Stress and immunity: An integrated view of relationships between the brain and the immune system

Physiological functions of glucocorticoids in stress and their relation to pharmacological actions

MUNCK, A., GUYRE, P. M., & HOLBROOK, N. J. (1984) · Endocrine Reviews · doi:10.1210/edrv-5-1-25 · Cited by 3,083

Cachectin and tumour necrosis factor as two sides of the same biological coin

Beutler, B., & Cerami, A. (1986) · Nature · doi:10.1038/320584a0 · Cited by 1,633

Biology of interleukin 1

Dinarello, C. A. (1988) · The FASEB Journal · doi:10.1096/fasebj.2.2.3277884 · Cited by 1,532

Interleukin-1 stimulates the secretion of hypothalamic corticotropin-releasing factor

Sapolsky, R., Rivier, C., Yamamoto, G., Plotsky, P., & Vale, W. (1987) · Science · doi:10.1126/science.2821621 · Cited by 1,504

Corticotropin-releasing factor-producing neurons in the rat activated by interleukin-1

Berkenbosch, F., van Oers, J., del Rey, A., Tilders, F., & Besedovsky, H. (1987) · Science · doi:10.1126/science.2443979 · Cited by 1,151

DEPRESSED LYMPHOCYTE FUNCTION AFTER BEREAVEMENT

Bartrop, R. W., Lazarus, L., Luckhurst, E., Kiloh, L. G., & Penny, R. (1977) · The Lancet · doi:10.1016/s0140-6736(77)92780-5 · Cited by 931

PSYCHOLOGICAL RESPONSE TO BREAST CANCER: EFFECT ON OUTCOME

Greer, S., Morris, T., & Pettingale, K. W. (1979) · The Lancet · doi:10.1016/s0140-6736(79)92127-5 · Cited by 774

Psychoneuroendocrine influences on immunocompetence and neoplasia

Riley, V. (1981) · Science · doi:10.1126/science.7233204 · Cited by 756

Noradrenergic Sympathetic Neural Interactions with the Immune System: Structure and Function

Felten, D. L., Felten, S. Y., Bellinger, D. L., Carlson, S. L., Ackerman, K. D., Madden, K. S., Olschowki, J. A., & Livnat, S. (1987) · Immunological Reviews · doi:10.1111/j.1600-065x.1987.tb00534.x · Cited by 746

Cachectin/tumor necrosis factor induces cachexia, anemia, and inflammation.

Tracey, K. J., He, W., Manogue, K. R., Fong, Y., HESSE, D. G., Nguyen, H. T., Kuo, G. C., Beutler, B., Cotran, R. S., & Cerami, A. (1988) · The Journal of Experimental Medicine · doi:10.1084/jem.167.3.1211 · Cited by 730

Profile of Chicken Macrophage Functions After Exposure to CatecholaminesIn Vitro

Ali, R. A., Qureshi, M. A., & McCorkle, F. M. (1994) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923979409019742 · Cited by 33

Cytokines, Sickness Behavior, and Depression

Dantzer, R., Bluthé, R.-M., Castanon, N., Kelley, K. W., Konsman, J. P., Layé, S., Lestage, J., & Parnet, P. (2007) · Elsevier eBooks · doi:10.1016/b978-012088576-3/50019-8 · Cited by 32

Met-enkephalin modulates stress-induced alterations of the immune response in mice

Marotti, T., Gabrilovac, J., Rabatić, S., Šmejkal-Jagar, L., Ročić, B., & Haberstock, H. (1996) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(95)02112-4 · Cited by 32

Role of central nervous system and behaviour in the immune response

Husband, A. J. (1993) · Vaccine · doi:10.1016/0264-410x(93)90355-2 · Cited by 32

β-Endorphin's modulation of lymphocyte proliferation is dose, donor, and time dependent

Millar, D., Hough, C., Mazorow, D. L., & Gootenberg, J. (1990) · Brain Behavior and Immunity · doi:10.1016/0889-1591(90)90025-l · Cited by 35

Identification of causes of the occupational stress for health providers at different levels of health care

Trifunovic, N., Jatic, Z., & DzuburKulenovic, A. (2017) · Medical Archives · doi:10.5455/medarh.2017.71.169-172 · Cited by 31

