Neural-immune interactions in health and disease.

Functional diversity of helper T lymphocytes

Abbas, A. K., MURPHY, K. M. M., & Sher, A. (1996) · Nature · doi:10.1038/383787a0 · Cited by 4,432

Cytokine-to-brain communication: A review & analysis of alternative mechanisms

Watkins, L. R., Maier, S. F., & Goehler, L. E. (1995) · Life Sciences · doi:10.1016/0024-3205(95)02047-m · Cited by 597

A central nervous system defect in biosynthesis of corticotropin-releasing hormone is associated with susceptibility to streptococcal cell wall-induced arthritis in Lewis rats.

Sternberg, E. M., Young, W. S., Bernardini, R., Calogero, A. E., Chrousos, G. P., Gold, P. W., & Wilder, R. L. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.12.4771 · Cited by 568

Negative cross-talk between RelA and the glucocorticoid receptor: a possible mechanism for the antiinflammatory action of glucocorticoids.

Caldenhoven, E., Lidén, J., Wissink, S., van de Stolpe, A., Raaijmakers, J. A. M., Koenderman, L., Okret, S., Gustafsson, J., & van der Saag, P. T. (1995) · Molecular Endocrinology · doi:10.1210/mend.9.4.7659084 · Cited by 490

Autocrine or Paracrine Inflammatory Actions of Corticotropin-Releasing Hormone in Vivo

Karalis, K. P., Sano, H., Redwine, J. M., LISTWAK, S. J., Wilder, R. L., & Chrousos, G. P. (1991) · Science · doi:10.1126/science.1925600 · Cited by 482

Type 1 interleukin‐1 receptor in the rat brain: Distribution, regulation, and relationship to sites of IL‐1–induced cellular activation

Ericsson, A., Liu, C., Hart, R. P., & Sawchenko, P. E. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903610410 · Cited by 471

Subdiaphragmatic vagotomy blocks induction of IL-1 beta mRNA in mice brain in response to peripheral LPS

Layé, S., Bluthé, R.-M., Kent, S., Combe, C., Medina, C. F., Parnet, P., Kelley, K., & Dantzer, R. (1995) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1995.268.5.r1327 · Cited by 303

Inducible nitric oxide synthase gene expression in the brain during systemic inflammation

Wong, M.-L., Rettori, V., AL-Shekhlee, A., Bongiorno, P. B., Canteros, G., McCann, S. M., Gold, P. W., & Licinio, J. (1996) · Nature Medicine · doi:10.1038/nm0596-581 · Cited by 286

Neuropeptides and Inflammation: The Role of Substance P

Payan, D. G. (1989) · Annual Review of Medicine · doi:10.1146/annurev.me.40.020189.002013 · Cited by 284

The role of interleukin 1 in acute neurodegeneration and stroke: pathophysiological and therapeutic implications.

Rothwell, N. J., Allan, S. M., & Toulmond, S. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119808 · Cited by 270

Cytokines and sickness behavior: implications from knockout animal models

Inui, A. (2001) · Trends in Immunology · doi:10.1016/s1471-4906(01)01981-0 · Cited by 61

Nocebo and the contribution of psychosocial factors to the generation of pain

Benedetti, F., Frisaldi, E., Barbiani, D., Camerone, E. M., & Shaibani, A. I. (2019) · Journal of Neural Transmission · doi:10.1007/s00702-019-02104-x · Cited by 69

Expression of IL-17B in neurons and evaluation of its possible role in the chromosome 5q-linked form of Charcot–Marie–Tooth disease

Moore, E. E., Presnell, S., Garrigues, U., Guilbot, A., Leguern, É., Smith, D. L., Yao, L. Y., Whitmore, T. E., Gilbert, T., Palmer, T. D., et al. (2002) · Neuromuscular Disorders · doi:10.1016/s0960-8966(01)00250-4 · Cited by 58

Influence of Acute Epinephrine Infusion on Endotoxin-Induced Parameters of Heart Rate Variability

