy/Chemical immunology and allergy · doi:10.1159/000336503 · Cited by 14

Pre and post-natal antigen exposure can program the stress axis of adult zebra finches: Evidence for environment matching

Merrill, L., & Grindstaff, J. L. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.12.013 · Cited by 14

Central adaptation to chronic administration of interleukin-1β (IL-1β) in rats

MohanKumar, S. M. J., Smith, C. L., & MohanKumar, P. S. (2003) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2003.09.001 · Cited by 14

Mechanisms of Behavioral and Neuroendocrine Effects of Interleukin‐1 in Mice

Neveu, P. J., & Liège, S. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05382.x · Cited by 14

gp130-Related Cytokines and Their Receptors in the Pituitary

Melmed, S. K. (1997) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(97)00156-2 · Cited by 14

Seasonal Allergy and Seasonal Decrements in Athletic Performance

Komarow, H. D., & Postolache, T. T. (2005) · Clinics in Sports Medicine · doi:10.1016/j.csm.2004.12.006 · Cited by 15

Exposure to Workplace Bullying, Distress, and Insomnia: The Moderating Role of the miR-146a Genotype

Rajalingam, D., Jacobsen, D. P., Nielsen, M. B., Einarsen, S. V., & Gjerstad, J. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.01204 · Cited by 13

Interleukin 2 up-regulates glucocorticoid receptor number in human peripheral blood mononuclear cells and the osteosarcoma cell line Saos-2 in vitro.

Sartori, M., Masera, R., Staurenghi, A., Racca, S., & Angeli, A. (1998) · Steroids · doi:10.1016/s0039-128x(98)00023-3 · Cited by 12

Neuroendocrine and immune interactions with airway macrophages

James, D., & Nijkamp, F. P. (2000) · Inflammation Research · doi:10.1007/pl00000205 · Cited by 12

Role of Nitric Oxide and Carbon Monoxide in Modulating the Activity of the Rodent Hypothalamic-Pituitary-Adrenal Axis

RIVIER, C. L. (2001) · KARGER eBooks · doi:10.1159/000061057 · Cited by 13

Psychoneuroendocrine immunology: perception of stress can alter body temperature and natural killer cell activity.

Hiramoto, R., Solvason, H., Hsueh, C.-M., Rogers, C. F., Demissie, S., Hiramoto, N., Gauthier, D., Lorden, J., & Ghanta, V. (1999) · International Journal of Neuroscience · doi:10.3109/00207459908994795 · Cited by 15

Endotoxin induced increases in rat plasma pituitary-adrenocortical hormones are better reflected by alterations in tumor necrosis factorα than interleukin-1β

Takao, T., Nanamiya, W., Takemura, T., Nishiyama, M., Asaba, K., Makino, S., Hashimoto, K., & Souza, E. B. D. (1997) · Life Sciences · doi:10.1016/s0024-3205(97)00780-7 · Cited by 12

A comparison between the equine and bovine hypothalamus-pituitary-adrenocortical axis

van der Kolk, J. H., Fouché, N., Gross, J. J., Gerber, V., & Bruckmaier, R. M. (2016) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2016.02.008 · Cited by 12

Histomorphometric evaluation of mice testicular tissue following short- and long-term effects of lipopolysaccharide-induced endotoxemia.

Jafari, O., Babaei, H., Kheirandish, R., Samimi, A. S., & Zahmatkesh, A. (2018) · PubMed Central · doi:10.22038/ijbms.2017.24415.6083 · Cited by 11

Mouse Testing Methods in Psychoneuroimmunology 2.0: Measuring Behavioral Responses

Towers, A. E., York, J. M., Baynard, T., Gainey, S. J., & Freund, G. G. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7828-1_13 · Cited by 11

Distribution of interleukin-1 receptor in chicken and quail brain

Wang, R., Millam, J. R., & Klasing, K. C. (2003) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/s1095-6433(03)00219-8 · Cited by 11

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