Inflammatory markers and negative mood symptoms following exercise withdrawal

Kop, W. J., Weinstein, A. A., Deuster, P. A., Whittaker, K. S., & Tracy, R. P. (2008) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2008.05.011 · Cited by 42

Behavioral and neurochemical responses in mice bearing tumors submitted to social stress

Vegas, Ó., Beitia, G., Sánchez‐Martín, J. R., Arregi, A., & Azpiroz, A. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.04.006 · Cited by 31

Immunoendocrine aspects of anorexia nervosa

Brambilla, F., Ferrari, E., Brunetta, M., Peirone, A., Draisci, A., Sacerdote, P., & Panerai, A. E. (1996) · Psychiatry Research · doi:10.1016/0165-1781(96)02992-7 · Cited by 31

Prenatal Alcohol Exposure Blunts Interleukin‐1‐Induced ACTH and β‐Endorphin Secretion by Immature Rats

Lee, S., & RIVIER, C. L. (1993) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.1993.tb05645.x · Cited by 31

Interleukin-1β stimulates the release of vasopressin from rat neurohypophysis

Christensen, J. D., Hansen, E. W., & Fjalland, B. (1989) · European Journal of Pharmacology · doi:10.1016/0014-2999(89)90112-x · Cited by 31

Hormones in self Tolerance and Autoimmunity: A role in the Pathogenesis of Rheumatoid Arthritis?

Berczi, I., Baragar, F. D., Chalmers, I. M., Keystone, E. C., Nagy, E., & Warrington, R. (1993) · Autoimmunity · doi:10.3109/08916939309010647 · Cited by 31

Assessing chronic pelvic pain syndrome patients: Blood plasma factors and cortisol saliva

Lundh, D., Hedelin, H. H., Jönsson, K., Gifford, M., & Larsson, D. (2013) · Scandinavian Journal of Urology · doi:10.3109/21681805.2013.769460 · Cited by 30

Changes with aging in the modulation of macrophages by norepinephrine

Ortega, E., García, J. J., Sáez, M. C., & la Fuente, M. D. (2000) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(00)00160-3 · Cited by 30

Opposite Effects of Gentle Handling on Body Temperature and Body Weight in Rats

Michel, C., & Cabanac, M. (1999) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00118-3 · Cited by 30

The glucocorticoid sensitivity of lymphocytes changes according to the activity of the hypothalamic-pituitary-adrenocortical system

Sauer, J., Polack, E., Wikinski, S., Holsboer, F., Stalla, G. K., & ARZT, E. S. (1995) · Psychoneuroendocrinology · doi:10.1016/0306-4530(94)00058-i · Cited by 29

Chronic stress from adolescence to aging in the prefrontal cortex: A neuroimmune perspective

Macht, V. A., & Reagan, L. P. (2017) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.12.001 · Cited by 34

Effect of cervical vagotomy on sympathetic nerve responses to peripheral interleukin-1β

Saindon, C. S., Blecha, F., Musch, T. I., Morgan, D. A., Fels, R. J., & Kenney, M. (2001) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00280-0 · Cited by 29

Central Interleukin‐1 Receptors as Mediators of Sicknessa

Kelley, K. W., Hutchison, K. A., French, R. A., Bluthé, R.-M., Parnet, P., Johnson, R. W., & Dantzer, R. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb48395.x · Cited by 29

Biochemical correlates of in vivo cell-mediated immune dysfunction in patients with depression: A preliminary report

Hickie, I. B., Hickie, C., Bennett, B. K., Wakefield, D., Silove, D. M., Mitchell, P. B., & Lloyd, A. R. (1995) · International Journal of Immunopharmacology · doi:10.1016/0192-0561(95)00055-7 · Cited by 29

Immune System

Schuurman, H., den Hondel-Franken, M. A. M. V., Kuper, C. F., Loveren, H. V., & Vos, J. G. (1991) · Elsevier eBooks · doi:10.1016/b978-0-12-330220-5.50022-x · Cited by 29

Breakdown of the Blood-Brain Barrier in Stress Alters Cognitive Dysfunction and Induces Brain Pathology: New Perspectives for Neuroprotective Strategies

Sharma, H. S., & Sharma, A. (2010) · Springer eBooks · doi:10.1007/978-90-481-8553-5_9 · Cited by 27

Psychophysiological Bases of Disease ☆

Steptoe, A., & Poole, L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.05144-0 · Cited by 28