Jan, B. U., Coyle, S. M., Oikawa, L. O., Lu, S., Calvano, S. E., Lehrer, P. M., & Lowry, S. F. (2009) · Annals of Surgery · doi:10.1097/sla.0b013e3181a40193 · Cited by 57

Leukemia Inhibitory Factor Mediates the Hypothalamic Pituitary Adrenal Axis Response to Inflammation

Chesnokova, V., & Melmed, S. K. (2000) · Endocrinology · doi:10.1210/endo.141.11.7778 · Cited by 59

Pituitary-Adrenal Axis Regulation in Crh-Deficient Mice

Muglia, L. J., Bethin, K. E., Jacobson, L., Vogt, S. K., & Majzoub, J. A. (2000) · Endocrine Research · doi:10.3109/07435800009048638 · Cited by 56

Glutathione in metastases: From mechanisms to clinical applications

Estrela, J. M., Ortega, Á., Mena, S., Sirerol, J. A., & Obrador, E. (2016) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2015.1136259 · Cited by 56

Myelinolytic lesions in spinal cord of cobalamin‐deficient rats are TNF‐α‐mediated

Buccellato, F. R., Miloso, M., Braga, M., Nicolini, G., Morabito, A., PRAVETTONI, G., Tredici, G., & Scalabrino, G. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.2.297 · Cited by 54

Integrative role of neuropeptides and cytokines in cancer anorexia–cachexia syndrome

Patra, S. K., & Arora, S. (2012) · Clinica Chimica Acta · doi:10.1016/j.cca.2011.12.008 · Cited by 55

Growth differentiation factor 15 as a potential therapeutic for treating obesity

Hale, C., & Véniant, M. M. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101117 · Cited by 54

IL-1β immunoreactive neurons in the human hypothalamus: reduced numbers in multiple sclerosis

Huitinga, I., van der Cammen, M., Salm, L. P., Erkut, Z. A., van Dam, A., Tilders, F. J. H., & Swaab, D. F. (2000) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(00)00248-4 · Cited by 54

Crosstalk between anticancer drugs and mitochondrial functions

Sahu, K., Langeh, U., Singh, C., & Singh, A. (2021) · Current Research in Pharmacology and Drug Discovery · doi:10.1016/j.crphar.2021.100047 · Cited by 52

Neurobiology of cancer: Interactions between nervous, endocrine and immune systems as a base for monitoring and modulating the tumorigenesis by the brain

Mravec, B., Gidron, Y., & Hulín, I. (2007) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2007.12.002 · Cited by 47

Fluoxetine suppresses the immune responses of blood clams by reducing haemocyte viability, disturbing signal transduction and imposing physiological stress

Shi, W. M., Han, Y., Guan, X., Rong, J., Su, W., Zha, S., Tang, Y., Du, X., & Liu, G. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.05.308 · Cited by 48

Suppression of human anti-inflammatory plasma cytokines IL-10 and IL-1RA with elevation of proinflammatory cytokine IFN-γ during the isolation of the Antarctic winter

Shearer, W. T., Lee, B.-N., Cron, S. G., Rosenblatt, H. M., Smith, E. O., Lugg, D. J., Nickolls, P. M., Sharp, R. M., Rollings, K., & Reuben, J. M. (2002) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2002.123873 · Cited by 47

How Should Alternative Medicine Be Taught to Medical Students and Physicians?

Marcus, D. M. (2001) · Academic Medicine · doi:10.1097/00001888-200103000-00007 · Cited by 47

Mind over matter in the postinfective irritable bowel

Drossman, D. A. (1999) · Gut · doi:10.1136/gut.44.3.306 · Cited by 47

Vagus nerve modulation of inflammation: Cardiovascular implications

Olshansky, B. (2015) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2015.03.016 · Cited by 46

Neural concomitants of immunity—Focus on the vagus nerve

Thayer, J. F., & Sternberg, E. M. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.058 · Cited by 46

From feedback loop transitions to biomarkers in the psycho-immune-neuroendocrine network: Detecting the critical transition from health to major depression

Stapelberg, N. J. C., Pratt, R., Neumann, D. L., Shum, D., Brandis, S. J., Muthukkumarasamy, V., Stantić, B., Blumenstein, M., & Headrick, J. P. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.03.005 · Cited by 45

Cortisol, Amyloid-β, and Reserve Predicts Alzheimer’s Disease Progression for Cognitively Normal Older Adults

Udeh‐Momoh, C. T., Initiative, A. D. N., Su, B., Evans, S., Zheng, B., Sindi, S., Tzoulaki, I., Perneczky, R., & Middleton, L. T. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181030 · Cited by 48

Stress-Related Programming of Autonomic Imbalance: Role in Allergy and Asthma

Wright, R. J. (2012) · Chemical immunology/Fortschritte der Allergielehre/Progress in allergy/Chemical immunology and allergy · doi:10.1159/000336496 · Cited by 45

Protection of early phase hepatic ischemia-reperfusion injury by cholinergic agonists

Crockett, E. T., Galligan, J. J., Uhal, B. D., Harkema, J. R., Roth, R. A., & Pandya, K. (2006) · BMC Clinical Pathology · doi:10.1186/1472-6890-6-3 · Cited by 45

Lasting Neuroendocrine-Immune Effects of Traumatic Brain Injury in Rats

Taylor, A. N., Rahman, S. U., Tio, D. L., Sanders, M. J., Bando, J. K., Truong, A. H., & Prolo, P. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.1802 · Cited by 45

The Proinflammatory Cytokines Tumor Necrosis Factor-α and Interleukin-1 Stimulate Neuropeptide Gene Transcription and Secretion in Adrenochromaffin Cells via Activation of Extracellularly Regulated Kinase 1/2 and p38 Protein Kinases, and Activator Protein-1 Transcription Factors

Aït‐Ali, D., Turquier, V., Grumolato, L., Yon, L., Jourdain, M., Alexandre, D., Eiden, L. E., Vaudry, H., & Anouar, Y. (2004) · Molecular Endocrinology · doi:10.1210/me.2003-0129 · Cited by 44

Emotions and Family Factors in Childhood Asthma: Psychobiologic Mechanisms and Pathways of Effect

Miller, B., & Wood, B. L. (2003) · KARGER eBooks · doi:10.1159/000073785 · Cited by 45

Enhancing the tourist experience with emotional intelligence

Prentice, C. (2020) · Tourism Review · doi:10.1108/tr-06-2019-0254 · Cited by 44

Neuropeptide Y: a key molecule in anorexia and cachexia in wasting disorders?

Inui, A. (1999) · Molecular Medicine Today · doi:10.1016/s1357-4310(98)01395-1 · Cited by 44

Chronic stress and insulin resistance-related indices of cardiovascular disease risk, part I: neurophysiological responses and pathological sequelae.

Innes, K. E., Vincent, H. K., & Taylor, A. G. (2007) · PubMed · Cited by 43

Series Introduction: The immuno-neuroendocrine interface

Melmed, S. K. (2001) · Journal of Clinical Investigation · doi:10.1172/jci200114604 · Cited by 43

Mental wellbeing and quality of sexual life in women with primary Sjögren's syndrome are related to circulating dehydroepiandrosterone sulphate

Valtýsdóttir, S. T., Wide, L., & Hallgren, R. (2003) · Annals of the Rheumatic Diseases · doi:10.1136/ard.62.9.875 · Cited by 42

Adenosine‐induced IL‐6 expression in pituitary folliculostellate cells is mediated via A2b adenosine receptors coupled to PKC and p38 MAPK

Rees, A., Lewis, B. M., Lewis, M. D., Francis, K., Scanlon, M. F., & Ham, J. (2003) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705488 · Cited by 42