Stress and Immunity

Moynihan, J. A., Cohen, N., & Ader, R. (1994) · Springer eBooks · doi:10.1007/978-3-642-78480-4_8 · Cited by 28

Effect of variable moderate chronic stress on ligature‐induced periodontal disease in Wistar rats

Susin, C., & Rõsing, C. K. (2003) · Acta Odontologica Scandinavica · doi:10.1080/00016350310005574 · Cited by 27

Influence of Interleukin‐1β on the Secretion of Oxytoxin and Vasopressin from the Isolated Rat Neurohypophysis

Christensen, J. D., Hansen, E. W., & Fjalland, B. (1990) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.1990.tb00787.x · Cited by 27

Influence of CRF and α-MSH on the migration of human monocytes in vitro

Genedani, S., Bernardi, M. M., Baldini, M. G., & Bertolini, A. (1992) · Neuropeptides · doi:10.1016/0143-4179(92)90085-b · Cited by 26

Cold stress-induced neuroinvasiveness of attenuated arboviruses is not solely mediated by corticosterone

Ben‐Nathan, D., Lustig, S., & Kobiler, D. (1996) · Archives of Virology · doi:10.1007/bf01718826 · Cited by 27

Psychiatric-medical comorbidity: Implications for health services delivery and for research on depression

Katz, I. R., Streim, J. E., & Parmelee, P. A. (1994) · Biological Psychiatry · doi:10.1016/0006-3223(94)91219-x · Cited by 27

Fish oil ameliorates sickness behavior induced by lipopolysaccharide in aged mice through the modulation of kynurenine pathway

de Gomes, M. G., Souza, L. C., Goes, A. T. R., Fabbro, L. D., Filho, C. B., Donato, F., Prigol, M., Luchese, C., Roman, S. S., Puntel, R. L., et al. (2018) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2018.05.002 · Cited by 26

Adolescent social instability stress leads to immediate and lasting sex-specific changes in the neuroendocrine-immune-gut axis in rats

McCormick, C. M., Smith, K. B., Baumbach, J. L., de Lima, A. P. N., Shaver, M., Hodges, T. E., Marcolin, M. L., & Ismail, N. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104845 · Cited by 30

Sickness and the Social Brain: How the Immune System Regulates Behavior across Species

Devlin, B. A., Smith, C. J. W., & Bilbo, S. D. (2021) · Brain Behavior and Evolution · doi:10.1159/000521476 · Cited by 30

Impact of cage stocking density on egg laying characteristics and related stress and immunity parameters of Japanese quails in subtropics

EL-TARABANY, M. S. (2015) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.12404 · Cited by 26

Role of dopaminergic mechanisms in the regulation of stress responses in experimental animals

Puri, S., Ray, A., Chakravarti, A. K., & Sen, P. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90497-9 · Cited by 26

Adrenalectomy enhances endotoxemia-induced hypophagia: higher activation of corticotrophin-releasing-factor and proopiomelanocortin hypothalamic neurons

Rorato, R. C., de Castro, M., Borges, B. C., Benedetti, M., Germano, C. M. R., Antunes‐Rodrigues, J., & Elias, L. L. K. (2008) · Hormones and Behavior · doi:10.1016/j.yhbeh.2008.02.011 · Cited by 26

Immunolocalization of thioredoxin and glutaredoxin in mammalian hypophysis

Padilla, C. A., Martı́nez-Galisteo, E., López‐Barea, J., Holmgren, A., & Bárcena, J. A. (1992) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(92)90119-q · Cited by 26

Role of arachidonic acid metabolism on corticotropin-releasing factor (CRF)-release induced by interleukin-1 from superfused rat hypothalami

Cambronero, J. C., Rivas, F. J., Borrell, J. I., & Guaza, C. (1992) · Journal of Neuroimmunology · doi:10.1016/0165-5728(92)90174-j · Cited by 26

Drug actions on delayed-type hypersensitivity in rats with developing and established adjuvant arthritis

Hambleton, P. T., & McMahon, S. (1990) · Inflammation Research · doi:10.1007/bf01966465 · Cited by 26

Differences in the effects of dexamethasone on macrophage nitrite production: Dependence on exposure regimen (in vivo or in vitro) and activation stimuli