Constitutive Expression of Interleukin-1beta (IL-1beta) in Rat Oligodendrocytes

Blasi, F., Riccio, M., Brogi, A., Strazza, M., Taddei, L., Romagnoli, S., Luddi, A., D’Angelo, R., Santi, S., Costantino‐Ceccarini, E., et al. (1999) · Biological Chemistry · doi:10.1515/bc.1999.034 · Cited by 43

Diversity, the Individual, and Proof of Efficacy: Complementary and Alternative Medicine in Medical Education

Park, C. M. (2002) · American Journal of Public Health · doi:10.2105/ajph.92.10.1568 · Cited by 41

Emerging Evidence for Inflammation in Conditions Frequently Affecting Older Adults: Report of a Symposium

Hamerman, D., Berman, J. W., Albers, G. W., Brown, D. L., & Silver, D. A. (1999) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1999.tb01299.x · Cited by 41

Shift Work in Rats Results in Increased Inflammatory Response after Lipopolysaccharide Administration

Guerrero‐Vargas, N. N., Guzmán‐Ruiz, M. A., Fuentes, R., García, J., Salgado‐Delgado, R., Basualdo, M. D. C., Escobar, C., Markus, R. P., & Buijs, R. M. (2015) · Journal of Biological Rhythms · doi:10.1177/0748730415586482 · Cited by 43

Neural influence on immune responses: underlying suppositions and basic principles of neural-immune signaling

Felten, D. L. (2000) · Progress in brain research · doi:10.1016/s0079-6123(08)62152-4 · Cited by 39

Hypothalamic inflammation and the central nervous system control of energy homeostasis

Pimentel, G. D., Ganeshan, K., & Carvalheira, J. B. C. (2014) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.06.005 · Cited by 42

Bilateral vagotomy or atropine pre-treatment reduces experimental diesel-soot induced lung inflammation

McQueen, D. S., Donaldson, K., Bond, S. M., McNeilly, J., Newman, S., Barton, N., & Duffin, R. (2006) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2006.11.034 · Cited by 40

Transgenic models for cytokine-induced neurological disease

Campbell, I. L., Hofer, M. J., & Pagenstecher, A. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.10.004 · Cited by 39

Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stress

Evans, C. A., Harbuz, M. S., Ostenfeld, T., Norrish, A. R., & Blackwell, J. M. (2001) · Neurogenetics · doi:10.1007/s100480100105 · Cited by 37

Neuromodulation by a Cytokine: Interferon-β Differentially Augments Neocortical Neuronal Activity and Excitability

Hadjilambreva, G., Mix, E., Rolfs, A., Müller, J. A., & Strauß, U. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01224.2003 · Cited by 38

Cachexia and obesity: two sides of one coin?

Inui, A., & Meguid, M. M. (2003) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/01.mco.0000078989.18774.74 · Cited by 38

Protozoan programmed cell death – insights from Blastocystis deathstyles

Tan, K. S. W., & Nasirudeen, A. M. A. (2005) · Trends in Parasitology · doi:10.1016/j.pt.2005.09.006 · Cited by 37

Cytokine production in motor neurons by poliovirus replicon vector gene delivery

Bledsoe, A., Jackson, C. A., McPherson, S. A., & Morrow, C. D. (2000) · Nature Biotechnology · doi:10.1038/79455 · 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

Acute Neuroimmune Modulation Attenuates the Development of Anxiety-Like Freezing Behavior in an Animal Model of Traumatic Brain Injury

Rodgers, K. M., Bercum, F. M., McCallum, D. L., Rudy, J. W., Frey, L. C., Johnson, K. W., Watkins, L. R., & Barth, D. S. (2012) · Journal of Neurotrauma · doi:10.1089/neu.2011.2273 · Cited by 37

Sympathetic nerves control bacterial clearance

Lankadeva, Y. R., May, C. N., McKinley, M. J., Neeland, M. R., Ma, S., Hocking, D. M., Robins-Browne, R. M., Bedoui, S., Farmer, D., Bailey, S. R., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-72008-4 · Cited by 38

Cancer Cachexia Pathophysiology and Translational Aspect of Herbal Medicine

Suzuki, H., Asakawa, A., Amitani, H., Fujitsuka, N., Nakamura, N., & Inui, A. (2013) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyt075 · Cited by 36

Melanocortins and the Cholinergic Anti-Inflammatory Pathway

Giuliani, D., Ottani, A., Altavilla, D., Bazzani, C., Squadrito, F., & Guarini, S. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6354-3_6 · Cited by 34

Glucocorticoid and type 1 interferon interactions at the blood–brain barrier: relevance for drug therapies for multiple sclerosis

Gaillard, P. J., van der Meide, P. H., de Boer, A. G., & Breimer, D. D. (2001) · Neuroreport · doi:10.1097/00001756-200107200-00029 · Cited by 34

Reversal of Established Traumatic Brain Injury-Induced, Anxiety-Like Behavior in Rats after Delayed, Post-Injury Neuroimmune Suppression

Rodgers, K. M., Deming, Y. K., Bercum, F. M., Chumachenko, S. Y., Wieseler, J. L., Johnson, K. W., Watkins, L. R., & Barth, D. S. (2013) · Journal of Neurotrauma · doi:10.1089/neu.2013.3090 · Cited by 33

The enkephalinergic nervous system and its immunomodulation on the developing immune system during the ontogenesis of oyster Crassostrea gigas

Liu, Z., Zhou, Z., Wang, L., Song, X., Chen, H., Wang, W., Liu, R., Wang, M., Wang, H., & Song, L. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.03.041 · Cited by 30

Immunomodulatory effect of antidepressants

Szelényi, J. (2002) · Current Opinion in Pharmacology · doi:10.1016/s1471-4892(02)00173-x · Cited by 31

The α2 Na+/K+-ATPase isoform mediates LPS-induced neuroinflammation

Leite, J. A., Isaksen, T. J., Heuck, A., Scavone, C., & Lykke‐Hartmann, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-71027-5 · Cited by 32

Neuropeptide Y regulates catecholamine release evoked by interleukin-1β in mouse chromaffin cells

Rosmaninho‐Salgado, J., Álvaro, A. R., Grouzmann, E., Duarte, E. P., & Cavadas, C. (2007) · Peptides · doi:10.1016/j.peptides.2006.11.015 · Cited by 30

Differential Reduction of IP-10 and C-Reactive Protein via Aerobic Exercise or Mindfulness-Based Stress-Reduction Training in a Large Randomized Controlled Trial

Meyer, J. D., Hayney, M. S., Coe, C. L., Ninos, C. L., & Barrett, B. P. (2019) · Journal of Sport and Exercise Psychology · doi:10.1123/jsep.2018-0214 · Cited by 29

Hematopoietic response of rats exposed to the impact of an acute psychophysiological stressor on responsiveness to an in vivo challenge with Listeria monocytogenes: Modulation by Chlorella vulgaris prophylactic treatment

Queiroz, J. D. S., Torello, C. O., Palermo‐Neto, J., Valadares, M. C., & Queiroz, M. L. S. (2008) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2008.03.002 · Cited by 29

Possible contribution of interferon-α to febrile seizures in influenza

Masuyama, T., Matsuo, M., Ichimaru, T., Ishii, K., Tsuchiya, K., & Hamasaki, Y. (2002) · Pediatric Neurology · doi:10.1016/s0887-8994(02)00452-6 · Cited by 28

The Relationship between Chronic Pain, Immune Function, Depression, and Health Behaviors

Vines, S. W., Gupta, S., Whiteside, T. L., Dostal-Johnson, D. A., & Hummler-Davis, A. (2003) · Biological Research For Nursing · doi:10.1177/1099800403005001002 · Cited by 29