Keil, D. E., Luebke, R. W., & Pruett, S. B. (1995) · International Journal of Immunopharmacology · doi:10.1016/0192-0561(95)00008-p · Cited by 26

Theoretical and practical considerations behind the use of laboratory animals for the study of Tourette syndrome

Macrı̀, S., Onori, M. P., & Laviola, G. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.03.014 · Cited by 26

Acute restraint stress enhances calcium mobilization and proliferative response in splenic lymphocytes from mice

Satoh, E., Edamatsu, H., & Omata, Y. (2006) · Stress · doi:10.1080/10253890601095794 · Cited by 25

Methylenedioxymethamphetamine-induced suppression of interleukin-1β and tumour necrosis factor-α is not mediated by serotonin

Connor, T. J., Dennedy, M. C., Harkin, A., & Kelly, J. P. (2001) · European Journal of Pharmacology · doi:10.1016/s0014-2999(01)00928-1 · Cited by 25

Effect of physical activity stress on the phagocytic process of peritoneal macrophages from old guinea pigs

Ortega, E., Collazos, M. E., Barriga, C., & la Fuente, M. D. (1992) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(92)90032-9 · Cited by 25

Hormonal aspects of postnatal depression

Harris, B. (1996) · International Review of Psychiatry · doi:10.3109/09540269609037815 · Cited by 24

The immunopathology of chronic inflammatory periodontal disease

Sosroseno, W., & Herminajeng, E. (1995) · FEMS Immunology & Medical Microbiology · doi:10.1016/0928-8244(94)00089-c · Cited by 25

Immunosuppression elicited by stressors and stressor-related odors

Zalcman, S., Kerr, L., & Anisman, H. (1991) · Brain Behavior and Immunity · doi:10.1016/0889-1591(91)90022-3 · Cited by 25

Targeting improved resilience in Merino sheep – Correlations between immune competence and health and fitness traits

Hine, B. C., Acton, G. A., Elks, D., Niemeyer, D. D. O., Bell, A., Colditz, I. G., Ingham, A. B., & Smith, J. L. (2022) · animal · doi:10.1016/j.animal.2022.100544 · Cited by 24

Influence of Stress on DDT-Induced Humoral Immune Responsiveness in Mice

Banerjee, B., Koner, B. C., & Ray, A. (1997) · Environmental Research · doi:10.1006/enrs.1997.3749 · Cited by 24

Central Regulation of Adaptive Responses to Heat and Cold

Zeisberger, E., & Roth, J. (1996) · Comprehensive physiology · doi:10.1002/cphy.cp040126 · Cited by 24

The effect of stocking density and social regrouping stressors on growth performance, carcass characteristics, nutrient digestibility and physiological stress responses in pigs

Leek, A. B. G., Sweeney, T., Duffy, P., Beattie, V. E., & O’Doherty, J. V. (2004) · Animal Science · doi:10.1017/s1357729800054588 · Cited by 23

Effect of a conditioned aversive stimulus on the immune response in three strains of rats

Shurin, M. R., Kusnecov, A. W., Riechman, S. E., & Rabin, B. S. (1995) · Psychoneuroendocrinology · doi:10.1016/0306-4530(95)00010-0 · Cited by 23

Effects of long-term dehydration on stress markers, blood parameters, and tissue morphology in the dromedary camel (Camelus dromedarius)

Ali, M. A., Damir, H. A., Adem, M. A., Ali, O., Amir, N., Shah, A. A. M., Muhairi, S. S. M. A., Abdouli, K. O. S. A., Khawaja, J. R., Fagieri, T. A., et al. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2023.1236425 · Cited by 27

Endocrine and immunological correlates of behaviorally identified swim stress resilient and vulnerable rats

Levay, E. A., Govic, A., Hazi, A., Flannery, G. R., Christianson, J. P., Drugan, R. C., & Kent, S. (2005) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2005.10.004 · Cited by 22

Psychoneuroimmunological effects of Qi-therapy: preliminary study on the changes of level of anxiety, mood, cortisol and melatonin and cellular function of neutrophil and natural killer cells

Lee, M. S., Huh, H. J., Hong, S.-S., Jang, H.-S., Ryu, H., Lee, H.-S., & Chung, H. (2001) · Stress and Health · doi:10.1002/1532-2998(200101)17:1 · Cited by 46