Plasma concentrations of tumor necrosis factor‐α (TNF‐α) and soluble TNF receptors in patients with bulimia nervosa

Nakai, Y., Hamagaki, S., Takagi, R., Taniguchi, A., & Kurimoto, F. (2000) · Clinical Endocrinology · doi:10.1046/j.1365-2265.2000.01091.x · Cited by 29

Bacterial DNA induced iNOS expression through MyD88-p38 MAP kinase in mouse primary cultured glial cells

Hosoi, T., Suzuki, S., Nomura, J., Ono, A., Okuma, Y., Akira, S., & Nomura, Y. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.02.014 · Cited by 29

Role of vasopressin and its antagonism in stroke related edema

Ameli, P. A., Ameli, N. J., Gubernick, D., Ansari, S., Mohan, S., Satriotomo, I., Buckley, A. K., Maxwell, C. W., Nayak, V. H., & Hedna, V. S. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23407 · Cited by 28

Effect of lesions of cerebellar fastigial nuclei on lymphocyte functions of rats

Peng, Y.-P., Qiu, Y., Chao, B.-B., & Wang, J. (2005) · Neuroscience Research · doi:10.1016/j.neures.2004.11.010 · Cited by 28

Interleukin-4 and Interleukin-10 Gene Polymorphisms in Patients with Inflammatory Bowel Disease

Daryani, N. E., Saghazadeh, A., Moossavi, S., Sadr, M., Shahkarami, S., Soltani, S., Farhadi, E., & Rezaei, N. (2017) · Immunological Investigations · doi:10.1080/08820139.2017.1360343 · Cited by 28

Bacterial endotoxin induces IL-20 expression in the glial cells

Hosoi, T., Wada, S., Suzuki, S., Okuma, Y., Akira, S., Matsuda, T., & Nomura, Y. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.07.005 · Cited by 28

Molecular Basis of Neuroimmune Interaction in an In Vitro Coculture Approach

Nakanishi, M., & Furuno, T. (2008) · Cellular and Molecular Immunology · doi:10.1038/cmi.2008.31 · Cited by 27

The immunomodulation mediated by a delta-opioid receptor for [Met5]-enkephalin in oyster Crassostrea gigas

Liu, Z., Zhou, Z., Wang, L., Jiang, S., Wang, W., Zhang, R., & Song, L. (2014) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2014.11.017 · Cited by 26

Chemical Neuroimmunology: Health in a Nutshell Bidirectional Communication between Immune and Stress (Limbic‐Hypothalamic‐Pituitary‐Adrenal) Systems

Lozovaya, N. P., & Miller, A. D. (2003) · ChemBioChem · doi:10.1002/cbic.200200492 · Cited by 28

Dietary n-3 fatty acids selectively attenuate LPS-induced behavioral depression in mice

Watanabe, S., Kanada, S., Takenaka, M., & Hamazaki, T. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.02.021 · Cited by 26

Neural–endocrine–immune complex in the central modulation of tumorigenesis: Facts, assumptions, and hypotheses

Mravec, B., Gidron, Y., Kukanova, B., Bízik, J., Kiss, A., & Hulín, I. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.07.003 · Cited by 26

Anesthesia-specific protection from endotoxic shock is not mediated through the vagus nerve

Fuentes, J. M., Hanly, E. J., Aurora, A. R., Maio, A. D., & Talamini, M. A. (2005) · Surgery · doi:10.1016/j.surg.2005.06.057 · Cited by 25

Specific up-regulation of CRH or AVP secretion by acetylcholine or lipopolysaccharide in inflammatory susceptible Lewis rat fetal hypothalamic cells

Wei, R., Phillips, T. M., & Sternberg, E. M. (2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00251-5 · Cited by 26

Sympathoadrenal and immune system activation during the periparturient period and their association with bovine coliform mastitis. A review

Diez‐Fraile, A., Meyer, E., & Burvenich, C. (2003) · Veterinary Quarterly · doi:10.1080/01652176.2003.9695142 · Cited by 25

Transforming Growth Factor-β1 and Cortisol in Differentially Reared Primates

Smith, E. L., Batuman, O., Trost, R. C., Coplan, J. D., & Rosenblum, L. A. (2002) · Brain Behavior and Immunity · doi:10.1006/brbi.2001.0629 · Cited by 25

Interactions between the immune and neuroendocrine systems

Sternberg, E. M. (2000) · Progress in brain research · doi:10.1016/s0079-6123(08)62129-9 · Cited by 25

Animal models of neuroimmune interactions in inflammatory diseases

Jafarian-Tehrani, M., & Sternberg, E. M. (1999) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(99)00207-6 · Cited by 25

Relationship between Rainfall andNeospora caninum‐associated Abortion in Two Dairy Herds in a Dry Environment

López-Gatius, F., Garcia-Ispierto, I., Santolaria, P., Yániz, J. L., López‐Béjar, M., Nogareda, C., & Almería, S. (2005) · Journal of Veterinary Medicine Series B · doi:10.1111/j.1439-0450.2005.00831.x · Cited by 24

Expression of glia maturation factor during retinal development in the rat

Nishiwaki, A., Asai, K., Tada, T., Ueda, T., Shimada, S., Ogura, Y., & Kato, T. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00252-2 · Cited by 24

Tumor necrosis factor (TNF) induces astrogliosis, microgliosis and promotes survival of cortical neurons

Abd‐El‐Basset, E. M., Rao, M. S. R., Alshawaf, S. M., Ashkanani, H. K. A. H. A., & Kabli, A. H. (2021) · AIMS neuroscience · doi:10.3934/neuroscience.2021031 · Cited by 24

Wellness interventions for anesthesiologists

Saadat, H., & Kain, Z. N. (2018) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0000000000000598 · Cited by 24

Increased interleukin-6 receptor expression in the paraventricular nucleus of rats with heart failure

Helwig, B. G., Musch, T. I., Craig, R. A., & Kenney, M. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00507.2006 · Cited by 23

Involvement of interleukin-1 in glial responses to lipopolysaccharide: endogenous versus exogenous interleukin-1 actions

Molina‐Holgado, F., Toulmond, S., & Rothwell, N. J. (2000) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(00)00344-1 · Cited by 22

Novel insights into how purines regulate pituitary cell function

Rees, A., Scanlon, M. F., & Ham, J. (2003) · Clinical Science · doi:10.1042/cs20030053 · Cited by 22

Visceral Obesity and the Metabolic Syndrome

Rosmond, R. (2001) · Wiley eBooks · doi:10.1002/0470846739.ch23 · Cited by 21

Blunted IL-6 and IL-10 response to maximal aerobic exercise in patients with traumatic brain injury

Timmerman, K. L., Amonette, W. E., Markofski, M. M., Ansinelli, H. A., Gleason, E. A., Rasmussen, B. B., & Mossberg, K. A. (2014) · European Journal of Applied Physiology · doi:10.1007/s00421-014-2997-4 · Cited by 20

Chronic traumatic stress impairs memory in mice: Potential roles of acetylcholine, neuroinflammation and corticotropin releasing factor expression in the hippocampus

Bhakta, A., Gavini, K., Yang, E., Lyman-Henley, L., & Parameshwaran, K. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.08.013 · Cited by 21

Cytokine expression in colostrum-deprived pigs immunized and challenged with Haemophilus parasuis

de la Fuente, A. J. M., Ferri, E. F. R., Tejerina, F., Frandoloso, R., Martínez-Martínez, S., & Gutiérrez-Martín, C. B. (2009) · Research in Veterinary Science · doi:10.1016/j.rvsc.2008.12.012 · Cited by 19

Cerebellar interposed nucleus lesions suppress lymphocyte function in rats

Peng, Y.-P., Qiu, Y., Qiu, J., & Wang, J. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.07.017 · Cited by 19