Modulation by naltrexone of stress-induced changes in humoral immune responsiveness and gastric mucosal integrity in rats

RAY, A., Mediratta, P. K., & Sen, P. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90143-p · Cited by 22

The Effects of Voluntary Exercise and Immobilization on Humoral Immunity and Endocrine Responses in Rats

BALDWIN, D., Wilcox, Z. C., & ZHENG, G. (1997) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00459-3 · Cited by 22

Enhancement by Restraint Stress of Natural Killer Cell Activity and Splenocyte Responsiveness to Concanavalin A in Fischer 344 Rats

Jain, S., & Stevenson, J. R. (1991) · Immunological Investigations · doi:10.3109/08820139109057762 · Cited by 22

Immunoenhancing effects of alprazolam in mice

Fride, E., Skolnick, P., & Pk, A. (1990) · Life Sciences · doi:10.1016/0024-3205(90)90485-a · Cited by 22

Behavioral, neuroendocrine, and immunological outcomes of escapable or inescapable shocks

Sandi, C., Borrell, J. I., & Guaza, C. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90192-5 · Cited by 22

Evolutionary Aspects of Infections: Inflammation and Sickness Behaviors

Dantzer, R. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_363 · Cited by 24

Phenytoin promotes Th2 type immune response in mice

Okada, K., Sugiura, T., Kuroda, E., Tsuji, S., & Yamashita, U. (2001) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.2001.01491.x · Cited by 21

Salivary markers of work stress in an emergency team of urban police (1 degree step).

Zefferino, R., Facciorusso, A., Lasalvia, M., Narciso, M., Nuzzaco, A., Lucchini, R. G., & L'ABBATE, N. (2006) · PubMed · Cited by 21

Splenic immunomodulation with swimming-induced stress in rats

Ferry, A., Weill, B. J., Amiridis, I. G., Laziry, F., & Rieu, M. (1991) · Immunology Letters · doi:10.1016/0165-2478(91)90180-i · Cited by 21

Electrolytic lesions of the lateral hypothalamus influence peripheral blood NK cytotoxicity in rats

Wrona, D., Jurkowski, M. K., Trojniar, W., Staszewska, M., & Tokarski, J. (1994) · Journal of Neuroimmunology · doi:10.1016/0165-5728(94)90145-7 · Cited by 21

Curcumin-loaded lipid-core nanocapsules attenuates the immune challenge LPS-induced in rats: Neuroinflammatory and behavioral response in sickness behavior

de Gomes, M. G., Teixeira, F. E. G., de Carvalho, F. B., Pacheco, C. O., Neto, M. R. D. S., Giacomeli, R., Ramalho, J. B., dos Santos, R. B., Domingues, W. B., Campos, V. F., et al. (2020) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2020.577270 · Cited by 20

Is there a relationship between morphological and functional platelet changes and depressive disorder?

Tagliarini, C., Carbone, M. G., Pagni, G., Marazziti, D., & Pomara, N. (2020) · CNS Spectrums · doi:10.1017/s1092852920001959 · Cited by 21

A Brief History of Immunological Research into Psychosis and Pathways for Immune Influence of the Brain

Müller, N. (2019) · Current topics in behavioral neurosciences · doi:10.1007/7854_2018_82 · Cited by 20

Effect of prenatal ambient temperature on the performance physiological parameters, and oxidative metabolism of Japanese quail (Coturnix coturnix japonica) layers exposed to heat stress during growth

Santana, T. P., Gasparino, E., Khatlab, A. D. S., Brito, C. O., Barbosa, L. T., Lamont, S. J., & Vesco, A. P. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-89306-0 · Cited by 20

Effects of human recombinant interleukins on stimulation-evoked noradrenaline overflow from the rat perfused spleen

Bognar, I. T., Albrecht, S. A., Ghazwiny, M. F., Schmitt, E., Seidel, G., & FUDER, H. (1994) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00169139 · Cited by 20

The effects of lateral hypothalamic lesions on peripheral blood natural killer cell cytotoxicity in rats hyper- and hyporesponsive to novelty

Wrona, D., Jurkowski, M. K., Luszawska, D., Tokarski, J., & Trojniar, W. (2003) · Brain Behavior and Immunity · doi:10.1016/s0889-1591(03)00065-5 · Cited by 20