Acute ileal inflammatory cytokine response induced by irradiation is modulated by subdiaphragmatic vagotomy

Linard, C., Marquette, C., Clarençon, D., Galonnier, M., Mathieu, J., Pennequin, A., Benderitter, M., & Gourmelon, P. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.07.007 · Cited by 19

The Wistar Kyoto (RT1l) rat is resistant to myelin basic protein-induced experimental autoimmune encephalomyelitis: comparison with the susceptible Lewis (RT1l) strain with regard to the MBP-directed CD4+ T cell repertoire and its regulation

Stevens, D. B., Gold, D. P., Sercarz, E. E., & Moudgil, K. D. (2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00045-0 · Cited by 19

Experimental Model of Acute Pancreatitis in Wistar Rat: Glucocorticoid Treatment Profile

Cosen-Binker, L. I., Binker, M. G., Negri, G. A., & Tiscornia, O. M. (2003) · Digestive Diseases and Sciences · doi:10.1023/a:1024791101859 · Cited by 19

Relative Contribution of Different Receptor Subtypes in the Response of Neuroblastoma Cells to Tumor Necrosis Factor‐α

Condorelli, F., Sortino, M. A., Stella, A. M. G., & Canonico, P. L. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0751172.x · Cited by 19

Blood-Brain Barrier Breakdown and Blood-Brain Communication in Neurological and Psychiatric Diseases

Friedman, A., & Kaufer, D. (2011) · Cardiovascular Psychiatry and Neurology · doi:10.1155/2011/431470 · Cited by 18

Increased pro-inflammatory cytokines, glial activation and oxidative stress in the hippocampus after short-term bilateral adrenalectomy

Hamadi, N. K., Sheikh, A., Madjid, N., Lubbad, L., Amir, N., Shehab, S. A. S., Khelifi‐Touhami, F., & Adem, A. (2016) · BMC Neuroscience · doi:10.1186/s12868-016-0296-1 · Cited by 18

Induction of preprotachykinin-I and neurokinin-1 by adrenocorticotropin and prolactin. Implication for neuroendocrine-immune-hematopoietic axis

Maloof, P., Joshi, D. D., Qian, J., Gascón, P., Singh, D., & Rameshwar, P. (2001) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(00)00405-7 · Cited by 18

Complement C5a receptors in the pituitary gland: expression and function

Francis, K. L., Lewis, B. M., Monk, P. N., & Ham, J. (2008) · Journal of Endocrinology · doi:10.1677/joe-08-0110 · Cited by 17

Microglia as a Source and Target of Cytokine Activities in the Brain

Hanisch, U. (2002) · Springer eBooks · doi:10.1007/978-1-4757-4139-1_5 · Cited by 17

Anaphylactoid reactions activate hypothalamo-pituitary-adrenocortical axis: comparison with endotoxic reactions

Földes, A., Némethy, Z., Szalay, O., & Kovács, K. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00299-9 · Cited by 17

Body temperature, behavior, and plasma cortisol changes induced by chronic infusion of Staphylococcus aureus in goats

Mphahlele, N. R., Fuller, A., Roth, J., & Kamerman, P. R. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00064.2004 · Cited by 16

Editorial [Exploring Neural-Immune System Interactions]

Lombardi, V. (2012) · Current Immunology Reviews · doi:10.2174/157339512798991191 · Cited by 1

Neural-immune interactions — NeuroImmune modulation

Waksman, B. H. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)91260-7

Experimental basis for neural-immune interactions

Madden, K. S., & Felten, D. L. (1995) · Physiological Reviews · doi:10.1152/physrev.1995.75.1.77 · Cited by 385

Neuroendocrine-Immune Interactions

(2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00012-7 · Cited by 1

Neuroimmune interactions

Borek, F. (1988) · Journal of Immunological Methods · doi:10.1016/0022-1759(88)90233-5 · Cited by 27