Neuroendocrine-Immune Interactions

Kelley, K. W., & Dantzer, R. (1990) · Advances in veterinary science and comparative medicine · doi:10.1016/b978-0-12-039235-3.50017-4 · Cited by 20

Combining inflammatory miRNA molecules as diagnostic biomarkers for depression: a clinical study

Brás, J. P., Pinto, S., von Doellinger, O., Prata, J., Coelho, R. C., Barbosa, M. A., Almeida, M. I., & Santos, S. G. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1227618 · Cited by 21

Poor self-reported health and its association with biomarkers among Canadian Inuit

Saudny-Unterberger, H., Cao, Z., & Egeland, G. M. (2012) · International Journal of Circumpolar Health · doi:10.3402/ijch.v71i0.18589 · Cited by 19

Effect of lipopolysaccharide on sickness behaviour in hens kept in cage and free range environments

Gregory, N. G., Payne, S. R., Devine, C. D., & Cook, C. J. (2009) · Research in Veterinary Science · doi:10.1016/j.rvsc.2009.01.003 · Cited by 21

Stress, Immunity, and Health

Keller, S. E., Shiflett, S. C., Schleifer, S. J., & Bartlett, J. A. (1994) · Elsevier eBooks · doi:10.1016/b978-0-12-285960-1.50013-7 · Cited by 19

The effects of the opiate antagonist naloxone on measures of cellular immunity during rest and brief psychological stress

Naliboff, B. D., Solomon, G. F., Gilmore, S. L., Benton, D. M., Morley, J. E., & Fahey, J. L. (1995) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(94)00142-r · Cited by 19

Effects of immobilization stress on the pathogenesis of acute murine toxoplasmosis

Chao, C. C., Peterson, P. K., FILICE, G. A., Pomeroy, C., & Sharp, B. M. (1990) · Brain Behavior and Immunity · doi:10.1016/0889-1591(90)90018-l · Cited by 19

Time-dependent in vivo mesolimbic dopamine variations following antigenic challenge

Lacosta, S., Merali, Z., Zalcman, S. S., & Anisman, H. (1994) · Brain Research · doi:10.1016/0006-8993(94)91976-3 · Cited by 19

Effect of physical exhaustion and glucocorticoids (dexamethasone) on T-cells of trained rats

Ferry, A., Rieu, P., Page, C. L., Elhabazi, A., Laziri, F., & Rieu, M. (1993) · European Journal of Applied Physiology · doi:10.1007/bf00599621 · Cited by 19

Segregated early weaning

Fangman, T., & Tubbs, R. C. (1997) · Journal of Swine Health and Production · Cited by 19

Applications cliniques en psychologie de la santé

Gauchet, A., Shankland, R., Dantzer, C., Pelissier, S., & Aguerre, C. (2012) · Psychologie Francaise · doi:10.1016/j.psfr.2012.03.005 · Cited by 18

Peripheral Biomarkers of Inflammation in Depression: Evidence from Animal Models and Clinical Studies

Brás, J. P., Pinto, S. F. T., Almeida, M. I., Prata, J., von Doellinger, O., Coelho, R. C., Barbosa, M. A., & Santos, S. G. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9554-7_28 · Cited by 19

Effect of the Tea Tree Oil on Growth Performance, Meat Quality, Serum Biochemical Indices, and Antioxidant Capacity in Finishing Pigs

Yang, T., Feifei, F., Zhan, K., Ma, X., Jiang, M., Datsomor, O., Zhu, X., Huo, Y., & Zhao, G. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.916625 · Cited by 18

Neuroimmune networks and communication pathways: the importance of location

Banks, W. A. (2003) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2003.11.003 · Cited by 18

Immunomodulatory role of the corticotropin-releasing factor.

Radulović, M., & Spiess, J. (2001) · PubMed · Cited by 18

Changes with aging and physical exercise in ascorbic acid content and proliferative response of murine lymphocytes

la Fuente, M. D., Ferrández, M. D., Miquel, J., & Hernánz, Á. (1992) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(92)90034-b · Cited by 18

Association of Low Job Control with a Decrease in Memory(CD4+CD45RO+) T Lymphocytes in Japanese Middle-Aged Male Workers in an Electric Power Plant.

Nakata, A., Tanigawa, T., Fujioka, Y., Kitamura, F., Iso, H., & Shimamoto, T. (2002) · Industrial Health · doi:10.2486/indhealth.40.142 · Cited by 18

Effects of a diverse prebiotic fibre blend on inflammation, the gut microbiota and affective symptoms in metabolic syndrome: a pilot open-label randomised controlled trial

Hall, C. V., Hepsomali, P., Dalile, B., Scapozza, L., & Gurry, T. (2024) · British Journal Of Nutrition · doi:10.1017/s0007114524002186 · Cited by 20

Pharmacological and biochemical studies on the role of free radicals during stress-induced immunomodulation in rats

Pal, R., Gulati, K., Banerjee, B., & Ray, A. (2011) · International Immunopharmacology · doi:10.1016/j.intimp.2011.05.026 · Cited by 17

Modulation of the immune response by changing neuromediator systems activity under stress

Idova, G. V., Чейдо, М. А., & Devoino, L. V. (1997) · International Journal of Immunopharmacology · doi:10.1016/s0192-0561(97)00077-5 · Cited by 17

Neuroimmunological Effects of Exposure to Methylmercury Forms in the Sprague-Dawley Rats. Activation of the Hypothalamic-Pituitary-Adrenal Axis and Lymphocyte Responsiveness

Ortega, H. G., Lopez, M., Takaki, A., Huang, Q.-H., Arimura, A., & Salvaggio, J. E. (1997) · Toxicology and Industrial Health · doi:10.1177/074823379701300105 · Cited by 17

Effects of HPA hormones on adapted lymphocyte responsiveness to repeated stress

Sandi, C., Cambronero, J. C., Borrell, J. I., & Guaza, C. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90106-8 · Cited by 17

Neuropharmacology of antidepressants that modify central noradrenergic and serotonergic function: a short review

Leonard, B. E. (1999) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/(sici)1099-1077(199903)14:2 · Cited by 16

The questionable wisdom of a low-fat diet and cholesterol reduction

Atrens, D. M. (1994) · Social Science & Medicine · doi:10.1016/0277-9536(94)90141-4 · Cited by 17

Stressor-induced alterations of natural killer cell activity and central catecholamines in mice

Zalcman, S., Irwin, J., & Anisman, H. (1991) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(91)90192-5 · Cited by 17

challenge of producing health in modern economiesPreprint

Stoddart, G. L. (1995) · RePEc: Research Papers in Economics · Cited by 17

Infection, learning, and memory: Focus on immune activation and aversive conditioning

Bishnoi, I. R., Cloutier, C. J., Tyson, C.-D., Matic, V. M., Kavaliers, M., & Ossenkopp, K. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104898 · Cited by 16

Relation between stress and cytokine responses in inner-city mothers

Gruenberg, D. A., Wright, R. J., Visness, C. M., Jaffee, K. F., Bloomberg, G. R., Cruikshank, W. W., Kattan, M., Sandel, M. T., Wood, R. A., & Gern, J. E. (2015) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2015.07.021 · Cited by 16

Prospective associations between cardiovascular reactions to acute psychological stress and change in physical disability in a large community sample

Phillips, A. C., Der, G., Shipton, D., & Benzeval, M. (2011) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2011.08.002 · Cited by 16

Blood and spleen natural killer cell cytotoxicity after exposure to open field stress in rats: the effect of spontaneous locomotor activity

Wrona, D., Jurkowski, M. K., & Tokarski, J. (2004) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2004.01.023 · Cited by 15

[Psychoneuroimmunology. A new approach to the function of immunological system].

Lutz, W., Tarkowski, M., & Dudek, B. (2001) · PubMed · Cited by 2

Stress-Induced Immune Changes, and Brain-Immune Interaction

Nagata, S. (1993) · Journal of UOEH · doi:10.7888/juoeh.15.161 · Cited by 2

Nervous System-Immune System Interactions: An Overview

Dunn, A. J. (1988) · Journal of Receptor Research · doi:10.3109/10799898809049013 · Cited by 55

[Stress and susceptibility to infection].

Kaulfersch, W., Kurz, R., & Hitzig, W. H. (1992) · PubMed

Stress and the Immune System

BALLIEUX, R. E., & Heijnen, C. J. (1987) · Springer eBooks · doi:10.1007/978-94-009-3339-2_3 · Cited by 7